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2018

Allegrini AG et al. Genetic vulnerability for smoking and cannabis use: associations with e-cigarette and water pipe use. Nicotine & Tobacco Research, Accepted Article
Supplementary Material

Auwera S van der et al. Genome-wide gene-environment interaction in depression: A systematic evaluation of candidate genes. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, Volume 177
Supporting Information

Baselmans BML et al. Unraveling the Genetic and Environmental Relationship Between Well-Being and Depressive Symptoms Throughout the Lifespan. Frontiers in Psychiatry, Volume 9
Supplementary Material (ZIP-file)

Baselmans BML & Bartels M. A genetic perspective on the relationship between eudaimonic -and hedonic well-being. Nature Scientific Reports, Volume 8
Supplementary Figures
Supplementary Tables

Beaumont RN et al. Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics. Human Molecular Genetics, In Press
Supplementary Tables
Supplementary Data

Bergen E van et al. Why do children read more? The influence of reading ability on voluntary reading practices. Journal of Child Psychology and Psychiatry, Volume 59
Supplementary Information

Brainstorm Consortium. Analysis of shared heritability in common disorders of the brain. Science, Volume 360
Supplement
Table S7
Table S12
Table S13

Demenais F et al. Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks. Nature Genetics, Volume 50
Supplementary Information

Demontis D et al. Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. Nature Genetics, Early View
Supplementary Materials on the NG Website

Dongen J van et al. DNA methylation signatures of educational attainment. npj Science of Learning, Volume 3
Supplemental Material
Supplemental Tables

Doorweerd S et al. Brain reward responses to food stimuli among female monozygotic twins discordant for BMI. Brain Imaging and Behavior, Volume 12
Supplementary Material

Finnicum CT et al. Metataxonomic Analysis of Individuals at BMI Extremes and Monozygotic Twins Discordant for BMI. Twin Research and Human Genetics, Volume 21
Supplementary Materials (ZIP-file)

Gormley P et al. Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families. Neuron, In Press
Supplemental Information

Gudmundsdottir V et al. Integrative network analysis highlights biological processes underlying GLP-1 stimulated insulin secretion: A DIRECT study. PLOS ONE, Volume 13
Supporting Information

Hagenbeek FA et al. Adult aggressive behavior in humans and biomarkers: a focus on lipids and methylation. Journal of Pediatric and Neonatal Individualized Medicine, Volume 7
Supplementary Material

Hancock DB et al. Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence. Molecular Psychiatry, Volume 23
Supplementary Methods

Hart LM 't et al. Blood metabolomic measures associate with present and future glycemic control in type 2 diabetes. Journal of Clinical Endocrinology & Metabolism, Volume 103
Supplementary Material

Heikkilä K et al. Triplets, birthweight, and handedness. PNAS, Volume 115
Supporting Information

Hysi PG et al. Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability. Nature Genetics, Volume 50
Supplementary Figures
Reporting Summary
Supplementary Note and Supplementary Tables

Ip HF et al. Characterizing the Relation Between Expression QTLs and Complex Traits: Exploring the Role of Tissue Specificity. Behavior Genetics, Volume 48
Supplementary Materials (ZIP-file)

Jelenkovic A et al. Associations between birth size and later height from infancy through adulthood: An individual based pooled analysis of 28 twin cohorts participating in the CODATwins project. Early Human Development, Volume 120
Supplementary Data

Jong S de et al. Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder. Communications Biology, Volume 1
Supplementary Figures

Kate M ten et al. White matter hyperintensities and vascular risk factors in monozygotic twins. Neurobiology of Aging, Volume 66
Online Supplement

Koenis MMG et al. Association between structural brain network efficiency and intelligence increases during adolescence. Human Brain Mapping, Volume 39
Supplemental Material

Korpela K et al. Selective maternal seeding and environment shape the human gut microbiome. Genome Research, Volume 28
Supplemental Material (ZIP-file)

Kreeke JA van de et al. Retinal and Cerebral Microvasculopathy: Relationships and Their Genetic Contributions. Investigative Ophthalmology & Visual Science, Volume 59
Supplementary Material

Lee JJ et al. Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. Nature Genetics, Volume 50
Supplementary Text and Figures
Reporting Summary
Supplementary Tables

Ligthart S et al. Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. The American Journal of Human Genetics, Volume 103
Supplemental Document S1
Supplemental Spreadsheet S1

Luijk R et al. Genome-wide identification of directed gene networks using large-scale population genomics data. Nature Communications, 9(1):3097
Supplementary Materials on the NC Website

Malanchini M et al. Aggressive behaviour in childhood and adolescence: the role of smoking during pregnancy, evidence from four twin cohorts in the EU-ACTION consortium. Psychological Medicine, Original Article
Supplementary Material

Minica CC et al. Extending Causality Tests with Genetic Instruments: An Integration of Mendelian Randomization with the Classical Twin Design. Behavior Genetics, Volume 48
Supplementary Material

Minica CC et al. Genome-Wide Association Meta-Analysis of Age at First Cannabis Use. Addiction, Volume 113
Supporting Information (ZIP-file)

Molnos S et al. Metabolite ratios as potential biomarkers for type 2 diabetes: a DIRECT study. Diabetologia, Volume 61
Supplementary Material

Moore R et al. A linear mixed-model approach to study multivariate gene–environment interactions. Nature Genetics, Early View
Supplementary Materials on the NG Website

Ouwens KG et al. A characterization of post-zygotic mutations identified in monozygotic twins. Human Mutation, Volume 39
Supporting Material
Supporting Table S3

Parmar P et al. Association of maternal prenatal smoking GFI1-locus and cardio-metabolic phenotypes in 18,212 adults. EBioMedicine, Open Access
Appendix A and B
Supplementary Material 1
Supplementary Material 2

Peyrot WJ et al. Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium. Biological Psychiatry, Volume 84
Supplemental Information

Piirtola M et al. Association of current and former smoking with body mass index: A study of smoking discordant twin pairs from 21 twin cohorts. PLOS One, Volume 13
Supporting Information (ZIP-file)

Qi T et al. Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood. Nature Communications, Open, Volume 9
Supplementary Information

Sandanger TM et al. DNA methylation and associated gene expression in blood prior to lung cancer diagnosis in the Norwegian Women and Cancer cohort. Scientific Reports, Volume 8
Supplementary Material

Smit DJA et al. Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. Human Brain Mapping, Volume 39
Supporting Information Figures
Supporting Information Methods
Supporting Information Note

Treur JL et al. Testing familial transmission of smoking with two different research designs. Nicotine and Tobacco Research, Volume 20
Supplementary Data on the NaTR Website

Waage J et al. Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis. Nature Genetics, Volume 50
Supplementary Text and Figures
Reporting Summary
Supplementary Tables

Walters RK et al. Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders. Nature Neuroscience, Volume 21
Supplementary Material on the NG Website

Wang J et al. Meta-analysis of human genome-microbiome association studies: the MiBioGen consortium initiative. Microbiome, Volume 6
Additional file 1
Additional file 2

Ward-Caviness CK et al. DNA methylation age is associated with an altered hemostatic profile in a multi-ethnic meta-analysis. Blood, Volume 132
Supplemental Methods and Figures
Supplemental Tables

Warrier V et al. Genome-wide meta-analysis of cognitive empathy: heritability, and correlates with sex, neuropsychiatric conditions and cognition. Molecular Psychiatry, Volume 23
Supplementary Note
Supplementary Tables 1–8
Supplementary males and females
Supplementary males
Supplementary females

Wesseldijk LW et al. Risk factors for parental psychopathology: a study in families with children or adolescents with psychopathology. European Child & Adolescent Psychiatry, Volume 27
Supplementary Material

Wesseldijk LW et al. Genetic and environmental influences on conduct and antisocial personality problems in childhood, adolescence, and adulthood. European Child & Adolescent Psychiatry, Volume 27
Supplementary Material

Willems YE et al. Genetic and Environmental Influences on Self-Control: Assessing Self-Control with the ASEBA Self-Control Scale. Behavior Genetics, Volume 48
Supplementary Material

Wray NR et al. Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nature Genetics, Volume 50
Supplementary Information

Yang Y et al. Molecular genetic overlap between migraine and major depressive disorder. European Journal of Human Genetics, Volume 26
Supplementary Information

Yokoyama Y et al. Genetic and environmental factors affecting birth size variation: a pooled individual-based analysis of secular trends and global geographical differences using 26 twin cohorts. International Journal of Epidemiology, Volume 47
Supplementary Data

Xue A et al. Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. Nature Communications, Volume 9
Supplementary Material (ZIP-file)

