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Raquel Martin

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Assistant ProfessorDepartment of Human GeneticsMcGill University

Raquel Martin

Assistant Professor

Department of Human Genetics

Faculty of Medicine and Health Sciences

McGill University

Montreal, Quebec, Canada

Supervision signals

Professors usually supervise graduate students in their department's programs.
10 publications in the last five years, latest in 2026.
Senior (last) author on 3 recent papers, a sign of leading a research group.

These signals come from public records, including federal and provincial funding decisions. Ask the professor or the graduate program whether they are taking new students.

Academic metrics

Publications

1,138

Citations

Collaborators

Publications by year

Counts cover the publications linked to this profile. Citations and the h-index appear when the source records them.

Roles and appointments

Canada Excellence Research Chair in Genomic Medicine Investigator, Victor Phillip Dahdaleh Institute of Genomic Medicine

Profiles and links

University Profile

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Signals and details

Research

Read how they describe their research on their McGill University profile.

Latest papers

Anticipating on-target resistance to WRN inhibitors in microsatellite unstable cancers
bioRxiv (Cold Spring Harbor Laboratory) · 2026 · senior author
Multimodal analysis of a rare BARD1 missense variant suggests its pathogenicity is conditional.
NPJ breast cancer · 2026
A base editing resource for functional annotation of DNA repair variants in breast-derived cell models.
Frontiers in cell and developmental biology · 2026

All 21 publications

21 publications.

Anticipating on-target resistance to WRN inhibitors in microsatellite unstable cancers

Mark E. Orcholski, Nancy Laterreur, Wardah Masud, Shamika Shenoy, Vincent Chapdelaine-Trépanier, Julian Bowlan, Amisha Minju-OP, Júlia-Jié Cabré-Romans, Tanja Sack, Chris Fiore, Jordan T.F. Young, Alejandro Álvarez-Quilón, Raquel Cuella-Martin

bioRxiv (Cold Spring Harbor Laboratory)20261 citationsSenior authorOpen Access

DOI: 10.64898/2026.01.22.700152

Multimodal analysis of a rare BARD1 missense variant suggests its pathogenicity is conditional.

Chan-Pak-Choon F, Gao Y, Camacho-Valenzuela J, Cabré-Romans JJ, Minju-Op A, Fu L, Polak P, Rivera B, Cuella-Martin R, Foulkes WD

NPJ breast cancer2026Open Access

DOI: 10.1038/s41523-026-00955-8 PMID: 42014738

A base editing resource for functional annotation of DNA repair variants in breast-derived cell models.

Masud W, Russo L, Chapdelaine-Trépanier V, Hayward SB, He W, Cirò M, Mercurio C, Xu H, Ciccia A, Cuella-Martin R, Leuzzi G

Frontiers in cell and developmental biology2026Open Access

DOI: 10.3389/fcell.2026.1714494 PMID: 41970959

CRISPR-dependent base editing as a therapeutic strategy for rare monogenic disorders.

Cabré-Romans JJ, Cuella-Martin R

Frontiers in genome editing202524 citationsSenior authorOpen Access

DOI: 10.3389/fgeed.2025.1553590 PMID: 40242216

Divergent roles of DNA methylation, TRIM28, and p53 surveillance in human embryonic and trophoblast stem cells.

Saini D, Katz MS, Beck SGA, Ireland TE, Ray S, Niloy AJ, Mazloomnejad R, Fleming A, Vetrici SC, Cinkornpumin JK, Sack T, Duhamel S, Slim R, Park M, Frost JM, Paul S, Martin RC, Pastor WA

bioRxiv : the preprint server for biology20252 citationsOpen Access

DOI: 10.1101/2025.10.19.683051 PMID: 41279747

CRISPR-BEasy: a free web-based service for designing sgRNA tiling libraries for CRISPR-dependent base editing screens.

