Roel Ophoff
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Dutch human geneticist
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Roel Ophoffbiology Degrees
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Biology
Roel Ophoff's Degrees
- Bachelors Biology University of Groningen
- Masters Molecular Biology University of Groningen
- PhD Genetics University of Groningen
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Why Is Roel Ophoff Influential?
(Suggest an Edit or Addition)According to Wikipedia, Roel André Ophoff is a Dutch human geneticist who is Professor of Psychiatry and Human Genetics in the David Geffen School of Medicine at the University of California, Los Angeles. He received his PhD in human genetics from Leiden University with a dissertation titled "The molecular basis of familial hemiplegic migraine".
Roel Ophoff's Published Works
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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)
- Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4 (1996) (2260)
- Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs (2013) (2011)
- Large recurrent microdeletions associated with schizophrenia (2008) (1790)
- Genome-wide association study identifies five new schizophrenia loci (2011) (1680)
- Common variants conferring risk of schizophrenia (2009) (1653)
- 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)
- Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47 (2011) (1315)
- 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 30 Loci Associated with Bipolar Disorder (2017) (998)
- Multiple common variants for celiac disease influencing immune gene expression (2010) (958)
- Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium (2015) (810)
- Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects (2016) (736)
- Common genetic variants influence human subcortical brain structures (2015) (731)
- Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders (2019) (724)
- Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) (676)
- The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data (2014) (646)
- Aging effects on DNA methylation modules in human brain and blood tissue (2012) (539)
- Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (2017) (517)
- Rare and low-frequency coding variants alter human adult height (2016) (511)
- Cortical abnormalities in bipolar disorder: an MRI analysis of 6503 individuals from the ENIGMA Bipolar Disorder Working Group (2017) (482)
- Disruption of the neurexin 1 gene is associated with schizophrenia. (2009) (469)
- Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis (2016) (424)
- Trans-eQTLs Reveal That Independent Genetic Variants Associated with a Complex Phenotype Converge on Intermediate Genes, with a Major Role for the HLA (2011) (394)
- Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus (2010) (377)
- Subcortical volumetric abnormalities in bipolar disorder (2016) (371)
- Mapping genomic loci implicates genes and synaptic biology in schizophrenia (2022) (361)
- Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis (2009) (358)
- The genetic architecture of the human cerebral cortex (2018) (355)
- Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction (2010) (345)
- The Relationship of DNA Methylation with Age, Gender and Genotype in Twins and Healthy Controls (2009) (343)
- Cortical Brain Abnormalities in 4474 Individuals With Schizophrenia and 5098 Control Subjects via the Enhancing Neuro Imaging Genetics Through Meta Analysis (ENIGMA) Consortium (2018) (343)
- Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights (2016) (327)
- Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa (2019) (314)
- CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy (2008) (297)
- Evaluating Historical Candidate Genes for Schizophrenia (2015) (293)
- Recurrent CNVs disrupt three candidate genes in schizophrenia patients. (2008) (281)
- Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture (2013) (280)
- Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p. (1997) (277)
- Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration (2008) (274)
- 5‐HTTLPR genotype and anxiety‐related personality traits: A meta‐analysis and new data (2009) (270)
- Copy number variations of chromosome 16p13.1 region associated with schizophrenia (2011) (253)
- Common variants on 8p12 and 1q24.2 confer risk of schizophrenia (2011) (243)
- Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology (2021) (240)
- Novel genetic loci associated with hippocampal volume (2017) (238)
- Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis (2008) (232)
- Unraveling the Regulatory Mechanisms Underlying Tissue-Dependent Genetic Variation of Gene Expression (2012) (224)
- ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study (2007) (215)
- Common variants at VRK2 and TCF4 conferring risk of schizophrenia. (2011) (210)
- Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder (2015) (206)
- Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis (2009) (197)
- Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects (2012) (194)
- Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure underpinning obesity (2017) (193)
- Novel genetic loci underlying human intracranial volume identified through genome-wide association (2016) (192)
- Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis (2011) (184)
