GGrantIndex
← Leaderboards

Yoseph Barash

University Of Pennsylvania

$7,413,836
Attributed
$10,057,328
Total exposure
5
Grants
4
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 $3.7M · FY201425
$5M$3.8M$2.5M$1.3M$0
'14
'15
'16
'17
'18
'19
'20
'21
'22
'23
'24
'25

Funding mix

By agency

NIH$10,057,328 · 5

By mechanism

R01$6,519,870 · 4
U01$3,537,458 · 1

Top collaborators

Most similar at University Of Pennsylvania

Same institution · by research overlap

Others in their field

Top investigators on “Code

Research focus

CodeVariantGenesData SetCellsRna SplicingMutationTranscriptome SequencingGenetic VariantAffectExonsProtein IsoformsSamplingValidationMapsGenomicsAlternative SplicingEventRna ProcessingComplexCohortBaseTissuesHeritability

Grant awards (23)

Identifying regulatory uORFs as a targetable axis for hereditary disease$404,023
R01 · FY2025 · GM · contact PI
Identifying regulatory uORFs as a targetable axis for hereditary disease$404,023
R01 · FY2024 · GM · contact PI
Identifying regulatory uORFs as a targetable axis for hereditary disease$66,558
R01 · FY2024 · GM · contact PI
Identifying regulatory uORFs as a targetable axis for hereditary disease$404,023
R01 · FY2023 · GM · contact PI
Methods for improving clinical diagnostic by detection, prediction, interpretation and prioritization of aberrant transcriptome variations$339,916
R01 · FY2023 · LM · contact PI
Identifying regulatory uORFs as a targetable axis for hereditary disease$76,447
R01 · FY2023 · GM · contact PI
Cassette exons in neoplastic pro-B-cells: implications for immunotherapy$420,362
U01 · FY2022 · CA
Identifying regulatory uORFs as a targetable axis for hereditary disease$394,453
R01 · FY2022 · GM · contact PI
Methods for improving clinical diagnostic by detection, prediction, interpretation and prioritization of aberrant transcriptome variations$339,881
R01 · FY2022 · LM · contact PI
Methods for RNA splicing variations detection, quantification, visualization, and association from large heterogeneous datasets$432,541
R01 · FY2021 · GM · contact PI
Methods for improving clinical diagnostic by detection, prediction, interpretation and prioritization of aberrant transcriptome variations$346,597
R01 · FY2021 · LM · contact PI
Methods for RNA splicing variations detection, quantification, visualization, and association from large heterogeneous datasets$432,541
R01 · FY2020 · GM · contact PI
Methods for improving clinical diagnostic by detection, prediction, interpretation and prioritization of aberrant transcriptome variations$347,736
R01 · FY2020 · LM · contact PI
Cassette exons in neoplastic pro-B-cells: implications for immunotherapy$185,346
U01 · FY2020 · CA
Methods for RNA splicing variations detection, quantification, visualization, and association from large heterogeneous datasets$432,541
R01 · FY2019 · GM · contact PI
Methods for RNA splicing variations detection, quantification, visualization, and association from large heterogeneous datasets$71,698
R01 · FY2019 · GM · contact PI
Cassette exons in neoplastic pro-B-cells: implications for immunotherapy$2,931,750
U01 · FY2018 · CA
Methods for RNA splicing variations detection, quantification, visualization, and association from large heterogeneous datasets$432,541
R01 · FY2018 · GM · contact PI
Modeling Splicing in normal tissues and neurodegenerative disease$323,005
R01 · FY2018 · AG · contact PI
Modeling Splicing in normal tissues and neurodegenerative disease$323,151
R01 · FY2017 · AG · contact PI
Modeling Splicing in normal tissues and neurodegenerative disease$323,292
R01 · FY2016 · AG · contact PI
Modeling Splicing in normal tissues and neurodegenerative disease$309,681
R01 · FY2015 · AG · contact PI
Modeling Splicing in normal tissues and neurodegenerative disease$315,222
R01 · FY2014 · AG · contact PI