Publications by authors named "Michael Feolo"

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Whole genome DNA and RNA sequencing of whole blood elucidates the genetic architecture of gene expression underlying a wide range of diseases.
Chunyu Liu, Roby Joehanes, Jiantao Ma, Yuxuan Wang, Xianbang Sun, Michael Feolo

Sci Rep· November 2022

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Identifying Datasets for Cross-Study Analysis in dbGaP using PhenX.
Huaqin Pan, Vesselina Bakalov, Lisa Cox, Michelle L Engle, Stephen W Erickson, Michael Feolo

Sci Data· September 2022

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Whole Genome DNA and RNA Sequencing of Whole Blood Elucidates the Genetic Architecture of Gene Expression Underlying a Wide Range of Diseases.
Chunyu Liu, Roby Joehanes, Jiantao Ma, Yuxuan Wang, Xianbang Sun, Michael Feolo

medRxiv· May 2022

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Whole Genome DNA and RNA Sequencing of Whole Blood Elucidates the Genetic Architecture of Gene Expression Underlying a Wide Range of Diseases.
Chunyu Liu, Roby Joehanes, Jiantao Ma, Yuxuan Wang, Xianbang Sun, Michael Feolo

Res Sq· May 2022

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GRAF-pop: A Fast Distance-Based Method To Infer Subject Ancestry from Multiple Genotype Datasets Without Principal Components Analysis.
Yumi Jin, Alejandro A Schaffer, Michael Feolo, J Bradley Holmes, Brandi L Kattman

G3 (Bethesda)· August 2019

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Quickly identifying identical and closely related subjects in large databases using genotype data.
Yumi Jin, Alejandro A Schäffer, Stephen T Sherry, Michael Feolo

PLoS One· September 2017

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Integrated genome-wide analysis of expression quantitative trait loci aids interpretation of genomic association studies.
Roby Joehanes, Xiaoling Zhang, Tianxiao Huan, Chen Yao, Sai-Xia Ying, Michael L Feolo

Genome Biol· January 2017

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HLA diversity in the 1000 genomes dataset.
Pierre-Antoine Gourraud, Pouya Khankhanian, Nezih Cereb, Soo Young Yang, Michael Feolo

PLoS One· October 2015

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Data use under the NIH GWAS data sharing policy and future directions.
Dina N Paltoo, Laura Lyman Rodriguez, Michael Feolo, Elizabeth Gillanders, Erin M Ramos

Nat Genet· September 2014

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NCBI's Database of Genotypes and Phenotypes: dbGaP.
Kimberly A Tryka, Luning Hao, Anne Sturcke, Yumi Jin, Zhen Y Wang, Michael Feolo

Nucleic Acids Res· January 2014

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Database resources of the National Center for Biotechnology Information.
Eric W Sayers, Tanya Barrett, Dennis A Benson, Evan Bolton, Stephen H Bryant, Michael Feolo

Nucleic Acids Res· January 2012

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Assessing and managing risk when sharing aggregate genetic variant data.
David W Craig, Robert M Goor, Zhenyuan Wang, Justin Paschall, Jim Ostell, Michael Feolo

Nat Rev Genet· September 2011

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Database resources of the National Center for Biotechnology Information.
Eric W Sayers, Tanya Barrett, Dennis A Benson, Evan Bolton, Stephen H Bryant, Michael Feolo

Nucleic Acids Res· January 2011

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Novel sequence feature variant type analysis of the HLA genetic association in systemic sclerosis.
David R Karp, Nishanth Marthandan, Steven G E Marsh, Chul Ahn, Frank C Arnett, Michael Feolo

Hum Mol Genet· February 2010

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Database resources of the National Center for Biotechnology Information.
Eric W Sayers, Tanya Barrett, Dennis A Benson, Evan Bolton, Stephen H Bryant, Michael Feolo

Nucleic Acids Res· January 2010

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Supplementing high-density SNP microarrays for additional coverage of disease-related genes: addiction as a paradigm.
Scott F Saccone, Laura J Bierut, Elissa J Chesler, Peter W Kalivas, Caryn Lerman, Michael Feolo

PLoS One· July 2009

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Database resources of the National Center for Biotechnology Information.
Eric W Sayers, Tanya Barrett, Dennis A Benson, Stephen H Bryant, Kathi Canese, Michael Feolo

Nucleic Acids Res· January 2009

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Database resources of the National Center for Biotechnology Information.
David L Wheeler, Tanya Barrett, Dennis A Benson, Stephen H Bryant, Kathi Canese, Michael Feolo

Nucleic Acids Res· January 2008

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The NCBI dbGaP database of genotypes and phenotypes.
Matthew D Mailman, Michael Feolo, Yumi Jin, Masato Kimura, Kimberly Tryka

Nat Genet· October 2007

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A second generation human haplotype map of over 3.1 million SNPs.

Nature· October 2007

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Genome-wide detection and characterization of positive selection in human populations.
Pardis C Sabeti, Patrick Varilly, Ben Fry, Jason Lohmueller, Elizabeth Hostetter, Michael Feolo

Nature· October 2007

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Inference and analysis of haplotypes from combined genotyping studies deposited in dbSNP.
Noah A Zaitlen, Hyun Min Kang, Michael L Feolo, Stephen T Sherry, Eran Halperin

Genome Res· November 2005

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The sequencing-based typing tool of dbMHC: typing highly polymorphic gene sequences.
Wolfgang Helmberg, Raymond Dunivin, Michael Feolo

Nucleic Acids Res· July 2004

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