Pasquale Striano

Istituto Giannina Gaslini

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 2%percentile

2.9Author DataRank

Indexed papers

2in 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 2 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 55 papers — median percentile 80. Top paper: “Consensus on diagnosis and management of JME: From founder's observations to current trends”.

Consensus on diagnosis and management of JME: From founder's observations to current trends

Epilepsy & Behavior(2013)10.1016/j.yebeh.2012.11.051

N/A

5.6DataRank · unranked

166 citations

Bettina Schmitz, Dieter Janz, Antonio V. Delgado-Escueta, Pierre Thomas, Edouard Hirsch +40 more

Genotype-phenotype correlations in SCN8A -related disorders reveal prognostic and therapeutic implications

Brain(2021)10.1093/brain/awab321

N/A

2.9DataRank · unranked

149 citations

Yuanyuan Liu, Mahmoud Koko, Cathrine E. Gjerulfsen, Lukas Sonnenberg, Julian Schubert +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

A randomized, double‐blind trial of triheptanoin for drug‐resistant epilepsy in glucose transporter 1 deficiency syndrome

Epilepsia(2022)10.1111/epi.17263

N/A

0.944DataRank · unranked

27 citations

Stéphane Auvin, Abigail Collins, Rita Horváth, Ingrid E Scheffer, Michal Tzadok +11 more

SLC6A1 variant pathogenicity, molecular function and phenotype: a genetic and clinical analysis

Brain(2023)10.1093/brain/awad292

Top 30%

0.660DataRank

Top 30%23 citations

Eduardo Pérez‐Palma, Tobias Brünger, Ludovica Montanucci, Cornelius Gati, Chiara Klöckner +41 more

Comment to: Addition of verapamil in the treatment of severe myoclonic epilepsy in infancy (Iannetti et al.)

Epilepsy Research(2009)10.1016/j.eplepsyres.2009.04.006

N/A

0.208DataRank · unranked

3 citations

Pasquale Striano

Interpretable surface-based detection of focal cortical dysplasias: a MELD study

medRxiv(2021)10.1101/2021.12.13.21267721

N/A

0.208DataRank · unranked

3 citations

Mathilde Ripart, Kirstie Whitaker, Antonio Napolitano, Luca De Palma, Alessandro De Benedictis +89 more

Network-based atrophy modelling in the common epilepsies: a worldwide ENIGMA study

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.04.076836

N/A

0DataRank · unranked

7 citations

Raúl Rodríguez‐Cruces, Jessica Royer, Maria Eugenia Caligiuri, Antonio Gambardella, Luis Concha +57 more

Atlas of lesion locations and postsurgical seizure freedom in focal cortical dysplasia: A MELD study

Epilepsia(2021)10.1111/epi.17130

N/A

0DataRank · unranked

109 citations

Kirstie Whitaker, Armin Raznahan, Jakob Seidlitz, Petra E. Vértes, Stephen T. Foldes +62 more

Progressive myoclonus epilepsies—Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.03.013

N/A

0DataRank · unranked

86 citations

Karen Oliver, Eon Joo Park, Jillian M. Cameron, Kariona A. Grabińska, Mikko Muona +34 more

Artificial intelligence for classification of temporal lobe epilepsy with ROI-level MRI data: A worldwide ENIGMA-Epilepsy study

NeuroImage Clinical(2021)10.1016/j.nicl.2021.102765

N/A

0DataRank · unranked

78 citations

Brent C. Munsell, Saud Alhusaini, Marina K. M. Alvim, Núria Bargalló, Benjamin Bender +61 more

Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.04.009

N/A

0DataRank · unranked

60 citations

Gundula Povysil, Ryan S. Dhindsa, Kate E. Stanley, Andrew S. Allen, Yen‐Chen Anne Feng +95 more

A systems‐level analysis highlights microglial activation as a modifying factor in common epilepsies

Neuropathology and Applied Neurobiology(2021)10.1111/nan.12758

N/A

0DataRank · unranked

54 citations

Mina Ryten, Martina Di Nunzio, Teresa Ravizza, Daniele Tolomeo, Regina Hertfelder Reynolds +95 more

Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.08.003

N/A

0DataRank · unranked

42 citations

Somayeh Bakhtiari, Ashley P.L. Marsh, Rauan Kaiyrzhanov, Matias Wagner, Sheetal Shetty +95 more

Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.11.003

N/A

0DataRank · unranked

34 citations

Stéphanie Efthymiou, Simone Seiffert, Karen Vargas Parra, Sukyeong Lee, Alessia Nasca +35 more

Variants in ATP6V0A1 cause progressive myoclonus epilepsy and developmental and epileptic encephalopathy

Brain Communications(2021)10.1093/braincomms/fcab245

N/A

0DataRank · unranked

32 citations

Mitra Forouhan, Maria Lieto, Ambre J. Sala, Ruth Ellerington, Janel O. Johnson +53 more

De novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathies

Brain(2021)10.1093/brain/awab409

N/A

0DataRank · unranked

17 citations

Jolien Roovers, Noor Smal, Candace T. Myers, Dilşad Türkdoğan, Filip Roelens +29 more

mTORC1 functional assay reveals SZT2 loss-of-function variants and a founder in-frame deletion

Brain(2021)10.1093/brain/awab451

N/A

0DataRank · unranked

9 citations

Miriam C. Aziz, Hannah C. Happ, Jonathan Gunti, Colleen Gleason, Najma Mohamed +24 more

Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy

Brain(2021)10.1093/brain/awab417

N/A

0DataRank · unranked

3 citations

Sara Larivière, Raúl Rodríguez‐Cruces, Jessica Royer, Shahin Tavakol, Yezhou Wang +82 more

Genotype-phenotype correlations in SCN8A -related disorders reveal prognostic and therapeutic implications

medRxiv(2021)10.1101/2021.03.22.21253711

N/A

0DataRank · unranked

5 citations

Yuanyuan Liu, Cathrine E. Gjerulfsen, Mahmoud Koko, Lukas Sonnenberg, Julian Schubert +95 more

Topographic Divergence of Atypical Cortical Asymmetry and Regional Atrophy Patterns in Temporal Lobe Epilepsy: A Worldwide ENIGMA Study

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.04.30.442117

N/A

0DataRank · unranked

1 citations

Sara Larivière, Raúl Rodríguez‐Cruces, Jessica Royer, Shahin Tavakol, Yezhou Wang +79 more

Determining the pathogenicity of variants of uncertain significance and identification of a founder variant in the epilepsy-associated gene, SZT2

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.01.06.425612

N/A

0DataRank · unranked

0 citations

Miriam C. Aziz, Hannah C. Happ, Jonathan Gunti, Colleen Gleason, Najma Mohamed +24 more

Biallelic and de novo variants in ATP6V0A1 cause progressive myoclonus epilepsy and developmental and epileptic encephalopathy

medRxiv(2021)10.1101/2021.06.01.21257500

N/A

0DataRank · unranked

0 citations

Mitra Forouhan, Maria Lieto, Ambre J. Sala, Ruth Ellerington, Janel O. Johnson +21 more

Structural network alterations in focal and generalized epilepsy follow axes of epilepsy risk gene expression: An ENIGMA study

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.10.18.464713

N/A

0DataRank · unranked

0 citations

Jessica Royer, Raúl Rodríguez‐Cruces, Maria Eugenia Caligiuri, Antonio Gambardella, Luis Concha +63 more

Interpretable surface-based detection of focal cortical dysplasias: a Multi-centre Epilepsy Lesion Detection study

Brain(2022)10.1093/brain/awac224

N/A

0DataRank · unranked

135 citations

Mathilde Ripart, Kirstie Whitaker, Felice D’Arco, Kshitij Mankad, Andrew A. Chen +72 more

Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expression

Nature Communications(2022)10.1038/s41467-022-31730-5

N/A

0DataRank · unranked

107 citations

Jessica Royer, Raúl Rodríguez‐Cruces, Casey Paquola, Maria Eugenia Caligiuri, Antonio Gambardella +69 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

Epilepsy Course and Developmental Trajectories in STXBP1 -DEE

Neurology Genetics(2022)10.1212/nxg.0000000000000676

N/A

0DataRank · unranked

49 citations

Julie Xian, Antonella Riva, Francesca Marchese, Bruria Ben Zeev, Loreto Ríos +53 more

