Thomas H. Wassink

Department of Psychiatry, University of Iowa

Research Area

Biography

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 4	2022

Other Publications

Article	Year
Prevalence of depressive symptoms early in the course of schizophrenia. The American journal of psychiatry\| PubMed ID: 9989572	1999
Heritability of BDNF alleles and their effect on brain morphology in schizophrenia. American journal of medical genetics\| PubMed ID: 10581496	1999
Tumor necrosis factor receptor-II: heritability and effect on brain morphology in schizophrenia. Molecular psychiatry\| PubMed ID: 11126399	2000
Evidence supporting WNT2 as an autism susceptibility gene. American journal of medical genetics\| PubMed ID: 11449391	2001
Chromosomal abnormalities in a clinic sample of individuals with autistic disorder. Psychiatric genetics\| PubMed ID: 11525418	2001
Evaluation of FOXP2 as an autism susceptibility gene. American journal of medical genetics\| PubMed ID: 12116195	2002
NOTCH4 and the frontal lobe in schizophrenia. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics\| PubMed ID: 12627456	2003
Examination of AVPR1a as an autism susceptibility gene. Molecular psychiatry\| PubMed ID: 15098001	2004
An association study of PCQAP polymorphisms and schizophrenia. Psychiatric genetics\| PubMed ID: 15318033	2004
The search for autism disease genes. Mental retardation and developmental disabilities research reviews\| PubMed ID: 15666342	2004
A case of autism and uniparental disomy of chromosome 1. Human genetics\| PubMed ID: 15887000	2005
Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics\| PubMed ID: 15892143	2005
Cognitive and magnetic resonance imaging brain morphometric correlates of brain-derived neurotrophic factor Val66Met gene polymorphism in patients with schizophrenia and healthy volunteers. Archives of general psychiatry\| PubMed ID: 16818862	2006
Systematic screening for subtelomeric anomalies in a clinical sample of autism. Journal of autism and developmental disorders\| PubMed ID: 17004120	2007
Cerebral cortical gray matter overgrowth and functional variation of the serotonin transporter gene in autism. Archives of general psychiatry\| PubMed ID: 17548752	2007
Association between brain-derived neurotrophic factor Val66Met gene polymorphism and progressive brain volume changes in schizophrenia. The American journal of psychiatry\| PubMed ID: 18056245	2007
Posterior probability of linkage analysis of autism dataset identifies linkage to chromosome 16. Psychiatric genetics\| PubMed ID: 18349700	2008
Cortical enlargement in autism is associated with a functional VNTR in the monoamine oxidase A gene. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics\| PubMed ID: 18361446	2008
Basic helix-loop-helix transcription factor NEUROG1 and schizophrenia: effects on illness susceptibility, MRI brain morphometry and cognitive abilities. Schizophrenia research\| PubMed ID: 18799289	2008
MTHFR 677C --> T genotype disrupts prefrontal function in schizophrenia through an interaction with COMT 158Val --> Met. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 18988738	2008
Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature\| PubMed ID: 19404256	2009
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature\| PubMed ID: 19404257	2009
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. PLoS genetics\| PubMed ID: 19557195	2009
G72 influences longitudinal change in frontal lobe volume in schizophrenia. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics\| PubMed ID: 19760675	2010
Functional impact of global rare copy number variation in autism spectrum disorders. Nature\| PubMed ID: 20531469	2010
A genome-wide scan for common alleles affecting risk for autism. Human molecular genetics\| PubMed ID: 20663923	2010
Genome-wide analysis of copy number variants in age-related macular degeneration. Human genetics\| PubMed ID: 20981449	2011
Copy number variations and primary open-angle glaucoma. Investigative ophthalmology & visual science\| PubMed ID: 21310917	2011
Cannabinoid receptor 1 gene polymorphisms and marijuana misuse interactions on white matter and cognitive deficits in schizophrenia. Schizophrenia research\| PubMed ID: 21420833	2011
Copy number variations on chromosome 12q14 in patients with normal tension glaucoma. Human molecular genetics\| PubMed ID: 21447600	2011
DISC1 is associated with cortical thickness and neural efficiency. NeuroImage\| PubMed ID: 21642004	2011
Germline mosaic transmission of a novel duplication of PXDN and MYT1L to two male half-siblings with autism. Psychiatric genetics\| PubMed ID: 22157634	2012
Multifaceted genomic risk for brain function in schizophrenia. NeuroImage\| PubMed ID: 22440650	2012
Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Human molecular genetics\| PubMed ID: 22843504	2012
Influence of ZNF804a on brain structure volumes and symptom severity in individuals with schizophrenia. Archives of general psychiatry\| PubMed ID: 22945618	2012
The impact of copy number deletions on general cognitive ability and ventricle size in patients with schizophrenia and healthy control subjects. Biological psychiatry\| PubMed ID: 23237311	2013
Genetic variation in GAD1 is associated with cortical thickness in the parahippocampal gyrus. Journal of psychiatric research\| PubMed ID: 23566421	2013
Prefrontal inefficiency is associated with polygenic risk for schizophrenia. Schizophrenia bulletin\| PubMed ID: 24327754	2014
Testing for association of the monoamine oxidase A promoter polymorphism with brain structure volumes in both autism and the fragile X syndrome. Journal of neurodevelopmental disorders\| PubMed ID: 24669826	2014
Genetic influences on cognitive endophenotypes in schizophrenia. Schizophrenia research\| PubMed ID: 24768440	2014
A genome-wide CNV analysis of schizophrenia reveals a potential role for a multiple-hit model. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics\| PubMed ID: 25228354	2014
Common genetic variants influence human subcortical brain structures. Nature\| PubMed ID: 25607358	2015
Novel genetic loci underlying human intracranial volume identified through genome-wide association. Nature neuroscience\| PubMed ID: 27694991	2016
Novel genetic loci associated with hippocampal volume. Nature communications\| PubMed ID: 28098162	2017
Genetic architecture of subcortical brain structures in 38,851 individuals. Nature genetics\| PubMed ID: 31636452	2019
Subcortical volumes across the lifespan: Data from 18,605 healthy individuals aged 3-90 years. Human brain mapping\| PubMed ID: 33570244	2021
Cortical thickness across the lifespan: Data from 17,075 healthy individuals aged 3-90 years. Human brain mapping\| PubMed ID: 33595143	2021