Fay Rodger
Cambridge, ENG CB20QQ, United Kingdom
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 10 publications
Germline variants in UHRF1 are associated with multilocus imprinting disturbance in humans and mice.
Germline variants in UHRF1 are associated with multilocus imprinting disturbance in humans and mice.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: August 18, 2025
Familial NSD1 Exon 3 Deletion Associated with Phenotypic and Epigenetic Variability.
Journal: Genes
Published: August 06, 2025
Germline pathogenic variants in HNRNPU are associated with alterations in blood methylome.
Journal: European journal of human genetics : EJHG
Published: March 03, 2023
Epigenotype-genotype-phenotype correlations in SETD1A and SETD2 chromatin disorders.
Journal: Human molecular genetics
Published: February 16, 2023
Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach.
Journal: Clinical epigenetics
Published: January 28, 2023
Comparison of methylation episignatures in KMT2B- and KMT2D-related human disorders.
Journal: Epigenomics
Published: May 04, 2022
SDHC epi-mutation testing in gastrointestinal stromal tumours and related tumours in clinical practice.
Journal: Scientific reports
Published: March 18, 2019
Clinical and Molecular Features of Renal and Pheochromocytoma/Paraganglioma Tumor Association Syndrome (RAPTAS): Case Series and Literature Review.
Journal: The Journal of clinical endocrinology and metabolism
Published: March 03, 2017
Profiling of somatic mutations in phaeochromocytoma and paraganglioma by targeted next generation sequencing analysis.
Journal: International journal of endocrinology
Published: June 27, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026