Complex traits

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
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
Haplotypes of the inducible nitric oxide synthase gene are strongly associated with exhaled nitric oxide levels in adults: a population-based study
Santosh Dahgam, Lars Modig, Åsa Torinsson Naluai, Anna-Carin Olin, Fredrik Nyberg

Journal of Medical Genetics Jul 2014, 51 (7) 449-454; DOI: 10.1136/jmedgenet-2013-101897
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
Loss-of-function de novo mutations play an important role in severe human neural tube defects
Philippe Lemay, Marie-Claude Guyot, Élizabeth Tremblay, Alexandre Dionne-Laporte, Dan Spiegelman, Édouard Henrion, Ousmane Diallo, Patrizia De Marco, Elisa Merello, Christine Massicotte, Valérie Désilets, Jacques L Michaud, Guy A Rouleau, Valeria Capra, Zoha Kibar

Journal of Medical Genetics Jul 2015, 52 (7) 493-497; DOI: 10.1136/jmedgenet-2015-103027
Associations of common variants in HFE and TMPRSS6 with iron parameters are independent of serum hepcidin in a general population: a replication study
Tessel E Galesloot, Anneke J Geurts-Moespot, Martin den Heijer, Fred C G J Sweep, Robert E Fleming, Lambertus A L M Kiemeney, Sita H Vermeulen, Dorine W Swinkels

Journal of Medical Genetics Sep 2013, 50 (9) 593-598; DOI: 10.1136/jmedgenet-2013-101673
Large-scale genotyping identifies a new locus at 22q13.2 associated with female breast size
Jingmei Li, Jia Nee Foo, Nils Schoof, Jajini S Varghese, Pablo Fernandez-Navarro, Gretchen L Gierach, Swee Tian Quek, Mikael Hartman, Silje Nord, Vessela N Kristensen, Marina Pollán, Jonine D Figueroa, Deborah J Thompson, Yi Li, Chiea Chuen Khor, Keith Humphreys, Jianjun Liu, Kamila Czene, Per Hall

Journal of Medical Genetics Oct 2013, 50 (10) 666-673; DOI: 10.1136/jmedgenet-2013-101708
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
Rare and low-frequency variants in human common diseases and other complex traits
Guillaume Lettre

Journal of Medical Genetics Nov 2014, 51 (11) 705-714; DOI: 10.1136/jmedgenet-2014-102437
Support of the histaminergic hypothesis in Tourette Syndrome: association of the histamine decarboxylase gene in a large sample of families
Iordanis Karagiannidis, Sandra Dehning, Paul Sandor, Zsanett Tarnok, Renata Rizzo, Tomasz Wolanczyk, Marcos Madruga-Garrido, Johannes Hebebrand, Markus M Nöthen, Gerd Lehmkuhl, Luca Farkas, Peter Nagy, Urszula Szymanska, Zachos Anastasiou, Vasileios Stathias, Christos Androutsos, Vaia Tsironi, Anastasia Koumoula, Csaba Barta, Peter Zill, Pablo Mir, Norbert Müller, Cathy Barr, Peristera Paschou

Journal of Medical Genetics Nov 2013, 50 (11) 760-764; DOI: 10.1136/jmedgenet-2013-101637

Main menu

Complex traits

Pages

Log in using your username and password

Main menu

Log in using your username and password

You are here

Complex traits

Pages