Dawn L. DeMeo
Dawn L. DeMeo
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Cited by
Cited by
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ...
Nature 590 (7845), 290-299, 2021
Sex and gender: modifiers of health, disease, and medicine
F Mauvais-Jarvis, NB Merz, PJ Barnes, RD Brinton, JJ Carrero, ...
The Lancet 396 (10250), 565-582, 2020
DNA methylation in newborns and maternal smoking in pregnancy: genome-wide consortium meta-analysis
BR Joubert, JF Felix, P Yousefi, KM Bakulski, AC Just, C Breton, ...
The American Journal of Human Genetics 98 (4), 680-696, 2016
Epigenetic signatures of cigarette smoking
R Joehanes, AC Just, RE Marioni, LC Pilling, LM Reynolds, ...
Circulation: cardiovascular genetics 9 (5), 436-447, 2016
Transmission of lymphocytic choriomeningitis virus by organ transplantation
SA Fischer, MB Graham, MJ Kuehnert, CN Kotton, A Srinivasan, FM Marty, ...
New England Journal of Medicine 354 (21), 2235-2249, 2006
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
Clinical and radiologic disease in smokers with normal spirometry
EA Regan, DA Lynch, D Curran-Everett, JL Curtis, JHM Austin, ...
JAMA internal medicine 175 (9), 1539-1549, 2015
Gender differences in COPD: are women more susceptible to smoking effects than men?
IC Sørheim, A Johannessen, A Gulsvik, PS Bakke, EK Silverman, ...
Thorax 65 (6), 480-485, 2010
α1-Antitrypsin deficiency· 2: Genetic aspects of α1-antitrypsin deficiency: phenotypes and genetic modifiers of emphysema risk
DL DeMeo, EK Silverman
Thorax 59 (3), 259-264, 2004
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries
N Shrine, AL Guyatt, AM Erzurumluoglu, VE Jackson, BD Hobbs, ...
Nature genetics 51 (3), 481-493, 2019
Understanding tissue-specific gene regulation
AR Sonawane, J Platig, M Fagny, CY Chen, JN Paulson, ...
Cell reports 21 (4), 1077-1088, 2017
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
Cigarette smoking behaviors and time since quitting are associated with differential DNA methylation across the human genome
ES Wan, W Qiu, A Baccarelli, VJ Carey, H Bacherman, SI Rennard, ...
Human molecular genetics 21 (13), 3073-3082, 2012
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
Early-onset chronic obstructive pulmonary disease is associated with female sex, maternal factors, and African American race in the COPDGene Study
MG Foreman, L Zhang, J Murphy, NN Hansel, B Make, JE Hokanson, ...
American journal of respiratory and critical care medicine 184 (4), 414-420, 2011
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
Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations
P Sakornsakolpat, D Prokopenko, M Lamontagne, NF Reeve, AL Guyatt, ...
Nature genetics 51 (3), 494-505, 2019
A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13
MH Cho, PJ Castaldi, ES Wan, M Siedlinski, CP Hersh, DL Demeo, ...
Human molecular genetics 21 (4), 947-957, 2012
Optimism and cause-specific mortality: a prospective cohort study
ES Kim, KA Hagan, F Grodstein, DL DeMeo, I De Vivo, LD Kubzansky
American journal of epidemiology 185 (1), 21-29, 2017
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