Sunwoo Lee

University of Cambridge — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

7h-index156citations18works0.32yr avg
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Research Topics

Epigenetics and DNA Methylation(7), Genomics and Rare Diseases(5), Genetic Syndromes and Imprinting(5), Histone Deacetylase Inhibitors Research(3), Genomics and Chromatin Dynamics(2)

Publications18 total

Familial pneumothorax in twins with Tatton-Brown-Rahman DNMT3A overgrowth syndrome
European Journal of Human Genetics·2026Open Access
Proteasome Cap Targeting Chimeras for Ubiquitination‐Independent Targeted Protein Degradation
Angewandte Chemie·2026
Proteasome Cap Targeting Chimeras for Ubiquitination‐Independent Targeted Protein Degradation
Angewandte Chemie International Edition·2026
Abstract C031: Disarming colorectal plasticity: Dual HDAC1/2 inhibition reprograms tumor cell fate via H3K27ac-dependent differentiation
Molecular Cancer Therapeutics·2025
Familial NSD1 Exon 3 Deletion Associated with Phenotypic and Epigenetic Variability
Genes·2025Open Access
Germline variants in <i>UHRF1</i> are associated with multilocus imprinting disturbance in humans and mice
Proceedings of the National Academy of Sciences·2025Open Access
Chemical Perturbations Impacting Histone Acetylation Govern Colorectal Cancer Differentiation
Gastroenterology·2025· 2 cited
Differential neuropilin isoform expressions highlight plasticity in macrophages in the heterogenous TME through in-silico profiling
Frontiers in Immunology·2025Open Access
Chemical perturbations impacting histone acetylation govern colorectal cancer differentiation
2024· 1 citedOpen Access
Germline pathogenic variants in HNRNPU are associated with alterations in blood methylome
European Journal of Human Genetics·2023· 17 citedOpen Access
Epigenotype–genotype–phenotype correlations in <i>SETD1A</i> and <i>SETD2</i> chromatin disorders
Human Molecular Genetics·2023· 13 citedOpen Access
Germline pathogenic variants in HNRNPU are associated with alterations in blood methylome
Research Square (Research Square)·2023Open Access
Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach
Clinical Epigenetics·2023· 15 citedOpen Access
Additional file 1 of Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach
Figshare·2023Open Access
Comparison of Methylation Episignatures in <i>KMT2B</i> - and <i>KMT2D</i> -Related Human Disorders
Epigenomics·2022· 20 citedOpen Access
ImprintSeq, a novel tool to interrogate DNA methylation at human imprinted regions and diagnose multilocus imprinting disturbance
Genetics in Medicine·2021· 23 cited
High-Throughput Mechanobiology Screening Platform Using Micro- and Nanotopography
Nano Letters·2016· 50 citedOpen Access
Differential Expression of MicroRNAs in Patients with Glioblastoma after Concomitant Chemoradiotherapy
OMICS A Journal of Integrative Biology·2013· 15 cited

Frequent Co-authors

Eguzkine Ochoa(9), Eamonn R. Maher(9), Fay Rodger(8), France Docquier(8), Ana Luisa Toribio(7), Jose‐Ezequiel Martín(6), Leonardo Bottolo(4), Meena Balasubramanian(4), Graeme M. Clark(3), Pornlada Likasitwatanakul(3), Zhixin Li(3), Khoa Doan(3), Sándor Spisák(3), Qi Liu(3), Priscilla Liow(3), David J. Chen(3), Pratyusha Bala(3), Daulet Aitymbayev(3), Jennifer S. Thalappillil(3), Malvina Papanastasiou(3)