Himani R. Pandey

Greater Noida, UP, India

Last Updated: 09/26/2026

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Found 24 publications

CTC1 mutation causing cerebro-retinal microangiopathy with calcifications and cysts type 1, masquerading as TORCH Infection.

CTC1 mutation causing cerebro-retinal microangiopathy with calcifications and cysts type 1, masquerading as TORCH Infection.

Journal: BMJ case reports

Published: January 19, 2026

Phyto-Nanotherapeutics for Alzheimer's Disease: Current Progress and Future Perspectives.

Phyto-Nanotherapeutics for Alzheimer's Disease: Current Progress and Future Perspectives.

Journal: Central nervous system agents in medicinal chemistry

Published: October 13, 2025

Gene-Dosage Effect of V89L Variants in Steroid 5α-Reductase Type 2 and Increased Risk of 46, XY Disorders of Sex Development: A Systematic Review and Meta-Analysis.

Gene-Dosage Effect of V89L Variants in Steroid 5α-Reductase Type 2 and Increased Risk of 46, XY Disorders of Sex Development: A Systematic Review and Meta-Analysis.

Journal: Journal of Indian Association of Pediatric Surgeons

Published: August 29, 2025

MicroRNA-21 in Cancer and Fibrosis: Molecular Mechanisms and Therapeutic Progress.

MicroRNA-21 in Cancer and Fibrosis: Molecular Mechanisms and Therapeutic Progress.

Journal: Anti-cancer agents in medicinal chemistry

Published: August 28, 2025

Expanding the Genetic Blueprint of Wilms Tumor: An Account of 71 Novel Variants across 16 Genes with Novel Implications for Wilms Tumor Pathogenesis.

Expanding the Genetic Blueprint of Wilms Tumor: An Account of 71 Novel Variants across 16 Genes with Novel Implications for Wilms Tumor Pathogenesis.

Journal: Journal of Indian Association of Pediatric Surgeons

Published: August 17, 2025

Nanomedicine for Alzheimer's Disease: Diagnostic and Therapeutic Progress.

Nanomedicine for Alzheimer's Disease: Diagnostic and Therapeutic Progress.

Journal: MicroRNA (Shariqah, United Arab Emirates)

Published: July 28, 2025

Novel CTNNB1 gene mutations reveal critical pathogenic mechanisms in pediatric hepatoblastoma.

Novel CTNNB1 gene mutations reveal critical pathogenic mechanisms in pediatric hepatoblastoma.

Journal: Pediatric surgery international

Published: July 04, 2025

USP18 gene mutation associated with recurrent encephalopathy, intracranial calcification, and microcephaly: case report, long-term follow-up, and literature review.

USP18 gene mutation associated with recurrent encephalopathy, intracranial calcification, and microcephaly: case report, long-term follow-up, and literature review.

Journal: Clinical dysmorphology

Published: April 28, 2025

FREM2 as a candidate gene for posterior urethral valves: Evidence from a case-parent cohort.

FREM2 as a candidate gene for posterior urethral valves: Evidence from a case-parent cohort.

Journal: Journal of pediatric urology

Published: April 03, 2025

Clinical and neuroimaging variability in two siblings with a novel PCDH12 variant: a case report.

Clinical and neuroimaging variability in two siblings with a novel PCDH12 variant: a case report.

Journal: Clinical dysmorphology

Published: March 12, 2025

Gut microbiota in non-alcoholic fatty liver disease: Pathophysiology, diagnosis, and therapeutics.

Gut microbiota in non-alcoholic fatty liver disease: Pathophysiology, diagnosis, and therapeutics.

Journal: World journal of hepatology

Published: March 09, 2025

Expanding the Phenotypic Spectrum of DPH2 -Related Disorder.

Expanding the Phenotypic Spectrum of DPH2 -Related Disorder.

Journal: American journal of medical genetics. Part A

Published: October 03, 2024

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Last Updated: 09/26/2026