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Interaction of developmental factors and ordinary stressful life events on brain structure in adults. NEUROIMAGE-CLINICAL 42.
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Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. MOLECULAR PSYCHIATRY (2020)
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87 (5), pp. 419 - 430 (2020)
Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression. BIOLOGICAL PSYCHIATRY 44.
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18 (1), 298 (2020)
Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. BMC MEDICINE 45.
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16 (2), e1007616 (2020)
DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learning. PLOS COMPUTATIONAL BIOLOGY 46.
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52 (4), pp. 437 - 447 (2020)
Minimal phenotyping yields genome-wide association signals of low specificity for major depression. NATURE GENETICS 47.
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139 (1), pp. 45 - 59 (2020)
A different view on fine-scale population structure in Western African populations. SI 48.
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25 (7), pp. 1430 - 1446 (2020)
Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank. MOLECULAR PSYCHIATRY 49.
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11, 2165 (2020)
Gene Expression in Spontaneous Experimental Autoimmune Encephalomyelitis Is Linked to Human Multiple Sclerosis Risk Genes. FRONTIERS IN IMMUNOLOGY 50.
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10 (1), 106 (2020)
Transcriptome signatures from discordant sibling pairs reveal changes in peripheral blood immune cell composition in Autism Spectrum Disorder. TRANSLATIONAL PSYCHIATRY 51.
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13 (6), pp. 569 - 575 (2020)
Population Bias in Polygenic Risk Prediction Models for Coronary Artery Disease. CIRCULATION-GENOMIC AND PRECISION MEDICINE 52.
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84 (4-5), pp. 209 - 210 (2020)
Population Stratification in Polygenic Risk Prediction Models for Coronary Artery Disease. HUMAN HEREDITY 53.
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44 (2), pp. 125 - 138 (2020)
Polygenic risk scores outperform machine learning methods in predicting coronary artery disease status. GENETIC EPIDEMIOLOGY 54.
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367 (6484), pp. 1340 - + (2020)
The genetic architecture of the human cerebral cortex. SI 55.
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48 (6), pp. 478 - 489 (2020)
A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4q. ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 56.
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183 (6), pp. 309 - 330 (2020)
Genetic comorbidity between major depression and cardio-metabolic traits, stratified by age at onset of major depression. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 57.
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46, pp. S35 - S36 (2020)
IMPACT OF POLYGENIC AND POLY-ENVIRONMENTAL RISK FACTORS ON A PSYCHOSIS RISK PHENOTYPE EXPLAINED THROUGH BRAIN STRUCTURE. SCHIZOPHRENIA BULLETIN 58.
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28 (SUPPL 1), p. 415 - 415 (2020)
Deep targeted-NGS identifies RLS genes by differential burden with low-frequency variants and differential target sequencing depth. EUROPEAN JOURNAL OF HUMAN GENETICS 59.
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87 (2), pp. 184 - 193 (2020)
Identification of Restless Legs Syndrome Genes by Mutational Load Analysis. ANNALS OF NEUROLOGY 60.
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116, 104685 (2020)
Salivary cortisol response to psychosocial stress in the late evening depends on CRHR1 genotype. PSYCHONEUROENDOCRINOLOGY