Christoph Lange
Christoph Lange
Biostatistics Department, Harvard School of Public Health
Verified email at
Cited by
Cited by
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
Family-based designs in the age of large-scale gene-association studies
NM Laird, C Lange
Nature Reviews Genetics 7 (5), 385-394, 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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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