Daniele Ghezzi

Fondazione IRCCS Istituto Neurologico Carlo Besta

Biochemistry, Genetics and Molecular BiologyNeuroscience

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 7 papers. Top paper: “Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians”.

Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians

European Journal of Human Genetics(2005)10.1038/sj.ejhg.5201425

N/A

0.801DataRank · unranked

207 citations

Cecilia Marelli, Alessandro Achilli, Stefano Goldwurm, Gianni Pezzoli, Paolo Barone +19 more

Systematic analysis of NDUFAF6 in complex I assembly and mitochondrial disease

Nature Metabolism(2024)10.1038/s42255-024-01039-2

N/A

0.470DataRank · unranked

22 citations

Rachel M. Guerra, Laura Steenberge, Charlotte L. Alston, Kei Murayama, Yasushi Okazaki +10 more

Biallelic USP14 variants cause a syndromic neurodevelopmental disorder

Genetics in Medicine(2024)10.1016/j.gim.2024.101120

N/A

0.170DataRank · unranked

2 citations

Xénia Latypova, Ka Ying Sharon Hung, Miguel A. Prado, Byung‐Hoon Lee, Sophie Möller +19 more

ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy

Annals of Neurology(2020)10.1002/ana.25723

N/A

0DataRank · unranked

53 citations

Stefania Magri, Andrea Legati, Valentina Del Dotto, Francesca Tagliavini, Francesca Balistreri +26 more

Systematic analysis of NDUFAF6 in complex I assembly and mitochondrial disease

Research Square(2023)10.21203/rs.3.rs-3332602/v1

N/A

0DataRank · unranked

0 citations

Andrew Y. Sung, Rachel M. Guerra, Laura Steenberge, Charlotte L. Alston, Kei Murayama +10 more

Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.11.003

N/A

0DataRank · unranked

34 citations

Stéphanie Efthymiou, Simone Seiffert, Karen Vargas Parra, Sukyeong Lee, Alessia Nasca +35 more

Clinical implementation of RNA sequencing for Mendelian disease diagnostics

medRxiv(2021)10.1101/2021.04.01.21254633

N/A

0DataRank · unranked

33 citations

Mirjana Gušić, Robert Kopajtich, Christian Mertes, Nicholas H. Smith, Charlotte L. Alston +48 more