Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: HUS1[original query] |
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Evaluating new candidate SNPs as low penetrance risk factors in sporadic breast cancer: a two-stage Spanish case-control study. Gynecologic oncology 2009 Jan 112 (1): 210-4. Vega Ana, Salas Antonio, Milne Roger L, Carracedo Begoña, Ribas Gloria, Ruibal Alvaro, de León Antonio Cabrera, González-Hernández Ana, Benítez Javier, Carracedo Ang |
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis. Human molecular genetics 2009 Apr 18 (8): 1524-32. Chiò Adriano, Schymick Jennifer C, Restagno Gabriella, Scholz Sonja W, Lombardo Federica, Lai Shiao-Lin, Mora Gabriele, Fung Hon-Chung, Britton Angela, Arepalli Sampath, Gibbs J Raphael, Nalls Michael, Berger Stephen, Kwee Lydia Coulter, Oddone Eugene Z, Ding Jinhui, Crews Cynthia, Rafferty Ian, Washecka Nicole, Hernandez Dena, Ferrucci Luigi, Bandinelli Stefania, Guralnik Jack, Macciardi Fabio, Torri Federica, Lupoli Sara, Chanock Stephen J, Thomas Gilles, Hunter David J, Gieger Christian, Wichmann H Erich, Calvo Andrea, Mutani Roberto, Battistini Stefania, Giannini Fabio, Caponnetto Claudia, Mancardi Giovanni Luigi, La Bella Vincenzo, Valentino Francesca, Monsurrò Maria Rosaria, Tedeschi Gioacchino, Marinou Kalliopi, Sabatelli Mario, Conte Amelia, Mandrioli Jessica, Sola Patrizia, Salvi Fabrizio, Bartolomei Ilaria, Siciliano Gabriele, Carlesi Cecilia, Orrell Richard W, Talbot Kevin, Simmons Zachary, Connor James, Pioro Erik P, Dunkley Travis, Stephan Dietrich A, Kasperaviciute Dalia, Fisher Elizabeth M, Jabonka Sibylle, Sendtner Michael, Beck Marcus, Bruijn Lucie, Rothstein Jeffrey, Schmidt Silke, Singleton Andrew, Hardy John, Traynor Bryan |
Common genetic variants related to genomic integrity and risk of papillary thyroid cancer. Carcinogenesis 2011 Aug 32 (8): 1231-7. Neta Gila, Brenner Alina V, Sturgis Erich M, Pfeiffer Ruth M, Hutchinson Amy A, Aschebrook-Kilfoy Briseis, Yeager Meredith, Xu Li, Wheeler William, Abend Michael, Ron Elaine, Tucker Margaret A, Chanock Stephen J, Sigurdson Alice |
Low penetrance alleles as risk modifiers in familial and sporadic breast cancer. Familial cancer 2012 Dec 11 (4): 629-36. Esteban Cardeñosa Eva, de Juan Jiménez Inmaculada, Palanca Suela Sarai, Chirivella González Isabel, Segura Huerta Angel, Santaballa Beltran Ana, Casals El Busto María, Barragán González Eva, Fuster Lluch Oscar, Bermúdez Edo José, Bolufer Gilabert Pascu |
Associations between polymorphisms in target, metabolism, or transport proteins of mycophenolate sodium and therapeutic or adverse effects in kidney transplant patients. Pharmacogenetics and genomics 2014 May 24 (5): 256-62. Woillard Jean-Baptiste, Picard Nicolas, Thierry Antoine, Touchard Guy, Marquet Pierre, |
Evaluation of the RHINO gene for breast cancer predisposition in Finnish breast cancer families. Breast cancer research and treatment 2014 Apr 144 (2): 437-41. Heikkinen Tuomas, Khan Sofia, Huovari Elina, Vilske Sara, Schleutker Johanna, Kallioniemi Anne, Blomqvist Carl, Aittomäki Kristiina, Nevanlinna He |
A Comprehensive Meta-analysis of Case-Control Association Studies to Evaluate Polymorphisms Associated with the Risk of Differentiated Thyroid Carcinoma. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2016 Feb . Figlioli Gisella, Elisei Rossella, Romei Cristina, Melaiu Ombretta, Cipollini Monica, Bambi Franco, Chen Bowang, Köhler Aleksandra, Cristaudo Alfonso, Hemminki Kari, Gemignani Federica, Försti Asta, Landi Stefa |
Amplification of 7p12 Is Associated with Pathologic Nonresponse to Neoadjuvant Chemotherapy in Muscle-Invasive Bladder Cancer. The American journal of pathology 2019 Dec . Pichler Renate, Lindner Andrea K, Compérat Eva, Obrist Peter, Schäfer Georg, Todenhöfer Tilman, Horninger Wolfgang, Culig Zoran, Untergasser Gero |
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- Page last updated:Apr 22, 2024
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