← Leaderboards
Bernice E. Morrow
Albert Einstein College Of Medicine
$29,775,627
Attributed
$35,820,246
Total exposure
26
Grants
23
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 $4M · FY2005–25$5M$3.8M$2.5M$1.3M$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$49,836,083 · 27
By mechanism
P01$22,465,172 · 9
R01$22,121,095 · 8
P30$1,697,098 · 2
R21$1,286,736 · 3
U54$1,051,728 · 1
R56$704,727 · 1
Top collaborators
- Bin Zhou10 shared
- Deyou Zheng9 shared
- Chenleng Cai1 shared
Most similar at Albert Einstein College Of Medicine
Same institution · by research overlap
- Bin Zhou$15,116,959
- Daniella Miller$108,512
- Deyou Zheng$6,936,375
Others in their field
Top investigators on “Genes”
- David Heimbrook · Leidos Biomedical Research, Inc.$413,811,031
- Richard A Gibbs · Baylor College Of Medicine$338,750,128
- Barton F Haynes · Duke University$304,076,400
- Stacey Gabriel · Massachusetts Institute Of Technology$241,252,013
- Eric S Lander · Whitehead Institute For Biomedical Res$211,825,987
- Richard K. Wilson · Washington University$195,881,965
Research focus
GenesProgramsGeneticBaseMolecularDefect22q11.2PhenotypeDigeorge SyndromeEmbryoCardiacMouse ModelGenotype22q11CellsInterestHuman GeneticsTranscription FactorShprintzen SyndromeTissuesSyndromeAffectAnimal ModelPharyngeal Apparatus
Grant awards (119)
Cell fate choices by Tbx1 in forming the mammalian heart$786,783
R01 · FY2025 · HL · contact PI
Genetic modifiers of congenital heart disease in 22q11.2 deletion syndrome$763,060
R01 · FY2025 · HL · contact PI
Molecular pathogenesis of congenital heart disease mediated by neural crest and second heart field cells$630,208
R01 · FY2025 · HL · contact PI
NEUROGENOMICS CORE$85,462
P50 · FY2025 · HD · contact PI
Genetic modifiers of congenital heart disease in 22q11.2 deletion syndrome$747,800
R01 · FY2024 · HL · contact PI
Molecular pathogenesis of congenital heart disease mediated by neural crest and second heart field cells$617,604
R01 · FY2024 · HL · contact PI
Molecular and cellular mechanisms in cardiac outflow tract formation and defects$579,364
R01 · FY2024 · HL
Molecular and cellular mechanisms in cardiac outflow tract formation and defects$527,857
R01 · FY2024 · HL
NEUROGENOMICS CORE$85,462
P50 · FY2024 · HD · contact PI
Genetic modifiers of congenital heart disease in 22q11.2 deletion syndrome$763,060
R01 · FY2023 · HL · contact PI
Molecular pathogenesis of congenital heart disease mediated by neural crest and second heart field cells$618,448
R01 · FY2023 · HL · contact PI
Cell fate choices by Tbx1 in forming the mammalian heart$605,558
R01 · FY2023 · HL · contact PI
NEUROGENOMICS CORE$85,462
P50 · FY2023 · HD · contact PI
Molecular and cellular mechanisms in cardiac outflow tract formation and defects$15,055
R01 · FY2023 · HL
Genetic modifiers of congenital heart disease in 22q11.2 deletion syndrome$797,060
R01 · FY2022 · HL · contact PI
Molecular and cellular mechanisms in cardiac outflow tract formation and defects$665,861
R01 · FY2022 · HL
Molecular pathogenesis of congenital heart disease mediated by neural crest and second heart field cells$618,448
R01 · FY2022 · HL · contact PI
Cell fate choices by Tbx1 in forming the mammalian heart$605,558
R01 · FY2022 · HL · contact PI
NEUROGENOMICS CORE$85,462
P50 · FY2022 · HD · contact PI
Molecular and cellular mechanisms in cardiac outflow tract formation and defects$663,602
R01 · FY2021 · HL
Cell fate choices by Tbx1 in forming the mammalian heart$605,558
R01 · FY2021 · HL · contact PI
NEUROGENOMICS CORE$166,666
P50 · FY2021 · HD · contact PI
Genomics & Computational Analysis$153,323
P30 · FY2021 · CA · contact PI
Developmental mechanisms of human congenital heart disease$1,497,819
P01 · FY2020 · HD · contact PI
Cell fate choices by Tbx1 in forming the mammalian heart$604,807
R01 · FY2020 · HL · contact PI
Genetic modifiers of congenital heart disease$374,455
P01 · FY2020 · HD · contact PI
