Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 52 Records) |
Query Trace: KCNJ2[original query] |
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Genetics of long-term treatment outcome in bipolar disorder.
Progress in neuro-psychopharmacology & biological psychiatry 2016 Feb 65 17-24. Fabbri Chiara, Serretti Alessand |
Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome. PloS one 2015 10 (7): e0133037. Allegue Catarina, Coll Mònica, Mates Jesus, Campuzano Oscar, Iglesias Anna, Sobrino Beatriz, Brion Maria, Amigo Jorge, Carracedo Angel, Brugada Pedro, Brugada Josep, Brugada Ram |
Coexistence of Andersen-Tawil Syndrome with Polymorphisms in hERG1 Gene (K897T) and SCN5A Gene (H558R) in One Family. Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc 2015 Jun . Jagodzi?ska Michalina, Szperl Ma?gorzata, Poni?ska Joanna, Kosiec Agnieszka, Gajda Robert, Kukla Piotr, Biernacka El?bieta Katarzy |
A genome-wide analysis of the response to inhaled ß2-agonists in chronic obstructive pulmonary disease.
The pharmacogenomics journal 2015 Oct . Hardin M, Cho M H, McDonald M-L, Wan E, Lomas D A, Coxson H O, MacNee W, Vestbo J, Yates J C, Agusti A, Calverley P M A, Celli B, Crim C, Rennard S, Wouters E, Bakke P, Bhatt S P, Kim V, Ramsdell J, Regan E A, Make B J, Hokanson J E, Crapo J D, Beaty T H, Hersh C P, , , |
Novel susceptibility gene for nonfamilial hypokalemic periodic paralysis. Neurology 2016 Mar . Song I-Wen, Sung Chih-Chien, Chen Chien-Hsiun, Cheng Chih-Jen, Yang Sung-Sen, Chou Yi-Chun, Yang Jenn-Hwai, Chen Yuan-Tsong, Wu Jer-Yuarn, Lin Shih-H |
TBX5 mutations contribute to early-onset atrial fibrillation in Chinese and Caucasians. Cardiovascular research 2016 Jan . Ma Ji-Fang, Yang Fan, Mahida Saagar N, Zhao Ling, Chen Xiaomin, Zhang Michael L, Sun Zhijun, Yao Yan, Zhang Yi-Xin, Zheng Gu-Yan, Dong Jie, Feng Ming-Jun, Zhang Rui, Sun Jian, Li Shuo, Wang Qun-Shan, Cao Huiqing, Benjamin Emelia J, Ellinor Patrick T, Li Yi-Gang, Tian Xiao- |
Novel lincRNA Susceptibility Gene and Its Role in Etiopathogenesis of Thyrotoxic Periodic Paralysis. Journal of the Endocrine Society 2017 Jul 1 (7): 809-815. Melo Maria Clara C, de Souza Janaína S, Kizys Marina M L, Vidi Angela C, Dorta Haron S, Kunii Ilda S, Giannocco Gisele, Carvalheira Gianna, Dias-da-Silva Magnus |
Replication Study for the Association of GWAS-associated Loci With Adolescent Idiopathic Scoliosis Susceptibility and Curve Progression in a Chinese Population. Spine 2018 Sep . Man Gene Chi-Wai, Tang Nelson Leung-Sang, Chan Ting Fung, Lam Tsz Ping, Li Jing Woei, Ng Bobby Kin-Wah, Zhu Zezhang, Qiu Yong, Cheng Jack Chun-Y |
Retrospective Genetic Analysis of 200 Cases of Sudden Infant Death Syndrome and Its Relationship with Long QT Syndrome in Korea. Journal of Korean medical science 2018 8 33 (32): e200. Son Min-Jeong, Kim Min-Kyoung, Yang Kyung-Moo, Choi Byung-Ha, Lee Bong Woo, Yoo Seong |
The Relationship between Single Nucleotide Polymorphisms in Taste Receptor Genes, Taste Function and Dietary Intake in Preschool-Aged Children and Adults in the Guelph Family Health Study. Nutrients 2018 Jul 10 (8): . Chamoun Elie, Carroll Nicholas A, Duizer Lisa M, Qi Wenjuan, Feng Zeny, Darlington Gerarda, Duncan Alison M, Haines Jess, Ma David W L, |
Whole-exome sequencing reveals microsatellite DNA markers for response to dofetilide initiation in patients with persistent atrial fibrillation: A pilot study. Clinical cardiology 2018 Apr . Kinney Nick, Larsen Timothy R, Kim David M, Varghese Robin T, Poelzing Steven, Garner Harold R, AlMahameed Soufian |
Association study between inwardly rectifying potassium channels 2.1 and 4.1 and autism spectrum disorders. Life sciences 2018 Oct . Sun Caihong, Zou Mingyang, Li Ling, Li Dexin, Ma Yongjuan, Xia Wei, Wu Lijie, Ren Hu |
