| A common genetic variant is associated with adult and childhood obesity A Herbert, NP Gerry, MB McQueen, IM Heid, A Pfeufer, T Illig, ... Science 312 (5771), 279-283, 2006 | 948 | 2006 |
| Family-based designs in the age of large-scale gene-association studies NM Laird, C Lange Nature Reviews Genetics 7 (5), 385-394, 2006 | 563 | 2006 |
| Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE L Bertram, C Lange, K Mullin, M Parkinson, M Hsiao, MF Hogan, ... The American Journal of Human Genetics 83 (5), 623-632, 2008 | 562 | 2008 |
| Genome‐wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations J Lasky‐Su, BM Neale, B Franke, RJL Anney, K Zhou, JB Maller, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147 …, 2008 | 488 | 2008 |
| MMP12, lung function, and COPD in high-risk populations GM Hunninghake, MH Cho, Y Tesfaigzi, ME Soto-Quiros, L Avila, ... New England Journal of Medicine 361 (27), 2599-2608, 2009 | 480 | 2009 |
| Variants in FAM13A are associated with chronic obstructive pulmonary disease MH Cho, N Boutaoui, BJ Klanderman, JS Sylvia, JP Ziniti, CP Hersh, ... Nature genetics 42 (3), 200-202, 2010 | 471 | 2010 |
| Genomewide association between GLCCI1 and response to glucocorticoid therapy in asthma KG Tantisira, J Lasky-Su, M Harada, A Murphy, AA Litonjua, BE Himes, ... New England Journal of Medicine 365 (13), 1173-1183, 2011 | 463 | 2011 |
| Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene BE Himes, GM Hunninghake, JW Baurley, NM Rafaels, P Sleiman, ... The American Journal of Human Genetics 84 (5), 581-593, 2009 | 381 | 2009 |
| Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci KU Ludwig, E Mangold, S Herms, S Nowak, H Reutter, A Paul, J Becker, ... Nature genetics 44 (9), 968-971, 2012 | 377 | 2012 |
| Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis MH Cho, MLN McDonald, X Zhou, M Mattheisen, PJ Castaldi, CP Hersh, ... The lancet Respiratory medicine 2 (3), 214-225, 2014 | 367 | 2014 |
| Association of vitamin D receptor gene polymorphisms with childhood and adult asthma BA Raby, R Lazarus, EK Silverman, S Lake, C Lange, M Wjst, ST Weiss American journal of respiratory and critical care medicine 170 (10), 1057-1065, 2004 | 350 | 2004 |
| Genome‐wide association scan of attention deficit hyperactivity disorder BM Neale, J Lasky‐Su, R Anney, B Franke, K Zhou, JB Maller, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147 …, 2008 | 341 | 2008 |
| Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS M Mattheisen, JF Samuels, Y Wang, BD Greenberg, AJ Fyer, ... Molecular psychiatry 20 (3), 337-344, 2015 | 336 | 2015 |
| The transforming growth factor-β1 (TGFB1) gene is associated with chronic obstructive pulmonary disease (COPD) JC Celedon, C Lange, BA Raby, AA Litonjua, LJ Palmer, DL DeMeo, ... Human molecular genetics 13 (15), 1649-1656, 2004 | 318 | 2004 |
| Genetic model testing and statistical power in population‐based association studies of quantitative traits G Lettre, C Lange, JN Hirschhorn Genetic Epidemiology: The Official Publication of the International Genetic …, 2007 | 302 | 2007 |
| Longitudinal multi-omics analyses identify responses of megakaryocytes, erythroid cells, and plasmablasts as hallmarks of severe COVID-19 JP Bernardes, N Mishra, F Tran, T Bahmer, L Best, JI Blase, D Bordoni, ... Immunity 53 (6), 1296-1314. e9, 2020 | 299 | 2020 |
| Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q MB McQueen, B Devlin, SV Faraone, VL Nimgaonkar, P Sklar, ... The American Journal of Human Genetics 77 (4), 582-595, 2005 | 299 | 2005 |
| PBAT: tools for family-based association studies C Lange, D DeMeo, EK Silverman, ST Weiss, NM Laird The American Journal of Human Genetics 74 (2), 367-369, 2004 | 294 | 2004 |
| Family-based association between Alzheimer's disease and variants in UBQLN1 L Bertram, M Hiltunen, M Parkinson, M Ingelsson, C Lange, K Ramasamy, ... New England Journal of Medicine 352 (9), 884-894, 2005 | 277 | 2005 |
| Genetic association analysis of copy-number variation (CNV) in human disease pathogenesis I Ionita-Laza, AJ Rogers, C Lange, BA Raby, C Lee Genomics 93 (1), 22-26, 2009 | 270 | 2009 |
Scott T. WeissProfessor of Medicine, Harvard Medical SchoolVerified email at channing.harvard.edu
