Caralyn R. Reisle
Vancouver, BC, Canada
Last Updated: 09/26/2026
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Found 18 publications
Evaluating Language Models for Biomedical Fact-Checking: A Benchmark Dataset for Cancer Variant Interpretation Verification.
Journal: bioRxiv : the preprint server for biology
Published: September 26, 2025
Uncovering the complexity of structural variants in four individuals with autism spectrum disorder.
Journal: Genome
Published: December 12, 2024
CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase.
Journal: Nucleic acids research
Published: September 01, 2022
Whole-genome and transcriptome analysis enhances precision cancer treatment options.
Journal: Annals of oncology : official journal of the European Society for Medical Oncology
Published: December 02, 2021
A platform for oncogenomic reporting and interpretation.
Journal: Nature communications
Published: September 08, 2021
Uncovering Clinically Relevant Gene Fusions with Integrated Genomic and Transcriptomic Profiling of Metastatic Cancers.
Journal: Clinical cancer research : an official journal of the American Association for Cancer Research
Published: May 17, 2020
Improved structural variant interpretation for hereditary cancer susceptibility using long-read sequencing.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: January 07, 2020
Therapeutic Implication of Genomic Landscape of Adult Metastatic Sarcoma.
Journal: JCO precision oncology
Published: December 01, 2019
Base excision repair deficiency signatures implicate germline and somatic MUTYH aberrations in pancreatic ductal adenocarcinoma and breast cancer oncogenesis.
Journal: Cold Spring Harbor molecular case studies
Published: November 15, 2018
Temporal Dynamics of Genomic Alterations in a BRCA1 Germline-Mutated Pancreatic Cancer With Low Genomic Instability Burden but Exceptional Response to Fluorouracil, Oxaliplatin, Leucovorin, and Irinotecan.
Journal: JCO precision oncology
Published: October 19, 2018
Corrigendum: Genomic profiling of pelvic genital type leiomyosarcoma in a woman with a germline CHEK2:c.1100delC mutation and a concomitant diagnosis of metastatic invasive ductal breast carcinoma.
Journal: Cold Spring Harbor molecular case studies
Published: August 03, 2018
Last Updated: 09/26/2026