← Leaderboards
Bruce D Gelb
Icahn School Of Medicine At Mount Sinai
$39,999,464
Attributed
$65,615,397
Total exposure
24
Grants
15
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 $9.1M · 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$65,615,397 · 24
By mechanism
U01$25,064,891 · 4
R01$10,632,128 · 4
T32$7,334,700 · 1
R35$6,103,136 · 1
OT2$5,712,150 · 1
UM1$3,215,241 · 2
Top collaborators
- Carol R Horowitz7 shared
- Manisha Balwani6 shared
- Eimear Elizabeth Kenny6 shared
- Melissa Pittel Wasserstein6 shared
- Wendy K Chung5 shared
- Roger J. Hajjar5 shared
- Yufeng Shen5 shared
- Ihor R Lemischka3 shared
Most similar at Icahn School Of Medicine At Mount Sinai
Same institution · by research overlap
- Manisha Balwani$4,522,531
- Girish Nitin Nadkarni$10,989,187
- Nandini Shroff$726,013
- Saskia Shuman$726,013
- Rong Chen$112,667
Others in their field
Top investigators on “Phenotype”
- David R. Weir · University Of Michigan At Ann Arbor$239,033,262
- David Heimbrook · Leidos Biomedical Research, Inc.$213,586,034
- Constance Ann Benson · University Of California, San Diego$187,132,366
- Richard A Gibbs · Baylor College Of Medicine$184,906,270
- James E. Gern · University Of Wisconsin-Madison$141,704,104
- Garret A Fitzgerald · University Of Pennsylvania$141,348,491
Research focus
PhenotypeGeneticGenesCardiacPathogenesisChildAffectChildhoodMutationComplexFamilyGenomicsCongenital Heart DefectsBaseClinical ResearchSignal TransductionCandidate Disease GeneCohortInsightProteinsCongenital Heart DisorderClinical CareMolecularMouse Model
Grant awards (115)
Mount Sinai Center for Undiagnosed Diseases$816,633
U01 · FY2025 · NS · contact PI
Therapy Development for Genetic Disorders of the RAS/MAPK Pathway$754,830
R01 · FY2025 · HL · contact PI
Using electronic medical record data to shorten diagnostic odysseys for rare genetic disorders in children and adults in two New York City health care settings$473,116
UH3 · FY2025 · TR · contact PI
Pediatric Heart Network New York Consortium$465,943
UM1 · FY2025 · HL
All of Us Research Program New York Consortium$5,712,150
OT2 · FY2024 · OD
Mount Sinai Center for Undiagnosed Diseases$822,709
U01 · FY2024 · NS · contact PI
Therapy Development for Genetic Disorders of the RAS/MAPK Pathway$759,920
R01 · FY2024 · HL · contact PI
Using electronic medical record data to shorten diagnostic odysseys for rare genetic disorders in children and adults in two New York City health care settings$490,366
UH3 · FY2024 · TR · contact PI
Pediatric Heart Network New York Consortium$482,068
UM1 · FY2024 · HL
Identifying and applying genetic variation relevant to clinical outcomes for individuals with congenital heart disease$445,762
U01 · FY2024 · HL
Congenital Heart Disease Expert Curation Panel$377,460
U24 · FY2024 · HD
Pediatric Heart Disease: Getting from Mutations to Therapeutics$860,739
R35 · FY2023 · HL · contact PI
Identifying and applying genetic variation relevant to clinical outcomes for individuals with congenital heart disease$454,859
U01 · FY2023 · HL
Congenital Heart Disease Expert Curation Panel$379,982
U24 · FY2023 · HD
Using electronic medical record data to shorten diagnostic odysseys for rare genetic disorders in children and adults in two New York City health care settings$338,000
UG3 · FY2023 · TR · contact PI
Pediatric Heart Disease: Getting from Mutations to Therapeutics$860,775
R35 · FY2022 · HL · contact PI
Identifying and applying genetic variation relevant to clinical outcomes for individuals with congenital heart disease$454,859
U01 · FY2022 · HL
Congenital Heart Disease Expert Curation Panel$413,438
U24 · FY2022 · HD
Using electronic medical record data to shorten diagnostic odysseys for rare genetic disorders in children and adults in two New York City health care settings$338,000
UG3 · FY2022 · TR · contact PI
Training Program in Molecular and Cellular Cardiology$251,845
T32 · FY2022 · HL · contact PI
Incorporating genomics into the clinical care of diverse NYC children$2,016,562
U01 · FY2021 · HG
Pediatric Heart Disease: Getting from Mutations to Therapeutics$860,810
R35 · FY2021 · HL · contact PI
Identifying and applying genetic variation relevant to clinical outcomes for individuals with congenital heart disease$454,859
