Faculty profile

Philip Awadalla

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 and email address may be missing. Find their university profile.

Philip Awadalla

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.
2 publications in the last five years, latest in 2026.
Principal investigator on 1 research grant (1 CIHR), most recently in 2019.

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

Publications

Citations

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Collaborators

Grants

Publications by year

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

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Signals and details

Research

Comparative Effectiveness And Safety Confounding Bias Exposure Measurement Errors Pharmacoepidemiology Prospective Studies Statistical Modelling

Latest papers

Genetic dissection of stool frequency implicates vitamin B1 metabolism and other actionable pathways in the modulation of gut motility.
Gut · 2026
Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin
Journal of the American Society of Nephrology · 2022
Effect of Cognitive Reserve on the Association of Vascular Brain Injury With Cognition
Neurology · 2021

All 23 publications

Latest funding

Enhancing CAN-AIM capacity to respond to drug safety and effectiveness queries
CIHR · 2019 · Principal investigator
$2,550,000
Air pollution and systemic autoimmune rheumatic diseases
CIHR · 2018 · Co-investigator
$772,650
Depression as a risk factor for type 2 diabetes: role of metabolic factors
CIHR · 2013 · Co-investigator
$334,770

All 3 grants and awards

23 publications.

Genetic dissection of stool frequency implicates vitamin B1 metabolism and other actionable pathways in the modulation of gut motility.

Díaz-Muñoz C, Bozzarelli I, Lopera-Maya EA, Belbasis L, Lo Faro V, Camargo Tavares L, Heredia-Fernández F, Di Lorenzo B, Sinha T, Esteban Blanco C, Favé MJ, Awadalla P, Walters RG, Bonfiglio F, Zhernakova A, Sanna S, D'Amato M

Gut2026

DOI: 10.1136/gutjnl-2025-337059 PMID: 41558814

Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin

Joseph CB, Mariniello M, Yoshifuji A, Schiano G, Lake J, Marten J, Richmond A, Huffman JE, Campbell A, Harris SE

Journal of the American Society of Nephrology202233 citations

DOI: 10.1681/asn.2021040491

Effect of Cognitive Reserve on the Association of Vascular Brain Injury With Cognition

Durrani R, Friedrich MG, Schulze KM, Awadalla P, Balasubramanian K, Black SE, Broet P, Busseuil D, Desai D, Dummer T

Neurology202132 citations

DOI: 10.1212/wnl.0000000000012765

Gene-by-environment interactions in urban populations modulate risk phenotypes.

Favé MJ, Lamaze FC, Soave D, Hodgkinson A, Gauvin H, Bruat V, Grenier JC, Gbeha E, Skead K, Smargiassi A, Johnson M, Idaghdour Y, Awadalla P

Nature communications2018Senior author

DOI: 10.1038/s41467-018-03202-2 PMID: 29511166

Clinical, Genetic, and Urinary Factors Associated with Uromodulin Excretion.

Troyanov S, Delmas-Frenette C, Bollée G, Youhanna S, Bruat V, Awadalla P, Devuyst O, Madore F

Clinical journal of the American Society of Nephrology : CJASN2016

DOI: 10.2215/cjn.04770415 PMID: 26683887

Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis.

Leblond CS, Gan-Or Z, Spiegelman D, Laurent SB, Szuto A, Hodgkinson A, Dionne-Laporte A, Provencher P, de Carvalho M, Orrù S, Brunet D, Bouchard JP, Awadalla P, Dupré N, Dion PA, Rouleau GA

Neurobiology of aging2016

DOI: 10.1016/j.neurobiolaging.2015.09.013 PMID: 26493020

Aortic Dilatation Associated With a De Novo Mutation in the SOX18 Gene: Expanding the Clinical Spectrum of Hypotrichosis-Lymphedema-Telangiectasia Syndrome.

Wünnemann F, Kokta V, Leclerc S, Thibeault M, McCuaig C, Hatami A, Stheneur C, Grenier JC, Awadalla P, Mitchell GA, Andelfinger G, Preuss C

The Canadian journal of cardiology2016

DOI: 10.1016/j.cjca.2015.04.004 PMID: 26148450

A haplotype-based normalization technique for the analysis and detection of allele specific expression.

Hodgkinson A, Grenier JC, Gbeha E, Awadalla P

BMC bioinformatics2016Senior author

DOI: 10.1186/s12859-016-1238-8 PMID: 27618913

Impact of the X Chromosome and sex on regulatory variation.

Kukurba KR, Parsana P, Balliu B, Smith KS, Zappala Z, Knowles DA, Favé MJ, Davis JR, Li X, Zhu X, Potash JB, Weissman MM, Shi J, Kundaje A, Levinson DF, Awadalla P, Mostafavi S, Battle A, Montgomery SB

Genome research2016

DOI: 10.1101/gr.197897.115 PMID: 27197214

Gain-of-function missense variant in SLC12A2, encoding the bumetanide-sensitive NKCC1 cotransporter, identified in human schizophrenia.

Merner ND, Mercado A, Khanna AR, Hodgkinson A, Bruat V, Awadalla P, Gamba G, Rouleau GA, Kahle KT

Journal of psychiatric research2016

DOI: 10.1016/j.jpsychires.2016.02.016 PMID: 26955005

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Philip Awadalla

Research

Latest papers

Latest funding

Genetic dissection of stool frequency implicates vitamin B1 metabolism and other actionable pathways in the modulation of gut motility.

Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin

Effect of Cognitive Reserve on the Association of Vascular Brain Injury With Cognition

Gene-by-environment interactions in urban populations modulate risk phenotypes.

Clinical, Genetic, and Urinary Factors Associated with Uromodulin Excretion.

Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis.

Aortic Dilatation Associated With a De Novo Mutation in&#xa0;the&#xa0;SOX18 Gene: Expanding the Clinical Spectrum of&#xa0;Hypotrichosis-Lymphedema-Telangiectasia Syndrome.

A haplotype-based normalization technique for the analysis and detection of allele specific expression.

Impact of the X Chromosome and sex on regulatory variation.

Gain-of-function missense variant in SLC12A2, encoding the bumetanide-sensitive NKCC1 cotransporter, identified in human schizophrenia.

Enhancing CAN-AIM capacity to respond to drug safety and effectiveness queries

Air pollution and systemic autoimmune rheumatic diseases

Depression as a risk factor for type 2 diabetes: role of metabolic factors

Frequent collaborators

Philip Awadalla

Philip Awadalla

Julie Hussin

Gregor Andelfinger

Trevor Dummer

Daniel Sinnett

Paul Poirier

David Conen

Michael Noseworthy

Ridha Joober

Elie Haddad

Paul Poirier

Jean-Claude Tardif

Pierre Drapeau

Jean-Claude Tardif

Bartha Knoppers

Jean-Claude Tardif

Laurent Mottron

Pavel Hamet

Grace Parraga

Michel Joffres

Salim Yusuf

Jonathon Leipsic

Audrey Smargiassi

Aortic Dilatation Associated With a De Novo Mutation in the SOX18 Gene: Expanding the Clinical Spectrum of Hypotrichosis-Lymphedema-Telangiectasia Syndrome.