Different responses to exercise between Andersen-Tawil syndrome and catecholaminergic polymorphic ventricular tachycardia. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2018 1 20 (10): 1675-1682. Inoue Yuko Y, Aiba Takeshi, Kawata Hiro, Sakaguchi Tomoko, Mitsuma Wataru, Morita Hiroshi, Noda Takashi, Takaki Hiroshi, Toyohara Keiko, Kanaya Yoshiaki, Itoi Toshiyuki, Mitsuhashi Takeshi, Sumitomo Naokata, Cho Yongkeun, Yasuda Satoshi, Kamakura Shiro, Kusano Kengo, Miyamoto Yoshihiro, Horie Minoru, Shimizu Wata |
Atypical periodic paralysis and myalgia: A novel RYR1 phenotype. Neurology 2018 1 90 (5): e412-e418. Matthews Emma, Neuwirth Christoph, Jaffer Fatima, Scalco Renata S, Fialho Doreen, Parton Matt, Raja Rayan Dipa, Suetterlin Karen, Sud Richa, Spiegel Roland, Mein Rachel, Houlden Henry, Schaefer Andrew, Healy Estelle, Palace Jacqueline, Quinlivan Ros, Treves Susan, Holton Janice L, Jungbluth Heinz, Hanna Michael |
Breast Cancer Clinical Trial of Chemotherapy and Trastuzumab: Potential Tool to Identify Cardiac Modifying Variants of Dilated Cardiomyopathy. Journal of cardiovascular development and disease 2018 1 4 (2): . Serie Daniel J, Crook Julia E, Necela Brian M, Axenfeld Bianca C, Dockter Travis J, Colon-Otero Gerardo, Perez Edith A, Thompson E Aubrey, Norton Nadi |
The research of ion channel-related gene polymorphisms with atrial fibrillation in the Chinese Han population. Molecular genetics & genomic medicine 2019 Jul e835. Liu Xiumin, Li Yujie, Zhang Huan, Ji Yuqiang, Zhao Zhao, Wang Chang |
Contribution of Asian Haplotype of KCNJ18 to Susceptibility to and Ethnic Differences in Thyrotoxic Periodic Paralysis. The Journal of clinical endocrinology and metabolism 2019 Jul . Noso Shinsuke, Babaya Naru, Hiromine Yoshihisa, Ito Hiroyuki, Taketomo Yasunori, Yoshida Sawa, Niwano Fumimaru, Monobe Keisuke, Minohara Tatsuro, Okada Takuya, Tsugawa Mamiko, Kawabata Yumiko, Ikegami Hiros |
Short QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare Variants. Journal of clinical medicine 2019 7 8 (7): . Campuzano Oscar, Fernandez-Falgueras Anna, Lemus Ximena, Sarquella-Brugada Georgia, Cesar Sergi, Coll Monica, Mates Jesus, Arbelo Elena, Jordà Paloma, Perez-Serra Alexandra, Del Olmo Bernat, Ferrer-Costa Carles, Iglesias Anna, Fiol Victoria, Puigmulé Marta, Lopez Laura, Pico Ferran, Brugada Josep, Brugada Ram |
Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults: A Population-Based Genome-Wide Association Study.
JAMA network open 2019 May 2 (5): e193348. Zhao Shuang-Xia, Liu Wei, Liang Jun, Gao Guan-Qi, Zhang Xiao-Mei, Yao Yu, Wang Hai-Ning, Yuan Fei-Fei, Xue Li-Qiong, Ma Yu-Ru, Zhang Le-Le, Ye Xiao-Ping, Zhang Qian-Yue, Sun Feng, Zhang Rui-Jia, Yang Shao-Ying, Zhan Ming, Du Wen-Hua, Liu Bing-Li, Chen Xia, Song Zhi-Yi, Li Xue-Song, Li Ping, Ru Ying, Zuo Chun-Lin, Li Sheng-Xian, Han Bing, Zhu Hui, Qiao Jie, Xuan Miao, Su Bin, Sun Fei, Ma Jun-Hua, Chen Jia-Lun, Tian Hao-Ming, Chen Sai-Juan, Song Huai-Dong, |
Identification of gene mutations in patients with primary periodic paralysis using targeted next-generation sequencing. BMC neurology 2019 5 19 (1): 92. Luo Sushan, Xu Minjie, Sun Jian, Qiao Kai, Song Jie, Cai Shuang, Zhu Wenhua, Zhou Lei, Xi Jianying, Lu Jiahong, Ni Xiaohua, Dou Tonghai, Zhao Chong |
Analysis of the genetic background associated with sporadic periodic paralysis in Japanese patients. Journal of the neurological sciences 2020 Mar 116795. Nakaza Maki, Kitamura Yuri, Furuta Mitsuru, Kubota Tomoya, Sasaki Ryogen, Takahashi Masanori |
Gene discovery for high-density lipoprotein cholesterol level change over time in prospective family studies.
