Francesca Mari

ORCID: 0000-0003-1992-1654

Also affiliated with Azienda Ospedaliera Universitaria Senese

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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 9 papers. Top paper: “Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative”.

Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative

PLoS Genetics(2022)10.1371/journal.pgen.1010367

N/A

0.635DataRank · unranked

68 citations

Gundula Povysil, Jack A. Kosmicki, Elizabeth T. Cirulli, Theodore G. Drivas, Simone Furini +95 more

ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population

10.1101/2020.04.03.20047977

N/A

0.564DataRank · unranked

42 citations

Tita Rossella, Ottavia Spiga, Andrea Ciolfi, Birolo Giovanni, Alessandro Bruselles +21 more

Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative

medRxiv(2022)10.1101/2022.03.28.22273040

N/A

0.312DataRank · unranked

7 citations

Gundula Povysil, Jack A. Kosmicki, Elizabeth T. Cirulli, Theodore G. Drivas, Simone Furini +95 more

ARID1B-related disorder in 87 adults: Natural history and self-sustainability

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101873

N/A

0.292DataRank · unranked

6 citations

M. Gösgens, Alexander J.M. Dingemans, P. Striano, Antonella Riva, C. Mignot +81 more

Genetic modifiers and ascertainment drive variable expressivity of complex disorders

medRxiv(2024)10.1101/2024.08.27.24312158

N/A

0.269DataRank · unranked

5 citations

Corrine Smolen, Anastasia Tyryshkina, Lucilla Pizzo, Deepro Banerjee, Matthew T. Oetjens +65 more

Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort

Genetics in Medicine(2022)10.1016/j.gim.2022.04.010

N/A

0DataRank · unranked

21 citations

Marieke Joosten, Caroline Alby, Tania Attié‐Bitach, Kelly L. Gilmore, Christèle Dubourg +50 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

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

Scientific Reports(2024)10.1038/s41598-024-53310-x

N/A

0DataRank · unranked

7 citations

Filippo Biscarini, Martina Esposito, Tommaso A. Dragani, Luís Bujanda, Souad Rahmouni +95 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