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

Chiara Fallerini

University of Siena

ORCID: 0000-0002-7386-3224

Also affiliated with Siena Biotech (Italy), Azienda Ospedaliera Universitaria Senese

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 8 papers. Top paper: “Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism”.

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

Cell(2020)10.1016/j.cell.2019.12.036

N/A

9.5DataRank · unranked

2470 citations

Jack A. Kosmicki, Jiebiao Wang, Michael S. Breen, Silvia De Rubeis, Joon‐Yong An +95 more

SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect

Brain(2020)10.1093/brain/awaa176

N/A

0DataRank · unranked

49 citations

Emanuela Iovino, Luke Mansard, Christel Vaché, David Baux, Emma Bedoukian +15 more

Human CRY1 variants associate with attention deficit/hyperactivity disorder

Journal of Clinical Investigation(2020)10.1172/jci135500

N/A

0DataRank · unranked

47 citations

Meltem Ece Kars, Şeref Gül, Kaya Bilgüvar, Yiming Wu, Ayşe Özhan +13 more

The polymorphism L412F in TLR3 inhibits autophagy and is a marker of severe COVID-19 in males

Autophagy(2021)10.1080/15548627.2021.1995152

N/A

0DataRank · unranked

43 citations

Mary Anna Venneri, Stefania Mantovani, Chiara Fallerini, Elisa Benetti, Nicola Picchiotti +28 more

Cryptic pathogen-sugar interactions revealed by universal saturation transfer analysis

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.04.14.439284

N/A

0DataRank · unranked

5 citations

Ben Gaunt, Peter J. Harrison, Yun Yang, Jiwei Liu, Aziz Khan +32 more

The microRNA processorDROSHAis a candidate gene for a severe progressive neurological disorder

Human Molecular Genetics(2022)10.1093/hmg/ddac085

N/A

0DataRank · unranked

17 citations

Mümine Şentürk, Kelly Schoch, Amanda L. Minogue, Diego Lopergolo, Chiara Fallerini +95 more

HLA‐DPB113:01 associates with enhanced, and KIR2DS4001 with diminished protection from developing severe COVID‐19

HLA(2023)10.1111/tan.15251

N/A

0DataRank · unranked

15 citations

Silvia Brugiapaglia, Susanna Croci, Paola Magistroni, Claudia Curcio, Kristina Zguro +19 more

A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death

Research Square(2023)10.21203/rs.3.rs-3316459/v1

N/A

0DataRank · unranked

0 citations

Francesca Minnai, Filippo Biscarini, Martina Esposito, Tommaso A. Dragani, Luís Bujanda +14 more