Atherosclerosis 2020 Feb 297 102-110. Feitosa Mary F, Lunetta Kathryn L, Wang Lihua, Wojczynski Mary K, Kammerer Candace M, Perls Thomas, Schupf Nicole, Christensen Kaare, Murabito Joanne M, Province Michael |
Genome-wide meta-analysis reveals novel susceptibility loci for thyrotoxic periodic paralysis.
European journal of endocrinology 2020 Dec 183 (6): 607-617. Hoi-Yee Li Gloria, Cheung Ching-Lung, Zhao Shuang-Xia, Song Huai-Dong, Wai-Chee Kung Ann |
A genome-wide association study of severe asthma exacerbations in Latino children and adolescents.
The European respiratory journal 2020 Oct . Yan Qi, Forno Erick, Herrera-Luis Esther, Pino-Yanes Maria, Qi Cancan, Rios Raimon, Han Yueh-Ying, Kim Soyeon, Oh Sam, Acosta-Pérez Edna, Zhang Rong, Hu Donglei, Eng Celeste, Huntsman Scott, Avila Lydiana, Boutaoui Nadia, Cloutier Michelle M, Soto-Quiros Manuel E, Xu Cheng-Jian, Weiss Scott T, Lasky-Su Jessica, Kiedrowski Megan R, Figueiredo Camila, Bomberger Jennifer, Barreto Mauricio L, Canino Glorisa, Chen Wei, Koppelman Gerard H, Burchard Esteban G, Celedón Juan |
Sour Taste SNP KCNJ2-rs236514 and Differences in Nutrient Intakes and Metabolic Health Markers in the Elderly. Frontiers in nutrition 2021 9 8 701588. Ferraris Celeste, Turner Alexandria, Scarlett Christopher J, Veysey Martin, Lucock Mark, Bucher Tamara, Beckett Emma |
Association analysis of SNPs in GRHL3, FAF1, and KCNJ2 with NSCPO sub-phenotypes in Han Chinese. Oral diseases 2021 7 28 (8): 2204-2214. Sun Jia-Lin, Shi Jia-Yu, Yin Bin, Lin Yan-Song, Shi Bing, Jia Zhong-L |
Association between Sour Taste SNP KCNJ2-rs236514, Diet Quality and Mild Cognitive Impairment in an Elderly Cohort. Nutrients 2021 Feb 13 (3): . Ferraris Celeste, Turner Alexandria, Scarlett Christopher, Veysey Martin, Lucock Mark, Bucher Tamara, Beckett Emma |
Mutational spectrum of congenital long QT syndrome in Turkey; identification of 12 novel mutations across KCNQ1, KCNH2, SCN5A, KCNJ2, CACNA1C, and CALM1. Journal of cardiovascular electrophysiology 2021 12 33 (2): 262-273. Akgun-Dogan Ozlem, A?ao?lu Nihat B, K Demirkol Yasemin, Do?anay Levent, Ergül Yakup, Karacan Mehm |
Twelve Loci Associated With Bone Density in Middle-aged and Elderly Chinese: The Shanghai Changfeng Study. The Journal of clinical endocrinology and metabolism 2022 10 108 (2): 295-305. Zeng Hailuan, Ge Jieyu, Xu Wenjie, Ma Hui, Chen Lingyan, Xia Mingfeng, Pan Baishen, Lin Huandong, Wang Sijia, Gao X |
Genetic analysis identifies the SLC4A3 anion exchanger as a major gene for short QT syndrome. Heart rhythm 2023 2 . Christiansen Morten Krogh, Kjær-Sørensen Kasper, Clavsen Natacha C, Dittmann Sven, Jensen Maja Fuhlendorff, Guldbrandsen Halvor Østerby, Pedersen Lisbeth Nørum, Sørensen Rikke Hasle, Lildballe Dorte Launholt, Müller Klara, Müller Patrick, Vogel Kira, Rudic Boris, Borggrefe Martin, Oxvig Claus, Aalkjær Christian, Schulze-Bahr Eric, Matchkov Vladimir, Bundgaard Henning, Jensen Henrik Kjæru |
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