Colin A. Ellis

Medicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 1%percentile

4.7Author DataRank

Indexed papers

3in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 3 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Assessing the landscape of STXBP1-related disorders in 534 individuals

Brain(2021)10.1093/brain/awab327

Top 9%

2.3DataRank

Top 9%125 citations

Shridhar Parthasarathy, Sarah M. Ruggiero, Ganna Balagura, Eryn Fitch, Katherine L. Helbig +48 more

Papers

Driven by 38 papers — median percentile 88. Top paper: “GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture”.

GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture

Nature Genetics(2023)10.1038/s41588-023-01485-w

N/A

2.9DataRank · unranked

217 citations

Ciarán Campbell, Siwei Chen, Bassel Abou‐Khalil, Oluyomi M. Adesoji, Zaid Afawi +95 more

Assessing the landscape of STXBP1-related disorders in 534 individuals

Brain(2021)10.1093/brain/awab327

Top 9%

2.3DataRank

Top 9%125 citations

Shridhar Parthasarathy, Sarah M. Ruggiero, Ganna Balagura, Eryn Fitch, Katherine L. Helbig +48 more

Computational analysis of 10,860 phenotypic annotations in individuals with SCN2A-related disorders

Genetics in Medicine(2021)10.1038/s41436-021-01120-1

Top 12%

1.7DataRank

Top 12%69 citations

Julie Xian, Katherine L. Helbig, Peter D. Galer, Shridhar Parthasarathy, David Lewis‐Smith +11 more

Modeling seizures in the Human Phenotype Ontology according to contemporary ILAE concepts makes big phenotypic data tractable

Epilepsia(2021)10.1111/epi.16908

Top 25%

0.794DataRank

Top 25%25 citations

Peter D. Galer, Ganna Balagura, Hugh Kearney, Shiva Ganesan, Mahgenn Cosico +8 more

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes

Nature Neuroscience(2024)10.1038/s41593-024-01747-8

N/A

0.612DataRank · unranked

58 citations

Siwei Chen, Bassel Abou‐Khalil, Zaid Afawi, Quratulain Zulfiqar Ali, Elisabetta Amadori +95 more

Epilepsy risk in offspring of affected parents; a cohort study of the “maternal effect” in epilepsy

Annals of Clinical and Translational Neurology(2020)10.1002/acn3.51258

N/A

0.464DataRank · unranked

21 citations

Colin A. Ellis, Samuel F. Berkovic, Chris Cotsapas, Ruth Ottman, Jakob Christensen +1 more

Phenotypic homogeneity in childhood epilepsies evolves in gene-specific patterns across 3251 patient-years of clinical data

European Journal of Human Genetics(2021)10.1038/s41431-021-00908-8

N/A

0.442DataRank · unranked

18 citations

Shiva Ganesan, Peter D. Galer, Katherine L. Helbig, Sarah McKeown, Margaret O’Brien +8 more

Generalized, focal, and combined epilepsies in families: New evidence for distinct genetic factors

Epilepsia(2020)10.1111/epi.16732

N/A

0.312DataRank · unranked

7 citations

Ruth Ottman, Michael P. Epstein, Samuel F. Berkovic, Colin A. Ellis

Generalization of finetuned transformer language models to new clinical contexts

JAMIA Open(2023)10.1093/jamiaopen/ooad070

N/A

0.269DataRank · unranked

5 citations

Samuel W. Terman, Ryan S. Gallagher, Chloé E. Hill, Kathryn A. Davis, Brian Litt +3 more

Variants in BSN, encoding the presynaptic protein Bassoon, result in a distinct neurodevelopmental disorder with a broad phenotypic range

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.04.011

N/A

0.241DataRank · unranked

4 citations

Sarah M. Ruggiero, Shiva Ganesan, Colin A. Ellis, Abiola Harrison, Katie Rose Sullivan +32 more

A pharmacokinetic model of antiseizure medication load to guide care in the epilepsy monitoring unit

Epilepsia(2023)10.1111/epi.17558

N/A

0DataRank · unranked

15 citations

Kevin Xie, Akash R. Pattnaik, James J. Gugger, Colin A. Ellis, Elizabeth Sweeney +7 more

Characterizing the treatment gap in the United States among adult patients with a new diagnosis of epilepsy

