Aanmelden
facebook twitter

2013

Abdellaoui A et al. Population structure, migration, and diversifying selection in the Netherlands. European Journal of Human Genetics, 21(11):1277-1285

Abdellaoui A et al. Association Between Autozygosity and Major Depression: Stratification Due to Religious Assortment. Behavior Genetics, 43(6):455-467

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, 21(8):876-882

Anttila V et al. Genome-wide meta-analysis identifies new susceptibility loci for migraine. Nature Genetics, 45(8):912-917

Bartels M et al. Exploring the Association Between Well-Being and Psychopathology in Adolescents. Behavior Genetics, 43(3):177-190

Beek JHDA van et al. The Genetic Architecture of Liver Enzyme Levels: GGT, ALT and AST. Behavior Genetics, 43(4):329-339

Beijsterveldt CEM van et al. The Young Netherlands Twin Register (YNTR): Longitudinal Twin and Family Studies in Over 70,000 Children. Twin Research and Human Genetics, 16(1):252-267

Berkelaar M et al. Effects of induced hyperinsulinaemia with and without hyperglycaemia on measures of cardiac vagal control. Diabetologia, 56(6):1436-1443

Berndt SI et al. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nature Genetics, 45(5):501-512

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, 3(1):50-60

Boomsma DI. Twin, association and current “omics” studies. Journal of Maternal-Fetal and Neonatal Medicine, 26(S2):9-12

Boomsma DI. Book Review: Far from the Tree by Andrew Solomon. Twin Research and Human Genetics, 16(4):922

Bot M et al. Exposure to secondhand smoke and depression and anxiety: A report from two studies in the Netherlands. Journal of Psychosomatic Research, 75(5):431-436

Braber A den et al. Obsessive–Compulsive Symptoms and Related Sex Differences in Brain Structure: An MRI Study in Dutch Twins. Twin Research and Human Genetics, 16(2):516-524

Braber A den et al. Heritability of subcortical brain measures: A perspective for future genome-wide association studies. NeuroImage, 83:98-102

Braber A den et al. Sex differences in gray and white matter structure in age-matched unrelated males and females and opposite-sex siblings. International Journal of Psychological Research, 6(Special Issue: Social Neuroscience):7-21

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, 14(6):441-451

Brant AM et al. The Nature and Nurture of High IQ: An Extended Sensitive Period for Intellectual Development. Psychological Science, 24(8):1487-1495

Broer L et al. Meta-analysis of telomere length in 19713 subjects reveals high heritability, stronger maternal inheritance and a paternal age effect. European Journal of Human Genetics, 21(10):1163-1168

Carpenter RW et al. Gene-Environment Studies and Borderline Personality Disorder: A Review. Current Psychiatry Reports, 15(1):336

Codd V et al. Identification of seven loci affecting mean telomere length and their association with disease. Nature Genetics, 45(4):422-427

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, 22(13):2735-2747

Cross-Disorder Group of the Psychiatric Genomics Consortium. Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. The Lancet, 381(9875):1371-1379

Cross-Disorder Group of the Psychiatric Genomics Consortium. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics, 45(9):984-994

Culverhouse RC et al. Protocol for a collaborative meta-analysis of 5-HTTLPR, stress, and depression. BMC Psychiatry, 13(304)

Diaz BA et al. The Amsterdam Resting-State Questionnaire reveals multiple phenotypes of resting-state cognition. Frontiers in Human Neuroscience, 7:446

Do R et al. Common variants associated with plasma triglycerides and risk for coronary artery disease. Nature Genetics, 45(11):1345-1352

Dongen J van et al. The evolutionary paradox and the missing heritability of schizophrenia. American Journal of Medical Genetics Part B. Neuropsychiatric Genetics, 162(2):122-136

Dongen J van et al. Heritability of metabolic syndrome traits in a large population-based sample. Journal of Lipid Research, 54(10):2914-2923

Draisma HHM et al. Hierarchical clustering analysis of blood plasma lipidomics profiles from mono- and dizygotic twin families. European Journal of Human Genetics, 21(1):95-101

Draisma HHM et al. Familial Resemblance for Serum Metabolite Concentrations. Twin Research and Human Genetics, 16(05):948-961

Fall T et al. The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis. PLOS Medicine, 10(6):e1001474

Fernández-Rhodes L et al. Association of Adiposity Genetic VariantsWith Menarche Timing in 92,105 Women of European Descent. American Journal of Epidemiology, 178(3):451-460

Franic S et al. Can Genetics Help Psychometrics? Improving Dimensionality Assessment Through Genetic Factor Modeling. Psychological Methods, 18(3):406-433

Geels LM et al. Increases in alcohol consumption in women and elderly groups: evidence from an epidemiological study. BMC Public Health, 13(207)

Global Lipids Genetics Consortium. Discovery and refinement of loci associated with lipid levels. Nature Genetics, 45(11):1274-1283

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, 162(5):457-465

't Hart LM et al. The CTRB1/2 locus affects diabetes susceptibility and treatment via the incretin pathway. Diabetes, 62(9):3275-3281 (Commentary by JC Florez)

Hek K et al. A Genome-Wide Association Study of Depressive Symptoms. Biological Psychiatry, 73(7):667-678

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, 93(5):865-875

Heuvel MP van den et al. Genetic control of functional brain network efficiency in children. European Neuropsychopharmacology, 23(1):19-23

