Human Genome Epidemiology Literature Finder
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Records 1 - 7 (of 7 Records) |
| Query Trace: Disease and XIRP2[original query] |
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| Distinct Subtypes of Gastric Cancer Defined by Molecular Characterization Include Novel Mutational Signatures with Prognostic Capability. Cancer research 2016 04 76 (7): 1724-32. Li Xiangchun, Wu William K K, Xing Rui, Wong Sunny H, Liu Yuexin, Fang Xiaodong, Zhang Yanlin, Wang Mengyao, Wang Jiaqian, Li Lin, Zhou Yong, Tang Senwei, Peng Shaoliang, Qiu Kunlong, Chen Longyun, Chen Kexin, Yang Huanming, Zhang Wei, Chan Matthew T V, Lu Youyong, Sung Joseph J Y, Yu J |
| Parkinson's disease: SNCA-, PARK2-, and LRRK2- targeting microRNAs elevated in cingulate gyrus. Parkinsonism & related disorders 2016 Sep . Tatura Roman, Kraus Theo, Giese Armin, Arzberger Thomas, Buchholz Malte, Höglinger Günter, Müller Ulri |
| Polymorphisms in selected genes and analysis of their relationship with osteochondrosis in Polish sport horse breeds. Animal genetics 2018 8 49 (6): 623-627. Wypch?o M, Korwin-Kossakowska A, Bereznowski A, Hecold M, Lewczuk |
| Germline but not somatic de novo mutations are common in human congenital diaphragmatic hernia. Birth defects research 2018 3 110 (7): 610-617. Matsunami Nori, Shanmugam Hari, Baird Lisa, Stevens Jeff, Byrne Janice L, Barnhart Douglas C, Rau Carrie, Feldkamp Marcia L, Yoder Bradley A, Leppert Mark F, Yost H Joseph, Brunelli Lu |
| Whole exome sequencing of high-risk neuroblastoma identifies novel non-synonymous variants. PloS one 2022 17 (8): e0273280. Przyby?a Weronika, Gjersvoll Paulsen Kirsti Marie, Mishra Charitra Kumar, Nygård Ståle, Engebretsen Solveig, Ruud Ellen, Trøen Gunhild, Beiske Klaus, Baumbusch Lars Oliv |
| Methylome analysis of ALS patients and presymptomatic mutation carriers in blood cells. Neurobiology of aging 2022 5 116 16-24. Ruf Wolfgang P, Hannon Eilis, Freischmidt Axel, Grozdanov Veselin, Brenner David, Müller Kathrin, Knehr Antje, Günther Kornelia, Dorst Johannes, Ammerpohl Ole, Danzer Karin M, Mill Jonathan, Ludolph Albert C, Weishaupt Jochen |
| Multi-ancestry genome-wide association study reveals novel genetic signals for lung function decline. medRxiv : the preprint server for health sciences 2024 12 . Bonnie K Patchen, Jingwen Zhang, Nathan Gaddis, Traci M Bartz, Jing Chen, Catherine Debban, Hampton Leonard, Ngoc Quynh Nguyen, Jungkun Seo, Courtney Tern, Richard Allen, Dawn L DeMeo, Myriam Fornage, Carl Melbourne, Melyssa Minto, Matthew Moll, George O'Connor, Tess Pottinger, Bruce M Psaty, Stephen S Rich, Jerome I Rotter, Edwin K Silverman, Jeran Stratford, R Graham Barr, Michael H Cho, Sina A Gharib, Ani Manichaikul, Kari North, Elizabeth C Oelsner, Eleanor M Simonsick, Martin D Tobin, Bing Yu, Seung Hoan Choi, Josee Dupuis, Patricia A Cassano, Dana B Hanco |
- Page last reviewed:Feb 1, 2024
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