Thomas H. Wassink

Prevalence of depressive symptoms early in the course of schizophrenia.

Heritability of BDNF alleles and their effect on brain morphology in schizophrenia.

Tumor necrosis factor receptor-II: heritability and effect on brain morphology in schizophrenia.

Evidence supporting WNT2 as an autism susceptibility gene.

Chromosomal abnormalities in a clinic sample of individuals with autistic disorder.

Evaluation of FOXP2 as an autism susceptibility gene.

NOTCH4 and the frontal lobe in schizophrenia.

Examination of AVPR1a as an autism susceptibility gene.

An association study of PCQAP polymorphisms and schizophrenia.

The search for autism disease genes.

A case of autism and uniparental disomy of chromosome 1.

Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene.

Cognitive and magnetic resonance imaging brain morphometric correlates of brain-derived neurotrophic factor Val66Met gene polymorphism in patients with schizophrenia and healthy volunteers.

Systematic screening for subtelomeric anomalies in a clinical sample of autism.

Cerebral cortical gray matter overgrowth and functional variation of the serotonin transporter gene in autism.

Association between brain-derived neurotrophic factor Val66Met gene polymorphism and progressive brain volume changes in schizophrenia.

Posterior probability of linkage analysis of autism dataset identifies linkage to chromosome 16.

Cortical enlargement in autism is associated with a functional VNTR in the monoamine oxidase A gene.

Basic helix-loop-helix transcription factor NEUROG1 and schizophrenia: effects on illness susceptibility, MRI brain morphometry and cognitive abilities.

MTHFR 677C --> T genotype disrupts prefrontal function in schizophrenia through an interaction with COMT 158Val --> Met.

Common genetic variants on 5p14.1 associate with autism spectrum disorders.

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.

G72 influences longitudinal change in frontal lobe volume in schizophrenia.

Functional impact of global rare copy number variation in autism spectrum disorders.

A genome-wide scan for common alleles affecting risk for autism.

Genome-wide analysis of copy number variants in age-related macular degeneration.

Copy number variations and primary open-angle glaucoma.

Cannabinoid receptor 1 gene polymorphisms and marijuana misuse interactions on white matter and cognitive deficits in schizophrenia.

Copy number variations on chromosome 12q14 in patients with normal tension glaucoma.

DISC1 is associated with cortical thickness and neural efficiency.

Germline mosaic transmission of a novel duplication of PXDN and MYT1L to two male half-siblings with autism.

Multifaceted genomic risk for brain function in schizophrenia.

Individual common variants exert weak effects on the risk for autism spectrum disorderspi.

Influence of ZNF804a on brain structure volumes and symptom severity in individuals with schizophrenia.

The impact of copy number deletions on general cognitive ability and ventricle size in patients with schizophrenia and healthy control subjects.

Genetic variation in GAD1 is associated with cortical thickness in the parahippocampal gyrus.

Prefrontal inefficiency is associated with polygenic risk for schizophrenia.

Testing for association of the monoamine oxidase A promoter polymorphism with brain structure volumes in both autism and the fragile X syndrome.

Genetic influences on cognitive endophenotypes in schizophrenia.

A genome-wide CNV analysis of schizophrenia reveals a potential role for a multiple-hit model.

Common genetic variants influence human subcortical brain structures.

Novel genetic loci underlying human intracranial volume identified through genome-wide association.

Novel genetic loci associated with hippocampal volume.

Genetic architecture of subcortical brain structures in 38,851 individuals.

Subcortical volumes across the lifespan: Data from 18,605 healthy individuals aged 3-90 years.

Cortical thickness across the lifespan: Data from 17,075 healthy individuals aged 3-90 years.