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Author Details
Full Name
Min He
Affiliation
ORCID
Career Start Year
2013
Papers
4
H Index
4
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
25074467
Phenome-wide association studies (PheWASs) for functional variants.
Eur J Hum Genet
2015
25587064
SeqHBase: a big data toolset for family based sequencing data analysis.
J Med Genet
2015
25250975
Use of an electronic medical record to create the marshfield clinic twin/multiple birth cohort.
Genet Epidemiol
2014
24008998
Some experiences and opportunities for big data in translational research.
Genet Med
2013
1 - 4 of 4
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Sean D Mooney
University of Washington
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Michael Brudno
University of Toronto
Career Start Year
2000
Number of shared co-authors
2
Eric Banks
Broad Institute of MIT and Harvard
Career Start Year
1999
Number of shared co-authors
0
Heidi L Rehm
The Broad Institute of MIT and Harvard
Career Start Year
1996
Number of shared co-authors
6
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Collaborators
Steven J Schrodi
University of Wisconsin Madison
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Simon Lin
The Research Institute at Nationwide Children's Hospital
Co-authored papers
2
Murray H Brilliant
Marshfield Clinic Research Institute
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2
Terrie Kitchner
Center for Precision Medicine Research, Marshfield Clinic Research Institute
Co-authored papers
1
Peggy L Peissig
Center for Precision Medicine Research, Marshfield Clinic Research Institute
Co-authored papers
1
Christopher G Chute
Brown University, Brown University Warren Alpert Medical School, Dartmouth-Hitchcock Medical Center, Harvard School of Public Health, Johns Hopkins Medicine, Mayo Clinic Minnesota
Co-authored papers
1
Kai Wang
University of Pennsylvania
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1
Grant M Wood
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1
Jyotishman Pathak
Cornell University
Co-authored papers
1
Gholson J Lyon
NYS Institute for Basic Research in Developmental Disabilities .
Co-authored papers
1
Mollie Ullman-Cullere
Dana-Farber Cancer Institute and Partners Healthcare
Co-authored papers
1
1 - 12