Possible association between genetic variants at the GRIN1 gene and schizophrenia with lifetime history of depressive symptoms in a German sample

Psychiatric Genetics

Volumn 17, Issue 5, 2007, Pages 308-310

  Georgi, Alexander ^a   Jamra, Rami Abou ^b   Klein, Katrin ^b   Villela, Angela Wolf ^b   Schumacher, Johannes ^b   Becker, Tim ^b   Paul, Torsten ^a   Schmael, Christine ^a   Höfels, Susanne ^c   Klopp, Norman ^c   Illig, Thomas ^c   Propping, Peter ^b   Cichon, Sven ^b   Nöthen, Markus M ^b   Schulze, Thomas G ^a   Rietschel, Marcella ^a  

^a CENTRAL INSTITUTE OF MENTAL HEALTH   (Germany)

^b UNIVERSITY OF BONN   (Germany)

^c INSTITUTE OF EPIDEMIOLOGY   (Germany)

Author keywords

Affective disorder; Depression; Genotype phenotype correlation; Glutamate; N methyl D aspartate; Psychosis

Indexed keywords

N METHYL DEXTRO ASPARTIC ACID RECEPTOR;

ADULT; ARTICLE; CONTROLLED STUDY; FEMALE; GENETIC ASSOCIATION; GENETIC VARIABILITY; GERMANY; HAPLOTYPE; HUMAN; LIFESPAN; MAJOR CLINICAL STUDY; MAJOR DEPRESSION; MALE; MARKER GENE; MICROSATELLITE MARKER; PHENOTYPE; PRIORITY JOURNAL; SCHIZOPHRENIA; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL SIGNIFICANCE; SYMPTOM;

CARRIER PROTEINS; DEPRESSIVE DISORDER; GERMANY; HUMANS; NERVE TISSUE PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTORS, N-METHYL-D-ASPARTATE; SCHIZOPHRENIA; VARIATION (GENETICS);

EID: 34548309202     PISSN: 09558829     EISSN: None     Source Type: Journal    
DOI: 10.1097/YPG.0b013e3280c1e5fb     Document Type: Article

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