Amal Rayan

Mutations in a Novel Isoform of TRIOBP That Encodes a Filamentous-Actin Binding Protein Are Responsible for DFNB28 Recessive Nonsyndromic Hearing Loss

Hashem Shahin, Tom Walsh, Tama Sobe et al. · The American Journal of Human Genetics · 2005 · 124 citations · Full text

Medicine, Molecular Biology, Molecular Genetics +8

Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population

Tom Walsh, Amal Rayan, Judeh Abu Sa’ed et al. · Human Genomics · 2006 · 56 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Nonsense mutation of the stereociliar membrane protein gene <i>PTPRQ</i> in human hearing loss <i>DFNB84</i>: Figure 1

Hashem Shahin, M. Rahil, Amal Rayan et al. · Journal of Medical Genetics · 2010 · 46 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Circulating microparticles and activated platelets as novel prognostic biomarkers in COVID-19; relation to cancer

Asmaa M. Zahran, Omnia El‐Badawy, Wageeh A. Ali et al. · PLoS ONE · 2021 · 35 citations · Full text

Medicine, Hematology, Oncology +17

Up-regulation of regulatory T cells, CD200 and TIM3 expression in cytogenetically normal acute myeloid leukemia

Asmaa M. Zahran, Mostafa Saleh, Mona M. Sayed et al. · Cancer Biomarkers · 2018 · 31 citations · Full text

Life Sciences, Hematology, Immunology +17