Systematic analysis and prediction of genes associated with monogenic disorders on human chromosome X

Nature Communications(2022)10.1038/s41467-022-34264-y

N/A

0DataRank · unranked

45 citations

Christopher Schröder, Ilaria Parenti, Carine Dalle, Agnès Rastetter, Theresa Kühnel +32 more

Association Between Lysine Reduction Therapies and Cognitive Outcomes in Patients With Pyridoxine-Dependent Epilepsy

Neurology(2022)10.1212/wnl.0000000000201222

N/A

0DataRank · unranked

42 citations

Laura A. Tseng, Levinus A. Bok, Hans Hartmann, Emma Footitt, Pasquale Striano +18 more

Event‐based modeling in temporal lobe epilepsy demonstrates progressive atrophy from cross‐sectional data

Epilepsia(2022)10.1111/epi.17316

N/A

0DataRank · unranked

27 citations

Leon Aksman, Neil P. Oxtoby, Sjoerd B. Vos, Jun Rao, Erik Kaestner +72 more

Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With KCNC2 Pathogenic Variants

Neurology(2022)10.1212/wnl.0000000000200660

N/A

0DataRank · unranked

21 citations

Simone Seiffert, Manuela Pendziwiat, Annika Rademacher, Tobias Brünger, Ulrike B. S. Hedrich +43 more

PIGNencephalopathy: Characterizing the epileptology

Epilepsia(2022)10.1111/epi.17173

N/A

0DataRank · unranked

8 citations

Guillem de Valles‐Ibáñez, Manuela Pendziwiat, Alexej Knaus, Kerstin Alt, Elisa Biamino +64 more

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

Nature Communications(2023)10.1038/s41467-023-39539-6

N/A

0DataRank · unranked

56 citations

David Lewis‐Smith, Ryan L. Collins, Lisa‐Marie Niestroj, Shridhar Parthasarathy, Julie Xian +94 more

Spliceosome malfunction causes neurodevelopmental disorders with overlapping features

Journal of Clinical Investigation(2023)10.1172/jci171235

N/A

0DataRank · unranked

44 citations

Qin Wang, Allan Bayat, Mark R. Battig, Yijing Zhou, Daniëlle G.M. Bosch +95 more

Clinical features, functional consequences, and rescue pharmacology of missense GRID1 and GRID2 human variants

Human Molecular Genetics(2023)10.1093/hmg/ddad188

N/A

0DataRank · unranked

13 citations

Kathryn B. Garber, Riley E. Perszyk, Cara T Khayat, Steven A. Kell, Maki Kaneko +22 more

Biallelic loss-of-function variants in CACHD1 cause a novel neurodevelopmental syndrome with facial dysmorphism and multisystem congenital abnormalities

Genetics in Medicine(2023)10.1016/j.gim.2023.101057

N/A

0DataRank · unranked

11 citations

Kamal Khan, Claire Bénéteau, Rachel Fox, Sandra von Hardenberg, Ayaz Khan +23 more

BRAT1–related disorders: phenotypic spectrum and phenotype-genotype correlations from 97 patients

European Journal of Human Genetics(2023)10.1038/s41431-023-01410-z

N/A

0DataRank · unranked

10 citations

Stéphanie Valence, Geoffroy Delplancq, Reza Maroofian, Andrea Accogli, Emanuele Agolini +85 more

Lunapark deficiency leads to an autosomal recessive neurodevelopmental phenotype with a degenerative course, epilepsy and distinct brain anomalies

Brain Communications(2023)10.1093/braincomms/fcad222

N/A

0DataRank · unranked

6 citations

Maha S. Zaki, Mohammed Al‐Owain, Mansour Y. Otaif, Adam Jackson, Emanuela Argilli +41 more

Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA-Epilepsy study

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.10.21.562994

N/A

0DataRank · unranked

4 citations

Andrew Perry, Lucy Vivash, Terence J. O’Brien, Marina K. M. Alvim, Donatello Arienzo +60 more

Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA‐Epilepsy study

Epilepsia(2024)10.1111/epi.17881

N/A

0DataRank · unranked

23 citations

Andrew Perry, Lucy Vivash, Terence J. O’Brien, Marina K. M. Alvim, Donatello Arienzo +59 more

