Human Genome Epidemiology Literature Finder
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Records 1 - 24 (of 24 Records) |
| Query Trace: Disease and KCNJ2[original query] |
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Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3.
Nature genetics 2012 Aug . Cheung CL, Lau KS, Ho AY, Lee KK, Tiu SC, Lau EY, Leung J, Tsang MW, Chan KW, Yeung CY, Woo YC, Cheung EY, Hung VH, Pang HK, Hung CS, Sham PC, Kung AW |
| Phenotype variability in patients carrying KCNJ2 mutations. Circulation. Cardiovascular genetics 2012 Jun 5 (3): 344-53. Kimura Hiromi, Zhou Jun, Kawamura Mihoko, Itoh Hideki, Mizusawa Yuka, Ding Wei-Guang, Wu Jie, Ohno Seiko, Makiyama Takeru, Miyamoto Akashi, Naiki Nobu, Wang Qi, Xie Yu, Suzuki Tsugutoshi, Tateno Shigeru, Nakamura Yoshihide, Zang Wei-Jin, Ito Makoto, Matsuura Hiroshi, Horie Mino |
| New exome data question the pathogenicity of genetic variants previously associated with catecholaminergic polymorphic ventricular tachycardia. Circulation. Cardiovascular genetics 2013 Oct 6 (5): 481-9. Jabbari Javad, Jabbari Reza, Nielsen Morten W, Holst Anders G, Nielsen Jonas B, Haunsø Stig, Tfelt-Hansen Jacob, Svendsen Jesper H, Olesen Morten |
| Results of genetic testing in 855 consecutive unrelated patients referred for long QT syndrome in a clinical laboratory. Genetic testing and molecular biomarkers 2013 Jul 17 (7): 553-61. Lieve Krystien V, Williams Leah, Daly Amy, Richard Gabriele, Bale Sherri, Macaya Daniela, Chung Wendy |
| Genetic background of catecholaminergic polymorphic ventricular tachycardia in Japan. Circulation journal : official journal of the Japanese Circulation Society 2013 77 (7): 1705-13. Kawamura Mihoko, Ohno Seiko, Naiki Nobu, Nagaoka Iori, Dochi Kenichi, Wang Qi, Hasegawa Kanae, Kimura Hiromi, Miyamoto Akashi, Mizusawa Yuka, Itoh Hideki, Makiyama Takeru, Sumitomo Naokata, Ushinohama Hiroya, Oyama Kotaro, Murakoshi Nobuyuki, Aonuma Kazutaka, Horigome Hitoshi, Honda Takafumi, Yoshinaga Masao, Ito Makoto, Horie Mino |
| Genome-wide association analysis identifies six new loci associated with forced vital capacity.
Nature genetics 2014 Jul 46 (7): 669-77. Loth Daan W, Artigas María Soler, Gharib Sina A, Wain Louise V, Franceschini Nora, Koch Beate, Pottinger Tess D, Smith Albert Vernon, Duan Qing, Oldmeadow Chris, Lee Mi Kyeong, Strachan David P, James Alan L, Huffman Jennifer E, Vitart Veronique, Ramasamy Adaikalavan, Wareham Nicholas J, Kaprio Jaakko, Wang Xin-Qun, Trochet Holly, Kähönen Mika, Flexeder Claudia, Albrecht Eva, Lopez Lorna M, de Jong Kim, Thyagarajan Bharat, Alves Alexessander Couto, Enroth Stefan, Omenaas Ernst, Joshi Peter K, Fall Tove, Viñuela Ana, Launer Lenore J, Loehr Laura R, Fornage Myriam, Li Guo, Wilk Jemma B, Tang Wenbo, Manichaikul Ani, Lahousse Lies, Harris Tamara B, North Kari E, Rudnicka Alicja R, Hui Jennie, Gu Xiangjun, Lumley Thomas, Wright Alan F, Hastie Nicholas D, Campbell Susan, Kumar Rajesh, Pin Isabelle, Scott Robert A, Pietiläinen Kirsi H, Surakka Ida, Liu Yongmei, Holliday Elizabeth G, Schulz Holger, Heinrich Joachim, Davies Gail, Vonk Judith M, Wojczynski Mary, Pouta Anneli, Johansson Asa, Wild Sarah H, Ingelsson Erik, Rivadeneira Fernando, Völzke Henry, Hysi Pirro G, Eiriksdottir Gudny, Morrison Alanna C, Rotter Jerome I, Gao Wei, Postma Dirkje S, White Wendy B, Rich Stephen S, Hofman Albert, Aspelund Thor, Couper David, Smith Lewis J, Psaty Bruce M, Lohman Kurt, Burchard Esteban G, Uitterlinden André G, Garcia Melissa, Joubert Bonnie R, McArdle Wendy L, Musk A Bill, Hansel Nadia, Heckbert Susan R, Zgaga Lina, van Meurs Joyce B J, Navarro Pau, Rudan Igor, Oh Yeon-Mok, Redline Susan, Jarvis Deborah L, Zhao Jing Hua, Rantanen Taina, O'Connor George T, Ripatti Samuli, Scott Rodney J, Karrasch Stefan, Grallert Harald, Gaddis Nathan C, Starr John M, Wijmenga Cisca, Minster Ryan L, Lederer David J, Pekkanen Juha, Gyllensten Ulf, Campbell Harry, Morris Andrew P, Gläser Sven, Hammond Christopher J, Burkart Kristin M, Beilby John, Kritchevsky Stephen B, Gudnason Vilmundur, Hancock Dana B, Williams O Dale, Polasek Ozren, Zemunik Tatijana, Kolcic Ivana, Petrini Marcy F, Wjst Matthias, Kim Woo Jin, Porteous David J, Scotland Generation, Smith Blair H, Viljanen Anne, Heliövaara Markku, Attia John R, Sayers Ian, Hampel Regina, Gieger Christian, Deary Ian J, Boezen H Marike, Newman Anne, Jarvelin Marjo-Riitta, Wilson James F, Lind Lars, Stricker Bruno H, Teumer Alexander, Spector Timothy D, Melén Erik, Peters Marjolein J, Lange Leslie A, Barr R Graham, Bracke Ken R, Verhamme Fien M, Sung Joohon, Hiemstra Pieter S, Cassano Patricia A, Sood Akshay, Hayward Caroline, Dupuis Josée, Hall Ian P, Brusselle Guy G, Tobin Martin D, London Stephanie |
| 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 markers of repolarization and arrhythmic events after acute coronary syndromes. American heart journal 2015 Apr 169 (4): 579-86.e3. Earle N J, Poppe K K, Pilbrow A P, Cameron V A, Troughton R W, Skinner J R, Love D R, Shelling A N, Whalley G A, Ellis C J, Richards A M, Doughty R |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| Rare variants at KCNJ2 are associated with LDL-cholesterol levels in a cross-population study. NPJ genomic medicine 2024 6 9 (1): 36. Niccolò Rossi, Najeeb Syed, Alessia Visconti, Elbay Aliyev, Sarah Berry, Mafalda Bourbon, Tim D Spector, Pirro G Hysi, Khalid A Fakhro, Mario Falc |
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