Epilepsia(2023)10.1111/epi.17641

N/A

0DataRank · unranked

6 citations

Colin A. Ellis, Emily Schriver, Kelly Fischbein, Debbie Smith, Jason T. Moyer +5 more

Alcohol for seizure induction in the epilepsy monitoring unit

Epilepsy & Behavior(2023)10.1016/j.yebeh.2023.109572

N/A

0DataRank · unranked

1 citations

Kevin Xie, Erin C. Conrad, Nina J Ghosn, Kristie Bauman, Jacob Korzun +14 more

Macrocephaly and developmental delay caused by missense variants in RAB5C

Human Molecular Genetics(2023)10.1093/hmg/ddad130

N/A

0DataRank · unranked

4 citations

Weimin Yuan, Federico Tessadori, Wilmer R. Rodriguez-Polanco, Jeremy J. Grubbs, Bo Zhang +94 more

Disparities in seizure outcomes revealed by large language models

medRxiv(2023)10.1101/2023.09.20.23295842

N/A

0DataRank · unranked

7 citations

William K.S. Ojemann, Ryan S. Gallagher, Alfredo Lucas, Chloé E. Hill, Roy H. Hamilton +5 more

Investigating the effect of polygenic background on epilepsy phenotype in ‘monogenic’ families

EBioMedicine(2024)10.1016/j.ebiom.2024.105404

N/A

0DataRank · unranked

30 citations

Ingrid E Scheffer, Colin A. Ellis, Bronwyn E. Grinton, Zaid Afawi, Dina Amrom +43 more

Disparities in Genetic Testing for Neurologic Disorders

Neurology(2024)10.1212/wnl.0000000000209161

N/A

0DataRank · unranked

25 citations

J. Nathan Copeland, Meron Azage, Laynie Dratch, Kelsey Johnson, Rachel Paul +16 more

Disparities in seizure outcomes revealed by large language models

Journal of the American Medical Informatics Association(2024)10.1093/jamia/ocae047

N/A

0DataRank · unranked

14 citations

William K.S. Ojemann, Ryan S. Gallagher, Russell T. Shinohara, Alfredo Lucas, Chloé E. Hill +6 more

Inflation of polygenic risk scores caused by sample overlap and relatedness: Examples of a major risk of bias

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.07.014

N/A

0DataRank · unranked

13 citations

Karen Oliver, Rebekah V. Harris, Ruth Ottman, Ingrid E Scheffer, Heather C Mefford +4 more

Artificial Intelligence in the Diagnosis and Quantitative Phenotyping of Hyperkinetic Movement Disorders: A Systematic Review

Journal of Clinical Medicine(2024)10.3390/jcm13237009

N/A

0DataRank · unranked

11 citations

Sushuma Yarlagadda, Kevin Xie, Colin A. Ellis, Meredith Spindler, Lauren H. Hammer +1 more

Interaction between visual impairment and genetic risk of dementia and psychosis in older adults

Age and Ageing(2024)10.1093/ageing/afae163

N/A

0DataRank · unranked

1 citations

Colin A. Ellis, Joshua R. Ehrlich, Allison W. Willis, Ali G. Hamedani

Familial aggregation of seizure outcomes in four familial epilepsy cohorts

Epilepsia(2024)10.1111/epi.18004

N/A

0DataRank · unranked

1 citations

Danni Tu, Karen Oliver, Heather C. Mefford, W. Allen Hauser, Jeffrey Buchhalter +5 more

Genome-wide association meta-analyses of drug-resistant epilepsy

EBioMedicine(2025)10.1016/j.ebiom.2025.105675

N/A

0DataRank · unranked

12 citations

Andreja Avberšek, Remi Stevelink, Helena Martins Custodio, Siwei Chen, Doug Speed +88 more

The Spectrum of Neurologic Phenotypes Associated With NUS1 Pathogenic Variants: A Comprehensive Case Series

Annals of Neurology(2025)10.1002/ana.27272

N/A

0DataRank · unranked

8 citations

María Novelli, Robert Coukos, Neha Prakash, Walaa A. Kamel, Marta Amengual‐Gual +75 more

Zero-Shot Extraction of Seizure Outcomes from Clinical Notes Using Generative Pretrained Transformers

