Mariasavina Severino

Also affiliated with Istituti di Ricovero e Cura a Carattere Scientifico

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 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 30 papers. Top paper: “Diagnostic Approach to Macrocephaly in Children”.

Diagnostic Approach to Macrocephaly in Children

Frontiers in Pediatrics(2022)10.3389/fped.2021.794069

N/A

0.604DataRank · unranked

55 citations

Ana Filipa Geraldo, Gianluca Piccolo, Antonella Riva, Marcello Scala, Ganna Balagura +9 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

0.601DataRank · unranked

54 citations

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

0.546DataRank · unranked

37 citations

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

Influence of adaptive denoising on Diffusion Kurtosis Imaging at 3T and 7T

Computer Methods and Programs in Biomedicine(2023)10.1016/j.cmpb.2023.107508

N/A

0.208DataRank · unranked

3 citations

Monica Roascio, Gabriele Arnulfo, Domenico Tortora, Mariasavina Severino, Andrea Rossi +3 more

Clinical and genetic characterization of a progressive RBL2-associated neurodevelopmental disorder

Brain(2024)10.1093/brain/awae363

N/A

0.104DataRank · unranked

1 citations

Elisa Calì, Reza Maroofian, Maha S. Zaki, Alistair T. Pagnamenta, Zafar Ali +51 more

Biallelic NDUFA9 variants cause a progressive neurodevelopmental disorder with prominent dystonia and mitochondrial complex I deficiency

Brain Communications(2025)10.1093/braincomms/fcaf369

N/A

0.104DataRank · unranked

1 citations

Lucie S Taylor, Sahar Sedighzadeh, Dalila Moualek, Mariasavina Severino, Daniel N. Grba +23 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

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

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

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

Genotype-Phenotype Correlation and Functional Insights for Two Monoallelic TREX1 Missense Variants Affecting the Catalytic Core

Genes(2022)10.3390/genes13071179

N/A

0DataRank · unranked

2 citations

Wayne O. Hemphill, Mariasavina Severino, Claudio Moratti, Rosario Pascarella, Marta Bertamino +9 more

Biallelic BORCS8 variants cause an infantile-onset neurodegenerative disorder with altered lysosome dynamics

Brain(2023)10.1093/brain/awad427

N/A

0DataRank · unranked

23 citations

Reza Maroofian, Adeline Paimboeuf, Mina Zamani, Maha S. Zaki, Saeid Sadeghian +18 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

Biallelic variants in SLC4A10 encoding a sodium-dependent bicarbonate transporter lead to a neurodevelopmental disorder

Genetics in Medicine(2023)10.1016/j.gim.2023.101034

N/A

0DataRank · unranked

8 citations

Mina Zamani, Rauan Kaiyrzhanov, Lutz Liebmann, Ehsan Ghayoor Karimiani, Barbara Vona +28 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

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

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

Variants in the WDR44 WD40-repeat domain cause a spectrum of ciliopathy by impairing ciliogenesis initiation

Nature Communications(2024)10.1038/s41467-023-44611-2

N/A

0DataRank · unranked

15 citations

Saurabh Shakya, Taewoo Yang, Christine Insinna, Soo Yeon Kim, David R. Bell +53 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

Novel loss-of-function variants expand ABCC9-related intellectual disability and myopathy syndrome

Brain(2024)10.1093/brain/awae010

N/A

0DataRank · unranked

14 citations

Marcello Scala, Vini Nagaraj, Katarzyna Ochenkowska, Fenne L. Komdeur, Robin A Liang +24 more

Biallelic loss-of-function variants of SLC12A9 cause lysosome dysfunction and a syndromic neurodevelopmental disorder

Genetics in Medicine(2024)10.1016/j.gim.2024.101097

N/A

0DataRank · unranked

10 citations

Young Nyun Park, Guy M. Lenk, Mariasavina Severino, Marcello Scala, Jonas Denecke +17 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

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

A STOP ‐Gain RNF213 Variant Causes Chorea, Stroke‐Like Episodes, and Leigh Syndrome‐Like Encephalopathy

Movement Disorders(2025)10.1002/mds.70077

N/A

0DataRank · unranked

0 citations

Mariasavina Severino, Jennifer Nichols, Fred Shen, Ignacio Juan Keller Sarmiento, Bernabé I. Bustos +4 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

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

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