Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: SLC12A6[original query] |
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Rare variants of the gene encoding the potassium chloride co-transporter 3 are associated with bipolar disorder. The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2005 Dec 8 (4): 495-504. Meyer Jobst, Johannssen Kirsten, Freitag Christine M, Schraut Kerstin, Teuber Isabel, Hahner Astrid, Mainhardt Christian, Mössner Rainald, Volz Hans-Peter, Wienker Thomas F, McKeane Darleen, Stephan Dietrich A, Rouleau Guy, Reif Andreas, Lesch Klaus-Pet |
Genetic factors underlying the risk of thalidomide-related neuropathy in patients with multiple myeloma. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2011 Mar 29 (7): 797-804. Johnson David C, Corthals Sophie L, Walker Brian A, Ross Fiona M, Gregory Walter M, Dickens Nicholas J, Lokhorst Henk M, Goldschmidt Hartmut, Davies Faith E, Durie Brian G M, Van Ness Brian, Child J Anthony, Sonneveld Pieter, Morgan Gareth |
ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease. Brain : a journal of neurology 2015 Nov . Montecchiani Celeste, Pedace Lucia, Lo Giudice Temistocle, Casella Antonella, Mearini Marzia, Gaudiello Fabrizio, Pedroso José L, Terracciano Chiara, Caltagirone Carlo, Massa Roberto, St George-Hyslop Peter H, Barsottini Orlando G P, Kawarai Toshitaka, Orlacchio Anton |
Interactions Between Genetic Variants and Environmental Factors Affect Risk of Esophageal Adenocarcinoma and Barrett's Esophagus.
Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association 2018 Mar . Dong Jing, Levine David M, Buas Matthew F, Zhang Rui, Onstad Lynn, Fitzgerald Rebecca C, , Corley Douglas A, Shaheen Nicholas J, Lagergren Jesper, Hardie Laura J, Reid Brian J, Iyer Prasad G, Risch Harvey A, Caldas Carlos, Caldas Isabel, Pharoah Paul D, Liu Geoffrey, Gammon Marilie D, Chow Wong-Ho, Bernstein Leslie, Bird Nigel C, Ye Weimin, Wu Anna H, Anderson Lesley A, MacGregor Stuart, Whiteman David C, Vaughan Thomas L, Thrift Aaron |
ACE2 Netlas: In silico Functional Characterization and Drug-Gene Interactions of ACE2 Gene Network to Understand Its Potential Involvement in COVID-19 Susceptibility. Frontiers in genetics 2021 9 12 698033. Pathak Gita A, Wendt Frank R, Goswami Aranyak, Koller Dora, De Angelis Flavio, , Polimanti Rena |
SLC gene mutations and pediatric neurological disorders: diverse clinical phenotypes in a Saudi Arabian population. Human genetics 2021 11 141 (1): 81-99. Mir Ali, Almudhry Montaha, Alghamdi Fouad, Albaradie Raidah, Ibrahim Mona, Aldurayhim Fatimah, Alhedaithy Abdullah, Alamr Mushari, Bawazir Maryam, Mohammad Sahar, Abdelhay Salma, Bashir Shahid, Housawi Yous |
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- Page last updated:Apr 29, 2024
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