2017

Bigdeli TB et al. Genetic effects influencing risk for major depressive disorder in China and Europe. Translational Psychiatry, 7:e1074
Supplementary Materials

Bogl LH et al. Does the sex of one’s co-twin affect height and BMI in adulthood? A study of dizygotic adult twins from 31 cohorts. Biology of Sex Differences, Volume 8
Additional Table S1
Additional Figure S1

Bolhuis K et al. Disentangling Heterogeneity of Childhood Disruptive Behavior Problems Into Dimensions and Subgroups. Journal of the American Academy of Child & Adolescent Psychiatry, Volume 56
Supplemental Material

Bonder MJ et al. Disease variants alter transcription factor levels and methylation of their binding sites. Nature Genetics, Volume 49
Supplementary Materials on the Nature Genetics website

Bot M. et al. Validity of LIDAS (LIfetime Depression Assessment Self-report): a self-report online assessment of lifetime major depressive disorder. Psychological Medicine, Volume 47
Supplementary Table S1
Supplementary Table S2

Brouwer RM et al. Genetic influences on individual differences in longitudinal changes in global and subcortical brain volumes: Results of the ENIGMA plasticity working group. Human Brain Mapping, Volume 38
Supporting Information Table 1
Supporting Information Table 2a
Supporting Information Table 2b
Supporting Information Table 3
Supporting Information Table 4
Supporting Information

Culverhouse RC et al. Collaborative meta-analysis finds no evidence of a strong interaction between stress and 5-HTTLPR genotype contributing to the development of depression. Molecular Psychiatry, Advance online publication
Supplementary Information on the MP website

Day FR et al. Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk. Nature Genetics, Volume 49
Supplementary Information on the NG website

Demuru M et al. Functional and effective whole brain connectivity using magnetoencephalography to identify monozygotic twin pairs. Nature Scientific Reports, Volume 7
Supporting Information

Direk N et al. An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype. Biological Psychiatry, Volume 82
Supplemental Information

Ehli EA et al. A method to customize population-specific arrays for genome-wide association testing. European Journal of Human Genetics, Volume 25

Supplementary Information on the EJHG website

Fedko IO et al. Heritability of Behavioral Problems in 7-Year Olds Based on Shared and Unique Aspects of Parental Views. Behavior Genetics, Volume 47
Supplementary Material

Ferreira MAR et al. Gene-based analysis of regulatory variants identifies 4 putative novel asthma risk genes related to nucleotide synthesis and signaling. Journal of Allergy and Clinical Immunology, Volume 139
Online Repository

Ferreira MAR et al. Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. Nature Genetics, Volume 49
Supplementary Figures and Note
Supplementary Tables

Francioli LC et al. A framework for the detection of de novo mutations in family-based sequencing data. European Journal of Human Genetics, Volume 25
Supplementary Materials on the EJHG website

Graff M et al. Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. PLOS Genetics, 13(4):e1006528
Supporting Information on the PLOS website

Hägg S et al. Short telomere length is associated with impaired cognitive performance in European ancestry cohorts. Translational Psychiatry, Volume 7
Supplementary Information
Supplementary Tables

Haller T et al. MixFit: Methodology for Computing Ancestry-Related Genetic Scores at the Individual Level and Its Application to the Estonian and Finnish Population Studies. PLOS ONE, Volume 12
Supplementary File S1
Supplementary File S2

Hibar DP et al. Novel genetic loci associated with hippocampal volume. Nature Communications, Volume 8

Supplementary Information
Supplementary Data

Houtem van CMHH et al. The factor structure of dental fear. European Journal of Oral Sciences, Volume 125
Supporting Information

Hu Y et al. MicroRNAs as biomarkers for psychiatric disorders with a focus on autism spectrum disorder: Current progress in genetic association studies, expression profiling, and translational research. Autism Research, Volume 10
Supplementary Table S1

Jansen R et al. Conditional eQTL Analysis Reveals Allelic Heterogeneity of Gene Expression. Human Molecular Genetics, Volume 26
Supplementary Data

Jelenkovic A et al. Association between birthweight and later body mass index: an individual-based pooled analysis of 27 twin cohorts participating in the CODATwins project. International Journal of Epidemiology, Volume 46
Supplementary Data

Justice AE et al. Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Nature Communications, 8:14977
Supplementary Information on NC website

Kluiver de H et al. Paternal age and psychiatric disorders: A review. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, Volume 174
Supplementary Table I
Supplementary Table II
Supplementary Table III
Supplementary Table IV
Supplementary Table V
Supplementary Table VI

Koenis MMG et al. Association between structural brain network efficiency and intelligence increases during adolescence. Human Brain Mapping, Early View
Supplemental Material

Lepik K et al. C-reactive protein upregulates the whole blood expression of CD59 - an integrative analysis. PLOS Computational Biology, Volume 13
Supporting Information on the PLOS website

Maes HH et al. A Genetic Epidemiological Mega Analysis of Smoking Initiation in Adolescents. Nicotine & Tobacco Research, Volume 19
maesEtal_OnlineMaterials2
maesEtal_eFigure1a
maesEtal_eFigure1b
maesEtal_eFigure2a
maesEtal_eFigure2b

Mbarek H et al. Genome-Wide Significance for PCLO as a Gene for Major Depressive Disorder. Twin Research and Human Genetics, Volume 20
Supplementary Information

Milaneschi Y et al. Genetic Association of Major Depression With Atypical Features and Obesity-Related Immunometabolic Dysregulations. JAMA Psychiatry, Volume 74
Supplementary Online Content

Minica CC et al. Pathways to smoking behaviours: biological insights from the Tobacco and Genetics Consortium meta-analysis. Molecular Psychiatry, Volume 22
Supplementary Materials on the Molecular Psychiatry website

Molnos S et al. Metabolite ratios as potential biomarkers for type 2 diabetes: a DIRECT study. Diabetologia, Open Access
Supplementary Material

Neumann A et al. The low single nucleotide polymorphism heritability of plasma and saliva cortisol levels. Psychoneuroendocrinology, Volume 85
Supplemental Tables
Supplementary Data

Nivard MG et al. Genetic Overlap Between Schizophrenia and Developmental Psychopathology: Longitudinal and Multivariate Polygenic Risk Prediction of Common Psychiatric Traits During Development. Schizophrenia Bulletin, Volume 43
Supplementary Materials on the journal website

Nolte IM et al. Genetic loci associated with heart rate variability and their effects on cardiac disease risk. Nature Communications, Open
Supplementary Materials on the Nature Communications website

Power RA et al. Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium. Biological Psychiatry, Volume 81

Supplementary Information

Richard MA et al. DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation. The American Journal of Human Genetics, Volume 101
Supplemental Data
Table S4
Table S10

Rietschel L et al. Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes.  Nature Scientific Reports, Volume 7
Supplementary Material

Robinson MR et al. Genetic evidence of assortative mating in humans. Nature Human Behaviour, Volume 1
Supplementary Materials on the Nature Human Behaviour website

Schwabe I et al. Mathematical Ability and Socio-Economic Background: IRT Modeling to Estimate Genotype by Environment Interaction. Twin Research and Human Genetics, Volume 20
Supplementary Material

Silventoinen K et al. Differences in genetic and environmental variation in adult body mass index by sex, age, time period, and region: an individual-based pooled analysis of 40 twin cohorts. The American Journal of Clinical Nutrition, Volume 106
Supplementary Figure 1
Supplementary Tables 1-3

Silventoinen K et al. Education in Twins and Their Parents Across Birth Cohorts Over 100 years: An Individual-Level Pooled Analysis of 42-Twin Cohorts. Twin Research and Human Genetics, Volume 20
Supplementary Materials

Slof-Op 't Landt MCT et al. Prevalence of dieting and fear of weight gain across ages: a community sample from adolescents to the elderly. International Journal of Public Health, Volume 62
Supplementary Material

Sohail M et al. Negative selection in humans and fruit flies involves synergistic epistasis. Science, Volume 356
Supplementary Material on the Science website

Treur JL et al. Smoking and caffeine consumption: a genetic analysis of their association. Addiction Biology, Volume 22

Supporting Tables & Figures

Verduijn J et al. Using Clinical Characteristics to Identify Which Patients With Major Depressive Disorder Have a Higher Genetic Load for Three Psychiatric Disorders. Biological Psychiatry, Volume 81
Supplementary Information

Verweij KJH et al. Heritability of lifetime ecstasy use. Drug and Alcohol Dependence, Volume 178
Supplementary Material

Vink JM et al. Differential gene expression patterns between smokers and non-smokers: cause or consequence? Addiction Biology, Volume 22
Supplementary Information (zip file)

Vries PS de et al. Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study. PLOS ONE, Volume 12
Supplementary Information (zip file)

