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David Curtis
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researcher (ORCID 0000-0002-4089-9183)
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Works
14
A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
scientific article
Gene–Brain Structure Relationships: Arbitrary Assumptions of Heterogeneity Generate Unfalsifiable Claims—Reply
article
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.
scientific article
The Epsin 4 gene on chromosome 5q, which encodes the clathrin-associated protein enthoprotin, is involved in the genetic susceptibility to schizophrenia
scientific article
Support of association between BRD1 and both schizophrenia and bipolar affective disorder.
scientific article published in March 2010
Fine mapping by genetic association implicates the chromosome 1q23.3 gene UHMK1, encoding a serine/threonine protein kinase, as a novel schizophrenia susceptibility gene
scientific article
Failure to confirm genetic association between schizophrenia and markers on chromosome 1q23.3 in the region of the gene encoding the regulator of G-protein signaling 4 protein (RGS4).
scientific article published in April 2006
Failure to confirm allelic association between markers at the CAPON gene locus and schizophrenia in a British sample
scientific article
Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes
scientific article
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