Skip to Main Content

Author Details

Andrew Crenshaw
Broad Institute
2004
34
27
PMIDPaper TitleJournal TitlePublished Year
29417738Genetic variants in sex hormone pathways and the risk of type 2 diabetes among African American, Hispanic American, and European American postmenopausal women in the US.J Diabetes2018
29417738Genetic variants in sex hormone pathways and the risk of type 2 diabetes among African American, Hispanic American, and European American postmenopausal women in the US.J Diabetes2018
26928769High-throughput identification of genotype-specific cancer vulnerabilities in mixtures of barcoded tumor cell lines.Nat Biotechnol2016
26928769High-throughput identification of genotype-specific cancer vulnerabilities in mixtures of barcoded tumor cell lines.Nat Biotechnol2016
25043339Limited clinical utility of a genetic risk score for the prediction of fracture risk in elderly subjects.J Bone Miner Res2015
26551672Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.Nat Genet2015
25043339Limited clinical utility of a genetic risk score for the prediction of fracture risk in elderly subjects.J Bone Miner Res2015
26551672Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.Nat Genet2015
24677197Epidermal growth factor receptor inhibition attenuates liver fibrosis and development of hepatocellular carcinoma.Hepatology2014
24677197Epidermal growth factor receptor inhibition attenuates liver fibrosis and development of hepatocellular carcinoma.Hepatology2014
24509480Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.Nat Genet2014
24509480Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.Nat Genet2014
22889921Genome-wide association study of obsessive-compulsive disorder.Mol Psychiatry2013
22889924Genome-wide association study of Tourette's syndrome.Mol Psychiatry2013
22889921Genome-wide association study of obsessive-compulsive disorder.Mol Psychiatry2013
23821607Evolutionary dynamics of the human NADPH oxidase genes CYBB, CYBA, NCF2, and NCF4: functional implications.Mol Biol Evol2013
23762230Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records.PLoS One2013
23314186Genetic variation associated with circulating monocyte count in the eMERGE Network.Hum Mol Genet2013
23267103Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association.Proc Natl Acad Sci U S A2013
23333348Prognostic gene expression signature for patients with hepatitis C-related early-stage cirrhosis.Gastroenterology2013
23821607Evolutionary dynamics of the human NADPH oxidase genes CYBB, CYBA, NCF2, and NCF4: functional implications.Mol Biol Evol2013
23762230Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records.PLoS One2013
23267103Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association.Proc Natl Acad Sci U S A2013
23314186Genetic variation associated with circulating monocyte count in the eMERGE Network.Hum Mol Genet2013
23333348Prognostic gene expression signature for patients with hepatitis C-related early-stage cirrhosis.Gastroenterology2013
22889924Genome-wide association study of Tourette's syndrome.Mol Psychiatry2013
22037903Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network.Hum Genet2012
22843986zCall: a rare variant caller for array-based genotyping: genetics and population analysis.Bioinformatics2012
22885922Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.Nat Genet2012
22923026Evaluating genetic risk for prostate cancer among Japanese and Latinos.Cancer Epidemiol Biomarkers Prev2012
22570617Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.PLoS Genet2012
22561516Detectable clonal mosaicism from birth to old age and its relationship to cancer.Nat Genet2012
22037903Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network.Hum Genet2012
22885922Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.Nat Genet2012
22843986zCall: a rare variant caller for array-based genotyping: genetics and population analysis.Bioinformatics2012
22923026Evaluating genetic risk for prostate cancer among Japanese and Latinos.Cancer Epidemiol Biomarkers Prev2012
22561516Detectable clonal mosaicism from birth to old age and its relationship to cancer.Nat Genet2012
22570617Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.PLoS Genet2012
21234875Quality control procedures for genome-wide association studies.Curr Protoc Hum Genet2011
21234875Quality control procedures for genome-wide association studies.Curr Protoc Hum Genet2011
21873608Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USA.Hum Mol Genet2011
22125226Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality.Genet Epidemiol2011
21597964Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers.Hum Genet2011
22125226Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality.Genet Epidemiol2011
21873608Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USA.Hum Mol Genet2011
21597964Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers.Hum Genet2011
20400780Candidate gene association resource (CARe): design, methods, and proof of concept.Circ Cardiovasc Genet2010
21051598The major genetic determinants of HIV-1 control affect HLA class I peptide presentation.Science2010
20352120Diversity in the glucose transporter-4 gene (SLC2A4) in humans reflects the action of natural selection along the old-world primates evolution.PLoS One2010
20520743Feasibility of High-Throughput Genome-Wide Genotyping using DNA from Stored Buccal Cell Samples.Biomark Insights2010
  • 1 - 50 of 68

