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2018

Abdellaoui A et al. Predicting Loneliness with Polygenic Scores of Social, Psychological, and Psychiatric Traits. Genes, Brain and Behavior, 17(6):e12472

Abdellaoui A et al. Associations between Loneliness and Personality are Mostly Driven by a Genetic Association with Neuroticism. Journal of Personality, Accepted Article

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

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, 177(1):40-49

Bartels M et al. Childhood aggression and the co-occurrence of behavioural and emotional problems: results across ages 3–16 years from multiple raters in six cohorts in the EU-ACTION project. European Child & Adolescent Psychiatry, 27(9):1105-1121

Baselmans BML et al. Unraveling the Genetic and Environmental Relationship Between Well-Being and Depressive Symptoms Throughout the Lifespan. Frontiers in Psychiatry, 9:261

Baselmans BML & Bartels M. A genetic perspective on the relationship between eudaimonic -and hedonic well-being. Nature Scientific Reports, 8(1):14610

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, 27(4):742-756

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, 59(11):1205-1214

Boomsma DI et al. An Extended Twin-Pedigree Study of Neuroticism in the Netherlands Twin Register. Behavior Genetics, 48(1):1-11

Brainstorm Consortium. Analysis of shared heritability in common disorders of the brain. Science, 360(6395):eaap8757

Colodro-Conde L et al. Association Between Population Density and Genetic Risk for Schizophrenia. JAMA Psychiatry, 75(9):901-910

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, 23(1):133-142

Demenais F et al. Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks. Nature Genetics, 50(1):42-53

Dongen J van et al. DNA methylation signatures of educational attainment. npj Science of Learning, 3(7)

Dongen J van et al. Genome-wide analysis of DNA methylation in buccal cells: a study of monozygotic twins and mQTLs. Epigenetics & Chromatin, 11(54)

Doornweerd S et al. Brain reward responses to food stimuli among female monozygotic twins discordant for BMI. Brain Imaging and Behavior, 12(3):718-727

Evangelou E et al. Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nature Genetics, 50(10):1412-1425

Ferreira MAR et al. Eleven loci with new reproducible genetic associations with allergic disease risk. Journal of Allergy and Clinical Immunology, Accepted Manuscript

Finnicum CT et al. Metataxonomic Analysis of Individuals at BMI Extremes and Monozygotic Twins Discordant for BMI. Twin Research and Human Genetics, 21(3):203-213

Gormley P et al. Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families. Neuron, 98(4):743-753

Gudmundsdottir V et al. Integrative network analysis highlights biological processes underlying GLP-1 stimulated insulin secretion: A DIRECT study. PLOS ONE, 13(1):e0189886

Hagenbeek FA et al. Adult aggressive behavior in humans and biomarkers: a focus on lipids and methylation. Journal of Pediatric and Neonatal Individualized Medicine, 7(2):e070204

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, 23(9):1-9

Hart LM 't et al. Blood metabolomic measures associate with present and future glycemic control in type 2 diabetes.  Journal of Clinical Endocrinology & Metabolism, 103(12):4569-4579

Heikkilä K et al. Triplets, birthweight, and handedness. PNAS, 115(23):6076-6081

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, 50(5):652-656

Ip HF et al. Characterizing the Relation Between Expression QTLs and Complex Traits: Exploring the Role of Tissue Specificity. Behavior Genetics, 48(5):374-385

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, 120:53-60

Jelenkovic A et al. Birth size and gestational age in opposite-sex twins as compared to same-sex twins: An individual-based pooled analysis of 21 cohorts. Nature Scientific Reports, Open Access

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, 1(163)

Kate M ten et al. White matter hyperintensities and vascular risk factors in monozygotic twins. Neurobiology of Aging, 66:40-48

Koenis MMG et al. Association between structural brain network efficiency and intelligence increases during adolescence. Human Brain Mapping, 39(2):822-836

Konijnenberg E et al. The EMIF-AD PreclinAD study: study design and baseline cohort overview. Alzheimer's Research & Therapy, 10(75)

Korpela K et al. Selective maternal seeding and environment shape the human gut microbiome. Genome Research, 28(4):561-568

Kreeke JA van de et al. Retinal and Cerebral Microvasculopathy: Relationships and Their Genetic Contributions. Investigative Ophthalmology & Visual Science, 59(12):5025-5031

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, 50(8):1112-1121

Ligthart L et al. Are Migraine and Tension-Type Headache Genetically Related? An Investigation of Twin Family Data. Twin Research and Human Genetics, 21(2):112-118

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, 103(5):691-706

Lubke GH et al. Genetic and Environmental Contributions to the Development of Childhood Aggression. Developmental Psychology, 54(1):39-50

Luijk R et al. Genome-wide identification of directed gene networks using large-scale population genomics data. Nature Communications, 9:3097

