Concepedia

Alison Foster

AF

Statistics

Publications

16

Citations

1.1K

H-Index

13

Active since

2004

Affiliations

Birmingham Women’s and Children’s NHS Foundation Trust(Current)

St George’s University Hospitals NHS Foundation Trust

Inserm

University of Manchester

Institute of Cancer Research

Alison Foster is an author at Birmingham Women’s and Children’s NHS Foundation Trust specializing in human genetics, molecular genetics, and genetics.

ORCID

Publications per year

2004–2024

16

Publications

16

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

Tarjinder Singh, Mitja Kurki, David Curtis et al. · Nature Neuroscience · 2016 · 476 citations · Full text

, , +14

Poly(A)-specific ribonuclease deficiency impacts telomere biology and causes dyskeratosis congenita

Hemanth Tummala, Amanda J. Walne, Laura C. Collopy et al. · Journal of Clinical Investigation · 2015 · 199 citations · Full text

, , +17

Further delineation of Malan syndrome

Manuela Priolo, Denny Schanze, Katrin Tatton-Brown et al. · Human Mutation · 2018 · 80 citations · Full text

, , +14

<i>CREBBP</i> mutations in individuals without Rubinstein–Taybi syndrome phenotype

Leonie A. Menke, Martine J. van Belzen, Mariëlle Alders et al. · American Journal of Medical Genetics Part A · 2016 · 68 citations · Full text

, , +16

The <i>CHD8</i> overgrowth syndrome: A detailed evaluation of an emerging overgrowth phenotype in 27 patients

Philip J. Ostrowski, Anna Zachariou, Chey Loveday et al. · American Journal of Medical Genetics Part C Seminars in Medical Genetics · 2019 · 53 citations

, , +17

1–5 of 16