Human Genome Epidemiology Literature Finder
Records 1 - 19 (of 19 Records) |
Query Trace: KCNMA1[original query] |
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Genetic variation in the KCNMA1 potassium channel alpha subunit as risk factor for severe essential hypertension and myocardial infarction. Journal of hypertension 2008 Nov 26 (11): 2147-53. Tomás Marta, Vázquez Esther, Fernández-Fernández José M, Subirana Isaac, Plata Cristina, Heras Magda, Vila Joan, Marrugat Jaume, Valverde Miguel A, Sentí Maria |
Genome wide association study identifies KCNMA1 contributing to human obesity.
BMC medical genomics 2011 Jun 4 (1): 1. Jiao H, Arner P, Hoffstedt J, Brodin D, Dubern B, Czernichow S, Van't Hooft F, Axelsson T, Pedersen O, Hansen T, Sorensen TI, Hedebrand J, Kere J, Dahlman-Wright K, Hamsten A, Clement K, Dahlman I |
Replication study of genome-wide associated SNPs with late-onset Alzheimer's disease. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2011 Jun 156B (4): 507-12. Burns L C, Minster R L, Demirci F Y, Barmada M M, Ganguli M, Lopez O L, DeKosky S T, Kamboh M |
Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample.
Alcoholism, clinical and experimental research 2011 May 35 (5): 963-75. Kendler Kenneth S, Kalsi Gursharan, Holmans Peter A, Sanders Alan R, Aggen Steven H, Dick Danielle M, Aliev Fazil, Shi Jianxin, Levinson Douglas F, Gejman Pablo |
Genetic variation in genes encoding airway epithelial potassium channels is associated with chronic rhinosinusitis in a pediatric population. PloS one 2014 9 (3): e89329. Purkey Michael T, Li Jin, Mentch Frank, Grant Struan F A, Desrosiers Martin, Hakonarson Hakon, Toskala Eli |
Thiopurine pharmacogenomics: association of SNPs with clinical response and functional validation of candidate genes. Pharmacogenomics 2014 Mar 15 (4): 433-47. Matimba Alice, Li Fang, Livshits Alina, Cartwright Cher S, Scully Stephen, Fridley Brooke L, Jenkins Gregory, Batzler Anthony, Wang Liewei, Weinshilboum Richard, Lennard Lyn |
Identification of TWIST-interacting genes in prostate cancer. Science China. Life sciences 2017 1 60 (4): 386-396. Lyu Peng, Zhang Shu-Dong, Yuen Hiu-Fung, McCrudden Cian M, Wen Qing, Chan Kwok-Wah, Kwok Hang F |
Genome-wide association study suggests four variants influencing outcomes with ranibizumab therapy in exudative age-related macular degeneration.
Journal of human genetics 2018 Oct 63 (10): 1083-1091. Akiyama Masato, Takahashi Atsushi, Momozawa Yukihide, Arakawa Satoshi, Miya Fuyuki, Tsunoda Tatsuhiko, Ashikawa Kyota, Oshima Yuji, Yasuda Miho, Yoshida Shigeo, Enaida Hiroshi, Tan Xue, Yanagi Yasuo, Yasukawa Tsutomu, Ogura Yuichiro, Nagai Yoshimi, Takahashi Kanji, Fujisawa Kimihiko, Inoue Maiko, Arakawa Akira, Tanaka Koji, Yuzawa Mitsuko, Kadonosono Kazuaki, Sonoda Koh-Hei, Ishibashi Tatsuro, Kubo Michia |
Multi-gene panel testing in Korean patients with common genetic generalized epilepsy syndromes. PloS one 2018 13 (6): e0199321. Lee Cha Gon, Lee Jeehun, Lee Munhya |
The genetics of smoking in individuals with chronic obstructive pulmonary disease.
