Danielle Posthuma

Danielle Posthuma's AcademicInfluence.com Rankings

Danielle Posthuma

Biology

#6814

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#9614

Historical Rank

Genetics

#643

World Rank

#727

Historical Rank

Neuroscience

#940

World Rank

#979

Historical Rank

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Biology

Danielle Posthuma's Degrees

Bachelors Psychology University of Amsterdam

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According to Wikipedia, Danielle Posthuma is a Dutch behavior and psychiatric geneticist who specializes in statistical genetics. She is a University Research Chair professor at VU University Amsterdam, where she is also head of the Department of Complex Trait Genetics. She has been a member of the Young Academy of the Royal Dutch Academy of Sciences since 2005. She is known for studying the genetics of psychiatric and cognitive traits, including schizophrenia, neuroticism, Alzheimer's disease, insomnia, as well as genetics of intelligence, which she first became interested in researching in the 1990s. In 2019 Posthuma became a member of the Royal Netherlands Academy of Arts and Sciences.

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Danielle Posthuma's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Biological Insights From 108 Schizophrenia-Associated Genetic Loci (2014) (6445)
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (2010) (2087)
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs (2013) (2011)
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression (2018) (1816)
Functional mapping and annotation of genetic associations with FUMA (2017) (1787)
MAGMA: Generalized Gene-Set Analysis of GWAS Data (2015) (1780)
Genome-wide association study identifies five new schizophrenia loci (2011) (1680)
Meta-analysis of the heritability of human traits based on fifty years of twin studies (2015) (1545)
Genome-wide Association Analysis Identifies 14 New Risk Loci for Schizophrenia (2013) (1455)
Analysis of shared heritability in common disorders of the brain (2016) (1385)
Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk (2019) (1232)
A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium (2016) (1125)
Genome-wide association study identifies 74 loci associated with educational attainment (2016) (1114)
Genome-wide meta-analyses identify multiple loci associated with smoking behavior (2010) (1107)
Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder (2017) (998)
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use (2018) (914)
GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment (2013) (803)
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects (2016) (736)
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders (2019) (724)
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence (2018) (705)
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) (676)
Author Correction: A global overview of pleiotropy and genetic architecture in complex traits (2018) (551)
The heritability of general cognitive ability increases linearly from childhood to young adulthood (2010) (546)
Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (2017) (517)
Rare and low-frequency coding variants alter human adult height (2016) (511)
Integrative functional genomic analysis of human brain development and neuropsychiatric risks (2018) (464)
Mapping the human genetic architecture of COVID-19 (2021) (455)
Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways (2018) (450)
Netherlands Twin Register: from twins to twin families. (2006) (421)
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) (421)
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) (421)
Genomewide Association for Major Depressive Disorder: A possible role for the presynaptic protein Piccolo (2008) (410)
Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways (2019) (396)
Theory and practice in quantitative genetics. (2003) (389)
Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence (2017) (380)
The association between brain volume and intelligence is of genetic origin (2002) (372)
Mapping genomic loci implicates genes and synaptic biology in schizophrenia (2022) (361)
The genetic architecture of the human cerebral cortex (2018) (355)
Quantitative genetic modeling of variation in human brain morphology. (2001) (333)
SynGO: An Evidence-Based, Expert-Curated Knowledge Base for the Synapse (2019) (328)
Poor replication of candidate genes for major depressive disorder using genome-wide association data (2011) (317)
The Construction and Validation of an Abridged Version of the Autism-Spectrum Quotient (AQ-Short) (2010) (317)
GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal effect of schizophrenia liability (2018) (316)
Netherlands Twin Register: A Focus on Longitudinal Research (2002) (310)
A Note on the Statistical Power in Extended Twin Designs (2000) (299)
Revealing the complex genetic architecture of obsessive–compulsive disorder using meta-analysis (2018) (294)
Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture (2013) (280)
Physical activity and cognitive function in a cross-section of younger and older community-dwelling individuals. (2006) (270)
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method (2014) (262)
Genome-wide association study of obsessive-compulsive disorder (2013) (256)
Heritability of “small‐world” networks in the brain: A graph theoretical analysis of resting‐state EEG functional connectivity (2008) (253)
Childhood intelligence is heritable, highly polygenic and associated with FNBP1L (2014) (247)
New insights into the genetic etiology of Alzheimer’s disease and related dementias (2022) (246)
Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology (2021) (240)
CYFIP1 Coordinates mRNA Translation and Cytoskeleton Remodeling to Ensure Proper Dendritic Spine Formation (2013) (223)
MAGMA: Generalized Gene-Set Analysis of GWAS Data (2015) (216)
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits (2017) (215)
The statistical properties of gene-set analysis (2016) (214)
Accounting for sequential trial effects in the flanker task: Conflict adaptation or associative priming? (2006) (213)
A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease (2021) (207)
Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder (2015) (206)
Heritability of Daytime Ambulatory Blood Pressure in an Extended Twin Design (2005) (203)
TATES: Efficient Multivariate Genotype-Phenotype Analysis for Genome-Wide Association Studies (2013) (201)
Are Smarter Brains Running Faster? Heritability of Alpha Peak Frequency, IQ, and Their Interrelation (2001) (200)
Heritability estimates of innate immunity: an extended twin study (2005) (194)
