Subin K. Choi
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 16 publications
Cancer Variant Interpretation Group UK (CanVIG-UK): updates on an exemplar national subspecialty multidisciplinary network.
Journal: Journal of medical genetics
Published: March 22, 2026
Association of Y-chromosomal gr/gr deletions with testicular germ cell tumor: whole-genome analysis of 198,306 individuals.
Journal: medRxiv : the preprint server for health sciences
Published: February 12, 2026
Routine germline genetic testing in 3552 unselected NHS breast cancer patients: evidence informing testing criteria and implementation of a 'BRCA-DIRECT' mainstreaming pathway.
Journal: NPJ breast cancer
Published: January 27, 2026
Understanding the rationale for metronidazole use in dogs and cats.
Journal: The Journal of small animal practice
Published: April 03, 2025
Meta-analysis of Germline Whole-exome Sequencing in 1435 Cases of Testicular Germ Cell Tumour to Evaluate Disruptive Mutations Under Dominant, Recessive, and X-linked Inheritance Models.
Journal: European urology open science
Published: January 30, 2025
Potent and Selective Human 5-HT2B Serotonin Receptor Antagonists: 4'-Cyano-(N)-methanocarba-adenosines by Synthetic Serendipity.
Journal: Journal of medicinal chemistry
Published: November 26, 2024
Uptake, utility and resource requirements of a genetic counselling telephone helpline within the BRCA-DIRECT digital pathway for mainstreamed BRCA testing in patients with breast cancer.
Journal: Journal of medical genetics
Published: October 08, 2024
BRCA-DIRECT digital pathway for diagnostic germline genetic testing within a UK breast oncology setting: a randomised, non-inferiority trial.
Journal: British journal of cancer
Published: May 10, 2024
A digital pathway for genetic testing in UK NHS patients with cancer: BRCA-DIRECT randomised study internal pilot.
Journal: Journal of medical genetics
Published: April 25, 2022
Reclassification of clinically-detected sequence variants: Framework for genetic clinicians and clinical scientists by CanVIG-UK (Cancer Variant Interpretation Group UK).
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: September 20, 2021
Quantifying prediction of pathogenicity for within-codon concordance (PM5) using 7541 functional classifications of BRCA1 and MSH2 missense variants.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: August 04, 2021
Quantifying evidence toward pathogenicity for rare phenotypes: The case of succinate dehydrogenase genes, SDHB and SDHD.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 26, 2021
Last Updated: 09/26/2026