Shruti Shenbagam

Dubai, DU, United Arab Emirates

Last Updated: 09/26/2026

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Found 13 publications

Citywide implementation of a rapid whole-genome sequencing program for critically ill pediatric patients.

Citywide implementation of a rapid whole-genome sequencing program for critically ill pediatric patients.

Journal: Nature medicine

Published: February 26, 2026

Citywide premarital genomic screening in a Middle Eastern population.

Citywide premarital genomic screening in a Middle Eastern population.

Journal: Nature medicine

Published: October 09, 2025

Genetic counseling in the Middle East: provider perspectives of patient attitudes and cultural challenges.

Genetic counseling in the Middle East: provider perspectives of patient attitudes and cultural challenges.

Journal: Human genomics

Published: March 26, 2025

Pathogenic variation underlying rare diseases in an Arab population: Implications for screening programs.

Pathogenic variation underlying rare diseases in an Arab population: Implications for screening programs.

Journal: Genetics in medicine open

Published: December 04, 2024

FBXO22 deficiency defines a pleiotropic syndrome of growth restriction and multi-system anomalies associated with a unique epigenetic signature.

FBXO22 deficiency defines a pleiotropic syndrome of growth restriction and multi-system anomalies associated with a unique epigenetic signature.

Journal: American journal of human genetics

Published: October 08, 2024

Genomics of rare diseases in the Greater Middle East.

Genomics of rare diseases in the Greater Middle East.

Journal: Nature genetics

Published: September 23, 2024

Virtual Gene Panels Have a Superior Diagnostic Yield for Inherited Rare Diseases Relative to Static Panels.

Virtual Gene Panels Have a Superior Diagnostic Yield for Inherited Rare Diseases Relative to Static Panels.

Journal: Clinical chemistry

Published: July 06, 2024

Long read sequencing enhances pathogenic and novel variation discovery in patients with rare diseases.

Long read sequencing enhances pathogenic and novel variation discovery in patients with rare diseases.

Journal: Nature communications

Published: April 18, 2024

The impact of clinical genome sequencing in a global population with suspected rare genetic disease.

The impact of clinical genome sequencing in a global population with suspected rare genetic disease.

Journal: American journal of human genetics

Published: November 27, 2023

Genetic determinants of severe COVID-19 in young Asian and Middle Eastern patients: a case series.

Genetic determinants of severe COVID-19 in young Asian and Middle Eastern patients: a case series.

Journal: Scientific reports

Published: August 17, 2023

The genomic landscape of rare disorders in the Middle East.

The genomic landscape of rare disorders in the Middle East.

Journal: Genome medicine

Published: September 02, 2022

Rapid whole genome sequencing of critically ill pediatric patients from genetically underrepresented populations.

Rapid whole genome sequencing of critically ill pediatric patients from genetically underrepresented populations.

Journal: Genome medicine

Published: March 11, 2022

Showing 1-12 of 13

Last Updated: 09/26/2026