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Shamil Sunyaev
Brigham And Women'S Hospital
$29,625,063
Attributed
$54,179,155
Total exposure
11
Grants
7
Lead (contact PI)
Attributed= this PI's even-split share of every grant they're on (the fair, additive number). Exposure = full size of all those grants.
Funding over time
peak $5.5M · FY2005–25$10M$7.5M$5M$2.5M$0
'05
'06
'07
'08
'09
'10
'11
'12
'13
'14
'15
'16
'17
'18
'19
'20
'21
'22
'23
'24
'25
Funding mix
By agency
NIH$54,179,155 · 11
By mechanism
U01$25,937,333 · 3
R01$19,114,631 · 6
R35$7,230,394 · 1
RL1$1,896,797 · 1
Top collaborators
- Benjamin Michael Neale12 shared
- Alkes L Price9 shared
- Xihong Lin8 shared
- Luda Diatchenko6 shared
- Roger B Fillingim6 shared
- Joel D. Greenspan6 shared
- William Maixner6 shared
- Richard Ohrbach6 shared
Most similar at Brigham And Women'S Hospital
Same institution · by research overlap
- Richard L Maas$32,489,019
- Edwin K Silverman$89,199,838
- Soumya Raychaudhuri$22,210,777
- Thomas A Gaziano$8,815,166
- Gail Kurr Adler$16,472,973
Others in their field
Top investigators on “Genetic”
- Richard A Gibbs · Baylor College Of Medicine$577,061,667
- Eric S Lander · Whitehead Institute For Biomedical Res$560,806,052
- David R. Weir · University Of Michigan At Ann Arbor$322,225,557
- Richard K. Wilson · Washington University$316,685,275
- Lawrence Corey · Fred Hutchinson Cancer Center$312,182,347
- Margaret Juliana McElrath · Fred Hutchinson Cancer Center$302,429,647
Research focus
GeneticPhenotypeGenesComplexVariantBaseComputer SoftwareComputing MethodologiesData SetSamplingDesignAllelesStatistical MethodsProgramsTraitCodeGenome SequencingHeritabilityGenome Wide Association StudyRare VariantUntranslated RnaBiologicalHuman DiseaseHuman Genetics
Grant awards (75)
The origin, the function and the phenotypic impact of human alleles$904,819
R35 · FY2025 · GM · contact PI
Predicting the impact of genetic variants, genes and pathways on human Disease$773,162
U01 · FY2025 · HG
Functional and population genetic architectures of complex disease$770,304
R01 · FY2025 · MH · contact PI
The origin, the function and the phenotypic impact of human alleles$904,819
R35 · FY2024 · GM · contact PI
Functional and population genetic architectures of complex disease$788,253
R01 · FY2024 · MH · contact PI
Predicting the impact of genetic variants, genes and pathways on human Disease$773,161
U01 · FY2024 · HG
The origin, the function and the phenotypic impact of human alleles$904,819
R35 · FY2023 · GM · contact PI
Functional and population genetic architectures of complex disease$804,835
R01 · FY2023 · MH · contact PI
Predicting the impact of genetic variants, genes and pathways on human Disease$788,939
U01 · FY2023 · HG
The origin, the function and the phenotypic impact of human alleles$896,692
R35 · FY2022 · GM · contact PI
Functional and population genetic architectures of complex disease$839,908
R01 · FY2022 · MH · contact PI
Predicting the impact of genetic variants, genes and pathways on human Disease$788,939
U01 · FY2022 · HG
The origin, the function and the phenotypic impact of human alleles$583,645
R35 · FY2021 · GM · contact PI
Rare and common variants in complex disease$496,215
R01 · FY2021 · MH · contact PI
Predicting the impact of genetic variants, genes and pathways on human Disease$409,010
U01 · FY2021 · HG
The origin, the function and the phenotypic impact of human alleles$295,265
R35 · FY2021 · GM · contact PI
Rare and common variants in complex disease$243,449
R01 · FY2021 · MH · contact PI
Powering whole genome sequence-based genetic discovery for common human diseases- Extended 2021-2022.$99,999
U01 · FY2021 · HG
The origin, the function and the phenotypic impact of human alleles$913,445
R35 · FY2020 · GM · contact PI
Powering whole genome sequence-based genetic discovery for common human diseases$884,756
U01 · FY2020 · HG
Rare and common variants in complex disease$690,534
R01 · FY2020 · MH · contact PI
Powering whole genome sequence-based genetic discovery for common human diseases$250,000
U01 · FY2020 · HG
The origin, the function and the phenotypic impact of human alleles$913,445
R35 · FY2019 · GM · contact PI
Powering whole genome sequence-based genetic discovery for common human diseases$884,756
U01 · FY2019 · HG
Rare and common variants in complex disease$691,264
R01 · FY2019 · MH · contact PI
Powering whole genome sequence-based genetic discovery for common human diseases$300,000
U01 · FY2019 · HG
The origin, the function and the phenotypic impact of human alleles$913,445
R35 · FY2018 · GM · contact PI
Powering whole genome sequence-based genetic discovery for common human diseases$886,871
U01 · FY2018 · HG
Rare and common variants in complex disease$700,491