Respiratory research 2018 04 19 (1): 59. Obeidat Ma'en, Zhou Guohai, Li Xuan, Hansel Nadia N, Rafaels Nicholas, Mathias Rasika, Ruczinski Ingo, Beaty Terri H, Barnes Kathleen C, Paré Peter D, Sin Don |
Screening of noise-induced hearing loss (NIHL)-associated SNPs and the assessment of its genetic susceptibility. Environmental health : a global access science source 2019 Apr 18 (1): 30. Zhang Xuhui, Ni Yaqin, Liu Yi, Zhang Lei, Zhang Meibian, Fang Xinyan, Yang Zhangping, Wang Qiang, Li Hao, Xia Yuyong, Zhu Yim |
Pathway genes and metabolites in thiopurine therapy in Korean children with acute lymphoblastic leukaemia. British journal of clinical pharmacology 2019 Mar . Choi Rihwa, Sohn Insuk, Kim Min-Ji, Woo Hye In, Lee Ji Won, Ma Youngeun, Yi Eun Sang, Koo Hong Hoe, Lee Soo-Yo |
Phenotype-to-genotype approach reveals head-circumference-associated genes in an autism spectrum disorder cohort. Clinical genetics 2019 Nov . Wu Huidan, Li Honghui, Bai Ting, Han Lin, Ou Jianjun, Xun Guanglei, Zhang Yu, Wang Yazhe, Duan Guiqin, Zhao Ningxia, Chen Biyuan, Du Xiaogang, Yao Meiling, Zou Xiaobing, Zhao Jingping, Hu Zhengmao, Eichler Evan E, Guo Hui, Xia K |
Genetic factors for susceptibility to and manifestations of neuromyelitis optica. Annals of clinical and translational neurology 2020 9 7 (11): 2082-2093. Matsushita Takuya, Masaki Katsuhisa, Isobe Noriko, Sato Shinya, Yamamoto Ken, Nakamura Yuri, Watanabe Mitsuru, Suenaga Toshihiko, Kira Jun-Ichi, |
Gene-gene and gene-lifestyle interactions of AKAP11, KCNMA1, PUM1, SPTBN1, and EPDR1 on osteoporosis risk in middle-aged adults. Nutrition (Burbank, Los Angeles County, Calif.) 2020 7 79-80 110859. Park Sunmin, Daily James W, Song Mi Young, Kwon Hyuk- |
Genome-wide association study of angioedema induced by angiotensin-converting enzyme inhibitor and angiotensin receptor blocker treatment.
The pharmacogenomics journal 2020 Feb . Rasmussen Eva Rye, Hallberg Pär, Baranova Ekaterina V, Eriksson Niclas, Karawajczyk Malgorzata, Johansson Caroline, Cavalli Marco, Maroteau Cyrielle, Veluchamy Abirami, Islander Gunilla, Hugosson Svante, Terreehorst Ingrid, Asselbergs Folkert W, Norling Pia, Johansson Hans-Erik, Kohnke Hugo, Syvänen Ann-Christine, Siddiqui Moneeza K, Lang Chim C, Magnusson Patrik K E, Yue Qun-Ying, Wadelius Claes, von Buchwald Christian, Bygum Anette, Alfirevic Ana, Maitland-van der Zee Anke H, Palmer Colin N A, Wadelius M |
An emerging spectrum of variants and clinical features in KCNMA1-linked channelopathy. Channels (Austin, Tex.) 2021 7 15 (1): 447-464. Miller Jacob P, Moldenhauer Hans J, Keros Sotirios, Meredith Andrea |
Genes and SNPs Involved with Scrotal and Umbilical Hernia in Pigs. Genes 2021 1 12 (2): . Rodrigues Ariene Fernanda Grando, Ibelli Adriana Mércia Guaratini, Peixoto Jane de Oliveira, Cantão Maurício Egídio, Oliveira Haniel Cedraz de, Savoldi Igor Ricardo, Souza Mayla Regina, Mores Marcos Antônio Zanella, Carreño Luis Orlando Duitama, Ledur Mônica Corr |
Genetic polymorphisms are associated with individual susceptibility to dexmedetomidine. Frontiers in genetics 2023 9 14 1187415. Yuanyuan Ding, Aiqing Liu, Yafeng Wang, Shuai Zhao, Shiqian Huang, Hongyu Zhu, Lulin Ma, Linlin Han, Shaofang Shu, Lidong Zheng, Xiangdong Ch |
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- Page last updated:Mar 18, 2024
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