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Alessandra Renieri | Researchclopedia

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Alessandra Renieri

University of Siena ORCID

570

Works

31,434

Citations

72

h-index

307

i10-index

Research Topics

Genetics and Neurodevelopmental Disorders Genomic variations and chromosomal abnormalities Genomics and Rare Diseases

Affiliations

University of Siena1985–2025

Broad Institute2023–2024

Università di Camerino2017–2019

Mount Sinai Health System2019–2019

University of Bonn2021–2021

Top Works

Genetic mechanisms of critical illness in COVID-19

The GenOMICC Investigators,Erola Pairo‐Castineira,et al.

20201,485 citations

Cell Adhesion Molecules Research

Autism Spectrum Disorder Research

Rett syndrome: Revised diagnostic criteria and nomenclature

Jeffrey L. Neul,Walter E. Kaufmann,et al.

20101,367 citations

Mapping the human genetic architecture of COVID-19

COVID-19 Host Genetics Initiative,COVID-19 Host Genetics InitiativeLeadership,et al.

20211,105 citations

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

Jack Fu,F. Kyle Satterstrom,et al.

2022583 citations

X-linked Alport Syndrome

Jean Philippe Jaïs,Bertrand Knebelmann,et al.

2000581 citations

X-Linked Alport Syndrome

Jean Philippe Jaïs,Bertrand Knebelmann,et al.

2003474 citations

FOXG1 Is Responsible for the Congenital Variant of Rett Syndrome

Francesca Ariani,Joussef Hayek,et al.

2008432 citations

CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome

Francesca Mari,Sara Azimonti,et al.

2005317 citations

MYH9-Related Disease

Marco Seri,Alessandro Pecci,et al.

2003308 citations