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Records 1-6

Query Trace: Bipolar Disorder and KCNN3[orginal query]

CAG repeat polymorphism within the KCNN3 gene is a significant contributor to susceptibility to anorexia nervosa: a case-control study of female patients and several ethnic groups in the Israeli Jewish population. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004 Nov 131B (1): 76-80. Koronyo-Hamaoui Maya, Gak Eva, Stein Daniel, Frisch Amos, Danziger Yardena, Leor Shani, Michaelovsky Elena, Laufer Neil, Carel Cynthia, Fennig Silvana, Mimouni Marc, Apter Alan, Goldman Boleslav, Barkai Gad, Weizman Abrah Similar articles in PubMed
CAG-repeat length in exon 1 of KCNN3 does not influence risk for schizophrenia or bipolar disorder: a meta-analysis of association studies. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003 Aug 121B (1): 14-20. Glatt Stephen J, Faraone Stephen V, Tsuang Ming Similar articles in PubMed
Association and linkage studies between bipolar affective disorder and the polymorphic CAG/CTG repeat loci ERDA1, SEF2-1B, MAB21L and KCNN3. Molecular psychiatry 2001 Sep 6 (5): 565-9. Meira-Lima I V, Zhao J, Sham P, Pereira A C, Krieger J E, Vallada Similar articles in PubMed
CAG repeats of CTG18.1 and KCNN3 in Korean patients with bipolar affective disorder. Journal of affective disorders 2001 Sep 66 (1): 19-24. Jin D K, Hwang H Z, Oh M R, Kim J S, Lee M, Kim S, Lim S W, Seo M Y, Kim J H, Kim D Similar articles in PubMed
Association study of CAG repeats in the KCNN3 gene in Japanese patients with schizophrenia, schizoaffective disorder and bipolar disorder. Psychiatry research 2001 Apr 101 (3): 203-7. Ujike H, Yamamoto A, Tanaka Y, Takehisa Y, Takaki M, Taked T, Kodama M, Kuroda Similar articles in PubMed
Association analysis of CAG repeats at the KCNN3 locus in Indian patients with bipolar disorder and schizophrenia. American journal of medical genetics 2000 Dec 96 (6): 744-8. Saleem Q, Sreevidya V S, Sudhir J, Savithri J V, Gowda Y, B-Rao C, Benegal V, Majumder P P, Anand A, Brahmachari S K, Jain Similar articles in PubMed

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