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Genetic epidemiology

  • Meta-analysis of genome-wide studies identifies MEF2C SNPs associated with bone mineral density at forearm
    Hou-Feng Zheng, Emma L Duncan, Laura M Yerges-Armstrong, Joel Eriksson, Ulrica Bergström, Paul J Leo, William D Leslie, David Goltzman, John Blangero, David A Hanley, Melanie A Carless, Elizabeth A Streeten, Mattias Lorentzon, Matthew A Brown, Tim D Spector, Ulrika Pettersson-Kymmer, Claes Ohlsson, Braxton D Mitchell, J Brent Richards
    Journal of Medical Genetics Jul 2013, 50 (7) 473-478; DOI: 10.1136/jmedgenet-2012-101287
  • Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci
    Daphna Weissglas-Volkov, Carlos A Aguilar-Salinas, Elina Nikkola, Kerry A Deere, Ivette Cruz-Bautista, Olimpia Arellano-Campos, Linda Liliana Muñoz-Hernandez, Lizeth Gomez-Munguia, Maria Luisa Ordoñez-Sánchez, Prasad M V Linga Reddy, Aldons J Lusis, Niina Matikainen, Marja-Riitta Taskinen, Laura Riba, Rita M Cantor, Janet S Sinsheimer, Teresa Tusie-Luna, Päivi Pajukanta
    Journal of Medical Genetics May 2013, 50 (5) 298-308; DOI: 10.1136/jmedgenet-2012-101461
  • Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk
    Christina M Lill, Brit-Maren M Schjeide, Christiane Graetz, Tian Liu, Vincent Damotte, Denis A Akkad, Paul Blaschke, Lisa-Ann Gerdes, Antje Kroner, Felix Luessi, Isabelle Cournu-Rebeix, Sabine Hoffjan, Alexander Winkelmann, Emmanuel Touze, Fernando Pico, Philippe Corcia, David Otaegui, Alfredo Antigüedad, Antonio Alcina, Manuel Comabella, Xavier Montalban, Javier Olascoaga, Fuencisla Matesanz, Thomas Dörner, Shu-Chen Li, Elisabeth Steinhagen-Thiessen, Ulman Lindenberger, Andrew Chan, Peter Rieckmann, Hans-Peter Hartung, Orhan Aktas, Peter Lohse, Mathias Buttmann, Tania Kümpfel, Christian Kubisch, Uwe K Zettl, Joerg T Epplen, Bertrand Fontaine, Frauke Zipp, Koen Vandenbroeck, Lars Bertram
    Journal of Medical Genetics Mar 2013, 50 (3) 140-143; DOI: 10.1136/jmedgenet-2012-101411
  • IL12B SNPs and copy number variation in IL23R gene associated with susceptibility to leprosy
    Shafat Ali, Amit Kumar Srivastava, Rupali Chopra, Shweta Aggarwal, Vijay Kumar Garg, Sambit Nath Bhattacharya, Rameshwar Nath Koul Bamezai
    Journal of Medical Genetics Jan 2013, 50 (1) 34-42; DOI: 10.1136/jmedgenet-2012-101214
  • An Italian association study and meta-analysis with previous GWAS confirm WNT4, CDKN2BAS and FN1 as the first identified susceptibility loci for endometriosis
    Luca Pagliardini, Davide Gentilini, Paola Vigano’, Paola Panina-Bordignon, Mauro Busacca, Massimo Candiani, Anna Maria Di Blasio
    Journal of Medical Genetics Jan 2013, 50 (1) 43-46; DOI: 10.1136/jmedgenet-2012-101257
  • Distinct and replicable genetic risk factors for acute respiratory distress syndrome of pulmonary or extrapulmonary origin
    Paula Tejera, Nuala J Meyer, Feng Chen, Rui Feng, Yang Zhao, D Shane O'Mahony, Lin Li, Chau-Chyun Sheu, Rihong Zhai, Zhaoxi Wang, Li Su, Ed Bajwa, Amy M Ahasic, Peter F Clardy, Michelle N Gong, Angela J Frank, Paul N Lanken, B Taylor Thompson, Jason D Christie, Mark M Wurfel, Grant E O'Keefe, David C Christiani
    Journal of Medical Genetics Nov 2012, 49 (11) 671-680; DOI: 10.1136/jmedgenet-2012-100972
  • A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants
    Manu Sharma, John P A Ioannidis, Jan O Aasly, Grazia Annesi, Alexis Brice, Lars Bertram, Maria Bozi, Maria Barcikowska, David Crosiers, Carl E Clarke, Maurizio F Facheris, Matthew Farrer, Gaetan Garraux, Suzana Gispert, Georg Auburger, Carles Vilariño-Güell, Georgios M Hadjigeorgiou, Andrew A Hicks, Nobutaka Hattori, Beom S Jeon, Zygmunt Jamrozik, Anna Krygowska-Wajs, Suzanne Lesage, Christina M Lill, Juei-Jueng Lin, Timothy Lynch, Peter Lichtner, Anthony E Lang, Cecile Libioulle, Miho Murata, Vincent Mok, Barbara Jasinska-Myga, George D Mellick, Karen E Morrison, Thomas Meitnger, Alexander Zimprich, Grzegorz Opala, Peter P Pramstaller, Irene Pichler, Sung Sup Park, Aldo Quattrone, Ekaterina Rogaeva, Owen A. Ross, Leonidas Stefanis, Joanne D Stockton, Wataru Satake, Peter A Silburn, Tim M Strom, Jessie Theuns, Eng- King Tan, Tatsushi Toda, Hiroyuki Tomiyama, Ryan J Uitti, Christine Van Broeckhoven, Karin Wirdefeldt, Zbigniew Wszolek, Georgia Xiromerisiou, Harumi S Yomono, Kuo-Chu Yueh, Yi Zhao, Thomas Gasser, Demetrius Maraganore, Rejko Krüger, on behalf of GEOPD consortium
    Journal of Medical Genetics Nov 2012, 49 (11) 721-726; DOI: 10.1136/jmedgenet-2012-101155
  • Rare variants in XRCC2 as breast cancer susceptibility alleles
    Florentine S Hilbers, Juul T Wijnen, Nicoline Hoogerbrugge, Jan C Oosterwijk, Margriet J Collee, Paolo Peterlongo, Paolo Radice, Siranoush Manoukian, Irene Feroce, Fabio Capra, Fergus J Couch, Xianshu Wang, Lucia Guidugli, Kenneth Offit, Sohela Shah, Ian G Campbell, Ella R Thompson, Paul A James, Alison H Trainer, Javier Gracia, Javier Benitez, Christi J van Asperen, Peter Devilee
    Journal of Medical Genetics Oct 2012, 49 (10) 618-620; DOI: 10.1136/jmedgenet-2012-101191

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