World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
66
Citations
14208
World Ranking
2630
National Ranking
88

Overview

Peter N. Ray is affiliated with the University of Toronto in Canada and has contributed to research primarily within the fields of Medicine and Social Sciences. Their scholarly work spans several interconnected subfields, including Public Health, Environmental and Occupational Health, Gender Studies, Pulmonary and Respiratory Medicine, Genetics, and Emergency Medical Services.

The scientist's research covers a range of topics, with a focus on Diversity and Career in Medicine, Medical Education and Admissions, Innovations in Medical Education, Cystic Fibrosis Research Advances, Tracheal and airway disorders, Neurogenetic and Muscular Disorders Research, and Global Health Workforce Issues.

Peter N. Ray has authored several recent papers, including:

  • Navigating the American Board of Surgery In-Training Examination (ABSITE) Success: Insights From Pre-assessment Practices in Preparing Surgical Residents for Competitive Sub-specialties, 2024, Cureus
  • Whole-Exome Sequencing and Targeted Copy Number Analysis in Primary Ciliary Dyskinesia, 2020, UNC Libraries
  • A Comparative American Board of Surgery In-Training Examination (ABSITE) Performance Analysis Between International vs. Domestic Graduates and Doctor of Medicine (MD) vs. Doctor of Osteopathic Medicine (DO) Medical Degrees, 2024, Cureus

Their work is frequently published in venues such as Cureus and UNC Libraries. Peter N. Ray's collaborative efforts include frequent co-authors:

  • Armein Rahimpour
  • Missy Morrison
  • David Denning
  • Paul Bown
  • Rahman Barry

This profile reflects a multidisciplinary approach that encompasses clinical, educational, and public health perspectives. The scientist's research interest in medical education and career diversity indicates a focus on factors influencing healthcare workforce development and the academic progression of medical professionals.

Overall, Peter N. Ray's academic contributions integrate various specialized topics in medicine with social science dimensions, addressing both scientific and systemic aspects of healthcare delivery and education.

Best Publications

  • The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle

    Elizabeth E. Zubrzycka-Gaarn;Dennis E. Bulman;George Karpati;Arthur H. M. Burghes

  • Identification of Proximal Spinal Muscular Atrophy Carriers and Patients by Analysis of SMNT and SMNC Gene Copy Number

    P.E. McAndrew;D.W. Parsons;L.R. Simard;C. Rochette

  • Whole-genome sequencing of quartet families with autism spectrum disorder

    Ryan K C Yuen;Bhooma Thiruvahindrapuram;Daniele Merico;Susan Walker

  • Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test.

    Anath C Lionel;Gregory Costain;Nasim Monfared;Susan Walker

  • Subgroup-Specific Prognostic Implications of TP53 Mutation in Medulloblastoma

    Nataliya Zhukova;Vijay Ramaswamy;Marc Remke;Elke Pfaff

  • Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy.

    Peter N. Ray;Bonnie Belfall;Catherine Duff;Cairine Logan

  • Whole-genome sequencing expands diagnostic utility and improves clinical management in paediatric medicine

    Dimitri J. Stavropoulos;Daniele Merico;Rebekah Jobling;Sarah Bowdin

  • Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy

    S. B. Malhotra;K. A. Hart;H. J. Klamut;N. S. T. Thomas

  • A cDNA clone from the Duchenne/Becker muscular dystrophy gene

    Arthur H. M. Burghes;Cairine Logan;Xiuyuan Hu;Bonnie Belfall

  • A novel dystrophin isoform is required for normal retinal electrophysiology

    Vinita N. D'Souza;Nguyen thi Man;Glenn E. Morris;Wolfram Karges

  • Duplicational mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin, and phenotypegenotype correlation.

    Xiuyuang Hu;P. N. Ray;E. G. Murphy;M. W. Thompson

  • BRAF mutation and CDKN2A deletion define a clinically distinct subgroup of childhood secondary high-grade glioma

    Matthew Mistry;Matthew Mistry;Nataliya Zhukova;Daniele Merico;Patricia Rakopoulos

  • Tumor development in the Beckwith–Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1

    Rosanna Weksberg;Joy Nishikawa;Oana Caluseriu;Yan-Ling Fei

  • Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene.

    E. F. Gillard;J. S. Chamberlain;E. G. Murphy;C. L. Duff

  • PhenoTips: patient phenotyping software for clinical and research use.

    Marta Girdea;Sergiu Dumitriu;Marc Fiume;Sarah Bowdin

  • Universal Poor Survival in Children With Medulloblastoma Harboring Somatic TP53 Mutations

    Uri Tabori;Berivan Baskin;Mary Shago;Noa Alon

  • Dystrophin expression in the human retina is required for normal function as defined by electroretinography

    De Ann M. Pillers;Dennis E. Bulman;Richard G. Weleber;Dayle A. Sigesmund

  • TP53 Alterations Determine Clinical Subgroups and Survival of Patients With Choroid Plexus Tumors

    Uri Tabori;Adam Shlien;Berivan Baskin;Sarah Levitt

  • Recurrent focal copy-number changes and loss of heterozygosity implicate two noncoding RNAs and one tumor suppressor gene at chromosome 3q13.31 in osteosarcoma.

    Ivan Pasic;Adam Shlien;Adam D. Durbin;Dimitrios J. Stavropoulos

  • Human ribosomal RNA genes: orientation of the tandem array and conservation of the 5' end.

    Ronald G. Worton;Joanne Sutherland;James E. Sylvester;Huntington F. Willard

Frequent Co-Authors

Christian R. Marshall
Christian R. Marshall University of Toronto
Stephen W. Scherer
Stephen W. Scherer University of Toronto
Rosanna Weksberg
Rosanna Weksberg University of Toronto
Dennis E. Bulman
Dennis E. Bulman Children's Hospital of Eastern Ontario
David Chitayat
David Chitayat University of Toronto
Cynthia Hawkins
Cynthia Hawkins University of Toronto
Arthur H.M. Burghes
Arthur H.M. Burghes The Ohio State University
Uri Tabori
Uri Tabori University of Toronto
Daniele Merico
Daniele Merico University of Toronto
Eric Bouffet
Eric Bouffet University of Toronto

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