Richa Sud

1.3k total citations
35 papers, 903 citations indexed

About

Richa Sud is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cellular and Molecular Neuroscience. According to data from OpenAlex, Richa Sud has authored 35 papers receiving a total of 903 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 20 papers in Cardiology and Cardiovascular Medicine and 17 papers in Cellular and Molecular Neuroscience. Recurrent topics in Richa Sud's work include Ion channel regulation and function (24 papers), Cardiac electrophysiology and arrhythmias (15 papers) and Genetic Neurodegenerative Diseases (14 papers). Richa Sud is often cited by papers focused on Ion channel regulation and function (24 papers), Cardiac electrophysiology and arrhythmias (15 papers) and Genetic Neurodegenerative Diseases (14 papers). Richa Sud collaborates with scholars based in United Kingdom, Italy and Finland. Richa Sud's co-authors include Michael G. Hanna, Emma Matthews, Mary B. Davis, A. Haworth, Doreen Fialho, Stéphanie Schorge, Dimitri M. Kullmann, Simona Portaro, J. Burge and Andrea Haworth and has published in prestigious journals such as Brain, Neurology and Annals of Neurology.

In The Last Decade

Richa Sud

32 papers receiving 882 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Richa Sud United Kingdom 17 761 518 476 84 69 35 903
Emmanuelle Plassart France 10 404 0.5× 221 0.4× 227 0.5× 56 0.7× 50 0.7× 11 513
Robyn Labrum United Kingdom 14 488 0.6× 145 0.3× 400 0.8× 23 0.3× 175 2.5× 21 772
Svetlana Maugenre France 16 842 1.1× 434 0.8× 228 0.5× 73 0.9× 32 0.5× 18 1.1k
Angelo G. Torrente France 18 659 0.9× 616 1.2× 225 0.5× 50 0.6× 9 0.1× 34 985
Yi‐Je Chen United States 13 276 0.4× 70 0.1× 171 0.4× 29 0.3× 48 0.7× 31 566
Søren Grubb Denmark 12 332 0.4× 235 0.5× 134 0.3× 36 0.4× 48 0.7× 24 573
Lan Wei‐LaPierre United States 12 599 0.8× 57 0.1× 174 0.4× 104 1.2× 44 0.6× 19 760
Alejandro Moreno‐Domínguez Spain 13 346 0.5× 196 0.4× 61 0.1× 41 0.5× 12 0.2× 16 592
Lama Al‐Qusairi United States 10 458 0.6× 105 0.2× 90 0.2× 17 0.2× 17 0.2× 25 564
Ali Lourhmati Germany 10 233 0.3× 40 0.1× 162 0.3× 20 0.2× 51 0.7× 11 592