Heritability of background EEG across the power spectrum. (2005) (186)
Exploring the association between severe respiratory syncytial virus infection and asthma: a registry-based twin study. (2009) (185)
Genetics of Cognition: Outline of a Collaborative Twin Study (2001) (182)
Heritability of life satisfaction in adults: a twin-family study (2005) (180)
Across the continuum of attention skills: a twin study of the SWAN ADHD rating scale. (2007) (176)
Gene expression in major depressive disorder (2016) (175)
Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder (2011) (173)
Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia (2011) (165)
Item-level analyses reveal genetic heterogeneity in neuroticism (2018) (157)
Genome-Wide Association Studies of a Broad Spectrum of Antisocial Behavior (2017) (155)
Genome-wide association studies (2021) (153)
Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. (2019) (153)
Perceptual Speed and IQ Are Associated Through Common Genetic Factors (2001) (148)
Genetic mapping of cell type specificity for complex traits (2019) (148)
A genomewide scan for intelligence identifies quantitative trait loci on 2q and 6p. (2005) (146)
Genome-wide analysis reveals extensive genetic overlap between schizophrenia, bipolar disorder, and intelligence (2019) (144)
Genetic correlations between brain volumes and the WAIS-III dimensions of verbal comprehension, working memory, perceptual organization, and processing speed. (2003) (140)
What Twin Studies Tell Us About the Heritability of Brain Development, Morphology, and Function: A Review (2015) (138)
Multivariate Genetic Analysis of Brain Structure in an Extended Twin Design (2000) (136)
Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus. (2013) (136)
A longitudinal twin study on IQ, executive functioning, and attention problems during childhood and early adolescence. (2006) (136)
The flexible mind is associated with the catechol-O-methyltransferase (COMT) Val158Met polymorphism: Evidence for a role of dopamine in the control of task-switching (2010) (132)
Functional Gene Group Analysis Reveals a Role of Synaptic Heterotrimeric G Proteins in Cognitive Ability (2010) (132)
Phenotypic Complexity, Measurement Bias, and Poor Phenotypic Resolution Contribute to the Missing Heritability Problem in Genetic Association Studies (2010) (127)
De Novo Coding Variants Are Strongly Associated with Tourette Disorder (2017) (125)
A Note on False Positives and Power in G × E Modelling of Twin Data (2011) (124)
Event-related alpha and theta responses in a visuo-spatial working memory task (2002) (124)
Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. (2015) (123)
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome (2016) (123)
Heritability and stability of resting blood pressure. (2005) (122)
The relation between frontal EEG asymmetry and the risk for anxiety and depression (2007) (119)
A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric Cohorts. (2016) (118)
Translating genome-wide association findings into new therapeutics for psychiatry (2016) (113)
The co-occurrence of autistic and ADHD dimensions in adults: an etiological study in 17 770 twins (2014) (110)
Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study. (2014) (109)
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia (2017) (107)
Heritability of Ambulatory Heart Rate Variability (2004) (106)
Twin–singleton differences in intelligence? (2000) (105)
Genome-wide association study of Tourette Syndrome (2012) (102)
Brain Plasticity and Intellectual Ability Are Influenced by Shared Genes (2010) (100)
Specific glial functions contribute to schizophrenia susceptibility. (2014) (100)
The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls (2018) (99)
The ongoing adaptive evolution of ASPM and Microcephalin is not explained by increased intelligence. (2007) (99)
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine (2015) (98)
Genome-wide association study of exercise behavior in Dutch and American adults. (2009) (97)
Endophenotypes in a Dynamically Connected Brain (2010) (96)
Association of Genetic Liability to Psychotic Experiences With Neuropsychotic Disorders and Traits (2019) (95)
ADHD: Sibling Interaction or Dominance: An Evaluation of Statistical Power (2003) (95)
The SNAP-25 gene is associated with cognitive ability: evidence from a family-based study in two independent Dutch cohorts (2006) (95)
Complement genes contribute sex-biased vulnerability in diverse illnesses (2020) (92)
The Heritability of Aptitude and Exceptional Talent Across Different Domains in Adolescents and Young Adults (2009) (89)
Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium (2017) (87)
Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores (2021) (85)
The Biological Contributions to Gender Identity and Gender Diversity: Bringing Data to the Table (2018) (85)
What have we learned from recent twin studies about the etiology of neurodevelopmental disorders? (2013) (82)
Genetic analyses of the stability of executive functioning during childhood (2007) (81)
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals (2022) (80)
Environmental factors determine where the Dutch live: results from the Netherlands twin register. (2005) (80)
Genetic mapping and evolutionary analysis of human-expanded cognitive networks (2019) (80)
Dissecting the genetic relationship between cardiovascular risk factors and Alzheimer’s disease (2018) (79)
Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls (2018) (77)
A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity (2019) (77)
Linkage analysis of smoking initiation and quantity in Dutch sibling pairs (2004) (77)
Sex differences on the Dutch WAIS-III (2006) (76)
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis (2018) (74)
Additive genetic variation in schizophrenia risk is shared by populations of African and European descent. (2013) (74)
Incidental Findings on Brain Imaging in the General Pediatric Population. (2017) (73)
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci (2019) (72)
Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank (2019) (72)
Power in GWAS: lifting the curse of the clinical cut-off (2013) (70)
FUMA: Functional mapping and annotation of genetic associations (2017) (70)
Genetic Regulation of Growth in Height and Weight from 3 to 12 Years of Age: A Longitudinal Study of Dutch Twin Children (2007) (70)
Attention problems, inhibitory control, and intelligence index overlapping genetic factors: a study in 9-, 12-, and 18-year-old twins. (2009) (69)
Genetic contributions to the association between height and intelligence: evidence from Dutch twin data from childhood to middle age (2006) (68)
