Faculty profile

Frank Rauch

ResearcherMcGill University

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

Frank Rauch

Researcher

Health Sciences

McGill University

Montreal, Quebec, Canada

Supervision signals

Has led research grants, which requires an independent research appointment. Ask their department whether they supervise graduate students.
63 publications in the last five years, latest in 2026.
Senior (last) author on 21 recent papers, a sign of leading a research group.
Principal investigator on 4 research grants (4 CIHR), most recently in 2022.

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

237

Publications

686

Citations

h-index

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

Osteogenesis Imperfecta Bone Mechanical Forces Osteocytes Genetic Disorders Glucose Insulin Metabolism

Latest papers

Factors Associated With Functional Mobility in 256 Children With Arthrogryposis Multiplex Congenita: A Multicentric Cross-Sectional Study.
Archives of physical medicine and rehabilitation · 2026
Arthrogryposis With CNS Involvement in AFF3-Related KINSSHIP Syndrome: A Detailed Phenotypic Characterization From a Mexican Patient and Review of the Literature.
American journal of medical genetics. Part A · 2026 · senior author
Osteocalcin-dependent and -independent metabolic dysregulation in a mouse model of Osteogenesis imperfecta.
Bone research · 2026

All 237 publications

Latest funding

Mechano-adaptation in Osteogenesis Imperfecta
CIHR · 2022 · Principal investigator
$868,276
Osteocalcin-driven metabolic changes in osteogenesis imperfecta
CIHR · 2016 · Principal investigator
$696,150
Novel functional outcomes of vitamin D in infancy; can correction of low vitamin D status program for a leaner body composition phenotype?
CIHR · 2015 · Co-investigator
$1,015,521

All 7 grants and awards

From the 150 most recent of 237 publications.

Factors Associated With Functional Mobility in 256 Children With Arthrogryposis Multiplex Congenita: A Multicentric Cross-Sectional Study.

Zidan A, Snider L, Rampakakis E, Hamdy R, Rauch F, Hyer LC, Manske MCB, Altiok H, Freese K, Mielke C, Nossov SB, Tavukcu S, Giampietro PF, Dahan-Oliel N

Archives of physical medicine and rehabilitation2026

DOI: 10.1016/j.apmr.2025.12.014 PMID: 41475428

Arthrogryposis With CNS Involvement in AFF3-Related KINSSHIP Syndrome: A Detailed Phenotypic Characterization From a Mexican Patient and Review of the Literature.

Ordaz-Robles T, Ramírez-García D, Dahan-Oliel N, Tavukcu S, Giampietro PF, Ríos-Ruíz JG, Cárdenas-Conejo A, Gustafson AG, Bardai G, Rauch F

American journal of medical genetics. Part A2026Senior author

DOI: 10.1002/ajmg.a.70257 PMID: 42499216

Osteocalcin-dependent and -independent metabolic dysregulation in a mouse model of Osteogenesis imperfecta.

Tauer JT, Rauch F, Ferron M, Komarova SV

Bone research2026

DOI: 10.1038/s41413-026-00553-1 PMID: 42463636

The Muscle-Bone Unit in Children and Adolescents: Insights from the Canadian Health Measures Survey.

Li O, Ward LM, Griffith LE, Anderson LN, Wong AKO, Adachi JD, Ma J, Rauch F

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2026Senior author

DOI: 10.1093/jbmr/zjag143 PMID: 42789064

Two Novel ACTC1 Variants Cause Arthrogryposis Multiplex Congenita.

Kerr L, Moffatt P, Hyer L, Nossov S, Dahan-Oliel N, Rauch F

Clinical genetics2026Senior author

DOI: 10.1111/cge.70218 PMID: 42458772

Psychometric properties of functional mobility outcome measures in children with arthrogryposis multiplex congenita.

Zidan A, Snider L, Rampakakis E, Hamdy R, Rauch F, Dahan-Oliel N

Developmental medicine and child neurology2026

DOI: 10.1111/dmcn.70036 PMID: 41124586

Mindful Self-Compassion to Reduce Pain Interference Among Adults with Osteogenesis Imperfecta.

Sediqi A, Al-Khalili R, Dover S, Peeters C, Khalif A, Sutton VR, Rauch F, Lee B, Storch EA, Robinson ME

Journal of clinical psychology in medical settings2026

DOI: 10.1007/s10880-025-10092-2 PMID: 40813548

Bone microstructural and strength changes over 1 year in children with osteogenesis imperfecta are comparable to age- and sex-matched healthy controls.

Hosseinitabatabaei S, McCluskey S, Denton C, Zimmermann EA, Glorieux FH, Charbonneau F, Rauch F, Willie BM

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2026

DOI: 10.1093/jbmr/zjaf112 PMID: 41045134

A Novel Splice Variant in ERGIC1 Causes Arthrogryposis Multiplex Congenita-Characterization Using Urine-Derived Cells.

Kerr L, McKay P, Marulanda J, Wu Z, Hamdy R, Tavukcu S, Dahan-Oliel N, Rauch F

American journal of medical genetics. Part C, Seminars in medical genetics2026Senior author

DOI: 10.1002/ajmg.c.70012 PMID: 42140882

Characterisation of Urine-Derived Cells for the Molecular Diagnosis of Rare Disorders.

