about
Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorderMicroduplications of 16p11.2 are associated with schizophreniaMutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1)A genome-wide association study of attempted suicide.Association study of serotonin pathway genes in attempted suicide.Family-based association study of Neuregulin 1 with psychotic bipolar disorderFurther development of YBOCS dimensions in the OCD Collaborative Genetics study: symptoms vs. categories.Assessment of the effect of age at onset on linkage to bipolar disorder: evidence on chromosomes 18p and 21qChronic corticosterone exposure increases expression and decreases deoxyribonucleic acid methylation of Fkbp5 in miceAssociation study of Wnt signaling pathway genes in bipolar disorderMonoamine oxidase A regulates antisocial personality in whites with no history of physical abuseFamily-based association of FKBP5 in bipolar disorder.Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms.Investigating the role of early childhood abuse and HPA axis genes in suicide attempters with bipolar disorder.Targeted Sequencing of FKBP5 in Suicide Attempters with Bipolar Disorder.Case-control association study of TGOLN2 in attempted suicideNeurotransmission and bipolar disorder: a systematic family-based association study.Clock genes may influence bipolar disorder susceptibility and dysfunctional circadian rhythm.Further evidence for an association of G72/G30 with schizophrenia in Chinese.Genome-wide association study of suicide attempts in mood disorder patientsFamily-based SNP association study on 8q24 in bipolar disorder.Common and rare variants of DAOA in bipolar disorderSNP fine mapping of chromosome 8q24 in bipolar disorder.Exome Sequencing of Familial Bipolar Disorder.Mood-incongruent psychotic features in bipolar disorder: familial aggregation and suggestive linkage to 2p11-q14 and 13q21-33.Demographic and clinical characteristics associated with treatment status in family members with obsessive-compulsive disorder.Familiality of factor analysis-derived YBOCS dimensions in OCD-affected sibling pairs from the OCD Collaborative Genetics Study.Sapap3 and pathological grooming in humans: Results from the OCD collaborative genetics study.Clinical correlates and familial aggregation of age at onset in bipolar disorder.A targeted sequencing study of glutamatergic candidate genes in suicide attempters with bipolar disorder.Whole-gene sequencing investigation of SAT1 in attempted suicide.Genome-wide linkage scan of 98 bipolar pedigrees and analysis of clinical covariates.Genome-wide scan and conditional analysis in bipolar disorder: evidence for genomic interaction in the National Institute of Mental Health genetics initiative bipolar pedigrees.CRELD1 mutations contribute to the occurrence of cardiac atrioventricular septal defects in Down syndrome.Attempted Suicide in Bipolar Disorder Pedigrees: Evidence for Linkage to 2p12Genome-wide scan of bipolar disorder in 65 pedigrees: supportive evidence for linkage at 8q24, 18q22, 4q32, 2p12, and 13q12Suggestive Linkage to Chromosomal Regions 13q31 and 22q12 in Families With Psychotic Bipolar DisorderThe Familial Aggregation of Psychotic Symptoms in Bipolar Disorder PedigreesHoarding in obsessive–compulsive disorder: Results from the OCD Collaborative Genetics StudyRare plus common SERT variants in obsessive-compulsive disorder
P50
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P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0002-6639-487X
@en
name
Virginia L Willour
@ast
Virginia L Willour
@en
Virginia L Willour
@es
Virginia L Willour
@nl
type
label
Virginia L Willour
@ast
Virginia L Willour
@en
Virginia L Willour
@es
Virginia L Willour
@nl
prefLabel
Virginia L Willour
@ast
Virginia L Willour
@en
Virginia L Willour
@es
Virginia L Willour
@nl
P106
P21
P31
P496
0000-0002-6639-487X