A Twin Study of the Genetics of High Cognitive Ability Selected from 11,000 Twin Pairs in Six Studies from Four Countries (2009) (68)
Associations of autozygosity with a broad range of human phenotypes (2019) (68)
Modeling psychiatric disorders: from genomic findings to cellular phenotypes (2016) (67)
Gene-Environment Interaction in Adults’ IQ Scores: Measures of Past and Present Environment (2008) (65)
A saturated map of common genetic variants associated with human height (2022) (65)
New insights on the genetic etiology of Alzheimer’s and related dementia (2020) (64)
Polygenic scores for schizophrenia and educational attainment are associated with behavioural problems in early childhood in the general population (2018) (62)
Association between the CHRM2 gene and intelligence in a sample of 304 Dutch families (2006) (62)
Common variants underlying cognitive ability: further evidence for association between the SNAP‐25 gene and cognition using a family‐based study in two independent Dutch cohorts (2008) (61)
Sexual dimorphism in innate immunity. (2002) (61)
Catechol O-methyl transferase and dopamine D2 receptor gene polymorphisms: evidence of positive heterosis and gene–gene interaction on working memory functioning (2008) (61)
The phenotypic and genotypic relation between working memory speed and capacity (2006) (60)
Genetic analysis of IQ, processing speed and stimulus-response incongruency effects (2002) (60)
An epigenome-wide association study meta-analysis of educational attainment (2017) (60)
A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts (2020) (60)
Fifty Years of Twin Studies : A Meta-Analysis of the Heritability of Human Traits (2015) (59)
Comparing Blood Pressure of Twins and Their Singleton Siblings: Being a Twin Does Not Affect Adult Blood Pressure (2001) (59)
Genetic influences on ‘environmental’ factors (2010) (59)
Association between obesity and asthma in a twin cohort (2007) (58)
Heritability of reproductive hormones in adult male twins. (2007) (58)
Reconsidering the Heritability of Intelligence in Adulthood: Taking Assortative Mating and Cultural Transmission into Account (2011) (58)
New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. (2015) (58)
Attentional switching forms a genetic link between attention problems and autistic traits in adults (2012) (58)
A genetic analysis of ambulatory cardiorespiratory coupling. (2005) (57)
Genetic components of functional connectivity in the brain: The heritability of synchronization likelihood (2005) (57)
GWAS Meta-Analysis of Neuroticism (N=449,484) Identifies Novel Genetic Loci and Pathways (2017) (56)
Perceptual speed does not cause intelligence, and intelligence does not cause perceptual speed (2005) (56)
Twin-singleton differences in brain structure using structural equation modelling. (2002) (54)
An integrated framework for local genetic correlation analysis (2021) (53)
Conditional and interaction gene-set analysis reveals novel functional pathways for blood pressure (2018) (53)
Genetic association signal near NTN4 in Tourette syndrome (2014) (51)
Statistical Power to Detect Genetic Loci Affecting Environmental Sensitivity (2010) (51)
Netherlands Twin Register: From Twins to Twin Families (2006) (51)
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families (2018) (50)
Erratum: Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence (2017) (50)
Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia (2017) (48)
MIR137 schizophrenia-associated locus controls synaptic function by regulating synaptogenesis, synapse maturation and synaptic transmission (2018) (48)
Exploring the functional role of the CHRM2 gene in human cognition: results from a dense genotyping and brain expression study (2007) (47)
Genome-wide linkage scan for exercise participation in Dutch sibling pairs (2007) (47)
Biological annotation of genetic loci associated with intelligence in a meta-analysis of 87,740 individuals (2019) (47)
Meta-analysis of four new genome scans for lipid parameters and analysis of positional candidates in positive linkage regions (2005) (47)
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depressive disorder (2017) (47)
Progress in the Molecular-Genetic Study of Intelligence (2006) (45)
Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women. (2016) (45)
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use (2019) (45)
A global overview of pleiotropy and genetic architecture in complex traits (2019) (44)
Genetic Analyses of Teacher Ratings of Problem Behavior in 5-Year-Old Twins (2006) (44)
Imaging the genetics of brain structure and function (2008) (43)
Genetic meta-analysis identifies 9 novel loci and functional pathways for Alzheimer’s disease risk (2018) (41)
Genetic Linkage and Association Analysis for Loneliness in Dutch Twin and Sibling Pairs Points to a Region on Chromosome 12q23–24 (2006) (41)
Linkage on chromosome 14 in a genome-wide linkage study of a broad anxiety phenotype (2008) (41)
Mx Scripts Library: Structural Equation Modeling Scripts for Twin and Family Data (2005) (41)
Genetic Influences Are Virtually Absent for Trust (2014) (40)
Joint reanalysis of 29 correlated SNPs supports the role of PCLO/Piccolo as a causal risk factor for major depressive disorder (2009) (39)
MGAS: a powerful tool for multivariate gene-based genome-wide association analysis (2014) (39)
Sex differences on the WISC-R in Belgium and The Netherlands (2008) (39)
Do twins have lower cognitive ability than singletons (2008) (39)
Association of polygenic score for major depression with response to lithium in patients with bipolar disorder (2020) (37)
Genetically-Informed Patient Selection for iPSC Studies of Complex Diseases May Aid in Reducing Cellular Heterogeneity (2017) (37)
Genetic and Environmental Factors Affecting Self-Rated Health from Age 16–25: A Longitudinal Study of Finnish Twins (2007) (37)
Meta‐analysis of the serotonin transporter promoter variant (5‐HTTLPR) in relation to adverse environment and antisocial behavior (2016) (36)
Genome-wide Analysis of Insomnia (N=1,331,010) Identifies Novel Loci and Functional Pathways (2018) (35)
QTLs for height: results of a full genome scan in Dutch sibling pairs (2004) (34)
Cortical thickness and inattention/hyperactivity symptoms in young children: a population-based study (2014) (34)
Heritability and Stability of Resting Blood Pressure (2005) (33)
Genome-wide association study of obsessive-compulsive disorder (2013) (33)
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use (2019) (33)
Combined Linkage and Association Tests in Mx (2004) (32)
Functional mapping and annotation of genetic associations with FUMA (2017) (32)
Genome-wide Linkage Scan to Identify Loci for Age at First Cigarette in Dutch Sibling Pairs (2006) (32)
