Mutation screening for thalassaemia in the Jino ethnic minority population of Yunnan Province, Southwest ChinaShiyun Wang, Rong Zhang, Guangxin Xiang, Yang Li, Xuhong Hou, Fusong Jiang, Feng Jiang, Cheng Hu, Weiping Jia
29 December 2015
Effect of smoking on physical and cognitive capability in later life: a multicohort study using observational and genetic approachesTeri-Louise North, Tom M Palmer, Sarah J Lewis, Rachel Cooper, Chris Power, Alison Pattie, John M Starr, Ian J Deary, Richard M Martin, Avan Aihie Sayer, Meena Kumari, Cyrus Cooper, Mika Kivimaki, Diana Kuh, Yoav Ben-ShlomoSee the full list of authors
15 December 2015
Association of GDF1 rs4808863 with fetal congenital heart defects: a case–control studyJuan Zhang, Qingqing Wu, Li Wang, Xiaofei Li, Yuqing Ma, Ling Yao
11 December 2015
Protocol of the adaptive study of IL-2 dose frequency on regulatory T cells in type 1 diabetes (DILfrequency): a mechanistic, non-randomised, repeat dose, open-label, response-adaptive studyLucy A Truman, Marcin L Pekalski, Paula Kareclas, Marina Evangelou, Neil M Walker, James Howlett, Adrian P Mander, Jane Kennet, Linda S Wicker, Simon Bond, John A Todd, Frank Waldron-Lynch
8 December 2015
Discovery of URAT1 SNPs and association between serum uric acid levels and URAT1Sung Kweon Cho, Soriul Kim, Jae-Yong Chung, Sun Ha Jee
24 November 2015
Evidence used in model-based economic evaluations for evaluating pharmacogenetic and pharmacogenomic tests: a systematic review protocolJaime L Peters, Chris Cooper, James Buchanan
11 November 2015
Association between COX-2 gene polymorphisms and risk of hepatocellular carcinoma development: a meta-analysisSi-Cong Lu, Jian-Hong Zhong, Jun-Tao Tan, Hua-Lin Tang, Xiao-Guang Liu, Bang-De Xiang, Le-Qun Li, Tao Peng
5 October 2015
Cohort profile: LifeLines DEEP, a prospective, general population cohort study in the northern Netherlands: study design and baseline characteristicsEttje F Tigchelaar, Alexandra Zhernakova, Jackie A M Dekens, Gerben Hermes, Agnieszka Baranska, Zlatan Mujagic, Morris A Swertz, Angélica M Muñoz, Patrick Deelen, Maria C Cénit, Lude Franke, Salome Scholtens, Ronald P Stolk, Cisca Wijmenga, Edith J M Feskens
28 August 2015
Non-invasive prenatal diagnosis using fetal DNA in maternal plasma: a preliminary study for identification of paternally-inherited alleles using single nucleotide polymorphismsJ J Chen, J A M A Tan, K H Chua, P C Tan, E George
22 July 2015
Association of endothelial lipase gene−384A/C with coronary artery disease in Han Chinese peopleLiang Xie, Yan Sun, Yu Tong, Ying Liu, Ying Deng
29 June 2015