- Association between common variants near the melanocortin 4 receptor gene and severe antipsychotic drug-induced weight gain. (2012) (181)
- Migraine: a complex genetic disorder (2007) (181)
- A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer (2010) (174)
- Genetic demography of Antioquia (Colombia) and the Central Valley of Costa Rica (2003) (171)
- Expanding the range of ZNF804A variants conferring risk of psychosis (2011) (169)
- Wnt signaling and Dupuytren's disease. (2011) (169)
- Genetic heterogeneity of familial hemiplegic migraine. (1994) (164)
- Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci (2013) (162)
- Identification of Novel Genetic Markers Associated with Clinical Phenotypes of Systemic Sclerosis through a Genome-Wide Association Strategy (2011) (158)
- Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients (2009) (155)
- Rare coding variants in ten genes confer substantial risk for schizophrenia (2022) (154)
- Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. (2019) (153)
- Genetic architecture of subcortical brain structures in 38,851 individuals (2019) (148)
- Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2. (2001) (145)
- Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura (2001) (144)
- A comprehensive family-based replication study of schizophrenia genes. (2013) (144)
- GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores. (2019) (144)
- Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine (1998) (138)
- Genetic contributions to social impulsivity and aggressiveness in vervet monkeys (2004) (136)
- Erratum: Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium (Molecular Psychiatry (2015) DOI:10.1038/mp.2015.63) (2016) (136)
- Gene-Network Analysis Identifies Susceptibility Genes Related to Glycobiology in Autism (2009) (135)
- Pharmacogenetic Associations of Antipsychotic Drug-Related Weight Gain: A Systematic Review and Meta-analysis. (2016) (135)
- Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia (2010) (134)
- European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene. (2011) (133)
- An Integrative Multi-scale Analysis of the Dynamic DNA Methylation Landscape in Aging (2015) (131)
- A Gene Co-Expression Network in Whole Blood of Schizophrenia Patients Is Independent of Antipsychotic-Use and Enriched for Brain-Expressed Genes (2012) (131)
- Connectome Disconnectivity and Cortical Gene Expression in Patients With Schizophrenia (2017) (130)
- Three ulcerative colitis susceptibility loci are associated with primary sclerosing cholangitis and indicate a role for IL2, REL, and CARD9 (2011) (128)
- Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3. (2001) (127)
- A sensitive and simple ultra-high-performance-liquid chromatography-tandem mass spectrometry based method for the quantification of D-amino acids in body fluids. (2011) (127)
- Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe (2012) (124)
- Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura (1995) (123)
- Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. (2015) (123)
- Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenon. (1998) (122)
- Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex (2016) (120)
- Genome Arrays for the Detection of Copy Number Variations in Idiopathic Mental Retardation, Idiopathic Generalized Epilepsy and Neuropsychiatric Disorders: Lessons for Diagnostic Workflow and Research (2011) (116)
- Whole genome sequencing in psychiatric disorders: the WGSPD consortium (2017) (115)
- A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathy. (2014) (112)
- An association screen of myelin-related genes implicates the chromosome 22q11 PIK4CA gene in schizophrenia (2008) (111)
- Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families. (1995) (111)
- At-Risk Variant in TCF7L2 for Type II Diabetes Increases Risk of Schizophrenia (2011) (109)
- Genetic correlation between amyotrophic lateral sclerosis and schizophrenia (2017) (107)
- Genetic Schizophrenia Risk Variants Jointly Modulate Total Brain and White Matter Volume (2013) (106)
- Is human blood a good surrogate for brain tissue in transcriptional studies? (2010) (105)
- Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (2021) (104)
- Genome-wide association study of Tourette Syndrome (2012) (102)
- Common variant at 16p11.2 conferring risk of psychosis (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)
- Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen (2008) (95)
- Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness. (2011) (94)
- Complement genes contribute sex-biased vulnerability in diverse illnesses (2020) (92)
- Complement genes contribute sex-biased vulnerability in diverse illnesses (2020) (92)
- Complement genes contribute sex-biased vulnerability in diverse illnesses (2020) (92)
- The genome-wide distribution of background linkage disequilibrium in a population isolate. (2001) (89)
- Virtual Histology of Cortical Thickness and Shared Neurobiology in 6 Psychiatric Disorders. (2020) (89)
- Paternal age and psychiatric disorders: Findings from a Dutch population registry (2011) (86)
- Brain network analysis reveals affected connectome structure in bipolar I disorder (2016) (85)
- Common Genetic Variations in CCK, Leptin, and Leptin Receptor Genes Are Associated With Specific Human Eating Patterns (2007) (85)
- Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium. (2016) (84)
- GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia (2011) (83)
