Nanda A. Singh

3.2k citations
12 papers · 2.4k · 2 hit papers · h-index 11

Impact in

Papers in

Nanda A. Singh

12 papers receiving 2.4k citations

Nanda A. Singh's Hit Papers

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family 1998 · 731 citations
7310+9+18Years since publication250500750

Peers

Nanda A. Singh
Comparison fields: 5 of 86
  • Cellular and Molecular Neuroscience 1.2k
  • Psychiatry and Mental health 666
  • Cardiology and Cardiovascular Medicine 667
  • Molecular Biology 1.6k
  • Genetics 462
Replace Christoph Lossin with:
Christoph Lossin United States
Wangzhen Shen United States
Emi Mazaki Japan
Leanne M. Dibbens Australia
Edward Glasscock United States
Denys Chaigne France
Qun-Yong Zhou United States
Duncan P. McHale United Kingdom
Marco Weiergräber Germany
Sheila Christie United Kingdom
Nanda A. Singh relative to Christoph Lossin United States Christoph Lossin's profile →
Citations per field
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Citations per year

Countries citing papers authored by Nanda A. Singh

Since Specialization
Citations

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

Fields of papers citing papers by Nanda A. Singh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nanda A. Singh. 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 Nanda A. Singh. The network helps show where Nanda A. Singh may publish in the future.

Co-authors

The 25 scholars most cited alongside Nanda A. Singh, 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 Nanda A. Singh Line = papers co-authored together Nanda A. Singh links everyone, so they are left out of the graph.

All Works

12 of 12 papers shown
#Work
1
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
Hit paper breakdown →
1998943
2
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
Hit paper breakdown →
1998731
3 2008205
4 2009204
5 2021106
6 2008105
7 200933
8 199133
9 199029
10 199428
11 199216
12 20033

About Nanda A. Singh

Nanda A. Singh is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Cardiology and Cardiovascular Medicine and Surgery, having authored 12 papers that have together received 2.4k indexed citations. Recurring topics across this work include Neuroscience and Neuropharmacology Research (4 papers), Neuropeptides and Animal Physiology (4 papers), Ion channel regulation and function (3 papers), Receptor Mechanisms and Signaling (3 papers), Cardiac electrophysiology and arrhythmias (2 papers), DNA Repair Mechanisms (1 paper), Cancer Genomics and Diagnostics (1 paper) and Epilepsy research and treatment (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (1.2k citations), Psychiatry and Mental health (666 citations), Cardiology and Cardiovascular Medicine (667 citations), Molecular Biology (1.6k citations) and Genetics (462 citations). Nanda A. Singh has collaborated with scholars based in United States, Poland and Sweden. Frequent co-authors include Robin J. Leach, Carole Charlier, Mark Leppert, Stephen G. Ryan, Tracey Lewis, B.E. Reus, Andy Peiffer, Barbara R. DuPont, Vernon Anderson and Jerome V. Murphy. Their work appears in journals such as Brain Research, Nature Genetics, PLoS Genetics, European Journal of Pharmacology and Annual Review of Genomics and Human Genetics.

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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