Ebtesam Qasem

Riyadh, 11211, Saudi Arabia

Last Updated: 09/26/2026

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Found 17 publications

A Unique Genotype of Pseudohypoaldosteronism Type 1b in a Highly Consanguineous Population.

A Unique Genotype of Pseudohypoaldosteronism Type 1b in a Highly Consanguineous Population.

Journal: Journal of the Endocrine Society

Published: July 14, 2021

Analysis of ALK, IDH1, IDH2 and MMP8 somatic mutations in differentiated thyroid cancers.

Analysis of ALK, IDH1, IDH2 and MMP8 somatic mutations in differentiated thyroid cancers.

Journal: Molecular and clinical oncology

Published: March 11, 2020

Correction to: Absence of EIF1AX, PPM1D, and CHEK2 mutations reported in Thyroid Cancer Genome Atlas (TCGA) in a large series of thyroid cancer.

Correction to: Absence of EIF1AX, PPM1D, and CHEK2 mutations reported in Thyroid Cancer Genome Atlas (TCGA) in a large series of thyroid cancer.

Journal: Endocrine

Published: June 27, 2019

GPCR-mediated PI3K pathway mutations in pediatric and adult thyroid cancer.

GPCR-mediated PI3K pathway mutations in pediatric and adult thyroid cancer.

Journal: Oncotarget

Published: February 21, 2019

Lung Metastasis in Pediatric Thyroid Cancer: Radiological Pattern, Molecular Genetics, Response to Therapy, and Outcome.

Lung Metastasis in Pediatric Thyroid Cancer: Radiological Pattern, Molecular Genetics, Response to Therapy, and Outcome.

Journal: The Journal of clinical endocrinology and metabolism

Published: August 09, 2018

Absence of EIF1AX, PPM1D, and CHEK2 mutations reported in Thyroid Cancer Genome Atlas (TCGA) in a large series of thyroid cancer.

Absence of EIF1AX, PPM1D, and CHEK2 mutations reported in Thyroid Cancer Genome Atlas (TCGA) in a large series of thyroid cancer.

Journal: Endocrine

Published: June 08, 2018

Molecular genetics and phenotype/genotype correlation of 5-α reductase deficiency in a highly consanguineous population.

Molecular genetics and phenotype/genotype correlation of 5-α reductase deficiency in a highly consanguineous population.

Journal: Endocrine

Published: June 08, 2018

Mutational analysis of rare subtypes of congenital adrenal hyperplasia in a highly inbred population.

Mutational analysis of rare subtypes of congenital adrenal hyperplasia in a highly inbred population.

Journal: Molecular and cellular endocrinology

Published: July 14, 2017

A high rate of novel CYP11B1 mutations in Saudi Arabia.

A high rate of novel CYP11B1 mutations in Saudi Arabia.

Journal: The Journal of steroid biochemistry and molecular biology

Published: July 05, 2017

Single Point Mutations in Pediatric Differentiated Thyroid Cancer.

Single Point Mutations in Pediatric Differentiated Thyroid Cancer.

Journal: Thyroid : official journal of the American Thyroid Association

Published: November 09, 2016

Classical V600E and other non-hotspot BRAF mutations in adult differentiated thyroid cancer.

Classical V600E and other non-hotspot BRAF mutations in adult differentiated thyroid cancer.

Journal: Journal of translational medicine

Published: April 29, 2016

HABP2 Gene Mutations Do Not Cause Familial or Sporadic Non-Medullary Thyroid Cancer in a Highly Inbred Middle Eastern Population.

HABP2 Gene Mutations Do Not Cause Familial or Sporadic Non-Medullary Thyroid Cancer in a Highly Inbred Middle Eastern Population.

Journal: Thyroid : official journal of the American Thyroid Association

Published: February 25, 2016

Showing 1-12 of 17

Last Updated: 09/26/2026