Gianpiero L. Cavalleri

Also affiliated with Ollscoil na Gaillimhe – University of Galway, Future Analytics

Biochemistry, Genetics and Molecular BiologyHealth Professions

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 100%percentile

0Author 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 →

Papers

Driven by 29 papers. Top paper: “Germline mosaicism in a family withMBD5haploinsufficiency”.

Germline mosaicism in a family withMBD5haploinsufficiency

Molecular Case Studies(2022)10.1101/mcs.a006253

N/A

0.287DataRank · unranked

4 citations

Gianpiero L. Cavalleri, Máire White, Norman Delanty, Brian J. Sweeney, Daniel J. Costello +3 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

SJS/TEN 2019: From science to translation

Journal of Dermatological Science(2020)10.1016/j.jdermsci.2020.02.003

N/A

0DataRank · unranked

76 citations

Riichiro Abe, Paul Anderson, Wanpen Anderson, Michael R. Ardern‐Jones, Thomas M. Beachkofsky +65 more

Genetic and Clinical Predictors of Age of ESKD in Individuals With Autosomal Dominant Tubulointerstitial Kidney Disease Due to UMOD Mutations

Kidney International Reports(2020)10.1016/j.ekir.2020.06.029

N/A

0DataRank · unranked

54 citations

Petr Vyleťal, Céline Schaeffer, Eric Olinger, Martina Živná, Kateřina Hodaňová +37 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

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

Postictal Psychosis in Epilepsy: A Clinicogenetic Study

Annals of Neurology(2021)10.1002/ana.26174

N/A

0DataRank · unranked

32 citations

Helena Martins Custodio, Costin Leu, Luigi Agrò, Baihan Wang, Stella Calafato +15 more

A Rare Autosomal Dominant Variant in Regulator of Calcineurin Type 1 (RCAN1) Gene Confers Enhanced Calcineurin Activity and May Cause FSGS

Journal of the American Society of Nephrology(2021)10.1681/asn.2020081234

N/A

0DataRank · unranked

7 citations

Susan Murray, Katherine A. Benson, Agnieszka Bierżyńska, Megan Chryst-Stangl, Liming Wang +21 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

Corrigendum to ‘SJS/TEN 2019: From science to translation’ [J. Dermatol. Sci. 98/1 (2020) 2–12]

Journal of Dermatological Science(2021)10.1016/j.jdermsci.2021.09.008

N/A

0DataRank · unranked

2 citations

Riichiro Abe, Paul Anderson, Wanpen Anderson, Michael R. Ardern‐Jones, Thomas M. Beachkofsky +65 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

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

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

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

0DataRank · unranked

217 citations

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

Updates in SJS/TEN: collaboration, innovation, and community

Frontiers in Medicine(2023)10.3389/fmed.2023.1213889

N/A

0DataRank · unranked

34 citations

Ramya Krishna Botta, Riichiro Abe, Thomas M. Beachkofsky, Isabelle Boothman, Bruce Carleton +57 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

0DataRank · unranked

58 citations

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

Somatic variants as a cause of drug‐resistant epilepsy including mesial temporal lobe epilepsy with hippocampal sclerosis

Epilepsia(2024)10.1111/epi.17943

N/A

0DataRank · unranked

10 citations

Michael G. Doyle, Hugh Kearney, Charles A. Steward, Nicholas Lench, Anthony S. Rogers +19 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

Somatic variants as a cause of drug-resistant epilepsy including mesial temporal lobe epilepsy with hippocampal sclerosis

UNC Libraries(2024)10.17615/a6yq-ff48

N/A

0DataRank · unranked

0 citations

Francesca Brett, Seamus McDonald, Gianpiero L. Cavalleri, Lacey, Austin, Charles A. Steward +19 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

Adaptive PRKAA1 variant in Andeans is associated with improved ventilation and sleep phenotypes

iScience(2025)10.1016/j.isci.2025.112911

N/A

0DataRank · unranked

2 citations

Wanjun Gu, Mitchell C. Kong, Santiago Fassardi, Cecilia Anza‐Ramirez, Esteban A. Moya +23 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

Long-Read Sequencing of the MUC1 VNTR: Genomic Variation, Mutational Landscape, and Its Impact on ADTKD Diagnosis and Progression

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.09.06.673538

N/A

0DataRank · unranked

3 citations

Anna Přistoupilová, Kendrah Kidd, Václav Janoušek, Martin Radina, Petr Vyleťal +38 more

The impact of a secondary, rare, non-pathogenic PKD1 variant on disease progression in autosomal dominant polycystic kidney disease

Journal of Nephrology(2025)10.1007/s40620-025-02211-x

N/A

0DataRank · unranked

0 citations

Kane E. Collins, Sophia Heneghan, Edmund Gilbert, Hana Yang, Sarah R. Senum +82 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