Countries citing papers authored by Richa Sud

Since Specialization
Citations

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

Fields of papers citing papers by Richa Sud

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Richa Sud

This figure shows the co-authorship network connecting the top 25 collaborators of Richa Sud. A scholar is included among the top collaborators of Richa Sud 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 Richa Sud. Richa Sud 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.
Vivekanandam, Vinojini, Richa Sud, Iwona Skorupinska, et al.. (2023). Prevalence of genetically confirmed skeletal muscle channelopathies in the era of next generation sequencing. Neuromuscular Disorders. 33(3). 270–273. 10 indexed citations
2.
Vivekanandam, Vinojini, Roope Männikkö, Iwona Skorupinska, et al.. (2021). Andersen–Tawil syndrome: deep phenotyping reveals significant cardiac and neuromuscular morbidity. Brain. 145(6). 2108–2120. 14 indexed citations
3.
Suetterlin, Karen, Emma Matthews, Richa Sud, et al.. (2021). Translating genetic and functional data into clinical practice: a series of 223 families with myotonia. Brain. 145(2). 607–620. 14 indexed citations
4.
Suetterlin, Karen, Vinojini Vivekanandam, Natalie James, et al.. (2020). Annual Renal Ultrasound May Prevent Acute Presentation With Acetazolamide-Associated Urolithiasis. Neurology Clinical Practice. 11(1). e40–e42. 4 indexed citations
5.
Suetterlin, Karen, Roope Männikkö, Enrico Floßmann, et al.. (2020). Andersen-Tawil Syndrome Presenting with Complete Heart Block. Journal of Neuromuscular Diseases. 8(1). 151–154. 4 indexed citations
6.
Vivekanandam, Vinojini, S. Veronica Tan, Karen Suetterlin, et al.. (2019). Myotonia in a patient with a mutation in an S4 arginine residue associated with hypokalaemic periodic paralysis and a concomitant synonymous CLCN1 mutation. Scientific Reports. 9(1). 17560–17560. 15 indexed citations
7.
Luo, Sushan, Emma Matthews, Richa Sud, et al.. (2018). Hypokalaemic periodic paralysis and myotonia in a patient with homozygous mutation p.R1451L in NaV1.4. Scientific Reports. 8(1). 9714–9714. 21 indexed citations
8.
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
9.
Stevens, Julia, Emma Matthews, Michael G. Hanna, et al.. (2017). Actazolamide to treat congenital myopathy caused by SCN4A mutation. European Journal of Paediatric Neurology. 21. e224–e225.
10.
Matthews, Emma, James Miller, Malcolm Macleod, et al.. (2011). Sodium and chloride channelopathies with myositis: Coincidence or connection?. Muscle & Nerve. 44(2). 283–288. 2 indexed citations
11.
Tan, S. Veronica, Emma Matthews, Melissa Barber, et al.. (2011). Refined exercise testing can aid dna‐based diagnosis in muscle channelopathies. Annals of Neurology. 69(2). 328–340. 72 indexed citations
12.
Matthews, Emma, Adnan Y. Manzur, Richa Sud, Francesco Muntoni, & Michael G. Hanna. (2011). Stridor as a Neonatal Presentation of Skeletal Muscle Sodium Channelopathy. Archives of Neurology. 68(1). 127–9. 25 indexed citations
13.
Matthews, Emma, Robyn Labrum, Mary G. Sweeney, et al.. (2008). Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis. Neurology. 72(18). 1544–1547. 144 indexed citations
14.
Matthews, Emma, S. Veronica Tan, Doreen Fialho, et al.. (2007). What causes paramyotonia in the United Kingdom?. Neurology. 70(1). 50–53. 49 indexed citations
15.
Sud, Richa, Chris M. Jones, Sandro Banfi, & Sally J. Dawson. (2005). Transcriptional regulation by Barhl1 and Brn-3c in organ of corti derived cell lines. Molecular Brain Research. 141(2). 174–180. 5 indexed citations
16.
Clough, R. Lee, Richa Sud, Ronna Hertzano, et al.. (2004). Brn-3c (POU4F3) regulates BDNF and NT-3 promoter activity. Biochemical and Biophysical Research Communications. 324(1). 372–381. 33 indexed citations
17.
Sud, Richa, et al.. (2001). Genetic alterations in gastric cancers from British patients. Cancer Genetics and Cytogenetics. 126(2). 111–119. 36 indexed citations
18.
Sud, Richa. (2000). Cell Lineage of Vein Formation in Variegated Leaves of the C4Grass Stenotaphrum secundatum. Annals of Botany. 86(1). 99–112. 17 indexed citations
19.
Sud, Richa, et al.. (1996). Infrequent alterations of the APC and MCC genes in gastric cancers from British patients. British Journal of Cancer. 74(7). 1104–1108. 16 indexed citations
20.
Gayther, Simon A., et al.. (1995). Rapid detection of rare variants and common polymorphisms in the APC gene by PCR-SSCP for presymptomatic diagnosis and showing allele loss.. Journal of Medical Genetics. 32(7). 568–571. 7 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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