Sunwoo L. Lee
Cambridge, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 8 publications
Familial pneumothorax in twins with Tatton-Brown-Rahman DNMT3A overgrowth syndrome.
Journal: European journal of human genetics : EJHG
Published: September 26, 2025
Familial NSD1 Exon 3 Deletion Associated with Phenotypic and Epigenetic Variability.
Journal: Genes
Published: August 06, 2025
Differential neuropilin isoform expressions highlight plasticity in macrophages in the heterogenous TME through in-silico profiling.
Journal: Frontiers in immunology
Published: December 18, 2024
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
ImprintSeq, a novel tool to interrogate DNA methylation at human imprinted regions and diagnose multilocus imprinting disturbance.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 19, 2021
Showing 1-8 of 8
Last Updated: 09/26/2026