Richa Sud

1.3k citations

35 papers · 903 indexed · h-index 17

Impact in

Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases
- Neuroscience and Neuropharmacology Research
Cardiology and Cardiovascular Medicine top 5%
- Cardiac electrophysiology and arrhythmias
- Cardiomyopathy and Myosin Studies

Papers in

Sensory Systems 5
- Hearing, Cochlea, Tinnitus, Genetics 3
Cellular and Molecular Neuroscience 17
- Genetic Neurodegenerative Diseases 14

Co-authors: Michael G. Hanna Emma Matthews Mary B. Davis A. Haworth Doreen Fialho Stéphanie Schorge Dimitri M. Kullmann J. Burge
Journals: Neurology (8 papers)Brain (4 papers)Neuromuscular Disorders (3 papers)Scientific Reports (2 papers)The Journal of Pediatrics (1 paper)
Partner nations: United Kingdom Italy Finland

In The Last Decade

Richa Sud

32 papers receiving 882 citations

Peers

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-authors

The 25 scholars most cited alongside Richa Sud, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Richa Sud Line = papers co-authored together Richa Sud links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Prevalence of genetically confirmed skeletal muscle channelopathies in the era of next generation sequencing Neuromuscular Disorders ·Vinojini Vivekanandam, Rawan Jaibaji, Richa Sud, Rebecca Ellmers, Iwona Skorupinska, Louise Germaine, Natalie James, Sarah Holmes, Roope Männikkö, Dipa Jayaseelan, Michael G. Hanna	2023	10
2	Andersen–Tawil syndrome: deep phenotyping reveals significant cardiac and neuromuscular morbidity Brain ·Vinojini Vivekanandam, Roope Männikkö, Iwona Skorupinska, Louise Germain, Belinda Gray, Sarah Wedderburn, Damian Kozyra, Richa Sud, Natalie James, Sarah Holmes, Konstantinos Savvatis, Doreen Fialho, Ashirwad Merve, J. Pattni, Maria Elena Farrugia, Elijah R. Behr, Chiara Marini‐Bettolo, Michael G. Hanna, Emma Matthews	2021	14
3	Translating genetic and functional data into clinical practice: a series of 223 families with myotonia Brain ·Karen Suetterlin, Emma Matthews, Richa Sud, Samuel McCall, Doreen Fialho, J. Burge, Dipa Jayaseelan, Andrea Haworth, Mary G. Sweeney, Dimitri M. Kullmann, Stéphanie Schorge, Michael G. Hanna, Roope Männikkö	2021	14
4	Annual Renal Ultrasound May Prevent Acute Presentation With Acetazolamide-Associated Urolithiasis Neurology Clinical Practice ·Karen Suetterlin, Vinojini Vivekanandam, Natalie James, Richa Sud, Sarah J. Holmes, Doreen Fialho, Michael G. Hanna, Emma Matthews	2020	4
5	Andersen-Tawil Syndrome Presenting with Complete Heart Block Journal of Neuromuscular Diseases ·Karen Suetterlin, Roope Männikkö, Enrico Floßmann, Richa Sud, Doreen Fialho, Vinojini Vivekanandam, Natalie James, Thomas Gossios, Michael G. Hanna, Kostas Savvatis, Emma Matthews	2020	4
6	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 ·Michael G. Thor, Vinojini Vivekanandam, Marisol Sampedro Castañeda, S. Veronica Tan, Karen Suetterlin, Richa Sud, S. Durran, Stéphanie Schorge, Dimitri M. Kullmann, Michael G. Hanna, Emma Matthews, Roope Männikkö	2019	15
7	Hypokalaemic periodic paralysis and myotonia in a patient with homozygous mutation p.R1451L in NaV1.4 Scientific Reports ·Sushan Luo, Marisol Sampedro Castañeda, Emma Matthews, Richa Sud, Michael G. Hanna, Jian Sun, Jie Song, Jiahong Lu, Kai Qiao, Chongbo Zhao, Roope Männikkö	2018	21
8	Skeletal Muscle Channelopathies: Rare Disorders with Common Pediatric Symptoms The Journal of Pediatrics ·Emma Matthews, Arpana Silwal, Richa Sud, Michael G. Hanna, Adnan Y. Manzur, Francesco Muntoni, Pinki Munot	2017	19
9	A new explanation for recessive myotonia congenita Neurology ·D.L. Raja Rayan, A. Haworth, Richa Sud, Emma Matthews, Doreen Fialho, J. Burge, Simona Portaro, Stéphanie Schorge, K. van devan der Tuin, Peter Lunt, Meriel McEntagart, António Toscano, Mary B. Davis, Michael G. Hanna	2012	27
10	1154 Skeletal muscle chloride channel gene (CLCN1) copy number variation can cause myotonia congenita Journal of Neurology Neurosurgery & Psychiatry ·Dipa Raja Rayan, A. Haworth, Richa Sud, Emma Matthews, Doreen Fialho, J. Burge, Simona Portaro, António Toscano, Mary Dabney Davis, Michael G. Hanna	2012	1
11	Refined exercise testing can aid dna‐based diagnosis in muscle channelopathies Annals of Neurology ·S. Veronica Tan, Emma Matthews, Melissa Barber, J. Burge, Sanjeev Rajakulendran, Doreen Fialho, Richa Sud, Andrea Haworth, Martin Koltzenburg, Michael G. Hanna	2011	72
12	Sodium and chloride channelopathies with myositis: Coincidence or connection? Muscle & Nerve ·Emma Matthews, James Miller, Malcolm Macleod, James W. Ironside, Gareth Ambler, Robin Labrum, Richa Sud, Janice L. Holton, Michael G. Hanna	2011	2
13	Stridor as a Neonatal Presentation of Skeletal Muscle Sodium Channelopathy Archives of Neurology ·Emma Matthews, Adnan Y. Manzur, Richa Sud, Francesco Muntoni, Michael G. Hanna	2011	25
14	A PATIENT WITH EPISODIC ATAXIA AND PARAMYOTONIA CONGENITA DUE TO MUTATIONS IN KCNA1 AND SCN4A Neurology ·Sanjeev Rajakulendran, S. Veronica Tan, Emma Matthews, Susan E Tomlinson, Robyn Labrum, Richa Sud, Dimitri M. Kullmann, Stéphanie Schorge, Michael G. Hanna	2009	7
15	Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis Neurology ·Emma Matthews, Robyn Labrum, Mary G. Sweeney, Richa Sud, A. Haworth, Patrick F. Chinnery, G. Meola, Stéphanie Schorge, Dimitri M. Kullmann, Mary B. Davis, Michael G. Hanna	2008	144
16	What causes paramyotonia in the United Kingdom? Neurology ·Emma Matthews, S. Veronica Tan, Doreen Fialho, M G Sweeney, Richa Sud, A. Haworth, Edouard G. Stanley, Gabriel Cea, Mary B. Davis, Michael G. Hanna	2007	49
17	Transcriptional regulation by Barhl1 and Brn-3c in organ of corti derived cell lines Molecular Brain Research ·Richa Sud, Chris M. Jones, Sandro Banfi, Sally J. Dawson	2005	5
18	Brn-3c (POU4F3) regulates BDNF and NT-3 promoter activity Biochemical and Biophysical Research Communications ·R. Lee Clough, Richa Sud, Noa Davis-Silberman, Ronna Hertzano, Karen B. Avraham, Matthew C. Holley, Sally J. Dawson	2004	33
19	Genetic alterations in gastric cancers from British patients Cancer Genetics and Cytogenetics ·Richa Sud, Dagan Wells, Ian Talbot, Joy Delhanty	2001	36
20	Infrequent alterations of the APC and MCC genes in gastric cancers from British patients British Journal of Cancer ·Richa Sud, IC Talbot, JDA Delhanty	1996	16

