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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 7 (of 7 Records)

Query Trace: Disease and KCNN3[original query]
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
Association analysis of a highly polymorphic CAG Repeat in the human potassium channel gene KCNN3 and migraine susceptibility.
BMC medical genetics 2005 Sep 6 (): 32.
Curtain Robert, Sundholm James, Lea Rod, Ovcaric Mick, MacMillan John, Griffiths L
Common variants in KCNN3 are associated with lone atrial fibrillation. GWAS Catalog
Nature genetics 2010 Mar 42 (3): 240-4.
Ellinor Patrick T, Lunetta Kathryn L, Glazer Nicole L, Pfeufer Arne, Alonso Alvaro, Chung Mina K, Sinner Moritz F, de Bakker Paul I W, Mueller Martina, Lubitz Steven A, Fox Ervin, Darbar Dawood, Smith Nicholas L, Smith Jonathan D, Schnabel Renate B, Soliman Elsayed Z, Rice Kenneth M, Van Wagoner David R, Beckmann Britt-M, van Noord Charlotte, Wang Ke, Ehret Georg B, Rotter Jerome I, Hazen Stanley L, Steinbeck Gerhard, Smith Albert V, Launer Lenore J, Harris Tamara B, Makino Seiko, Nelis Mari, Milan David J, Perz Siegfried, Esko Tõnu, Köttgen Anna, Moebus Susanne, Newton-Cheh Christopher, Li Man, Möhlenkamp Stefan, Wang Thomas J, Kao W H Linda, Vasan Ramachandran S, Nöthen Markus M, MacRae Calum A, Stricker Bruno H Ch, Hofman Albert, Uitterlinden André G, Levy Daniel, Boerwinkle Eric, Metspalu Andres, Topol Eric J, Chakravarti Aravinda, Gudnason Vilmundur, Psaty Bruce M, Roden Dan M, Meitinger Thomas, Wichmann H-Erich, Witteman Jacqueline C M, Barnard John, Arking Dan E, Benjamin Emelia J, Heckbert Susan R, Kääb Stef
Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population.
Human genetics 2011 Mar 129 (3): 239-46.
Li Cong, Wang Fan, Yang Yanzong, Fu Fenfen, Xu Chengqi, Shi Lisong, Li Sisi, Xia Yunlong, Wu Gang, Cheng Xiang, Liu Hui, Wang Chuchu, Wang Pengyun, Hao Jianjun, Ke Yuhe, Zhao Yuanyuan, Liu Mugen, Zhang Rongfeng, Gao Lianjun, Yu Bo, Zeng Qiutang, Liao Yuhua, Yang Bo, Tu Xin, Wang Qing
Severity of obstructive sleep apnea influences the effect of genotype on response to anti-arrhythmic drug therapy for atrial fibrillation.
Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine 2014 May 10 (5): 503-7.
Goyal Sandeep K, Wang Li, Upender Raghu, Darbar Dawood, Monahan K
Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation.
Journal of medical genetics 2015 Jan 52 (1): 28-36.
Tsai Chia-Ti, Hsieh Chia-Shan, Chang Sheng-Nan, Chuang Eric Y, Juang Jyh-Ming Jimmy, Lin Lian-Yu, Lai Ling-Ping, Hwang Juey-Jen, Chiang Fu-Tien, Lin Jiunn-L
[Rs17042171 at chromosome 4q25 is associated with atrial fibrillation in the Chinese Han population from the central plains].
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2018 Jun 43 (6): 594-603.
Wang Xu, Nie Yali, Ning Shuwei, Shi Yong, Zhao Yujie, Niu Siquan, Guo Chengxian, Meng Xiangguang, Yuan Yiqia
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