Psychiatric Polygenic Risk Scores as Predictor for Attention Deficit/Hyperactivity Disorder and Autism Spectrum Disorder in a Clinical Child and Adolescent Sample (2019) (32)
Largest GWAS (N=1,126,563) of Alzheimer's Disease Implicates Microglia and Immune Cells (2020) (32)
Genome-wide meta-analysis of brain volume identifies genomic loci and genes shared with intelligence (2020) (31)
A polygenic resilience score moderates the genetic risk for schizophrenia (2019) (31)
GWAS meta-analysis (N=279,930) identifies new genes and functional links to intelligence (2017) (31)
Detecting genotype-environment interaction in monozygotic twin data: comparing the Jinks and Fulker test and a new test based on Marginal Maximum Likelihood estimation. (2006) (30)
Gene-set analysis shows association between FMRP targets and autism spectrum disorder (2017) (30)
Common Polygenic Variations for Psychiatric Disorders and Cognition in Relation to Brain Morphology in the General Pediatric Population. (2019) (30)
Common variants in Alzheimer’s disease: Novel association of six genetic variants with AD and risk stratification by polygenic risk scores (2019) (30)
Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS (2017) (29)
Replicated Linkage for Eye Color on 15q Using Comparative Ratings of Sibling Pairs (2006) (29)
Blood sample stability at room temperature for counting red and white blood cells and platelets. (2002) (29)
Power Calculations Using Exact Data Simulation: A Useful Tool for Genetic Study Designs (2007) (29)
Gene expression in major depressive disorder. (2016) (28)
Myelination-related genes are associated with decreased white matter integrity in schizophrenia (2015) (26)
Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium (2018) (26)
Genetic contributions to anatomical, behavioral and neurophysiological indices of cognition (2002) (26)
A General Test for Gene–Environment Interaction in Sib Pair-based Association Analysis of Quantitative Traits (2008) (25)
Emerging Methods and Resources for Biological Interrogation of Neuropsychiatric Polygenic Signal (2020) (25)
The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: Evidence from a large collaborative study totaling 4,963 Subjects (2010) (25)
Complement genes contribute sex-biased vulnerability in diverse disorders (2020) (25)
Genetic Contribution to the P3 in Young and Middle-Aged Adults (2007) (24)
Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia (2022) (24)
Author Correction: GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal effect of schizophrenia liability (2019) (24)
Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache (2020) (23)
Involvement of astrocyte metabolic coupling in Tourette syndrome pathogenesis (2015) (23)
Schizophrenia and a high-resolution map of the three-dimensional chromatin interactome of adult and fetal cortex (2018) (23)
Genome-wide association study identifies 30 loci associated with bipolar disorder (2019) (22)
Genome-wide study identifies 611 loci associated with risk tolerance and risky behaviors (2018) (21)
Multivariate Genetic Analysis (2009) (20)
Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression (2020) (20)
FADS2 Genetic Variance in Combination with Fatty Acid Intake Might Alter Composition of the Fatty Acids in Brain (2013) (20)
Biological pathways and networks implicated in psychiatric disorders (2015) (20)
Genome-wide Association Study of Exercise Behavior in Dutch (2011) (20)
Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Nature Genetics (2010) 42 (105-116)) (2010) (20)
A Functional Polymorphism under Positive Evolutionary Selection in ADRB2 is Associated with Human Intelligence with Opposite Effects in the Young and the Elderly (2009) (20)
EXOME SEQUENCING IN BIPOLAR DISORDER REVEALS SHARED RISK GENE AKAP11 WITH SCHIZOPHRENIA (2021) (19)
Genetic correlation of antisocial behaviour with alcohol, nicotine, and cannabis use. (2018) (19)
Association of Genetic Risk for Schizophrenia and Bipolar Disorder With Infant Neuromotor Development (2018) (19)
Genetic Correlations Between Brain Volumes and the WAIS-III Dimensions of Verbal Comprehension, Working Memory, Perceptual Organization, and Processing Speed (2003) (18)
Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank (2019) (18)
Gyrification differences in children and adolescents with velocardiofacial syndrome and attention-deficit/hyperactivity disorder: A pilot study (2014) (18)
Higher Polygenetic Predisposition for Asthma in Cow’s Milk Allergic Children (2018) (18)
Heritability of anterior and posterior visual N1. (2007) (18)
Genome-Wide Scan for Blood Pressure in Australian and Dutch Subjects Suggests Linkage at 5P, 14Q, and 17P (2007) (18)
A whole-genome scan for 24-hour respiration rate: a major locus at 10q26 influences respiration during sleep. (2005) (17)
Majority of human traits do not show evidence for sex-specific genetic and environmental effects (2017) (17)
Core dimensions of personality broadly account for the link from perceived social support to symptoms of depression and anxiety. (2014) (17)
Combined cellomics and proteomics analysis reveals shared neuronal morphology and molecular pathway phenotypes for multiple schizophrenia risk genes (2019) (16)
Sex differences in adults' motivation to achieve (2010) (16)
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder (2021) (16)
Life events moderate variation in cognitive ability (g) in adults (2011) (15)
Global similarity with local differences in linkage disequilibrium between the Dutch and HapMap–CEU populations (2009) (15)
Genome-wide association analysis of lifetime cannabis use (N=184,765) identifies new risk loci, genetic overlap with mental health, and a causal influence of schizophrenia on cannabis use (2018) (15)
Model-based assessment of replicability for genome-wide association meta-analysis (2021) (15)
Combined association and linkage analysis applied to the APOE locus (2004) (15)
JAG: A Computational Tool to Evaluate the Role of Gene-Sets in Complex Traits (2015) (15)
Gamma frailty model for linkage analysis with application to interval-censored migraine data. (2008) (14)
Genome-wide association study of pediatric obsessive-compulsive traits: shared genetic risk between traits and disorder (2019) (14)
Human cytokine response to ex vivo amyloid-beta stimulation is mediated by genetic factors. (2005) (14)
Statistical testing in transcriptomic‐neuroimaging studies: A how‐to and evaluation of methods assessing spatial and gene specificity (2021) (14)
Exploring the genetic correlations of antisocial behaviour and life history traits (2018) (14)
Generation of Isogenic Controls for In Vitro Disease Modelling of X-Chromosomal Disorders (2018) (13)