Hoed M den et al. Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders. Nature Genetics, 45(6):621-631

Horikoshi M et al. New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism. Nature Genetics, 45(1):76-82

Houtem CMHH van et al. A review and meta-analysis of the heritability of specific phobia subtypes and corresponding fears. Journal of Anxiety Disorders, 27(4):379-388

Hu Y-J et al. Meta-analysis of Gene-Level Associations for Rare Variants Based on Single-Variant Statistics. American Journal of Human Genetics, 93(2):236-248

Kan KJ et al. Genetic and Environmental Stability in Attention Problems Across the Lifespan: Evidence From the Netherlands Twin Register. Journal of the American Academy of Child & Adolescent Psychiatry, 52(1):12-25

Kan KJ et al. On the Nature and Nurture of Intelligence and Specific Cognitive Abilities: The More Heritable, the More Culture Dependent. Psychological Science, 24(12):2420-2428

Kiezun A et al. Deleterious Alleles in the Human Genome Are on Average Younger Than Neutral Alleles of the Same Frequency. PLOS Genetics, 9(2):e1003301

Koenis MMG et al. Longitudinal Study of Hormonal and Physical Development in Young Twins. The Journal of Clinical Endocrinology & Metabolism, 98(3):518-527

Ligthart L et al. Anxiety and Depression Are Associated With Migraine and Pain in General: An Investigation of the Interrelationships. The Journal of Pain, 14(4):363-370

Loos MJHM van der et al. The Molecular Genetic Architecture of Self-Employment. PLOS One, 8(4):e60542

Lubke GH et al. Gradient Boosting as a SNP Filter: an Evaluation Using Simulated and Hair Morphology Data. Journal of Datamining in Genomics & Proteomics, 4(4)

Major Depressive Disorder Working Group of the Psychiatric GWAS Consortium. A mega-analysis of genome-wide association studies for major depressive disorder. Molecular Psychiatry, 18(4):497-511

Minica CC et al. The Use of Imputed Sibling Genotypes in Sibship-Based Association Analysis: On Modeling Alternatives, Power and Model Misspecification. Behavior Genetics, 43(3):254-266

Molenaar D et al. Genotype by Environment Interactions in Cognitive Ability: A Survey of 14 Studies from Four Countries Covering Four Age Groups. Behavior Genetics, 43(3):208-219

Neijts M et al. Genetic Architecture of the Pro-Inflammatory State in an Extended Twin-Family Design. Twin Research and Human Genetics, 16(05):931-940

Ordoñana JR et al. Biological pathways and genetic mechanisms involved in social functioning. Quality of Life Research, 22(6):1189-1200

Peyrot WJ et al. Strong effects of environmental factors on prevalence and course of major depressive disorder are not moderated by 5-HTTLPR polymorphisms in a large Dutch sample. Journal of Affective Disorders, 146(1):91-99

Randall JC et al. Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits. PLOS Genetics, 9(6):e1003500

Revez JA et al. A new regulatory variant in the interleukin-6 receptor gene associates with asthma risk. Genes and Immunity, 14(7):441-446

Rietveld CA et al. Molecular genetics and subjective well-being. Proceedings of the National Academy of Sciences of the United States of America, 110(24):9692-9697

Rietveld CA et al. GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment. Science, 340(6139):1467-1471

Sabater-Lleal M et al. 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, 128(12):1310-1324

Schork AJ et al. All SNPs Are Not Created Equal: Genome-Wide Association Studies Reveal a Consistent Pattern of Enrichment among Functionally Annotated SNPs. PLOS Genetics, 9(4):e1003449

Schutte NM et al. Heritability of Resting State EEG Functional Connectivity Patterns. Twin Research and Human Genetics, 16(05):962-969

Slof MCT et al. Genetic Variation at the TPH2 Gene Influences Impulsivity in Addition to Eating Disorders. Behavior Genetics, 43(1):24-33

Soelen ILC van et al. Heritability of Volumetric Brain Changes and Height in Children Entering Puberty. Human Brain Mapping, 34(3):713-725

Stephens SH et al. Distinct Loci in the CHRNA5/CHRNA3/CHRNB4 Gene Cluster Are Associated With Onset of Regular Smoking. Genetic Epidemiology, 37(8):846-859

Stroom EMC van der et al. Ovarian Reserve and Anti-Mullerian Hormone (AMH) in Mothers of Dizygotic Twins. Twin Research and Human Genetics, 16(2):634-638

Velde SJ te et al. Genetic and Environmental Influences on Individual Differences in Sleep Duration During Adolescence. Twin Research and Human Genetics, 16(06):1015-1025

Verbeek EC et al. Resequencing Three Candidate Genes for Major Depressive Disorder in a Dutch Cohort. PLOS ONE, 8(11):e79921

Vimaleswaran KS et al. Causal Relationship between Obesity and Vitamin D Status: Bi-Directional Mendelian Randomization Analysis of Multiple Cohorts. PLOS Medicine, 10(2):e1001383

Willemsen G et al. The Adult Netherlands Twin Register: Twenty-Five Years of Survey and Biological Data Collection. Twin Research and Human Genetics, 16(1):271-281

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, 16(06):1026-132

Zhernakova DV et al. DeepSAGE Reveals Genetic Variants Associated with Alternative Polyadenylation and Expression of Coding and Non-coding Transcripts. PLOS Genetics, 9(6):e1003594