Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: PNKD[original query] |
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Common polymorphisms in dystonia-linked genes and susceptibility to the sporadic primary dystonias. Parkinsonism & related disorders 2012 May 18 (4): 351-7. Newman Jeremy R B, Sutherland Greg T, Boyle Richard S, Limberg Nicole, Blum Stefan, O'Sullivan John D, Silburn Peter A, Mellick George |
Spectrum of diverse genomic alterations define non-clear cell renal carcinoma subtypes. Nature genetics 2015 Jan 47 (1): 13-21. Durinck Steffen, Stawiski Eric W, Pavía-Jiménez Andrea, Modrusan Zora, Kapur Payal, Jaiswal Bijay S, Zhang Na, Toffessi-Tcheuyap Vanina, Nguyen Thong T, Pahuja Kanika Bajaj, Chen Ying-Jiun, Saleem Sadia, Chaudhuri Subhra, Heldens Sherry, Jackson Marlena, Peña-Llopis Samuel, Guillory Joseph, Toy Karen, Ha Connie, Harris Corissa J, Holloman Eboni, Hill Haley M, Stinson Jeremy, Rivers Celina Sanchez, Janakiraman Vasantharajan, Wang Weiru, Kinch Lisa N, Grishin Nick V, Haverty Peter M, Chow Bernard, Gehring Julian S, Reeder Jens, Pau Gregoire, Wu Thomas D, Margulis Vitaly, Lotan Yair, Sagalowsky Arthur, Pedrosa Ivan, de Sauvage Frederic J, Brugarolas James, Seshagiri Somasek |
Mutation Analysis of MR-1, SLC2A1, and CLCN1 in 28 PRRT2-negative Paroxysmal Kinesigenic Dyskinesia Patients. Chinese medical journal 0 129 (9): 1017-1021. Wang Hong-Xia, Li Hong-Fu, Liu Gong-Lu, Wen Xiao-Dan, Wu Zhi-Yi |
Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease. Human molecular genetics 2016 Mar . Orlando Giulia, Law Philip J, Palin Kimmo, Tuupanen Sari, Gylfe Alexandra, Hänninen Ulrika, Cajuso Tatiana, Tanskanen Tomas, Kondelin Johanna, Kaasinen Eevi, Sarin Antti-Pekka, Kaprio Jaakko, Eriksson Johan G, Rissanen Harri, Knekt Paul, Pukkala Eero, Jousilahti Pekka, Salomaa Veikko, Ripatti Samuli, Palotie Aarno, Järvinen Heikki, Renkonen-Sinisalo Laura, Lepistö Anna, Böhm Jan, Meklin Jukka-Pekka, Al-Tassan Nada A, Palles Claire, Martin Lynn, Barclay Ella, Tenesa Albert, Farrington Susan, Timofeeva Maria N, Meyer Brian F, Wakil Salma M, Campbell Harry, Smith Christopher G, Idziaszczyk Shelley, Maughan Timothy S, Kaplan Richard, Kerr Rachel, Kerr David, Buchanan Daniel D, Win Aung Ko, Hopper John, Jenkins Mark, Lindor Noralane M, Newcomb Polly A, Gallinger Steve, Conti David, Schumacher Fred, Casey Graham, Taipale Jussi, Cheadle Jeremy P, Dunlop Malcolm G, Tomlinson Ian P, Aaltonen Lauri A, Houlston Richard |
Paroxysmal Dyskinesia in Children: from Genes to the Clinic. Journal of clinical neurology (Seoul, Korea) 2018 Jul . Kim Soo Yeon, Lee Jin Sook, Kim Woo Joong, Kim Hyuna, Choi Sun Ah, Lim Byung Chan, Kim Ki Joong, Chae Jong H |
Molecular Profiling for Predictors of Radiosensitivity in Patients with Breast or Head-and-Neck Cancer. Cancers 2020 4 12 (3): . Drobin Kimi, Marczyk Michal, Halle Martin, Danielsson Daniel, Papiez Anna, Sangsuwan Traimate, Bendes Annika, Hong Mun-Gwan, Qundos Ulrika, Harms-Ringdahl Mats, Wersäll Peter, Polanska Joanna, Schwenk Jochen M, Haghdoost Siam |
Screening Gene Mutations in Chinese Patients With Benign Essential Blepharospasm. Frontiers in neurology 2020 2 10 1387. Dong Hongjuan, Luo Ying, Fan Shanghua, Yin Bo, Weng Chao, Peng B |
Comprehensive Exonic Sequencing of Hemiplegic Migraine-Related Genes in a Cohort of Suspected Probands Identifies Known and Potential Pathogenic Variants. Cells 2020 10 9 (11): . Sutherland Heidi G, Maksemous Neven, Albury Cassie L, Ibrahim Omar, Smith Robert A, Lea Rod A, Haupt Larisa M, Jenkins Bronwyn, Tsang Benjamin, Griffiths Lyn |
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- Page last updated:Apr 22, 2024
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