Search Results - "WASSINK, H"
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Association Between Brain-Derived Neurotrophic Factor Val66Met Gene Polymorphism and Progressive Brain Volume Changes in Schizophrenia
Published in The American journal of psychiatry (01-12-2007)“…Objective: Factors underlying progressive brain volume changes in schizophrenia remain poorly understood. The authors investigated whether a gene polymorphism…”
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2
Prefrontal Inefficiency Is Associated With Polygenic Risk for Schizophrenia
Published in Schizophrenia bulletin (01-11-2014)“…Considering the diverse clinical presentation and likely polygenic etiology of schizophrenia, this investigation examined the effect of polygenic risk on a…”
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3
Examination of AVPR1a as an autism susceptibility gene
Published in Molecular psychiatry (01-10-2004)“…Impaired reciprocal social interaction is one of the core features of autism. While its determinants are complex, one biomolecular pathway that clearly…”
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4
Pax6 3′ deletion results in aniridia, autism and mental retardation
Published in Human genetics (01-05-2008)“…The PAX6 gene is a transcription factor expressed early in development, predominantly in the eye, brain and gut. It is well known that mutations in PAX6 may…”
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5
Inflammatory bowel disease, cancer and medication: Cancer risk in the Dutch population‐based IBDSL cohort
Published in International journal of cancer (15-09-2016)“…The management of inflammatory bowel disease (IBD) has changed since the mid‐1990s (e.g., use of thiopurines/anti‐TNFα agents, improved surveillance programs),…”
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6
MAPK14 and CNR1 gene variant interactions: effects on brain volume deficits in schizophrenia patients with marijuana misuse
Published in Psychological medicine (01-03-2013)“…Adolescent marijuana use is associated with increased risk for schizophrenia. We previously reported that marijuana misuse in conjunction with specific…”
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7
MTHFR 677C [rightward arrow] T genotype disrupts prefrontal function in schizophrenia through an interaction with COMT 158Val [rightward arrow] Met
Published in Proceedings of the National Academy of Sciences - PNAS (11-11-2008)“…Understanding how risk genes cumulatively impair brain function in schizophrenia could provide critical insights into its pathophysiology. Working memory…”
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8
Copy number variations and primary open-angle glaucoma
Published in Investigative ophthalmology & visual science (2011)“…This study sought to investigate the role of rare copy number variation (CNV) in age-related disorders of blindness, with a focus on primary open-angle…”
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9
Linkage Disequilibrium at the Angelman Syndrome Gene UBE3A in Autism Families
Published in Genomics (San Diego, Calif.) (01-09-2001)“…Autistic disorder is a neurodevelopmental disorder with a complex genetic etiology. Observations of maternal duplications affecting chromosome 15q11–q13 in…”
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10
G72 influences longitudinal change in frontal lobe volume in schizophrenia
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01-03-2010)“…Schizophrenia is a neurodevelopmental psychiatric disorder characterized by a variety of structural brain abnormalities that appear to progress across the…”
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11
Cerebellar morphology as a predictor of symptom and psychosocial outcome in schizophrenia
Published in Biological psychiatry (1969) (1999)“…Background: In this study, we examined whether brain morphology assessed early in the course of schizophrenia predicted psychosocial or symptomatic outcome…”
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12
Cannabinoid receptor 1 gene polymorphisms and marijuana misuse interactions on white matter and cognitive deficits in schizophrenia
Published in Schizophrenia research (01-05-2011)“…Abstract Marijuana exposure during the critical period of adolescent brain maturation may disrupt neuro-modulatory influences of endocannabinoids and increase…”
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13
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
Published in Nature (28-05-2009)“…Autism spectrum disorders (ASDs) are childhood neurodevelopmental disorders with complex genetic origins. Previous studies focusing on candidate genes or…”
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14
Evaluation of FOXP2 as an autism susceptibility gene
Published in American journal of medical genetics (08-07-2002)“…A mutation in the gene FOXP2 was recently identified as being responsible for a complicated speech and language phenotype in a single large extended pedigree…”
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15
Germline mosaic transmission of a novel duplication of PXDN and MYT1L to two male half-siblings with autism
Published in Psychiatric genetics (01-06-2012)“…Autism is a neurodevelopmental disorder with a strong genetic component to susceptibility. In this study, we report the molecular characterization of an…”
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Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder
Published in Molecular psychiatry (01-03-2001)“…Autistic disorder (MIM 209850) is currently viewed as a neurodevelopmental disease. Reelin plays a pivotal role in the development of laminar structures…”
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Common genetic variants on 5p14.1 associate with autism spectrum disorders
Published in Nature (28-05-2009)“…Autism spectrum disorders (ASDs) represent a group of childhood neurodevelopmental and neuropsychiatric disorders characterized by deficits in verbal…”
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18
Prevalence of Depressive Symptoms Early in the Course of Schizophrenia
Published in The American journal of psychiatry (01-02-1999)“…OBJECTIVE: The rate of depressive symptoms early in the course of schizophrenia was determined. METHOD: Seventy subjects with recent-onset schizophrenia were…”
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Chromosomal abnormalities in a clinic sample of individuals with autistic disorder
Published in Psychiatric genetics (01-06-2001)“…We examined data from the largest reported sample of autistic individuals who have been karyotyped with the aim of providing additional information in the…”
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20
Copy number variations on chromosome 12q14 in patients with normal tension glaucoma
Published in Human molecular genetics (15-06-2011)“…We report identification of a novel genetic locus (GLC1P) for normal tension glaucoma (NTG) on chromosome 12q14 using linkage studies of an African-American…”
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