Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: CLCN6[original query] |
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Polygenic prediction of preeclampsia and gestational hypertension.
Nature medicine 2023 5 29 (6): 1540-1549. Honigberg Michael C, Truong Buu, Khan Raiyan R, Xiao Brenda, Bhatta Laxmi, Vy Ha My T, Guerrero Rafael F, Schuermans Art, Selvaraj Margaret Sunitha, Patel Aniruddh P, Koyama Satoshi, Cho So Mi Jemma, Vellarikkal Shamsudheen Karuthedath, Trinder Mark, Urbut Sarah M, Gray Kathryn J, Brumpton Ben M, Patil Snehal, Zöllner Sebastian, Antopia Mariah C, Saxena Richa, Nadkarni Girish N, Do Ron, Yan Qi, Pe'er Itsik, Verma Shefali Setia, Gupta Rajat M, Haas David M, Martin Hilary C, van Heel David A, Laisk Triin, Natarajan Prade |
Genetic architecture of ambulatory blood pressure in the general population: insights from cardiovascular gene-centric array. Hypertension 2010 Dec 56 (6): 1069-76. Tomaszewski Maciej, Debiec Radoslaw, Braund Peter S, Nelson Christopher P, Hardwick Robert, Christofidou Paraskevi, Denniff Matthew, Codd Veryan, Rafelt Suzanne, van der Harst Pim, Waterworth Dawn, Song Kijoung, Vollenweider Peter, Waeber Gerard, Zukowska-Szczechowska Ewa, Burton Paul R, Mooser Vincent, Charchar Fadi J, Thompson John R, Tobin Martin D, Samani Nilesh |
Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster.
Human molecular genetics 2011 Apr 20 (8): 1660-71. Del Greco M Fabiola, Pattaro Cristian, Luchner Andreas, Pichler Irene, Winkler Thomas, Hicks Andrew A, Fuchsberger Christian, Franke Andre, Melville Scott A, Peters Annette, Wichmann H Erich, Schreiber Stefan, Heid Iris M, Krawczak Michael, Minelli Cosetta, Wiedermann Christian J, Pramstaller Peter |
Circulating atrial natriuretic peptide genetic association study identifies a novel gene cluster associated with stroke in whites. Circulation. Cardiovascular genetics 2015 Feb 8 (1): 141-9. Pereira Naveen L, Tosakulwong Nirubol, Scott Christopher G, Jenkins Gregory D, Prodduturi Naresh, Chai Yubo, Olson Timothy M, Rodeheffer Richard J, Redfield Margaret M, Weinshilboum Richard M, Burnett John |
Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk. Circulation. Cardiovascular genetics 2015 Dec . Yu Bing, Pulit Sara L, Hwang Shih-Jen, Brody Jennifer A, Amin Najaf, Auer Paul L, Bis Joshua C, Boerwinkle Eric, Burke Gregory L, Chakravarti Aravinda, Correa Adolfo, Dreisbach Albert W, Franco Oscar H, Ehret Georg B, Franceschini Nora, Hofman Albert, Lin Dan-Yu, Metcalf Ginger A, Musani Solomon K, Muzny Donna, Palmas Walter, Raffel Leslie, Reiner Alex, Rice Ken, Rotter Jerome I, Veeraraghavan Narayanan, Fox Ervin, Guo Xiuqing, North Kari E, Gibbs Richard A, van Duijn Cornelia M, Psaty Bruce M, Levy Daniel, Newton-Cheh Christopher, Morrison Alanna C, , |
Are genetic polymorphisms in the renin-angiotensin-aldosterone system associated with essential hypertension? Evidence from genome-wide association studies. Journal of human hypertension 2017 Apr . Ji L-D, Li J-Y, Yao B-B, Cai X-B, Shen Q-J, Xu |
Genetic Variants Identified from Epilepsy of Unknown Etiology in Chinese Children by Targeted Exome Sequencing. Scientific reports 2017 Jan 7 40319. Wang Yimin, Du Xiaonan, Bin Rao, Yu Shanshan, Xia Zhezhi, Zheng Guo, Zhong Jianmin, Zhang Yunjian, Jiang Yong-Hui, Wang |
Novel West syndrome candidate genes in a Chinese cohort. CNS neuroscience & therapeutics 2018 4 24 (12): 1196-1206. Peng Jing, Wang Ying, He Fang, Chen Chen, Wu Li-Wen, Yang Li-Fen, Ma Yu-Ping, Zhang Wen, Shi Zi-Qing, Chen Chao, Xia Kun, Guo Hui, Yin Fei, Pang N |
Genetic modifiers of long-term survival in sickle cell anemia. Clinical and translational medicine 2020 Aug 10 (4): e152. Wonkam Ambroise, Chimusa Emile R, Mnika Khuthala, Pule Gift Dineo, Ngo Bitoungui Valentina Josiane, Mulder Nicola, Shriner Daniel, Rotimi Charles N, Adeyemo Adebowa |
Impact of natriuretic peptide polymorphisms on diastolic and metabolic function in a populational cohort: insights from the STANISLAS cohort.
ESC heart failure 2021 Nov . Xhaard Constance, Rouget Raphaël, Vodovar Nicolas, Le Floch Edith, Dandine-Roulland Claire, Wagner Sandra, Bacq-Daian Delphine, Thuillier Quentin, Boivin Jean-Marc, Branlant Christiane, Deleuze Jean-François, Behm-Ansmant Isabelle, Zannad Faiez, Rossignol Patrick, Girerd Nicol |
Genetic polymorphism in Methylenetetrahydrofolate Reductase chloride transport protein 6 (MTHFR CLCN6) gene is associated with keratinocyte skin cancer in a cohort of renal transplant recipients. Skin health and disease 2022 Jun 2 (2): e95. Griffin L, Ho L, Akhurst R J, Arron S T, Boggs J M E, Conlon P, O'Kelly P, Toland A E, Epstein E H, Balmain A, Bastian B C, Moloney F J, Murphy G M, Laing M |
Genetic Variants Associated with Poor Responsiveness to Sulfonylureas in Filipinos with Type 2 Diabetes Mellitus. Journal of the ASEAN Federation of Endocrine Societies 2023 5 38 (1): 31-40. Elizabeth Paz-Pacheco, Jose Nevado, Eva Maria Cutiongco-De La Paz, Gabriel Jasul, Aimee Yvonne Criselle Aman, Elizabeth Laurize Alejandro-Ribaya, Mark David Francisco, Ma Luz Vicenta Guanzon, May Uyking-Naranjo, Cecille Añonuevo-Cruz, Maria Patricia Deanna Maningat, Cristina Jaring, Paulette Nacpil-Dominguez, Aniza Pala-Mohamad, Abigail Uy-Canto, John Paul Quisumbing, Annabelle Marie Lat, Diane Carla Bernardo, Noemie Marie Mansibang, Vincent Sean Ribaya, Karell Jo Angelique Calpito, Julius Patrick Ferrer, Jessica Biwang, Jodelyn Melegrito, Christian Deo Deguit, Carlos Emmanuel Paner |
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- Page last updated:Apr 16, 2024
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