Wain LV et al. Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney. Hypertension, Volume 70
Supplemental PDF File
Supplemental Excel File

Warren HR et al. Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk. Nature Genetics, Volume 49
Supplementary Information on the Nature Genetics website

Wesseldijk LW et al. Psychopathology in 7-year-old children: Differences in maternal and paternal ratings and the genetic epidemiology. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, Volume 174
Supplementary Tables 1 & 2

Wheeler E et al. Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis. PLOS Medicine, Volume 14
Supporting Information

Witt SH et al. Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia. Translational Psychiatry, Volume 7
Supplementary Information

Zeeuw EL de et al. Attention Deficit Hyperactivity Disorder Symptoms and Low Educational Achievement: Evidence Supporting A Causal Hypothesis. Behavior Genetics, Volume 47
Supplementary Material

Zhernakova DV et al.  Identification of context-dependent expression quantitative trait loci in whole blood. Nature Genetics, Volume 49
Supplementary Materials on the Nature Genetics website

Zilhão NR et al. Heritability of tic disorders: a twin-family study. Psychological Medicine, Volume 47
Supplementary Materials

2016

Adams HHH et al. Novel genetic loci underlying human intracranial volume identified through genome-wide association. Nature Neuroscience, Volume 19
Supplementary Information

Amin N et al. Genetic variants in RBFOX3 are associated with sleep latency. European Journal of Human Genetics, Volume 24
Supplementary Material (Tables, Text, Figures)

Antonakakis M et al. Genetic effects on source level evoked and induced oscillatory brain responses in a visual oddball task. Biological Psychology, Volume 114
Supplementary Material

Barban N et al. Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Nature Genetics, Volume 48
Supplementary Material on the NG website

Beijsterveldt CEM van et al. Chorionicity and Heritability Estimates from Twin Studies: The Prenatal Environment of Twins and Their Resemblance Across a Large Number of Traits. Behavior Genetics, Volume 46
Supplementary material I – Tables S1 – S6
Supplementary material II – Sensitivity analysis

Berg SM van den et al. Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium. Behavior Genetics, Volume 46
Supplementary Materials

Braber A den et al. Obsessive–compulsive symptoms in a large population-based twin-family sample are predicted by clinically based polygenic scores and by genome-wide SNPs. Translational Psychiatry, Volume 6
Supplementary Files

Chen J et al. Genetic Relationship between Schizophrenia and Nicotine Dependence. Scientific Reports, Volume 6
Supplementary Material

Dekkers KF et al. Blood lipids influence DNA methylation in circulating cells. Genome Biology, Volume 17
Supplementary Material at PMC

Dongen J van et al. Genetic and environmental influences interact with age and sex in shaping the human methylome. Nature Communications, Volume 7

Supplementary Information
Supplementary Data 1
Supplementary Data 2
Supplementary Data 3
Supplementary Data 4
Supplementary Data 5
Supplementary Data 6
Supplementary Data 7
Supplementary Data 8
Supplementary Data 9
Supplementary Data 10
Supplementary Data 11
Supplementary Data 12

Ehret GB et al. The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. Nature Genetics, Volume 48

Supplementary Materials

Eising E et al. Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas. Human Genetics, Volume 135
Supplemental Information

Felix JF et al. Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index. Human Molecular Genetics, Volume 25
Supplementary Data
Supplementary Table 1
Supplementary Table 5
Supplementary Table 6
Supplementary Table 8

Franke B et al. Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept. Nature Neuroscience, Volume 19

Supplementary Information (on the NN website)

Gale CR et al. Pleiotropy between neuroticism and physical and mental health: findings from 108038 men and women in UK Biobank. Translational Psychiatry, Volume 6
Supplementary Material

Gormley P et al. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics, Volume 48
Supplementary Material on the Nature Genetics website

Gusev A et al. Integrative approaches for large-scale transcriptome-wide association studies. Nature Genetics, Volume 48
Supplementary Figures 1– 19 and Supplementary Note
Supplementary Tables 1– 17

Hagenbeek FA et al. Discovery of Biochemical Biomarkers for Aggression: A Role for Metabolomics in Psychiatry. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, Volume 171
Supplementary Tables SI-SIV

Hehir-Kwa JY et al. A high-quality human reference panel reveals the complexity and distribution of genomic structural variants. Nature Communications, Open
Supplementary Information
Supplementary Data 1
Supplementary Data 2
Supplementary Data 3
Supplementary Data 4
Supplementary Data 5
Supplementary Data 6
Supplementary Data 7

Hodkinson EC et al. Heritability of ECG Biomarkers in the Netherlands Twin Registry Measured from Holter ECGs. Frontiers in Physiology, Volume 7
Table 1
Table 2
Table 3
Table 4
Table 5
Image 1
Image 2
Image 3
Image 4
Image 5
Image 6

Horikoshi M et al. Genome-wide associations for birth weight and correlations with adult disease. Nature, Volume 538
Supplementary Information

Howrigan DP et al. Genome-wide autozygosity is associated with lower general cognitive ability. Molecular Psychiatry, Volume 21
Supplementary Information

Huppertz C et al. Individual Differences in Exercise Behavior: Stability and Change in Genetic and Environmental Determinants From Age 7 to 18. Behavior Genetics, Volume 46
Supplementary Material

Huppertz C et al. The effects of parental education on exercise behavior in childhood and youth: a study in Dutch and Finnish twins. Scandinavian Journal of Medicine & Science in Sports, Early View
Supplementary Tables

Jelenkovic A et al. Genetic and environmental influences on height from infancy to early adulthood: An individual-based pooled analysis of 45 twin cohorts. Scientific Reports, Volume 6
Supplementary Information

Johnson EC et al. No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study. PLOS Genetics, Volume 12
Supporting Information (zip file)

Kettunen J et al. Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Nature Communications, Volume 7
Supplementary Information
Supplementary Data 1
Supplementary Data 2
Supplementary Data 3

Leeuwen van EM et al. Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels. Journal of Medical Genetics, Volume 53
Supplementary Material

Li M et al. Transmission of human mtDNA heteroplasmy in the Genome of the Netherlands families: support for a variable-size bottleneck. Genome Research, Volume 26
Supplemental Material
Dataset S1 Heteroplasmy list

Lin BD et al. The Genetic Overlap Between Hair and Eye Color. Twin Research and Human Genetics, Volume 19
Supplementary Materials

Marceau K et al. The Prenatal Environment in Twin Studies: A Review on Chorionicity. Behavior Genetics, Volume 46

Supplementary Material

Marioni RE et al. Genetic variants linked to education predict longevity. Proceedings of the National Academy of Sciences, Volume 113
Supporting Information
Appendix

Mbarek H et al. Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility. American Journal of Human Genetics, Volume 98
Document S1
Table S7
Table S8

Mbarek H et al. Two SNPs Associated With Spontaneous Dizygotic Twinning: Effect Sizes and How We Communicate Them. Twin Research and Human Genetics, Volume 19
Supplemental Material

McCarthy S et al. A reference panel of 64,976 haplotypes for genotype imputation. Nature Genetics, Volume 48
Supplementary Information

Middeldorp CM et al. A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric Cohorts. Journal of the American Academy of Child & Adolescent Psychiatry, Volume 10
Figure S1
Figure S2
Table S1
Table S2
Table S3
Table S4

Milaneschi Y et al. Polygenic dissection of major depression clinical heterogeneity. Molecular Psychiatry, Volume 21
Supplementary Figure 1
Supplementary Figure 2
Supplementary Figure 3
Supplementary Information

Minica CC et al. Pathways to smoking behaviours: biological insights from the Tobacco and Genetics Consortium meta-analysis. Molecular Psychiatry, Advance Online Publication
Supplementary Materials (on the MP website)

Nivard MG et al. Detection of gene–environment interaction in pedigree data using genome-wide genotypes. European Journal of Human Genetics, Volume 24
Supplementary Figure S1
Supplementary Figure S2
Supplementary Figure S3
Supplementary Table 1

Okbay A et al. Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Nature Genetics, Advance Online Publication
Supplementary Figures 1–15 and Supplementary Note
Supplementary Tables 1–35

Okbay A et al. Genome-wide association study identifies 74 loci associated with educational attainment. Nature, Advance Online Publication
Supplementary Information
Supplementary Data

Otowa T et al. Meta-analysis of genome-wide association studies of anxiety disorders. Molecular Psychiatry, Volume 21
Supplementary Material

Pappa I et al. A genome-wide approach to children's aggressive behavior: The EAGLE consortium. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, Volume 171
Supplementary Material

