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Anne M. Slavotinek

University Of California San Francisco

$6,374,035
Attributed
$14,969,091
Total exposure
10
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 $3.8M · FY200525
$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$14,969,091 · 10

By mechanism

U01$10,724,450 · 1
R01$2,369,872 · 2
R21$838,463 · 2
K08$624,848 · 1
T32$190,778 · 1
R03$149,720 · 1

Top collaborators

Most similar at University Of California San Francisco

Same institution · by research overlap

Others in their field

Top investigators on “Affect

Research focus

AffectGenesCongenital AbnormalityGeneticPathogenesisGene ExpressionCounselingLoss Of FunctionDiagnosisVariantMolecular GeneticsEtiologyLifeBaseTissuesGenetic Predisposition To DiseaseMicrophthalmosAnophthalmosCandidate Disease GeneMortality Vital StatisticsPhenotypeEye DevelopmentColobomaVisual Impairment

Grant awards (27)

Microphthalmia, anophthalmia and coloboma (MAC) and retinoic acid pathway genes$341,063
R01 · FY2025 · EY · contact PI
Microphthalmia, anophthalmia and coloboma (MAC) and retinoic acid pathway genes$401,250
R01 · FY2024 · EY · contact PI
Microphthalmia, anophthalmia and coloboma (MAC) and retinoic acid pathway genes$361,125
R01 · FY2023 · EY · contact PI
Genomic analysis of microphthalmia, anophthalmia and coloboma$327,273
R01 · FY2023 · EY · contact PI
Genomic analysis of microphthalmia, anophthalmia and coloboma$462,429
R01 · FY2022 · EY · contact PI
Genomic analysis of microphthalmia, anophthalmia and coloboma$476,732
R01 · FY2021 · EY · contact PI
Genomic sequencing to aid diagnosis in pediatric and prenatal practice: Examining clinical utility, ethical implications, payer coverage, and data integration in a diverse population.$3,482,776
U01 · FY2019 · HG
Genomic sequencing to aid diagnosis in pediatric and prenatal practice: Examining clinical utility, ethical implications, payer coverage, and data integration in a diverse population.$166,973
U01 · FY2019 · HG
Genomic sequencing to aid diagnosis in pediatric and prenatal practice: Examining clinical utility, ethical implications, payer coverage, and data integration in a diverse population.$134,048
U01 · FY2019 · HG
Genomic sequencing to aid diagnosis in pediatric and prenatal practice: Examining clinical utility, ethical implications, payer coverage, and data integration in a diverse population.$3,845,228
U01 · FY2018 · HG
Genomic sequencing to aid diagnosis in pediatric and prenatal practice: Examining clinical utility, ethical implications, payer coverage, and data integration in a diverse population.$3,095,425
U01 · FY2017 · HG
Postdoctoral Training in Medical Genetics$190,778
T32 · FY2013 · GM · contact PI
Gene Discovery in Human Anopthalmia/Micropthalmia$186,438
R21 · FY2013 · EY · contact PI
Gene Discovery in Human Anopthalmia/Micropthalmia$234,875
R21 · FY2012 · EY · contact PI
Anopthalmia Spectrum Disorders$185,400
R21 · FY2011 · EY · contact PI
Molecular Genetic Analysis of Congenital Diaphragmatic Hernia$125,820
K08 · FY2011 · HD · contact PI
Anopthalmia Spectrum Disorders$231,750
R21 · FY2010 · EY · contact PI
Molecular Genetic Analysis of Congenital Diaphragmatic Hernia$125,820
K08 · FY2010 · HD · contact PI
Molecular Genetic Analysis of Congenital Diaphragmatic Hernia$125,415
K08 · FY2009 · HD · contact PI
Molecular Genetic Analysis of Congenital Diaphragmatic Hernia$124,200
K08 · FY2008 · HD · contact PI
Molecular Genetic Analysis of Congenital Diaphragmatic Hernia$123,593
K08 · FY2007 · HD · contact PI
Genetic analysis of congenital diaphragmatic hernia$73,970
R03 · FY2006 · HD · contact PI
Genetic analysis of congenital diaphragmatic hernia$75,750
R03 · FY2005 · HD
MOLECULAR GENETIC ANALYSIS OF FRASER SYNDROME AND FRYNS SYNDROME$19,210
M01 · FY2005 · RR
MOLECULAR GENETIC ANALYSIS OF MULTIPLE CONGENITAL ANOMALY SYNDROMES$16,862
M01 · FY2005 · RR
Molecular genetic analysis of Fraser Syndrome and Fryns Syndrome$25,269
M01 · FY2004 · RR
Molecular genetic investigation of multiple congenital anomaly syndromes$9,619
M01 · FY2004 · RR