Vandana Gupta

4.7k total citations · 1 hit paper
89 papers, 2.7k citations indexed

About

Vandana Gupta is a scholar working on Molecular Biology, Cell Biology and Oncology. According to data from OpenAlex, Vandana Gupta has authored 89 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 14 papers in Cell Biology and 11 papers in Oncology. Recurrent topics in Vandana Gupta's work include Muscle Physiology and Disorders (22 papers), Cardiomyopathy and Myosin Studies (8 papers) and Chronic Obstructive Pulmonary Disease (COPD) Research (6 papers). Vandana Gupta is often cited by papers focused on Muscle Physiology and Disorders (22 papers), Cardiomyopathy and Myosin Studies (8 papers) and Chronic Obstructive Pulmonary Disease (COPD) Research (6 papers). Vandana Gupta collaborates with scholars based in United States, India and United Kingdom. Vandana Gupta's co-authors include Alan H. Beggs, Laura L. Smith, Richard Booton, Saifudin Khalid, Mohammed Munavvar, J. M. Martín Martín, John Blaikley, Nazia Chaudhuri, Neal Navani and Najib M. Rahman and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Vandana Gupta

81 papers receiving 2.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

British Thoracic Society guideline for diagnostic flexible bronchoscopy in adults: accredited by NICE

2013 572 citations Vandana Gupta et al. profile →

Peers

Countries citing papers authored by Vandana Gupta

Since Specialization

Citations

This map shows the geographic impact of Vandana Gupta'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 Vandana Gupta with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Vandana Gupta more than expected).

Fields of papers citing papers by Vandana Gupta

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vandana Gupta. 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 Vandana Gupta. The network helps show where Vandana Gupta may publish in the future.

