Treena Cranston
Oxford, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 35 publications
Multiple endocrine neoplasia type 1 syndrome due to novel Alu insertion.
Journal: Cancer genetics
Published: June 18, 2025
EMQN best practice guidelines for analysis and reporting of microsatellite instability in solid tumours.
Journal: European journal of human genetics : EJHG
Published: December 16, 2024
Secondary (additional) findings from the 100,000 Genomes Project: Disease manifestation, health care outcomes, and costs of disclosure.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: July 13, 2023
GNA11 Variants Identified in Patients with Hypercalcemia or Hypocalcemia.
Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: January 18, 2023
Corrigendum to 'Multiple endocrine neoplasia type 1 in children and adolescents: Clinical features and treatment outcomes' [Surgery 171 (2021) 77-87].
Journal: Surgery
Published: April 16, 2022
UK recommendations for SDHA germline genetic testing and surveillance in clinical practice.
Journal: Journal of medical genetics
Published: November 22, 2021
Spectrum of germline AIRE mutations causing APS-1 and familial hypoparathyroidism.
Journal: European journal of endocrinology
Published: September 12, 2021
Multiple Endocrine Neoplasia Type 1 (MEN1) Phenocopy Due to a Cell Cycle Division 73 (CDC73) Variant.
Journal: Journal of the Endocrine Society
Published: August 21, 2020
Multiple Endocrine Neoplasia Type 1 (MEN1) 5'UTR Deletion, in MEN1 Family, Decreases Menin Expression.
Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: March 04, 2020
Cancer Variant Interpretation Group UK (CanVIG-UK): an exemplar national subspecialty multidisciplinary network.
Journal: Journal of medical genetics
Published: December 04, 2019
Last Updated: 09/26/2026