H Hindi-Al
Riyadh, Saudi Arabia
Last Updated: 09/26/2026
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Found 39 publications
LncRNA GAS8-AS1 is downregulated, correlates with early-stage disease and lymph node metastasis, and its knockdown promotes proliferation, migration, and invasion in differentiated thyroid cancer.
Journal: Frontiers in endocrinology
Published: March 25, 2026
Genome-wide methylation and copy number variation analysis of medulloblastoma in a Saudi Arabian pediatric population.
Journal: Annals of medicine and surgery (2012)
Published: March 14, 2025
LncRNA GAS8-AS1 dinucleotide genetic variantn.713A>G, n.714T>C is associated with early-stage disease, lymph node, and distant metastasis in differentiated thyroid cancer.
Journal: Endocrine
Published: January 31, 2024
EPAS1-related pheochromocytoma/paraganglioma.
Journal: Endocrine-related cancer
Published: October 04, 2023
Expanding the phenotypic and genotypic spectrum of GGPS1 related congenital muscular dystrophy.
Journal: American journal of medical genetics. Part A
Published: August 07, 2023
An aggressive cabergoline-resistant, temozolomide-responsive macroprolactinoma due to a germline SDHB pathogenic variant in the absence of paraganglioma or pheochromocytoma.
Journal: Frontiers in endocrinology
Published: August 05, 2023
Molecular Genetics of Diffuse Sclerosing Papillary Thyroid Cancer.
Journal: The Journal of clinical endocrinology and metabolism
Published: December 30, 2022
A molecular study of pediatric pilomyxoid and pilocytic astrocytomas: Genome-wide copy number screening, retrospective analysis of clinicopathological features and long-term clinical outcome.
Journal: Frontiers in oncology
Published: September 01, 2022
Thyroid Cancer, Neuroendocrine Tumor, Adrenal Adenoma, and Other Tumors in a Patient With a Germline PMS1 Mutation.
Journal: Journal of the Endocrine Society
Published: July 26, 2022
Clinicopathologic and genomic characterizations of brain metastases using a comprehensive genomic panel.
Journal: Frontiers in medicine
Published: May 18, 2022
A Unique Mechanism of a Novel Synonymous PHEX Variant Causing X-Linked Hypophosphatemia.
Journal: The Journal of clinical endocrinology and metabolism
Published: May 08, 2022
Fumarate Hydratase is a Novel Gene for Familial Non-Medullary Thyroid Cancer.
Journal: The Journal of clinical endocrinology and metabolism
Published: April 26, 2022
Last Updated: 09/26/2026