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David B. Goldstein

Duke University

$34,778,092
Attributed
$81,219,916
Total exposure
14
Grants
12
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 $13.8M · FY200720
$20M$15M$10M$5M$0
'07
'08
'09
'10
'11
'12
'13
'14
'15
'16
'17
'18
'19
'20

Funding mix

By agency

NIH$81,219,916 · 14

By mechanism

U01$31,109,839 · 4
OT2$24,000,000 · 1
R01$8,298,446 · 3
UG3$6,820,862 · 1
RC2$6,573,614 · 2
U19$3,482,015 · 1

Top collaborators

Most similar at Duke University

Same institution · by research overlap

Others in their field

Top investigators on “Variant

Research focus

VariantAffectGeneticPhenotypeFamilyGenomeBaseGenesGenome SequencingGenomicsGenetic VariantFamily MemberInterestResearch PersonnelGenotypeExome SequencingComplexMeetingsMemberBioinformaticsCase ControlMutationPathway InteractionsSampling

Grant awards (65)

New York City Consortium for Precision Medicine$12,000,000
OT2 · FY2020 · OD · contact PI
An integrated and diverse genomic medicine program for undiagnosed diseases$1,100,000
U01 · FY2020 · HG
Next Generation Rare Variant Discovery in Multiplex AD Families$156,267
R01 · FY2020 · AA
An integrated and diverse genomic medicine program for undiagnosed diseases$146,047
U01 · FY2020 · HG
New York City Consortium for Precision Medicine$12,000,000
OT2 · FY2019 · OD · contact PI
An integrated and diverse genomic medicine program for undiagnosed diseases$1,500,000
U01 · FY2019 · HG
Next Generation Rare Variant Discovery in Multiplex AD Families$300,751
R01 · FY2019 · AA
An integrated and diverse genomic medicine program for undiagnosed diseases$1,440,000
U01 · FY2018 · HG
1/3-ldentifying regulatory mutations that influence neuropsychiatric disease$334,142
U01 · FY2018 · MH · contact PI
Next Generation Rare Variant Discovery in Multiplex AD Families$299,708
R01 · FY2018 · AA
3 of 7 Epi4K: Sequencing, Biostatistics & Bioinformatics Core$160,000
U01 · FY2018 · NS · contact PI
An integrated and diverse genomic medicine program for undiagnosed diseases$2,289,986
U01 · FY2017 · HG
Columbia/Cornell/Harlem Hospital Precision Medicine Initiative HPO$2,128,967
UG3 · FY2017 · OD · contact PI
1/3-Identifying regulatory mutations that influence neuropsychiatric disease$1,374,267
U01 · FY2017 · MH · contact PI
Identifying de novo mutations causing OCD in trios by whole exome sequencing$880,214
R01 · FY2017 · MH · contact PI
Next Generation Rare Variant Discovery in Multiplex AD Families$443,741
R01 · FY2017 · AA
1 of 2: Identification of Rare Variants of OCD$349,910
R01 · FY2017 · MH · contact PI
Columbia/Cornell/Harlem Hospital Precision Medicine Initiative HPO$4,461,312
UG3 · FY2016 · OD · contact PI
An integrated and diverse genomic medicine program for undiagnosed diseases$2,300,000
U01 · FY2016 · HG
1/3-Identifying regulatory mutations that influence neuropsychiatric disease$1,373,814
U01 · FY2016 · MH · contact PI
Identifying de novo mutations causing OCD in trios by whole exome sequencing$881,166
R01 · FY2016 · MH · contact PI
Next Generation Rare Variant Discovery in Multiplex AD Families$440,636
R01 · FY2016 · AA
1 of 2: Identification of Rare Variants of OCD$358,265
R01 · FY2016 · MH · contact PI
Columbia/Cornell/Harlem Hospital Precision Medicine Initiative HPO$230,583
UG3 · FY2016 · OD · contact PI
An integrated and diverse genomic medicine program for undiagnosed diseases$77,391
U01 · FY2016 · HG
3 of 7 Epi4K: Sequencing, Biostatistics & Bioinformatics Core$2,610,991
U01 · FY2015 · NS · contact PI
An integrated and diverse genomic medicine program for undiagnosed diseases$1,573,904
U01 · FY2015 · HG
1/3-Identifying regulatory mutations that influence neuropsychiatric disease$1,379,311
U01 · FY2015 · MH · contact PI
