Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: SLC9A3R1[original query] |
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Analysis of polymorphisms in 16 genes in type 1 diabetes that have been associated with other immune-mediated diseases. BMC medical genetics 2006 7 (): 20. Smyth Deborah J, Howson Joanna M M, Payne Felicity, Maier Lisa M, Bailey Rebecca, Holland Kieran, Lowe Christopher E, Cooper Jason D, Hulme John S, Vella Adrian, Dahlman Ingrid, Lam Alex C, Nutland Sarah, Walker Neil M, Twells Rebecca C J, Todd John |
Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study.
Circulation. Cardiovascular genetics 2009 Apr 2 (2): 134-41. Danik Jacqueline S, Paré Guillaume, Chasman Daniel I, Zee Robert Y L, Kwiatkowski David J, Parker Alex, Miletich Joseph P, Ridker Paul |
Next Generation Sequencing and Animal Models Reveal SLC9A3R1 as a New Gene Involved in Human Age-Related Hearing Loss. Frontiers in genetics 2019 3 10 142. Girotto Giorgia, Morgan Anna, Krishnamoorthy Navaneethakrishnan, Cocca Massimiliano, Brumat Marco, Bassani Sissy, La Bianca Martina, Di Stazio Mariateresa, Gasparini Pao |
Genomic analysis of 21 patients with corneal neuralgia after refractive surgery. Pain reports 0 5 (4): e826. Yuan Jun-Hui, Schulman Betsy R, Effraim Philip R, Sulayman Dib-Hajj, Jacobs Deborah S, Waxman Stephen |
Synonymous variants associated with Alzheimer disease in multiplex families. Neurology. Genetics 2020 7 6 (4): e450. Tang Min, Alaniz Maria Eugenia, Felsky Daniel, Vardarajan Badri, Reyes-Dumeyer Dolly, Lantigua Rafael, Medrano Martin, Bennett David A, de Jager Philip L, Mayeux Richard, Santa-Maria Ismael, Reitz Christia |
Overlapping Phenotypes Associated With CYP24A1, SLC34A1, and SLC34A3 Mutations: A Cohort Study of Patients With Hypersensitivity to Vitamin D. Frontiers in endocrinology 2021 11 12 736240. Molin Arnaud, Lemoine Sandrine, Kaufmann Martin, Breton Pierre, Nowoczyn Marie, Ballandonne Céline, Coudray Nadia, Mittre Hervé, Richard Nicolas, Ryckwaert Amélie, Lavillaureix Alinoe, Jones Glenville, Bacchetta Justine, Kottler Marie-Lau |
Systematic assessment of monogenic etiology in adult-onset kidney stone formers undergoing urological intervention-evidence for genetic pretest probability. American journal of medical genetics. Part C, Seminars in medical genetics 2022 8 190 (3): 279-288. Schönauer Ria, Scherer Lotte, Nemitz-Kliemchen Melanie, Hagemann Tobias, Hantmann Elena, Seidel Anna, Müller Luise, Kehr Stephanie, Voigt Cornelia, Stolzenburg Jens-Uwe, Halbritter J |
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