Peyrot WJ et al. Disease and Polygenic Architecture: Avoid Trio Design and Appropriately Account for Unscreened Control Subjects for Common Disease. American Journal of Human Genetics, Volume 98
Supplemental data

Quteineh L et al. Association of CRTC1 polymorphisms with obesity markers in subjects from the general population with lifetime depression. Journal of Affective Disorders, Volume 198
Supplementary Material

Ricaño-Ponce I et al. Refined mapping of autoimmune disease associated genetic variants with gene expression suggests an important role for non-coding RNAs. Journal of Autoimmunity, Volume 68
Supplemental Materials (on the J of A website)

Ried JS et al. A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape. Nature Communications, Volume 7
Supplementary Information
Supplementary Data 1
Supplementary Data 2
Supplementary Data 3
Supplementary Data 4

Roos L et al. Integrative DNA methylome analysis of pan-cancer biomarkers in cancer discordant monozygotic twin-pairs. Clinical Epigenetics, Volume 8
Additional file 1
Additional file 2
Additional file 3
Additional file 4
Additional file 5

Schumann G et al. KLB is associated with alcohol drinking, and its gene product B-Klotho is necessary for FGF21 regulation of alcohol preference. Proceedings of the National Academy of Sciences, Volume 113
Supporting Information
Appendix
Dataset S01
Dataset S02

Schwabe I et al. A New Approach to Handle Missing Covariate Data in Twin Research. Behavior Genetics, Volume 46
Supplementary Material

Silventoinen K et al. Genetic and environmental effects on body mass index from infancy to the onset of adulthood: an individual-based pooled analysis of 45 twin cohorts participating in the COllaborative project of Development of Anthropometrical measures in Twins (CODATwins) study. The American Journal of Clinical Nutrition, Volume 104
Supplemental Figure 1
Supplemental Tables 1-5

Stringer S et al. Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium. Translational Psychiatry, Open Access 6
Supplementary Materials (on the TP website)

Swagerman SC et al.  The Computerized Neurocognitive Battery: Validation, aging effects, and heritability across cognitive domains. Neuropsychology, Volume 30
Supplementary Material

Treur JL et al. Associations between smoking and caffeine consumption in two European cohorts. Addiction, Early View
Supplemental Tables and Figures

Treur JL et al. Heritability of high sugar consumption through drinks and the genetic correlation with substance use. American Journal of Clinical Nutrition, Article in Press

Supporting Material

Tyrrell J et al. Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight. JAMA Journal of the American Medical Association, Volume 315
Supplementary Online Content

Vinciotti V et al. Consistency of biological networks inferred from microarray and sequencing data. BMC Bioinformatics, Volume 17

Additional File

Vink JM et al. Heritability of compulsive Internet use in adolescents. Addiction Biology, Volume 21
Frequency distribution for CIUS items split for boys and girls

Vries PS de et al. A meta-analysis of 120,246 individuals identifies 18 new loci for fibrinogen concentration. Human Molecular Genetics, Volume 25, Issue 2
Supplementary Materials
Supplementary Tables

Ware JJ et al. Genome-Wide Meta-Analysis of Cotinine Levels in Cigarette Smokers Identifies Locus at 4q13.2. Nature Scientific Reports, Volume 6
Supplementary Information

Weiss A et al. Personality Polygenes, Positive Affect, and Life Satisfaction. Twin Research and Human Genetics, Volume 19
Supplementary Material S1
Supplementary Material S2
Supplementary Table S3

Wesseldijk LW et al. Spousal resemblance in psychopathology: A comparison of parents of children with and without psychopathology. European Psychiatry, Volume 34
Supplementary Tables 1 & 2

Zanoni P et al. Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease. Science, Volume 351

Supplementary Materials

Zhao H et al. Gene-based pleiotropy across migraine with aura and migraine without aura patient groups. Cephalalgia, Volume 36
Supplementary material

2015

Baselmans BML et al. Epigenome-Wide Association Study of Wellbeing. Twin Research and Human Genetics, Volume 18, Issue 6
Supplemental Table S1
Supplemental Table S2
Supplemental Table S3
Supplemental Table S4
Supplementary Material

Beek JHDA van et al. Heritability of liver enzyme levels estimated from genome-wide SNP data. European Journal of Human Genetics, Volume 12, Issue 9
Supplementary Materials

Bootsman F et al. Contribution of genes and unique environment to cross-sectional and longitudinal measures of subcortical volumes in bipolar disorder. European Neuropsychopharmacology, Volume 25, Issue 12

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Brouwer RM et al. Longitudinal Development of Hormone Levels and Grey Matter Density in 9 and 12-Year-Old Twins. Behavior Genetics, Open Access
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The Coffee and Caffeine Genetics Consortium.  Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption. Molecular Psychiatry, Volume 20, Issue 05
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Davies MN et al. Generalised Anxiety Disorder – A Twin Study of Genetic Architecture, Genome-Wide Association and Differential Gene Expression. PLOS ONE, Volume 10, Issue 8
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Dongen J van et al. Epigenome-Wide Association Study of Aggressive Behavior. Twin Research and Human Genetics, FirstView Article
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Franic S et al. Mendelian and polygenic inheritance of intelligence: A common set of causal genes? Using next-generation sequencing to examine the effects of 168 intellectual disability genes on normal-range intelligence. Intelligence, Volume 49
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Franic S et al. Intelligence: shared genetic basis between Mendelian disorders and a polygenic trait. European Journal of Human Genetics, Advance Online Publication
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Gottlieb DJ et al. Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study. Molecular Psychiatry, Volume 20, Issue 10
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Hägg S et al. Adiposity as a cause of cardiovascular disease: a Mendelian randomization study. International Journal of Epidemiology, Volume 44, Issue 2
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Hansell NK et al. Genetic Basis of a Cognitive Complexity Metric. PLOS One, Open Access
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Hibar DP et al. Common genetic variants influence human subcortical brain structures. Nature, Volume 520
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Horikoshi M et al. Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation. PLoS Genetics, Volume 11, Issue 7 
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Jacobsen KK et al. Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder. Journal of Affective Disorders, Volume 172

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Jansen R et al. Gene expression in major depressive disorder. Molecular Psychiatry, Advance Online Publication
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Joshi PK et al. Directional dominance on stature and cognition in diverse human populations. Nature, Volume 523, Issue 7561
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Kloosterman WP et al. Characteristics of de novo structural changes in the human genome. Genome Research, Published in Advance
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Kochunov P et al. Heritability of fractional anisotropy in human white matter: A comparison of Human Connectome Project and ENIGMA-DTI data. NeuroImage, Volume 111
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Koenis MMG et al. Development of the brain's structural network efficiency in early adolescence: A longitudinal DTI twin study. Human Brain Mapping, Volume 36, Issue 12
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Leeuwen EM van et al. Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels. Nature Communications, Open Access
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Leeuwen EM van et al. Fine mapping the CETP region reveals a common intronic insertion associated to HDL-C. npj Aging and Mechanisms of Disease, Open Access
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Lin BD et al. Heritability and Genome-Wide Association Studies for Hair Color in a Dutch Twin Family Based Sample. Genes, Volume 6, Issue 3
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Luo X et al. Does refining the phenotype improve replication rates? A review and replication of candidate gene studies on Major Depressive Disorder and Chronic Major Depressive Disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, Early View
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Mbarek H et al. The genetics of alcohol dependence: Twin and SNP-based heritability, and genome-wide association study based on AUDIT scores. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, Volume 168, Issue 8
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Minica CC et al. Sandwich corrected standard errors in family-based genome-wide association studies. European Journal of Human Genetics, Volume 23, Issue 3
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Minica CC et al. Heritability, SNP- and Gene-Based Analyses of Cannabis Use Initiation and Age at Onset. Behavior Genetics, Open Access
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Molenaar D et al. Evidence for Gender-Dependent Genotype by Environment Interaction in Adult Depression. Behavior Genetics, Open Access
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Morris RW et al. Heavier smoking may lead to a relative increase in waist circumference: evidence for a causal relationship from a Mendelian randomisation meta-analysis. The CARTA consortium. BMJ Open, Volume 5, Issue 8
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Nivard MG et al. Stability in symptoms of anxiety and depression as a function of genotype and environment: a longitudinal twin study from ages 3 to 63 years. Psychological Medicine, Volume 45, Issue 05
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Nyholt DR et al. Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies. Cephalalgia, Volume 35, Issue 6
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Oh G et al. DNA Modification Study of Major Depressive Disorder: Beyond Locus-by-locus Comparisons. Biological Psychiatry, Volume 77, Issue 3
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Pappa I et al. Single Nucleotide Polymorphism Heritability of Behavior Problems in Childhood: Genome-Wide Complex Trait Analysis. Journal of the American Academy of Child & Adolescent Psychiatry, Volume 54, Issue 9

