A population-specific uncommon variant in GRIN3A associated with schizophrenia

Biological Psychiatry

Volumn 73, Issue 6, 2013, Pages 532-539

  Takata, Atsushi ^a,b,c   Iwayama, Yoshimi ^a   Fukuo, Yasuhisa ^b   Ikeda, Masashi ^b   Okochi, Tomo ^b   Maekawa, Motoko ^a   Toyota, Tomoko ^a   Yamada, Kazuo ^a   Hattori, Eiji ^a   Ohnishi, Tetsuo ^a   Toyoshima, Manabu ^a   Ujike, Hiroshi ^d   Inada, Toshiya ^e   Kunugi, Hiroshi ^f   Ozaki, Norio ^g   Nanko, Shinichiro ^h   Nakamura, Kazuhiko ⁱ   Mori, Norio ⁱ   Kanba, Shigenobu ^c   Iwata, Nakao ^b   Kato, Tadafumi ^a,b   Yoshikawa, Takeo ^a   more..

^a RIKEN BRAIN SCIENCE INSTITUTE   (Japan)

^b FUJITA HEALTH UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c KYUSHU UNIVERSITY   (Japan)

^d Ujike Nishiguchi Clinic   (Japan)

^e SEIWA HOSPITAL   (Japan)

^f NATIONAL INSTITUTE OF NEUROSCIENCE   (Japan)

^g NAGOYA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^h TEIKYO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

ⁱ HAMAMATSU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

Bipolar disorder; CFB; DNMT1; FAAH; GRIN3A; MYO18B; NR3A; rare variants

Indexed keywords

GLUTAMATE RECEPTOR; N METHYL DEXTRO ASPARTIC ACID RECEPTOR;

ADULT; ALLELE; ARTICLE; ATTENTION; BIPOLAR DISORDER; CHINESE; CONTROLLED STUDY; EFFECT SIZE; FEMALE; GENE; GENE FREQUENCY; GENE STRUCTURE; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HUMAN; JAPANESE; MAJOR CLINICAL STUDY; MALE; META ANALYSIS (TOPIC); MISSENSE MUTATION; N METHYL D ASPARTATE 3A GENE; NONSENSE MUTATION; PRIORITY JOURNAL; SCHIZOPHRENIA;

ASIAN CONTINENTAL ANCESTRY GROUP; BIPOLAR DISORDER; CASE-CONTROL STUDIES; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; MALE; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTORS, N-METHYL-D-ASPARTATE; SCHIZOPHRENIA;

EID: 84874529521     PISSN: 00063223     EISSN: 18732402     Source Type: Journal    
DOI: 10.1016/j.biopsych.2012.10.024     Document Type: Article

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