Gautam Wali

969 total citations
30 papers, 363 citations indexed

About

Gautam Wali is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Gautam Wali has authored 30 papers receiving a total of 363 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Cellular and Molecular Neuroscience, 13 papers in Neurology and 9 papers in Molecular Biology. Recurrent topics in Gautam Wali's work include Hereditary Neurological Disorders (11 papers), Neurogenetic and Muscular Disorders Research (7 papers) and Botulinum Toxin and Related Neurological Disorders (5 papers). Gautam Wali is often cited by papers focused on Hereditary Neurological Disorders (11 papers), Neurogenetic and Muscular Disorders Research (7 papers) and Botulinum Toxin and Related Neurological Disorders (5 papers). Gautam Wali collaborates with scholars based in Australia, India and United States. Gautam Wali's co-authors include Carolyn M. Sue, Alan Mackay‐Sim, Ratneswary Sutharsan, Kishore R. Kumar, Yongjun Fan, Bernadette Bellette, Denis I. Crane, Romal Stewart, Nicholas Matigian and David Veivers and has published in prestigious journals such as SHILAP Revista de lepidopterología, Analytical Chemistry and Scientific Reports.

In The Last Decade

Gautam Wali

28 papers receiving 357 citations

Peers

Countries citing papers authored by Gautam Wali

Since Specialization

Citations

This map shows the geographic impact of Gautam Wali's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Gautam Wali with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gautam Wali more than expected).

Fields of papers citing papers by Gautam Wali

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gautam Wali. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Gautam Wali. The network helps show where Gautam Wali may publish in the future.