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Paternoster L et al. Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis. Nature Genetics, Volume 47, Issue 12.
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Peyrot W et al. The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25 000 subjects. Molecular Psychiatry, Volume 20, Issue 6
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Power RA et al. Polygenic risk scores for schizophrenia and bipolar disorder predict creativity. Nature Neuroscience, Volume 18, Issue 7
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Rahmioglu N et al. Genome-wide Enrichment Analysis between Endometriosis and Obesity-related Traits Reveals Novel Susceptibility Loci. Human Molecular Genetics, Volume 24, Issue 4
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Robinson MR et al. Population genetic differentiation of height and body mass index across Europe. Nature Genetics, Volume 47, Issue 11
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Shah S et al. Improving Phenotypic Prediction by Combining Genetic and Epigenetic Associations. The American Journal of Human Genetics, Volume 97, Issue 1

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Shungin D et al. New genetic loci link adipose and insulin biology to body fat distribution. Nature, Volume 518, Issue 7538
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Silventoinen K et al. The CODATwins Project: The Cohort Description of Collaborative Project of Development of Anthropometrical Measures in Twins to Study Macro-Environmental Variation in Genetic and Environmental Effects on Anthropometric Traits. Twin Research and Human Genetics, Volume 18, Issue 04
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Sirota M et al. Effect of Genome and Environment on Metabolic and Inflammatory Profiles. PLOS One, Open Access
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Spjuth O et al. Harmonising and linking biomedical and clinical data across disparate data archives to enable integrative cross-biobank research. European Journal of Human Genetics EJHG Open, Advance Online Publication
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Surakka I et al. The impact of low-frequency and rare variants on lipid levels. Nature Genetics, Volume 47, Issue 6
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Toulopoulou T et al. Reciprocal causation models of cognitive vs volumetric cerebral intermediate phenotypes for schizophrenia in a pan-European twin cohort. Molecular Psychiatry, Volume 20, Issue 11
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Treur JL et al. Spousal resemblance for smoking: Underlying mechanismsand effects of cohort and age. Drug and Alcohol Dependence, Volume 153
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Treur JL et al. Smoking during adolescence as a risk factor for attention problems. Biological Psychiatry, Volume 78, Issue 9
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Valk RJP van der et al. A novel common variant in DCST2 is associated with length in early life and height in adulthood. Human Molecular Genetics, Volume 24, Issue 4
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Vink JM et al. Differential gene expression patterns between smokers and non-smokers: cause or consequence? Addiction Biology, Early View
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Winkler TW et al. The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. PLOS Genetics, Volume 11, Issue 10
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Winsvold BS et al. Genetic analysis for a shared biological basis between migraine and coronary artery disease. Neurology Genetics, Volume 1
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Table e1 - e-7
Coinvestigators

Xu T et al. Effects of Metformin on Metabolite Profiles and LDL Cholesterol in Patients With Type 2 Diabetes. Diabetes Care, Volume 38, Issue 10
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Zeeuw EL de et al. Childhood ODD and ADHD Behavior: The Effect of Classroom Sharing, Gender, Teacher Gender and Their Interactions. Behavior Genetics, Volume 45, Issue 4
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Zeeuw EL de et al. Meta-analysis of twin studies highlights the importance of genetic variation in primary school educational achievement. Trends in Neuroscience and Education, Volume 4, Issue 3
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Zilhão NR et al. Genetic and Environmental Contributions to Stability in Adult Obsessive Compulsive Behavior. Twin Research and Human Genetics, Volume 18, Issue 01

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Zilhão NR et al. Epigenome-Wide Association Study of Tic Disorders. Twin Research and Human Genetics, Volume 18, Issue 06
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2014

Aarts E et al. A solution to dependency: using multilevel analysis to accommodate nested data. Nature Neuroscience, Volume 17, Issue 4, 2014
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Akker EB van den et al. Meta-Analysis on Blood Transcriptomic Studies Identifies Consistently Co-Expressed PPI Modules as Robust Markers of Human Ageing. Aging Cell, Volume 13, Issue 2, 2014
Supporting information FigS1 TableS1 TableS2 TableS3 TableS4 TableS5 TableS6 TableS7 DataS1

Albrecht E et al. Telomere Length in Circulating Leukocytes is Associated with Lung Function and Disease. European Respiratory Journal, Volume 43, Issue 4, 2014
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Baumert J et al. No Evidence for Genome-Wide Interactions on Plasma Fibrinogen by Smoking, Alcohol Consumption and Body Mass Index: Results from Meta-Analyses of 80,607 Subjects. PLOS One, Volume 9, Issue 12, 2014
S1 fig
S2 fig
S1 Table - Basic information about studies
S2 Table - Genotype information about studies
S3 Table - Genomic inflation factor per study
S4 Table - Interaction with alcohol consumption for association with fibrinogen concentration (in g/L) among SNPs associated with circulating fibrinogen
S5 Table - Interaction with BMI for association with fibrinogen concentration (in g/L) among SNPs associated with circulating fibrinogen
S1 Funding
S1 Checklist - PRISMA checklist
S1 Methods - Additional information about study samples, fibrinogen measurements, genotyping/imputation and statistical analyses

Beek JHDA van et al. The association of alcohol intake with gamma-glutamyl transferase (GGT) levels: Evidence for correlated genetic effects. Drug and Alcohol Dependence, Volume 134, Issue 1, 2014
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Benyamin B et al. Childhood intelligence is heritable, highly polygenic and associated with FNBP1L. Molecular Psychiatry, Volume 19, Issue 2, 2014
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Berg SM van den et al. Harmonization of Neuroticism and Extraversion phenotypes across inventories and cohorts in the Genetics of Personality Consortium: an application of Item Response Theory. Behavior Genetics, Volume 44, Issue 4, 2014
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Bohlken MM et al. Genes contributing to subcortical volumes and intellectual ability implicate the thalamus. Human Brain Mapping, Early View, 2014
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Brouwer RM et al. Heritability of brain volume change and its relation to intelligence. NeuroImage, Volume 100, 2014
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Brouwer RM et al. Genetic Associations Between Intelligence and Cortical Thickness Emerge at the Start of Puberty. Human Brain Mapping, Volume 35, Issue 8, 2014
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Supporting Information Table 1
Supporting Information Table 2
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Supporting Information Table 4

Byrne EM et al. Applying polygenic risk scores to postpartum depression. Archives of Women's Mental Health, Volume 17, Issue 6, 2014
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ESM 2 (XLSX)
ESM 3 (PDF)

Cousminer DL et al. Genome-wide association study of sexual maturation in males and females highlights a role for body mass and menarche loci in male puberty. Human Molecular Genetics, Volume 23, Issue 16, 2014
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Dane AD et al. Integrating Metabolomics Profiling Measurements Across Multiple Biobanks. Analytical Chemistry, Volume 86, Issue 9, 2014
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Deelen J et al. Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age. Human Molecular Genetics, Volume 23, Issue 16, 2014
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Deelen J et al. Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'. European Journal of Human Genetics, Volume 22, Issue 11, 2014
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Derks EM et al. Genetic and environmental influences on the relationship between adult ADHD symptoms and self-reported problem drinking in 6024 Dutch twins. Psychological Medicine, Volume 44, Issue 12, 2014
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Dongen J van et al. The Contribution of the Functional IL6R Polymorphism rs2228145, eQTLs and Other Genome-Wide SNPs to the Heritability of Plasma sIL-6R Levels. Behavior Genetics, Volume 44, Issue 4, 2014
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Dongen J van et al. Epigenetic Variation in Monozygotic Twins: A Genome-Wide Analysis of DNA Methylation in Buccal Cells. Genes, Volume 5, Issue 2, 2014
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Franic S et al. Genetic and Environmental Stability of Intelligence in Childhood and Adolescence. Twin Research and Human Genetics, Volume 17, Issue 03, 2014
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Franic S et al. Three-and-a-Half-Factor Model? The Genetic and Environmental Structure of the CBCL/6–18 Internalizing Grouping. Behavior Genetics, Volume 44, Issue 3, 2014
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GoNL/Franciolo LC. Whole-genome sequence variation, population structure and demographic history of the Dutch population. Nature Genetics, Advance Online Publication, 2014
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Guigas B et al.  Sex-specific effects of naturally occurring variants in the dopamine receptor D2 locus on insulin secretion and Type 2 diabetes susceptibility. Diabetic Medicine, Volume 31, Issue 8, 2014
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Huppertz C et al. A Twin-Sibling Study on the Relationship Between Exercise Attitudes and Exercise Behavior. Behavior Genetics, Volume 44, Issue 1, 2014
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Jansen R et al. Sex differences in the human peripheral blood transcriptome. BMC Genomics, Volume 15, Issue 33, 2014
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Kochunov P et al. Multi-site study of additive genetic effects on fractional anisotropy of cerebral white matter: Comparing meta and megaanalytical approaches for data pooling. NeuroImage, Volume 95, 2014
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Korhonen T et al. Role of Nicotine Dependence in the Association between the Dopamine Receptor Gene DRD3 and Major Depressive Disorder. PLOS One, Volume 9, Issue 6, 2014
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Liu CT et al. Multi-ethnic fine-mapping of 14 central adiposity loci. Human Molecular Genetics, Volume 23, Issue 17, 2014
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Mathews CA et al. Partitioning the etiology of hoarding and obsessive–compulsive symptoms. Psychological Medicine, Volume 44, Issue 13, 2014
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Minica CC et al. MZ twin pairs or MZ singletons in population family-based GWAS? More power in pairs. Molecular Psychiatry, Volume 19, Issue 11, 2014
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Perry JRB et al. Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. Nature, Advance Online Publication, 2014

