Ioannis Kafetzopoulos

Cambridge, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 10 publications

Scaling and self-similarity in the formation of the embryonic epigenome.

Scaling and self-similarity in the formation of the embryonic epigenome.

Journal: Nature physics

Published: July 23, 2025

DNMT1 loss leads to hypermethylation of a subset of late replicating domains by DNMT3A.

DNMT1 loss leads to hypermethylation of a subset of late replicating domains by DNMT3A.

Journal: PLoS genetics

Published: May 22, 2025

Using CRISPR barcoding as a molecular clock to capture dynamic processes at single-cell resolution.

Using CRISPR barcoding as a molecular clock to capture dynamic processes at single-cell resolution.

Journal: Genome research

Published: May 12, 2025

Replication-associated mechanisms contribute to an increased CpG > TpG mutation burden in mismatch repair-deficient cancers.

Replication-associated mechanisms contribute to an increased CpG > TpG mutation burden in mismatch repair-deficient cancers.

Journal: Genome medicine

Published: February 26, 2025

Epigenetic priming of mammalian embryonic enhancer elements coordinates developmental gene networks.

Epigenetic priming of mammalian embryonic enhancer elements coordinates developmental gene networks.

Journal: Genome biology

Published: September 10, 2024

Author Correction: Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.

Author Correction: Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.

Journal: Nature communications

Published: June 28, 2023

Genome-wide single-molecule analysis of long-read DNA methylation reveals heterogeneous patterns at heterochromatin that reflect nucleosome organisation.

Genome-wide single-molecule analysis of long-read DNA methylation reveals heterogeneous patterns at heterochromatin that reflect nucleosome organisation.

Journal: PLoS genetics

Published: May 01, 2023

DNMT3B PWWP mutations cause hypermethylation of heterochromatin.

DNMT3B PWWP mutations cause hypermethylation of heterochromatin.

Journal: EMBO reports

Published: April 18, 2023

Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.

Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.

Journal: Nature communications

Published: November 20, 2022

De novo DNA methyltransferase activity in colorectal cancer is directed towards H3K36me3 marked CpG islands.

De novo DNA methyltransferase activity in colorectal cancer is directed towards H3K36me3 marked CpG islands.

Journal: Nature communications

Published: September 03, 2019

Showing 1-10 of 10

Last Updated: 09/26/2026