Khalda Amr

Identification of a Frameshift Mutation in Osterix in a Patient with Recessive Osteogenesis Imperfecta

Pablo Lapunzina, Mona Aglan, Samia A. Temtamy et al. · The American Journal of Human Genetics · 2010 · 283 citations · Full text

Bone Disease, Recessive Osteogenesis Imperfecta, Developmental Biology +7

LRP4 Mutations Alter Wnt/β-Catenin Signaling and Cause Limb and Kidney Malformations in Cenani-Lenz Syndrome

Yun Li, Barbara Pawlik, Nursel Elçioğlu et al. · The American Journal of Human Genetics · 2010 · 163 citations · Full text

A novel homozygous missense mutation of the leptin gene (N103K) in an obese Egyptian patient

Inas Mazen, Mona El Gammal, Mohamed S. Abdel‐Hamid et al. · Molecular Genetics and Metabolism · 2009 · 114 citations

Obesity, Metabolic Syndrome, Obese Egyptian Patient +10

Early diagnostic evaluation of miR-122 and miR-224 as biomarkers for hepatocellular carcinoma

Khalda Amr, Hanan Abd Elmawgoud Atia, Rehab Abd Elazeem Elbnhawy et al. · Genes & Diseases · 2017 · 96 citations · Full text

Mutations in PLOD2 cause autosomal-recessive connective tissue disorders within the Bruck syndrome-Osteogenesis imperfecta phenotypic spectrum

Maria Trinidad Puig-Hervás, Samia A. Temtamy, Mona Aglan et al. · Human Mutation · 2012 · 95 citations