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Power RA et al. A recessive genetic model and runs of homozygosity in major depressive disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, Volume 165, Issue 2, 2014
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Swagerman S et al. Development and heritability of subcortical brain volumes at age 9 and 12. Genes, Brain and Behavior, Volume 13, Issue 8, 2014
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Taylor AE et al. Investigating the possible causal association of smoking with depression and anxiety using Mendelian randomisation meta-analysis: the CARTA consortium. BMJ Open, Volume 4, Issue 10, 2014
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Taylor AE et al. Stratification by Smoking Status Reveals an Association of CHRNA5-A3-B4 Genotype with Body Mass Index in Never Smokers. PLOS Genetics, Volume 10, Issue 12, 2014
Text S1: Ethics approvals for individual contributing studies
Text S2: Smoking heaviness in the CARTA studies
Text S3: Data access arrangements for individual contributing studies

Treur JL et al. The Predictive Value of Smoking Expectancy and the Heritability of its Accuracy. Nicotine & Tobacco Research, Volume 16, Issue 3, 2014

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Verweij KJH et al. The Association of Genotype-Based Inbreeding Coefficient with a Range of Physical and Psychological Human Traits. PLOS One, Volume 9, Issue 7, 2014

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Vink JM et al. Polygenic risk scores for smoking: predictors for alcohol and cannabis use? Addiction, Volume 109, Issue 7, 2014
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Winkler TW et al. Quality control and conduct of genome-wide association meta-analyses. Nature Protocols, Volume 9, Number 5, 2014
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Wood AR et al. Defining the role of common variation in the genomic and biological architecture of adult human height. Nature Genetics, Advance Online Publication, 2014
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Wray NR et al. Research Review: Polygenic methods and their application to psychiatric traits. Journal of Child Psychology and Psychiatry, Volume 55, Issue 10, 2014
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Wright FA et al. Heritability and genomics of gene expression in peripheral blood. Nature Genetics, Volume 46, Number 5, 2014
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2013

Abdellaoui A et al. Population structure, migration, and diversifying selection in the Netherlands. European Journal of Human Genetics, Volume 21, Issue 11, 2013
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Amin N et al. Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions. European Journal of Human Genetics, Volume 21, Issue 8, 2013
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Anttila V et al. Genome-wide meta-analysis identifies new susceptibility loci for migraine. Nature Genetics, Volume 45, Number 8, 2013
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Beek JHDA van et al. The Genetic Architecture of Liver Enzyme Levels: GGT, ALT and AST. Behavior Genetics, Volume 43, Issue 4, 2013
Supplementary Materials

Berndt SI et al. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nature Genetics, Volume 45, Number 5, 2013
Supplementary text and figures

Boersma M et al. Growing trees in child brains: Graph theoretical analysis of EEG derived minimum spanning tree in 5 and 7 year old children reflects brain maturation. Brain Connectivity, Volume 3, Issue 1, 2013
Supplementary Data

Brandys MK et al. The Val66Met polymorphism of the BDNF gene in anorexia nervosa: New data and a meta-analysis. The World Journal of Biological Psychiatry, Volume 14, Issue 6, 2013Supplementary Material

Brant AM et al. The Nature and Nurture of High IQ: An Extended Sensitive Period for Intellectual Development. Psychological Science, Volume 24, Issue 8, 2013
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Broer L et al. Meta-analysis of telomere length in 19?713 subjects reveals high heritability, stronger maternal inheritance and a paternal age effect. European Journal of Human Genetics, Volume 21, Issue 10, 2013
Supplemental material

Codd V et al. Identification of seven loci affecting mean telomere length and their association with disease. Nature Genetics, Volume 45, Number 4, 2013

Supplementary text and figures

Cousminer DL et al. Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity. Human Molecular Genetics, Volume 22, Issue 13, 2013
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Cross-Disorder Group of the Psychiatric Genomics Consortium et al. Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. The Lancet, Volume 381, Issue 9875, 2013
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Culverhouse RC et al. Protocol for a collaborative meta-analysis of 5-HTTLPR, stress, and depression. BMC Psychiatry, 13(304)
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Do R et al. Common variants associated with plasma triglycerides and risk for coronary artery disease. Nature Genetics, Volume 45, Number 11, 2013
Supplementary Information

Dongen J van et al. The heritability of metabolic syndrome traits in a large population-based sample. Journal of Lipid Research, Volume 54, Issue 10, 2013
Supplemental Methods

Draisma HHM et al. Hierarchical clustering analysis of blood plasma lipidomics profiles from mono- and dizygotic twin families. European Journal of Human Genetics, Volume 21, Issue 1, 2013
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Fernández-Rhodes L et al. Association of Adiposity Genetic VariantsWith Menarche Timing in 92,105 Women of European Descent. American Journal of Epidemiology, Volume 178, Issue 3, 2013
Web Appendix

Global Lipids Genetics Consortium. Discovery and refinement of loci associated with lipid levels. Nature Genetics, Volume 45, Number 11, 2013
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Groen-Blokhuis MM et al. A prospective study of the effects of breastfeeding and FADS2 polymorphisms on cognition and hyperactivity/attention problems. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, Volume 162, Issue 5, 2013
TABLE SI
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't Hart LM et al. The CTRB1/2 locus affects diabetes susceptibility and treatment via the incretin pathway. Diabetes, Volume 62, Issue 9, 2013
Supplementary data

Hek K et al. A Genome-Wide Association Study of Depressive Symptoms. Biological Psychiatry, Volume 73, Issue 7, 2013
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Hemani G et al. Inference of the Genetic Architecture Underlying BMI and Height with the Use of 20,240 Sibling Pairs. American Journal of Human Genetics, Volume 93, Issue 5, 2013
Supplemental data

Hoed M den et al. Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders. Nature Genetics, Volume 45, Number 6, 2013
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Hong Lee S et al. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics, Volume 45, Number 9, 2013
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Hu Y-J et al. Meta-analysis of Gene-Level Associations for Rare Variants Based on Single-Variant Statistics. American Journal of Human Genetics, Volume 93, Issue 2, 2013
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Kan KJ et al. On the Nature and Nurture of Intelligence and Specific Cognitive Abilities: The More Heritable, the More Culture Dependent. Psychological Science, Volume 24, Issue 12, 2013
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Koenis MMG et al. Longitudinal Study of Hormonal and Physical Development in Young Twins. The Journal of Clinical Endocrinology & Metabolism, Volume 98, Issue 3, 2013
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Loos MJHM van der et al. The Molecular Genetic Architecture of Self-Employment. PLOS One, Volume 8, Issue 4, 2013
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Revez JA et al. A new regulatory variant in the interleukin-6 receptor gene associates with asthma risk. Genes and Immunity, Online First, 2013
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Rietveld CA et al. Molecular genetics and subjective well-being. Proceedings of the National Academy of Sciences of the United States of America, Volume 110, Number 24, 2013
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Rietveld CA et al. GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment. Science, Volume 340, Issue 6139, 2013
Supporting Information