Further Evidence for a QTL Influencing Body Mass Index on Chromosome 7p from a Genome-wide Scan in Dutch Families (2004) (13)
Involvement of astrocyte and oligodendrocyte gene sets in migraine (2016) (13)
Further evidence for a QTL influencing body mass index on chromosome 7p from a genome-wide scan in Dutch families. (2004) (13)
Sex differences and gender‐invariance of mother‐reported childhood problem behavior (2017) (13)
Functional characterization of the PCLO p.Ser4814Ala variant associated with major depressive disorder reveals cellular but not behavioral differences (2015) (13)
Polygenic Scores for Neuropsychiatric Traits and White Matter Microstructure in the Pediatric Population. (2019) (13)
Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways (2022) (12)
A response to Yurko et al: H-MAGMA, inheriting a shaky statistical foundation, yields excess false positives (2020) (12)
Individual Differences in Processing Speed and Working Memory Speed as Assessed with the Sternberg Memory Scanning Task (2009) (12)
Twins and the fetal origins hypothesis: an application to growth data (2005) (11)
Functional Gene-Set Analysis Does Not Support a Major Role for Synaptic Function in Attention Deficit/Hyperactivity Disorder (ADHD) (2014) (11)
Quantitative proteomic analysis of Rett iPSC-derived neuronal progenitors (2020) (11)
Phenotypic and genetic correlations between evoked EEG/ERP measures during the response anticipation period of a delayed response task. (2009) (10)
Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers (2022) (10)
Supporting the generalist genes hypothesis for intellectual ability/disability: the case of SNAP25 (2012) (10)
Exploring the role of low-frequency and rare exonic variants in alcohol and tobacco use. (2018) (10)
Erratum: Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families (Neuron (2018) 98(4) (743–753.e4), (S0896627318303222) (10.1016/j.neuron.2018.04.014)) (2018) (9)
A Population-Based Imaging Genetics Study of Inattention/Hyperactivity: Basal Ganglia and Genetic Pathways. (2015) (9)
Degree of genetic liability for Alzheimer's disease associated with specific proteomic profiles in cerebrospinal fluid (2020) (9)
A Longitudinal Genetic Study of Vocabulary Knowledge in Adults (2004) (9)
Genetic Variation and Cognitive Ability (2002) (9)
Understanding the assumptions underlying Mendelian randomization (2021) (8)
A longitudinal genetic study of vocabulary knowledge in adults. (2004) (8)
Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes (2021) (8)
17 FUMA: FUNCTIONAL MAPPING AND ANNOTATION OF GENETIC ASSOCIATIONS (2019) (8)
Author Correction: Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk (2020) (8)
Cortical morphology as a shared neurobiological substrate of attention-deficit/hyperactivity symptoms and executive functioning: a population-based pediatric neuroimaging study (2017) (8)
Testing replication of a 5-SNP set for general cognitive ability in six population samples (2008) (7)
Erratum: Modeling psychiatric disorders: from genomic findings to cellular phenotypes (2016) (7)
Genome-wide gene-environment interactions in neuroticism: an exploratory study across 25 environments (2021) (7)
Correction: Genome-wide analysis reveals extensive genetic overlap between schizophrenia, bipolar disorder, and intelligence (2019) (7)
Introduction to the Special Issue: Human Linkage Studies for Behavioral Traits (2006) (7)
Elevated Common Variant Genetic Risk for Tourette Syndrome in a Densely Affected Pedigree (2021) (7)
The Biological Contributions to Gender Identity and Gender Diversity: Bringing Data to the Table (2018) (7)
Genome-wide association study identifies new locus associated with OCD (2021) (7)
Interaction Between Experience Seeking and Genetic and Environmental Influences on General Cognitive Ability (2012) (6)
Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls – CORRIGENDUM (2018) (6)
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) (6)
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) (6)
Genomics of Alzheimer’s disease (2020) (6)
Genes Encoding Heterotrimeric G-proteins Are Associated with Gray Matter Volume Variations in the Medial Frontal Cortex (2012) (6)
High Performance Vehicle Chassis Structure for NVH Reduction (2006) (5)
Single Locus Association Models (2007) (5)
Exploring the genetic overlap between twelve psychiatric disorders (2022) (5)
Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms (2020) (5)
Additive Genetic Variance (2005) (5)
Eating Disorder Working Group of the PGC , Major Depressive Disorder Working Group of the PGC , Obsessive Compulsive Disorders and Tourette Syndrome Working Group of the PGC , Schizophrenia CLOZUK , Substance Use Disorder Working Group of the PGC (2018) (4)
Uncovering the Genetic Architecture of Broad Antisocial Behavior through a Genome-Wide Association Study Meta-analysis (2021) (4)
Multivariate Gene-Based Association Test on Family Data in MGAS (2016) (4)
Functional consequences of genetic loci associated with intelligence in a meta-analysis of 87,740 individuals (2017) (4)
GWAS of brain volume on 54,407 individuals and cross-trait analysis with intelligence identifies shared genomic loci and genes (2019) (4)
Brain Imaging and Cognition (2014) (4)
On the interpretation of transcriptome-wide association studies (2021) (4)
Genetic association study of psychotic experiences in UK Biobank (2019) (4)
Functional Gene Group Analysis Indicates No Role for Heterotrimeric G Proteins in Cognitive Ability (2014) (4)
Environmental Factors Determine Where the Dutch Live: Results From the Netherlands Twin Register (2005) (4)
Erratum: Common genetic variants associated with cognitive performance identified using the proxy-phenotype method (Proc Natl Acad Sci USA (2014) 111 (13790-13794) DOI: 10.1073/pnas.1404623111) (2015) (4)
Adding non-twin siblings to increase statistical power (1999) (3)
Family-based association approach provides further evidence for a role of the CHRM2 gene in cognition. (2006) (3)
An epigenome-wide association study of educational attainment (n = 10,767) (2017) (3)
Author Correction: A global overview of pleiotropy and genetic architecture in complex traits (2020) (3)
Demystifying non-coding GWAS variants: an overview of computational tools and methods (2022) (3)
A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank (2020) (3)
A Note on False Positives and Power in G × E Modelling of Twin Data (2011) (3)
Large-scale genetic study of risk tolerance and risky behaviors identifies new loci and reveals shared genetic influences (2017) (3)
Twin–singleton di fferences in intel l igence? (2007) (3)
Systematic assessment of variability in the proteome of iPSC derivatives. (2021) (3)
