Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: POLG2[original query] |
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Identification of two gene variants associated with risk of advanced fibrosis in patients with chronic hepatitis C. Gastroenterology 2006 May 130 (6): 1679-87. Huang Hongjin, Shiffman Mitchell L, Cheung Ramsey C, Layden Thomas J, Friedman Scott, Abar Olivia T, Yee Linda, Chokkalingam Anand P, Schrodi Steven J, Chan Jason, Catanese Joseph J, Leong Diane U, Ross David, Hu Xiaolan, Monto Alexander, McAllister Linda B, Broder Samuel, White Thomas, Sninsky John J, Wright Teresa |
Polymorphism discovery in 62 DNA repair genes and haplotype associations with risks for lung and head and neck cancers. Carcinogenesis 2007 Aug 28 (8): 1731-9. Michiels Stefan, Danoy Patrick, Dessen Philippe, Bera Alex, Boulet Thomas, Bouchardy Christine, Lathrop Mark, Sarasin Alain, Benhamou Simo |
Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegia. Journal of neurology 2008 Sep 255 (9): 1384-91. Virgilio Roberta, Ronchi Dario, Hadjigeorgiou Georgios M, Bordoni Andreina, Saladino Francesca, Moggio Maurizio, Adobbati Laura, Kafetsouli Demetra, Tsironi Evangelia, Previtali Stefano, Papadimitriou Alexandros, Bresolin Nereo, Comi Giacomo |
A polymorphism of the POLG2 gene is genetically associated with the invasiveness of urinary bladder cancer in Japanese males. Journal of human genetics 2011 Aug 56 (8): 572-6. Ratanajaraya Chanavee, Nishiyama Hiroyuki, Takahashi Meiko, Kawaguchi Takahisa, Saito Ryoichi, Mikami Yoshiki, Suyama Mikita, Lathrop Mark, Yamada Ryo, Ogawa Osamu, Matsuda Fumihi |
What is influencing the phenotype of the common homozygous polymerase-? mutation p.Ala467Thr? Brain : a journal of neurology 2012 Dec 135 (Pt 12): Pt 12. Neeve VC, Samuels DC, Bindoff LA, van den Bosch B, Van Goethem G, Smeets H, Lombès A, Jardel C, Hirano M, Dimauro S, De Vries M, Smeitink J, Smits BW, de Coo IF, Saft C, Klopstock T, Keiling BC, Czermin B, Abicht A, Lochmüller H, Hudson G, Gorman GG, Turnbull DM, Taylor RW, Holinski-Feder E, Chinnery PF, Horvath R |
Genome wide association and linkage analyses identified three loci-4q25, 17q23.2, and 10q11.21-associated with variation in leukocyte telomere length: the Long Life Family Study.
Frontiers in genetics 2013 4 310. Lee Joseph H, Cheng Rong, Honig Lawrence S, Feitosa Mary, Kammerer Candace M, Kang Min S, Schupf Nicole, Lin Shiow J, Sanders Jason L, Bae Harold, Druley Todd, Perls Thomas, Christensen Kaare, Province Michael, Mayeux Richa |
Association of DNA sequence variation in mitochondrial DNA polymerase with mitochondrial DNA synthesis and risk of oral cancer. Gene 2015 Sep . Datta Sayantan, Ray Anindita, Roy Roshni, Roy Bidy |
Mitochondrial pathology in inclusion body myositis. Neuromuscular disorders : NMD 2015 Apr 25 (4): 281-8. Lindgren Ulrika, Roos Sara, Hedberg Oldfors Carola, Moslemi Ali-Reza, Lindberg Christopher, Oldfors Ande |
Novel mutation in C10orf2 associated with multiple mtDNA deletions, chronic progressive external ophthalmoplegia and premature aging. Mitochondrion 2015 Dec 26 81-85. Paramasivam Arumugam, Meena Angamuthu Kannan, Pedaparthi Lalitha, Jyothi Vuskamalla, Uppin Megha S, Jabeen Shaikh Afshan, Sundaram Challa, Thangaraj Kumarasa |
Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR). BioData mining 2015 8 41. De Rishika, Verma Shefali S, Drenos Fotios, Holzinger Emily R, Holmes Michael V, Hall Molly A, Crosslin David R, Carrell David S, Hakonarson Hakon, Jarvik Gail, Larson Eric, Pacheco Jennifer A, Rasmussen-Torvik Laura J, Moore Carrie B, Asselbergs Folkert W, Moore Jason H, Ritchie Marylyn D, Keating Brendan J, Gilbert-Diamond Dia |
Clarification of undiagnosed ataxia using whole-exome sequencing with clinical implications. Parkinsonism & related disorders 2020 9 80 58-64. Kim Minkyeong, Kim Ah Reum, Kim Ji Sun, Park Jongkyu, Youn Jinyoung, Ahn Jong Hyeon, Mun Jun Kyu, Lee Chung, Kim Nam-Soon, Kim Nayoung K D, Park Woong-Yang, Cho Jin Wh |
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- Page last updated:Apr 22, 2024
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