M. Sabater-Lleal. A Multi-Ethnic Meta-Analysis of Genome-Wide Association Studies in Over 100,000 Subjects Identifies 23 Fibrinogen-Associated Loci but no Strong Evidence of a Causal Association between Circulating Fibrinogen and Cardiovascular Disease. Circulation, Volume 128, Issue 12, 2013
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Schutte NM et al. Heritability of Resting State EEG Functional Connectivity Patterns. Twin Research and Human Genetics, Volume 16, Issue 05, 2013
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Slof MCT et al.  Genetic Variation at the TPH2 Gene Influences Impulsivity in Addition to Eating Disorders. Behavior Genetics, Volume 43, Issue 1, 2013
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Stephens SH et al. Distinct Loci in the CHRNA5/CHRNA3/CHRNB4 Gene Cluster Are Associated With Onset of Regular Smoking. Genetic Epidemiology, Volume 37, Issue 8, 2013
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Velde SJ te et al.Genetic and Environmental Influences on Individual Differences in Sleep Duration During Adolescence. Twin Research and Human Genetics, Volume 16, Issue 06, 2013
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Vimaleswaran KS et al. Causal Relationship between Obesity and Vitamin D Status: Bi-Directional Mendelian Randomization Analysis of Multiple Cohorts. PLOS Medicine, Volume 10, Issue 2, 2013
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Ye K et al. Aging as Accelerated Accumulation of Somatic Variants: Whole-Genome Sequencing of Centenarian and Middle-Aged Monozygotic Twin Pairs. Twin Research and Human Genetics, Volume 16, Issue 06, 2013
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2012

Aa N van der et al. Genetic and Environmental Influences on Individual Differences in Sedentary Behavior During Adolescence. Archives of Pediatrics & Adolescent Medicine, Volume 166, Number 6, 2012
Supplementary Online Content

Abdellaoui A et al. Thought Problems from Adolescence to Adulthood: Measurement Invariance and Longitudinal Heritability. Behavior Genetics, Volume 42, Number 1, 2012
Supplementary material (Word document)

Amin N et al. Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM. Molecular Psychiatry, Volume 17, Issue 11, 2012
Supplemental material

Arfan Ikram M et al. Common variants at 6q22 and 17q21 are associated with intracranial volume. Nature Genetics, Volume 44, Number 5, 2012
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Boraska V et al. Genome-wide meta-analysis of common variant differences between men and women. Human Molecular Genetics, Volume 21, Number 21, 2012
Supplementary data

Bradfield JP et al. A genome-wide association meta-analysis identifies new childhood obesity loci. Nature Genetics, Volume 44, Number 5, 2012
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Dongen J van et al. The continuing value of twin studies in the omics era. Nature Reviews Genetics, Volume 13, Number 9, 2012
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Ehli EA et al. De novo and inherited CNVs in MZ twin pairs selected for discordance and concordance on Attention Problems. European Journal of Human Genetics, Volume 20, Issue 10, 2012
Supplementary Figure 1 Supplementary Figure 2 Supplementary Figure 3 Supplementary Information (doc) Readme File (txt) Perl Script 1 (txt) Perl Script 2 (txt) Perl Script 3 (txt) Perl Script 4 (txt)

Forsberg LA et al. Age-Related Somatic Structural Changes in the Nuclear Genome of Human Blood Cells. The American Journal of Human Genetics, Volume 90, Issue 2, 2012
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Geels LM et al. Trends in adolescent alcohol use: Effects of age, sex and cohort on prevalence and heritability. Addiction, Volume 107, Issue 3, 2012
Table S1-S10

Haren NEM van et al. The Genetic and Environmental Determinants of the Association Between Brain Abnormalities and Schizophrenia: The Schizophrenia Twins and Relatives Consortium. Biological Psychiatry, Volume 71, Issue 10, 2012
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Harst P van der et al. Seventy-five genetic loci influencing the human red blood cell. Nature, Volume 492, Issue 7429, 2012
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Supplementary Table 5

fileadmin/user_upload/publicaties/verslaggeving/NTR-publicaties_2012/Harst_Nature-s3.xlsxHulshoff Pol HE et al. Overlapping and Segregating Structural Brain Abnormalities in Twins With Schizophrenia or Bipolar Disorder. Archives of General Psychiatry, Volume 69, Issue 4, 2012
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Lamb DJ et al. Gene–environment interaction in teacher-rated internalizing and externalizing problem behavior in 7- to 12-year-old twins. Journal of Child Psychology and Psychiatry, Volume 53, Issue 8, 2012
Table S1

Lee PH et al. Multi-locus genome-wide association analysis supports the role of glutamatergic synaptic transmission in the etiology of major depressive disorder. Translational Psychiatry, Volume 2, e184, 2012
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Luciano M et al. Genome-Wide Association Uncovers Shared Genetic Effects Among Personality Traits and Mood States. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, Volume 159B, Issue 6, 2012
Table S1-S3

Manning AK et al. A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. Nature Genetics, Volume 44, Number 6, 2012
Supplementary Note & Figures

McEachin RC et al. Convergence of genetic influences in comorbidity. BMC Bioinformatics, Volume 13, Supplement 2, 2012
Additional background

Middelberg RP et al. Loci Affecting Gamma-Glutamyl Transferase in Adults and Adolescents Show Age X SNP Iinteraction and Cardiometabolic Disease Associations. Human Molecular Genetics, Volume 21, Issue 2, 2012
Supplementary Table 1

Mook-Kanamori DO et al. Heritability Estimates of Body Size in Fetal Life and Early Childhood. PLOS One, Volume 7, Issue 7, 2012
Supporting information

Moor MHM de et al. Meta-analysis of genome-wide association studies for personality. Molecular Psychiatry, Volume 17, Issue 3, 2012
Supplementary Information (Word document)

Nürnberg ST et al. A GWAS sequence variant for platelet volume marks an alternative DNM3 promoter in megakaryocytes near a MEIS1 binding site. Blood, Volume 120, Issue 24, 2012
Supplemental material
Supplemental material: list of 1,285 potentially MEIS1 regulated genes

Paternoster L et al. Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis. Nature Genetics, Volume 44, Issue 2, 2012
Supplementary material

Palmer ND et al. A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans. PLoS One, Volume 7, Issue 1, 2012
Supplementary figures and tables

Supplementary table 2 (Excel file)

Raalte DH van et al. Glucocorticoid receptor gene polymorphisms are associated with reduced first-phase glucose-stimulated insulin secretion and disposition index in women, but not in men. Diabetic Medicine, Volume 29, Issue 8, 2012
Supporting information

Scheet P et al. Twins, Tissue, and Time: An Assessment of SNPs and CNVs. Twin Research and Nature Genetics, Volume 15, Issue 6, 2012
Supplementary material

Scott RA et al. Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways. Nature Genetics, Volume 44, Number 9, 2012
Supplementary Note and Supplementary Figures 1–10
Supplementary tables 1-7
(Excel file)

Stein JL et al. Identification of common variants associated with human hippocampal and intracranial volumes. Nature Genetics, Volume 44, Number 5, 2012
Supplementary information

Stolk L et al. Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Nature Genetics, Volume 44, Issue 3, 2012
Supplementary material

Surakka I et al. A Genome-Wide Association Study of Monozygotic Twin-Pairs Suggests a Locus Related to Variability of Serum High-Density Lipoprotein Cholesterol. Twin Research and Nature Genetics, Volume 15, Issue 6, 2012
Supplementary material

Taal HR et al. Common variants at 12q15 and 12q24 are associated with infant head circumference. Nature Genetics, Volume 44, Number 5, 2012
Supplementary information
Supplementary table 1
(Excel file)
Supplementary table 2 (Excel file)

Talens RP et al. Epigenetic variation during the adult lifespan: cross-sectional and longitudinal data on monozygotic twin pairs. Aging Cell, Volume 11, Issue 4, 2012
Supporting information

Vink JM et al. Sex Differences in Genetic Architecture of Complex Phenotypes?. PLoS One, Volume 7, Issue 12, 2012
Supplementary materials

Vliet-Ostaptchouk JV et al. Common Variants in the Type 2 Diabetes KCNQ1 Gene Are Associated with Impairments in Insulin Secretion During Hyperglycaemic Glucose Clamp. PLoS O, Volume 7, Issue 3, 2012
Supplementary tables S1-S5

Webb BT et al. Meta-analyses of genome-wide linkage scans of anxiety-related phenotypes. European Journal of Human Genetics, Volume 20, Issue 10, 2012
Supplementary Figure 1 (gif)
Supplementary Figure 1 (gif)
Supplementary Table (xls)
Supplementary Information (doc)

Wray NR et al. Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned. Molecular Psychiatry, Volume 17, Issue 1, 2012
Supplementary file 1
Supplementary file 2

Supplementary file 3 (Excel file)

Supplementary file 4 (Excel file)

Yang J et al. FTO genotype is associated with phenotypic variability of body mass index. Nature, Volume 490, Issue 7419, 2012
Supplementary Information

