Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: PRKRA[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 |
Genome-wide copy number variation analysis identifies deletion variants associated with ankylosing spondylitis. Arthritis & rheumatology (Hoboken, N.J.) 2014 Aug 66 (8): 2103-12. Jung Seung-Hyun, Yim Seon-Hee, Hu Hae-Jin, Lee Kyu Hoon, Lee Joo-Hyun, Sheen Dong-Hyuk, Lim Mi-Kyoung, Kim Soon-Young, Park Sung-Won, Kim So-Hee, Han Kyudong, Kim Tae-Hwan, Shim Seung-Cheol, Chung Yeun-J |
Copy number variants in short children born small for gestational age. Hormone research in pædiatrics 2014 82 (5): 310-8. Wit Jan M, van Duyvenvoorde Hermine A, van Klinken Jan B, Caliebe Janina, Bosch Cathy A J, Lui Julian C, Gijsbers Antoinet C J, Bakker Egbert, Breuning Martijn H, Oostdijk Wilma, Losekoot Monique, Baron Jeffrey, Binder Gerhard, Ranke Michael B, Ruivenkamp Claudia A |
Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms.
American journal of human genetics 2015 Jan 96 (1): 104-20. Baurecht Hansjörg, Hotze Melanie, Brand Stephan, Büning Carsten, Cormican Paul, Corvin Aiden, Ellinghaus David, Ellinghaus Eva, Esparza-Gordillo Jorge, Fölster-Holst Regina, Franke Andre, Gieger Christian, Hubner Norbert, Illig Thomas, Irvine Alan D, Kabesch Michael, Lee Young A E, Lieb Wolfgang, Marenholz Ingo, McLean W H Irwin, Morris Derek W, Mrowietz Ulrich, Nair Rajan, Nöthen Markus M, Novak Natalija, O'Regan Grainne M, , Schreiber Stefan, Smith Catherine, Strauch Konstantin, Stuart Philip E, Trembath Richard, Tsoi Lam C, Weichenthal Michael, Barker Jonathan, Elder James T, Weidinger Stephan, Cordell Heather J, Brown Sara |
Impact of polymorphisms in microRNA biogenesis genes on colon cancer risk and microRNA expression levels: a population-based, case-control study. BMC medical genomics 2016 9 (1): 21. Mullany Lila E, Herrick Jennifer S, Wolff Roger K, Buas Matthew F, Slattery Martha |
Single nucleotide polymorphisms within MicroRNAs, MicroRNA targets, and MicroRNA biogenesis genes and their impact on colorectal cancer survival. Genes, chromosomes & cancer 2016 Nov . Mullany Lila E, Herrick Jennifer S, Wolff Roger K, Slattery Martha |
The prevalence of PRKRA mutations in idiopathic dystonia. Parkinsonism & related disorders 2017 Dec . Dos Santos Camila Oliveira, da Silva-Júnior Francisco Pereira, Puga Renato David, Barbosa Egberto Reis, Azevedo Silva Sonia Maria Cesar, Borges Vanderci, Limongi João Carlos Papaterra, Rocha Maria Sheila Guimarães, Ferraz Henrique Ballalai, de Carvalho Aguiar Patric |
Mutational analysis of GSC, HOXA2 and PRKRA in 106 Chinese patients with microtia. International journal of pediatric otorhinolaryngology 2017 1 93 78-82. Hao Shaojuan, Jin Lei, Li Chenlong, Wang Huijun, Zheng Fengyun, Ma Duan, Zhang Tian |
Han Chinese family with early-onset Parkinson's disease carries novel compound heterozygous mutations in the PARK2 gene. Brain and behavior 2019 8 9 (9): e01372. Huang Ting, Gao Chen-Yu, Wu Liang, Gong Peng-Yu, Wang Ji-Zheng, Tian You-Yong, Zhang Ying-Do |
Baseline Hepatic Levels of miR-29b and Claudin are Respectively Associated with the Stage of Fibrosis and HCV RNA in Hepatitis C. Clinical & experimental gastroenterology & hepatology 2019 4 1 (1): . Sendi Hossein, Mehrab-Mohseni Marjan, Russo Mark W, Steuerwald Nury, Jacobs Carl, Clemens Mark G, Bonkovsky Herbert |
Exome-wide analysis of copy number variation shows association of the human leukocyte antigen region with asthma in UK Biobank. BMC medical genomics 2022 May 15 (1): 119. Fawcett Katherine A, Demidov German, Shrine Nick, Paynton Megan L, Ossowski Stephan, Sayers Ian, Wain Louise V, Hollox Edward |
Uniparental disomy screen of Irish rare disorder cohort unmasks homozygous variants of clinical significance in the TMCO1 and PRKRA genes. Frontiers in genetics 2022 13 945296. Molloy B, Jones E R, Linhares N D, Buckley P G, Leahy T R, Lynch B, Knerr I, King M D, Gorman K |
Exome-wide association study of treatment-resistant depression suggests novel treatment targets. Scientific reports 2023 8 13 (1): 12467. Shrey B Shah, Teja N Peddada, Christopher Song, Maame Mensah, Heejong Sung, Mani Yavi, Peixiong Yuan, Carlos A Zarate, Brian J Mickey, Margit Burmeister, Nirmala Akula, Francis J McMah |
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- Page last updated:Mar 18, 2024
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