No evidence for an involvement of copy number variation in ABCA13 in schizophrenia, bipolar disorder, or major depressive disorder

Psychiatric Genetics

Volumn 23, Issue 1, 2013, Pages 45-46

  Degenhardt, Franziska ^a,b   Priebe, Lutz ^a,b   Strohmaier, Jana ^f   Herms, Stefan ^a,b   Hoffmann, Per ^a,b   Mattheisen, Manuel ^b,c,l   Mössner, Rainald ^d   Nenadic, Igor ^g   Sauer, Heinrich ^g   Rujescu, Dan ^h,i   Maier, Wolfgang ^d   Schulze, Thomas G ^e,j   Rietschel, Marcella ^f   Nöthen, Markus M ^a,b,e   Cichon, Sven ^a,b,k,l  

^a Institute of Human Genetics   (Germany)

^b Life and Brain Center   (Germany)

^c Institute for Genomic Mathematics   (Germany)

^d UNIVERSITY OF BONN   (Germany)

^e GERMAN CENTER FOR NEURODEGENERATIVE DISEASES DZNE   (Germany)

^f UNIVERSITY OF HEIDELBERG   (Germany)

^g JENA UNIVERSITY HOSPITAL   (Germany)

^h LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

ⁱ MARTIN LUTHER UNIVERSITY HALLE WITTENBERG   (Germany)

^j UNIVERSITY MEDICAL CENTER GÖTTINGEN   (Germany)

^k FORSCHUNGSZENTRUM JÜLICH   (Germany)

^l HARVARD MEDICAL SCHOOL   (United States)

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Author keywords

[No Author keywords available]

Indexed keywords

ABC TRANSPORTER; ABC TRANSPORTER A13; UNCLASSIFIED DRUG;

BIPOLAR DISORDER; CONTROLLED STUDY; COPY NUMBER VARIATION; GENE DELETION; GENE DUPLICATION; GENETIC ASSOCIATION; GENOTYPE; HUMAN; LETTER; MAJOR CLINICAL STUDY; MAJOR DEPRESSION; PRIORITY JOURNAL; SCHIZOPHRENIA;

ATP-BINDING CASSETTE TRANSPORTERS; BIPOLAR DISORDER; CASE-CONTROL STUDIES; DEPRESSIVE DISORDER, MAJOR; DNA COPY NUMBER VARIATIONS; GENETIC PREDISPOSITION TO DISEASE; HUMANS; SCHIZOPHRENIA;

EID: 84871748438     PISSN: 09558829     EISSN: 14735873     Source Type: Journal    
DOI: 10.1097/YPG.0b013e328358645b     Document Type: Letter

References (5)

1. Degenhardt F, Priebe L, Herms S, Mattheisen M, Mu? hleisen TW, Meier S, et al. (2012). Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample. Am J Med Genet B Neuropsychiatr Genet 159B:263-273.
2. Knight HM, Pickard BS, Maclean A, Malloy MP, Soares DC, Mcrae AF, et al. (2009). A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression. Am J Hum Genet 85:833-846.
3. Pickard BS, Van Den Bossche MJ, Malloy MP, Johnstone M, Lenaerts AS, Nordin A, et al. (2012). Multiplex amplicon quantification screening the ABCA13 gene for copy number variation in schizophrenia and bipolar disorder. Psychiatr Genet [Epub ahead of print].
4. Priebe L, Degenhardt FA, Herms S, Haenisch B, Mattheisen M, Nieratschker V, et al. (2012). Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder. Mol Psychiatry 17:421-432.
5. Rietschel M, Mattheisen M, Degenhardt F, Kahn RS, Linszen DH, Os JV, et al. GROUP Investigators Genetic Risk and Outcome in Psychosis (GROUP Investigators) (2011). Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe. Mol Psychiatry [Epub ahead of print].