2011

Bartels M et al. Adolescent Self-Report of Emotional and Behavioral Problems: Interactions of Genetic Factors with Sex and Age. Journal of the Canadian Academy of Child and Adolescent Psychiatry, Volume 20, Number 1, 2011
Supplementary tables

Chambers et al. Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. Nature Genetics, Volume 43, Number 11, 2011
Supplementary information

Deelen J et al. Genome-wide association study identifies a single major locus contributing to survival into old age; the APOE locus revisited. Aging Cell, Volume 10, Issue 4, 2011
Supplementary figures
Supplementary table (Excel file)

Dehghan A et al. Meta-Analysis of Genome-Wide Association Studies in >80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels. Circulation, Volume 123, Issue 7, 2011 
Supplemental material

Demirkan A et al. Genetic architecture of circulating lipid levels. European Journal of Human Genetics, Volume 19, Issue 7, 2011
Supplemental material

Ferreira MAR et al. Identification of IL6R and chromosome 11q13.5 as risk loci for asthma. The Lancet, Volume 378, Number 9795, 2011
Supplementary webappendix

Gieger C et al. New gene functions in megakaryopoiesis and platelet formation. Nature, Volume 480, Issue 7376, 2011
Supplementary information

Klok MD et al. A common and functional mineralocorticoid receptor haplotype enhances optimism and protects against depression in females. Translational Psychiatry, Volume 1, 2011 
Supplementary information

Ligthart L et al. Meta-analysis of genome-wide association for migraine in six population-based European cohorts. European Journal of Human Genetics, Volume 19, Issue 8, 2011
Supplementary table 1 (Excel file)
Supplementary table 2 (Excel file)
Supplementary table 3 (Word document)
Supplementary table 4 (Excel file)
Supplementary data

Liu Y et al. Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.  Molecular Psychiatry, Volume 16, Issue 1, 2011
Supplemental material

Maugeri N et al. LPAR1 and ITGA4 Regulate Peripheral Blood Monocyte Counts. Human Mutation, Volume 32, Issue 8, 2011
Supporting information

Pergadia ML et al. A 3p26-3p25 Genetic Linkage Finding for DSM-IV Major Depression in Heavy Smoking Families. The American Journal of Psychiatry, Volume 168, Issue 8, 2011
Supplementary table 1
Supplementary table 2

Saviouk V et al. ADHD in Dutch Adults: Heritability and Linkage Study. American Journal of Medical Genetics Part B, Neuropsychiatric Genetics, Volume 156, Issue 3, 2011
Supplemental materials

Schumann G et al. Genome-wide association and genetic functional studies identify   autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption. Proceedings of the National Academy of Sciences, Proceedings of the National Academy of Sciences, Volume 108, Number 17, 2011
Supporting information
Table S01-S07

Simonis-Bik AMC et al. The heritability of beta cell function parameters in a mixed meal test design. Diabetologia, Volume 54, Issue 5, 2011
Supplemental material

Speliotes EK et al. Genome-Wide Association Analysis Identifies Variants Associated with Nonalcoholic Fatty Liver Disease That Have Distinct Effects on Metabolic Traits. PLoS Genetics, Volume 7, Issue 3, 2011
Supplemental material (tables S1-S10)

Strawbridge RJ et al. Genome-Wide Association Identifies Nine Common Variants Associated With Fasting Proinsulin Levels and Provides New Insights Into the Pathophysiology of Type 2 Diabetes. Diabetes, Volume 60, Issue 10, 2011
Supplementary data

Supplemental table 1

Zhu H et al. The Lin28/let-7 Axis Regulates Glucose Metabolism. Cell, Volume 147, Issue 1, 2011
Supplemental text
Supplemental table

2010

Beekman M et al. Genome-wide association study (GWAS)-identified disease risk alleles do not compromise human longevity. Proceedings of the National Academy of Sciences USA, Vol. 107, No. 42, 2010
Dataset S01 (Excel file)
Supporting information

Brouwer RM et al. Heritability of DTI and MTR in nine-year-old children. NeuroImage, Volume 53, Issue 3, 2010 
Supplementary content

Draisma HHM et al. Equating, or Correction for Between-Block Effects with Application to Body Fluid LC-MS and NMR Metabolomics Data Sets. Analytical Chemistry, Volume 82, No. 3, 2010
Supporting information

Eijgelsheim M et al. Genome-wide association analysis identifies multiple loci related to resting heart rate. Human Molecular Genetics, Volume 19, No. 19, 2010
Supplementary data
Supplemental table (Excel file)

Elks et al. Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nature Genetics, Volume 42, Number 12, 2010
Supplementary information
Supplementary table (Excel file)

Freathy RM et al for the Early Growth Genetics (EGG) Consortium. Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight. Nature Genetics, Volume 42, Number 5, 2010
Supplementary table 1 (Excel file)
Supplementary table 2 (Excel file)
Supporting information

Gielen M et al. Secular trends in gestational age and birthweight in twins. Human Reproduction, Volume 25, Number 9, 2010
Supplementary tables

Haworth CMA et al. The heritability of general cognitive ability increases linearly from childhood to young adulthood. Molecular Psychiatry, Volume 15, Issue 11, 2010
Supplementary information

Heid IM et al on behalf of GIANT. Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nature, Volume 42, Number 11, 2010
Supplementary table 11 (Excel file)
Supplementary text and figures

Heni M et al. The Impact of Genetic Variation in the G6PC2 Gene on Insulin  Secretion Depends on Glycemia. The Journal of Clinical Endocrinology & Metabolism, Volume 95, Number 12, 2010
Supplemental data

Lango Allen et al on behalf of GIANT. Hundreds of variants clustered in genomic loci and biological pathways affect human heightNature, Volume 467, Number 7317, 2010
Supplementary information

MAGIC. New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nature Genetics, Volume 42, Number 2, 2010
Supplementary Text and Figures 
Supplementary Table 1 (Excel file)

Middeldorp CM et al. Anxiety and depression in children and adults: influence of serotonergic and neurotrophic genes? Genes, Brain and Behavior, Volume 9, Issue 7, 2010
Supplementary figure 1

Nettleton JA et al. Interactions of Dietary Whole-Grain Intake With Fasting Glucose– and Insulin-Related Genetic Loci in Individuals of European Descent. Diabetes Care, Volume 33, Number 12, 2010
Supplement

Perlis RH et al. Genome-Wide Association Study of Suicide Attempts in Mood Disorder Patients. The American Journal of Psychiatry, Volume 167, Issue 12, 2010
Supplement

Schot van der AC et al. Genetic and environmental influences on focal brain density in bipolar disorder. Brain, Volume 133, Issue 10, 2010
Supplementary data (TIF)

Soranzo N et al. Common Variants at 10 Genomic Loci Influence Hemoglobin A1C Levels via Glycemic and Nonglycemic Pathways. Diabetes, Volume 59, Number 12, 2010
Supporting online information
Institutional affiliations

Tables S1-S6 (Excel file)

Speliotes EK et al on behalf of GIANT. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nature, Volume 42, Issue 11, 2010
Supplementary information

Talens RP et al. Variation, patterns, and temporal stability of DNA methylation: considerations for epigenetic epidemiologyThe FASEB Journal, Volume 24, Issue 9, 2010
Supplementary material

Terracciano A et al. Genome-wide association scan for five major dimensions of personality. Molecular Psychiatry, Volume 15, Issue 6, 2010
Supplementary table A (Excel file)

Supplementary table B (Excel file)

Teslovich TM et al. Biological, clinical and population relevance of 95 loci for blood lipids. Nature, Volume 466, 2010
Supplementary information

Thorgeirsson TE et al. Sequence variants at CHRNB3CHRNA6 and CYP2A6 affect smoking behavior. Nature Genetics, Volume 42, Number 5, 2010
Supplementary information

The Tobacco and Genetics Consortium. Genome-wide meta-analyses identify multiple loci associated with smoking behavior. Nature Genetics, Volume 42, Number 5, 2010
Supplementary information

Supplementary table (Excel file)

2009

Aulchenko YS et al. Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nature Genetics, Volume 41, Number 1, 2009
Supplementary material

Estrada K et al. A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. Human Molecular Genetics, Volume 18, No. 18, 2009
Supplementary material

Sullivan PF et al. Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. Molecular Psychiatry, Volume 14, 2009
Supplementary information
Supplementary table (Excel file)

Vink JM et al. Genome-wide Association Study of Smoking Initiation and Current Smoking. The American Journal of Human Genetics, Volume 84, Issue 3, 2009
Supplemental data (Excel file)

2008

Bruder CEG et al. Phenotypically Concordant and Discordant Monozygotic Twins Display Different DNA Copy-Number-Variation Profiles. The American Journal of Human Genetics, Volume 82, 2008
Supplemental data