Huda A. BinEssa

Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid Dyshormonogenesis

Minjing Zou, Ali S. Alzahrani, Ali Al‐Odaib et al. · The Journal of Clinical Endocrinology & Metabolism · 2018 · 76 citations · Full text

TSH overcomes BrafV600E-induced senescence to promote tumor progression via downregulation of p53 expression in papillary thyroid cancer

Minjing Zou, Essa Y. Baitei, Roua A. Al‐Rijjal et al. · Oncogene · 2015 · 57 citations · Full text

Oncology, Brafv600e-induced Senescence, Medicine +10

Novel CYP27B1 Gene Mutations in Patients with Vitamin D-Dependent Rickets Type 1A

Korcan Demir, Walaa E. Kattan, Minjing Zou et al. · PLoS ONE · 2015 · 49 citations · Full text

Mendelian Disorder, Genetic Disorder, Medicine +12

Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3

Sezer Acar, Huda A. BinEssa, Korcan Demir et al. · PLoS ONE · 2018 · 33 citations · Full text

Functional analysis of 22 splice-site mutations in the PHEX, the causative gene in X-linked dominant hypophosphatemic rickets

Huda A. BinEssa, Minjing Zou, Anwar F Al-Enezi et al. · Bone · 2019 · 31 citations

Biology, Genetic Disorder, Splice-site Mutations +9