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Author Details
Full Name
Michael Feolo
Affiliation
University of Massachusetts Medical School
ORCID
Career Start Year
1994
Papers
39
H Index
22
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36050327
Identifying Datasets for Cross-Study Analysis in dbGaP using PhenX.
Sci Data
2022
35547845
Whole Genome DNA and RNA Sequencing of Whole Blood Elucidates the Genetic Architecture of Gene Expression Underlying a Wide Range of Diseases.
medRxiv
2022
35664994
Whole Genome DNA and RNA Sequencing of Whole Blood Elucidates the Genetic Architecture of Gene Expression Underlying a Wide Range of Diseases.
Res Sq
2022
36424512
Whole genome DNA and RNA sequencing of whole blood elucidates the genetic architecture of gene expression underlying a wide range of diseases.
Sci Rep
2022
36380121
Elucidating the genetic architecture of DNA methylation to identify promising molecular mechanisms of disease.
Sci Rep
2022
31151998
GRAF-pop: A Fast Distance-Based Method To Infer Subject Ancestry from Multiple Genotype Datasets Without Principal Components Analysis.
G3 (Bethesda)
2019
28609482
Quickly identifying identical and closely related subjects in large databases using genotype data.
PLoS One
2017
28122634
Integrated genome-wide analysis of expression quantitative trait loci aids interpretation of genomic association studies.
Genome Biol
2017
27350599
Rapid evaluation of phenotypes, SNPs and results through the dbGaP CHARGE Summary Results site.
Nat Genet
2016
23695286
Phenotype-Genotype Integrator (PheGenI): synthesizing genome-wide association study (GWAS) data with existing genomic resources.
Eur J Hum Genet
2014
24988075
HLA diversity in the 1000 genomes dataset.
PLoS One
2014
25162809
Data use under the NIH GWAS data sharing policy and future directions.
Nat Genet
2014
24297256
NCBI's Database of Genotypes and Phenotypes: dbGaP.
Nucleic Acids Res
2014
22140104
Database resources of the National Center for Biotechnology Information.
Nucleic Acids Res
2012
21097890
Database resources of the National Center for Biotechnology Information.
Nucleic Acids Res
2011
21921928
Assessing and managing risk when sharing aggregate genetic variant data.
Nat Rev Genet
2011
20030785
The Babel Tower revisited: SNPs - Indels - CNVs. Confusion in naming sequence variant always rises from ashes.
Tissue Antigens
2010
19910364
Database resources of the National Center for Biotechnology Information.
Nucleic Acids Res
2010
19933168
Novel sequence feature variant type analysis of the HLA genetic association in systemic sclerosis.
Hum Mol Genet
2010
18940862
Database resources of the National Center for Biotechnology Information.
Nucleic Acids Res
2009
19381300
Supplementing high-density SNP microarrays for additional coverage of disease-related genes: addiction as a paradigm.
PLoS One
2009
18045790
Database resources of the National Center for Biotechnology Information.
Nucleic Acids Res
2008
17445202
14th International HLA and Immunogenetics Workshop: report on mapping microsatellite markers in the major histocompatibility complex region.
Tissue Antigens
2007
17898773
The NCBI dbGaP database of genotypes and phenotypes.
Nat Genet
2007
17943131
Genome-wide detection and characterization of positive selection in human populations.
Nature
2007
17943122
A second generation human haplotype map of over 3.1 million SNPs.
Nature
2007
17445204
14th International HLA and Immunogenetics Workshop: report on the HLA component of type 1 diabetes.
Tissue Antigens
2007
17445203
Nomenclature for HLA microsatellites.
Tissue Antigens
2007
16671947
The dbMHC microsatellite portal: a public resource for the storage and display of MHC microsatellite information.
Tissue Antigens
2006
16251470
Inference and analysis of haplotypes from combined genotyping studies deposited in dbSNP.
Genome Res
2005
14705985
The reagent database at dbMHC.
Tissue Antigens
2004
15215374
The sequencing-based typing tool of dbMHC: typing highly polymorphic gene sequences.
Nucleic Acids Res
2004
12124726
Genome-wide linkage analysis for celiac disease in North American families.
Am J Med Genet
2002
11426458
Prevalence and clinical characteristics of celiac disease in Downs syndrome in a US study.
Am J Med Genet
2001
11684124
A strategy for high throughput HLA-DQ typing.
J Immunol Methods
2001
11737870
Linkage analysis of HLA and candidate genes for celiac disease in a North American family-based study.
BMC Med Genet
2001
12361089
NCBI genetic resources supporting immunogenetic research.
Rev Immunogenet
2000
7608450
Immune response factors in rheumatic heart disease: meta-analysis of HLA-DR associations and evaluation of additional class II alleles.
J Am Coll Cardiol
1995
7977121
Major histocompatibility complex class II gene frequencies by serologic and deoxyribonucleic acid genomic typing in idiopathic dilated cardiomyopathy.
Am J Cardiol
1994
1 - 39 of 39
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