Faculty profile

Pranesh Chakraborty

ResearcherPediatricsUniversity of Ottawa

This profile is built from public research funding records (CIHR, NSERC and SSHRC) and PubMed. We have not imported them from a University of Ottawa directory, so their courses and email address may be missing. Find their university profile.

Pranesh Chakraborty

Researcher

Pediatrics

Health Sciences

University of Ottawa

Ottawa, Ontario, Canada

Supervision signals

Has led research grants, which requires an independent research appointment. Ask their department whether they supervise graduate students.
43 publications in the last five years, latest in 2026.
Senior (last) author on 9 recent papers, a sign of leading a research group.
Principal investigator on 7 research grants (7 CIHR), most recently in 2021.

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

Academic metrics

137

Publications

462

Citations

h-index

121

Collaborators

Grants

Publications by year

Counts cover the works listed on the university profile; citation counts come from Dimensions.

Profiles and links

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Signals and details

Research

Newborn Screening Cytomegalovirus Congenital Infection Cost Effectiveness Diagnostics Pediatrics Cohort Study Hearing

Latest papers

Eye Findings Following Congenital Cytomegalovirus Newborn Screening.
Pediatrics · 2026
Development and content validation of the Clinician-reported Genetic testing Utility InDEx for genomic newborn screening (C-GUIDE NBS).
Genetics in medicine : official journal of the American College of Medical Genetics · 2026
General Population Screening for Type 1 Diabetes in Canada---CanScreenT1D.
Canadian journal of diabetes · 2026

All 137 publications

Latest funding

Developing and implementing a core outcome set for adolescents and adults with phenylketonuria
CIHR · 2026 · Co-investigator
$539,325
Developing and implementing a core outcome set for adolescents and adults with phenylketonuria
CIHR · 2025 · Co-investigator
$100,000
Congenital CMV ANd HEARing in Ontario: Optimizing Screening to Improve Child Health Outcomes (CAN HEAR ONTARIO)
CIHR · 2021 · Principal investigator
$950,896

All 14 grants and awards

137 publications.

Eye Findings Following Congenital Cytomegalovirus Newborn Screening.

Leahy KE, Dunn JKE, Gallagher L, Reuvers E, Chakraborty P, Bitnun A, Barton M, Leifso K, Pernica JM, Brophy J, O'Connor M, Makar I, Sharan S, Iordanous Y, Fournier A, Sabri K, Saleh S, Strube YNJ, Ali A, Mireskandari K

Pediatrics2026

DOI: 10.1542/peds.2025-075586 PMID: 42764171

Development and content validation of the Clinician-reported Genetic testing Utility InDEx for genomic newborn screening (C-GUIDE NBS).

Shickh S, Luca S, Fooks K, Poole E, Xiao B, Yan J, Pichini A, Ziff J, Stone K, Ungar WJ, Chakraborty P, Bick D, Hayeems RZ

Genetics in medicine : official journal of the American College of Medical Genetics2026

DOI: 10.1016/j.gim.2026.102611 PMID: 42200354

General Population Screening for Type 1 Diabetes in Canada---CanScreenT1D.

Senior PA, Marwaha A, Witteman HO, Chakraborty P, Hayeems RZ, Wherrett DK, CanScreenT1D Consortium

Canadian journal of diabetes2026

DOI: 10.1016/j.jcjd.2025.11.001 PMID: 41213473

Improved Performance of Newborn Screening for Congenital Adrenal Hyperplasia Using 21-deoxycortisol Measurement.

Lawrence SE, Marcadier J, Auger S, Bariciak E, Chakraborty P, Chambers A, Eagle S, Kowalski M, Marr A, McIntosh N, Saleh DS, Santander E, Sinclair G, Wherrett DK, Henderson MPA

Journal of the Endocrine Society2026

DOI: 10.1210/jendso/bvaf157 PMID: 41394115

The impacts of caring for children with inherited metabolic diseases for families: a cross-sectional study

Chow AJ, Jordan I, Pallone N, Smith M, Chakraborty P, Brehaut J, Chan AKJ, Cohen E, Dyack S, Graham ID

Orphanet Journal of Rare Diseases2026

DOI: 10.1186/s13023-026-04434-y

High precision newborn screening for mucopolysaccharidosis type I by enzymatic activity followed by endogenous, non-reducing end glycosaminoglycan analysis.

