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Michal Inbar-Feigenberg

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Associate ProfessorDepartment of PaediatricsUniversity of Toronto

Michal Inbar-Feigenberg

Associate Professor

Department of Paediatrics

Temerty Faculty of Medicine

University of Toronto

Toronto, Ontario, Canada

Supervision signals

Professors usually supervise graduate students in their department's programs.
19 publications in the last five years, latest in 2026.
Senior (last) author on 5 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

1,163

Citations

Collaborators

Publications by year

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

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Signals and details

Research

Read how they describe their research on their University of Toronto profile.

Latest papers

Case Report: Persistent isolated hyperhomocysteinemia in an adolescent with celiac disease and homozygous MTHFR c.665C>T polymorphism: a multifactorial disturbance of one-carbon metabolism.
Frontiers in genetics · 2026 · senior author
Intrathecal idursulfase-IT in children younger than 3 years with neuronopathic mucopolysaccharidosis II in a single-arm, open-label, phase 2/3 substudy and extension.
JIMD reports · 2026
Mitochondrial Complex V Deficiency Caused by a Homozygous Splice Variant in ATP5PO.
American journal of medical genetics. Part A · 2026

All 31 publications

31 publications.

Case Report: Persistent isolated hyperhomocysteinemia in an adolescent with celiac disease and homozygous MTHFR c.665C>T polymorphism: a multifactorial disturbance of one-carbon metabolism.

Al Masseri Z, Marshall CR, Martin N, Cordeiro D, Guilder L, Inbar-Feigenberg M

Frontiers in genetics2026Senior authorOpen Access

DOI: 10.3389/fgene.2026.1912912 PMID: 42713553

Intrathecal idursulfase-IT in children younger than 3 years with neuronopathic mucopolysaccharidosis II in a single-arm, open-label, phase 2/3 substudy and extension.

Muenzer J, Burton BK, Harmatz P, Gutiérrez-Solana LG, Ruiz-Garcia M, Jones SA, Guffon N, Inbar-Feigenberg M, Bratkovic D, Rust S, Hale M, Wu Y, Yee KS, Whiteman DAH, Alexanderian D

JIMD reports2026

DOI: 10.1002/jmd2.12443 PMID: 41737901

Mitochondrial Complex V Deficiency Caused by a Homozygous Splice Variant in ATP5PO.

Al Masseri Z, Guilder L, Inbar-Feigenberg M, Cameron J, Venkatachalam S, Chitayat D

American journal of medical genetics. Part A2026

DOI: 10.1002/ajmg.a.64239 PMID: 40913360

Impact of regular physiotherapy intervention on the function and quality of life of pediatric patients diagnosed with Mucopolysaccharidosis.

Dealy J, Inbar-Feigenberg M

Molecular genetics and metabolism reports2026Senior author

DOI: 10.1016/j.ymgmr.2026.101306 PMID: 41890541

Clinical applications of and molecular insights from RNA sequencing in a rare disease cohort.

Stark JC, Pipko N, Liang Y, Szuto A, Tsoi CT, Dickson MA, Yuki KE, Hou H, Scholten S, Pulsifer K, Acker M, Laver M, Murthy H, Moran OM, Bonnell E, Liang N, Sidhu J, Dupuis L, Seno MMG, Care4Rare Canada Consortium, Chard M, Jobling RK, Cameron J, Chami R, Inbar-Feigenberg M, Wilson MD, Chitayat DA, Boycott KM, Kyriakopoulou L, Mendoza-Londono R, Marshall CR, Dowling JJ, Costain G, Deshwar AR

Genome medicine202512 citationsOpen Access

DOI: 10.1186/s13073-025-01494-w PMID: 40597352

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 reports2025Open Access

DOI: 10.1002/jmd2.70042 PMID: 40901071

Early-Onset Hearing Loss in Leber's Hereditary Optic Neuropathy: A Case Report.

Al Bandari M, Nasr E, Cushing SL, Inbar-Feigenberg M

Ear, nose, & throat journal2025Senior author

DOI: 10.1177/01455613251347923 PMID: 40537415

Evaluation of early treatment with intravenous idursulfase and intrathecal idursulfase-IT on cognitive function in siblings with neuronopathic mucopolysaccharidosis II.

