Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: CECR1[original query] |
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COL4A2 is associated with lacunar ischemic stroke and deep ICH: Meta-analyses among 21,500 cases and 40,600 controls. Neurology 2017 Sep . Rannikmäe Kristiina, Sivakumaran Vhinoth, Millar Henry, Malik Rainer, Anderson Christopher D, Chong Mike, Dave Tushar, Falcone Guido J, Fernandez-Cadenas Israel, Jimenez-Conde Jordi, Lindgren Arne, Montaner Joan, O'Donnell Martin, Paré Guillaume, Radmanesh Farid, Rost Natalia S, Slowik Agnieszka, Söderholm Martin, Traylor Matthew, Pulit Sara L, Seshadri Sudha, Worrall Brad B, Woo Daniel, Markus Hugh S, Mitchell Braxton D, Dichgans Martin, Rosand Jonathan, Sudlow Cathie L M, |
Mutational profile of rare variants in inflammasome-related genes in Behçet disease: A Next Generation Sequencing approach. Scientific reports 2017 8 7 (1): 8453. Burillo-Sanz Sergio, Montes-Cano Marco-Antonio, García-Lozano José-Raúl, Ortiz-Fernández Lourdes, Ortego-Centeno Norberto, García-Hernández Francisco-José, Espinosa Gerard, Graña-Gil Genaro, Sánchez-Bursón Juan, Rosa Juliá María, Solans Roser, Blanco Ricardo, Barnosi-Marín Ana-Celia, Gómez De la Torre Ricardo, Fanlo Patricia, Rodríguez-Carballeira Mónica, Rodríguez-Rodríguez Luis, Camps Teresa, Castañeda Santos, Alegre-Sancho Juan-Jose, Martín Javier, González-Escribano María Francis |
The Genetic Landscape of Diamond-Blackfan Anemia. American journal of human genetics 2018 12 103 (6): 930-947. Ulirsch Jacob C, Verboon Jeffrey M, Kazerounian Shideh, Guo Michael H, Yuan Daniel, Ludwig Leif S, Handsaker Robert E, Abdulhay Nour J, Fiorini Claudia, Genovese Giulio, Lim Elaine T, Cheng Aaron, Cummings Beryl B, Chao Katherine R, Beggs Alan H, Genetti Casie A, Sieff Colin A, Newburger Peter E, Niewiadomska Edyta, Matysiak Michal, Vlachos Adrianna, Lipton Jeffrey M, Atsidaftos Eva, Glader Bertil, Narla Anupama, Gleizes Pierre-Emmanuel, O'Donohue Marie-Françoise, Montel-Lehry Nathalie, Amor David J, McCarroll Steven A, O'Donnell-Luria Anne H, Gupta Namrata, Gabriel Stacey B, MacArthur Daniel G, Lander Eric S, Lek Monkol, Da Costa Lydie, Nathan David G, Korostelev Andrei A, Do Ron, Sankaran Vijay G, Gazda Hanna |
Behçet's disease and genetic interactions between HLA-B*51 and variants in genes of autoinflammatory syndromes. Scientific reports 2019 2 9 (1): 2777. Burillo-Sanz Sergio, Montes-Cano Marco-Antonio, García-Lozano José-Raúl, Olivas-Martínez Israel, Ortego-Centeno Norberto, García-Hernández Francisco-José, Espinosa Gerard, Graña-Gil Genaro, Sánchez-Bursón Juan, Juliá María Rosa, Solans Roser, Blanco Ricardo, Barnosi-Marín Ana-Celia, Gómez de la Torre Ricardo, Fanlo Patricia, Rodríguez-Carballeira Mónica, Rodríguez-Rodríguez Luis, Camps Teresa, Castañeda Santos, Alegre-Sancho Juan-Jose, Martín Javier, González-Escribano María Francis |
[Prenatal genetic analysis of three fetuses with abnormalities of chromosome 22]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 3 37 (4): 405-409. Ge Yunsheng, Zhang Jian, Cai Meijiao, Chen Xiaolu, Zhou Yul |
Global Assessment of Mendelian Stroke Genetic Prevalence in 101 635 Individuals From 7 Ethnic Groups. Stroke 2020 Feb STROKEAHA119028840. Grami Nickrooz, Chong Michael, Lali Ricky, Mohammadi-Shemirani Pedrum, Henshall David E, Rannikmäe Kristiina, Paré Guillau |
A Novel LC-MS/MS-Based Method for the Diagnosis of ADA2 Deficiency from Dried Plasma Spot. Molecules (Basel, Switzerland) 2021 9 26 (18): . Cafaro Alessia, Pigliasco Federica, Barco Sebastiano, Penco Federica, Schena Francesca, Caorsi Roberta, Volpi Stefano, Tripodi Gino, Gattorno Marco, Cangemi Giulia |
Mediterranean fever gene variants modify clinical phenotypes of idiopathic multi-centric Castleman disease. Clinical and experimental immunology 2021 6 206 (1): 91-98. Endo Yushiro, Koga Tomohiro, Ubara Yoshihumi, Sumiyoshi Remi, Furukawa Kaori, Kawakami Atsus |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 29, 2024
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