R. Wallace

发表

A phenome-wide association study (PheWAS) in the Population Architecture using Genomics and Epidemiology (PAGE) study reveals potential pleiotropy in African Americans

Janina M. Jeff, A. Reiner, T. Matise, 2019, PloS one.

Phenome-Wide Association Study (PheWAS) for Detection of Pleiotropy within the Population Architecture using Genomics and Epidemiology (PAGE) Network

Marylyn D. Ritchie, Dana C. Crawford, Ewa Deelman, 2013, PLoS genetics.

Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project.

Benjamin A. Logsdon, Andrew D. Johnson, M. Nalls, 2012, American journal of human 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.

Genome-Wide Interaction Analyses between Genetic Variants and Alcohol Consumption and Smoking for Risk of Colorectal Cancer

Stephanie A. Bien, T. Hudson, P. Schrotz-King, 2016, PLoS genetics.

Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

Nicholette D. Palmer, Sina A. Gharib, M. Fornage, 2020, bioRxiv.

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Ivana V. Yang, Zhaohui S. Qin, Andrew D. Johnson, 2018, Nature Communications.

A common variant of the p16INK4a genetic region is associated with physical function in older people

S. Bandinelli, D. Melzer, L. Ferrucci, 2007, Mechanisms of Ageing and Development.

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.

Andrew D. Johnson, O. Franco, A. Hofman, 2016, American journal of human genetics.

Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Ryan D. Hernandez, May E. Montasser, Min A. Jhun, 2018, Nature Communications.

Confirmation of the Reported Association of Clonal Chromosomal Mosaicism with an Increased Risk of Incident Hematologic Cancer

Alex P. Reiner, David R. Crosslin, Gail P. Jarvik, 2013, PloS one.

Human longevity: 25 genetic loci associated in 389,166 UK biobank participants

D. Melzer, L. Pilling, L. Ferrucci, 2017, Aging.

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.

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.

The use of phenome‐wide association studies (PheWAS) for exploration of novel genotype‐phenotype relationships and pleiotropy discovery

C Kooperberg, Y Lin, A. Reiner, 2011, Genetic epidemiology.

Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children with asthma.

Ivana V. Yang, Andrew D. Johnson, Ryan D. Hernandez, 2019, Chest.

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.

Multi-ancestry genome-wide gene–sleep interactions identify novel loci for blood pressure

Nicholette D. Palmer, Sina A. Gharib, M. Fornage, 2021, Molecular Psychiatry.

Genetic Determinants of Pelvic Organ Prolapse among African American and Hispanic Women in the Women’s Health Initiative

Jennifer M Wu, A. Reiner, K. North, 2015, PloS one.

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

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

Admixture mapping of pelvic organ prolapse in African Americans from the Women’s Health Initiative Hormone Therapy trial

Jennifer M Wu, K. North, M. Aldrich, 2017, PloS one.

Erratum: Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis (American Journal of Human Genetics (2016) 99(2) (481–488)(S0002929716302208)(10.1016/j.ajhg.2016.06.016))

Andrew D. Johnson, O. Franco, A. Hofman, 2016 .

Large trans-ethnic meta-analysis identifies AKR1C4 as a novel gene associated with age at menarche.

K. Lunetta, H. Hakonarson, S. Grant, 2021, Human reproduction.

Impact of Ancestry and Common Genetic Variants on QT Interval in African Americans

Kathleen F. Kerr, Cameron D. Palmer, Toshiko Tanaka, 2012, Circulation. Cardiovascular genetics.

Characterization of the association between 8q24 and colon cancer: gene-environment exploration and meta-analysis

J. Potter, D. Duggan, Jill Muehling, 2010, BMC Cancer.

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.

Characterization of 9p24 Risk Locus and Colorectal Adenoma and Cancer: Gene–Environment Interaction and Meta-Analysis

R. Hayes, J. Potter, D. Duggan, 2010, Cancer Epidemiology, Biomarkers & Prevention.

Characterization of 9 p 24 Risk Locus and Colorectal Adenoma and Cancer : Gene – Environment Interaction and Meta-Analysis

R. Hayes, J. Potter, D. Duggan, 2010 .

Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium.

Benjamin D. Heavner, Kelsey E. Grinde, A. Reiner, 2021, EBioMedicine.

Genome-wide Association Study of Parental Life Span

Toshiko Tanaka, K. Lunetta, J. Murabito, 2016, The journals of gerontology. Series A, Biological sciences and medical sciences.

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.

Andrew D. Johnson, O. Franco, A. Hofman, 2016, American journal of human genetics.

Clonal haematopoiesis and risk of chronic liver disease

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

Assessment of immune cell profiles among post-menopausal women in the Women’s Health Initiative using DNA methylation-based methods

A. Reiner, B. Christensen, K. Kelsey, 2023, Clinical Epigenetics.

An APOO Pseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels

Ivana V. Yang, Andrew D. Johnson, Ryan D. Hernandez, 2018, Circulation.

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.

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.

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.

Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children with asthma.

Ivana V. Yang, Andrew D. Johnson, Benjamin D. Heavner, 2019, Chest.