- A CASE OF ALS-FTD IN A LARGE FALS PEDIGREE WITH A K17I ANG MUTATION (2009) (81)
- Current status and future prospects for epigenetic psychopharmacology (2012) (79)
- FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands. (2010) (76)
- Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder (2012) (76)
- Transcriptome analysis in whole blood reveals increased microbial diversity in schizophrenia (2018) (75)
- A genome-wide survey of segmental duplications that mediate common human genetic variation of chromosomal architecture (2004) (74)
- Genomewide linkage disequilibrium mapping of severe bipolar disorder in a population isolate. (2002) (74)
- Gene networks associated with conditional fear in mice identified using a systems genetics approach (2011) (73)
- Investigation of the Genetic Association between Quantitative Measures of Psychosis and Schizophrenia: A Polygenic Risk Score Analysis (2012) (71)
- The Relationship Between Polygenic Risk Scores and Cognition in Schizophrenia (2019) (69)
- High educational performance is a distinctive feature of bipolar disorder: a study on cognition in bipolar disorder, schizophrenia patients, relatives and controls (2015) (68)
- Transcriptome-wide mega-analyses reveal joint dysregulation of immunologic genes and transcription regulators in brain and blood in schizophrenia (2016) (68)
- Genome-Wide Analysis Shows Increased Frequency of Copy Number Variation Deletions in Dutch Schizophrenia Patients (2011) (68)
- Correction: Identification of Novel Genetic Markers Associated with Clinical Phenotypes of Systemic Sclerosis through a Genome-Wide Association Strategy (2011) (67)
- A double hit implicates DIAPH3 as an autism risk gene (2011) (67)
- The effect of childhood maltreatment and cannabis use on adult psychotic symptoms is modified by the COMT Val158Met polymorphism (2013) (66)
- Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors (2020) (66)
- 5‐HT1B Receptor Polymorphism and Clinical Response to Sumatriptan (1998) (65)
- Genome-wide association study identifies 48 common genetic variants associated with handedness (2019) (65)
- A Common Variant in DRD3 Receptor Is Associated with Autism Spectrum Disorder (2009) (65)
- Expression QTL analysis of top loci from GWAS meta-analysis highlights additional schizophrenia candidate genes (2012) (64)
- A Genome-wide Association Study of Dupuytren Disease Reveals 17 Additional Variants Implicated in Fibrosis (2017) (63)
- On the relationship between degree of hand-preference and degree of language lateralization (2015) (63)
- P/Q-type Ca2+ channel defects in migraine, ataxia and epilepsy. (1998) (62)
- A genetic linkage map of the vervet monkey (Chlorocebus aethiops sabaeus) (2007) (60)
- A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts (2020) (60)
- Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner (2012) (59)
- The genetics of symptom dimensions of schizophrenia: Review and meta-analysis (2008) (59)
- Shared vulnerability for connectome alterations across psychiatric and neurological brain disorders (2018) (58)
- New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. (2015) (58)
- The association of antipsychotic medication and lithium with brain measures in patients with bipolar disorder (2016) (58)
- Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid (2014) (55)
- A quantitative trait locus for variation in dopamine metabolism mapped in a primate model using reference sequences from related species (2007) (55)
- A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia. (2010) (55)
- Integrated Pathway-Based Approach Identifies Association between Genomic Regions at CTCF and CACNB2 and Schizophrenia (2014) (53)
- Finding Suitable Phenotypes for Genetic Studies of Schizophrenia: Heritability and Segregation Analysis (2008) (53)
- A large genome scan for rare CNVs in amyotrophic lateral sclerosis. (2010) (53)
- Association of the PIK4CA schizophrenia‐susceptibility gene in adults with the 22q11.2 deletion syndrome (2009) (52)
- Do mood symptoms subdivide the schizophrenia phenotype? association of the GMP6A gene with a depression subgroup (2008) (52)
- Mapping of Gene Expression Reveals CYP27A1 as a Susceptibility Gene for Sporadic ALS (2012) (52)
- Linkage Analysis in a Dutch Population Isolate Shows No Major Gene for Left-Handedness or Atypical Language Lateralization (2015) (49)
- Analysis of genome-wide copy number variation in Irish and Dutch ALS populations. (2008) (49)
- Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition. (2020) (47)
- Identification of schizophrenia-associated loci by combining DNA methylation and gene expression data from whole blood (2014) (47)
- What we learn about bipolar disorder from large‐scale neuroimaging: Findings and future directions from the ENIGMA Bipolar Disorder Working Group (2020) (47)
- A Genome-wide Association Analysis of a Broad Psychosis Phenotype Identifies Three Loci for Further Investigation (2014) (46)
- TCF4 (e2‐2; ITF2): A schizophrenia‐associated gene with pleiotropic effects on human disease (2013) (46)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2019) (45)
- Kraepelin was right: a latent class analysis of symptom dimensions in patients and controls. (2012) (45)
- Detection, imputation, and association analysis of small deletions and null alleles on oligonucleotide arrays. (2008) (45)
- White matter disruptions in patients with bipolar disorder (2018) (44)
