Nicholas P. Mancuso

Emergency Medicine

6379 Center Drive
Norfolk, VA 23502

Last Updated: 09/26/2026

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Found 84 publications

Highly efficient genotype compression leveraging genealogical relatedness.

Highly efficient genotype compression leveraging genealogical relatedness.

Journal: bioRxiv : the preprint server for biology

Published: May 07, 2026

Publisher Correction: Multi-ancestry genome-wide association study of severe pregnancy nausea and vomiting.

Publisher Correction: Multi-ancestry genome-wide association study of severe pregnancy nausea and vomiting.

Journal: Nature genetics

Published: April 28, 2026

Single-cell full-length transcriptome of human lung reveals genetic effects on isoform regulation beyond gene-level expression.

Single-cell full-length transcriptome of human lung reveals genetic effects on isoform regulation beyond gene-level expression.

Journal: bioRxiv : the preprint server for biology

Published: April 27, 2026

Single-cell lung eQTL dataset of Asian never-smokers highlights the roles of alveolar cells in lung cancer etiology.

Single-cell lung eQTL dataset of Asian never-smokers highlights the roles of alveolar cells in lung cancer etiology.

Journal: bioRxiv : the preprint server for biology

Published: April 03, 2026

Prioritizing context-specific genetic risk mechanisms in 11 solid cancers.

Prioritizing context-specific genetic risk mechanisms in 11 solid cancers.

Journal: medRxiv : the preprint server for health sciences

Published: November 24, 2025

Genome-wide association study and predictors of neonatal blood cell traits in Hispanic newborns.

Genome-wide association study and predictors of neonatal blood cell traits in Hispanic newborns.

Journal: American journal of human genetics

Published: October 09, 2025

traceax: a JAX-based framework for stochastic trace estimation.

traceax: a JAX-based framework for stochastic trace estimation.

Journal: bioRxiv : the preprint server for biology

Published: August 12, 2025

Identifying independent causal cell types for human diseases and risk variants.

Identifying independent causal cell types for human diseases and risk variants.

Journal: Cell genomics

Published: August 04, 2025

Author Correction: A likelihood-based framework for demographic inference from genealogical trees.

Author Correction: A likelihood-based framework for demographic inference from genealogical trees.

Journal: Nature genetics

Published: June 17, 2025

The impact of Indigenous American-like ancestry on the risk of acute lymphoblastic leukemia in Hispanic/Latino children.

The impact of Indigenous American-like ancestry on the risk of acute lymphoblastic leukemia in Hispanic/Latino children.

Journal: HGG advances

Published: April 10, 2025

Efficient count-based models improve power and robustness for large-scale single-cell eQTL mapping.

Efficient count-based models improve power and robustness for large-scale single-cell eQTL mapping.

Journal: medRxiv : the preprint server for health sciences

Published: March 17, 2025

The impact of Indigenous American-like ancestry on risk of acute lymphoblastic leukemia in Hispanic/Latino children.

The impact of Indigenous American-like ancestry on risk of acute lymphoblastic leukemia in Hispanic/Latino children.

Journal: medRxiv : the preprint server for health sciences

Published: January 27, 2025

Showing 1-12 of 84

Last Updated: 09/26/2026