Personal profile
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
-
SDG 3 Good Health and Well-being
Fingerprint
- 1 Similar Profiles
Collaborations and top research areas from the last five years
-
Inherited deficiency of DIAPH1 identifies a DNA double strand break repair pathway regulated by γ-actin
Woodward, B. L., Lahiri, S., Chauhan, A. S., Garcia, M. R., Goodley, L. E., Clarke, T. L., Pal, M., Agathanggelou, A., Jhujh, S. S., Ganesh, A. N., Hollins, F. M., Deforie, V. G., Maroofian, R., Efthymiou, S., Meinhardt, A., Mathew, C. G., Simpson, M. A., Mefford, H. C., Faqeih, E. A. & Rosenzweig, S. D. & 16 others, , Dec 2025, In: Nature Communications. 16, 1, 20 p., 4491.Research output: Contribution to journal › Article › peer-review
Open AccessFile59 Downloads (Pure) -
ATM germ line pathogenic variants affect outcomes in children with ataxia-telangiectasia and hematological malignancies
Elitzur, S., Shiloh, R., Loeffen, J. L. C., Pastorczak, A., Takagi, M., Bomken, S., Baruchel, A., Lehrnbecher, T., Tasian, S. K., Abla, O., Arad-Cohen, N., Astigarraga, I., Ben-Harosh, M., Bodmer, N., Brozou, T., Ceppi, F., Chugaeva, L., Dalla Pozza, L., Ducassou, S. & Escherich, G. & 33 others, , 12 Sept 2024, In: Blood. 144, 11, p. 1193-1205Research output: Contribution to journal › Article › peer-review
Open AccessFile40 Downloads (Pure) -
Genome-scale clustered regularly interspaced short palindromic repeats screen identifies nucleotide metabolism as an actionable therapeutic vulnerability in diffuse large B-cell lymphoma
Davies, N., Francis, T., Oldreive, C., Azam, M., Wilson, J., Byrd, P. J., Burley, M., Sharma-Oates, A., Keane, P., Alatawi, S., Higgs, M. R., Rudzki, Z., Ibrahim, M., Perry, T., Agathanggelou, A., Hewitt, A. M., Smith, E., Bonifer, C., O’Connor, M. & Forment, J. V. & 8 others, , Dec 2024, In: Haematologica. 109, 12, p. 3989-4006 18 p.Research output: Contribution to journal › Article › peer-review
Open AccessFile36 Downloads (Pure) -
Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly
Serey-Gaut, M., Cortes, M., Makrythanasis, P., Suri, M., Taylor, A. M. R., Sullivan, J. A., Asleh, A. N., Mitra, J., Dar, M. A., McNamara, A., Shashi, V., Dugan, S., Song, X., Rosenfeld, J. A., Cabrol, C., Iwaszkiewicz, J., Zoete, V., Pehlivan, D., Akdemir, Z. C. & Roeder, E. R. & 29 others, , 2 Mar 2023, In: American Journal of Human Genetics. 110, 3, p. 499-515 17 p.Research output: Contribution to journal › Article › peer-review
-
Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy
Grange, L. J., Reynolds, J. J., Ullah, F., Isidor, B., Shearer, R. F., Latypova, X., Baxley, R. M., Oliver, A. W., Ganesh, A., Cooke, S. L., Jhujh, S. S., McNee, G. S., Hollingworth, R., Higgs, M. R., Natsume, T., Khan, T., Martos-Moreno, G. Á., Chupp, S., Mathew, C. G. & Parry, D. & 28 others, , 4 Nov 2022, In: Nature Communications. 13, 1, 6664.Research output: Contribution to journal › Article › peer-review
Open AccessFile58 Downloads (Pure)
-
RNaseH2 inactivation in cancer cells: a pathogenic mechanism and therapeutic target
Stankovic, T. (Principal Investigator), Moss, P. (Co-Investigator), Stewart, G. (Co-Investigator) & Taylor, M. (Co-Investigator)
1/01/20 → 31/12/26
Project: Research
-
Survey of cancer in ataxia telangiectasia patients in the UK
Davies, N. (Co-Investigator) & Taylor, M. (Principal Investigator)
1/03/21 → 28/02/23
Project: Research
-
Defining novel targeted strategies for treating ATM deficient lymphomas using a new Atm null murine model that faithfully recapitulates the tumour spectrum observed in A-T patients
Stewart, G. (Co-Investigator), Stankovic, T. (Co-Investigator) & Taylor, M. (Principal Investigator)
15/01/18 → 14/01/20
Project: Research
-
Birmingham ECMC
Beggs, A. (Co-Investigator), Moss, P. (Co-Investigator), Kearns, P. (Co-Investigator), Craddock, C. (Co-Investigator), Nankivell, P. (Co-Investigator), Willcox, B. (Co-Investigator), Morton, D. (Co-Investigator), Middleton, G. (Principal Investigator), Khoja, L. (Researcher), Drayson, M. (Co-Investigator), Tomlinson, I. (Co-Investigator), Steven, N. (Co-Investigator), Taylor, M. (Co-Investigator), Watts, C. (Co-Investigator) & Mehanna, H. (Co-Investigator)
1/04/17 → 31/03/23
Project: Research
-
Investigating the pathogenic impact of mutations in C21 or F60 as the genetic cause of a novel developmental disorder in children
Taylor, M. (Co-Investigator) & Stewart, G. (Principal Investigator)
BIRMINGHAM CHILDRENS HOSPITAL RESEARCH FOUNDATION
4/01/16 → 3/01/20
Project: Research