arrow
B

Benetti, Elisa

IRCCS Ospedale San Raffaele
H指数:0
被引数:10

个人简介

暂无内容

教育背景

暂无内容

工作经历

暂无内容

荣誉奖项

暂无内容

A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing
2023-04-013
OAAI
SELP Asp603Asn and severe thrombosis in COVID-19 males (vol 14, 123, 2021)
2023-02-150
OAAI
High rate of HDR in gene editing of p.(Thr158Met) MECP2 mutational hotspot (FEB, 10.1038/s41431-020-0624-x, 2023)
2023-02-031
OA
The polymorphism L412F in TLR3 inhibits autophagy and is a marker of severe COVID-19 in males
AUTOPHAGY
IF14.3
2021-12-2925
OAAI
Rare variants in Toll-like receptor 7 results in functional impairment and downregulation of cytokine-mediated signaling in COVID-19 patients
2021-12-2443
OAAI
Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity
2021-12-1026
OAAI
Exome Sequencing in BRCA1-2 Candidate Familias: The Contribution of Other Cancer Susceptibility Genes (vol 11, 649435, 2021)
2021-08-171
OAAI
SELP Asp603Asn and severe thrombosis in COVID-19 males
2021-08-1610
OAAI
Severe COVID-19 in Hospitalized Carriers of Single CFTR Pathogenic Variants
2021-06-1520
OAAI
Whole Exome Sequencing in BRCA1-2 Candidate Families: The Contribution of Other Cancer Susceptibility Genes
2021-05-0713
OAAI
Association of Toll-like receptor 7 variants with life-threatening COVID-19 disease in males: findings from a nested case-control study
2021-03-02155
OAAI
Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in European males
2021-03-0146
OAAI
Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders
BRAIN
IF11.7
2020-11-2732
OAAI
ACE2gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population
2020-07-17176
OAAI
AAV-mediated FOXG1 gene editing in human Rett primary cells
2020-06-1511
OAAI