About Richa Sud

Richa Sud is a scholar working on Sensory Systems, Cellular and Molecular Neuroscience, Cardiology and Cardiovascular Medicine, Molecular Biology and Pathology and Forensic Medicine, having authored 35 papers that have together received 903 indexed citations. Recurring topics across this work include Ion channel regulation and function (24 papers), Cardiac electrophysiology and arrhythmias (15 papers), Genetic Neurodegenerative Diseases (14 papers), Cardiomyopathy and Myosin Studies (5 papers), Plant Molecular Biology Research (3 papers), Genetic factors in colorectal cancer (3 papers), Hearing, Cochlea, Tinnitus, Genetics (3 papers) and Ion Transport and Channel Regulation (3 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (476 citations), Cardiology and Cardiovascular Medicine (518 citations), Sensory Systems (84 citations), Molecular Biology (761 citations) and Neurology (69 citations). Richa Sud has collaborated with scholars based in United Kingdom, Italy and Finland. Frequent co-authors include Michael G. Hanna, Emma Matthews, Mary B. Davis, A. Haworth, Doreen Fialho, Stéphanie Schorge, Dimitri M. Kullmann, J. Burge, Simona Portaro and Andrea Haworth. Their work appears in journals such as Neurology, Brain, Neuromuscular Disorders, Scientific Reports and The Journal of Pediatrics.

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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