Publications by authors named "Fay Rodger"

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Familial Exon 3 Deletion Associated with Phenotypic and Epigenetic Variability.
Sunwoo Liv Lee, Alison Foster, Dalit May, Ciara Batterton, Eguzkine Ochoa, Fay Rodger

Genes (Basel)· October 2025

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Germline variants in are associated with multilocus imprinting disturbance in humans and mice.
Eguzkine Ochoa, Ilona Zvetkova, Sunwoo Liv Lee, Nozomi Takahashi, Benoit Lan-Leung, Fay Rodger

Proc Natl Acad Sci U S A· August 2025

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Epigenotype-genotype-phenotype correlations in SETD1A and SETD2 chromatin disorders.
Sunwoo Lee, Lara Menzies, Eleanor Hay, Eguzkine Ochoa, France Docquier, Fay Rodger

Hum Mol Genet· November 2023

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Germline pathogenic variants in HNRNPU are associated with alterations in blood methylome.
Sunwoo Lee, Eguzkine Ochoa, Magdalena Badura-Stronka, Deirdre Donnelly, Damien Lederer, Fay Rodger

Eur J Hum Genet· September 2023

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Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach.
Larissa Bilo, Eguzkine Ochoa, Sunwoo Lee, Daniela Dey, Ingo Kurth, Fay Rodger

Clin Epigenetics· March 2023

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Investigating the role of somatic sequencing platforms for phaeochromocytoma and paraganglioma in a large UK cohort.
Bettina Winzeler, Nicola Tufton, Eugenie S Lim, Ben G Challis, Soo-Mi Park, Fay Rodger

Clin Endocrinol (Oxf)· October 2022

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Comparison of methylation episignatures in - and -related human disorders.
Sunwoo Lee, Eguzkine Ochoa, Katy Barwick, Laura Cif, Fay Rodger

Epigenomics· May 2022

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SDHC epi-mutation testing in gastrointestinal stromal tumours and related tumours in clinical practice.
Ruth T Casey, Rogier Ten Hoopen, Eguzkine Ochoa, Benjamin G Challis, James Whitworth, Fay Rodger

Sci Rep· July 2019

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Clinical and Molecular Features of Renal and Pheochromocytoma/Paraganglioma Tumor Association Syndrome (RAPTAS): Case Series and Literature Review.
Ruth T Casey, Anne Y Warren, Jose Ezequiel Martin, Benjamin G Challis, Eleanor Rattenberry, Fay Rodger

J Clin Endocrinol Metab· November 2017

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Profiling of somatic mutations in phaeochromocytoma and paraganglioma by targeted next generation sequencing analysis.
Andrea Luchetti, Diana Walsh, Fay Rodger, Graeme Clark, Tom Martin

Int J Endocrinol· April 2015

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