R01 · FY2018 · MH · contact PI
Powering whole genome sequence-based genetic discovery for common human diseases$889,255
U01 · FY2017 · HG
Rare and common variants in complex disease$775,877
R01 · FY2017 · MH · contact PI
Improving Polygenic Prediction using Next-Generation Data Sets$491,613
R01 · FY2017 · GM · contact PI
New methods and enhanced software for predicting functional SNPs$362,387
R01 · FY2017 · GM · contact PI
Genetic and Psychosocial Influences on Transition to Chronic TMD and Related Pain$2,796,628
U01 · FY2016 · DE
Powering whole genome sequence-based genetic discovery for common human diseases$893,773
U01 · FY2016 · HG
Improving Polygenic Prediction using Next-Generation Data Sets$491,613
R01 · FY2016 · GM · contact PI
Statistical methods for studies of rare variants$451,985
R01 · FY2016 · MH · contact PI
New methods and enhanced software for predicting functional SNPs$378,516
R01 · FY2016 · GM · contact PI
Genetic and Psychosocial Influences on Transition to Chronic TMD and Related Pain$171,998
U01 · FY2016 · DE
Mutant mapping and identification in zebrafish by next generation sequencing$97,185
R01 · FY2016 · DK
Genetic and Psychosocial Influences on Transition to Chronic TMD and Related Pain$3,399,224
U01 · FY2015 · DE
Improving Polygenic Prediction using Next-Generation Data Sets$491,613
R01 · FY2015 · GM · contact PI
Statistical methods for studies of rare variants$451,985
R01 · FY2015 · MH · contact PI
Mutant mapping and identification in zebrafish by next generation sequencing$435,866
R01 · FY2015 · DK
New methods and enhanced software for predicting functional SNPs$365,925
R01 · FY2015 · GM · contact PI
Genetic and Psychosocial Influences on Transition to Chronic TMD and Related Pain$2,890,056
U01 · FY2014 · DE
Improving Polygenic Prediction using Next-Generation Data Sets$543,271
R01 · FY2014 · GM · contact PI
Statistical methods for studies of rare variants$451,871
R01 · FY2014 · MH · contact PI
Mutant mapping and identification in zebrafish by next generation sequencing$435,790
R01 · FY2014 · DK
New methods and enhanced software for predicting functional SNPs$365,925
R01 · FY2014 · GM · contact PI
Genetic and Psychosocial Influences on Transition to Chronic TMD and Related Pain$4,146,067
U01 · FY2013 · DE
Statistical methods for studies of rare variants$539,763
R01 · FY2013 · MH · contact PI
Mutant mapping and identification in zebrafish by next generation sequencing$419,650
R01 · FY2013 · DK
New methods and enhanced software for predicting functional SNPs$353,118
R01 · FY2013 · GM · contact PI
Genetic and Psychosocial Influences on Transition to Chronic TMD and Related Pain$3,910,739
U01 · FY2012 · DE
Mutant mapping and identification in zebrafish by next generation sequencing$530,443
R01 · FY2012 · DK
New methods and enhanced software for predicting functional SNPs$365,925
R01 · FY2012 · GM · contact PI
Mass Spectrometry of Proteins Involved in Organogenesis (5 of 10)$364,287
RL1 · FY2011 · DE · contact PI
Statistical Methods for the Design and Interpretation of Deep Resequencing Studie$434,795
R01 · FY2010 · MH · contact PI
Mass Spectrometry of Proteins Involved in Organogenesis (5 of 10)$379,467
RL1 · FY2010 · DE · contact PI
Statistical Methods for the Design and Interpretation of Deep Resequencing Studie$369,860
R01 · FY2010 · MH · contact PI
New Methods and Enhanced Software for Predicting Functional SNPs$334,748
R01 · FY2010 · GM · contact PI
Statistical Methods for the Design and Interpretation of Deep Resequencing Studie$444,264
R01 · FY2009 · MH · contact PI
Mass Spectrometry of Proteins Involved in Organogenesis (5 of 10)$383,300
RL1 · FY2009 · DE · contact PI
New Methods and Enhanced Software for Predicting Functional SNPs$332,589
R01 · FY2009 · GM · contact PI
Approaches to Multiorganismal Comparative Proteomics$249,426
R01 · FY2009 · GM · contact PI
Statistical Methods for the Design and Interpretation of Deep Resequencing Studie$462,728
R01 · FY2008 · MH · contact PI
Mass Spectrometry of Proteins Involved in Organogenesis (5 of 10)$382,743
RL1 · FY2008 · DE · contact PI
New Methods and Enhanced Software for Predicting Functional SNPs$326,359
R01 · FY2008 · GM · contact PI
Approaches to Multiorganismal Comparative Proteomics$249,426
R01 · FY2008 · GM · contact PI
Mass Spectrometry of Proteins Involved in Organogenesis (5 of 10)$387,000
RL1 · FY2007 · DE · contact PI
New Methods and Enhanced Software for Predicting Functional SNPs$326,139
R01 · FY2007 · GM · contact PI
Approaches to Multiorganismal Comparative Proteomics$249,426
R01 · FY2007 · GM · contact PI
Approaches to Multiorganismal Comparative Proteomics$256,875
R01 · FY2006 · GM · contact PI
Approaches to Multiorganismal Comparative Proteomics$252,422
R01 · FY2005 · GM