Author Correction: Genetic mapping of cell type specificity for complex traits (2020) (3)
Disentangling genetic and assortative mating effects on autistic traits: an extended twin family study in adults (2010) (3)
14GENETIC META-ANALYSIS IDENTIFIES 9 NOVEL LOCI AND FUNCTIONAL PATHWAYS FOR ALZHEIMER'S DISEASE RISK (2019) (3)
The more the merrier? Multivariate approaches to genome-wide association analysis (2019) (3)
Exploring the genetic overlap between 12 psychiatric disorders (2022) (3)
Human Cytokine Response to ex vivo Amyloid-β Stimulation is Mediated by Genetic Factors (2005) (3)
Lipid associated polygenic enrichment in Alzheimer’s disease (2018) (3)
Statistical testing in gene transcriptomic-neuroimaging associations: an evaluation of methods that assess spatial and gene specificity (2021) (3)
Data Related to Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use (2019) (3)
Molecular Signatures and Cellular Diversity During Mouse Habenula Development (2022) (2)
Imaging genetics & cognition: A pilot study involving the CHRM2 and SNAP-25 genes (2007) (2)
Testing replication of a 5-SNP set for general cognitive ability in six population samples (2008) (2)
Genome-wide meta-analysis of insomnia in over 2.3 million individuals indicates involvement of specific biological pathways through gene-prioritization (2020) (2)
Polygenic resilience scores capture protective genetic effects for Alzheimer’s disease (2022) (2)
Planar cell polarity pathway and development of the human visual cortex (2018) (2)
Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (2)
Association between apoE genotype, apoE-levels and cognitive performance (1999) (2)
Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS (2018) (2)
Correction to: Genome-wide gene-environment interactions in neuroticism: an exploratory study across 25 environments (2021) (2)
Gene Mapping Through Linkage and Association (2007) (2)
Exploring the genetic correlations of antisocial behavior and life history traits (2018) (2)
Gene expression imputation provides insight into the genetic architecture of frontotemporal dementia (2020) (2)
Phenotypic and genetic association between attention problems and autistic traits in adults is mainly mediated by attentional switching ability (2012) (2)
Quantitative genetic modelling of variation in the dynamics of human brain morphology: a longitudinal study in monozygotic and dizygotic twins and their siblings. (2004) (2)
Heritability of "small world'' architecture of functional brain connectivity. (2006) (2)
Genetics of loneliness: a study from the Netherlands Twin Register. (2004) (2)
Genes and behavior: A twin study of Executive functioning, IQ and attention problems in childhood and early adolescence. (2006) (2)
Specificity and overlap in the genetic architectures of functional and structural connectivity within cerebral resting-state networks (2022) (2)
Quantitative proteomic alterations of human iPSC-based neuronal development indicate early onset of Rett syndrome (2019) (2)
Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease (2022) (2)
A genome-wide association study for educational attainment. (2008) (2)
Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease (2021) (1)
Can the comorbidity of physical inactivity and cardiovascular risk factors help us find genes (2004) (1)
Using Gene-Set Analysis To Gain Biological Knowledge Based On GWAS Results (2019) (1)
What Twin Studies Tell Us About the Heritability of Brain Development, Morphology, and Function: A Review (2015) (1)
The genetic liability for insomnia is associated with lower amount of slow wave sleep in young and healthy individuals (2018) (1)
Correction: Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank (2020) (1)
The Establishment of a Biobank: Experiences of the Netherlands Twin Register (2004) (1)
Full genome scans for cognition in Dutch and Australian samples. (2004) (1)
Using genome-wide association results to identify drug repurposing candidates (2022) (1)
Gene finding for intelligence (2005) (1)
Theory and Practice in Quantitative Genetics (2003) (1)
Modeling GxE with categorical moderators in the presence of dominance (2007) (1)
Genome-wide association studies of polygenic risk score-derived phenotypes may lead to inflated false positive rates (2022) (1)
Exome chip meta-analysis elucidates the genetic architecture of rare coding variants in smoking and drinking behavior (2017) (1)
Increased coherence during visuospatial rehearsal: genes or environment? (2000) (1)
Genes and Intelligence (2013) (1)
Psychiatric Polygenic Risk Scores as Predictor for Attention Deficit/Hyperactivity Disorder and Autism Spectrum Disorder in a Clinical Child and Adolescent Sample (2019) (1)
Genome-wide association study for leisure-time exercise behavior (2008) (1)
Author Correction: Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk (2020) (1)
Genetics of smoking and nicotine dependence. (2004) (1)
Statistical testing and annotation of gene transcriptomic-neuroimaging associations (1)
Life events moderate variation in cognitive ability (g) in adults (2010) (1)
Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes (2017) (1)
Author Correction: Majority of human traits do not show evidence for sex-specific genetic and environmental effects (2018) (1)
Genetic correlation between inspection time and IQ (2001) (1)
Birth weight and tracking of blood pressure: A 15 year follow-up study of Dutch adolescents (2001) (1)
Intelligence and peak EEG alpha frequency (2000) (1)
A note on permutation tests for genetic association analysis of quantitative traits when variances are heterogeneous (2009) (1)
Are SNPs associated with educational attainment also associated with cognitive function (2013) (1)
Erratum: Testing replication of a 5-SNP set for general cognitive ability in six population samples (European Journal of Human Genetics (2008) 10.1038/ejhg.2008.100) (2008) (1)
Association between APOE genotype and cognitive functioning in adult twins (1999) (1)
Intelligence and the ‘Intelligence Quotient’ (2013) (0)
Author Correction: Majority of human traits do not show evidence for sex-specific genetic and environmental effects (2018) (0)
65. CURRENT ETHICAL AND SOCIETAL CHALLENGES WE ARE FACING AS A RESULT OF THE CURRENT STATE OF THE ART OF GWAS (2022) (0)
Are faster brains also smarter (2001) (0)
Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns (2019) (0)
SU92GENERAL COMMON POLYGENIC RISK IN PSYCHIATRIC DISORDERS (2019) (0)
Generation of Isogenic Controls for In Vitro Disease Modelling of X-Chromosomal Disorders (2018) (0)
50th European Mathematical Genetics Meeting (EMGM) 2022 (2022) (0)
Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (0)
PGC Data Access Committee: Methods To Access PGC Data (2019) (0)
