Ashirwad Merve

UCL Queen Square Institute Of Neurology
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 50 publications

A 5' UTR CCG expansion in TBC1D7 causes oculopharyngodistal myopathy.

A 5' UTR CCG expansion in TBC1D7 causes oculopharyngodistal myopathy.

Journal: medRxiv : the preprint server for health sciences
Published: April 10, 2026

Sellar-parasellar Epstein-Barr virus associated smooth muscle tumour mimicking a pituitary adenoma: A case report.

Sellar-parasellar Epstein-Barr virus associated smooth muscle tumour mimicking a pituitary adenoma: A case report.

Journal: Brain, behavior, & immunity - health
Published: March 04, 2026

Pediatric Pleomorphic Xanthoastrocytomas: A Multicenter Neuroradiological and Clinical Correlation Study.

Pediatric Pleomorphic Xanthoastrocytomas: A Multicenter Neuroradiological and Clinical Correlation Study.

Journal: AJNR. American journal of neuroradiology
Published: January 09, 2026

Pediatric Pleomorphic Xanthoastrocytomas: A Multicenter Neuroradiological and Clinical Correlation Study.

Pediatric Pleomorphic Xanthoastrocytomas: A Multicenter Neuroradiological and Clinical Correlation Study.

Journal: AJNR. American journal of neuroradiology
Published: January 09, 2026

Identifying virulent avian paramyxovirus type-1: A paediatric case of progressive encephalitis diagnosed by clinical metagenomics with case series review.

Identifying virulent avian paramyxovirus type-1: A paediatric case of progressive encephalitis diagnosed by clinical metagenomics with case series review.

Journal: IDCases
Published: October 23, 2025

Modeling medulloblastoma pathogenesis and treatment in human cerebellar organoids.

Modeling medulloblastoma pathogenesis and treatment in human cerebellar organoids.

Journal: Genes & development
Published: August 22, 2025

TDP-43 pathology induces CD8+ T cell activation through cryptic epitope recognition.

TDP-43 pathology induces CD8+ T cell activation through cryptic epitope recognition.

Journal: bioRxiv : the preprint server for biology
Published: July 16, 2025

Biallelic NSUN3 Variants Cause Diverse Phenotypic Spectrum Disease: From Isolated Optic Atrophy to Severe Early-Onset Mitochondrial Disorder.

Biallelic NSUN3 Variants Cause Diverse Phenotypic Spectrum Disease: From Isolated Optic Atrophy to Severe Early-Onset Mitochondrial Disorder.

Journal: Investigative ophthalmology & visual science
Published: June 04, 2025

Spatial transcriptomic analysis of muscle biopsy from patients with treatment-naive juvenile dermatomyositis reveals mitochondrial abnormalities despite disease-related interferon-driven signature.

Spatial transcriptomic analysis of muscle biopsy from patients with treatment-naive juvenile dermatomyositis reveals mitochondrial abnormalities despite disease-related interferon-driven signature.

Journal: Annals of the rheumatic diseases
Published: February 05, 2025

Testing Meningiomas With Methylation Arrays: Insights and Recommendations From a Large Single-Centre Study.

Testing Meningiomas With Methylation Arrays: Insights and Recommendations From a Large Single-Centre Study.

Journal: Neuropathology and applied neurobiology
Published: November 17, 2024

Author Correction: A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry.

Author Correction: A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry.

Journal: Nature communications
Published: October 17, 2024

Safety and Diagnostic Utility of Brain Biopsy and Metagenomics in Decision-Making for Patients with Inborn Errors of Immunity (IEI) and Unexplained Neurological Manifestations.

Safety and Diagnostic Utility of Brain Biopsy and Metagenomics in Decision-Making for Patients with Inborn Errors of Immunity (IEI) and Unexplained Neurological Manifestations.

Journal: Journal of clinical immunology
Published: June 24, 2024
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Last Updated: 09/26/2026