Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: KCNJ1[original query] |
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Rare independent mutations in renal salt handling genes contribute to blood pressure variation. Nature genetics 2008 May 40 (5): 592-9. Ji Weizhen, Foo Jia Nee, O'Roak Brian J, Zhao Hongyu, Larson Martin G, Simon David B, Newton-Cheh Christopher, State Matthew W, Levy Daniel, Lifton Richard |
Common variants in genes underlying monogenic hypertension and hypotension and blood pressure in the general population. Hypertension 2008 Jun 51 (6): 1658-64. Tobin Martin D, Tomaszewski Maciej, Braund Peter S, Hajat Cother, Raleigh Stuart M, Palmer Thomas M, Caulfield Mark, Burton Paul R, Samani Nilesh |
Association of KCNJ1 variation with change in fasting glucose and new onset diabetes during HCTZ treatment. The pharmacogenomics journal 2013 Oct 13 (5): 430-6. Karnes J H, McDonough C W, Gong Y, Vo T T, Langaee T Y, Chapman A B, Gums J G, Beitelshees A L, Bailey K R, Del-Aguila J L, Boerwinkle E A, Pepine C J, Turner S T, Johnson J A, Cooper-DeHoff R |
Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions. European journal of human genetics : EJHG 2012 Dec . Amin N, Hottenga JJ, Hansell NK, Janssens AC, de Moor MH, Madden PA, Zorkoltseva IV, Penninx BW, Terracciano A, Uda M, Tanaka T, Esko T, Realo A, Ferrucci L, Luciano M, Davies G, Metspalu A, Abecasis GR, Deary IJ, Raikkonen K, Bierut LJ, Costa PT, Saviouk V, Zhu G, Kirichenko AV, Isaacs A, Aulchenko YS, Willemsen G, Heath AC, Pergadia ML, Medland SE, Axenovich TI, de Geus E, Montgomery GW, Wright MJ, Oostra BA, Martin NG, Boomsma DI, van Duijn CM |
Calcium intake and ion transporter genetic polymorphisms interact in human colorectal neoplasia risk in a 2-phase study. The Journal of nutrition 2014 Nov 144 (11): 1734-41. Zhu Xiangzhu, Liang Ji, Shrubsole Martha J, Ness Reid M, Cai Qiuyin, Long Jirong, Chen Zhi, Li Guoliang, Wiese Dawn, Zhang Bing, Smalley Walter E, Edwards Todd L, Giovannucci Edward, Zheng Wei, Dai |
Common variants in UMOD associate with urinary uromodulin levels: a meta-analysis.
Journal of the American Society of Nephrology : JASN 2014 Aug 25 (8): 1869-82. Olden Matthias, Corre Tanguy, Hayward Caroline, Toniolo Daniela, Ulivi Sheila, Gasparini Paolo, Pistis Giorgio, Hwang Shih-Jen, Bergmann Sven, Campbell Harry, Cocca Massimiliano, Gandin Ilaria, Girotto Giorgia, Glaudemans Bob, Hastie Nicholas D, Loffing Johannes, Polasek Ozren, Rampoldi Luca, Rudan Igor, Sala Cinzia, Traglia Michela, Vollenweider Peter, Vuckovic Dragana, Youhanna Sonia, Weber Julien, Wright Alan F, Kutalik Zoltán, Bochud Murielle, Fox Caroline S, Devuyst Olivi |
Clinical and Genetic Factors Associated With Thiazide-Induced Hyponatremia. Medicine 2015 Aug 94 (34): e1422. Huang Chin-Chou, Chung Chia-Min, Hung Shuen-Iu, Pan Wen-Harn, Leu Hsin-Bang, Huang Po-Hsun, Chiu Chun-Chih, Lin Liang-Yu, Lin Chih-Ching, Yang Chih-Yu, Li Szu-Yuan, Chen Yen-Chia, Wu Tao-Cheng, Lin Shing-Jong, Chen Jaw-W |
Interactions between calcium intake and polymorphisms in genes essential for calcium reabsorption and risk of colorectal neoplasia in a two-phase study. Molecular carcinogenesis 2017 10 56 (10): 2258-2266. Zhao Jing, Zhu Xiangzhu, Shrubsole Martha J, Ness Reid M, Hibler Elizabeth A, Cai Qiuyin, Long Jirong, Chen Zhi, Jiang Ming, Kabagambe Edmond K, Zhang Bing, Hou Lifang, Smalley Walter E, Edwards Todd L, Giovannucci Edward L, Zheng Wei, Dai |