Endophenotypes for cognitive ability. (2006) (0)
Spatial and temporal structure of resting state EEG: Development and (genetic) stability (2009) (0)
DIFFERENTIAL EXPRESSION OF POLYGENIC RISK IN CEREBROSPINAL FLUID PROTEOMIC MEASURES IN ALZHEIMER’S DISEASE (2019) (0)
THE STATISTICAL PROPERTIES OF GENE-SET ANALYSIS FOR GWAS DATA (2017) (0)
Exploring EEG coherence during working memory as intermediate phenotype for linkage analysis (2000) (0)
SU86GENETIC INFLUENCES ON EIGHT PSYCHIATRIC DISORDERS BASED ON FAMILY DATA OF 4,408,646 FULL AND HALF SIBLINGS, AND GENETIC DATA OF 333,748 CASES AND CONTROLS (2019) (0)
GENETIC RISK ACROSS DOMAINS: GENOME-WIDE ANALYSIS OF INSOMNIA AND SLEEP-RELATED TRAITS IN OVER 2 MILLION INDIVIDUALS IDENTIFIES METABOLIC AND PSYCHIATRIC LINKS, AS WELL AS NOVEL LOCI, GENES, AND CELL TYPES (2019) (0)
The use of hybrid statistical models to chart the heterogeneity of internalizing problem behavior in child- and adolescent psychiatric patients (2013) (0)
GWAS: pathways/networks/multilocus analyses (2011) (0)
65GENOME-WIDE ANALYSIS OF INSOMNIA AND SLEEP-RELATED TRAITS IN OVER 1 MILLION INDIVIDUALS IDENTIFIES NOVEL GENES AND PATHWAYS (2019) (0)
Title : Gene-based association studies report four novel 1 genes in the etiology of clinical subtypes of 2 frontotemporal dementia 3 (2016) (0)
Reconsidering the Heritability of Intelligence in Adulthood: Taking Assortative Mating and Cultural Transmission into Account (2011) (0)
Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores (2023) (0)
Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways (2018) (0)
Genetic contribution to the tracking of blood pressure: 10-year follow-up of adolescent Dutch twins (2002) (0)
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture ofmajor depressive disorder (2018) (0)
Systematic Assessment of Variability in the Proteome of iPSC Derivatives (2021) (0)
Majority of human traits do not show evidence for sex-specific genetic and environmental effects (2017) (0)
Predicting resting blood pressure from cardiovascular stress reactivity over a 10 year follow-up period: No can do (2003) (0)
Linkage of the APOE locus with ApoE plasma levels in adolescent Dutch twins is completely explained by the APOE e2/e3/e4 alleles (2002) (0)
Development of brain organization: heritability and stability across the life span (2009) (0)
Current status of the migraine research in GenomEUtwin. (2004) (0)
Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome (2022) (0)
F85COMMON POLYGENIC VARIATIONS FOR PSYCHIATRIC DISORDERS AND COGNITION IN RELATION TO BRAIN MORPHOLOGY IN THE GENERAL PEDIATRIC POPULATION (2019) (0)
Genetics of Smoking and Nicotine Dependence - Session: Genetics of Nicotine Dependence (Symposium) (2004) (0)
Gene-based analysis detects novel loci associated with frontotemporal dementia and its clinical subtypes (2016) (0)
Genetic Enhancement of Human Beings: Reality or Fiction? (2013) (0)
Combining linkage scans from different samples: full genome scans for cognitive ability in Dutch and Australian samples. (2004) (0)
Sample stability and agreement of data after storage of blood for white blood cell count and differentials (2001) (0)
Local genetic correlation analysis links depression with molecular and brain imaging endophenotypes (2023) (0)
Running Head : GWAS Meta-Analysis of Alzheimer ’ s Disease 1 Genetic meta-analysis identifies 9 novel loci and functional pathways for Alzheimer ’ s disease risk (2019) (0)
Quantitative proteomic analysis shows alterations in patient Rett syndrome iPSC cultures at early neuronal progenitor stages (2020) (0)
Translating Genomewide Association Findings into New Therapeutics for Psychiatry 1 (2016) (0)
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals (2018) (0)
61ITEM-LEVEL STUDY OF NEUROTICISM REVEALS GENETIC HETEROGENEITY (2019) (0)
LOCAL GENETIC SEX DIFFERENCES IN QUANTITATIVE TRAITS (2022) (0)
Author Correction: GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal effect of schizophrenia liability (2019) (0)
Multivariate Linkage Methodology: An Application to Endophenotypes of Cardiovascular Disease (2004) (0)
SU27A GLOBAL VIEW OF GENETIC ARCHITECTURE AND PLEIOTROPY IN HUMAN COMPLEX TRAITS (2019) (0)
Correction: Genome-wide gene-environment interactions in neuroticism: an exploratory study across 25 environments (2022) (0)
Memories are made of THis (2000) (0)
Influence of autozygosity on common disease risk across the phenotypic spectrum (2023) (0)
Conditional and interaction gene-set analysis reveals novel functional pathways for blood pressure (2018) (0)
Our faces and brains (2021) (0)
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression (2018) (0)
Insights in the genetic architecture of impulsivity in mice (2012) (0)
Detecting Genotype–Environment Interaction in Monozygotic Twin Data: Comparing the Jinks and Fulker Test and a New Test Based on Marginal Maximum Likelihood Estimation (2006) (0)
Genetic associations between Attention, IQ and the Stroop effect during childhood (2007) (0)
Item-level analyses reveal genetic heterogeneity in neuroticism (2018) (0)
T82. RARE VARIANT AGGREGATION IN 148,508 EXOMES IDENTIFIES GENES ASSOCIATED WITH PROXY ALZHEIMER'S DISEASE/DEMENTIA (2022) (0)
S0033291718002039jra 1166..1173 (2019) (0)
Genetic variation in brain function (2002) (0)
Genome-wide association study of cerebellar volume provides insights into heritable mechanisms underlying brain development and mental health (2022) (0)
T15. DECODING GWAS SIGNALS: AN INTEGRATIVE METHOD FOR GENE PRIORITIZATION (2022) (0)
Genetic correlates of evolutionary adaptations in cognitive functional brain networks and their relationship to human cognitive functioning and disease (2019) (0)
UPDATE ON THE ANALYSES OF THE LARGEST BIPOLAR CASE-CONTROL EXOME SEQUENCING DATASET TO DATE (2019) (0)
A psychometric approach to gene-finding for complex traits (2009) (0)
13. DISTINGUISHING DIFFERENT PSYCHIATRIC DISORDERS USING DDX-PRS (2022) (0)
Importance of psychophysiolology for gene hunting (2000) (0)
Brain and cognition (2003) (0)
TU89. INVESTIGATING GENETIC HETEROGENEITY OF ALCOHOL MISUSE THROUGH THE LENS OF AN INTERNALIZING/EXTERNALIZING TYPOLOGY (2021) (0)
Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity (2020) (0)
S.10.01 MRI and GWAS reveal emotion regulation key to the biology of insomnia (2019) (0)
Abundant pleiotropy across neuroimaging modalities identified through a multivariate genome-wide association study (2022) (0)
Erratum: Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS (Scientific reports (2017) 7 1 (8899)) (2018) (0)
37 CONTRIBUTIONS OF COPY NUMBER VARIANTS TO HUMAN COMPLEX TRAITS (2019) (0)
Associated genetics and connectomic circuitry in schizophrenia and bipolar disorder (2022) (0)
