Chiara Fallerini

Employment

• University of Siena Dr.
  2010 - Present

Education

Education history is unavailable.

Projects & Funding

Projects & funding information is unavailable.

Publications (76)

• A Complex Case of Retinoblastoma Solved by the Combined Approach of Humor/Plasma cfDNA-NGS and LR-WGS
  Genes 2025 DOI: 10.3390/genes16121399
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• Carriers of ADAMTS13 Rare Variants Are at High Risk of Life-Threatening COVID-19
  Viruses 2022 DOI: 10.3390/v14061185
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• An explainable model of host genetic interactions linked to COVID-19 severity
  Communications Biology 2022 DOI: 10.1038/s42003-022-04073-6
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• Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity
  Chiara Fallerini, Nicola Picchiotti, Margherita Baldassarri +97 more
  Human Genetics 2022 DOI: 10.1007/s00439-021-02397-7
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• Host genetic basis of COVID-19: from methodologies to genes
  European Journal of Human Genetics 2022 DOI: 10.1038/s41431-022-01121-x
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• Nosological and Theranostic Approach to Vascular Malformation through cfDNA NGS Liquid Biopsy
  Journal of Clinical Medicine 2022 DOI: 10.3390/jcm11133740
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• Pathogen-sugar interactions revealed by universal saturation transfer analysis
  Science 2022 DOI: 10.1126/science.abm3125
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• Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
  Jack M. Fu, F. Kyle Satterstrom, Minshi Peng +97 more
  Nature Genetics 2022 DOI: 10.1038/s41588-022-01104-0
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• Rare variants in Toll-like receptor 7 results in functional impairment and downregulation of cytokine-mediated signaling in COVID-19 patients
  Genes and Immunity 2022 DOI: 10.1038/s41435-021-00157-1
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• The microRNA processor DROSHA is a candidate gene for a severe progressive neurological disorder
  Human Molecular Genetics 2022 DOI: 10.1093/hmg/ddac085
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• Understanding the new BRD4-related syndrome: Clinical and genomic delineation with an international cohort study
  Clinical Genetics 2022 DOI: 10.1111/cge.14141
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• Whole-genome sequencing reveals host factors underlying critical COVID-19
  Athanasios Kousathanas, Erola Pairo‐Castineira, Konrad Rawlik +97 more
  Nature 2022 DOI: 10.1038/s41586-022-04576-6
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• Exome Sequencing in 200 Intellectual Disability/Autistic Patients: New Candidates and Atypical Presentations
  Brain Sciences 2021 DOI: 10.3390/brainsci11070936
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• An explainable model of host genetic interactions linked to COVID-19 severity
  ResearchSquare 2021 DOI: 10.21203/rs.3.rs-1062190
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• Association of toll-like receptor 7 variants with life-threatening COVID-19 disease in males: Findings from a nested case-control study
  eLife 2021 DOI: 10.7554/eLife.67569
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• Autism spectrum disorders: Analysis of mobile elements at 7q11.23 williams–beuren region by comparative genomics
  Genes 2021 DOI: 10.3390/genes12101605
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• C9orf72 intermediate repeats confer genetic risk for severe covid-19 pneumonia independently of age
  International Journal of Molecular Sciences 2021 DOI: 10.3390/ijms22136991
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• Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity
  medRxiv 2021 DOI: 10.1101/2021.09.03.21262611
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• Corrigendum: Exome Sequencing in BRCA1-2 Candidate Familias: The Contribution of Other Cancer Susceptibility Genes (Front. Oncol., (2021), 11, 10.3389/fonc.2021.649435)
  Frontiers in Oncology 2021 DOI: 10.3389/fonc.2021.740860
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• Cryptic pathogen-sugar interactions revealed by universal saturation transfer analysis
  bioRxiv 2021 DOI: 10.1101/2021.04.14.439284
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