Catherine Shain

1.2k total citations
5 papers, 233 citations indexed

About

Catherine Shain is a scholar working on Genetics, Psychiatry and Mental health and Molecular Biology. According to data from OpenAlex, Catherine Shain has authored 5 papers receiving a total of 233 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 3 papers in Psychiatry and Mental health and 2 papers in Molecular Biology. Recurrent topics in Catherine Shain's work include Genomics and Rare Diseases (3 papers), Epilepsy research and treatment (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Catherine Shain is often cited by papers focused on Genomics and Rare Diseases (3 papers), Epilepsy research and treatment (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Catherine Shain collaborates with scholars based in United States, Canada and United Arab Emirates. Catherine Shain's co-authors include Annapurna Poduri, Heather E. Olson, Beth Rosen Sheidley, McKenna Kelly, Sriram Ramgopal, Anne Rochtus, Lacey Smith, Alan Taylor, Sonal Mahida and Shira Rockowitz and has published in prestigious journals such as Neurology, Annals of Neurology and Epilepsia.

In The Last Decade

Catherine Shain

5 papers receiving 232 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Catherine Shain United States	5	125	105	70	62	36	5	233
McKenna Kelly United States	6	136 1.1×	102 1.0×	75 1.1×	39 0.6×	39 1.1×	6	226
Viola Doccini Italy	9	182 1.5×	92 0.9×	109 1.6×	108 1.7×	58 1.6×	10	317
Sinéad B. Heavin Australia	3	85 0.7×	137 1.3×	66 0.9×	62 1.0×	45 1.3×	3	196
Ahmed Abdelmoity United States	11	95 0.8×	91 0.9×	55 0.8×	54 0.9×	33 0.9×	25	264
Vandana Shashi United States	4	77 0.6×	90 0.9×	76 1.1×	23 0.4×	45 1.3×	4	170
Cheuk Wing Fung China	9	54 0.4×	31 0.3×	67 1.0×	42 0.7×	21 0.6×	18	177
Agnès Gautier France	7	136 1.1×	130 1.2×	121 1.7×	38 0.6×	50 1.4×	14	295
Rebecca Pinsky United States	2	99 0.8×	46 0.4×	72 1.0×	22 0.4×	28 0.8×	2	157
Melanie Bonner United States	6	76 0.6×	148 1.4×	108 1.5×	55 0.9×	61 1.7×	9	249
E. Chung United Kingdom	8	103 0.8×	51 0.5×	98 1.4×	34 0.5×	28 0.8×	9	267

Countries citing papers authored by Catherine Shain

Since Specialization

Citations

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

Fields of papers citing papers by Catherine Shain

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine Shain

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

All Works

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5 of 5 papers shown

1.

Rochtus, Anne, Heather E. Olson, Lacey Smith, et al.. (2020). Genetic diagnoses in epilepsy: The impact of dynamic exome analysis in a pediatric cohort. Epilepsia. 61(2). 249–258. 88 indexed citations

2.

Olson, Heather E., McKenna Kelly, Christopher M. LaCoursiere, et al.. (2017). Genetics and genotype–phenotype correlations in early onset epileptic encephalopathy with burst suppression. Annals of Neurology. 81(3). 419–429. 94 indexed citations

3.

Tobochnik, Steven, et al.. (2017). Familial aggregation of focal seizure semiology in the Epilepsy Phenome/Genome Project. Neurology. 89(1). 22–28. 6 indexed citations

4.

Pardoe, Heath, Robert Bachman, Catherine Shain, et al.. (2015). Phenotypic and imaging features of FLNA-negative patients with bilateral periventricular nodular heterotopia and epilepsy. Epilepsy & Behavior. 51. 321–327. 11 indexed citations

5.

Shain, Catherine, et al.. (2013). Polymicrogyria‐associated epilepsy: A multicenter phenotypic study from the Epilepsy Phenome/Genome Project. Epilepsia. 54(8). 1368–1375. 34 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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