Genetic Epidemiology, Translational Neurogenomics, Psychiatric Genetics and Statistical Genetics Laboratories investigate the pattern of disease in families, particularly identical and non-identical twins, to assess the relative importance of genes and environment in a variety of important health problems.
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PMID
19944402
TITLE
A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression.
ABSTRACT
DATE PUBLISHED
2009 Dec
HISTORY
PUBSTATUS PUBSTATUSDATE
received 2009/08/20
revised 2009/10/14
accepted 2009/11/02
aheadofprint 2009/11/26
entrez 2009/12/01 06:00
pubmed 2009/12/01 06:00
medline 2010/01/15 06:00
AUTHORS
NAME COLLECTIVENAME LASTNAME FORENAME INITIALS AFFILIATION AFFILIATIONINFO
Knight HM Division of Psychiatry, University of Edinburgh, Royal Edinburgh Hospital, Edinburgh EH10 5HF, UK.
Pickard BS
Maclean A
Malloy MP
Soares DC
McRae AF
Condie A
White A
Hawkins W
McGhee K
van Beck M
MacIntyre DJ
Starr JM
Deary IJ
Visscher PM
Porteous DJ
Cannon RE
St Clair D
Muir WJ
Blackwood DH
INVESTIGATORS
JOURNAL
MEDLINE JOURNAL
MEDLINETA: Am J Hum Genet
COUNTRY: United States
ISSNLINKING: 0002-9297
NLMUNIQUEID: 0370475
PUBLICATION TYPE
PUBLICATIONTYPE TEXT
Journal Article
Research Support, Non-U.S. Gov't
COMMENTS AND CORRECTIONS
REFTYPE REFSOURCE REFPMID NOTE
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GRANTS
GRANTID AGENCY COUNTRY
CZB/4/498 Chief Scientist Office United Kingdom
G0100266 Medical Research Council United Kingdom
G0900627 Medical Research Council United Kingdom
Biotechnology and Biological Sciences Research Council United Kingdom
Medical Research Council United Kingdom
Wellcome Trust United Kingdom
GENERAL NOTE
KEYWORDS
MESH HEADINGS
DESCRIPTORNAME QUALIFIERNAME
ATP-Binding Cassette Transporters physiology
Amino Acid Sequence physiology
Bipolar Disorder genetics
Case-Control Studies genetics
Codon, Nonsense genetics
Cytogenetics genetics
DNA Mutational Analysis genetics
Depression genetics
Exons genetics
Female genetics
Genetic Linkage genetics
Genetic Predisposition to Disease genetics
Heterozygote genetics
Humans genetics
Male genetics
Middle Aged genetics
Molecular Sequence Data genetics
Mutation, Missense genetics
Polymorphism, Genetic genetics
Schizophrenia genetics
Sequence Homology, Amino Acid genetics
SUPPLEMENTARY MESH
GENE SYMBOLS
CHEMICALS
REGISTRYNUMBER NAMEOFSUBSTANCE
0 ABCA13 protein, human
0 Codon, Nonsense
OTHER ID's
OTHERID SOURCE
PMC2790560 NLM
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