🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Alberto Spalice

Policlinico Umberto I

ORCID: 0000-0002-8455-796X

Also affiliated with Sapienza University of Rome

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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 3 papers. Top paper: “Identification of ultra-rare genetic variants in Pediatric Acute Onset Neuropsychiatric Syndrome (PANS) by exome and whole genome sequencing”.

Identification of ultra-rare genetic variants in Pediatric Acute Onset Neuropsychiatric Syndrome (PANS) by exome and whole genome sequencing

medRxiv(2021)10.1101/2021.05.25.21257256

N/A

0DataRank · unranked

3 citations

Herbert M. Lachman, Olivia R. Manusama, Deyou Zheng, Alberto Spalice, Pietro Chiurazzi +6 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

Identification of ultra-rare genetic variants in pediatric acute onset neuropsychiatric syndrome (PANS) by exome and whole genome sequencing

Scientific Reports(2022)10.1038/s41598-022-15279-3

N/A

0DataRank · unranked

37 citations

Herbert M. Lachman, Olivia R. Manusama, Deyou Zheng, Alberto Spalice, Pietro Chiurazzi +7 more