Nada Alsahan

Riyadh, Saudi Arabia

Last Updated: 09/26/2026

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Found 16 publications

A Novel Uterus-Sparing Technique for Placenta Accreta Spectrum (PAS), at a Tertiary Center.

A Novel Uterus-Sparing Technique for Placenta Accreta Spectrum (PAS), at a Tertiary Center.

Journal: Obstetrics and gynecology international

Published: May 13, 2025

Missense Variants in GFRA1 and NPNT Are Associated with Congenital Anomalies of the Kidney and Urinary Tract.

Missense Variants in GFRA1 and NPNT Are Associated with Congenital Anomalies of the Kidney and Urinary Tract.

Journal: Genes

Published: August 06, 2022

A null founder variant in NPNT, encoding nephronectin, causes autosomal recessive renal agenesis.

A null founder variant in NPNT, encoding nephronectin, causes autosomal recessive renal agenesis.

Journal: Clinical genetics

Published: December 16, 2021

Prenatal exome sequencing and chromosomal microarray analysis in fetal structural anomalies in a highly consanguineous population reveals a propensity of ciliopathy genes causing multisystem phenotypes.

Prenatal exome sequencing and chromosomal microarray analysis in fetal structural anomalies in a highly consanguineous population reveals a propensity of ciliopathy genes causing multisystem phenotypes.

Journal: Human genetics

Published: August 18, 2021

Maternal Vitamin D Levels and Its Correlation With Low Birth Weight in Neonates: A Tertiary Care Hospital Experience in Saudi Arabia.

Maternal Vitamin D Levels and Its Correlation With Low Birth Weight in Neonates: A Tertiary Care Hospital Experience in Saudi Arabia.

Journal: Cureus

Published: May 20, 2021

Fetal Anomalies Associated with Novel Pathogenic Variants in TMEM94.

Fetal Anomalies Associated with Novel Pathogenic Variants in TMEM94.

Journal: Genes

Published: July 22, 2020

Confirming TBC1D32-related ciliopathy in humans.

Confirming TBC1D32-related ciliopathy in humans.

Journal: American journal of medical genetics. Part A

Published: April 02, 2020

Novel loss of function variants in FRAS1 AND FREM2 underlie renal agenesis in consanguineous families.

Novel loss of function variants in FRAS1 AND FREM2 underlie renal agenesis in consanguineous families.

Journal: Journal of nephrology

Published: March 26, 2020

Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population.

Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population.

Journal: American journal of human genetics

Published: October 05, 2019

Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population.

Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population.

Journal: American journal of human genetics

Published: December 19, 2018

Bialleleic PKD1 mutations underlie early-onset autosomal dominant polycystic kidney disease in Saudi Arabian families.

Bialleleic PKD1 mutations underlie early-onset autosomal dominant polycystic kidney disease in Saudi Arabian families.

Journal: Pediatric nephrology (Berlin, Germany)

Published: October 06, 2018

Molecular autopsy in maternal-fetal medicine.

Molecular autopsy in maternal-fetal medicine.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: May 17, 2017

Showing 1-12 of 16

Last Updated: 09/26/2026