Ludwig K, Wu Z, Bardai G, Marulanda J, Munns CF, Moffatt P, Rauch F

International journal of molecular sciences2026Senior author

DOI: 10.3390/ijms27072929 PMID: 41977117

Mechano-adaptation in Osteogenesis Imperfecta

Principal investigatorCIHR2022Project Grant

Principal investigators: Willie, Bettina M; Rauch, Frank

Keywords: Bone; Mechanical Forces; Osteocytes; Osteogenesis Imperfecta

$868,276

Osteocalcin-driven metabolic changes in osteogenesis imperfecta

Principal investigatorCIHR2016Project Grant

Principal investigators: Komarova, Svetlana V; Rauch, Frank

Keywords: Genetic Disorders; Glucose; Insulin; Metabolism; Osteocalcin; Osteoclast; Osteogenesis Imperfecta

$696,150

Novel functional outcomes of vitamin D in infancy; can correction of low vitamin D status program for a leaner body composition phenotype?

Co-investigatorCIHR2015Operating Grant

Principal investigators: Weiler, Hope A

Keywords: Adiposity; Bone Mass; Epigenetic Mechanisms; Infant; Lean Body Composition; Low Vitamin D Status; Programming; Rodent Epigenetic Validation; Trial

$1,015,521

The role of BRIL in the pathogenesis of osteogenesis imperfecta type V.

Co-investigatorCIHR2014Operating Grant

Principal investigators: Moffatt, Pierre

Keywords: Bone Physiology/Pathology; Cell Biology; Cell Culture; Micro Computed Tomography; Molecular Biology; Osteogenesis Imperfecta; Pcr; Transgenic/Knockin Mouse Models; Western Blotting

$549,170

Muscle-bone interactions in Canadians: a national, population-based study

Nominated PICIHR2014Operating Grant

Principal investigators: Rauch, Frank; Ward, Leanne M

Keywords: Bone Metabolism; Mechanography; Muscle Function; Osteoporosis; Peripheral Quantitative Computed Tomography; Population-Based

$1,334,440

The role of BRIL in the pathogenesis of osteogenesis imperfecta type V.

Co-investigatorCIHR2013Operating Grant - PA: Musculoskeletal Health, Arthritis, Skin and Oral Health

Principal investigators: Moffatt, Pierre

Keywords: Bone Physiology/Pathology; Cell Biology; Cell Culture; Micro Computed Tomography; Molecular Biology; Osteogenesis Imperfecta; Pcr; Transgenic/Knockin Mouse Models; Western Blotting

$100,000

The Role of Pigment Epithelium Derived Factor During Skeletal Development

Nominated PICIHR2011Operating Grant - PA: Musculoskeletal Health, Arthritis, Skin and Oral Health

Principal investigators: Rauch, Frank

Keywords: Biomineralization; Bone Development; Bone Histomorphometry; Bone Remodeling; Knock-Out Mouse

$100,000

From CIHR, NSERC and SSHRC funding decisions: CIHR since 2008, NSERC since 1991 and SSHRC since 1998, including their latest published competition results.

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Frank Rauch

Research

Latest papers

Latest funding

Factors Associated With Functional Mobility in 256 Children With Arthrogryposis Multiplex Congenita: A Multicentric Cross-Sectional Study.

Arthrogryposis With CNS Involvement in AFF3-Related KINSSHIP Syndrome: A Detailed Phenotypic Characterization From a Mexican Patient and Review of the Literature.

Osteocalcin-dependent and -independent metabolic dysregulation in a mouse model of Osteogenesis imperfecta.

The Muscle-Bone Unit in Children and Adolescents: Insights from the Canadian Health Measures Survey.

Two Novel ACTC1 Variants Cause Arthrogryposis Multiplex Congenita.

Psychometric properties of functional mobility outcome measures in children with arthrogryposis multiplex congenita.

Mindful Self-Compassion to Reduce Pain Interference Among Adults with Osteogenesis Imperfecta.

Bone microstructural and strength changes over 1&#xa0;year in children with osteogenesis imperfecta are comparable to age- and sex-matched healthy controls.

A Novel Splice Variant in ERGIC1 Causes Arthrogryposis Multiplex Congenita-Characterization Using Urine-Derived Cells.

Characterisation of Urine-Derived Cells for the Molecular Diagnosis of Rare Disorders.

Mechano-adaptation in Osteogenesis Imperfecta

Osteocalcin-driven metabolic changes in osteogenesis imperfecta

Novel functional outcomes of vitamin D in infancy; can correction of low vitamin D status program for a leaner body composition phenotype?

The role of BRIL in the pathogenesis of osteogenesis imperfecta type V.

Muscle-bone interactions in Canadians: a national, population-based study

The role of BRIL in the pathogenesis of osteogenesis imperfecta type V.

The Role of Pigment Epithelium Derived Factor During Skeletal Development

Frequent collaborators

Pierre Moffatt

Louis-Nicolas Veilleux

Jinhui Ma

Reggie Hamdy

Peter Roughley

Argerie Tsimicalis

Celia Rodd

Stephanie Atkinson

Jacek Majewski

Margaret Larche

Josephine Ho

Faleh Tamimi

Ronald Duncan Barr

Jean Ouellet

Noémi Dahan-Oliel

Christophe Bedos

Jonathan Derrick Adachi

Christophe Bedos

Johannes Roth

Sasha Carsen

Monzur Murshed

Craig Coblentz

Adam Huber

Victor Lewis

Daniel Sinnett

Nagwa Wilson

Shahrokh Esfandiari

David Moher

Glenville Jones

Alexandra Papaioannou

Sylvie Le May

Andrew Howard

Despoina Manousaki

Jacob Jaremko

Dora Liu

Frank Rauch

Alfredo Ribeiro-Da-Silva

Lauren Griffith

Waleed Kishta

Jennifer Stinson

Bone microstructural and strength changes over 1 year in children with osteogenesis imperfecta are comparable to age- and sex-matched healthy controls.