Pinki Munot

1.8k total citations
51 papers, 718 citations indexed

About

Pinki Munot is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Pinki Munot has authored 51 papers receiving a total of 718 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 18 papers in Genetics and 15 papers in Neurology. Recurrent topics in Pinki Munot's work include Neurogenetic and Muscular Disorders Research (18 papers), Muscle Physiology and Disorders (8 papers) and Congenital Anomalies and Fetal Surgery (8 papers). Pinki Munot is often cited by papers focused on Neurogenetic and Muscular Disorders Research (18 papers), Muscle Physiology and Disorders (8 papers) and Congenital Anomalies and Fetal Surgery (8 papers). Pinki Munot collaborates with scholars based in United Kingdom, Italy and United States. Pinki Munot's co-authors include Vijeya Ganesan, Francesco Muntoni, Yanick J. Crow, S. Robb, Sonal Gupta, Heinz Jungbluth, Francesco Muntoni, Suresh Pujar, Cheryl Hemingway and Dawn E. Saunders and has published in prestigious journals such as Brain, Neurology and Stroke.

In The Last Decade

Pinki Munot

45 papers receiving 694 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Pinki Munot United Kingdom 15 259 205 127 116 113 51 718
Tanya Stojkovic France 13 249 1.0× 138 0.7× 82 0.6× 44 0.4× 150 1.3× 37 713
Steve Verreault Canada 13 414 1.6× 135 0.7× 84 0.7× 85 0.7× 132 1.2× 20 782
Guilhem Solé France 15 250 1.0× 176 0.9× 94 0.7× 33 0.3× 152 1.3× 62 731
Ângela Romano Italy 16 351 1.4× 355 1.7× 223 1.8× 99 0.9× 126 1.1× 77 924
Tae Chung United States 11 266 1.0× 355 1.7× 136 1.1× 201 1.7× 122 1.1× 29 1.3k
J. Franques France 21 256 1.0× 533 2.6× 124 1.0× 91 0.8× 242 2.1× 44 927
Pierre Lozeron France 20 582 2.2× 455 2.2× 126 1.0× 36 0.3× 198 1.8× 65 1.2k
A. Cabello Spain 18 299 1.2× 215 1.0× 133 1.0× 48 0.4× 138 1.2× 37 735
James Miller United Kingdom 13 239 0.9× 126 0.6× 106 0.8× 74 0.6× 150 1.3× 28 573
Barend P. Lotz South Africa 12 368 1.4× 183 0.9× 91 0.7× 90 0.8× 144 1.3× 31 863

