Rahul Phadke

4.6k total citations
85 papers, 1.8k citations indexed

About

Rahul Phadke is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Rahul Phadke has authored 85 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 18 papers in Cardiology and Cardiovascular Medicine and 17 papers in Genetics. Recurrent topics in Rahul Phadke's work include Muscle Physiology and Disorders (32 papers), Cardiomyopathy and Myosin Studies (16 papers) and Neurogenetic and Muscular Disorders Research (16 papers). Rahul Phadke is often cited by papers focused on Muscle Physiology and Disorders (32 papers), Cardiomyopathy and Myosin Studies (16 papers) and Neurogenetic and Muscular Disorders Research (16 papers). Rahul Phadke collaborates with scholars based in United Kingdom, Italy and United States. Rahul Phadke's co-authors include Caroline A. Sewry, Francesco Muntoni, Heinz Jungbluth, Anna Sárközy, Francesco Zorzato, Julien Ochala, Mathias Gautel, Michael P. Lunn, Susan Treves and Samia N. Naccache and has published in prestigious journals such as The Journal of Experimental Medicine, SHILAP Revista de lepidopterología and The Journal of Cell Biology.

In The Last Decade

Rahul Phadke

78 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rahul Phadke United Kingdom 21 933 339 279 265 238 85 1.8k
Nir Yogev Germany 21 913 1.0× 183 0.5× 244 0.9× 118 0.4× 92 0.4× 29 3.1k
Alexis R. Demonbreun United States 25 1.2k 1.3× 217 0.6× 267 1.0× 138 0.5× 98 0.4× 59 1.7k
Linda N. Geng United States 15 1.3k 1.4× 251 0.7× 109 0.4× 125 0.5× 164 0.7× 35 1.7k
Jean‐Pierre Louboutin United States 29 921 1.0× 121 0.4× 317 1.1× 248 0.9× 83 0.3× 64 2.6k
Liesbet Martens Belgium 17 930 1.0× 144 0.4× 273 1.0× 188 0.7× 82 0.3× 24 3.0k
John T. Sladky United States 31 1.5k 1.6× 272 0.8× 416 1.5× 856 3.2× 908 3.8× 59 3.0k
Sofie De Prijck Belgium 13 831 0.9× 120 0.4× 235 0.8× 182 0.7× 88 0.4× 15 3.2k
Jonathan B. Strober United States 24 444 0.5× 144 0.4× 73 0.3× 224 0.8× 677 2.8× 43 1.9k
Jonathan D. Fratkin United States 23 608 0.7× 100 0.3× 343 1.2× 329 1.2× 223 0.9× 55 1.6k
Akira Naito Japan 23 337 0.4× 168 0.5× 181 0.6× 197 0.7× 112 0.5× 187 1.9k

Countries citing papers authored by Rahul Phadke

Since Specialization
Citations

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

Fields of papers citing papers by Rahul Phadke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rahul Phadke

