Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: MYO3A[original query] |
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Polymorphisms in the GAD2 gene-region are associated with susceptibility for unipolar depression and with a risk factor for anxiety disorders. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009 Dec 150B (8): 1100-9. Unschuld Paul G, Ising Marcus, Specht Michael, Erhardt Angelika, Ripke Stephan, Heck Angela, Kloiber Stefan, Straub Verica, Brueckl Tanja, Müller-Myhsok Bertram, Holsboer Florian, Binder Elisabeth |
Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility. Carcinogenesis 2010 Sep 31 (9): 1612-9. Lascorz Jesús, Försti Asta, Chen Bowang, Buch Stephan, Steinke Verena, Rahner Nils, Holinski-Feder Elke, Morak Monika, Schackert Hans K, Görgens Heike, Schulmann Karsten, Goecke Timm, Kloor Matthias, Engel Cristoph, Büttner Reinhard, Kunkel Nelli, Weires Marianne, Hoffmeister Michael, Pardini Barbara, Naccarati Alessio, Vodickova Ludmila, Novotny Jan, Schreiber Stefan, Krawczak Michael, Bröring Clemens D, Völzke Henry, Schafmayer Clemens, Vodicka Pavel, Chang-Claude Jenny, Brenner Hermann, Burwinkel Barbara, Propping Peter, Hampe Jochen, Hemminki Ka |
Supervised machine learning and logistic regression identifies novel epistatic risk factors with PTPN22 for rheumatoid arthritis. Genes and immunity 2010 Apr 11 (3): 199-208. Briggs F B S, Ramsay P P, Madden E, Norris J M, Holers V M, Mikuls T R, Sokka T, Seldin M F, Gregersen P K, Criswell L A, Barcellos L |
Genomic screening of ABCA4 and array CGH analysis underline the genetic variability of Greek patients with inherited retinal diseases. Meta gene 2016 Jun 8 37-43. Tsipi Maria, Tzetis Maria, Kosma Konstantina, Moschos Marilita, Braoudaki Maria, Poulou Myrto, Kanavakis Emmanuel, Kitsiou-Tzeli Sof |
Systematic Review of Hearing Loss Genes in the African American Population. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2019 5 40 (5): e488-e496. Worden Cameron P, Jeyakumar Ani |
Mutation screening in non-syndromic hearing loss patients with cochlear implantation by massive parallel sequencing in Taiwan. PloS one 2019 1 14 (1): e0211261. Liu Wei-Hsiu, Chang Pi-Yueh, Chang Shih-Cheng, Lu Jang-Jih, Wu Che-Mi |
Whole exome sequencing reveals pathogenic variants in MYO3A, MYO15A and COL9A3 and differential frequencies in ancestral alleles in hearing impairment genes among individuals from Cameroon. Human molecular genetics 2020 Oct . Wonkam Ambroise, Manyisa Noluthando, Bope Christian D, Dandara Collet, Chimusa Emile |
Whole-Exome Sequencing Targeting a Gene Panel for Sensorineural Hearing Loss: The First Portuguese Cohort Study. Cytogenetic and genome research 2022 5 162 (1-2): 1-9. Reis Cláudia Sousa, Quental Sofia, Fernandes Susana, Castedo Sérgio, Moura Carla Pin |
Gene-Set Enrichment Analysis for Identifying Genes and Biological Activities Associated with Growth Traits in Dromedaries. Animals : an open access journal from MDPI 2022 1 12 (2): . Sani Morteza Bitaraf, Roudbari Zahra, Karimi Omid, Banabazi Mohammad Hossein, Esmaeilkhanian Saeid, Asadzadeh Nader, Zare Harofte Javad, Shafei Naderi Ali, Burger Pamela An |
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- Page last updated:Apr 22, 2024
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