Anikha Bellad

International Technology Park
Bengaluru, KA, India

Last Updated: 09/26/2026

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Found 15 publications

A multiplexed LC-MS/MS assay for comprehensive screening of amino acid metabolism disorders.

A multiplexed LC-MS/MS assay for comprehensive screening of amino acid metabolism disorders.

Journal: Talanta open

Published: June 01, 2026

Hemoglobin alpha-like subunit mu is expressed during ontogeny and is elevated in alpha thalassemia.

Hemoglobin alpha-like subunit mu is expressed during ontogeny and is elevated in alpha thalassemia.

Journal: Blood. Red cells & iron

Published: April 20, 2026

A Mass Spectrometry-Based Multiplexed Targeted Assay for Detection of Hemoglobinopathies from Dried Blood Spots.

A Mass Spectrometry-Based Multiplexed Targeted Assay for Detection of Hemoglobinopathies from Dried Blood Spots.

Journal: The Journal of molecular diagnostics : JMD

Published: January 06, 2025

Conotruncal Heart Defects: A Narrative Review of Molecular Genetics, Genomics Research and Innovation.

Conotruncal Heart Defects: A Narrative Review of Molecular Genetics, Genomics Research and Innovation.

Journal: Omics : a journal of integrative biology

Published: July 10, 2024

Dysregulated Cerebrospinal Fluid Proteome of Spinocerebellar Ataxia Type 2 and its Clinical Implications.

Dysregulated Cerebrospinal Fluid Proteome of Spinocerebellar Ataxia Type 2 and its Clinical Implications.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: December 12, 2023

Identification of a rare [Gγ(Aγδβ)0] -thalassemia using tandem mass spectrometry.

Identification of a rare [Gγ(Aγδβ)0] -thalassemia using tandem mass spectrometry.

Journal: Proteomics

Published: November 04, 2023

Urinary Proteomics for Discovery of Gastric Cancer Biomarkers to Enable Precision Clinical Oncology.

Urinary Proteomics for Discovery of Gastric Cancer Biomarkers to Enable Precision Clinical Oncology.

Journal: Omics : a journal of integrative biology

Published: August 14, 2023

Loss of function variants in L2HGDH gene causing L-2-hydroxyglutaric aciduria.

Loss of function variants in L2HGDH gene causing L-2-hydroxyglutaric aciduria.

Journal: Acta neurologica Belgica

Published: February 17, 2023

PLA2G6-associated neurodegeneration in four different populations-case series and literature review.

PLA2G6-associated neurodegeneration in four different populations-case series and literature review.

Journal: Parkinsonism & related disorders

Published: March 02, 2022

Shukla-Vernon Syndrome: A Second Family with a Novel Variant in the BCORL1 Gene.

Shukla-Vernon Syndrome: A Second Family with a Novel Variant in the BCORL1 Gene.

Journal: Genes

Published: February 17, 2021

Applications of quantitative metabolomics to revolutionize early diagnosis of inborn errors of metabolism in India.

Applications of quantitative metabolomics to revolutionize early diagnosis of inborn errors of metabolism in India.

Journal: Analytical science advances

Published: February 06, 2021

A novel loss of function mutation in adaptor protein complex 4, subunit mu-1 causing autosomal recessive spastic paraplegia 50.

A novel loss of function mutation in adaptor protein complex 4, subunit mu-1 causing autosomal recessive spastic paraplegia 50.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: January 19, 2021

Showing 1-12 of 15

Last Updated: 09/26/2026