Renzo Guerrini

Also affiliated with University of Florence

MedicineBiochemistry, 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 2%percentile

2.6Author 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.

Lessons learned from 40 novel PIGA patients and a review of the literature

Epilepsia(2020)10.1111/epi.16545

Top 10%

2.0DataRank

Top 10%58 citations

Alexej Knaus, Manuela Pendziwiat, Alexandra Afenjar, Tahsin Stefan Barakat, Friedrich Bosch +49 more

Papers

Driven by 57 papers — median percentile 76. Top paper: “Genotype-phenotype correlations in SCN8A -related disorders reveal prognostic and therapeutic implications”.

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

Lessons learned from 40 novel PIGA patients and a review of the literature

Epilepsia(2020)10.1111/epi.16545

Top 10%

2.0DataRank

Top 10%58 citations

Alexej Knaus, Manuela Pendziwiat, Alexandra Afenjar, Tahsin Stefan Barakat, Friedrich Bosch +49 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

1.2DataRank · unranked

56 citations

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

Comprehensive multiomic profiling of somatic mutations in malformations of cortical development

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.04.07.487401

Top 37%

0.522DataRank

Top 37%11 citations

Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels +45 more

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

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

Somatic Focal Copy Number Gains of Noncoding Regions of Receptor Tyrosine Kinase Genes in Treatment-Resistant Epilepsy

Journal of Neuropathology & Experimental Neurology(2020)10.1093/jnen/nlaa137

N/A

0DataRank · unranked

11 citations

Javier Hernaez Rodriguez, Cristiana Pelorosso, Kaicen Zhu, Anna Maria Buccoliero, Maristela L. Onozato +23 more

Mutations in the exocyst component EXOC2 cause severe defects in human brain development

The Journal of Experimental Medicine(2020)10.1084/jem.20192040

N/A

0DataRank · unranked

40 citations

Syed Mukhtar Ahmed, Felicity Collins, Mark J. Cowley, Annalisa Vetro, Russell C. Dale +14 more

De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature

European Journal of Human Genetics(2020)10.1038/s41431-020-0571-6

N/A

0DataRank · unranked

38 citations

Sophie Nambot, Laurence Faivre, Ghayda Mirzaa, Julien Thévenon, Ange‐Line Bruel +60 more

Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy

Brain(2020)10.1093/brain/awaa085

N/A

0DataRank · unranked

32 citations

Felicitas Becker, Heba Morsy, Miriam Schmidts, Katia Hardies, Beyhan Tüysüz +40 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

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

Profiling PI3K-AKT-MTOR variants in focal brain malformations reveals new insights for diagnostic care

Brain(2021)10.1093/brain/awab376

N/A

0DataRank · unranked

55 citations

Matthew Berkseth, Rylee Shear, Lorenzo Gonzalez, Andrew E. Timms, Josef Šulc +19 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

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

Large-scale, cell-resolution volumetric mapping allows layer-specific investigation of human brain cytoarchitecture

Biomedical Optics Express(2021)10.1364/boe.415555

N/A

0DataRank · unranked

32 citations

Giacomo Mazzamuto, Matteo Roffilli, Annunziatina Laurino, Filippo Maria Castelli, Mattia Neri +10 more

Pathogenic MAST3 Variants in the STK Domain Are Associated with Epilepsy

Annals of Neurology(2021)10.1002/ana.26147

N/A

0DataRank · unranked

18 citations

Kyle R. Christensen, Emily Bryant, Amy Schneider, Jennifer Rakotomamonjy, Alison M. Muir +32 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

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

Drosophila functional screening of de novo variants in autism uncovers deleterious variants and facilitates discovery of rare neurodevelopmental diseases

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2020.12.30.424813

N/A

0DataRank · unranked

3 citations

Samantha L. Deal, Jonathan C. Andrews, J. Michael Harnish, Venkata Hemanjani Bhavana, Hillary K. Graves +39 more

Pathogenic MAST3 variants in the STK domain are associated with epilepsy

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.09.434675

N/A

0DataRank · unranked

2 citations

Kyle R. Christensen, Emily Bryant, Amy Schneider, Jennifer Rakotomamonjy, Alison M. Muir +25 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

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

Disrupters of the Thymidylate Synthase Homodimer Accelerate Its Proteasomal Degradation and Inhibit Cancer Growth.