Herbst ZM, Kubaski F, Pollard L, Basheeruddin K, Burton B, Orsini J, Henderson M, Chakraborty P, Gelb MH

Molecular genetics and metabolism2025

DOI: 10.1016/j.ymgme.2024.108612 PMID: 39645522

Metabolic Control and Frequency of Clinical Monitoring Among Canadian Children With Phenylalanine Hydroxylase Deficiency: A Retrospective Cohort Study.

Yuskiv N, Saad A, Potter BK, Stockler-Ipsiroglu S, Mitchell JJ, Hawken S, Tingley K, Pugliese M, Lamoureux M, Chow AJ, Kronick JB, Wilson K, Feigenbaum A, Goobie S, Inbar-Feigenberg M, Little J, Mercimek-Andrews S, Pender A, Prasad C, Schulze A, Trakadis Y, Ho G, Vallance H, Austin V, Vandersteen A, Yu AC, Rockman-Greenberg C, Mhanni AA, Chakraborty P

JIMD reports2025Senior author

DOI: 10.1002/jmd2.70042 PMID: 40901071

Systematic review for economic evaluations on newborn screening for spinal muscular atrophy.

Pace AC, Poon C, Chakraborty P, Oskoui M, McMillan H, Mackenzie A, Round J

Journal of neuromuscular diseases2025

DOI: 10.1177/22143602251336862 PMID: 40400315

A cost-utility analysis of newborn screening for spinal muscular atrophy in Canada.

Pace A, Roda W, Poon C, McMillan HJ, Oskoui M, MacKenzie A, Chakraborty P, Round J

Orphanet journal of rare diseases2025

DOI: 10.1186/s13023-025-03927-6 PMID: 40804727

Newborn screening for common genetic variants associated with permanent hearing loss: Implementation in Ontario and review of the first 3 years.

Kernohan KD, Gallagher L, Pigeon M, Yeh E, Lacaria M, Axford MM, MacCormick J, Papaioannou V, Quercia N, Rupar C, Zimmerman K, Weber S, Cushing SL, Chakraborty P

Genetics in medicine : official journal of the American College of Medical Genetics2025Senior author

DOI: 10.1016/j.gim.2025.101364 PMID: 39846246

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Pranesh Chakraborty

Research

Latest papers

Latest funding

Eye Findings Following Congenital Cytomegalovirus Newborn Screening.

Development and content validation of the Clinician-reported Genetic testing Utility InDEx for genomic newborn screening (C-GUIDE NBS).

General Population Screening for Type 1 Diabetes in Canada---CanScreenT1D.

Improved Performance of Newborn Screening for Congenital Adrenal Hyperplasia Using 21-deoxycortisol Measurement.

The impacts of caring for children with inherited metabolic diseases for families: a cross-sectional study

High precision newborn screening for mucopolysaccharidosis type I by enzymatic activity followed by endogenous, non-reducing end glycosaminoglycan analysis.

Metabolic Control and Frequency of Clinical Monitoring Among Canadian Children With Phenylalanine Hydroxylase Deficiency: A Retrospective Cohort Study.

Systematic review for economic evaluations on newborn screening for spinal muscular atrophy.

A cost-utility analysis of newborn screening for spinal muscular atrophy in Canada.

Newborn screening for common genetic variants associated with permanent hearing loss: Implementation in Ontario and review of the first 3&#xa0;years.

Frequent collaborators

Kumanan Wilson

Julian Little

Steven Hawken

Doug Coyle

Sylvia Stockler

Murray Alexander Potter

Jennifer MacKenzie

Astrid Guttmann

Martin Offringa

Maureen Smith

Mark Tarnopolsky

Mark Walker

Monica Taljaard

Yvonne Bombard

Jagdeep Walia

Robin Hayeems

Michael Geraghty

Martin Holcik

Jean Michaud

Jamie Brehaut

Melanie Lacaria

Mary-Ellen Harper

Maryam Oskoui

Nathalie Lepage

Beth Potter

Maureen Smith

Craig Campbell

Thierry Lacaze-Masmonteil

Clara van Karnebeek

Eyal Cohen

Linda Dodds

Anne-Marie Laberge

Brian Hutton

Jason Brophy

Kusum Menon

Meranda Nakhla

Meranda Nakhla

Kathy Speechley

Jesse Papenburg

Mark Dobrow

Newborn screening for common genetic variants associated with permanent hearing loss: Implementation in Ontario and review of the first 3 years.