Disentangling Genetic Risks for Metabolic Syndrome. (2022) (0)
295 GENETIC LINKAGE ANALYSIS AND META ANALYSIS OF STIMULATED CYTOKINE LEVELS IN DUTCH FAMILY BASED STUDIES (2007) (0)
50 FUNCTIONAL CONSEQUENCES OF GENETIC LOCI ASSOCIATED WITH IQ IN A META-ANALYSIS OF 87,740 INDIVIDUALS (2019) (0)
Multivariate linkage analysis: An application to endophenotypes of cardiovascular disease (2004) (0)
Collaborative projects making use of the MDD – GAIN data (2008) (0)
Heritability of the N1 in a visual oddball task. (2006) (0)
Examining the shared genetic architecture of risk tolerance and related behaviors (2017) (0)
SA72A HIGH-RESOLUTION MAP OF CHROMATIN INTERACTIONS IN ADULT AND FETAL CORTEX (2019) (0)
Genetic contribution to blood pressure: heritability and linkage results from Dutch twin and sibling pairs. (2004) (0)
Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk (2019) (0)
Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms (2020) (0)
A genetic basis for high-speed memory scanning (2007) (0)
F27GENE EXPRESSION DEPENDENCY AND INTERACTION OF FUNCTIONAL ANNOTATION IN GWAS (2019) (0)
Improved functional mapping with GSA-MiXeR implicates biologically specific gene-sets and estimates enrichment magnitude (2022) (0)
CORRECT FOR POPULATION STRATIFICATION USING DEEP NEURAL NETWORKS (2022) (0)
Linkage analysis of smoking initiation and quantity in Dutch sibling pairs (2004) (0)
INTRODUCTION TO GWAS (2021) (0)
Education, Religion, and Prosociality: A Study of Identical Twins (2016) (0)
Rare variant aggregation in 148,508 exomes identifies genes associated with proxy dementia (2023) (0)
14. DECOMPOSING GENETIC CORRELATIONS (2022) (0)
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence (2018) (0)
GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal effect of schizophrenia liability (2018) (0)
Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder (2021) (0)
A large-scale search for genes underlying behavior, cognition and depression. (2004) (0)
De Rubeis et al., Neuron, S1 (Supplemental Experimental Procedures and Figures S1–S6) (2015) (0)
Author Correction: Genome-wide meta-analysis of brain volume identifies genomic loci and genes shared with intelligence (2022) (0)
15. PREDICTING AN INDIVIDUAL'S DISORDER PROBABILITY WITH A WELL-CALIBRATED POLYGENIC RISK SCORE (2022) (0)
Genome-wide association study of cerebellar volume (2021) (0)
Sexual dimorphism in and HLA region influence on innate immunity (2002) (0)
Association between the SNAP-25 gene and attention in a twin sample (2007) (0)
Author Correction: Genetic mapping of cell type specificity for complex traits (2020) (0)
Correction (2019) (0)
Identification of common genetic risk variants for autism spectrum disorder (2019) (0)
Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS (2018) (0)
A genome-wide linkage scan for wellbeing. (2008) (0)
Genetically identical but cognitively different: twins discordant for migraine (2002) (0)
TH37. THE GENETIC ARCHITECTURE OF CEREBELLAR VOLUME (2021) (0)
Rare Variant Aggregation in 148,508 Exomes Identifies Genes Associated with Proxy Alzheimer's Disease (2021) (0)
F81A MENDELIAN RANDOMIZATION APPROACH TOWARDS MODEL SELECTION: STUDYING THE NATURE OF THE RELATIONS BETWEEN NEUROTICISM SYMPTOMS (2019) (0)
Genetic correlates of intelligence (2002) (0)
ASSOCIATION OF CSF TAU WITH HYPERPLASTICITY IN ALZHEIMER’S DISEASE (2019) (0)
ESTABLISHING THE EFFECT OF CODING VARIANTS ON ALZHEIMER’S DISEASE RELATED ENDOPHENOTYPES (2017) (0)
The genetics of processing speed (2007) (0)
Multivariate Gene-Based Association Test on Family Data in MGAS (2016) (0)
BMI and waist circumference: an expression of the same genes? (2006) (0)
Genetics of body mass index: Should we take the influence of child bearing into account? (2007) (0)
Does the SNAP-25 gene play a role in inhibitory control and attention? (2008) (0)
Autism-Spectrum Quotient-Short (2014) (0)
GWAS meta-analysis (N=279,930) identifies new genes and functional links to general cognitive ability (2018) (0)
Genetic timeline of human brain and cognitive traits (2023) (0)
VKučinskas-2001-2016 (2016) (0)
CHRM2 genetic variation and brain structure (2007) (0)
Fifty Years of Twin Studies On Psychiatric Traits Show That for the Majority of Traits Genetic Variation Is Mostly Additive (2017) (0)
SA54ARE INTERNALIZING DISORDERS GENETICALLY DISTINCT? LESSONS LEARNED FROM ITEM-LEVEL ANALYSES (2019) (0)
The genetic liability for insomnia is associated with the number of awakenings during sleep in young and healthy individuals (2018) (0)
Genome-wide meta-analysis identifies new loci and functional pathways influencing 1 Alzheimer ’ s disease risk 2 3 (2020) (0)
Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder (2018) (0)
The Genetic Architectures of Functional and Structural Connectivity Properties within Cerebral Resting-State Networks (2023) (0)
USING DRUG GENE-SET ANALYSIS TO IDENTIFY DRUG REPURPOSING CANDIDATES BASED ON GENOME-WIDE ASSOCIATION RESULTS (2022) (0)
12 GENOME-WIDE ASSOCIATION META-ANALYSIS IDENTIFIES NEW LOCI AND GENES INFLUENCING HUMAN INTELLIGENCE (2019) (0)
Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease (2020) (0)
Using The Lisa Genetic Cluster (2019) (0)
77. RECONSIDERING THE VALIDITY OF TRANSCRIPTOME-WIDE ASSOCIATION STUDIES (2021) (0)
ApoE genotype, aopE levels and cognitive performance in adult twins (2001) (0)
Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways (2019) (0)
Environmental moderation of the heritability of IQ in adults. (2008) (0)
Working memory in 12-year old twins and their siblings (2005) (0)
Variance Components Linkage Analysis for Quantitative Traits (2007) (0)
Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease (2021) (0)
2 Genetic Linkage and Association Analysis for Loneliness 3 in Dutch Twin and Sibling Pairs Points to a Region (2005) (0)
SU28MODELLING GENETIC ASSOCIATIONS VIA THE INTEGRATION OF GWAS AND EQTL DATA (2019) (0)
Causal relationships between migraine and microstructural white matter: a Mendelian randomization study (2023) (0)
A Comparison of the Heritability of Perceptual Discrimination Speed and IQ in Australian and Dutch Twins - Session: Behavioral Genetics (2004) (0)
Development of functional brain organization: Heritability and stability across the life span (2009) (0)
TU39. GENETICS OF DEPRESSION ELUCIDATED VIA LOCAL GENETIC CORRELATION ANALYSIS WITH MOLECULAR AND BRAIN IMAGING ENDOPHENOTYPES (2021) (0)
Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS (2017) (0)
The genetic overlap between Alzheimer’s disease, amyotrophic lateral sclerosis, Lewy body dementia, and Parkinson’s disease (2022) (0)

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