Jeremy A. Schwartzentruber

Montreal, QC, Canada

Last Updated: 09/26/2026

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Found 107 publications

An Alzheimer's disease-associated common regulatory variant in a PTK2B intron alters microglial function.

An Alzheimer's disease-associated common regulatory variant in a PTK2B intron alters microglial function.

Journal: iScience

Published: October 13, 2025

Predicting expression-altering promoter mutations with deep learning.

Predicting expression-altering promoter mutations with deep learning.

Journal: Science (New York, N.Y.)

Published: May 29, 2025

Estimation and mapping of the missing heritability of human phenotypes.

Estimation and mapping of the missing heritability of human phenotypes.

Journal: Nature

Published: January 12, 2025

Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery.

Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery.

Journal: Nucleic acids research

Published: September 13, 2024

Integrative GWAS and co-localisation analysis suggests novel genes associated with age-related multimorbidity.

Integrative GWAS and co-localisation analysis suggests novel genes associated with age-related multimorbidity.

Journal: Scientific data

Published: May 19, 2023

Artificial intelligence for dementia genetics and omics.

Artificial intelligence for dementia genetics and omics.

Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association

Published: April 05, 2023

The next-generation Open Targets Platform: reimagined, redesigned, rebuilt.

The next-generation Open Targets Platform: reimagined, redesigned, rebuilt.

Journal: Nucleic acids research

Published: September 15, 2022

Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia.

Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia.

Journal: Orphanet journal of rare diseases

Published: March 30, 2022

Multi-ancestry Mendelian randomization of omics traits revealing drug targets of COVID-19 severity.

Multi-ancestry Mendelian randomization of omics traits revealing drug targets of COVID-19 severity.

Journal: EBioMedicine

Published: March 08, 2022

Screening for functional regulatory variants in open chromatin using GenIE-ATAC.

Screening for functional regulatory variants in open chromatin using GenIE-ATAC.

Journal: Nucleic acids research

Published: February 09, 2022

Genetic variants associated with psychiatric disorders are enriched at epigenetically active sites in lymphoid cells.

Genetic variants associated with psychiatric disorders are enriched at epigenetically active sites in lymphoid cells.

Journal: Nature communications

Published: November 05, 2021

Mapping interindividual dynamics of innate immune response at single-cell resolution.

Mapping interindividual dynamics of innate immune response at single-cell resolution.

Journal: Nature genetics

Published: August 28, 2021

Showing 1-12 of 107

Last Updated: 09/26/2026