Muenzer J, Burton BK, Harmatz P, Gutiérrez-Solana LG, Ruiz-Garcia M, Jones SA, Guffon N, Inbar-Feigenberg M, Bratkovic D, Rust S, Hale M, Wu Y, Yee KS, Whiteman DAH, Alexanderian D

Journal of inherited metabolic disease2025

DOI: 10.1002/jimd.12790 PMID: 39252529

Family‐centred care interventions for children with chronic conditions: A scoping review

Chow AJ, Saad A, Al‐Baldawi Z, Iverson R, Skidmore B, Jordan I, Pallone N, Smith M, Chakraborty P, Brehaut J

Health Expectations202435 citationsOpen Access

DOI: 10.1111/hex.13897 PMID: W4391512486

Evaluation of the diagnostic accuracy of exome sequencing and its impact on diagnostic thinking for patients with rare disease in a publicly funded health care system: A prospective cohort study

Hartley T, Marshall D, Acker M, Fooks K, Gillespie MK, Price EM, Graham ID, White-Brown A, MacKay L, Macdonald SK

Genetics in Medicine202410 citationsOpen Access

DOI: 10.1016/j.gim.2023.101012

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

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Michal Inbar-Feigenberg

Research

Latest papers

Case Report: Persistent isolated hyperhomocysteinemia in an adolescent with celiac disease and homozygous MTHFR c.665C>T polymorphism: a multifactorial disturbance of one-carbon metabolism.

Intrathecal idursulfase-IT in children younger than 3 years with neuronopathic mucopolysaccharidosis II in a single-arm, open-label, phase 2/3 substudy and extension.

Mitochondrial Complex V Deficiency Caused by a Homozygous Splice Variant in ATP5PO.

Impact of regular physiotherapy intervention on the function and quality of life of pediatric patients diagnosed with Mucopolysaccharidosis.

Clinical applications of and molecular insights from RNA sequencing in a rare disease cohort.

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

Early-Onset Hearing Loss in Leber's Hereditary Optic Neuropathy: A Case Report.

Evaluation of early treatment with intravenous idursulfase and intrathecal idursulfase-IT on cognitive function in siblings with neuronopathic mucopolysaccharidosis II.

Family‐centred care interventions for children with chronic conditions: A scoping review

Evaluation of the diagnostic accuracy of exome sequencing and its impact on diagnostic thinking for patients with rare disease in a publicly funded health care system: A prospective cohort study

Frequent collaborators

Andreas Schulze

Pranesh Chakraborty

John Mitchell

Beth Potter

Roberto Mendoza-Londono

Greg Costain

David Chitayat

Komudi Siriwardena

Cheryl Rockman-Greenberg

Kumanan Wilson

Rosanna Weksberg

Gregory Costain

Jagdeep Walia

Christian Marshall

Robin Hayeems

James Dowling

Julian Little

Murray Alexander Potter

Neal Sondheimer

Yannis Trakadis

Jennifer MacKenzie

Bruno Maranda

Rebekah Jobling

Michal Inbar-Feigenberg

Research

Latest papers

Case Report: Persistent isolated hyperhomocysteinemia in an adolescent with celiac disease and homozygous MTHFR c.665C>T polymorphism: a multifactorial disturbance of one-carbon metabolism.

Intrathecal idursulfase-IT in children younger than 3&#x2009;years with neuronopathic mucopolysaccharidosis II in a single-arm, open-label, phase 2/3 substudy and extension.

Mitochondrial Complex V Deficiency Caused by a Homozygous Splice Variant in ATP5PO.

Impact of regular physiotherapy intervention on the function and quality of life of pediatric patients diagnosed with Mucopolysaccharidosis.

Clinical applications of and molecular insights from RNA sequencing in a rare disease cohort.

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

Early-Onset Hearing Loss in Leber's Hereditary Optic Neuropathy: A Case Report.

Evaluation of early treatment with intravenous idursulfase and intrathecal idursulfase-IT on cognitive function in siblings with neuronopathic mucopolysaccharidosis II.

Family‐centred care interventions for children with chronic conditions: A scoping review

Evaluation of the diagnostic accuracy of exome sequencing and its impact on diagnostic thinking for patients with rare disease in a publicly funded health care system: A prospective cohort study

Frequent collaborators

Andreas Schulze

Pranesh Chakraborty

John Mitchell

Beth Potter

Roberto Mendoza-Londono

Greg Costain

David Chitayat

Komudi Siriwardena

Cheryl Rockman-Greenberg

Kumanan Wilson

Rosanna Weksberg

Gregory Costain

Jagdeep Walia

Christian Marshall

Robin Hayeems

James Dowling

Julian Little

Murray Alexander Potter

Neal Sondheimer

Yannis Trakadis

Jennifer MacKenzie

Bruno Maranda

Rebekah Jobling

Intrathecal idursulfase-IT in children younger than 3 years with neuronopathic mucopolysaccharidosis II in a single-arm, open-label, phase 2/3 substudy and extension.