Cross-cohort analysis of expression and splicing quantitative trait loci in TOPMed
Peter Orchard, Thomas W. Blackwell, Linda Kachuri, Peter J. Castaldi et autres
15 citationsScience
Deborah A. Nickerson
Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.
654Publications signalées
98598Citations signalées
1Affiliations récentes
Institutions déclarées
Domaines associés
Genetic Associations and EpidemiologyGenomics and Rare DiseasesGenomic variations and chromosomal abnormalitiesRNA modifications and cancerConnective tissue disorders research
Publications récentes
Integration of DNA sequencing with population pharmacokinetics to improve the prediction of irinotecan exposure in cancer patients
Spinel Karas, Robert R. Bies, Federico Innocenti, Nancy J. Cox et autres
0 citationsCarolina Digital Repository (University of North Carolina at Chapel Hill)
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program
Braxton D. Mitchell, Rasika A. Mathias, Kāri Stefánsson, Joshua P. Lewis et autres
0 citationsCarolina Digital Repository (University of North Carolina at Chapel Hill)
Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification
Stephen S. Rich, Paul S. de Vries, HarshaVardhan Doddapaneni, David R. Jacobs et autres
0 citationsCarolina Digital Repository (University of North Carolina at Chapel Hill)
Whole genome sequence association with E-selectin levels reveals loss-of-function variant in African Americans
Arden Moscati, NHLBI Trans-Omics for Precision Medicine Consortium, Nathan Pankratz, Biqi Wang et autres
0 citationsCarolina Digital Repository (University of North Carolina at Chapel Hill)
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk
Seung Hoan Choi, Sean J. Jurgens, Ling Xiao, Matthew C. Hill et autres
32 citationsNature Genetics
A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies
Xihao Li, Han Chen, Margaret Sunitha Selvaraj, Eric Van Buren et autres
10 citationsNature Computational Science
Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease
Nathan Pankratz, Jacob C. Ulirsch, Alex P. Reiner, Gonçalo R. Abecasis et autres
0 citationsCarolina Digital Repository (University of North Carolina at Chapel Hill)
Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program
Nitin Gupta, Stephen S. Rich, Xin Hu, B.E Cade et autres
0 citationsCarolina Digital Repository (University of North Carolina at Chapel Hill)
Remote surveillance and detection of SARS-CoV-2 transmission among household members in King County, Washington
Anne Emanuels, Amanda M. Casto, Jessica Heimonen, Jessica O’Hanlon et autres
1 citationBMC Infectious Diseases
Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data
Denise M. Kay, Wendy N. Nembhard, Shiran Shapira, Andrew F. Olshan et autres
0 citationsCarolina Digital Repository (University of North Carolina at Chapel Hill)
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program
E. Boerwinkle, R. Duggirala, Qi Sun, P. Surendran et autres
0 citationsCarolina Digital Repository (University of North Carolina at Chapel Hill)
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