Countries citing papers authored by Pinki Munot

Since Specialization
Citations

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

Fields of papers citing papers by Pinki Munot

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pinki Munot

This figure shows the co-authorship network connecting the top 25 collaborators of Pinki Munot. A scholar is included among the top collaborators of Pinki Munot 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 Pinki Munot. Pinki Munot is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Main, Marion, Giovanni Baranello, Pinki Munot, et al.. (2025). Spinal presentations in children with type 1 spinal muscular atrophy on nusinersen treatment across the SMA-REACH UK network: a retrospective national observational study. BMJ Open. 15(1). e082240–e082240. 2 indexed citations
2.
3.
Everett, Ruth, Yan Dong, C. Marini Bettolo, et al.. (2024). 498P Neuromuscular centre effect on prevalence of congenital myasthenic syndrome (CMS) in the UK. Neuromuscular Disorders. 43. 104441.631–104441.631.
4.
Mohassel, Payam, Maike F. Dohrn, Museer A. Lone, et al.. (2023). P169 Childhood onset amyotrophic lateral sclerosis associated with SPTLC2 gain-of-function pathogenic variants: clinical, genetic, and biochemical insights. Neuromuscular Disorders. 33. S107–S107.
5.
Chaplin, Marty, Rebecca Bresnahan, Nigel Fleeman, et al.. (2023). Onasemnogene Abeparvovec for Treating Pre-symptomatic Spinal Muscular Atrophy: An External Assessment Group Perspective of the Partial Review of NICE Highly Specialised Technology Evaluation 15. PharmacoEconomics - Open. 7(6). 863–875. 6 indexed citations
6.
Sárközy, Anna, Mário Sá, Deborah Ridout, et al.. (2023). Long-term Natural History of Pediatric Dominant and Recessive RYR1 -Related Myopathy. Neurology. 101(15). e1495–e1508. 4 indexed citations
7.
Pipis, Menelaos, Roy Poh, Stéphanie Efthymiou, et al.. (2023). Post-transcriptional microRNA repression of PMP22 dose in severe Charcot-Marie-Tooth disease type 1. Brain. 146(10). 4025–4032. 3 indexed citations
8.
Samuels, Martin, Jacqueline Palace, David Beeson, et al.. (2023). Congenital myasthenic syndromes: a retrospective natural history study of respiratory outcomes in a single centre. Brain Communications. 5(6). fcad299–fcad299. 5 indexed citations
9.
Sabanathan, Saraswathy, Kshitij Mankad, James Davison, et al.. (2022). Expanding the phenotype of children presenting with hypoventilation with biallelic TBCK pathogenic variants and literature review. Neuromuscular Disorders. 33(1). 50–57. 3 indexed citations
10.
Field, Ella, Helen Walsh, Gabrielle Norrish, et al.. (2022). Cardiac Manifestations of Myotonic Dystrophy in a Pediatric Cohort. Frontiers in Pediatrics. 10. 910660–910660. 5 indexed citations
11.
Munot, Pinki, Silvia Torelli, Adnan Manzur, et al.. (2021). TRAPPC11 ‐related muscular dystrophy with hypoglycosylation of alpha‐dystroglycan in skeletal muscle and brain. Neuropathology and Applied Neurobiology. 48(2). e12771–e12771. 17 indexed citations
12.
Wilson, Louise C., et al.. (2021). Biallelic P4HTM variants associated with HIDEA syndrome and mitochondrial respiratory chain complex I deficiency. European Journal of Human Genetics. 29(10). 1536–1541. 5 indexed citations
13.
Wadman, Renske I., Ramona De Amicis, Alberto Battezzati, et al.. (2020). Feeding difficulties in children and adolescents with spinal muscular atrophy type 2. Neuromuscular Disorders. 31(2). 101–112. 16 indexed citations
14.
Vivekanandam, Vinojini, Pinki Munot, Michael G. Hanna, & Emma Matthews. (2020). Skeletal Muscle Channelopathies. Neurologic Clinics. 38(3). 481–491. 7 indexed citations
15.
Vecchio, Domizia, Sithara Ramdas, Pinki Munot, et al.. (2019). Paediatric myasthenia gravis: Prognostic factors for drug free remission. Neuromuscular Disorders. 30(2). 120–127. 24 indexed citations
16.
Pitt, Matthew, Rahul Phadke, Alexander M. Rossor, et al.. (2018). Clinical spectrum, treatment and outcome of children with suspected diagnosis of chronic inflammatory demyelinating polyradiculoneuropathy. Neuromuscular Disorders. 28(9). 757–765. 14 indexed citations
17.
Matthews, Emma, Richa Sud, Michael G. Hanna, et al.. (2017). Skeletal Muscle Channelopathies: Rare Disorders with Common Pediatric Symptoms. The Journal of Pediatrics. 188. 181–185.e6. 19 indexed citations
18.
Brunklaus, Andreas, S. Robb, Rosaline C. M. Quinlivan, et al.. (2016). Vitamin D in corticosteroid-naïve and corticosteroid-treated Duchenne muscular dystrophy: what dose achieves optimal 25(OH) vitamin D levels?. Archives of Disease in Childhood. 101(10). 957–961. 11 indexed citations
19.
Munot, Pinki, Yanick J. Crow, & Vijeya Ganesan. (2011). Paediatric stroke: genetic insights into disease mechanisms and treatment targets. The Lancet Neurology. 10(3). 264–274. 43 indexed citations
20.
Munot, Pinki, et al.. (2010). Severe iron deficiency anaemia and ischaemic stroke in children. Archives of Disease in Childhood. 96(3). 276–279. 37 indexed citations

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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