Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits A Scuteri, S Sanna, WM Chen, M Uda, G Albai, J Strait, S Najjar, ... PLoS Genet 3 (7), e115, 2007 | 1705 | 2007 |
Newly identified loci that influence lipid concentrations and risk of coronary artery disease CJ Willer, S Sanna, AU Jackson, A Scuteri, LL Bonnycastle, R Clarke, ... Nature genetics 40 (2), 161-169, 2008 | 1689 | 2008 |
Robust relationship inference in genome-wide association studies A Manichaikul, JC Mychaleckyj, SS Rich, K Daly, M Sale, WM Chen Bioinformatics 26 (22), 2867-2873, 2010 | 1213 | 2010 |
Variants in MTNR1B influence fasting glucose levels I Prokopenko, C Langenberg, JC Florez, R Saxena, N Soranzo, ... Nature genetics 41 (1), 77-81, 2009 | 762 | 2009 |
Analysis of shared heritability in common disorders of the brain V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ... Science 360 (6395), 2018 | 665 | 2018 |
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of β-thalassemia M Uda, R Galanello, S Sanna, G Lettre, VG Sankaran, W Chen, G Usala, ... Proceedings of the National Academy of Sciences 105 (5), 1620-1625, 2008 | 607 | 2008 |
Heritability of cardiovascular and personality traits in 6,148 Sardinians G Pilia, WM Chen, A Scuteri, M Orrú, G Albai, M Dei, S Lai, G Usala, M Lai, ... PLoS Genet 2 (8), e132, 2006 | 530 | 2006 |
Imputing amino acid polymorphisms in human leukocyte antigens X Jia, B Han, S Onengut-Gumuscu, WM Chen, PJ Concannon, SS Rich, ... PloS one 8 (6), e64683, 2013 | 491 | 2013 |
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies M Traylor, M Farrall, EG Holliday, C Sudlow, JC Hopewell, YC Cheng, ... The Lancet Neurology 11 (11), 951-962, 2012 | 491 | 2012 |
Family-based association tests for genomewide association scans WM Chen, GR Abecasis The American Journal of Human Genetics 81 (5), 913-926, 2007 | 474 | 2007 |
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers S Onengut-Gumuscu, WM Chen, O Burren, NJ Cooper, AR Quinlan, ... Nature genetics 47 (4), 381-386, 2015 | 426 | 2015 |
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes R Malik, G Chauhan, M Traylor, M Sargurupremraj, Y Okada, A Mishra, ... Nature genetics 50 (4), 524-537, 2018 | 417 | 2018 |
Common variants in the GDF5-UQCC region are associated with variation in human height S Sanna, AU Jackson, R Nagaraja, CJ Willer, WM Chen, LL Bonnycastle, ... Nature genetics 40 (2), 198-203, 2008 | 404 | 2008 |
Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis A Hinks, J Cobb, MC Marion, S Prahalad, M Sudman, J Bowes, P Martin, ... Nature genetics 45 (6), 664-669, 2013 | 325 | 2013 |
The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts S Li, S Sanna, A Maschio, F Busonero, G Usala, A Mulas, S Lai, M Dei, ... PLoS Genet 3 (11), e194, 2007 | 302 | 2007 |
Genome-wide association scan for five major dimensions of personality A Terracciano, S Sanna, M Uda, B Deiana, G Usala, F Busonero, ... Molecular psychiatry 15 (6), 647-656, 2010 | 279 | 2010 |
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry KL Monda, GK Chen, KC Taylor, C Palmer, TL Edwards, LA Lange, ... Nature genetics 45 (6), 690-696, 2013 | 248 | 2013 |
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis E Wheeler, A Leong, CT Liu, MF Hivert, RJ Strawbridge, C Podmore, M Li, ... PLoS medicine 14 (9), e1002383, 2017 | 220 | 2017 |
Genetic determination of Colles' fracture and differential bone mass in women with and without Colles' fracture HW Deng, WM Chen, S Recker, MR Stegman, JL Li, KM Davies, Y Zhou, ... Journal of Bone and Mineral Research 15 (7), 1243-1252, 2000 | 206 | 2000 |
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol LA Lange, Y Hu, H Zhang, C Xue, EM Schmidt, ZZ Tang, C Bizon, ... The American Journal of Human Genetics 94 (2), 233-245, 2014 | 201 | 2014 |