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Author Details

Brendan Blumenstiel
Broad Institute of MIT and Harvard
2001
26
22
PMIDPaper TitleJournal TitlePublished Year
34793200Donor Clonal Hematopoiesis and Recipient Outcomes After Transplantation.J Clin Oncol2022
34793200Donor Clonal Hematopoiesis and Recipient Outcomes After Transplantation.J Clin Oncol2022
35051367Transmission from vaccinated individuals in a large SARS-CoV-2 Delta variant outbreak.Cell2022
35051367Transmission from vaccinated individuals in a large SARS-CoV-2 Delta variant outbreak.Cell2022
32511487Using viral load and epidemic dynamics to optimize pooled testing in resource constrained settings.medRxiv2021
33619080Using viral load and epidemic dynamics to optimize pooled testing in resource-constrained settings.Sci Transl Med2021
32511487Using viral load and epidemic dynamics to optimize pooled testing in resource constrained settings.medRxiv2021
34976934Pooling for SARS-CoV2 Surveillance: Validation and Strategy for Implementation in K-12 Schools.Front Public Health2021
34704102Evidence of transmission from fully vaccinated individuals in a large outbreak of the SARS-CoV-2 Delta variant in Provincetown, Massachusetts.medRxiv2021
33619080Using viral load and epidemic dynamics to optimize pooled testing in resource-constrained settings.Sci Transl Med2021
34976934Pooling for SARS-CoV2 Surveillance: Validation and Strategy for Implementation in K-12 Schools.Front Public Health2021
34704102Evidence of transmission from fully vaccinated individuals in a large outbreak of the SARS-CoV-2 Delta variant in Provincetown, Massachusetts.medRxiv2021
31337885Outcomes of patient self-referral for the diagnosis of several rare inherited kidney diseases.Genet Med2020
32170028Sensitive Detection of Minimal Residual Disease in Patients Treated for Early-Stage Breast Cancer.Clin Cancer Res2020
31337885Outcomes of patient self-referral for the diagnosis of several rare inherited kidney diseases.Genet Med2020
32170028Sensitive Detection of Minimal Residual Disease in Patients Treated for Early-Stage Breast Cancer.Clin Cancer Res2020
29967284Noninvasive Immunohistochemical Diagnosis and Novel <i>MUC1</i> Mutations Causing Autosomal Dominant Tubulointerstitial Kidney Disease.J Am Soc Nephrol2018
29967284Noninvasive Immunohistochemical Diagnosis and Novel <i>MUC1</i> Mutations Causing Autosomal Dominant Tubulointerstitial Kidney Disease.J Am Soc Nephrol2018
27157321Development and Validation of a Mass Spectrometry-Based Assay for the Molecular Diagnosis of Mucin-1 Kidney Disease.J Mol Diagn2016
27157321Development and Validation of a Mass Spectrometry-Based Assay for the Molecular Diagnosis of Mucin-1 Kidney Disease.J Mol Diagn2016
24893890EGFR variant heterogeneity in glioblastoma resolved through single-nucleus sequencing.Cancer Discov2014
25186949The genomic landscape of pediatric Ewing sarcoma.Cancer Discov2014
24893890EGFR variant heterogeneity in glioblastoma resolved through single-nucleus sequencing.Cancer Discov2014
24752078Whole-exome sequencing of circulating tumor cells provides a window into metastatic prostate cancer.Nat Biotechnol2014
25186949The genomic landscape of pediatric Ewing sarcoma.Cancer Discov2014
24752078Whole-exome sequencing of circulating tumor cells provides a window into metastatic prostate cancer.Nat Biotechnol2014
23396133Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing.Nat Genet2013
23396133Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing.Nat Genet2013
22585170High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing.Cancer Discov2012
22585170High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing.Cancer Discov2012
23114594DGAT1 mutation is linked to a congenital diarrheal disorder.J Clin Invest2012
23114594DGAT1 mutation is linked to a congenital diarrheal disorder.J Clin Invest2012
21205303A scalable, fully automated process for construction of sequence-ready human exome targeted capture libraries.Genome Biol2011
21205303A scalable, fully automated process for construction of sequence-ready human exome targeted capture libraries.Genome Biol2011
20582916Targeted exon sequencing by in-solution hybrid selection.Curr Protoc Hum Genet2010
20582916Targeted exon sequencing by in-solution hybrid selection.Curr Protoc Hum Genet2010
18317468Whole-genome association study of bipolar disorder.Mol Psychiatry2008
18317468Whole-genome association study of bipolar disorder.Mol Psychiatry2008
18711365Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.Nat Genet2008
18711365Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.Nat Genet2008
17463246Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.Science2007
17943131Genome-wide detection and characterization of positive selection in human populations.Nature2007
17463246Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.Science2007
17943122A second generation human haplotype map of over 3.1 million SNPs.Nature2007
17982456Two independent alleles at 6q23 associated with risk of rheumatoid arthritis.Nat Genet2007
17982456Two independent alleles at 6q23 associated with risk of rheumatoid arthritis.Nat Genet2007
17943131Genome-wide detection and characterization of positive selection in human populations.Nature2007
17943122A second generation human haplotype map of over 3.1 million SNPs.Nature2007
12029063The structure of haplotype blocks in the human genome.Science2002
12029063The structure of haplotype blocks in the human genome.Science2002
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Collaborators

Matthew DeFelice
Broad Institute of Harvard and MIT
Co-authored papers 17
Stacey Gabriel
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Co-authored papers 12
Mark J Daly
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Co-authored papers 10
Shaun Purcell
Brigham and Women's Hospital
Co-authored papers 6
Niall J Lennon
Broad Institute of MIT and Harvard.
Co-authored papers 6
David Altshuler
Broad Institute of Harvard and Massachusetts Institute of Technology (MIT)
Co-authored papers 6
Stephen F Schaffner
Broad Institute of Massachusetts Institute of Technology (MIT) and Harvard
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Kristian Cibulskis
Co-authored papers 5
Eric S Lander
Vanderbilt-Ingram Cancer Center, Vanderbilt University
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Paul I W de Bakker
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Melissa Parkin
The Broad Institute of MIT and Harvard
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Matthew Meyerson
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Carrie Sougnez
The Broad Institute of Harvard and MIT
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Michelle Cipicchio
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St. James's Hospital
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Maegan Harden
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Jessica Roy
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Maura Faggart
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Lincoln Stein
Ontario Institute for Cancer Research, University Avenue
Co-authored papers 3
Todd R Golub
Broad Institute of MIT and Harvard
Co-authored papers 3
Alkes L Price
Broad Institute of MIT and Harvard
Co-authored papers 3
Gad Getz
Broad Institute of the Massachusetts Institute of Technology and Harvard
Co-authored papers 3
Charles N Rotimi
Center for Research on Genomics and Global Health, National Institutes of Health
Co-authored papers 3
Jane Rogers
The Wellcome Trust Sanger Institute
Co-authored papers 3
Stacey B Gabriel
Whitehead/MIT Center for Genome Research
Co-authored papers 3
Stephen T Sherry
National Center for Biotechnology Information, National Institutes of Health
Co-authored papers 3
Andrew Kirby
Co-authored papers 3
David Willey
Institute of Biotechnology, University of Cambridge
Co-authored papers 3
Jamie M Moore
Late Stage Pharmaceutical Development
Co-authored papers 3
Release 1.2