Co-authorship network of co-authors of Gautam Wali

This figure shows the co-authorship network connecting the top 25 collaborators of Gautam Wali. A scholar is included among the top collaborators of Gautam Wali based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Gautam Wali. Gautam Wali is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Dopamine and cortical neurons with different Parkinsonian mutations show variation in lysosomal and mitochondrial dysfunction 2025 ·npj Parkinson s Disease ·(unknown), Yan Li, Adahir Labrador‐Garrido, Dad Abu-Bonsrah, (unknown), (unknown), Dmitry A. Ovchinnikov, Meizuo Zhong, Ryan L. Davis, Dario Strbenac, Jennifer Johnston, Lachlan H. Thompson, Deniz Kirik, Clare L. Parish, Glenda M. Halliday, Carolyn M. Sue, Gautam Wali, Nicolas Dzamko	1
2	Reduced acetylated α-tubulin in SPAST hereditary spastic paraplegia patient PBMCs 2023 ·Frontiers in Neuroscience ·Gautam Wali, (unknown), (unknown), Kishore R. Kumar, Alan Mackay‐Sim, Carolyn M. Sue	2
3	Outcome Measures and Biomarkers for Clinical Trials in Hereditary Spastic Paraplegia: A Scoping Review 2023 ·Genes ·(unknown), (unknown), (unknown), Fangzhi Jia, Gautam Wali, Carolyn M. Sue, Kishore R. Kumar	7
4	Generation of human-induced pluripotent-stem-cell-derived cortical neurons for high-throughput imaging of neurite morphology and neuron maturation 2023 ·STAR Protocols ·Gautam Wali, Yan Li, Dad Abu-Bonsrah, Deniz Kirik, Clare L. Parish, Carolyn M. Sue	7
5	Pharmacological rescue of mitochondrial and neuronal defects in SPG7 hereditary spastic paraplegia patient neurons using high throughput assays 2023 ·Frontiers in Neuroscience ·Gautam Wali, Yan Li, (unknown), Kishore R. Kumar, Margot L. Day, Carolyn M. Sue	8
6	PIGG gene mutation associated with Uner Tan syndrome 2021 ·Gautam Wali, (unknown), (unknown)	1
7	Mitochondrial Function in Hereditary Spastic Paraplegia: Deficits in SPG7 but Not SPAST Patient-Derived Stem Cells 2020 ·Frontiers in Neuroscience ·Gautam Wali, Kishore R. Kumar, (unknown), Ryan L. Davis, Alan Mackay‐Sim, Carolyn M. Sue	21
8	Antibody-Free Targeted Proteomics Assay for Absolute Measurement of α-Tubulin Acetylation 2020 ·Analytical Chemistry ·Alok K. Shah, Gautam Wali, Carolyn M. Sue, Alan Mackay‐Sim, Michelle M. Hill	2
9	Long‐Term Follow‐Up and Evolution of ADCY5—From a Ballistic to Dystonic Phenotype 2020 ·Movement Disorders Clinical Practice ·(unknown), Gautam Wali, Kishore R. Kumar, Carolyn M. Sue	3
10	Expanding the spectrum of PEX16 mutations and novel insights into disease mechanisms 2018 ·Molecular Genetics and Metabolism Reports ·Kishore R. Kumar, Gautam Wali, Ryan L. Davis, Amali Mallawaarachchi, Elizabeth E. Palmer, Velimir Gayevskiy, André E. Minoche, David Veivers, Marcel E. Dinger, Alan Mackay‐Sim, Mark J. Cowley, Carolyn M. Sue	13
11	Patient-Derived Stem Cell Models in SPAST HSP: Disease Modelling and Drug Discovery 2018 ·Brain Sciences ·Gautam Wali, Carolyn M. Sue, Alan Mackay‐Sim	9
12	A Patient-Specific Stem Cell Model to Investigate the Neurological Phenotype Observed in Ataxia-Telangiectasia 2017 ·Methods in molecular biology ·Romal Stewart, Gautam Wali, Chris Perry, Martin F. Lavin, François Féron, Alan Mackay‐Sim, Ratneswary Sutharsan	3
13	Defining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencing 2016 ·Neurogenetics ·Kishore R. Kumar, Gautam Wali, Mahesh Kamate, André E. Minoche, Clare Puttick, Mark Pinese, Velimir Gayevskiy, Marcel E. Dinger, Tony Roscioli, Carolyn M. Sue, Mark J. Cowley	22
14	Mechanism of impaired microtubule-dependent peroxisome trafficking and oxidative stress in SPAST-mutated cells from patients with Hereditary Spastic Paraplegia 2016 ·Scientific Reports ·Gautam Wali, Ratneswary Sutharsan, Yongjun Fan, Romal Stewart, Johana Tello Velasquez, Carolyn M. Sue, Denis I. Crane, Alan Mackay‐Sim	37
15	Molecular analysis of α-synuclein gene in Parkinson′s disease in North Karnataka, India 2014 ·Neurology India ·(unknown), (unknown), Suyamindra S. Kulkarni, Gautam Wali	6
16	Low dose tubulin-binding drugs rescue peroxisome trafficking deficit in patient-derived stem cells in Hereditary Spastic Paraplegia 2014 ·Biology Open ·Yongjun Fan, Gautam Wali, Ratneswary Sutharsan, Bernadette Bellette, Denis I. Crane, Carolyn M. Sue, Alan Mackay‐Sim	37
17	A patient-derived olfactory stem cell disease model for ataxia-telangiectasia 2013 ·Human Molecular Genetics ·Romal Stewart, Sergei Kozlov, Nicholas Matigian, Gautam Wali, Magtouf Gatei, Ratneswary Sutharsan, Bernadette Bellette, Amanda W. Kijas, J. Cochrane, M G Coulthard, Chris Perry, Kate Sinclair, Alan Mackay‐Sim, Martin F. Lavin	26
18	Mutation analysis of the sodium/hydrogen exchanger gene (NHE5) in familial paroxysmal kinesigenic dyskinesia 2002 ·Journal of Neural Transmission ·Sian Spacey, (unknown), John E. McRory, Gautam Wali, Nicholas Wood, Terrance P. Snutch	7
19	Asymmetrical blepharospasm associated with a left frontal cortical infarct 2001 ·Movement Disorders ·Gautam Wali	8
20	Friedreich ataxia associated with dystonic head tremor provoked by prolonged exercise 2000 ·Movement Disorders ·Gautam Wali	3

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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