Faculty profile

Geoff Hicks

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ProfessorUniversity of Manitoba

Geoff Hicks

Professor

Max Rady College of Medicine

University of Manitoba

Winnipeg, Manitoba, Canada

Supervision signals

Professors usually supervise graduate students in their department's programs.
6 publications in the last five years, latest in 2025.
Senior (last) author on 4 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

5,714

Citations

Collaborators

Publications by year

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

Profiles and links

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Signals and details

Research

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

Latest papers

Barriers and enablers to evidence-based practice for the initial management of women with early pregnancy bleeding in the Emergency Department
International Emergency Nursing · 2025
Risk and Resilience Variants in the Retinoic Acid Metabolic and Developmental Pathways Associated with Risk of FASD Outcomes.
Biomolecules · 2024 · senior author
Genetically programmed retinoic acid deficiency during gastrulation phenocopies most known developmental defects due to acute prenatal alcohol exposure in FASD
Frontiers in Cell and Developmental Biology · 2023 · senior author

All 78 publications

78 publications.

Barriers and enablers to evidence-based practice for the initial management of women with early pregnancy bleeding in the Emergency Department

Baylie Trostian, Kate Anne Curtis, Sameer Dikshit, Simon Binks, Anne Smith, Belinda Munroe, Geoffrey G. Hicks, Andrea McCloughen

International Emergency Nursing20252 citationsOpen Access

DOI: 10.1016/j.ienj.2025.101693 PMID: 41106240

Risk and Resilience Variants in the Retinoic Acid Metabolic and Developmental Pathways Associated with Risk of FASD Outcomes.

McKay L, Petrelli B, Pind M, Reynolds JN, Wintle RF, Chudley AE, Drögemöller B, Fainsod A, Scherer SW, Hanlon-Dearman A, Hicks GG

Biomolecules20243 citationsSenior authorOpen Access

DOI: 10.3390/biom14050569 PMID: 38785976

Genetically programmed retinoic acid deficiency during gastrulation phenocopies most known developmental defects due to acute prenatal alcohol exposure in FASD

Berardino Petrelli, Ahmet Öztürk, Molly Pind, Henok Tadesse Ayele, Abraham Fainsod, Geoffrey G. Hicks

Frontiers in Cell and Developmental Biology20236 citationsSenior authorOpen Access

DOI: 10.3389/fcell.2023.1208279 PMID: 37397253

Genetic, Epigenetic, and Environmental Influences on Fetal Alcohol Spectrum Disorder: Implications for Diagnosis, Research and Clinical Practice

Alexandre A. Lussier, Berardino Petrelli, Geoffrey G. Hicks, Joanne Weinberg

20232 citations

DOI: 10.1007/978-3-031-20792-1_28

Genetics of FASD: Confounding Rare Craniofacial and Neurodevelopmental Disorders May Identify Ethanol-Sensitizing Genetic Variants of FASD

Leo McKay, Berardino Petrelli, Albert E. Chudley, Geoffrey G. Hicks

Neuromethods20223 citationsSenior author

DOI: 10.1007/978-1-0716-2613-9_5

Dental Signatures as a Potential Biomarker of FASD

Berardino Petrelli, Noriko B. Boorberg, Geoffrey G. Hicks

Neuromethods20222 citationsSenior author

DOI: 10.1007/978-1-0716-2613-9_12

A novel, ataxic mouse model of ataxia telangiectasia caused by a clinically relevant nonsense mutation

H. Daniel Perez, May F. Abdallah, Jose I Chavira, Angelina S Norris, Martin T. Egeland, Karen L. Vo, Callan L Buechsenschuetz, Valentina Sanghez, Jeannie L Kim, Molly Pind, Kotoka Nakamura, Geoffrey G. Hicks, Richard A. Gatti, Joaquı́n Madrenas, Michelina Iacovino, Peter J. McKinnon, Paul J. Mathews

eLife202130 citationsOpen Access

DOI: 10.7554/elife.64695 PMID: 34723800

Budget Impact Analysis of an Epigenetic Test Used for Diagnosing Fetal Alcohol Spectrum Disorder from the Perspective of a Laboratory Budget Holder in Manitoba, Canada

Patrick Berrigan, Geoffrey G. Hicks, Wendy J. Ungar, Jennifer D. Zwicker

PharmacoEconomics - Open20211 citationsOpen Access

DOI: 10.1007/s41669-021-00304-4 PMID: 34628597

Author response: A novel, ataxic mouse model of ataxia telangiectasia caused by a clinically relevant nonsense mutation

2021Open Access

DOI: 10.7554/elife.64695.sa2

The Canadian Rare Diseases Models and Mechanisms (RDMM) Network: Connecting Understudied Genes to Model Organisms.

Boycott KM, Campeau PM, Howley HE, Pavlidis P, Rogic S, Oriel C, Berman JN, Hamilton RM, Hicks GG, Lipshitz HD, Masson JY, Shoubridge EA, Junker A, Leroux MR, McMaster CR, Michaud JL, Turvey SE, Dyment D, Innes AM, van Karnebeek CD, Lehman A, Cohn RD, MacDonald IM, Rachubinski RA, Frosk P, Vandersteen A, Wozniak RW, Pena IA, Wen XY, Lacaze-Masmonteil T, Rankin C, Hieter P

American journal of human genetics202051 citationsOpen Access

DOI: 10.1016/j.ajhg.2020.01.009 PMID: 32032513

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

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Geoff Hicks

Research

Latest papers

Barriers and enablers to evidence-based practice for the initial management of women with early pregnancy bleeding in the Emergency Department

Risk and Resilience Variants in the Retinoic Acid Metabolic and Developmental Pathways Associated with Risk of FASD Outcomes.

Genetically programmed retinoic acid deficiency during gastrulation phenocopies most known developmental defects due to acute prenatal alcohol exposure in FASD

Genetic, Epigenetic, and Environmental Influences on Fetal Alcohol Spectrum Disorder: Implications for Diagnosis, Research and Clinical Practice

Genetics of FASD: Confounding Rare Craniofacial and Neurodevelopmental Disorders May Identify Ethanol-Sensitizing Genetic Variants of FASD

Dental Signatures as a Potential Biomarker of FASD

A novel, ataxic mouse model of ataxia telangiectasia caused by a clinically relevant nonsense mutation

Budget Impact Analysis of an Epigenetic Test Used for Diagnosing Fetal Alcohol Spectrum Disorder from the Perspective of a Laboratory Budget Holder in Manitoba, Canada

Author response: A novel, ataxic mouse model of ataxia telangiectasia caused by a clinically relevant nonsense mutation

The Canadian Rare Diseases Models and Mechanisms (RDMM) Network: Connecting Understudied Genes to Model Organisms.

Frequent collaborators

Janet Rossant

Michael Mowat

Andras Nagy

Sean Egan

Joaquin Madrenas

William Stanford

Barry Rosen

Kym Boycott

Christopher McMaster

James Reynolds

Elizabeth Simpson

Jiuyong Xie

Ana Hanlon-Dearman

Stephen Scherer

Sabine Mai

Christian Marshall

Wendy Ungar

Stuart Turvey

Paul Pavlidis

Mojgan Rastegar

Eric Shoubridge