Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Next-generation sequencing[original query] |
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| Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
PLoS genetics 2012 8 (3): e1002548. Lill Christina M, Roehr Johannes T, McQueen Matthew B, Kavvoura Fotini K, Bagade Sachin, Schjeide Brit-Maren M, Schjeide Leif M, Meissner Esther, Zauft Ute, Allen Nicole C, Liu Tian, Schilling Marcel, Anderson Kari J, Beecham Gary, Berg Daniela, Biernacka Joanna M, Brice Alexis, DeStefano Anita L, Do Chuong B, Eriksson Nicholas, Factor Stewart A, Farrer Matthew J, Foroud Tatiana, Gasser Thomas, Hamza Taye, Hardy John A, Heutink Peter, Hill-Burns Erin M, Klein Christine, Latourelle Jeanne C, Maraganore Demetrius M, Martin Eden R, Martinez Maria, Myers Richard H, Nalls Michael A, Pankratz Nathan, Payami Haydeh, Satake Wataru, Scott William K, Sharma Manu, Singleton Andrew B, Stefansson Kari, Toda Tatsushi, Tung Joyce Y, Vance Jeffery, Wood Nick W, Zabetian Cyrus P, , , , , Young Peter, Tanzi Rudolph E, Khoury Muin J, Zipp Frauke, Lehrach Hans, Ioannidis John P A, Bertram La |
| Identification of a melanoma susceptibility locus and somatic mutation in TET2.
Carcinogenesis 2014 Sep 35 (9): 2097-101. Song Fengju, Amos Christopher I, Lee Jeffrey E, Lian Christine G, Fang Shenying, Liu Hongliang, MacGregor Stuart, Iles Mark M, Law Matthew H, Lindeman Neal I, Montgomery Grant W, Duffy David L, Cust Anne E, Jenkins Mark A, Whiteman David C, Kefford Richard F, Giles Graham G, Armstrong Bruce K, Aitken Joanne F, Hopper John L, Brown Kevin M, Martin Nicholas G, Mann Graham J, Bishop D Timothy, Bishop Julia A Newton, , Kraft Peter, Qureshi Abrar A, Kanetsky Peter A, Hayward Nicholas K, Hunter David J, Wei Qingyi, Han Jia |
| Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism.
Blood 2016 Dec . Rühle Frank, Witten Anika, Barysenka Andrei, Huge Andreas, Arning Astrid, Heller Christine, Krümpel Anne, Mesters Rolf, Franke Andre, Lieb Wolfgang, Riemenschneider Mona, Hiersche Milan, Limperger Verena, Nowak-Göttl Ulrike, Stoll Moni |
| Investigation of the predisposing factor of pemphigus and its clinical subtype through a genome-wide association and next generation sequence analysis.
Journal of the European Academy of Dermatology and Venereology : JEADV 2018 Aug . Sun Y, Liu H, Yang B, Wang C, Foo J N, Bao F, Irwanto A, Yu G, Fu X, Wang Z, You J, Liu J, Zhou G, Liu J, Zhang |
| Genome wide association study of HTLV-1-associated myelopathy/tropical spastic paraparesis in the Japanese population.
Proceedings of the National Academy of Sciences of the United States of America 2021 3 118 (11): . Penova Marina, Kawaguchi Shuji, Yasunaga Jun-Ichirou, Kawaguchi Takahisa, Sato Tomoo, Takahashi Meiko, Shimizu Masakazu, Saito Mineki, Tsukasaki Kunihiro, Nakagawa Masanori, Takenouchi Norihiro, Hara Hideo, Matsuura Eiji, Nozuma Satoshi, Takashima Hiroshi, Izumo Shuji, Watanabe Toshiki, Uchimaru Kaoru, Iwanaga Masako, Utsunomiya Atae, Tabara Yasuharu, Paul Richard, Yamano Yoshihisa, Matsuoka Masao, Matsuda Fumihi |
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