[Risk of type 2 diabetes mellitus in the Kyrgyz population in the presence of ADIPOQ (G276T), KCNJ11 (Glu23Lys), TCF7L2 (IVS3C>T) gene polymorphisms]. Terapevticheskii arkhiv 0 89 (10): 40-47. Isakova Zh T, Talaibekova E T, Asambaeva D A, Kerimkulova A S, Lunegova O S, Aldasheva N M, Aldashev A |
Contributions of rare coding variants in hypotension syndrome genes to population blood pressure variation. Medicine 2018 Aug 97 (33): e11865. Nandakumar Priyanka, Morrison Alanna C, Grove Megan L, Boerwinkle Eric, Chakravarti Aravin |
Genetic screening for Bartter syndrome and Gitelman syndrome pathogenic genes among individuals with hypertension and hypokalemia. Clinical and experimental hypertension (New York, N.Y. : 1993) 2018 Jun 1-8. Bao Minghui, Cai Jun, Yang Xinchun, Ma Wenj |
Impact of variants on type-2 diabetes risk genes identified through genomewide association studies in polycystic ovary syndrome: a case-control study. Journal of genetics 2018 Dec 97 (5): 1213-1223. Ezzidi Intissar, Mtiraoui Nabil, Mohmmed Ali Mohammed Eltigani, Masoudi Aqeel Al, Abu Duhier Fais |
Polymorphisms in PCSK9, LDLR, BCMO1, SLC12A3, and KCNJ1 are Associated with Serum Lipid Profile in Chinese Han Population. International journal of environmental research and public health 2019 Sep 16 (17): . Li Zheng, Zhao Tianyu, Tan Xiaohua, Lei Song, Huang Liu, Yang L |
Maturity-Onset Diabetes of the Young Identified Among Algerian Probands with Early-Onset Diabetes. Diabetes, metabolic syndrome and obesity : targets and therapy 2020 12 13 4829-4837. Bouldjennet Faiza, Gjesing Anette P, Azzouz Malha, Abderrahman Samir Ait, El Guecier Amina, Ali Said, Oudjit Brahim, Mennadi-Lacete Farida, Yargui Lyèce, Boudiba Aissa, Chibane Ahcène, Touil-Boukoffa Chafia, Hansen Torben, Raache Rachi |
Clinical Course of Patients with Bartter Syndrome. Iranian journal of kidney diseases 2022 6 16 (3): 162-170. Rodriges Jose Henrique Paiva, Menezes Silva Luiz Alberto Wanderley, Soares Silvia Bouissou Morais, Cruz Raissa Ritielle Oliveira, Mrad Flavia Cristina De Carvalho, Simoes E Silva Ana Cristi |
Genetic variants for prediction of gestational diabetes mellitus and modulation of susceptibility by a nutritional intervention based on a Mediterranean diet. Frontiers in endocrinology 2022 10 13 1036088. Ramos-Levi Ana, Barabash Ana, Valerio Johanna, García de la Torre Nuria, Mendizabal Leire, Zulueta Mirella, de Miguel Maria Paz, Diaz Angel, Duran Alejandra, Familiar Cristina, Jimenez Inés, Del Valle Laura, Melero Veronica, Moraga Inmaculada, Herraiz Miguel A, Torrejon María José, Arregi Maddi, Simón Laureano, Rubio Miguel A, Calle-Pascual Alfonso |
Phenotypic and genotypic characteristics of children with Bartter syndrome. The Turkish journal of pediatrics 2022 10 64 (5): 825-838. Güven Serçin, Gökçe ?brahim, Alavanda Ceren, Çiçek Neslihan, Demirci Ece Bodur, Sak Mehtap, Pul Serim, Türkkan Özde Nisa, Y?ld?z Nurdan, Ata P?nar, Alpay Hari |
Association of polymorphisms of calcium reabsorption genes SLC12A1, KCNJ1 and SLC8A1 with colorectal adenoma. Journal of cancer research and clinical oncology 2023 4 . Xiaolian Lai, Shuoyan Lu, Jia Jiang, Hanqun Zhang, Qinglin Yang, Yuncong Liu, Libo Li, Sanming Li, Si Dai, Yanping Chen, Yan Chen, Jun Liu, Yong |
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