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: Exome Sequence Findings and Bleeding Manifestations for Uncharacterized Platelet Function Disorders with Impaired Aggregation Responses and/or Non‐syndromic Dense Granule Deficiency: Results from the Hamilton Platelet Disorder Study

Researchers

Presenter

  • J. Brunet

Principal Investigators

  • M. Badin

  • M. Chong

  • J. Iyer

  • S. Tasneem

  • L. Graf

  • G.E. Rivard

  • A.D. Paterson

  • G. Pare

  • C. Hayward

Medical Centers

  • McMaster University, Department of Pathology and Molecular Medicine, Hamilton,Canada

  • Centre for Laboratory Medicine and Hemophilia and Hemostasis Centre, St. Gallen, Switzerland

  • Centre Hospitalier Universitaire Sainte Justine, Montreal, QC, Canada

  • The Hospital for Sick Children, Genetics and Genome Biology, Toronto, Canada

  • University of Toronto, The Dalla Lana School of Public Health and Institute of Medical Sciences, Toronto, Canada

  • Pathology and Molecular Medicine, Hamilton, Canada

  • McMaster University, Pathology and Molecular Medicine, and Medicine, Hamilton, Canada

  • Hamilton Regional Laboratory Medicine Program, Hamilton, ON, Canada

Locations

  • Canada

  • Switzerland

Companies

  • N/A

Study Components

Therapeutic Area

  • N/A

Disease

  • N/A

Biomarkers

  • ETV6-RUNX1

  • Fli-1 proto-oncogene, ETS transcription factor

Drug/Treatment

  • N/A

Outcome

  • N/A

Study Design

  • Cohort

Phase

  • NA

Study Id's

  • N/A

Sponsors

  • N/A

Result

  • N/A

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