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Himani Pandey

Observed names: H. Pandey, Himani P Pandey, Himani Reddy Pandey
ORCID: 0000-0002-1243-4370
Observed ORCID: 0000-0002-1243-4370
OpenAlex ID: A5102815497
Gut Microbiota in Colorectal Cancer: Biological Role and Therapeutic Opportunities
2023 · Himani Pandey, Daryl W. T. Tang, et al. · Cancers · 178
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Gut microbiota in pathophysiology, diagnosis, and therapeutics of inflammatory bowel disease
2023 · Himani Pandey, Dheeraj Jain, et al. · Intestinal Research · 97
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Connexin 26 (GJB2) Mutations Associated with Non-Syndromic Hearing Loss (NSHL)
2018 · Shivani Mishra, Himani Pandey, et al. · The Indian Journal of Pediatrics · 35
Gut microbiota in non-alcoholic fatty liver disease: Pathophysiology, diagnosis, and therapeutics
2025 · Himani Pandey, Prabudh Goel, et al. · World Journal of Hepatology · 20
Spondyloepiphyseal dysplasia Omani type: CHST3 mutation spectrum and phenotypes in three Indian families
2016 · Priyanka Srivastava, Himani Pandey, et al. · American Journal of Medical Genetics Part A · 18
Hotspots in PTPN11 gene among Indian children with Noonan syndrome
2017 · Dhanya Lakshmi Narayanan, Himani Pandey, et al. · Indian Pediatrics · 14
Mitochondrial Dna Variation and Population Genetic Structure of Snow Trout from Kumaun and Garhwal Himalayan Regions of India
2014 · S. Ali, A. Barat, et al. · Journal of Ecophysiology and Occupational Health · 11
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Helminths in alternative therapeutics of inflammatory bowel disease
2024 · Himani Pandey, Daryl W. T. Tang, et al. · Intestinal Research · 10
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Novel CTNNB1 gene mutations reveal critical pathogenic mechanisms in pediatric hepatoblastoma
2025 · Sourabh Kumar, Jyoti Sharma, et al. · Pediatric Surgery International · 5
Expanding the Phenotype of NRROS ‐Related SENEBAC Syndrome
2024 · Varunvenkat M. Srinivasan, Vykuntaraju K. Gowda, et al. · American Journal of Medical Genetics Part A · 5
Von Hippel–Lindau (VHL) disease and VHL-associated tumors in Indian subjects: VHL gene testing in a resource constraint setting
2022 · Aradhana Dwivedi, Amita Moirangthem, et al. · Egyptian Journal of Medical Human Genetics · 4
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CTC1 mutation causing cerebro-retinal microangiopathy with calcifications and cysts type 1, masquerading as TORCH Infection
2026 · Vykuntaraju K Gowda, Varunvenkat M Srinivasan, et al. · BMJ Case Reports · 2
Expanding the Genetic Blueprint of Wilms Tumor: An Account of 71 Novel Variants across 16 Genes with Novel Implications for Wilms Tumor Pathogenesis
2026 · Sourabh Kumar, Jyoti Sharma, et al. · Journal of Indian Association of Pediatric Surgeons · 1
Integrated Multi-Omics Analysis Identifies Novel Prognostic and Diagnostic Hub Genes in Colorectal Cancer
2025 · Devi Lal, Himani Pandey · Onco · 1
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Expanding the Phenotypic Spectrum of DPH2 ‐Related Disorder
2025 · Vykuntaraju K. Gowda, Varunvenkat M. Srinivasan, et al. · American Journal of Medical Genetics Part A · 1
Clinical and neuroimaging variability in two siblings with a novel PCDH12 variant: a case report
2025 · Vykuntaraju K. Gowda, Varunvenkat M. Srinivasan, et al. · Clinical Dysmorphology · 1
Genetic Markers of Spina Bifida: Enrichment of Pathogenic Variants and Variants of Uncertain Significance
2025 · Jyoti Sharma, Mahima Sharma, et al. · Journal of Indian Association of Pediatric Surgeons · 1
KMT2C Polymorphism in Familial Hypospadias
2025 · Sourabh Kumar, Jyoti Sharma, et al. · The Indian Journal of Pediatrics · 1
Kohlschutter-Tonz syndrome (amelo-cerebro-hypohidrotic syndrome) in an Indian family with a novel ROGD1 mutation
2023 · Vykuntaraju K. Gowda, Arun Y. Bylappa, et al. · Clinical Dysmorphology · 1
Beyond dysbiosis: Reframing microbiome-associated diseases from taxonomy to functional and ecological models
2026 · Devi Lal, Himani Pandey, et al. · World Journal of Gastrointestinal Oncology
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Nonimmune hydrops fetalis with skeletal dysplasia due to a novel homozygous recessive TAPT1 splice-donor variant
2026 · Naren Satya Srinivas M., Shivani Mishra, et al. · Clinical Dysmorphology
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
2026 · Farah Deeba, Prativa Choudhury, et al. · Journal of Indian Association of Pediatric Surgeons
FREM2 as a candidate gene for posterior urethral valves: Evidence from a case-parent cohort
2026 · Jyoti Sharma, Sourabh Kumar, et al. · Journal of Pediatric Urology
Hypomagnesaemia with secondary hypocalcaemia due to a novel TRPM6 mutation
2025 · Vykuntaraju K Gowda, Rajesh R N, et al. · BMJ Case Reports
USP18 gene mutation associated with recurrent encephalopathy, intracranial calcification, and microcephaly: case report, long-term follow-up, and literature review
2025 · Vykuntaraju K. Gowda, Varunvenkat M. Srinivasan, et al. · Clinical Dysmorphology
Works count: 27
Citation count: 406
H-index: 8
I10-index: 8
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