- Genetic studies of neuropsychiatric disorders in Costa Rica: a model for the use of isolated populations (2004) (43)
- WNT2 locus is involved in genetic susceptibility of Peyronie's disease. (2012) (41)
- Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia (2018) (40)
- Genetic liability for schizophrenia predicts risk of immune disorders (2014) (40)
- Genetic Overlap Among Intelligence and Other Candidate Endophenotypes for Schizophrenia (2009) (39)
- The impact of pharmacogenetics for migraine. (2001) (39)
- Functionally distinct ERAP1 and ERAP2 are a hallmark of HLA-A29-(Birdshot) Uveitis (2018) (39)
- Increased paternal age and the influence on burden of genomic copy number variation in the general population (2013) (38)
- Epigenetic age analysis of children who seem to evade aging (2015) (37)
- Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders: A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches (2019) (37)
- Hyperekplexia-like syndromes without mutations in the GLRA1 gene (1997) (37)
- Genetic causes of developmental disorders. (2013) (37)
- Seasonal changes in gene expression represent cell-type composition in whole blood. (2014) (36)
- The Val66Met polymorphism of the BDNF gene in anorexia nervosa: New data and a meta-analysis (2013) (36)
- An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis (2014) (36)
- No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder (2011) (36)
- Epigenome-wide meta-analysis of blood DNA methylation and its association with subcortical volumes: findings from the ENIGMA Epigenetics Working Group (2018) (35)
- Sex-Dependent Novelty Response in Neurexin-1α Mutant Mice (2012) (35)
- Using ancestry-informative markers to identify fine structure across 15 populations of European origin (2014) (34)
- Involvement of a Ca 2+ Channel Gene in Familial Hemiplegic Migraine and Migraine With and Without Aura (1997) (34)
- The characteristics of psychotic features in bipolar disorder (2018) (33)
- The association of the alpha-5 subunit of the nicotinic acetylcholine receptor gene and the brain-derived neurotrophic factor gene with different aspects of smoking behavior. (2012) (33)
- Chromosome 19p13 loci in Finnish migraine with aura families (2005) (32)
- Chromosomal localization of the 5-HT1F receptor gene: no evidence for involvement in response to sumatriptan in migraine patients. (1998) (31)
- Towards a unified nomenclature describing voltage-gated calcium channel genes (1997) (31)
- Identification of an Amino Acid Motif in HLA–DRβ1 That Distinguishes Uveitis in Patients With Juvenile Idiopathic Arthritis (2018) (31)
- Recurrent Inversion Events at 17q21.31 Microdeletion Locus Are Linked to the MAPT H2 Haplotype (2010) (31)
- A polygenic resilience score moderates the genetic risk for schizophrenia (2019) (31)
- Accurate and fast multiple-testing correction in eQTL studies. (2015) (30)
- The involvement of GSK3β in bipolar disorder: Integrating evidence from multiple types of genetic studies (2010) (30)
- Network analysis of positional candidate genes of schizophrenia highlights myelin-related pathways (2009) (28)
- Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide (2017) (28)
- Vitamin B-6 vitamers in human plasma and cerebrospinal fluid. (2014) (27)
- Genetic variants associated with longitudinal changes in brain structure across the lifespan (2021) (27)
- RECONSTRUCTING DNA COPY NUMBER BY PENALIZED ESTIMATION AND IMPUTATION. (2009) (26)
- Anorexia nervosa and the Val158Met polymorphism of the COMT gene: meta-analysis and new data (2012) (26)
- Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium (2018) (26)
- No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis. (2014) (26)
- Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (2021) (26)
- Identification of novel genetic markers associated with the clinical phenotypes of systemic sclerosis through a genome wide association strategy (2010) (26)
- Genome-wide burden of deleterious coding variants increased in schizophrenia (2015) (25)
- Complement genes contribute sex-biased vulnerability in diverse disorders (2020) (25)
- Complement genes contribute sex-biased vulnerability in diverse disorders (2020) (25)
- Complement genes contribute sex-biased vulnerability in diverse disorders (2020) (25)
- Familial hemiplegic migraine: involvement of a calcium neuronal channel. (1997) (25)
- Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis. (1995) (24)
- Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia (2022) (24)
- No evidence that common genetic risk variation is shared between schizophrenia and autism (2013) (24)
- Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosis (2009) (24)
- Season of Sampling and Season of Birth Influence Serotonin Metabolite Levels in Human Cerebrospinal Fluid (2012) (24)
- Seasonal variation of serotonin turnover in human cerebrospinal fluid, depressive symptoms and the role of the 5-HTTLPR (2013) (23)
- Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates (2018) (23)
- Structural brain alterations in youth with psychosis and bipolar spectrum symptoms (2018) (22)
- Sleep Disturbances, Psychosocial Difficulties, and Health Risk Behavior in 16,781 Dutch Adolescents. (2018) (22)
- Genome-wide association study identifies 30 loci associated with bipolar disorder (2019) (22)
- Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia. (2014) (21)
- A Genetic Deconstruction of Neurocognitive Traits in Schizophrenia and Bipolar Disorder (2013) (21)
