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

Orsetta Zuffardi

University of Pavia

ORCID: 0000-0002-1466-4559
Biochemistry, Genetics and Molecular BiologyAgricultural and Biological Sciences

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 7 papers. Top paper: “Balanced chromosomal rearrangements offer insights into coding and noncoding genomic features associated with developmental disorders”.

Balanced chromosomal rearrangements offer insights into coding and noncoding genomic features associated with developmental disorders

medRxiv(2022)10.1101/2022.02.15.22270795
N/A
0.373DataRank · unranked
11 citations

Mana M. Mehrjouy, Ryan L. Collins, Mads Bak, Olga Dudchenko, Harrison Brand +95 more

NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain

Molecular Cell(2021)10.1016/j.molcel.2021.10.023
N/A
0DataRank · unranked
14 citations

Kimberly A. Aldinger, Chi Vicky Cheng, Takae Kiyama, Mitali Dave, Hanna K. McNamara +22 more

NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.30.437620
N/A
0DataRank · unranked
2 citations

Kimberly A. Aldinger, Chi Vicky Cheng, Takae Kiyama, Mitali Dave, Hanna K. McNamara +17 more

NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain

Molecular Cell(2021)10.1016/j.molcel.2021.09.020
N/A
0DataRank · unranked
57 citations

Kimberly A. Aldinger, Chi Vicky Cheng, Takae Kiyama, Mitali Dave, Hanna K. McNamara +21 more

Bi-allelic variants in the ESAM tight-junction gene cause a neurodevelopmental disorder associated with fetal intracranial hemorrhage

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.03.005
N/A
0DataRank · unranked
17 citations

Davut Pehli̇van, Damián Heine‐Suñer, Karin Weiss, Thibault Coste, Markus Zweier +42 more

Further Delineation of the AUTS2 HX Repeat Domain‐Related Phenotype

American Journal of Medical Genetics Part A(2025)10.1002/ajmg.a.64093
N/A
0DataRank · unranked
2 citations

Chi Vicky Cheng, Stefano Giuseppe Caraffi, Ivan Ivanovski, Gianluca Piatelli, Edoardo Errichiello +29 more

Seamless Gene Correction in the Human Cystic Fibrosis Transmembrane Conductance Regulator Locus by Vector Replacement and Vector Insertion Events

Frontiers in Genome Editing(2022)10.3389/fgeed.2022.843885
N/A
0DataRank · unranked
3 citations

Keisuke Chosa, C. Barillà, Michael Yao, Orsetta Zuffardi, Hirofumi Kai +6 more