Shiva Ganesan

1.9k total citations
15 papers, 143 citations indexed

About

Shiva Ganesan is a scholar working on Genetics, Psychiatry and Mental health and Molecular Biology. According to data from OpenAlex, Shiva Ganesan has authored 15 papers receiving a total of 143 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 5 papers in Psychiatry and Mental health and 4 papers in Molecular Biology. Recurrent topics in Shiva Ganesan's work include Genomics and Rare Diseases (9 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Epilepsy research and treatment (5 papers). Shiva Ganesan is often cited by papers focused on Genomics and Rare Diseases (9 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Epilepsy research and treatment (5 papers). Shiva Ganesan collaborates with scholars based in United States, United Kingdom and Luxembourg. Shiva Ganesan's co-authors include Ingo Helbig, Peter D. Galer, David Lewis‐Smith, Katherine L. Helbig, Colin A. Ellis, Margaret O’Brien, Julie Xian, Roland Krause, Michael C. Kaufman and Shridhar Parthasarathy and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Brain and Neurology.

In The Last Decade

Shiva Ganesan

11 papers receiving 142 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Shiva Ganesan United States	8	91	64	60	14	13	15	143
Shridhar Parthasarathy United States	7	60 0.7×	61 1.0×	38 0.6×	5 0.4×	8 0.6×	14	145
Anil P. S. Ori Netherlands	5	43 0.5×	103 1.6×	25 0.4×	6 0.4×	4 0.3×	6	170
Sonal Mahida United States	8	124 1.4×	93 1.5×	63 1.1×	19 1.4×		13	210
Jianmin Zhong China	10	54 0.6×	107 1.7×	68 1.1×	34 2.4×		27	216
Leslie Myint United States	6	27 0.3×	69 1.1×	28 0.5×	8 0.6×	4 0.3×	10	135
Danielle Nolan United States	6	75 0.8×	46 0.7×	33 0.6×	23 1.6×		10	129
Anaïs Begemann Switzerland	3	47 0.5×	51 0.8×	26 0.4×	9 0.6×		4	108
Philip Holmgren Belgium	5	88 1.0×	66 1.0×	48 0.8×	20 1.4×	1 0.1×	5	174
Meghan Candee United States	6	71 0.8×	31 0.5×	40 0.7×	17 1.2×	1 0.1×	10	123
Sarah M. Ruggiero United States	6	40 0.4×	26 0.4×	26 0.4×	7 0.5×	1 0.1×	10	81

Countries citing papers authored by Shiva Ganesan

Since Specialization

Citations

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

Fields of papers citing papers by Shiva Ganesan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shiva Ganesan

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

All Works

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15 of 15 papers shown

Shimelis, Hermela, et al.. (2026). Shared and distinct phenotypic profiles among neurodevelopmental disorder genes. medRxiv.

Galer, Peter D., Jillian L. McKee, Sarah M. Ruggiero, et al.. (2025). Quantitative EEG Biomarkers in the Genetic Epilepsies and Associations With Neurologic Outcomes. Neurology. 105(8). e214148–e214148.

Cuddapah, Vishnu Anand, Dechun Chen, Bumsik Cho, et al.. (2025). Rare variants in BMAL1 are associated with a neurodevelopmental syndrome. Proceedings of the National Academy of Sciences. 122(31). e2427085122–e2427085122.

Harrison, Abiola, Shiva Ganesan, Samuel R. Pierce, et al.. (2025). Familial SYNGAP1 variants define the boundaries of a complex neurodevelopmental disorder with epilepsy. Epilepsia. 66(9). 3505–3515.

Ruggiero, Sarah M., Julie Xian, Shridhar Parthasarathy, et al.. (2024). The clinical and genetic spectrum of paediatric speech and language disorders. Brain. 148(2). 663–674. 4 indexed citations

Parthasarathy, Shridhar, et al.. (2024). Advances in big data and omics: Paving the way for discovery in childhood epilepsies. Current problems in pediatric and adolescent health care. 54(8). 101634–101634. 2 indexed citations

Oliver, Karen, Colin A. Ellis, Ingrid E. Scheffer, et al.. (2022). Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery. EBioMedicine. 81. 104079–104079. 17 indexed citations

Lewis‐Smith, David, Shridhar Parthasarathy, Julie Xian, et al.. (2022). Computational analysis of neurodevelopmental phenotypes: Harmonization empowers clinical discovery. Human Mutation. 43(11). 1642–1658. 11 indexed citations

Lewis‐Smith, David, Shiva Ganesan, Peter D. Galer, et al.. (2021). Phenotypic homogeneity in childhood epilepsies evolves in gene-specific patterns across 3251 patient-years of clinical data. European Journal of Human Genetics. 29(11). 1690–1700. 8 indexed citations

10.

Crawford, Katherine, Julie Xian, Katherine L. Helbig, et al.. (2021). Computational analysis of 10,860 phenotypic annotations in individuals with SCN2A-related disorders. Genetics in Medicine. 23(7). 1263–1272. 32 indexed citations

11.

Lewis‐Smith, David, Peter D. Galer, Ganna Balagura, et al.. (2021). Modeling seizures in the Human Phenotype Ontology according to contemporary ILAE concepts makes big phenotypic data tractable. Epilepsia. 62(6). 1293–1305. 13 indexed citations

12.

Ganesan, Shiva, Peter D. Galer, Katherine L. Helbig, et al.. (2020). A longitudinal footprint of genetic epilepsies using automated electronic medical record interpretation. Genetics in Medicine. 22(12). 2060–2070. 17 indexed citations

13.

Ganesan, Shiva, David Lewis‐Smith, Manuela Pendziwiat, et al.. (2020). Semantic Similarity Analysis Reveals Robust Gene-Disease Relationships in Developmental and Epileptic Encephalopathies. The American Journal of Human Genetics. 107(4). 683–697. 22 indexed citations

14.

Felmeister, Alex, Angela J. Waanders, Jennifer L. Mason, et al.. (2020). A Framework for Analysis, Ontological Evaluation, and Visualization in Preparation to Predictive Analytics in Pediatric Brain Tumor Research. 1 indexed citations

15.

Helbig, Ingo, Giulia Barcia, Manuela Pendziwiat, et al.. (2020). Whole‐exome and HLA sequencing in Febrile infection‐related epilepsy syndrome. Annals of Clinical and Translational Neurology. 7(8). 1429–1435. 16 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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