Identifying de novo mutations causing OCD in trios by whole exome sequencing$888,420
R01 · FY2015 · MH · contact PI
Next Generation Rare Variant Discovery in Multiplex AD Families$445,805
R01 · FY2015 · AA
1 of 2: Identification of Rare Variants of OCD$379,011
R01 · FY2015 · MH · contact PI
1 of 7 Epi4K: Gene discovery in 4,000 epilepsy genomes - Administrative Core$149,993
U01 · FY2015 · NS · contact PI
3 of 7 Epi4K: Sequencing, Biostatistics & Bioinformatics Core$2,087,831
U01 · FY2014 · NS · contact PI
1/3-Identifying regulatory mutations that influence neuropsychiatric disease$1,274,060
U01 · FY2014 · MH · contact PI
An integrated and diverse genomic medicine program for undiagnosed diseases$799,429
U01 · FY2014 · HG
Identifying de novo mutations causing OCD in trios by whole exome sequencing$599,590
R01 · FY2014 · MH · contact PI
3 of 7 Epi4K: Sequencing, Biostatistics & Bioinformatics Core$375,853
U01 · FY2014 · NS · contact PI
1 of 2: Identification of Rare Variants of OCD$251,906
R01 · FY2014 · MH · contact PI
Identifying de novo mutations causing OCD in trios by whole exome sequencing$158,639
R01 · FY2014 · MH · contact PI
3 of 7 Epi4K: Sequencing, Biostatistics & Bioinformatics Core$157,166
U01 · FY2014 · NS · contact PI
1 of 2: Identification of Rare Variants of OCD$129,718
R01 · FY2014 · MH · contact PI
Identifying de novo mutations causing OCD in trios by whole exome sequencing$128,759
R01 · FY2014 · MH · contact PI
1/3-Identifying regulatory mutations that influence neuropsychiatric disease$120,641
U01 · FY2014 · MH · contact PI
1 of 7 Epi4K: Gene discovery in 4,000 epilepsy genomes - Administrative Core$74,637
U01 · FY2014 · NS · contact PI
1 of 7 Epi4K: Gene discovery in 4,000 epilepsy genomes - Administrative Core$72,914
U01 · FY2014 · NS · contact PI
3 of 7 Epi4K: Gene discovery in 4,000 epilepsy genomes$30,246
U01 · FY2014 · NS · contact PI
3 of 7 Epi4K: Sequencing, Biostatistics & Bioinformatics Core$1,919,296
U01 · FY2013 · NS · contact PI
Identifying de novo mutations causing OCD in trios by whole exome sequencing$791,759
R01 · FY2013 · MH · contact PI
1 of 2: Identification of Rare Variants of OCD$414,181
R01 · FY2013 · MH · contact PI
Genomics scientific research support component$200,630
UM1 · FY2013 · AI · contact PI
1 of 7 Epi4K: Gene discovery in 4,000 epilepsy genomes - Administrative Core$149,796
U01 · FY2013 · NS · contact PI
3 of 7 Epi4K: Sequencing, Biostatistics & Bioinformatics Core$2,871,102
U01 · FY2012 · NS · contact PI
Determinants of protection in HIV-exposed seronegative men$499,010
R56 · FY2012 · AI · contact PI
Genomics scientific research support component$235,500
UM1 · FY2012 · AI · contact PI
1 of 7 Epi4K: Gene discovery in 4,000 epilepsy genomes - Administrative Core$159,404
U01 · FY2012 · NS · contact PI
3 of 7 Epi4K: Sequencing, Biostatistics & Bioinformatics Core$3,037,863
U01 · FY2011 · NS · contact PI
Whole-genome sequencing for rare highly penetrant gene variants in schizophrenia$1,440,617
RC2 · FY2011 · MH · contact PI
1 of 7 Epi4K: Gene discovery in 4,000 epilepsy genomes - Administrative Core$169,755
U01 · FY2011 · NS · contact PI
Whole-genome sequencing for rare highly penetrant gene variants in schizophrenia$1,461,725
RC2 · FY2010 · MH · contact PI
Whole-genome sequencing in multiplex epilepsy families$900,501
RC2 · FY2010 · NS · contact PI
Whole-genome sequencing for rare highly penetrant gene variants in schizophrenia$1,671,247
RC2 · FY2009 · MH · contact PI
Whole-genome sequencing in multiplex epilepsy families$1,099,524
RC2 · FY2009 · NS · contact PI
Host and Viral Genetics Core$1,081,268
U19 · FY2009 · AI · contact PI
Host and Viral Genetics Core$1,072,115
U19 · FY2008 · AI · contact PI
Host and Viral Genetics Core$1,328,632
U19 · FY2007 · AI · contact PI