This figure shows the co-authorship network connecting the top 25 collaborators of Rahul Phadke. A scholar is included among the top collaborators of Rahul Phadke 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 Rahul Phadke. Rahul Phadke 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.
Butler, James J., et al.. (2025). Outcomes Following Achilles Tendon Ruptures in the National Hockey League: A Retrospective Sports Database Study. Journal of Clinical Medicine. 14(15). 5471–5471.
2.
Müller, Juliane S., Irina Zaharieva, Vicente A. Yépez, et al.. (2025). Multi-omics approach identifies a novel recessive pathogenic variant in the TNNT3 gene in two siblings with congenital myopathy. Neuromuscular Disorders. 52. 105415–105415.
3.
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
4.
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
5.
Zambon, Alberto A., François Abel, Barry Linnane, et al.. (2022). Troponin-T type 1 (TNNT1)-related nemaline myopathy: unique respiratory phenotype and muscle pathology findings. Neuromuscular Disorders. 32(3). 245–254. 5 indexed citations
6.
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
7.
Suetterlin, Karen, S. Veronica Tan, Roope Männikkö, et al.. (2021). Ageing contributes to phenotype transition in a mouse model of periodic paralysis. SHILAP Revista de lepidopterología. 4(2). 245–259. 6 indexed citations
8.
Sewry, Caroline A., L. Feng, D. Chambers, Emma Matthews, & Rahul Phadke. (2021). Importance of immunohistochemical evaluation of developmentally regulated myosin heavy chains in human muscle biopsies. Neuromuscular Disorders. 31(5). 371–384. 7 indexed citations
9.
Aartsma‐Rus, Annemieke, Jennifer E. Morgan, Hendrik Neubert, et al.. (2019). Report of a TREAT-NMD/World Duchenne Organisation Meeting on Dystrophin Quantification Methodology. Journal of Neuromuscular Diseases. 6(1). 147–159. 44 indexed citations
10.
Ravenscroft, Gianina, Irina Zaharieva, Carlo Augusto Bortolotti, et al.. (2018). Bi-allelic mutations in MYL1 cause a severe congenital myopathy. Human Molecular Genetics. 27(24). 4263–4272. 29 indexed citations
11.
Hafner, Patricia, Rahul Phadke, Adnan Manzur, et al.. (2018). Electromyography and muscle biopsy in paediatric neuromuscular disorders – Evaluation of current practice and literature review. Neuromuscular Disorders. 29(1). 14–20. 11 indexed citations
12.
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
13.
Ullmann, Urielle, L. D'Argenzio, Shrey Mathur, et al.. (2018). ECEL1 gene related contractural syndrome: Long-term follow-up and update on clinical and pathological aspects. Neuromuscular Disorders. 28(9). 741–749. 10 indexed citations
14.
Pavlidou, Efterpi, Vincenzo Salpietro, Rahul Phadke, et al.. (2016). Pontocerebellar hypoplasia type 2D and optic nerve atrophy further expand the spectrum associated with selenoprotein biosynthesis deficiency. European Journal of Paediatric Neurology. 20(3). 483–488. 30 indexed citations
15.
Goede, Christian de, et al.. (2015). Choline Kinase Beta–Related Muscular Dystrophy, Appearance of Muscle Involvement on Magnetic Resonance Imaging. Pediatric Neurology. 54. 49–54. 5 indexed citations
16.
Steel, Dora, Vincenzo Salpietro, Rahul Phadke, et al.. (2015). Whole exome sequencing reveals a MLL de novo mutation associated with mild developmental delay and without ‘hairy elbows’: expanding the phenotype of Wiedemann–Steiner syndrome. Journal of Genetics. 94(4). 755–758. 20 indexed citations
17.
18.
Stevens, Elizabeth, Silvia Torelli, Lucy Feng, et al.. (2013). Flow Cytometry for the Analysis of α-Dystroglycan Glycosylation in Fibroblasts from Patients with Dystroglycanopathies. PLoS ONE. 8(7). e68958–e68958. 13 indexed citations
19.
Borg, Anouk, George Samandouras, Rahul Phadke, & Neil Kitchen. (2010). An unusual cerebellar cyst. Journal of Clinical Neuroscience. 17(8). 1023–1023. 1 indexed citations
20.
Ali, Nadeem, Mary G. Sweeney, Rahul Phadke, et al.. (2010). Pupillary Dysfunction in an Atypical Case of Mitochondrial Myopathy With Tubular Aggregates. Journal of Neuro-Ophthalmology. 30(2). 153–156. 1 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Nir Yogev Breakdown of academic impact, for papers by Alexis R. Demonbreun Breakdown of academic impact, for papers by Linda N. Geng Breakdown of academic impact, for papers by Jean‐Pierre Louboutin Breakdown of academic impact, for papers by Liesbet Martens Breakdown of academic impact, for papers by John T. Sladky Breakdown of academic impact, for papers by Sofie De Prijck Breakdown of academic impact, for papers by Jonathan B. Strober Breakdown of academic impact, for papers by Jonathan D. Fratkin Breakdown of academic impact, for papers by Akira Naito
Rankless by CCL
2026