Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: SH3GL2[original query] |
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Replication of top markers of a genome-wide association study in multiple sclerosis in Spain. Genes and immunity 2011 Mar 12 (2): 110-5. Cavanillas M L, Fernández O, Comabella M, Alcina A, Fedetz M, Izquierdo G, Lucas M, Cénit M C, Arroyo R, Vandenbroeck K, Alloza I, García-Barcina M, Antigüedad A, Leyva L, Gómez C L, Olascoaga J, Otaegui D, Blanco Y, Saiz A, Montalbán X, Matesanz F, Urcelay |
Comprehensive replication of the relationship between myopia-related genes and refractive errors in a large Japanese cohort. Investigative ophthalmology & visual science 2014 Nov 55 (11): 7343-54. Yoshikawa Munemitsu, Yamashiro Kenji, Miyake Masahiro, Oishi Maho, Akagi-Kurashige Yumiko, Kumagai Kyoko, Nakata Isao, Nakanishi Hideo, Oishi Akio, Gotoh Norimoto, Yamada Ryo, Matsuda Fumihiko, Yoshimura Nagahisa, |
SNP rs1049430 in the 3'-UTR of SH3GL2 regulates its expression: Clinical and prognostic implications in head and neck squamous cell carcinoma. Biochimica et biophysica acta 2015 May 1852 (5): 1059-67. Maiti Guru Prasad, Ghosh Amlan, Mondal Pinaki, Baral Aradhita, Datta Sayantan, Samadder Sudip, Nayak Sandeep P, Chakrabarti Jayanta, Biswas Jaydeep, Sikdar Nilabja, Chowdhury Shantanu, Roy Bidyut, Roychowdhury Susanta, Panda Chinmay Kum |
Germline Genetic Biomarkers of Sunitinib Efficacy in Advanced Renal Cell Carcinoma: Results From the RENAL EFFECT Trial. Clinical genitourinary cancer 2017 Feb . Motzer Robert J, Figlin Robert A, Martini Jean-François, Hariharan Subramanian, Agarwal Neeraj, Li Chun Xiao, Williams J Andrew, Hutson Thomas |
Independent Maternal and Fetal Genetic Effects on Midgestational Circulating Levels of Environmental Pollutants.
G3 (Bethesda, Md.) 2017 Feb . Traglia Michela, Croen Lisa A, Lyall Kristen, Windham Gayle C, Kharrazi Marty, DeLorenze Gerald N, Torres Anthony R, Weiss Lauren |
Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study.
Translational psychiatry 2017 Oct 7 (10): e1249. Lencer R, Mills L J, Alliey-Rodriguez N, Shafee R, Lee A M, Reilly J L, Sprenger A, McDowell J E, McCarroll S A, Keshavan M S, Pearlson G D, Tamminga C A, Clementz B A, Gershon E S, Sweeney J A, Bishop J |
The Role of Rare Coding Variants in Parkinson's Disease GWAS Loci. Frontiers in neurology 2020 1 10 1284. Germer Elisabeth Luisa, Imhoff Sophie, Vilariño-Güell Carles, Kasten Meike, Seibler Philip, Brüggemann Norbert, , Klein Christine, Trinh Joan |
Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor Subtypes.
Neurology. Genetics 2021 Apr 7 (2): e557. Alfradique-Dunham Isabel, Al-Ouran Rami, von Coelln Rainer, Blauwendraat Cornelis, Hill Emily, Luo Lan, Stillwell Amanda, Young Emily, Kaw Anita, Tan Manuela, Liao Calwing, Hernandez Dena, Pihlstrom Lasse, Grosset Donald, Shulman Lisa M, Liu Zhandong, Rouleau Guy A, Nalls Mike, Singleton Andrew B, Morris Huw, Jankovic Joseph, Shulman Joshua |
Axial Impairment Following Deep Brain Stimulation in Parkinson's Disease: A Surgicogenomic Approach. Journal of Parkinson's disease 2021 Sep . Visanji Naomi P, Ghani Mahdi, Yu Eric, Kakhki Erfan Ghani, Sato Christine, Moreno Danielle, Naranian Taline, Poon Yu-Yan, Abdollahi Maryam, Naghibzadeh Maryam, Rajalingam Rajasumi, Lozano Andres M, Kalia Suneil K, Hodaie Mojgan, Cohn Melanie, Statucka Marta, Boutet Alexandre, Elias Gavin J B, Germann Jürgen, Munhoz Renato, Lang Anthony E, Gan-Or Ziv, Rogaeva Ekaterina, Fasano Alfon |
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- Page last updated:Apr 22, 2024
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