Pouria Mashouri

University Health Network — Canada

Biochemistry, Genetics and Molecular Biology · Life Sciences

10h-index632citations19works5.72yr avg
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Research Topics

Genomics and Rare Diseases(5), Artificial Intelligence in Healthcare and Education(4), Surgical Simulation and Training(3), COVID-19 Clinical Research Studies(2), Asthma and respiratory diseases(2)

Publications19 total

Predicting Surgical Versus Nonsurgical Management of Acute Isolated Distal Radius Fractures in Patients Under Age 60 Using a Convolutional Neural Network
The Journal Of Hand Surgery·2025· 3 citedOpen Access
645P The utility and limitations of artificial intelligence in diagnosing rare disorders
Neuromuscular Disorders·2024
Development, deployment and scaling of operating room-ready artificial intelligence for real-time surgical decision support
npj Digital Medicine·2024· 14 citedOpen Access
What is the educational value and clinical utility of artificial intelligence for intraoperative and postoperative video analysis? A survey of surgeons and trainees
Surgical Endoscopy·2023· 17 cited
Use of artificial intelligence for decision-support to avoid high-risk behaviors during laparoscopic cholecystectomy
Surgical Endoscopy·2023· 12 cited
Genomics4RD: An integrated platform to share Canadian deep-phenotype and multiomic data for international rare disease gene discovery.
PubMed·2022· 17 citedOpen Access
Assessment of Machine Learning–Based Medical Directives to Expedite Care in Pediatric Emergency Medicine
JAMA Network Open·2022· 35 citedOpen Access
Prospective observational study and serosurvey of SARS-CoV-2 infection in asymptomatic healthcare workers at a Canadian tertiary care center
PLoS ONE·2021· 18 citedOpen Access
Achieving Clinical Automation in Emergency Medicine with Machine Learning Medical Directives
SSRN Electronic Journal·2021· 1 citedOpen Access
Prospective Observational Study of Screening Asymptomatic Healthcare Workers for SARS-CoV-2 at a Canadian Tertiary Care Center
2020· 7 citedOpen Access
EpigenCentral: Portal for DNA methylation data analysis and classification in rare diseases
Human Mutation·2020· 31 cited
Correction: Phenotate: crowdsourcing phenotype annotations as exercises in undergraduate classes
Genetics in Medicine·2020Open Access
Phenotate: crowdsourcing phenotype annotations as exercises in undergraduate classes
Genetics in Medicine·2020· 6 citedOpen Access
Quality Indicators as Predictors of Future Inspection Performance in Ontario Nursing Homes
Journal of the American Medical Directors Association·2019· 14 cited
Extract and component‐specific sensitization patterns in Canadian moderate‐to‐severe preschool asthmatics
Allergy·2019· 8 cited
Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease
The American Journal of Human Genetics·2019· 214 citedOpen Access
Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease
The American Journal of Human Genetics·2019· 235 citedOpen Access
Characterization Of Allergen Sensitization Patterns In Canadian Preschool Children With Severe Wheezing
Journal of Allergy and Clinical Immunology·2019Open Access
NEXT GENERATION SEQUENCING AND EXPERIMENTAL MYOLOGY
Neuromuscular Disorders·2018

Frequent Co-authors

Michael Brudno(15), Arun Ramani(6), Hao Chi Zhang(4), Amin Madani(4), Hernán Gonorazky(3), Sergey Naumenko(3), Mark A. Tarnopolsky(3), Caterina Masino(3), Sergey Protserov(3), Viswateja Nelakuditi(2), Peiqui Wang(2), Dennis Kao(2), Krish Ohri(2), Senthuri Viththiyapaskaran(2), Katherine D. Mathews(2), Steven A. Moore(2), Andres Nascimiento Osorio(2), David Villanova(2), Dwi U. Kemaladewi(2), Ronald D. Cohn(2)