Human mutations in SLITRK3 implicated in GABAergic synapse development in mice

Frontiers in Molecular Neuroscience(2024)10.3389/fnmol.2024.1222935

N/A

0DataRank · unranked

5 citations

Wenyan Han, Muhammad Ilyas, Jun Li, Yichao Yu, Marcello Scala +22 more

A worldwide ENIGMA study on epilepsy-related gray and white matter compromise across the adult lifespan

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.03.02.583073

N/A

0DataRank · unranked

6 citations

Alexander Ngo, Raúl Rodríguez‐Cruces, Jessica Royer, Maria Eugenia Caligiuri, Antonio Gambardella +83 more

Genome-wide association study of long COVID

Nature Genetics(2025)10.1038/s41588-025-02100-w

N/A

0DataRank · unranked

36 citations

Tomoko Nakanishi, Samuel E. Jones, Shea J. Andrews, Juha Karjalainen, Beatriz Cortés +95 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

ELFN1 deficiency: The mechanistic basis and phenotypic spectrum of a neurodevelopmental disorder with epilepsy

Genetics in Medicine(2025)10.1016/j.gim.2025.101506

N/A

0DataRank · unranked

3 citations

Chu-Ting Chang, A. Declève, Gloria Brunori, W.H. Ludlam, Alden Huang +93 more

Pathogenic variants in TMEM184B cause a neurodevelopmental syndrome associated with alteration of metabolic signaling

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.08.004

N/A

0DataRank · unranked

1 citations

Farid Ullah, Zachary A Yahiku, Sheraz Jamal Khan, Sri Varsha Kodiparthi, Georgios Kellaris +22 more

SLK is mutated in individuals with a neurodevelopmental disorder

EBioMedicine(2025)10.1016/j.ebiom.2025.105725

N/A

0DataRank · unranked

2 citations

Norah Altuwaijri, Jun‐yi Zhu, Stéphanie Efthymiou, Hangnoh Lee, Jianli Duan +94 more

Associations between epilepsy-related polygenic risk and brain morphology in childhood

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.01.17.633277

N/A

0DataRank · unranked

0 citations

Lang Liu, Sara Larivière, Valeria Kebets, Serena Fett, Clara F. Weber +50 more

Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA study

Science Advances(2020)10.1126/sciadv.abc6457

N/A

0DataRank · unranked

200 citations

Raúl Rodríguez‐Cruces, Jessica Royer, Maria Eugenia Caligiuri, Antonio Gambardella, Luis Concha +57 more

White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study

Brain(2020)10.1093/brain/awaa200

N/A

0DataRank · unranked

235 citations

Khoa H Huynh, Leonardo Bonilha, Eugenio Abela, Saud Alhusaini, André Altmann +71 more

Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects

Brain(2020)10.1093/brain/awaa171

N/A

0DataRank · unranked

81 citations

Eduardo Pérez‐Palma, Daniel P. Howrigan, Yadi Zhou, Feixiong Cheng, Elmo Saarentaus +86 more

The ENIGMA‐Epilepsy working group: Mapping disease from large data sets

Human Brain Mapping(2020)10.1002/hbm.25037

N/A

0DataRank · unranked

79 citations

Christopher D. Whelan, Sean N. Hatton, Khoa H Huynh, André Altmann, Mina Ryten +67 more

Damaging de novo missense variants inEEF1A2lead to a developmental and degenerative epileptic‐dyskinetic encephalopathy

Human Mutation(2020)10.1002/humu.24015

N/A

0DataRank · unranked

40 citations

Katherine L. Helbig, Candace T. Myers, Marcello Scala, Robert Huether, Sara A. Lewis +40 more

Biallelic MFSD2A variants associated with congenital microcephaly, developmental delay, and recognizable neuroimaging features

European Journal of Human Genetics(2020)10.1038/s41431-020-0669-x

N/A

0DataRank · unranked

36 citations

Geok Lin Chua, Cheen Fei Chin, Hessa S. Alsaif, Artem Borovikov, Saima Riazuddin +25 more

Pasquale Striano

Indexed papers

Top data-sharing exemplar

Papers