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Laxmi Kirola

Identification of a novel homozygous mutation Arg459Pro in SYNJ1 gene of an Indian family with autosomal recessive juvenile Parkinsonism
2016 · Laxmi Kirola, Madhuri Behari, et al. · Parkinsonism & Related Disorders · 83
Recent Updates on the Genetics of Amyotrophic Lateral Sclerosis and Frontotemporal Dementia
2022 · Laxmi Kirola, Ashim Mukherjee, et al. · Molecular Neurobiology · 77
Genetic emergence of B.1.617.2 in COVID-19
2021 · L. Kirola · New Microbes and New Infections · 52
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Does gut brain axis has an impact on Parkinson’s disease (PD)?
2023 · Ajay Elangovan, Bhawna Dahiya, et al. · Ageing Research Reviews · 22
Association Study Between Kynurenine 3-Monooxygenase (KMO) Gene and Parkinson’s Disease Patients
2023 · Harysh Winster Suresh Babu, Ajay Elangovan, et al. · Molecular Neurobiology · 11
New insights on the regulators and inhibitors of RhoA-ROCK signalling in Parkinson’s disease
2025 · Nandita Ravichandran, Mahalaxmi Iyer, et al. · Metabolic Brain Disease · 7
Identification and molecular characterization of two recurrent missense mutations in the RS1 gene in two families with X‐linked retinoschisis from North India
2023 · Souradip Chatterjee, Shashank Gupta, et al. · American Journal of Medical Genetics Part A · 5
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Lack of evidence supporting a role for DPP6 sequence variants in Alzheimer’s disease in the European American population
2021 · NIA-LOAD family study group, NCRAD, the ADSP project, Laxmi Kirola, et al. · Acta Neuropathologica · 4
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Identification of a compound heterozygous mutation in GDAP1 gene in a consanguineous South Indian family with Charcot–Marie–Tooth (CMT) Disease
2025 · Laxmi Kirola, Deepika Joshi, et al. · Egyptian Journal of Medical Human Genetics · 1
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A novel partial duplication in OPHN1, associated with vermis cerebellar hypoplasia, seizures and developmental delay
2022 · Laxmi Kirola, Joy Norris, et al. · Gene Reports · 1
Genetics of Parkinson's Disease: Contributions from India
2026 · Laxmi Kirola, Madhuri Behari, et al. · CRC Press eBooks
Brain organoids in bipolar disorder: Unraveling mechanisms and therapeutic approaches
2025 · Souradip Chaterjee, Laxmi Kirola · Elsevier eBooks
"Harnessing the power of organoids for improved outcomes in pancreatic cancer"
2025 · Laxmi Kirola, Saurabh Kedia, et al. · Pancreatology
Identification of a novel compound heterozygous mutation in RyR1 gene in an Indian family affected with congenital myopathy
2024 · Laxmi Kirola, Deepika Joshi, et al.
Gene Regulation, DNA and RNA Structure and Sequencing
2023 · Neetu Verma, Deepa Bhatt, et al. · Bioinformatics and Computational Biology
Review of: "The Truth about the Origin of Omicron"
2022 · Laxmi Kirola
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A novel leaky splice variant in centromere protein J (CENPJ)‐associated Seckel syndrome
2022 · Navneesh Yadav, Laxmi Kirola, et al. · Annals of Human Genetics
Genetic emergence of B.1.617 in COVID-19 (Preprint)
2021 · Laxmi Kirola
DPP6 gene in European American Alzheimer’s Disease
2020 · Laxmi Kirola, John P. Budde, et al. · medRxiv
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Phenotypic and molecular description of an individual with a disruptive variant in the SULF2 gene
2019 · Laxmi Kirola, Courtney L. Edgar-Zarate, et al. · Clinical Dysmorphology
A novel de novo heterozygous deletion at 13q14.2-q21.1 in two siblings with mild intellectual disability
2018 · Kirti Mittal, Laxmi Kirola, et al. · Gene Reports
Works count: 24
Citation count: 263
H-index: 6
I10-index: 5
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