Luijk R et al. Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation. Nature Communications, 9:3738

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

Mee DJ van der et al. Dopaminergic Genetic Variants and Voluntary Externally Paced Exercise Behavior. Medicine & Science in Sports & Exercise, 50(4):700-708

Mies GW et al. Polygenic risk for alcohol consumption and its association with alcohol-related phenotypes: Do stress and life satisfaction moderate these relationships?. Drug and Alcohol Dependence, 183:7-12

Minica CC et al. Extending Causality Tests with Genetic Instruments: An Integration of Mendelian Randomization with the Classical Twin Design. Behavior Genetics, 48(4):337-349

Minica CC et al. Genome-Wide Association Meta-Analysis of Age at First Cannabis Use. Addiction, 113(11):2073-2086

Molnos S et al. Metabolite ratios as potential biomarkers for type 2 diabetes: a DIRECT study. Diabetologia, 61(1):117-129

Odintsova VV et al. Establishing a Twin Register: An Invaluable Resource for (Behavior) Genetic, Epidemiological, Biomarker, and 'Omics' Studies. Twin Research and Human Genetics, 21(3):239-252

Ouwens KG et al. A characterization of post-zygotic mutations identified in monozygotic twins. Human Mutation, 39(10):1393-1401

Parmar P et al. Association of maternal prenatal smoking GFI1-locus and cardio-metabolic phenotypes in 18,212 adults. EBioMedicine, 38:206-216

Pasman JA et al. GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal influence of schizophrenia. Nature Neuroscience, 21(9):1161-1170

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, 84(2):138-147

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, 13(7)

Qi T et al. Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood. Nature Communications, 9:2282

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, 8(1):16714

Shvetsova E et al. Skewed X-inactivation is common in the general female population. European Journal of Human Genetics, Open

Smit DJA et al. Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. Human Brain Mapping, 39(11):4183-4195

Teeuw J et al. Genetic Influences on the Development of Cerebral Cortical Thickness During Childhood and Adolescence in a Dutch Longitudinal Twin Sample: The Brainscale Study. Cerebral Cortex, Advance Article

Timmermans EJ et al. Cohort profile: the Geoscience and Health Cohort Consortium (GECCO) in the Netherlands. BMJ Open, 8:e021597

Treur JL et al. Testing familial transmission of smoking with two different research designs. Nicotine and Tobacco Research, 20(7):836-842

Visscher CM et al. Shared Genetics of Temporomandibular Disorder Pain and Neck Pain: Results of a Twin Study. Journal of Oral & Facial Pain & Headache, 32(2):107-112

Waage J et al. Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis. Nature Genetics, 50(8):1072-1080

Walters RK et al. Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders. Nature Neuroscience, 21(12):1656-1669

Wang J et al. Meta-analysis of human genome-microbiome association studies: the MiBioGen consortium initiative. Microbiome, 6(1):101

Ward-Caviness CK et al. DNA methylation age is associated with an altered hemostatic profile in a multi-ethnic meta-analysis. Blood, 132(17):1842-1850

Warrier V et al. Genome-wide meta-analysis of cognitive empathy: heritability, and correlates with sex, neuropsychiatric conditions and cognition. Molecular Psychiatry, 23(6):1402-1409

Wesseldijk LW et al. Risk factors for parental psychopathology: a study in families with children or adolescents with psychopathology. European Child & Adolescent Psychiatry, 27(12):1575-1584

Wesseldijk LW et al. Genetic and environmental influences on conduct and antisocial personality problems in childhood, adolescence, and adulthood. European Child & Adolescent Psychiatry, 27(9):1123-1132

Wesseldijk LW et al. Do Parental Psychiatric Symptoms Predict Outcome in Children With Psychiatric Disorders? A Naturalistic Clinical Study. Journal of the American Academy of Child & Adolescent Psychiatry, 57(9):669-677

Willems YE et al. Genetic and Environmental Influences on Self-Control: Assessing Self-Control with the ASEBA Self-Control Scale. Behavior Genetics, 48(2):135-146

Willems YE et al. The Relationship between Family Violence and Self-Control in Adolescence: A Multi-Level Meta-Analysis. International Journal of Environmental Research and Public Health, 15(11):2468

Wray NR et al. Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nature Genetics, 50(5):668-681

Yang Y et al. Molecular genetic overlap between migraine and major depressive disorder. European Journal of Human Genetics, 26(8):1202-1216

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, 47(4):1195-1206

Yousefi S et al. A SNP panel for identification of DNA and RNA specimens. BMC Genomics, 19(90)

Xue A et al. Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. Nature Communications, 9(1):2941

Zilhão NR et al. Polygenic prediction of obsessive compulsive symptoms. Molecular Psychiatry, 23(2):168-169