Chapdelaine-Trépanier V, Shenoy S, Masud W, Minju-Op A, Bérubé MA, Schönherr S, Forer L, Fradet-Turcotte A, Taliun D, Cuella-Martin R

Nucleic acids research20252 citationsSenior authorOpen Access

DOI: 10.1093/nar/gkaf382 PMID: 40377102

SMARCAL1 is a dual regulator of innate immune signaling and PD-L1 expression that promotes tumor immune evasion

Giuseppe Leuzzi, Alessandro Vasciaveo, Angelo Taglialatela, Xiao Chen, Tessa M. Firestone, Allison R. Hickman, Wendy Mao, Tanay Thakar, Alina Vaitsiankova, Jen‐Wei Huang, Raquel Cuella-Martin, Samuel B. Hayward, Jordan S. Kesner, Ali Ghasemzadeh, Tarun S. Nambiar, Patricia L. Ho, Alexander Rialdi, Maxime Hebrard, Yinglu Li, Jinmei Gao, Saarang Gopinath, Oluwatobi A. Adeleke, Bryan J. Venters, Charles G. Drake, Richard J. Baer, Benjamin Izar, Ernesto Guccione, Michael‐Christopher Keogh, Raphaël Guérois, Lu Sun, et al. (33 authors)

Cell2024105 citationsOpen Access

DOI: 10.1016/j.cell.2024.01.008 PMID: 38301646

Rare splice and missense variants with evidence of pathogenicity in consanguineous families with autosomal recessive intellectual disability from Pakistan

Abdul A Waheed, Robert J. M. Eveleigh, Danielle S. Perley, Janick St-Cyr, François Lefebvre, Abdul Hameed Khan, Zarqash Majeed, Abrish Majeed, Katerina Trajanoska, Raquel Cuella-Martin, Claude Bhérer, Ghazanfar Ali, Vincent Mooser, Daniel Taliun

medRxiv2024Open Access

DOI: 10.1101/2024.01.08.23299914

Abstract PR009: SMARCAL1 is a dual regulator of innate immune signaling and PD-L1 expression that promotes tumor immune evasion

Cancer Research2024

DOI: 10.1158/1538-7445.dnarepair24-pr009

Systematic proximal mapping of the classical RAD51 paralogs unravel functionally and clinically relevant interactors for genome stability.

Simo Cheyou E, Boni J, Boulais J, Pinedo-Carpio E, Malina A, Sherill-Rofe D, Luo VM, Goncalves C, Bagci H, Maters A, Cuella-Martin R, Tabach Y, Del Rincon S, Côté JF, Rivera B, Orthwein A

PLoS genetics20222 citationsOpen Access

DOI: 10.1371/journal.pgen.1010495 PMID: 36374936

Profile data last refreshed on September 29, 2026 from the university directory, publication records and public research funding records.

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Raquel Martin

Research

Latest papers

Anticipating on-target resistance to WRN inhibitors in microsatellite unstable cancers

Multimodal analysis of a rare BARD1 missense variant suggests its pathogenicity is conditional.

A base editing resource for functional annotation of DNA repair variants in breast-derived cell models.

CRISPR-dependent base editing as a therapeutic strategy for rare monogenic disorders.

Divergent roles of DNA methylation, TRIM28, and p53 surveillance in human embryonic and trophoblast stem cells.

CRISPR-BEasy: a free web-based service for designing sgRNA tiling libraries for CRISPR-dependent base editing screens.

SMARCAL1 is a dual regulator of innate immune signaling and PD-L1 expression that promotes tumor immune evasion

Rare splice and missense variants with evidence of pathogenicity in consanguineous families with autosomal recessive intellectual disability from Pakistan

Abstract PR009: SMARCAL1 is a dual regulator of innate immune signaling and PD-L1 expression that promotes tumor immune evasion

Systematic proximal mapping of the classical RAD51 paralogs unravel functionally and clinically relevant interactors for genome stability.

Frequent collaborators

Raquel Cuella Martin

Daniel Taliun

Morag Park

Alexandre Orthwein

Amélie Fradet-Turcotte

Sonia Del Rincon

Rima Slim

Vincent Mooser

Claude Bhérer

Pierre Billon

William Pastor

William Foulkes