Stephen G. Ryan

2.3k total citations · 1 hit paper
10 papers, 1.7k citations indexed

About

Stephen G. Ryan is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Stephen G. Ryan has authored 10 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Cellular and Molecular Neuroscience and 2 papers in Genetics. Recurrent topics in Stephen G. Ryan's work include Ion channel regulation and function (4 papers), Neuroscience and Neuropharmacology Research (4 papers) and Ion Transport and Channel Regulation (2 papers). Stephen G. Ryan is often cited by papers focused on Ion channel regulation and function (4 papers), Neuroscience and Neuropharmacology Research (4 papers) and Ion Transport and Channel Regulation (2 papers). Stephen G. Ryan collaborates with scholars based in United States, Australia and Poland. Stephen G. Ryan's co-authors include Tracey Lewis, Robin J. Leach, Carole Charlier, Mark Leppert, Nanda A. Singh, B.E. Reus, John J. Wasmuth, Rita Shiang, P. O’Connell and Yazhen Zhu and has published in prestigious journals such as Nature Genetics, Annals of Neurology and Journal of Child Neurology.

In The Last Decade

Stephen G. Ryan

10 papers receiving 1.6k citations

Hit Papers

A pore mutation in a novel KQT-like potassium channel gen... 1998 2026 2007 2016 1998 200 400 600
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
    1998 729 citations Carole Charlier, Nanda A. Singh et al. Nature Genetics profile →

Peers

Stephen G. Ryan
Patrick Cossette Canada
Claudia A. Sailer Austria
Heather A. O’Malley United States
Jack Kronengold United States
Vostrikov Vm Russia
Kamna Das United States
Li‐Dong Huang China
Elena Pravettoni Italy
Federica Bertaso France
Véronique André United States
Patrick Cossette Canada
Stephen G. Ryan
Citations per year, relative to Stephen G. Ryan Stephen G. Ryan (= 1×) peers Patrick Cossette

Countries citing papers authored by Stephen G. Ryan

Since Specialization
Citations

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

Fields of papers citing papers by Stephen G. Ryan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephen G. Ryan. 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 Stephen G. Ryan. The network helps show where Stephen G. Ryan may publish in the future.

Co-authorship network of co-authors of Stephen G. Ryan

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

All Works

10 of 10 papers shown
1.
Miller, Adam D., et al.. (2004). Mitochondrial 12S rRNA sequences support the existence of a third species of freshwater blackfish (Percicthyidae: Gadopsis) from south-eastern Australia. Memoirs of Museum Victoria. 61(2). 121–127. 20 indexed citations
2.
Miller, Van S. & Stephen G. Ryan. (1999). Hypertonia, hyperreflexia, and excessive startle response in a neonate. Seminars in Pediatric Neurology. 6(3). 158–163. 1 indexed citations
3.
Charlier, Carole, Nanda A. Singh, Stephen G. Ryan, et al.. (1998). A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family. Nature Genetics. 18(1). 53–55. 729 indexed citations breakdown →
4.
Ryan, Stephen G., et al.. (1997). Epilepsy and mental retardation limited to females: an X-linked dominant disorder with male sparing. Nature Genetics. 17(1). 92–95. 96 indexed citations
5.
Shiang, Rita, Stephen G. Ryan, Yazhen Zhu, et al.. (1995). Mutational analysis of familial and sporadic hyperekplexia. Annals of Neurology. 38(1). 85–91. 100 indexed citations
6.
Ryan, Stephen G., Marion S. Buckwalter, Cheryl A. Handford, et al.. (1994). A missense mutation in the gene encoding the α1 subunit of the inhibitory glycine receptor in the spasmodic mouse. Nature Genetics. 7(2). 131–135. 146 indexed citations
7.
Ryan, Stephen G., et al.. (1994). Paroxysmal Kinesigenic Dystonia After Methylphenidate Administration. Journal of Child Neurology. 9(1). 45–46. 29 indexed citations
8.
Shiang, Rita, Stephen G. Ryan, Yazhen Zhu, et al.. (1993). Mutations in the α1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia. Nature Genetics. 5(4). 351–358. 384 indexed citations
9.
Ryan, Stephen G., et al.. (1992). Startle disease, or hyperekplexia: Response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysis. Annals of Neurology. 31(6). 663–668. 92 indexed citations
10.
Ryan, Stephen G., et al.. (1991). Benign familial neonatal convulsions: Evidence for clinical and genetic heterogeneity. Annals of Neurology. 29(5). 469–473. 69 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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