Moriel Singer‐Berk

Broad Institute

Associate Professor(heuristic)

Genomics and Rare Diseases · Genetics

h-index21

i10-index34

Publications58

Citations15,157

Grants

No NSF/NIH grants on record.

Lab Funding Health

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In-Field Influence

0.0024

PageRank within Genetics co-authorship network

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Admission Signals

New paper: Unifying the Communities of Early‐Onset Glycogen Storage Disease Type <scp>IV</scp> and Adult Polyglucosan Body Disease Through a Genetic Prevalence Study of <scp> <i>GBE1</i> </scp> ‐Related Disease (JIMD Reports)2026-04-06
New preprint: Unifying the communities of early-onset glycogen storage disease type IV and adult polyglucosan body disease through a genetic prevalence study of <i>GBE1</i> -related disease2025-12-17

Data Freshness

Publications as of 2026-07-01
Grants as of 2026-06-30

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ORCID: 0000-0001-8148-0648

Career Trajectory

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Recent Publications

Last 2 years · showing 5 of 5

Unifying the Communities of Early‐Onset Glycogen Storage Disease Type <scp>IV</scp> and Adult Polyglucosan Body Disease Through a Genetic Prevalence Study of <scp> <i>GBE1</i> </scp> ‐Related Disease
JIMD Reports · 2026-04-06
Unifying the communities of early-onset glycogen storage disease type IV and adult polyglucosan body disease through a genetic prevalence study of <i>GBE1</i> -related diseasePreprint
medRxiv · 2025-12-17
Exploring penetrance of clinically relevant variants in over 800,000 humans from the Genome Aggregation Database
Nature Communications · 2025-10-31 · 11 citations
An estimation of global genetic prevalence of PLA2G6-associated neurodegeneration
Orphanet Journal of Rare Diseases · 2024-10-18 · 10 citations
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders
Genetics in Medicine · 2024-07-17 · 16 citations

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