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Genetics

D-Index
45
Citations
7036
World Ranking
4230
National Ranking
157

Overview

Peter K. Rogan is affiliated with the University of Western Ontario in Canada, contributing extensively to research at the intersection of medicine, biochemistry, genetics, and molecular biology. Their work spans multiple specialized fields including molecular biology, radiology, nuclear medicine and imaging, pulmonary and respiratory medicine, epidemiology, and mechanical engineering.

The scientist has contributed significantly to topics such as mineral processing and grinding, radioactivity and radon measurements, data-driven disease surveillance, radiation therapy and dosimetry, gene expression and cancer classification, lung cancer treatments and mutations, and DNA repair mechanisms.

Recent scholarly publications authored or co-authored by Peter K. Rogan include:

  • "Collaborative, Multidisciplinary Evaluation of Cancer Variants Through Virtual Molecular Tumor Boards Informs Local Clinical Practices" (2020) in JCO Clinical Cancer Informatics
  • "Expression Changes Confirm Genomic Variants Predicted to Result in Allele-Specific, Alternative mRNA Splicing" (2020) in Frontiers in Genetics
  • "Gene expression for biodosimetry and effect prediction purposes: promises, pitfalls and future directions - key session ConRad 2021" (2021) in International Journal of Radiation Biology
  • "Estimating partial-body ionizing radiation exposure by automated cytogenetic biodosimetry" (2020) in International Journal of Radiation Biology
  • "Pathway-extended gene expression signatures integrate novel biomarkers that improve predictions of patient responses to kinase inhibitors" (2020) in MedComm

Peter K. Rogan has frequently collaborated with several researchers, including:

  • Eliseos J. Mucaki
  • Ben C. Shirley
  • Joan H.M. Knoll
  • Ruipeng Lu
  • EJ Mucaki

The scientist often publishes in venues such as Zenodo (CERN European Organization for Nuclear Research), Faculty Opinions - Post-Publication Peer Review of the Biomedical Literature, bioRxiv (Cold Spring Harbor Laboratory), F1000Research, and the International Journal of Radiation Biology, with multiple papers appearing in each of these outlets.

Best Publications

  • Hepatic CYP2B6 expression: gender and ethnic differences and relationship to CYP2B6 genotype and CAR (constitutive androstane receptor) expression.

    Vishal Lamba;Jatinder Lamba;Kazuto Yasuda;Stephen Strom

  • Imprinting-Mutation Mechanisms in Prader-Willi Syndrome

    T. Ohta;T. A. Gray;P. K. Rogan;K. Buiting

  • Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints.

    James M. Amos-Landgraf;Yonggang Ji;Wayne Gottlieb;Theresa Depinet

  • The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis.

    Maria J. Mascari;Wayne Gottlieb;Peter K. Rogan;Merlin G. Butler

  • Information analysis of human splice site mutations.

    Peter K. Rogan;Brian M. Faux;Thomas D. Schneider

  • Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.

    Shinji Saitoh;Karin Buiting;Peter K. Rogan;Jessica L. Buxton

  • Automated splicing mutation analysis by information theory.

    Vijay K. Nalla;Peter K. Rogan

  • Autosomal dominant zonular cataract with sutural opacities is associated with a splice mutation in the betaA3/A1-crystallin gene.

    Kannabiran C;Rogan Pk;Olmos L;Basti S

  • Predicting responses to platin chemotherapy agents with biochemically-inspired machine learning.

    Eliseos J. Mucaki;Jonathan Z. L. Zhao;Daniel J. Lizotte;Peter K. Rogan

  • Nondisjunction of human acrocentric chromosomes : studies of 432 trisomic fetuses and liveborns

    Michael V. Zaragoza;Patricia A. Jacobs;Rowena S. James;Peter Rogan

  • Mutations that alter RNA splicing of the human HPRT gene: a review of the spectrum.

    J.Patrick O'Neill;Peter K Rogan;Neal Cariello;Janice A Nicklas

  • Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation.

    Shinji Saitoh;Karin Buiting;Suzanne B. Cassidy;Jeffrey M. Conroy

  • Method for rapid identification of prokaryotic and eukaryotic organisms

    Peter K. Rogan

  • Interpretation of mRNA splicing mutations in genetic disease: review of the literature and guidelines for information-theoretical analysis.

    Natasha G. Caminsky;Eliseos J. Mucaki;Peter K. Rogan

  • Genomic signatures for paclitaxel and gemcitabine resistance in breast cancer derived by machine learning

    Stephanie N. Dorman;Katherina Baranova;Joan H.M. Knoll;Joan H.M. Knoll;Brad L. Urquhart

  • FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor

    Paolo Peterlongo;Irene Catucci;Mara Colombo;Laura Caleca

  • Human SP-A locus: allele frequencies and linkage disequilibrium between the two surfactant protein A genes.

    Joanna Floros;Susan DiAngelo;Michael Koptides;Anne M. Karinch

  • Information theory-based analysis of CYP2C19, CYP2D6 and CYP3A5 splicing mutations.

    Peter K Rogan;Stan Svojanovsky;J Steven Leeder

  • Bloom syndrome and maternal uniparental disomy for chromosome 15

    Trevor Woodage;Madhuri Prasad;Joanne W. Dixon;Roslyn E. Selby

  • Organization of the ABCR gene: analysis of promoter and splice junction sequences

    Rando Allikmets;Wyeth W. Wasserman;Amy Hutchinson;Philip Smallwood

Frequent Co-Authors

Robert D. Nicholls
Robert D. Nicholls University of Pittsburgh
Bernhard Horsthemke
Bernhard Horsthemke University of Duisburg-Essen
Jeffrey S. Hoch
Jeffrey S. Hoch University of California, Davis
Paolo Radice
Paolo Radice Fondazione IRCCS Istituto Nazionale dei Tumori
Joanna Floros
Joanna Floros Pennsylvania State University
J. Steven Leeder
J. Steven Leeder Children's Mercy Hospital
Stuart Schwartz
Stuart Schwartz LabCorp (United States)
Michael Dean
Michael Dean National Institutes of Health
Fergus J. Couch
Fergus J. Couch Mayo Clinic

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