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Ashitha S. Niranjana Murthy

Observed names: Ashitha S Niranjana Murthy, Ashitha S.Niranjana Murthy, Ashitha Siddappa Niranjana Murthy
ORCID: 0000-0001-7651-0670
Observed ORCID: 0000-0001-7651-0670
OpenAlex ID: A5111357077
Visceral Adiposity Index and Lipid Accumulation Product as diagnostic markers of Metabolic Syndrome in South Indians with Polycystic Ovary Syndrome
2021 · Zeinab Naghshband, Lakshmi Kumar, et al. · Journal of Human Reproductive Sciences · 29
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SHH Signaling as a Key Player in Endometrial Cancer: Unveiling the Correlation with Good Prognosis, Low Proliferation, and Anti-Tumor Immune Milieu
2024 · V. P. Snijesh, Shivakumar Krishnamurthy, et al. · International Journal of Molecular Sciences · 10
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Assessment and Establishment of Correlation between Reactive Oxidation Species, Citric Acid, and Fructose Level in Infertile Male Individuals
2021 · Golnaz Shemshaki, Ashitha S. Niranjana Murthy, et al. · Journal of Human Reproductive Sciences · 10
Comprehensive in silico mutational-sensitivity analysis of PTEN establishes signature regions implicated in pathogenesis of Autism Spectrum Disorders
2020 · Ashitha S. Niranjana Murthy, Raviraj V. Suresh, et al. · Genomics · 6
Whole Exome Sequencing of a Multiplex Family of Indian Origin Identifies Variants in the RAI1 and FLII Genes within the 17p11.2 Region in Siblings with Autism and Smith Magenis Syndrome
2024 · Durbagula Srividhya, Snijesh Valiya Parambath, et al. · Molecular Syndromology · 5
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Novel association of PhosphoSerine PHosphatase (PSPH) gene mutations with male infertility identified through whole exome sequencing of South Indians
2021 · Golnaz Shemshaki, Mohsen Najafi, et al. · Meta Gene · 5
Best Practices for Variant Calling Using the Genome Analysis Toolkit
2025 · V. P. Snijesh, K Shivakumar, et al. · CRC Press eBooks · 3
Genetic insights into male autism spectrum disorder in a small cohort of Indian simplex families: findings from whole exome sequencing
2024 · Srividhya Durbagula, Snijesh Valiya Parambath, et al. · General Psychiatry · 2
Integrated in silico functional analysis predicts autism spectrum disorders to be burdened by deleterious variations within CHD8 core domains and its CHD7-binding motif
2022 · Ashitha S. Niranjana Murthy, Suryanarayanan Thangalazhi Balakrishnan, et al. · Network Modeling Analysis in Health Informatics and Bioinformatics · 2
Lack of association of OXTR variants with autism spectrum disorders in a south Indian population
2019 · Dhanesh Mandamkulathil, Anitha Ayyappan Pillai, et al. · Journal of Indian Association for Child and Adolescent Mental Health · 2
Including lived experience voices in science communication to combat mental illness stigma: insights from India
2026 · Kadambari Patil, Anushka Banerjee, et al. · Journal of Science Communication
In silico Genotype-Phenotype Correlation Analysis of Inherited Variations in Autism Spectrum Disorder Families Identify an Interplay between Sensory Function and Repetitive-behaviour Genes
2026 · Meghana Kommerahalli RameshRaju, Snijesh Valiya Parambath, et al. · Journal of Molecular Neuroscience
Generation of iPSC line NIMHi033-A from an Indian patient with Autism Spectrum Disorder carrying mutation in DYNC1H1 gene
2026 · Ashitha Siddappa Niranjana Murthy, Princy Choudhary, et al. · Stem Cell Research
Human-induced pluripotent stem cells in psychiatric disorders: An inflammatory perspective
2026 · Varsha Vishnu, Ashitha Siddappa Niranjana Murthy, et al. · Advances in immunology
A Novel Homozygous Variant in CPLANE1 Gene in a Patient with Developmental Deficits
2024 · Bhagyalakshmi Shankarappa, Vishnu P. Prasad, et al. · Molecular Syndromology
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Whole exome sequencing of discordant diseases in Monozygotic twins with Down syndrome reveals mutations for Congenital Heart Defect and epileptic seizures
2017 · Ashitha S. Niranjana Murthy, Avinash M. Veerappa, et al. · Meta Gene
Works count: 16
Citation count: 74
H-index: 5
I10-index: 3
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