Ashwin B. Dalal

Hyderabad, TG, India

Last Updated: 09/26/2026

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Found 169 publications

Spinal Muscular Atrophy in Adult Neurology Services in India.

Spinal Muscular Atrophy in Adult Neurology Services in India.

Journal: Clinical genetics
Published: May 06, 2026

Clinical, biochemical and molecular spectrum of acute neuronopathic type 2 Gaucher disease from India.

Clinical, biochemical and molecular spectrum of acute neuronopathic type 2 Gaucher disease from India.

Journal: BMC pediatrics
Published: April 02, 2026

Integrative approach for delineating structural variants using optical genome mapping and long-read genome sequencing.

Integrative approach for delineating structural variants using optical genome mapping and long-read genome sequencing.

Journal: Molecular biology reports
Published: March 27, 2026

Experience of Prenatal Diagnosis for β-Thalassemia and Major Hemoglobinopathies in the Last Decade from Seven Tertiary-Care Referral Centers in India.

Experience of Prenatal Diagnosis for β-Thalassemia and Major Hemoglobinopathies in the Last Decade from Seven Tertiary-Care Referral Centers in India.

Journal: Indian journal of pediatrics
Published: February 14, 2026

Skewed X-Chromosome Inactivation in a Child with Fungal Pneumonia and a Pathogenic de novo CYBB Variant.

Skewed X-Chromosome Inactivation in a Child with Fungal Pneumonia and a Pathogenic de novo CYBB Variant.

Journal: Indian journal of pediatrics
Published: December 05, 2025

Development of national biobank for lysosomal storage disorders in India- a step towards advancing research and precision medicine.

Development of national biobank for lysosomal storage disorders in India- a step towards advancing research and precision medicine.

Journal: Orphanet journal of rare diseases
Published: October 31, 2025

Spinal muscular atrophy in India: Patient journey, access to care, treatment barriers, and strategic recommendations: Insights from experts.

Spinal muscular atrophy in India: Patient journey, access to care, treatment barriers, and strategic recommendations: Insights from experts.

Journal: Journal of neuromuscular diseases
Published: October 23, 2025

Deciphering the Structural Variants by Long-Read Genome Sequencing: Technology, Applications, and Case Illustrations.

Deciphering the Structural Variants by Long-Read Genome Sequencing: Technology, Applications, and Case Illustrations.

Journal: Cytogenetic and genome research
Published: August 11, 2025

Expanding the Phenotypic Spectrum of Syndromic Arthrogryposis Multiplex Congenita: Role of Biallelic Variants in COL25A1 Across Fetal and Pediatric Periods.

Expanding the Phenotypic Spectrum of Syndromic Arthrogryposis Multiplex Congenita: Role of Biallelic Variants in COL25A1 Across Fetal and Pediatric Periods.

Journal: Indian journal of pediatrics
Published: July 30, 2025

Quality Issues in Medical Genetics Laboratories: "What a Clinician Needs to Know?"

Quality Issues in Medical Genetics Laboratories: "What a Clinician Needs to Know?"

Journal: Indian journal of pediatrics
Published: July 16, 2025

Corrigendum to "Integrated genomic, proteomic and cognitive assessment in Duchenne Muscular Dystrophy suggest astrocyte centric pathology" [Heliyon Volume 9, Issue 8, August 2023, Article e18530].

Corrigendum to "Integrated genomic, proteomic and cognitive assessment in Duchenne Muscular Dystrophy suggest astrocyte centric pathology" [Heliyon Volume 9, Issue 8, August 2023, Article e18530].

Journal: Heliyon
Published: June 19, 2025

Author Correction: Mapping genetic diversity with the GenomeIndia project.

Author Correction: Mapping genetic diversity with the GenomeIndia project.

Journal: Nature genetics
Published: May 09, 2025
Showing 1-12 of 169

Last Updated: 09/26/2026