Browsing Centre for Genomics and Child Health by Author "Rahman, S"
Now showing items 1-3 of 3
-
Influence of autozygosity on common disease risk across the phenotypic spectrum.
Malawsky, DS; van Walree, E; Jacobs, BM; Heng, TH; Huang, QQ; Sabir, AH; Rahman, S; Sharif, SM; Khan, A; Mirkov, MU (2023-09-20)Autozygosity is associated with rare Mendelian disorders and clinically relevant quantitative traits. We investigated associations between the fraction of the genome in runs of homozygosity (FROH) and common diseases in ... -
Phenotype association with filaggrin loss-of-function variants in 349 individuals with eczema from the Tower Hamlets Eczema Assessment (THEA)
Thomas, BR; Tan, XL; Javadzadeh, S; Robinson, EJ; McDonald, BS; Dhoat, S; Krupiczojc, MA; Rahman, SR; Hogan, S; Rahman, S (2021-07) -
Synergy between histone deacetylase inhibitors and DNA-damaging agents is mediated by histone deacetylase 2 in colorectal cancer
Alzoubi, S; Brody, L; Rahman, S; Mahul-Mellier, A-L; Mercado, N; Ito, K; El-Bahrawy, M; Silver, A; Boobis, A; Bell, JD (2016-07-12)