Co-authorship network of co-authors of Vandana Gupta

This figure shows the co-authorship network connecting the top 25 collaborators of Vandana Gupta. A scholar is included among the top collaborators of Vandana Gupta 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 Vandana Gupta. Vandana Gupta 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	Standardization of zebrafish drug testing parameters for muscle diseases 2024 ·Disease Models & Mechanisms ·(unknown), (unknown), Clarissa A. Henry, M. Chiara Manzini, John M. Parant, (unknown), Avnika A. Ruparelia, Peter D. Currie, Vandana Gupta, James J. Dowling, Lisa Maves, Matthew S. Alexander	13
2	NRAP reduction rescues sarcomere defects in nebulin-related nemaline myopathy 2023 ·Human Molecular Genetics ·(unknown), (unknown), (unknown), Frank Li, Henk Granzier, Vandana Gupta	3
3	Pediatric Nemaline Myopathy: A Systematic Review Using Individual Patient Data 2022 ·Journal of Child Neurology ·Briana Christophers, Michael A. Lopez, Vandana Gupta, Hannes Vogel, Mary K. Baylies	4
4	Bi‐allelic loss of function variants in GOLGA2 are associated with a complex neurological phenotype: Report of a second family 2021 ·Clinical Genetics ·(unknown), Mehul Mistri, Nidhi Shah, Parth Shah, Vandana Gupta	7
5	Know the unknown fact of novel COVID -19 corona virus 2020 ·Letters in Applied NanoBioScience ·Vandana Gupta, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	2
6	Novel Recessive TNNT1 Congenital Core‐Rod Myopathy in French Canadians 2020 ·Annals of Neurology ·David Pellerin, (unknown), Benjamin Ellezam, Emily C. Troiano, Jason Karamchandani, Marie‐Josée Dicaire, (unknown), Rebecca Robertson, (unknown), Denis Brunet, Chamindra G. Konersman, Jean Mathieu, Jodi Warman‐Chardon, Vandana Gupta, Alan H. Beggs, Bernard Brais, Nicolas Chrestian	15
7	Homozygous TRPV4 mutation causes congenital distal spinal muscular atrophy and arthrogryposis 2019 ·Neurology Genetics ·(unknown), (unknown), Ágnes Tóth-Petróczy, (unknown), (unknown), Nikkola Carmichael, Elicia Estrella, Basil T. Darras, Natasha Y. Frank, Joel B. Krier, Rachelle Gaudet, Vandana Gupta	16
8	Dysregulation of NRAP degradation by KLHL41 contributes to pathophysiology in nemaline myopathy 2019 ·Human Molecular Genetics ·(unknown), (unknown), (unknown), (unknown), Vandana Gupta	23
9	ACTN2 mutations cause “Multiple structured Core Disease” (MsCD) 2019 ·Acta Neuropathologica ·Xavière Lornage, Norma B. Romero, (unknown), (unknown), Sandra Donkervoort, (unknown), Sarah Neuhaus, A. Reghan Foley, C. Labasse, Raphaël Schneider, Robert Carlier, Katherine R. Chao, Līvija Medne, Jean‐François Deleuze, David Orlikowski, Carsten G. Bönnemann, Vandana Gupta, Michel Fardeau, Johann Böhm, Jocelyn Laporte	35
10	Association of A:O ratio with metabolic risk markers in North Indian women 2018 ·Clinical Epidemiology and Global Health ·Supriya Mishra, (unknown), (unknown), (unknown), (unknown), Rekha Sachan, Abbas Ali Mahdi, Vandana Gupta	1
11	Association of acylation stimulating protein and adiponectin with metabolic risk marker in North Indian obese women 2018 ·Diabetes & Metabolic Syndrome Clinical Research & Reviews ·Supriya Mishra, (unknown), (unknown), (unknown), (unknown), Sandeep Kumar, Vandana Gupta, Rekha Sachan, Abbas Ali Mahdi	6
12	Association of Leptin: Adiponectin ratio and metabolic risk markers in postmenopausal women 2018 ·Immunology Letters ·Vandana Gupta, (unknown), Supriya Mishra, Sandeep Kumar, (unknown), (unknown)	19
13	RNA helicase, DDX27 regulates skeletal muscle growth and regeneration by modulation of translational processes 2018 ·PLoS Genetics ·(unknown), Marie-Françoise O’Donohue, (unknown), (unknown), Jeffrey J. Widrick, Isabelle Draper, Anirban Chakraborty, Yi Zhou, Leonard I. Zon, Pierre‐Emmanuel Gleizes, Alan H. Beggs, Vandana Gupta	34
14	Secondary Prevention of Cervical Cancer: ASCO Resource-Stratified Clinical Practice Guideline 2017 ·Obstetrical & Gynecological Survey ·José Jerónimo, Philip E. Castle, Sarah Temin, Lynette Denny, Vandana Gupta, Jane J. Kim, Silvana Luciani, Daniel Murokora, Twalib Ngoma, You‐Lin Qiao, Michael Quinn, Rengaswamy Sankaranarayanan, Peter Sasieni, Kathleen M. Schmeler, Surendra S. Shastri	2
15	GOLGA2, encoding a master regulator of golgi apparatus, is mutated in a patient with a neuromuscular disorder 2016 ·Human Genetics ·Hanan E. Shamseldin, (unknown), Majid Alfadhel, Vandana Gupta, Fowzan S. Alkuraya	31
16	A comparative study of Shilajatu and Asanadi Ghana Vati in the management of Madhumeha w.s.r. to type-2 diabetes mellitus 2016 ·AYU (An International Quarterly Journal of Research in Ayurveda) ·(unknown), Vandana Gupta, (unknown), (unknown)	6
17	Mutation of the mitochondrial carrier SLC25A42 causes a novel form of mitochondrial myopathy in humans 2015 ·Human Genetics ·Hanan E. Shamseldin, Laura L. Smith, Amal Y. Kentab, Hisham Alkhalidi, Brady J. Summers, (unknown), Yong Xiong, Vandana Gupta, Fowzan S. Alkuraya	34
18	Bridging integrator 1 (Bin1) deficiency in zebrafish results in centronuclear myopathy 2014 ·Human Molecular Genetics ·Laura L. Smith, Vandana Gupta, Alan H. Beggs	21
19	POMK mutations disrupt muscle development leading to a spectrum of neuromuscular presentations 2014 ·Human Molecular Genetics ·Stefania Di Costanzo, Anuradha Balasubramanian, (unknown), Anete Rozkalne, Chiara Pantaleoni, S. Saredi, Vandana Gupta, (unknown), Timothy W. Yu, Peter B. Kang, Mustafa A. Salih, Marina Mora, Emanuela Gussoni, Christopher A. Walsh, M. Chiara Manzini	58
20	Loss of Catalytically Inactive Lipid Phosphatase Myotubularin-related Protein 12 Impairs Myotubularin Stability and Promotes Centronuclear Myopathy in Zebrafish 2013 ·PLoS Genetics ·Vandana Gupta, Karim Hnia, Laura L. Smith, (unknown), (unknown), (unknown), (unknown), (unknown), Leonela Amoasii, (unknown), Jocelyn Laporte, Alan H. Beggs	24

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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