Bio-analytics and Administration Core$374,455
P01 · FY2020 · HD · contact PI
Mouse functional analysis of genes for congenital heart disease$374,454
P01 · FY2020 · HD · contact PI
Project: Genetic basis of intellectual disability in 22q11.2 deletion syndrome$200,400
U54 · FY2020 · HD · contact PI
Genomics & Computational Analysis$152,023
P30 · FY2020 · CA · contact PI
Developmental mechanisms of human congenital heart disease$1,498,873
P01 · FY2019 · HD · contact PI
Molecular aspects of CRKL in heart development and human disease$809,950
R01 · FY2019 · HL · contact PI
Bio-analytics and Administration Core$374,719
P01 · FY2019 · HD · contact PI
Mouse functional analysis of genes for congenital heart disease$374,718
P01 · FY2019 · HD · contact PI
Genetic modifiers of congenital heart disease$374,718
P01 · FY2019 · HD · contact PI
Project: Genetic basis of intellectual disability in 22q11.2 deletion syndrome$211,554
U54 · FY2019 · HD · contact PI
Genomics & Computational Analysis$152,023
P30 · FY2019 · CA · contact PI
Developmental mechanisms of human congenital heart disease$747,328
P01 · FY2018 · HD · contact PI
Developmental mechanisms of human congenital heart disease$734,162
P01 · FY2018 · HD · contact PI
Genetic modifiers of congenital heart disease$510,115
P01 · FY2018 · HD · contact PI
Mouse functional analysis of genes for congenital heart disease$437,784
P01 · FY2018 · HD · contact PI
Molecular aspects of CRKL in heart development and human disease$416,613
R01 · FY2018 · HL · contact PI
Molecular aspects of CRKL in heart development and human disease$393,337
R01 · FY2018 · HL · contact PI
Genetic modifiers of congenital heart disease$260,922
P01 · FY2018 · HD · contact PI
Mouse functional analysis of genes for congenital heart disease$206,322
P01 · FY2018 · HD · contact PI
Project: Genetic basis of intellectual disability in 22q11.2 deletion syndrome$134,175
U54 · FY2018 · HD · contact PI
Project: Genetic basis of intellectual disability in 22q11.2 deletion syndrome$82,488
U54 · FY2018 · HD · contact PI
Bio-analytics and Administration Core$74,388
P01 · FY2018 · HD · contact PI
Bio-analytics and Administration Core$37,756
P01 · FY2018 · HD · contact PI
Developmental mechanisms of human congenital heart disease$1,483,245
P01 · FY2017 · HD · contact PI
Molecular aspects of CRKL in heart development and human disease$809,950
R01 · FY2017 · HL · contact PI
Genetic modifiers of congenital heart disease$508,933
P01 · FY2017 · HD · contact PI
Mouse functional analysis of genes for congenital heart disease$437,696
P01 · FY2017 · HD · contact PI
Project: Genetic basis of intellectual disability in 22q11.2 deletion syndrome$211,555
U54 · FY2017 · HD · contact PI
Bio-analytics and Administration Core$80,189
P01 · FY2017 · HD · contact PI
Developmental mechanisms of human congenital heart disease$1,553,251
P01 · FY2016 · HD · contact PI
Molecular aspects of CRKL in heart development and human disease$809,950
R01 · FY2016 · HL · contact PI
Genetic modifiers of congenital heart disease$529,689
P01 · FY2016 · HD · contact PI
Mouse functional analysis of genes for congenital heart disease$447,885
P01 · FY2016 · HD · contact PI
Project: Genetic basis of intellectual disability in 22q11.2 deletion syndrome$211,556
U54 · FY2016 · HD · contact PI
Bio-analytics and Administration Core$99,110
P01 · FY2016 · HD · contact PI
Genetic Basis of Syndromic and Non-Syndromic Congential Heart Defects$1,274,277
P01 · FY2015 · HD · contact PI
Tbx1 and canonical Wnt signaling in the second heart field$704,727
R56 · FY2015 · HL · contact PI
Mouse Models of Human Conotruncal Defects$275,255
P01 · FY2015 · HD · contact PI
Clinical and Administrative Core$118,108
P01 · FY2015 · HD · contact PI
Genetic Basis of Syndromic and Non-Syndromic Congential Heart Defects$1,262,786
P01 · FY2014 · HD · contact PI
Mouse Models of Human Conotruncal Defects$271,357
P01 · FY2014 · HD · contact PI