ChemRxiv(2021)10.26434/chemrxiv.14156918

N/A

0DataRank · unranked

0 citations

Stefania Ferrari, Matteo Santucci, Outi M. Salo-Ahen, Emanuele Carosati, Silvia Franchini +32 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

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

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

Clinical Features, Neuropathology, and Surgical Outcome in Patients With Refractory Epilepsy and Brain Somatic Variants in the SLC35A2 Gene

Neurology(2022)10.1212/wnl.0000000000201471

N/A

0DataRank · unranked

55 citations

Ingmar Blümcke, Melodie R. Winawer, Till Hartlieb, Hoon‐Chul Kang, Laura Grisotto +31 more

Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases

Cell Reports(2022)10.1016/j.celrep.2022.110517

N/A

0DataRank · unranked

52 citations

Samantha L. Deal, Jonathan C. Andrews, J. Michael Harnish, Venkata Hemanjani Bhavana, Hillary K. Graves +56 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

Phenotypic and genetic spectrum of ATP6V1A encephalopathy: a disorder of lysosomal homeostasis

Brain(2022)10.1093/brain/awac145

N/A

0DataRank · unranked

36 citations

Davide Mei, Katalin Kerti‐Szigeti, Sara Pepe, Mary Kay Koenig, Gretchen Von Allmen +48 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

Monoallelic and biallelic mutations inRELNunderlie a graded series of neurodevelopmental disorders

Brain(2022)10.1093/brain/awac164

N/A

0DataRank · unranked

22 citations

Renzo Guerrini, Charles J. Billington, A. James Barkovich, Philine Dinkel, Elena Freri +21 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

SEMA6B variants cause intellectual disability and alter dendritic spine density and axon guidance

Human Molecular Genetics(2022)10.1093/hmg/ddac114

N/A

0DataRank · unranked

17 citations

Martina Schaettin, Médéric Jeanne, Veranika Panasenkava, Anne‐Sophie Denommé‐Pichon, Boris Keren +43 more

Destabilizers of the thymidylate synthase homodimer accelerate its proteasomal degradation and inhibit cancer growth

eLife(2022)10.7554/elife.73862

N/A

0DataRank · unranked

14 citations

Stefania Ferrari, Matteo Santucci, Outi M. H. Salo‐Ahen, Emanuele Carosati, Silvia Franchini +34 more

Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development

Nature Genetics(2023)10.1038/s41588-022-01276-9

N/A

0DataRank · unranked

112 citations

Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels +76 more

Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.06.013

N/A

0DataRank · unranked

43 citations

Tianyu Guo, Chen Wang, Lillian Garrett, Angad Jolly, Moez Dawood +63 more

Developmental epileptic encephalopathy in DLG4‐related synaptopathy

Epilepsia(2023)10.1111/epi.17876

N/A

0DataRank · unranked

15 citations

Amanda M. Levy, Elena Gardella, Ángel Aledo‐Serrano, Amitha Ananth, Alejandro Brea‐Fernández +59 more

Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders

Brain(2023)10.1093/brain/awad380

N/A

0DataRank · unranked

19 citations

Abolfazl Rad, Sheng‐Jia Lin, Aida M. Bertoli‐Avella, Wouter W. Kallemeijn, Annie Godwin +84 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

Clinical and molecular characterization of patients with YWHAG‐related epilepsy

Epilepsia(2024)10.1111/epi.17939

N/A

0DataRank · unranked

11 citations

Tiziana Pisano, Gaëtan Lesca, Dana Marafi, Laura Licchetta, Florence Riccardi +30 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

High-resolution electrophysiological mapping of effective connectivity of lateral prefrontal cortex

Brain(2025)10.1093/brain/awaf317

N/A

0DataRank · unranked

9 citations

Maciej Jedynak, Anthony Boyer, Blandine Chanteloup-Forêt, Cristiana Pinheiro, Christopher C. Cline +91 more

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

Brain(2025)10.1093/brain/awaf259

N/A

0DataRank · unranked

3 citations

Lang Liu, Sara Larivière, Valeria Kebets, Serena Fett, Clara F. Weber +81 more

Quantitative cytoarchitectural phenotyping of deparaffinized human brain tissues

Communications Biology(2025)10.1038/s42003-025-08887-y

N/A

0DataRank · unranked

1 citations

Michele Sorelli, Josephine Ramazzotti, Franco Cheli, Samuel Bradley, Laura Perego +13 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

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

Renzo Guerrini

Indexed papers

Top data-sharing exemplar

Papers