Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: GALM[original query] |
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A non-synonymous polymorphism in galactose mutarotase (GALM) is associated with serotonin transporter binding potential in the human thalamus: results of a genome-wide association study.
Molecular psychiatry 2011 Jun 16 (6): 584-5. Liu X, Cannon D M, Akula N, Moya P R, Knudsen G M, Arentzen T E, Steele J, Laje G, Drevets W C, McMahon F |
Epigenetic dysregulation of secreted frizzled-related proteins in myeloproliferative neoplasms complements the JAK2V617F-mutation. Clinical epigenetics 2012 Aug 4 (1): 1. Bennemann K, Galm O, Wilop S, Schubert C, Bruemmendorf TH, Jost E |
The genome-wide landscape of copy number variations in the MUSGEN study provides evidence for a founder effect in the isolated Finnish population. European journal of human genetics : EJHG 2013 Dec 21 (12): 1411-6. Kanduri Chakravarthi, Ukkola-Vuoti Liisa, Oikkonen Jaana, Buck Gemma, Blancher Christine, Raijas Pirre, Karma Kai, Lähdesmäki Harri, Järvelä Ir |
Genome-wide copy number variation analysis in extended families and unrelated individuals characterized for musical aptitude and creativity in music. PloS one 2013 8 (2): 2. Ukkola-Vuoti L, Kanduri C, Oikkonen J, Buck G, Blancher C, Raijas P, Karma K, Lähdesmäki H, Järvelä I |
Serotonin-Related Gene Polymorphisms and Asymptomatic Neurocognitive Impairment in HIV-Infected Alcohol Abusers. Genetics research international 2016 2016 7169172. Villalba Karina, Dévieux Jessy G, Rosenberg Rhonda, Cadet Jean L |
Two locus inheritance of non-syndromic midline craniosynostosis via rare SMAD6 and common BMP2 alleles. eLife 2016 Sep 5 . Timberlake Andrew T, Choi Jungmin, Zaidi Samir, Lu Qiongshi, Nelson-Williams Carol, Brooks Eric D, Bilguvar Kaya, Tikhonova Irina, Mane Shrikant, Yang Jenny F, Sawh-Martinez Rajendra, Persing Sarah, Zellner Elizabeth G, Loring Erin, Chuang Carolyn, Galm Amy, Hashim Peter W, Steinbacher Derek M, DiLuna Michael L, Duncan Charles C, Pelphrey Kevin A, Zhao Hongyu, Persing John A, Lifton Richard |
De novo mutations in inhibitors of Wnt, BMP, and Ras/ERK signaling pathways in non-syndromic midline craniosynostosis. Proceedings of the National Academy of Sciences of the United States of America 2017 8 114 (35): E7341-E7347. Timberlake Andrew T, Furey Charuta G, Choi Jungmin, Nelson-Williams Carol, , Loring Erin, Galm Amy, Kahle Kristopher T, Steinbacher Derek M, Larysz Dawid, Persing John A, Lifton Richard |
Mutations in TFAP2B and previously unimplicated genes of the BMP, Wnt, and Hedgehog pathways in syndromic craniosynostosis. Proceedings of the National Academy of Sciences of the United States of America 2019 7 116 (30): 15116-15121. Timberlake Andrew T, Jin Sheng Chih, Nelson-Williams Carol, Wu Robin, Furey Charuta G, Islam Barira, Haider Shozeb, Loring Erin, Galm Amy, , Steinbacher Derek M, Larysz Dawid, Staffenberg David A, Flores Roberto L, Rodriguez Eduardo D, Boggon Titus J, Persing John A, Lifton Richard |
The Discovery of GALM Deficiency (Type IV Galactosemia) and Newborn Screening System for Galactosemia in Japan. International journal of neonatal screening 2021 Oct 7 (4): . Kikuchi Atsuo, Wada Yoichi, Ohura Toshihiro, Kure Shig |
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- Page last updated:Mar 25, 2024
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