J. Pankow

发表

Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies

Andrew D. Johnson, May E. Montasser, Nicholette D. Palmer, 2022, Nature Genetics.

Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole genome sequencing studies at scale

Ivana V. Yang, Andrew D. Johnson, Ryan D. Hernandez, 2020, Nature Genetics.

Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals

Andrew D. Johnson, Benjamin D. Heavner, Michael E. Hall, 2022, Nature Communications.

Genome sequencing unveils a regulatory landscape of platelet reactivity

Benjamin D. Heavner, May E. Montasser, Nicholette D. Palmer, 2019, Nature Communications.

Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

Andrew D. Johnson, Benjamin D. Heavner, Ryan D. Hernandez, 2022, Nature Genetics.

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

Ivana V. Yang, Sebastian M. Armasu, Andrew D. Johnson, 2020, Nature.

Rare loss of function variants in candidate genes and risk of colorectal cancer

Taylor J. Maxwell, Jennifer G. Robinson, Andrew J. Sanford, 2018, Human Genetics.

Reply by Elmaleh-Sachs et al. to Townsend and Cowl, and to Miller et al.

Benjamin M. Smith, J. Hankinson, R. Barr, 2022, American journal of respiratory and critical care medicine.

Pulmonary Blood Volume Among Older Adults in the Community: The MESA Lung Study

Benjamin M. Smith, David W. Kaczka, Sanjiv J. Shah, 2022, Circulation. Cardiovascular imaging.

Distribution of Lewis (FUT3) genotype and allele: frequencies in a biethnic United States population

D. Couper, G. Heiss, B. Çakır, 2002, Annals of Hematology.

Weight-Loss Induced Changes in Plasma Factor VII Coagulant Activity and Relation to the Factor VII Arg/Gln353 Polymorphism in Moderately Obese Adults

A. Folsom, R. Wing, R. Jeffery, 1998, Thrombosis and Haemostasis.

Clonal haematopoiesis and risk of chronic liver disease

Andrew D. Johnson, Benjamin D. Heavner, May E. Montasser, 2023, Nature.

Omega-3 Fatty Acid Biomarkers and Incident Atrial Fibrillation.

W. Guan, D. Mozaffarian, E. Rimm, 2023, Journal of the American College of Cardiology.

Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

Ross M. Fraser, May E. Montasser, Sara M. Willems, 2020, Nature Communications.

Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

Andrew D. Johnson, Benjamin D. Heavner, May E. Montasser, 2023, EBioMedicine.

Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

Andrew D. Johnson, May E. Montasser, Nicholette D. Palmer, 2020, Nature Genetics.

Genetic and non-genetic factors affecting the expression of COVID-19-relevant genes in the large airway epithelium

Andrew D. Johnson, Benjamin D. Heavner, May E. Montasser, 2020, Genome Medicine.

Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People with Type 2 Diabetes Mellitus

Lynn K. Carmichael, Philip H. Schroeder, David E. Condon, 2023, medRxiv.

Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge

Alex Doney, Beverley Balkau, Meena Kumari, 2010, Nature Genetics.

WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE

Benjamin D. Heavner, Nancy L. Heard Costa, Nicholette D. Palmer, 2023, medRxiv.

Genetic analysis of mammographic breast density in adult women: evidence of a gene effect.

J. Pankow, D. Grabrick, T. Sellers, 1997, Journal of the National Cancer Institute.

Alcohol consumption and plasminogen activator inhibitor type 1: the National Heart, Lung, and Blood Institute Family Heart Study.

J. Pankow, M. Province, Yuling Hong, 2000, American heart journal.

Association of coronary artery calcified plaque with clinical coronary heart disease in the National Heart, Lung, and Blood Institute's Family Heart Study.

J. Pankow, C. Lewis, M. Province, 2006, The American journal of cardiology.

Variant-specific inflation factors for assessing population stratification at the phenotypic variance level

Andrew D. Johnson, Benjamin D. Heavner, May E. Montasser, 2021, Nature Communications.

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

Tanya M. Teslovich, J. Pankow, M. McCarthy, 2014 .

A framework for detecting noncoding rare variant associations of large-scale whole-genome sequencing studies

Benjamin D. Heavner, May E. Montasser, Nicholette D. Palmer, 2021, bioRxiv.

Lack of association between the angiotensin-converting enzyme insertion/deletion polymorphism and plasminogen activator inhibitor-1 antigen levels in the National Heart, Lung, and Blood Institute Family Heart Study

J. Pankow, I. Borecki, A. Folsom, 2000, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Antithrombin, Protein C, and Protein S: Genome and Transcriptome-Wide Association Studies Identify 7 Novel Loci Regulating Plasma Levels

C. Sitlani, A. Morrison, M. Kleber, 2023 .

Transcriptome-wide association study and Mendelian randomization in pancreatic cancer identifies susceptibility genes and causal relationships with type 2 diabetes and venous thromboembolism

Sebastian M. Armasu, D. Chasman, M. Germain, 2024, EBioMedicine.

Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge

E. Zeggini, N. Grarup, M. Weedon, 2010, Nature Genetics.