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Chiara Fallerini
Observed names:
C. Fallerini,
Chiara Fallerini (9265073),
Fallerini, Chiara
Institutions:
University of Siena,
Siena Biotech (Italy),
Azienda Ospedaliera Universitaria Senese
Observed institutions:
University of Siena,
Universitat Autònoma de Barcelona,
Max Planck Society,
University of Michigan,
Ospedale Santa Maria alle Scotte,
Meyer Children's Hospital,
Siena Biotech (Italy),
Azienda Ospedaliera Universitaria Senese,
IRCCS Humanitas Research Hospital
show all 9
ORCID:
0000-0002-7386-3224
Observed ORCID:
0000-0002-7386-3224
OpenAlex ID:
A5068548633
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
2019
·
F. Kyle Satterstrom
, Jack A. Kosmicki
, et al.
·
Cell
·
2,305
PDF
Mapping the human genetic architecture of COVID-19
2021
·
COVID-19 Host Genetics Initiative
, COVID-19 Host Genetics InitiativeLeadership
, et al.
·
Nature
·
983
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
2022
·
Jack M. Fu
, F. Kyle Satterstrom
, et al.
·
Nature Genetics
·
625
PDF
Whole-genome sequencing reveals host factors underlying critical COVID-19
2022
·
Athanasios Kousathanas
, Erola Pairo-Castineira
, et al.
·
Nature
·
327
PDF
ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population
2020
·
Elisa Benetti
, Rossella Tita
, et al.
·
European Journal of Human Genetics
·
263
PDF
Association of Toll-like receptor 7 variants with life-threatening COVID-19 disease in males: findings from a nested case-control study
2021
·
Chiara Fallerini
, Sergio Daga
, et al.
·
eLife
·
198
A first update on mapping the human genetic architecture of COVID-19
2022
·
COVID-19 Host Genetics Initiative
, COVID-19 Host Genetics Initiative
, et al.
·
Nature
·
181
PDF
Evidence of digenic inheritance in Alport syndrome
2015
·
Maria Antonietta Mencarelli
, Laurence Heidet
, et al.
·
Journal of Medical Genetics
·
163
Unbiased next generation sequencing analysis confirms the existence of autosomal dominant Alport syndrome in a relevant fraction of cases
2013
·
C. Fallerini
, L. Dosa
, et al.
·
Clinical Genetics
·
145
PDF
Genome-wide association study of long COVID
2025
·
Vilma Lammi
, Tomoko Nakanishi
, et al.
·
Nature Genetics
·
86
PDF
Advances in Alport syndrome diagnosis using next-generation sequencing
2011
·
Rosangela Artuso
, Chiara Fallerini
, et al.
·
European Journal of Human Genetics
·
85
PDF
Rare variants in Toll-like receptor 7 results in functional impairment and downregulation of cytokine-mediated signaling in COVID-19 patients
2021
·
Stefania Mantovani
, Sergio Daga
, et al.
·
Genes and Immunity
·
69
PDF
Alport syndrome: impact of digenic inheritance in patients management
2016
·
C. Fallerini
, M. Baldassarri
, et al.
·
Clinical Genetics
·
65
Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in European males
2021
·
Margherita Baldassarri
, Nicola Picchiotti
, et al.
·
EBioMedicine
·
62
PDF
Protective Role of a TMPRSS2 Variant on Severe COVID-19 Outcome in Young Males and Elderly Women
2021
·
Maria Monticelli
, Bruno Hay Mele
, et al.
·
Genes
·
60
PDF
New Candidates for Autism/Intellectual Disability Identified by Whole-Exome Sequencing
2021
·
Lucia Pia Bruno
, Gabriella Doddato
, et al.
·
International Journal of Molecular Sciences
·
57
PDF
Pathogen-sugar interactions revealed by universal saturation transfer analysis
2022
·
Charles J. Buchanan
, Ben Gaunt
, et al.
·
Science
·
56
New frontiers to cure Alport syndrome: COL4A3 and COL4A5 gene editing in podocyte-lineage cells
2019
·
Sergio Daga
, Francesco Donati
, et al.
·
European Journal of Human Genetics
·
53
PDF
iPSC-derived neurons profiling reveals GABAergic circuit disruption and acetylated α-tubulin defect which improves after iHDAC6 treatment in Rett syndrome
2018
·
Elisa Landucci
, Margherita Brindisi
, et al.
·
Experimental Cell Research
·
52
PDF
SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect
2020
·
Alisdair McNeill
, Emanuela Iovino
, et al.
·
Brain
·
50
PDF
Human CRY1 variants associate with attention deficit/hyperactivity disorder
2020
·
O. Emre Onat
, M. Ece Kars
, et al.
·
Journal of Clinical Investigation
·
47
PDF
Employing a systematic approach to biobanking and analyzing clinical and genetic data for advancing COVID-19 research
2021
·
Sergio Daga
, Chiara Fallerini
, et al.
·
European Journal of Human Genetics
·
46
PDF
SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues
2021
·
Matteo D’Antonio
, Jennifer P. Nguyen
, et al.
·
Cell Reports
·
45
PDF
The polymorphism L412F in TLR3 inhibits autophagy and is a marker of severe COVID-19 in males
2021
·
Susanna Croci
, Mary Anna Venneri
, et al.
·
Autophagy
·
44
Clinical and molecular characterization of COVID-19 hospitalized patients
2020
·
Elisa Benetti
, Annarita Giliberti
, et al.
·
PLoS ONE
·
43
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Works count:
106
Citation count:
6,892
H-index:
30
I10-index:
54
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