Edoardo Errichiello

ORCID: 0000-0001-6346-1988

Also affiliated with Foundation Center, Fondazione Istituto Neurologico Nazionale Casimiro Mondino, Urology Foundation

Biochemistry, 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 6 papers. Top paper: “A Genome-Wide Association Study of Myasthenia Gravis”.

A Genome-Wide Association Study of Myasthenia Gravis

UNC Libraries(2020)10.17615/hk4s-3m41

N/A

0DataRank · unranked

0 citations

Emanuela Bartoccioni, Michael A. Nalls, Mamatha Pasnoor, Mario Sabatelli, April McVey +27 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

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

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