Malcom A Taylor

7PUBLICATIONS
78CO-AUTHORS
Cell and nuclear divisionInfant and child healthEpigenetics (incl. genome methylation and epigenomics)Anthropological genetics
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Publications (7)

|May 14, 2025
Inherited deficiency of DIAPH1 identifies a DNA double strand break repair pathway regulated by γ-actin.

Beth L Woodward, Sudipta Lahiri, Anoop S Chauhan

|Jun 25, 2024
ATM germ line pathogenic variants affect outcomes in children with ataxia-telangiectasia and hematological malignancies.

Sarah Elitzur, Ruth Shiloh, Jan L C Loeffen

|Nov 05, 2022
Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy.

Laura J Grange, John J Reynolds, Farid Ullah

|Dec 01, 2021
Biallelic Mutation of SETX and Additional Likely "In Cis" SETX Sequence Change in Ataxia with Oculomotor Apraxia Type 2.

Michael D Perry, Martin J Evans, Philip J Byrd

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Frequent Collaborators

3 joint publications

Grant S Stewart

2 joint publications

Ferran Nadeu

2 joint publications

Holger Heyn

2 joint publications

Satpal S Jhujh