Anne O’Donnell‐Luria

Broad Institute

Full Professor(heuristic)

Genomics and Rare Diseases · Genetics

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h-index63
i10-index147
Publications272
Citations39,542

Grants

8 total · 2 active

NIH #R01HG013986

Advancing rare disease discovery through technological and methodological approaches using an intuitive platform, seqr

Active
Amount
$3M–$4M
Period
2025-09-082029-06-30
PIs
2

Awarded at BROAD INSTITUTE, INC.

NIH #R01HG012781

Improving Genetic Diagnosis for African Ancestry Populations

Active
Amount
$600K–$700K
Period
2023-09-202028-01-31
PIs
1

Awarded at BROAD INSTITUTE, INC.

NIH #U01HG011755

Broad Institute Mendelian Genomic Research Center

Amount
$2M–$3M
Period
2021-06-012026-03-31
PIs
3

Awarded at BROAD INSTITUTE, INC.

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All Grants

8 total · 2 active

NIH #R01HG013986

Advancing rare disease discovery through technological and methodological approaches using an intuitive platform, seqr

Active
Amount
$3M–$4M
Period
2025-09-082029-06-30
PIs
2

Awarded at BROAD INSTITUTE, INC.

NIH #R01HG012781

Improving Genetic Diagnosis for African Ancestry Populations

Active
Amount
$600K–$700K
Period
2023-09-202028-01-31
PIs
1

Awarded at BROAD INSTITUTE, INC.

NIH #U01HG011755

Broad Institute Mendelian Genomic Research Center

Amount
$2M–$3M
Period
2021-06-012026-03-31
PIs
3

Awarded at BROAD INSTITUTE, INC.

NIH #U24HD104591

Gene Curation Expert Panel for Syndromic Disorders

Amount
$300K–$400K
Period
2022-08-172025-07-31
PIs
1

Awarded at BOSTON CHILDREN'S HOSPITAL

NIH #R21HG012397

Understanding Disparities in Genomic Medicine

Amount
$200K–$300K
Period
2022-07-012024-12-31
PIs
2

Awarded at BOSTON CHILDREN'S HOSPITAL

NIH #U01MH119689

Rare genetic disorders in NeuroDev: Insight into the genetic and phenotypic heterogeneity of ID, ASD and ADHD in South African Populations

Amount
$1M–$2M
Period
2019-06-012024-03-31
PIs
3

Awarded at BROAD INSTITUTE, INC.

NIH #UM1HG008900

Joint Center for Mendelian Genomics

Amount
$3M–$4M
Period
2016-01-142021-11-30
PIs
2

Awarded at BROAD INSTITUTE, INC.

NIH #F30MH085471

Epigenetic Profiling of Major Depression

Amount
<$100K
Period
2009-01-152011-10-14
PIs
1

Awarded at COLUMBIA UNIVERSITY HEALTH SCIENCES

Recent Public Signals

  1. New preprint: Structural variant discovery and diagnostic impact in rare diseases from short-read and long-read sequencing2026-06-24
  2. New paper: Automated reanalysis of genomic data for rare disease diagnostics at scale (Nature Medicine)2026-06-24
  3. New NIH award: Advancing rare disease discovery through technological and methodological approaches using an intuitive platform, seqr2025-09-08

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Data Freshness

  • Publications as of 2026-07-09
  • Grants as of 2026-09-05

Data may not be current

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ORCID: 0000-0001-6418-9592

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