Clinical and Administrative Core$115,792
P01 · FY2014 · HD · contact PI
Genetic Basis of Syndromic and Non-Syndromic Congential Heart Defects$1,229,041
P01 · FY2013 · HD · contact PI
Genetic Analysis of Tbx1 in Ear Disorders$321,144
R01 · FY2013 · DC · contact PI
Mouse Models of Human Conotruncal Defects$261,178
P01 · FY2013 · HD · contact PI
Clinical and Administrative Core$107,167
P01 · FY2013 · HD · contact PI
Genetic Basis of Syndromic and Non-Syndromic Congential Heart Defects$1,324,263
P01 · FY2012 · HD · contact PI
Genetic Analysis of Tbx1 in Ear Disorders$363,462
R01 · FY2012 · DC · contact PI
Mouse Models of Human Conotruncal Defects$281,762
P01 · FY2012 · HD · contact PI
Clinical and Administrative Core$129,271
P01 · FY2012 · HD · contact PI
GENETIC CORE$19,045
P01 · FY2012 · AG · contact PI
Genetic Basis of Syndromic and Non-Syndromic Congential Heart Defects$1,410,792
P01 · FY2011 · HD · contact PI
Genetic Analysis of Tbx1 in Ear Disorders$399,467
R01 · FY2011 · DC · contact PI
Mouse Models of Human Conotruncal Defects$359,287
P01 · FY2011 · HD · contact PI
GENOMICS SHARED RESOURCE$345,544
P30 · FY2011 · CA · contact PI
Clinical and Administrative Core$108,630
P01 · FY2011 · HD · contact PI
GENETIC CORE$84,028
P01 · FY2011 · AG · contact PI
Genetic Modifiers for 22q 11.2 Deletion Syndrome$783,313
R01 · FY2010 · HL · contact PI
Developmental Genetics of the Pharyngeal Apparatus$411,635
R01 · FY2010 · HL · contact PI
Genetic Analysis of Tbx1 in Ear Disorders$349,223
R01 · FY2010 · DC · contact PI
Genetic Basis of Birth Defects in 22q11 Deletion Syndrome$246,510
R21 · FY2010 · NS · contact PI
GENOMICS SHARED RESOURCE$229,271
P30 · FY2010 · CA · contact PI
Sequence Variations in Low Copy Repeats on 22q11.2$207,500
R21 · FY2010 · MH · contact PI
GENETIC CORE$85,182
P01 · FY2010 · AG · contact PI
Genetic Analysis of Tbx1 in Ear Disorders$36,952
R01 · FY2010 · DC · contact PI
Genetic Modifiers for 22q 11.2 Deletion Syndrome$800,208
R01 · FY2009 · HL · contact PI
Developmental Genetics of the Pharyngeal Apparatus$415,000
R01 · FY2009 · HL · contact PI
Genetic Analysis of Tbx1 in Ear Disorders$352,750
R01 · FY2009 · DC · contact PI
GENOMICS SHARED RESOURCE$251,169
P30 · FY2009 · CA · contact PI
Sequence Variations in Low Copy Repeats on 22q11.2$245,656
R21 · FY2009 · MH · contact PI
Genetic Basis of Birth Defects in 22q11 Deletion Syndrome$207,500
R21 · FY2009 · NS · contact PI
GENETIC CORE$83,667
P01 · FY2009 · AG · contact PI
Genetic Modifiers for 22q 11.2 Deletion Syndrome$802,221
R01 · FY2008 · HL · contact PI
GENOMICS SHARED RESOURCE$235,892
P30 · FY2008 · CA · contact PI
GENETIC CORE$134,851
P01 · FY2008 · AG · contact PI
HEARING LOSS$1,013
M01 · FY2008 · RR · contact PI
Genetic Modifiers for 22q 11.2 Deletion Syndrome$872,292
R01 · FY2007 · HL · contact PI
Genetic Analysis of Tbx1 in Ear Disorders$327,731
R01 · FY2007 · DC · contact PI
GENOMICS SHARED RESOURCE$177,853
P30 · FY2007 · CA · contact PI
GENETIC CORE$136,447
P01 · FY2007 · AG · contact PI
Genetic Analysis of Tbx1 in Ear Disorders$338,407
R01 · FY2006 · DC · contact PI
Molecular Basis of Monosomy 1p36$164,934
R21 · FY2006 · NS · contact PI
Genetic Analysis of Tbx1 in Ear Disorders$347,433
R01 · FY2005 · DC
Molecular Basis of Monosomy 1p36$214,636
R21 · FY2005 · NS
Genetic Analysis of Tbx1 in Ear Disorders$342,194
R01 · FY2004 · DC
Genetic Analysis of Tbx1 in Ear Disorders$352,172
R01 · FY2003 · DC
Genetic Analysis of Tbx1 in Ear Disorders$50,000
R01 · FY2003 · DC
Molecular mechanism of recurrent rearrangements$0
P01 · FY2002 · HD
MOLECULAR MECHANISMS AND GENOTYPE-PHENOTYPE IN VCFS/DGS$0
P01 · FY2002 · HD
MOLECULAR MECHANISMS AND GENOTYPE-PHENOTYPE IN VCFS/DGS$0
P01 · FY2001 · HD
Molecular mechanism of recurrent rearrangements$0
P01 · FY2001 · HD
MOLECULAR MECHANISMS AND GENOTYPE-PHENOTYPE IN VCFS/DGS$0
P01 · FY2001 · HD
MOLECULAR MECHANISMS AND GENOTYPE-PHENOTYPE IN VCFS/DGS$0
P01 · FY2000 · HD