- Markov Models for Inferring Copy Number Variations from Genotype Data on Illumina Platforms (2009) (21)
- Familial clustering of schizophrenia, bipolar disorder, and major depressive disorder (2012) (21)
- Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders (2021) (21)
- Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies (2019) (20)
- 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans (2021) (20)
- A Common Variant in ERBB4 Regulates GABA Concentrations in Human Cerebrospinal Fluid (2012) (20)
- Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2017) (20)
- Association between body mass index and subcortical brain volumes in bipolar disorders–ENIGMA study in 2735 individuals (2021) (20)
- D-Amino Acid Aberrations in Cerebrospinal Fluid and Plasma of Smokers (2013) (19)
- EXOME SEQUENCING IN BIPOLAR DISORDER REVEALS SHARED RISK GENE AKAP11 WITH SCHIZOPHRENIA (2021) (19)
- Title Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects Permalink (2012) (19)
- Effects of season of birth and a common MTHFR gene variant on the risk of schizophrenia (2011) (19)
- A four-generation Dutch family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), linked to chromosome 19p13 (1995) (19)
- Replication Study and Meta-Analysis in European Samples Supports Association of the 3p21.1 Locus with Bipolar Disorder (2012) (18)
- Missense Mutation Carried by Patients with Episodic Ataxia Type 2 (18)
- An actigraphy study investigating sleep in bipolar I patients, unaffected siblings and controls. (2017) (17)
- Transcriptomic abnormalities in peripheral blood in bipolar disorder, and discrimination of the major psychoses (2020) (17)
- Dupuytren's disease susceptibility gene, EPDR1, is involved in myofibroblast contractility. (2016) (17)
- Accelerated aging in the brain, epigenetic aging in blood, and polygenic risk for schizophrenia (2020) (17)
- Prediction of serotonin transporter promoter polymorphism genotypes from single nucleotide polymorphism arrays using machine learning methods (2012) (17)
- The association of sleep and physical activity with integrity of white matter microstructure in bipolar disorder patients and healthy controls (2017) (16)
- Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder (2021) (16)
- Gene expression profiling in C57BL/6J and A/J mouse inbred strains reveals gene networks specific for brain regions independent of genetic background (2010) (16)
- Dynamics of Brain Structure and its Genetic Architecture over the Lifespan (2020) (16)
- Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study (2020) (15)
- Whole blood transcriptome analysis in bipolar disorder reveals strong lithium effect (2019) (15)
- Peripheral blood gene expression profiles linked to monoamine metabolite levels in cerebrospinal fluid (2016) (15)
- The relationship between brain volumes and intelligence in bipolar disorder. (2017) (14)
- Genome-wide association study of NMDA receptor coagonists in human cerebrospinal fluid and plasma (2015) (13)
- BDNF Val66Met homozygosity does not influence plasma BDNF levels in healthy human subjects (2013) (13)
- Erratum: Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47 (Nature Genetics (2011) 43 (246-252)) (2011) (13)
- Methylation age acceleration does not predict mortality in schizophrenia (2019) (13)
- Wolff Award 1997. Involvement of a Ca2+ channel gene in familial hemiplegic migraine and migraine with and without aura. Dutch Migraine Genetics Research Group. (1997) (12)
- Genetic Variation and the Risk of Haloperidol-Related Parkinsonism in Elderly Patients: A Candidate Gene Approach (2013) (12)
- Total RNA Sequencing reveals microbial communities in human blood and disease specific effects (2016) (12)
- Characterization of Genome-Methylome Interactions in 22 Nuclear Pedigrees (2014) (12)
- Exploring the clinical utility of two staging models for bipolar disorder (2019) (12)
- The Alkaline Phosphatase (ALPL) Locus Is Associated with B6 Vitamer Levels in CSF and Plasma (2018) (11)
- Hippocampal Gene Expression Analysis Highlights Ly6a/Sca-1 as Candidate Gene for Previously Mapped Novelty Induced Behaviors in Mice (2011) (11)
- Accommodating chromosome inversions in linkage analysis. (2006) (10)
- Analysis of segmental duplications reveals a distinct pattern of continuation-of-synteny between human and mouse genomes (2007) (10)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (10)
- Association study of copy number variants with brain volume in schizophrenia patients and healthy controls (2012) (10)
- State-Dependent Functional Dysconnectivity in Youth With Psychosis Spectrum Symptoms (2019) (10)
- Segment-Wise Genome-Wide Association Analysis Identifies a Candidate Region Associated with Schizophrenia in Three Independent Samples (2012) (9)
- Genome-wide Association Study of Clinical Features in the Schizophrenia Psychiatric Genomics Consortium: Confirmation of Polygenic Effect on Negative Symptoms (2017) (9)
- Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes (2021) (8)
- Sex-Dependent Shared and Non-Shared Genetic Architecture Across Mood and Psychotic Disorders (2020) (8)
- Genetic and clinical analyses of psychosis spectrum symptoms in a large multiethnic youth cohort reveal significant link with ADHD (2019) (8)
- Extensions of Multiple-Group Item Response Theory Alignment: Application to Psychiatric Phenotypes in an International Genomics Consortium (2020) (8)