U01 · FY2021 · HL
Training Program in Molecular and Cellular Cardiology$358,890
T32 · FY2021 · HL · contact PI
Incorporating genomics into the clinical care of diverse NYC children$3,105,550
U01 · FY2020 · HG
Pediatric Heart Disease: Getting from Mutations to Therapeutics$860,844
R35 · FY2020 · HL · contact PI
Training Program in Molecular and Cellular Cardiology$597,383
T32 · FY2020 · HL · contact PI
Identifying and applying genetic variation relevant to clinical outcomes for individuals with congenital heart disease$470,359
U01 · FY2020 · HL
Incorporating genomics into the clinical care of diverse NYC children$3,784,706
U01 · FY2019 · HG
Pediatric Heart Disease: Getting from Mutations to Therapeutics$860,875
R35 · FY2019 · HL · contact PI
Training Program in Molecular and Cellular Cardiology$571,260
T32 · FY2019 · HL · contact PI
Genetics of conotruncal defects and associated neurodevelopmental outcomes$453,446
UM1 · FY2019 · HL · contact PI
Incorporating genomics into the clinical care of diverse NYC children$4,186,045
U01 · FY2018 · HG
Pediatric Heart Disease: Getting from Mutations to Therapeutics$860,906
R35 · FY2018 · HL · contact PI
Incorporating genomics into the clinical care of diverse NYC children$591,057
U01 · FY2018 · HG
Training Program in Molecular and Cellular Cardiology$534,587
T32 · FY2018 · HL · contact PI
Genetics of conotruncal defects and associated neurodevelopmental outcomes$453,446
UM1 · FY2018 · HL · contact PI
Pediatric Heart Disease: Getting from Mutations to Therapeutics$62,733
R35 · FY2018 · HL · contact PI
Incorporating genomics into the clinical care of diverse NYC children$3,352,780
U01 · FY2017 · HG
Pediatric Heart Disease: Getting from Mutations to Therapeutics$856,106
R35 · FY2017 · HL · contact PI
Genetics of conotruncal defects and associated neurodevelopmental outcomes$453,446
UM1 · FY2017 · HL · contact PI
Training Program in Molecular and Cellular Cardiology$157,548
T32 · FY2017 · HL · contact PI
Pediatric Heart Disease: Getting from Mutations to Therapeutics$19,348
R35 · FY2017 · HL · contact PI
Training Program in Molecular and Cellular Cardiology$553,293
T32 · FY2016 · HL · contact PI
Human Induced Pluripotent Cell Models of Pediatric Cardiac Disorders$488,181
R01 · FY2016 · HL · contact PI
Molecular Basis of Noonan Syndrome and Related Disorder$465,369
R01 · FY2016 · HL · contact PI
Genetics of conotruncal defects and associated neurodevelopmental outcomes$453,446
UM1 · FY2016 · HL · contact PI
Training Program in Molecular and Cellular Cardiology$537,538
T32 · FY2015 · HL · contact PI
Human Induced Pluripotent Cell Models of Pediatric Cardiac Disorders$480,857
R01 · FY2015 · HL · contact PI
Genetics of conotruncal defects and associated neurodevelopmental outcomes$453,446
UM1 · FY2015 · HL · contact PI
Molecular Basis of Noonan Syndrome and Related Disorder$433,856
R01 · FY2015 · HL · contact PI
Genomic studies of secundum atrial septal defects$766,273
U01 · FY2014 · HL · contact PI
Training Program in Molecular and Cellular Cardiology$506,732
T32 · FY2014 · HL · contact PI
Human Induced Pluripotent Cell Models of Pediatric Cardiac Disorders$478,418
R01 · FY2014 · HL · contact PI
Molecular Basis of Noonan Syndrome and Related Disorder$466,425
R01 · FY2014 · HL · contact PI
Human Induced Pluripotent Cell Models of Pediatric Cardiac Disorders$43,519
R01 · FY2014 · HL · contact PI
Genomic studies of secundum atrial septal defects$744,670
U01 · FY2013 · HL · contact PI
Molecular Basis of Noonan Syndrome and Related Disorder$475,742
R01 · FY2013 · HL · contact PI
Training Program in Molecular and Cellular Cardiology$412,043
T32 · FY2013 · HL · contact PI
Human Induced Pluripotent Cell Models of Pediatric Cardiac Disorders$403,410
R01 · FY2013 · HL · contact PI
Understanding intellectual disability in Noonan syndrome and related disorders$48,735
R03 · FY2013 · TW · contact PI
Genomic studies of secundum atrial septal defects$768,797
U01 · FY2012 · HL · contact PI
Molecular studies of Noonan syndrome and related disorders$414,309
R01 · FY2012 · HL · contact PI
Training Program in Molecular and Cellular Cardiology$157,318
T32 · FY2012 · HL · contact PI
