Sameer M. Zuberi

Also affiliated with University of Glasgow

MedicineNeuroscienceBiochemistry, Genetics and Molecular Biology

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

5.6Author DataRank

Indexed papers

1in 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 1 indexed paper 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.

ILAE definition of the Idiopathic Generalized Epilepsy Syndromes: Position statement by the ILAE Task Force on Nosology and Definitions

Epilepsia(2022)10.1111/epi.17236

Top 4%

5.6DataRank

Top 4%449 citations

Jacqueline A. French, Ingrid E Scheffer, Alicia Bogacz, Taoufik Alsaadi, Michael R. Sperling +17 more

Papers

Driven by 14 papers — median percentile 96. Top paper: “ILAE definition of the Idiopathic Generalized Epilepsy Syndromes: Position statement by the ILAE Task Force on Nosology and Definitions”.

ILAE definition of the Idiopathic Generalized Epilepsy Syndromes: Position statement by the ILAE Task Force on Nosology and Definitions

Epilepsia(2022)10.1111/epi.17236

Top 4%

5.6DataRank

Top 4%449 citations

Jacqueline A. French, Ingrid E Scheffer, Alicia Bogacz, Taoufik Alsaadi, Michael R. Sperling +17 more

Genetic and phenotypic spectrum associated with IFIH1 gain‐of‐function

Human Mutation(2020)10.1002/humu.23975

N/A

0DataRank · unranked

113 citations

Sehoon Park, Francesco Gavazzi, Laura Adang, Loveline A. Ayuk, Lien Van Eyck +58 more

NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns

Genetics in Medicine(2020)10.1038/s41436-020-00988-9

N/A

0DataRank · unranked

56 citations

Trine Bjørg Hammer, Elena Gardella, Danique R.M. Vlaskamp, Birgitte Bertelsen, Simone Mandelstam +80 more

International League Against Epilepsy classification and definition of epilepsy syndromes with onset in childhood: Position paper by the ILAE Task Force on Nosology and Definitions

Epilepsia(2022)10.1111/epi.17241

N/A

0DataRank · unranked

902 citations

Elaine C Wirrell, Ingrid E Scheffer, Rima Nabbout, Kate Riney, Pauline Samia +14 more

Methodology for classification and definition of epilepsy syndromes with list of syndromes: Report of the ILAE Task Force on Nosology and Definitions

Epilepsia(2022)10.1111/epi.17237

N/A

0DataRank · unranked

276 citations

Rima Nabbout, Ingrid E Scheffer, Taoufik Alsaadi, Alicia Bogacz, Jacqueline A. French +17 more

International League Against Epilepsy classification and definition of epilepsy syndromes with onset at a variable age: position statement by the ILAE Task Force on Nosology and Definitions

Epilepsia(2022)10.1111/epi.17240

N/A

0DataRank · unranked

262 citations

Alicia Bogacz, Ernest Somerville, Édouard Hirsch, Rima Nabbout, Ingrid E Scheffer +15 more

The gain of function SCN1A disorder spectrum: novel epilepsy phenotypes and therapeutic implications

Brain(2022)10.1093/brain/awac210

N/A

0DataRank · unranked

158 citations

Tobias Brünger, Tony Feng, Carmen Fons, Anni Lehikoinen, Eleni Panagiotakaki +30 more

Development and Validation of a Prediction Model for Early Diagnosis of SCN1A -Related Epilepsies

Neurology(2022)10.1212/wnl.0000000000200028

N/A

0DataRank · unranked

73 citations

Eduardo Pérez‐Palma, Ismael Ghanty, Xinge Ji, Eva H. Brilstra, Berten Ceulemans +17 more

Fenfluramine provides clinically meaningful reduction in frequency of drop seizures in patients with Lennox–Gastaut syndrome: Interim analysis of an open‐label extension study

Epilepsia(2022)10.1111/epi.17431

N/A

0DataRank · unranked

50 citations

Ingrid E Scheffer, Berten Ceulemans, Joseph Sullivan, Katherine Nickels, Lieven Lagae +14 more

Conserved patterns across ion channels correlate with variant pathogenicity and clinical phenotypes

Brain(2022)10.1093/brain/awac305

N/A

0DataRank · unranked

26 citations

Eduardo Pérez‐Palma, Ludovica Montanucci, Michael Nothnagel, Rikke S. Møller, Stéphanie Schorge +8 more

Severe communication delays are independent of seizure burden and persist despite contemporary treatments in SCN1A+ Dravet syndrome: Insights from the ENVISION natural history study

Epilepsia(2023)10.1111/epi.17850

N/A

0DataRank · unranked

24 citations

Ingrid E Scheffer, Joseph Sullivan, Andreas Brunklaus, Susana Boronat, James W. Wheless +24 more

Solving the Etiology of Developmental and Epileptic Encephalopathy with Spike–Wave Activation in Sleep (D/EE‐SWAS)

Annals of Neurology(2024)10.1002/ana.27041

N/A

0DataRank · unranked

18 citations

Karen Oliver, Brigid M. Regan, Amy Schneider, Candace T. Myers, Michele G. Mehaffey +22 more

Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group

Epilepsia Open(2020)10.1002/epi4.12414

N/A

0DataRank · unranked

276 citations

Cigdem I. Akman, Marisa Armeno, Stéphane Auvin, Mackenzie C. Cervenka, J. Helen Cross +19 more

Cognitive stagnation and executive function deficits in young children with SCN1A + Dravet syndrome: Detailed characterization of onset, progression, and impact in the ENVISION natural history study

Epilepsia(2025)10.1111/epi.70015

N/A

0DataRank · unranked

1 citations

M. Scott Perry, Ingrid E Scheffer, James W. Wheless, Susana Boronat, Andreas Brunklaus +24 more

Sameer M. Zuberi

Indexed papers

Top data-sharing exemplar

Papers