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L. Adrienne Cupples

Child Health and Development Institute · US
Area of research
Genetics · Endocrinology, Diabetes and Metabolism
Research interest
L. Adrienne Cupples, Ph.D. is Professor of Biostatistics and of Epidemiology. She has a long standing interest in statistical methods for epidemiologic studies, for survival data analysis and for genetic epidemiology. She has taught for thirty years at both the introductory and advanced levels. She developed several of the courses in the Biostatistics curriculum, including Statistical Methods for Epidemiology (BS852) and has received numerous teaching awards, including the Norman A Scotch Award for Excellence in Teaching at the School of Public Health. For her efforts in research she received the BUSPH Faculty Career Award in Research & Scholarship as the First Recipient. And she received the Janet L. Norwood Award for Outstanding Achievement by a Woman in the Statistical Sciences as the ninth recipient in 2010.
h-index
176
citations
139,305
works
1,054
NIH funding
primary concept
email

Recent publications

Cross-cohort analysis of expression and splicing quantitative trait loci in TOPMed
2025cited by 13position: contributordoi
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
Nature Communications 2025cited by 6position: contributordoi
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes
Nature Communications 2024cited by 7position: middledoi
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes
Nature Communications 2024cited by 5position: contributordoi
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification
Nature Genetics 2023cited by 147position: middledoi
Clonal Hematopoiesis of Indeterminate Potential (CHIP) and Incident Type 2 Diabetes Risk
Diabetes Care 2023cited by 63position: middledoi
Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma
EBioMedicine 2023cited by 19position: middledoi
The impact of obesity on lung function measurements and respiratory disease: A Mendelian randomization study
Annals of Human Genetics 2023cited by 19position: middledoi
WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE
2023cited by 2position: contributordoi
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data
Nature Genetics 2022cited by 312position: contributordoi
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
Nature Genetics 2022cited by 230position: middledoi
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies
Nature Methods 2022cited by 109position: middledoi
Recommendations on the use and reporting of race, ethnicity, and ancestry in genetic research: Experiences from the NHLBI TOPMed program
Cell Genomics 2022cited by 98position: middledoi
Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential
Science Advances 2022cited by 89position: middledoi
Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed
Cell Genomics 2022cited by 80position: middledoi
Whole genome sequence analysis of blood lipid levels in >66,000 individuals
Nature Communications 2022cited by 73position: middledoi
Whole genome sequence analysis of blood lipid levels in >66,000 individuals
Nature Communications 2022cited by 69position: contributordoi
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies
Nature Genetics 2022cited by 60position: middledoi
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies
Nature Genetics 2022cited by 54position: contributordoi
Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels
Communications Biology 2022cited by 38position: middledoi
Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels
Communications Biology 2022cited by 35position: contributordoi
Rare genetic variants explain missing heritability in smoking
Nature Human Behaviour 2022cited by 30position: middledoi
Gene-lifestyle interactions in the genomics of human complex traits
European Journal of Human Genetics 2022cited by 29position: middledoi
Gene-lifestyle interactions in the genomics of human complex traits.
2022cited by 28position: contributordoi
Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program
The American Journal of Human Genetics 2022cited by 24position: middledoi
Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program
Communications Biology 2022cited by 16position: contributordoi
Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program
Communications Biology 2022cited by 16position: middledoi
Sociodemographic Patterns of Exposure to Civil Aircraft Noise in the United States
Environmental Health Perspectives 2022cited by 13position: middledoi
Rare coding variants in RCN3 are associated with blood pressure
BMC Genomics 2022cited by 10position: middledoi
Lymphocyte activation gene-3-associated protein networks are associated with HDL-cholesterol and mortality in the Trans-omics for Precision Medicine program
Communications Biology 2022cited by 8position: contributordoi

Grants

No grants ingested yet.

Frequent collaborators

Douglas P. Kiel · Harvard University14 papers (2012–2018) · 13 papers (2019–2025)Ramachandran S. Vasan · Department of Public Health12 papers (2013–2025)Ching‐Ti Liu · Boston University11 papers (2012–2023) · 10 papers (2013–2018)Caroline S. Fox · Tallaght University Hospital8 papers (2012–2016)Daniel Levy · Icahn School of Medicine at Mount Sinai7 papers (2012–2021) · 7 papers (2019–2025)Mary Bouxsein · Massachusetts Institute of Technology7 papers (2013–2018)Julius S. Ngwa · Children's National7 papers (2012–2019)Nancy L. Heard‐Costa · Boston University7 papers (2012–2016)Kari E. North · Uganda Virus Research Institute6 papers (2014–2018) · 6 papers (2013–2018)Robert R. McLean · Navitas Systems (United States)6 papers (2013–2018)Anne E. Justice · Geisinger Health System5 papers (2014–2017)Marian T. Hannan · University of San Francisco5 papers (2013–2018)Christopher J. O’Donnell · Boston Biomedical Research Institute5 papers (2012–2016)Ingrid B. Borecki · Washington University in St. Louis5 papers (2012–2018)Thomas W. Winkler · University of North Carolina at Chapel Hill5 papers (2014–2017)Amanda L. Lorbergs · McMaster University5 papers (2016–2018)