Understanding intellectual disability in Noonan syndrome and related disorders$51,300
R03 · FY2012 · TW · contact PI
Genomic studies of secundum atrial septal defects$784,125
U01 · FY2011 · HL · contact PI
Molecular studies of Noonan syndrome and related disorders$418,647
R01 · FY2011 · HL · contact PI
Training Program in Molecular and Cellular Cardiology$395,642
T32 · FY2011 · HL · contact PI
Impact of CNVs on outcomes for infants with single ventricle heart defects$211,875
R21 · FY2011 · HL · contact PI
Understanding intellectual disability in Noonan syndrome and related disorders$57,932
R03 · FY2011 · TW · contact PI
International Meeting on Genetic Syndromes of the Ras/MAPK Pathway$50,000
R13 · FY2011 · HL · contact PI
Molecular studies of Noonan syndrome and related disorders$28,815
R01 · FY2011 · HL · contact PI
Genomic studies of secundum atrial septal defects$763,414
U01 · FY2010 · HL · contact PI
Training Program in Molecular and Cellular Cardiology$487,413
T32 · FY2010 · HL · contact PI
Molecular studies of Noonan syndrome and related disorders$457,780
R01 · FY2010 · HL · contact PI
Impact of CNVs on outcomes for infants with single ventricle heart defects$254,250
R21 · FY2010 · HL · contact PI
Molecular studies of Noonan syndrome and related disorders$3,390
R01 · FY2010 · HL · contact PI
Training Program in Molecular and Cellular Cardiology$483,330
T32 · FY2009 · HL · contact PI
Molecular studies of Noonan syndrome and related disorders$418,940
R01 · FY2009 · HL · contact PI
Genomic studies of secundum atrial septal defects$280,872
U01 · FY2009 · HL · contact PI
THE PATHOGENESIS OF PTPN11 MUTATIONS IN HUMAN DISEASE$638,795
P50 · FY2008 · HL · contact PI
Training Program in Molecular and Cellular Cardiology$462,167
T32 · FY2008 · HL · contact PI
Molecular studies of Noonan syndrome and related disorders$419,428
R01 · FY2008 · HL · contact PI
Disease pathogenesis of Noonan syndrome and related disorders$145,913
K24 · FY2008 · HD · contact PI
THE PATHOGENESIS OF PTPN11 MUTATIONS IN HUMAN DISEASE$653,598
P50 · FY2007 · HL · contact PI
Disease pathogenesis of Noonan syndrome and related disorders$145,913
K24 · FY2007 · HD · contact PI
THE PATHOGENESIS OF PTPN11 MUTATIONS IN HUMAN DISEASE$471,357
P50 · FY2006 · HL · contact PI
Molecular Basis of Noonan Syndrome and Related Disorders$371,056
R01 · FY2006 · HL · contact PI
Disease pathogenesis/Noonan syndrome/related disorders$145,913
K24 · FY2006 · HD · contact PI
THE PATHOGENESIS OF PTPN11 MUTATIONS IN HUMAN DISEASE$460,308
P50 · FY2005 · HL
Molecular Basis of Noonan Syndrome and Related Disorders$379,985
R01 · FY2005 · HL
Disease pathogenesis/Noonan syndrome/related disorders$145,913
K24 · FY2005 · HD
THE PATHOGENESIS OF PTPN11 MUTATIONS IN HUMAN DISEASE$461,582
P50 · FY2004 · HL
Molecular Basis of Noonan Syndrome and Related Disorders$379,985
R01 · FY2004 · HL
Training Program in Molecular and Cellular Cardiology$360,523
T32 · FY2004 · HL
FAMILIAL PATENT DUCTUS ARTERIOSUS$261,959
R01 · FY2004 · HD
Disease pathogenesis/Noonan syndrome/related disorders$145,913
K24 · FY2004 · HD
TRAINING PROGRAM IN MOLECULAR AND CELLULAR CARDIOLOGY$507,188
T32 · FY2003 · HL
Molecular Basis of Noonan Syndrome and Related Disorders$379,985
R01 · FY2003 · HL
FAMILIAL PATENT DUCTUS ARTERIOSUS$261,959
R01 · FY2003 · HD
OSTEOSCLEROTIC BONE DISORDERS$112,523
K24 · FY2003 · HD
Molecular Basis of Noonan Syndrome and Related Disorders$375,815
R01 · FY2002 · HL
FAMILIAL PATENT DUCTUS ARTERIOSUS$261,959
R01 · FY2002 · HD
OSTEOSCLEROTIC BONE DISORDERS$112,523
K24 · FY2002 · HD
FAMILIAL PATENT DUCTUS ARTERIOSUS$16,386
R01 · FY2002 · HD
FAMILIAL PATENT DUCTUS ARTERIOSUS$12,289
R01 · FY2002 · HD
OSTEOSCLEROTIC BONE DISORDERS$0
M01 · FY2002 · RR
FAMILIAL PATENT DUCTUS ARTERIOSUS$261,959
R01 · FY2001 · HD
OSTEOSCLEROTIC BONE DISORDERS$112,523
K24 · FY2001 · HD
OSTEOSCLEROTIC BONE DISORDERS$0
M01 · FY2001 · RR
FAMILIAL PATENT DUCTUS ARTERIOSUS$256,955
R01 · FY2000 · HD
POSITIONAL CLONING OF PYCNODYSOSTOSIS$118,650
R29 · FY2000 · AR
OSTEOSCLEROTIC BONE DISORDERS$112,523
K24 · FY2000 · HD
GENE DISCOVERY FOR THE KENNY CAFFEY SYNDROME$84,750
R03 · FY2000 · HD
OSTEOSCLEROTIC BONE DISORDERS$0
M01 · FY2000 · RR