- Integrative analysis of Dupuytren's disease identifies novel risk locus and reveals a shared genetic etiology with BMI (2018) (7)
- Genetics and pathology of voltage-gated Ca2+ channels. (1998) (7)
- Characterisation of age and polarity at onset in bipolar disorder (2021) (7)
- Elevated Common Variant Genetic Risk for Tourette Syndrome in a Densely Affected Pedigree (2021) (7)
- A Genetic Population Isolate in The Netherlands Showing Extensive Haplotype Sharing and Long Regions of Homozygosity (2017) (7)
- Corrigendum: Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus (2011) (7)
- Double hits in schizophrenia (2018) (6)
- The association between antibodies to neurotropic pathogens and bipolar disorder (2019) (6)
- Systematic genotype–phenotype analysis of autism susceptibility loci implicates additional symptoms to co-occur with autism (2010) (6)
- Genome-wide association study of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores (2018) (6)
- A Longitudinal Model of Human Neuronal Differentiation for Functional Investigation of Schizophrenia Polygenic Risk (2019) (6)
- Dumpster diving in RNA-sequencing to find the source of every last read (2016) (6)
- Genome-wide analyses of smoking behaviors in schizophrenia: Findings from the Psychiatric Genomics Consortium. (2021) (6)
- Efficient Strategy for Detecting Gene × Gene Joint Action and Its Application in Schizophrenia (2014) (5)
- Title Gene expression profiling in C 57 BL / 6 J and A / J mouse inbred strains reveals gene networks specific for brain regions independent of genetic background Permalink (2010) (5)
- The quest for migraine genes (1997) (5)
- Corrigendum: Multiple common variants for celiac disease influencing immune gene expression (2010) (5)
- No association between anti-thyroidperoxidase antibodies and bipolar disorder: a study in the Dutch Bipolar Cohort and a meta-analysis (2019) (5)
- Schizophrenia is characterized by age- and sex-specific effects on epigenetic aging (2019) (5)
- Lithium Use during Pregnancy and the Risk of Miscarriage (2020) (4)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (4)
- Genome-wide association study identifies 48 common genetic variants associated with handedness (2020) (4)
- A summary-statistics-based approach to examine the role of serotonin transporter promoter tandem repeat polymorphism in psychiatric phenotypes (2021) (4)
- Reply to: New Meta- and Mega-analyses of Magnetic Resonance Imaging Findings in Schizophrenia: Do They Really Increase Our Knowledge About the Nature of the Disease Process? (2019) (4)
- Common Genetic Variation and Age of Onset of Anorexia Nervosa (2021) (3)
- A systematic evaluation of 41 DNA methylation predictors across 101 data preprocessing and normalization strategies highlights considerable variation in algorithm performance (2021) (3)
- Powerful eQTL mapping through low coverage RNA sequencing (2021) (3)
- Diagnosis of bipolar disorders and body mass index predict clustering based on similarities in cortical thickness—ENIGMA study in 2436 individuals (2021) (3)
- Identifying tissues implicated in Anorexia Nervosa using Transcriptomic Imputation (2018) (3)
- Bipolar episodes after reproductive events in women with bipolar I disorder, A study of 919 pregnancies. (2021) (3)
- Genetic analysis of activity, brain and behavioral associations in extended families with heavy genetic loading for bipolar disorder (2019) (3)
- Epigenetic age is accelerated in schizophrenia with age- and sex-specific effects and associated with polygenic disease risk (2019) (3)
- Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1 (2022) (3)
- Wnt Signaling and Dupuytren's Disease REPLY (2011) (3)
- Correction: Identification of Novel Genetic Markers Associated with Clinical Phenotypes of Systemic Sclerosis through a Genome-Wide Association Strategy (2011) (3)
- Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium (2018) (3)
- ROP: dumpster diving in RNA-sequencing to find the source of 1 trillion reads across diverse adult human tissues (2018) (3)
- Complement component 4 genes contribute sex-specific vulnerability in diverse illnesses (2019) (3)
- Common Variants near the Melanocortin 4 Receptor Gene are Associated with Severe Antipsychotic Drug-induced Weight Gain (2014) (3)
- An amino acid motif in HLA-DRβ1 distinguishes patients with uveitis in juvenile idiopathic arthritis (2017) (2)
- The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data (2014) (2)
- A Clinical Genetic Study of Familial Dupuytren’s Disease in the Netherlands (2012) (2)
- Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (2)
- Gene expression imputation provides insight into the genetic architecture of frontotemporal dementia (2020) (2)
- Liprin alfa 2 gene expression is increased by cannabis use and associated with neuropsychological function (2019) (2)
- Replication and refinement of the role of rs548181 in schizophrenia: Results from a family based study (2013) (2)
- Poster #120 THE GENETICS OF LANGUAGE LATERALIZATION AND LEFT-HANDEDNESS: LINKAGE ANALYSIS IN A DUTCH POPULATION ISOLATE (2012) (2)
- Comparison of Clustering Methods for Time Course Genomic Data: Applications to Aging Effects (2014) (2)
- Significant variation in the performance of DNA methylation predictors across data preprocessing and normalization strategies (2022) (2)
- No neuronal autoantibodies detected in plasma of patients with a bipolar I disorder (2018) (2)
- Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects (2012) (1)