Recommended Authors

University of Pennsylvania
Career Start Year 2013
Number of shared co-authors 65
Mayo Clinic
Career Start Year 2012
Number of shared co-authors 21
University of Texas Health Science Center at Houston
Career Start Year 2012
Number of shared co-authors 62
Broad Institute of MIT and Harvard
Career Start Year 2010
Number of shared co-authors 33
Ontario Institute for Cancer Research
Career Start Year 2009
Number of shared co-authors 47
National Cancer Institute, 9609 Medical Center Drive
Career Start Year 2007
Number of shared co-authors 105
Cleveland Institute for Computational Biology, Case Western Reserve University
Career Start Year 2006
Number of shared co-authors 71
Kidney Research Institute and Division of Nephrology, University of Washington
Career Start Year 2006
Number of shared co-authors 27
University of Southern California
Career Start Year 2004
Number of shared co-authors 28
Genentech Inc.
Career Start Year 2004
Number of shared co-authors 57
Vanderbilt University Medical Center
Career Start Year 2004
Number of shared co-authors 110
University of California San Diego Health System
Career Start Year 2004
Number of shared co-authors 86
Icahn School of Medicine at Mount Sinai, NY Institute for Genomic Health
Career Start Year 2003
Number of shared co-authors 53
Marshfield Clinic Research Institute
Career Start Year 2003
Number of shared co-authors 40
Department of Pediatrics and Rady's Children's Hospital, University of California
Career Start Year 2002
Number of shared co-authors 86
East China University of Science and Technology
Career Start Year 2002
Number of shared co-authors 32
The University of Chicago
Career Start Year 2001
Number of shared co-authors 34
University of Pennsylvania
Career Start Year 2001
Number of shared co-authors 50
National Human Genome Research Institute, National Institutes of Health
Career Start Year 2001
Number of shared co-authors 104
University of Texas M.D. Anderson Cancer Center
Career Start Year 2001
Number of shared co-authors 82
University of Groningen, University Medical Center Groningen
Career Start Year 2000
Number of shared co-authors 107
Wellcome Sanger Institute
Career Start Year 1998
Number of shared co-authors 108
The Hospital for Sick Children
Career Start Year 1997
Number of shared co-authors 36
Barcelona Institute of Science and Technology (BIST)
Career Start Year 1995
Number of shared co-authors 76
University of Maryland School of Medicine
Career Start Year 1995
Number of shared co-authors 115
Kaiser Permanente Research Bank
Career Start Year 1994
Number of shared co-authors 104
23andMe Inc.
Career Start Year 1992
Number of shared co-authors 85
Ontario Institute for Cancer Research
Career Start Year 1991
Number of shared co-authors 75
University of Washington
Career Start Year 1976
Number of shared co-authors 109
University of California, USA Institute for Genomic Medicine
Career Start Year 1967
Number of shared co-authors 42

Collaborators

Broad Institute of Harvard and MIT
Co-authored papers 14
National Cancer Institute, National Institutes of Health
Co-authored papers 10
Frederick National Laboratory for Cancer Research
Co-authored papers 8
Mayo Clinic
Co-authored papers 6
Cleveland Institute for Computational Biology, Case Western Reserve University
Co-authored papers 6
University of Minnesota Medical School, 1035 University Drive duluth
Co-authored papers 6
Center for Inherited Disease Research, Johns Hopkins School of Medicine
Co-authored papers 6
University of Washington Medical Center
Co-authored papers 6
Feinberg School of Medicine, Northwestern University
Co-authored papers 5
Harvard T. H. Chan School of Public Health
Co-authored papers 5
Baylor College of Medicine
Co-authored papers 5
Center for Systems Genomics, Pennsylvania State University, University Park
Co-authored papers 5
The Kolling Institute, University of Sydney, and Royal North Shore Hospital
Co-authored papers 5
University of Washington
Co-authored papers 5
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 5
The Broad Institute of MIT and Harvard
Co-authored papers 5
Co-authored papers 5
Mayo Clinic
Co-authored papers 5
National Cancer Institute, Frederick National Laboratory for Cancer Research
Co-authored papers 4
Broad Institute of Harvard and Massachusetts Institute of Technology (MIT)
Co-authored papers 4
Broad Institute of MIT and Harvard
Co-authored papers 4
University of Washington Medical Center
Co-authored papers 4
University of Oxford
Co-authored papers 4
Cleveland Institute for Computational Biology, Case Western Reserve University
Co-authored papers 4
Co-authored papers 4
Icahn School of Medicine at Mount Sinai
Co-authored papers 4
Co-authored papers 4
Lung and Blood Institute's (NHLBI) Framingham Heart Study
Co-authored papers 4
Co-authored papers 4
Co-authored papers 4