Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Disease and SLC8A1[original query] |
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| A custom correlation coefficient (CCC) approach for fast identification of multi-SNP association patterns in genome-wide SNPs data. Genetic epidemiology 2014 Nov 38 (7): 610-21. Climer Sharlee, Yang Wei, de las Fuentes Lisa, Dávila-Román Victor G, Gu C Charl |
A common variant in RAB27A gene is associated with fractional exhaled nitric oxide levels in adults.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2015 Apr 45 (4): 797-806. Bouzigon E, Nadif R, Thompson E E, Concas M P, Kuldanek S, Du G, Brossard M, Lavielle N, Sarnowski C, Vaysse A, Dessen P, van der Valk R J P, Duijts L, Henderson A J, Jaddoe V W V, de Jongste J C, , Casula S, Biino G, Dizier M-H, Pin I, Matran R, Lathrop M, Pirastu M, Demenais F, Ober C, |
| Genome-wide rare copy number variations contribute to genetic risk for transposition of the great arteries. International journal of cardiology 2015 Nov 204 115-121. Costain Gregory, Lionel Anath C, Ogura Lucas, Marshall Christian R, Scherer Stephen W, Silversides Candice K, Bassett Anne |
| Genetic Variation in the SLC8A1 Calcium Signaling Pathway Is Associated With Susceptibility to Kawasaki Disease and Coronary Artery Abnormalities. Circulation. Cardiovascular genetics 2016 Dec 9 (6): 559-568. Shimizu Chisato, Eleftherohorinou Hariklia, Wright Victoria J, Kim Jihoon, Alphonse Martin P, Perry James C, Cimaz Rolando, Burgner David, Dahdah Nagib, Hoang Long T, Khor Chiea Chuen, Salgado Andrea, Tremoulet Adriana H, Davila Sonia, Kuijpers Taco W, Hibberd Martin L, Johnson Todd A, Takahashi Atsushi, Tsunoda Tatsuhiko, Kubo Michiaki, Tanaka Toshihiro, Onouchi Yoshihiro, Yeung Rae S M, Coin Lachlan J M, Levin Michael, Burns Jane C, |
| Genetics of ion homeostasis in Ménière's Disease. European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2016 Nov . Teggi Roberto, Zagato Laura, Delli Carpini Simona, Citterio Lorena, Cassandro Claudia, Albera Roberto, Yang Wen-Yi, Staessen Jan A, Bussi Mario, Manunta Paolo, Lanzani Chia |
| Urotensin 2 in Kawasaki disease pathogenesis. Pediatric research 2017 Dec 82 (6): 1048-1055. Huang Cassidy Y, Burns Jane C, Shimizu Chisa |
| Genetic susceptibility to salt-sensitive hypertension in a Han Chinese population: a validation study of candidate genes. Hypertension research : official journal of the Japanese Society of Hypertension 2017 Apr . Liu Zheng, Qi Han, Liu Bin, Liu Kuo, Wu Jingjing, Cao Han, Zhang Jie, Yan Yuxiang, He Yan, Zhang Li |
| Size matters: Large copy number losses in Hirschsprung disease patients reveal genes involved in enteric nervous system development. PLoS genetics 2021 8 17 (8): e1009698. Kuil Laura E, MacKenzie Katherine C, Tang Clara S, Windster Jonathan D, Le Thuy Linh, Karim Anwarul, de Graaf Bianca M, van der Helm Robert, van Bever Yolande, Sloots Cornelius E J, Meeussen Conny, Tibboel Dick, de Klein Annelies, Wijnen René M H, Amiel Jeanne, Lyonnet Stanislas, Garcia-Barcelo Maria-Mercè, Tam Paul K H, Alves Maria M, Brooks Alice S, Hofstra Robert M W, Brosens Erw |
| Could ionic regulation disorders explain the overlap between meniere's disease and migraine? Journal of vestibular research : equilibrium & orientation 2021 2 31 (4): 297-301. Teggi Roberto, Colombo Bruno, Zagato Laura, Filippi Massi |
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