Journal of Healthcare Informatics Research(2025)10.1007/s41666-025-00198-5

N/A

0DataRank · unranked

6 citations

Kevin Xie, Kevin Liu, Ellie Chang, Dan Roth, Brian Litt +2 more

Mesial‐to‐lateral gradients of epileptiform activity to localize mesial temporal lobe epilepsy

Epilepsia(2025)10.1111/epi.18462

N/A

0DataRank · unranked

3 citations

Alfredo Lucas, Sarah Lavelle, Akash R. Pattnaik, Juri Kim, William K.S. Ojemann +12 more

USP25 in genetic generalized epilepsy: a gene under scrutiny

Brain(2025)10.1093/brain/awaf406

N/A

0DataRank · unranked

1 citations

Jill R. Murrell, Anna J. Prentice, Ingo Helbig, Holger Lerche, Patrick May +90 more

Variants in BSN , encoding the presynaptic protein Bassoon, result in a novel neurodevelopmental disorder with a broad phenotypic range

medRxiv(2025)10.1101/2025.02.10.25321755

N/A

0DataRank · unranked

0 citations

Sarah M. Ruggiero, Shiva Ganesan, Colin A. Ellis, Abiola Harrison, Katie Rose Sullivan +34 more

Seizure characteristics and outcomes in patients with pleomorphic xanthoastrocytoma

Neuro-Oncology Advances(2025)10.1093/noajnl/vdaf134

N/A

0DataRank · unranked

0 citations

Colin A. Ellis, Kevin Xie, Nishant Sinha, Sharon X. Xie, Kathryn A. Davis +8 more

Early-onset genetic epilepsies reaching adult clinics

Brain(2020)10.1093/brain/awaa029

N/A

0DataRank · unranked

19 citations

Colin A. Ellis, Ingo Helbig, Rhys H. Thomas, David Lewis‐Smith

Low rate of glutamic acid decarboxylase 65 (GAD-65) antibodies in chronic epilepsy

Seizure(2020)10.1016/j.seizure.2020.05.008

N/A

0DataRank · unranked

9 citations

Colin A. Ellis, Julia Reichert, Eric Lancaster, Etsegenet F. Tizazu

Semantic Similarity Analysis Reveals Robust Gene-Disease Relationships in Developmental and Epileptic Encephalopathies

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.08.003

N/A

0DataRank · unranked

46 citations

Shiva Ganesan, David Lewis‐Smith, Sarah McKeown, Manuela Pendziwiat, Katherine L. Helbig +13 more

A longitudinal footprint of genetic epilepsies using automated electronic medical record interpretation

Genetics in Medicine(2020)10.1038/s41436-020-0923-1

N/A

0DataRank · unranked

40 citations

Peter D. Galer, Katherine L. Helbig, Sarah McKeown, Margaret O’Brien, Alexander K. Gonzalez +5 more

De novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonus

Brain(2021)10.1093/brain/awab299

N/A

0DataRank · unranked

42 citations

Ban H. Edani, Simone Martinelli, Hana Hansíková, Erik A. Eklund, Caterina Caputi +45 more

Natural History Study of STXBP1-Developmental and Epileptic Encephalopathy Into Adulthood

Neurology(2022)10.1212/wnl.0000000000200715

N/A

0DataRank · unranked

58 citations

David Crosiers, Ganna Balagura, Claudia Bonardi, Anna Basu, Gaetano Cantalupo +36 more

Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery

EBioMedicine(2022)10.1016/j.ebiom.2022.104079

N/A

0DataRank · unranked

41 citations

Colin A. Ellis, Ingrid E Scheffer, Shiva Ganesan, Costin Leu, Lynette G. Sadleir +12 more

Quantifying Clinical Outcome Measures in Patients with Epilepsy Using the Electronic Health Record

(2022)10.18653/v1/2022.bionlp-1.36

N/A

0DataRank · unranked

10 citations

Brian Litt, Dan Roth, Colin A. Ellis, Kevin Xie

Long‐term epilepsy outcome dynamics revealed by natural language processing of clinic notes

Epilepsia(2023)10.1111/epi.17633

N/A

0DataRank · unranked

33 citations

Ryan S. Gallagher, Russell T. Shinohara, Sharon X. Xie, Chloé E. Hill, Erin C. Conrad +5 more

Colin A. Ellis

Indexed papers

Top data-sharing exemplar

Papers