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Malcom A Taylor

7PUBLICATIONS

78CO-AUTHORS

Cell and nuclear divisionInfant and child healthEpigenetics (incl. genome methylation and epigenomics)Anthropological geneticsHaematological tumours

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Publications (7)

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|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

|Dec 05, 2022

Correction: ATM germline variants in a young adult with chronic lymphocytic leukemia: 8 years of genomic evolution.

Romina Royo, Laura Magnano, Julio Delgado

|Nov 05, 2022

Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy.

Laura J Grange, John J Reynolds, Farid Ullah

|Jun 07, 2022

ATM germline variants in a young adult with chronic lymphocytic leukemia: 8 years of genomic evolution.

Romina Royo, Laura Magnano, Julio Delgado

|Dec 01, 2021

Biallelic Mutation of <i>SETX</i> and Additional Likely "In Cis" <i>SETX</i> 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

2 joint publications

Elías Campo

2 joint publications

Xose S Puente

2 joint publications

Laura Magnano

2 joint publications

Christopher G Mathew

2 joint publications

Michael A Simpson

1 joint publications

Thomas L Clarke

Frequent Collaborators

3 joint publications

Grant S Stewart

2 joint publications

Ferran Nadeu

2 joint publications

Holger Heyn

2 joint publications

Satpal S Jhujh

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