- Whole blood transcriptome analysis in bipolar disorder reveals strong lithium effect Authors (2018) (1)
- SA102GENETIC AND CLINICAL ANALYSES OF PSYCHOSIS SPECTRUM IN A LARGE MULTI-ETHNIC YOUTH COHORT (N>8,000) REVEAL SIGNIFICANT LINK WITH ADHD (2019) (1)
- 30 SCHIZOPHRENIA IS CHARACTERIZED BY AGE- AND SEX-SPECIFIC EFFECTS ON EPIGENETIC AGING (2019) (1)
- FIBROBLAST GROWTH FACTORS AND BRAIN VOLUME IN SCHIZOPHRENIA PATIENTS AND HEALTHY CONTROLS (2010) (1)
- Genetic architecture of subcortical brain structures in 38,851 individuals (2019) (1)
- Aging effects on DNA methylation modules in human brain and blood tissue (2012) (1)
- Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex (2016) (1)
- University of Groningen Gene expression profiling in C 57 BL / 6 J and A / J mouse inbred strains reveals gene networks specific for brain regions independent of genetic background (2018) (1)
- Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner (2012) (1)
- Characterization of Age and Polarity at Onset in Bipolar Disorder (2021) (1)
- M14 DISCRIMINATION OF MAJOR NEUROPSYCHIATRIC DISORDERS USING BLOOD-BASED TRANSCRIPTOMIC SIGNATURES (2019) (1)
- ASSOCIATION STUDY OF CNVS WITH BRAIN VOLUME AND BRAIN VOLUME CHANGE OVER 5 YEARS IN SCHIZOPHRENIA PATIENTS AND HEALTHY CONTROLS (2010) (1)
- Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia (2019) (1)
- IMPROVEMENT OF PHENOTYPING IN GENOME WIDE ASSOCIATION STUDIES ON SCHIZOPHRENIA: AN APPLICATION OF LATENT CLASS FACTOR ANALYSIS (2010) (1)
- ASSOCIATION OF FIBROBLAST GROWTH FACTOR 2 (FGF2) WITH HIPPOCAMPAL VOLUME IN DUTCH SCHIZOPHRENIA PATIENTS (2008) (1)
- Comprehensive analysis of RNA-sequencing to find the source of 1 trillion reads across diverse adult human tissues (2017) (1)
- Hypokalemic Periodic Paralysis andtheDihydropyridine Receptor (CACNLIA3):Genotype/Phenotype Correlations forTwo Predominant Mutations andEvidence fortheAbsenceofa Founder Effect in16Caucasian Families (1995) (1)
- PHENOTYPES IN THE WHOLE GENOME SEQUENCING FOR PSYCHIATRIC DISORDERS CONSORTIUM (2019) (1)
- Genome‐wide Quantitative Trait Loci (QTL) Mapping of Metabolites in Human Cerebrospinal Fluid (2020) (0)
- P.1.a.024 Deoxyribonucleic acid methylation marks of psychotropic drug use in bipolar disorder patients; an explorative pilot study (2015) (0)
- P.4.16 Cannabis use and subclinical psychotic symptoms: is the public mental health at risk? (2009) (0)
- Functional Characterisation of a GWAS Risk Locus Identifies GPX3 as a Lead Candidate Gene in ALS (2020) (0)
- Epigenetic age analysis of human children who seem to evade aging (2015) (0)
- Transient patterns of functional dysconnectivity in youth with psychosis spectrum symptoms (2018) (0)
- University of Groningen A Genetic Population Isolate in The Netherlands Showing Extensive Haplotype Sharing and Long Regions of (2017) (0)
- T46 In Vitro Human Neuronal Differentiation Validated As Genomic Model System To Study Major Psychiatric Illnesses (2017) (0)
- Mutation inDHP receptorcxlsubunit (CACLN1A3)gene ina Dutchfamily with hypokalaemic periodic paralysis (1995) (0)
- T225. Burden of Rare Coding Variants in the 22q11.2 Deletion Syndrome Region is Associated With Educational Attainment and Schizophrenia Risk (2018) (0)
- T71. FIBROBLASTS AS AN IN VITRO MODEL OF CIRCADIAN GENETIC AND GENOMIC STUDIES (2022) (0)
- Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling (2017) (0)
- Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome (2022) (0)
- PARENTAL AGE AND THE RISK OF PSYCHIATRIC DISORDERS (2010) (0)
- Mutation inDHP receptorcxlsubunit (CACLN1A3)gene ina Dutchfamily with hypokalaemic periodic paralysis (1995) (0)
- Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder (2018) (0)
- STATISTICAL PHENOTYPES OF SCHIZOPHRENIA; WHAT IS THEIR PURPOSE? (2008) (0)
- SA132THE RELATIONSHIP BETWEEN POLYGENIC RISK SCORES AND G IN PGC2 SCHIZOPHRENIA CASES (2019) (0)
- Human Genetic Studies of Dupuytren Disease: A Primer (2017) (0)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2019) (0)
- Increased paternal age and the influence on burden of genomic copy number variation in the general population (2013) (0)
- UPDATE ON THE ANALYSES OF THE LARGEST BIPOLAR CASE-CONTROL EXOME SEQUENCING DATASET TO DATE (2019) (0)
- Poster #105 MONOZYGOTIC TWINS DISCORDANT FOR BIPOLAR DISORDER SHOW FUNCTIONAL DNA METHYLATION CHANGES IN WHOLE BLOOD AND BRAIN (2012) (0)
- P.4.007 Human schizophrenia and autism candidate gene neurexin1a regulates behavioural habituation in mice (2011) (0)
- SEGMENT-WISE GENOME-WIDE ASSOCIATION ANALYSIS IDENTIFIES A LIMITED NUMBER OF REPLICABLE CANDIDATE REGIONS ASSOCIATED WITH SCHIZOPHRENIA (2010) (0)
- Mega-analysis of association between obesity and cortical morphology in bipolar disorders: ENIGMA study in 2832 participants. (2023) (0)
- S.24.02 Cognitive endophenotypes in schizophrenia (2010) (0)
- Poster #112 NO EVIDENCE THAT COMMON GENETIC RISK VARIANTS ARE SHARED BETWEEN SCHIZOPHRENIA AND AUTISM (2012) (0)
- Genome-Wide Association Study of Gilles de la Tourette Syndrome (IN10-1.002) (2012) (0)
- Correction: Investigation of the Genetic Association between Quantitative Measures of Psychosis and Schizophrenia: A Polygenic Risk Score Analysis (2013) (0)
- University of Groningen Identification of Novel Genetic Markers Associated with Clinical Phenotypes of Systemic Sclerosis through a Genome-Wide Association Strategy Gorlova, (2011) (0)
- Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (0)
- Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights (2018) (0)
- SHARED GENETICS OF CANDIDATE ENDOPHENOTYPES FOR SCHIZOPHRENIA: MULTIVARIATE HERITABILITY ANALYSIS (2008) (0)
- SU98 THE DISTRIBUTION OF AMINO ACID CHANGES FROM CODING VARIANTS IS ALTERED IN SCHIZOPHRENIA (2019) (0)
- Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease (2020) (0)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (0)
- ORIGINAL RESEARCH—PEYRONIE'S DISEASE WNT2 Locus Is Involved in Genetic Susceptibility of (2012) (0)
- 14:00 COMMON POLYGENIC VARIATION CONTRIBUTING TO SCHIZOPHRENIA RISK EXPLAINS VARIATION IN TOTAL BRAIN VOLUME (2012) (0)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (0)
- Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium (2018) (0)
- Poster #106 IN A NORMAL POPULATION SAMPLE SCHIZOPHRENIA ASSOCIATED COPY NUMBER VARIATIONS IN GENOMIC REGIONS 1Q21.1, 15Q11.2 ARE MORE FREQUENT IN FEMALE AND ARE ASSOCIATED WITH LOWER SOCIOECONOMIC STATUS, OBESITY AND HIGHER CHOLESTEROL LEVELS (2012) (0)
- Contents Vol. 129, 2010 (2010) (0)
- Explorer Epigenome-wide meta-analyses of blood DNA methylation and its association with subcortical volumes (2019) (0)
- GENETICS OF SEVERE MENTAL ILLNESS IN SOUTH AMERICA (2022) (0)
- Shared vulnerability for connectome alterations across psychiatric and neurological brain disorders (2019) (0)
- Powerful eQTL mapping through low-coverage RNA sequencing (2022) (0)
- Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (2022) (0)
- ReplicationStudyandMeta-AnalysisinEuropean SamplesSupportsAssociationofthe3p21.1Locuswith (2012) (0)
- University of Groningen Mapping of Gene Expression Reveals CYP 27 A 1 as a Susceptibility Gene for Sporadic (2012) (0)
- [Genetic variation with increased risk of schizophrenia]. (2010) (0)
- SU109 SCHIZOPHRENIA AND ADULT HEIGHT SHOW AN INVERSE POLYGENIC CORRELATION WITHIN SPECIFIC FUNCTIONAL DOMAINS OF THE GENOME (2019) (0)
- REVEALING THE GENETIC ARCHITECTURE OF BIPOLAR DISORDER AND SUBTYPES PROVIDES BIOLOGICAL INSIGHT (2021) (0)
- P.1.005 Season of sampling and season of birth determine serotonin metabolite levels in human cerebrospinal fluid (2012) (0)
- Effects of psychosis on brain volume in bipolar disorder (2013) (0)
- Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder (2021) (0)
- Pharmacogenetics of Antipsychotic-Induced Weight Gain in Multiple Medication-Naive Cohorts (2017) (0)
- Cognitive endophenotypes in schizophrenia (2010) (0)
- Whole genome sequencing in psychiatric disorders: the WGSPD consortium (2017) (0)
- AGE AT ONSET CHARACTERISTICS OF BIPOLAR DISORDER IN A COHORT OF 13,700 PATIENTS (2019) (0)
- European Mathematical Genetics Meeting, Rotterdam, the Netherlands, 10th–11th April 2008 (2008) (0)
- O12.1. EXAMINING THE NEUROBIOLOGICAL IMPACT OF CHILDHOOD TRAUMA: AN IMPORTANT ROLE FOR FRONTAL AND INSULAR REGIONS (2018) (0)
- SUB-PHENOTYPE ANALYSES OF BIPOLAR DISORDER IN DATA FROM THE PGC BIPOLAR DISORDER WORKING GROUP (2019) (0)
- 18. CELL TYPE DECONVOLUTION OF BULK BLOOD RNA-SEQ TO REVEAL BIOLOGICAL INSIGHTS OF PSYCHIATRIC DISEASE (2022) (0)
- Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1 (2022) (0)
- P.1.04 Schizophrenia and cytogenetic aberrations: in search of susceptibility genes and pathways (2009) (0)
- P.3.007 A common variant in human ErbB4 regulates GABA cerebrospinal fluid concentrations (2012) (0)
- A longitudinal model of human neuronal differentiation for functional investigation of schizophrenia disease susceptibility (2017) (0)
- F124EPIGENETIC AGING IN BLOOD IS AFFECTED IN SCHIZOPHRENIA (2019) (0)
- Eichler , EE Re : Proposal for Construction a Human Haploid BAC library from Hydaditiform Mole Source Material (2002) (0)
- An association study of the total genome in Amyotrophic Lateral Sclerosis in a Dutch polulation (2007) (0)
- A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling (2017) (0)
- Edinburgh Research Explorer Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia (2017) (0)
- (2018). Cortical Brain Abnormalities in 4474 Individuals With Schizophrenia and 5098 Control Subjects via the Enhancing Neuro Imaging Genetics Through Meta Analysis (0)
- T33. USING GENOMICS TO AID EARLY DIFFERENTIAL DIAGNOSIS BETWEEN BIPOLAR DISORDER AND MAJOR DEPRESSION (2022) (0)
- Genome-Wide Association Study of Gilles de la Tourette Syndrome (2012) (0)
- P538. Rare Damaging Variants and Phenotypic Variability in Schizophrenia (2022) (0)
- Contents Vol. 135, 2011 (2011) (0)
- [Channelopathies: a genetic explanation of migraine and other paroxysmal neurologic disorders]. (1998) (0)
- Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa (2019) (0)
- Genetic Susceptibility Factors in ALS (2002) (0)
- No evidence for common genetic variants shared between multiple sclerosis (MS) and amyotrophic lateral sclerosis (ALS) (2011) (0)
- VKučinskas-2001-2016 (2016) (0)
- haracterization of a Family with Rare Deletions in NTNAP5 and DOCK4 Suggests Novel Risk Loci for utism and Dyslexia (0)
- 91. Structural Brain Volumes in Youth With Psychotic and Bipolar Spectrum Symptoms (2017) (0)
- A GENOME-WIDE LINKAGE SCAN OF THETA BAND ACTIVITY AS AN ENDOPHENOTYPE FOR SCHIZOPHRENIA (2010) (0)
- Flowchart for (1) detection and replication of schizophrenia associated pathways and (2) identification of the most informative genes, and (3) functional annotation of single nucleotide polymorphisms in the genes of interest. (2014) (0)
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