Huda A. BinEssa - Concepedia

Author

Huda A. BinEssa

King Faisal Specialist Hospital & Research Centre

Also Known As

H A Binessa, Huda A BinEssa, Huda A. BinEssa, Huda BinEssa

Publications

380

Citations

H-Index

Concepts

All Affiliations

King Faisal Specialist Hospital & Research Centre National Cancer Institute National Institutes of Health University of Leicester Alfaisal University

About

Huda A. BinEssa is an author at King Faisal Specialist Hospital & Research Centre specializing in medicine, molecular genetics, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	137
2	Natural Sciences	1	1	31
3	Biology	1	1	31
4	Cell Biology	1	1	57
5	Molecular Biology	1	1	31

Huda A. BinEssa

Publications

357

Citations

H-Index

Page 1

	Year	Citations
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, The Journal of Clinical Endocrinology & Metabolism	2018	76
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, Oncogene OncologyBrafv600e-induced SenescenceMedicineP53 ExpressionPapillary Thyroid Cancer	2015	57
Novel CYP27B1 Gene Mutations in Patients with Vitamin D-Dependent Rickets Type 1A Korcan Demir, Walaa E. Kattan, Minjing Zou, PLoS ONE Mendelian DisorderGenetic DisorderMedicineGeneticsInherited Metabolic Disease	2015	49
Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3 Sezer Acar, Huda A. BinEssa, Korcan Demir, PLoS ONE	2018	33
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, Bone BiologyGenetic DisorderSplice-site MutationsGeneticsNatural Sciences	2019	31
Mutational analysis of <i>PHEX</i>,<i> FGF23</i> and <i>CLCN5</i> in patients with hypophosphataemic rickets Ayla Güven, Roua A. Al‐Rijjal, Huda A. BinEssa, Clinical Endocrinology	2017	29
<i>Cyp24a1</i> Attenuation Limits Progression of <i>BrafV600E</i> -Induced Papillary Thyroid Cancer Cells and Sensitizes Them to BRAFV600E Inhibitor PLX4720 Minjing Zou, Essa Y. Baitei, Huda A. BinEssa, Cancer Research	2017	20
Mutation of SGK3, a Novel Regulator of Renal Phosphate Transport, Causes Autosomal Dominant Hypophosphatemic Rickets Ayşe Cebeci, Minjing Zou, Huda A. BinEssa, The Journal of Clinical Endocrinology & Metabolism	2019	15
Mutation spectrum of EXT1 and EXT2 in the Saudi patients with hereditary multiple exostoses Zayed Al‐Zayed, Roua A. Al‐Rijjal, Lamya Al-Ghofaili, Orphanet Journal of Rare Diseases	2021	14
KRAS-mediated oncogenic transformation of thyroid follicular cells requires long-term TSH stimulation and is regulated by SPRY1 Minjing Zou, Essa Y. Baitei, Roua A. Al‐Rijjal, Laboratory Investigation	2015	13

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