RENIERI, ALESSANDRA
 Distribuzione geografica
Continente #
NA - Nord America 195
EU - Europa 163
AF - Africa 12
AS - Asia 11
OC - Oceania 1
Totale 382
Nazione #
US - Stati Uniti d'America 195
IT - Italia 113
NL - Olanda 38
CI - Costa d'Avorio 11
CN - Cina 9
CH - Svizzera 3
DE - Germania 3
GB - Regno Unito 2
AT - Austria 1
AU - Australia 1
FI - Finlandia 1
FR - Francia 1
NG - Nigeria 1
TR - Turchia 1
UA - Ucraina 1
VN - Vietnam 1
Totale 382
Città #
Naples 52
Amsterdam 38
Chandler 34
Ashburn 24
Millbury 11
Lawrence 9
Napoli 7
Los Angeles 6
Selargius 6
Boston 5
Wilmington 5
Des Moines 4
Rome 4
Washington 4
Zola Predosa 4
Basel 3
Fairfield 2
London 2
Merano 2
New York 2
Bussolengo 1
Caserta 1
Castel Morrone 1
Chicago 1
Council Bluffs 1
Crispano 1
Formia 1
Frankfurt am Main 1
Giugliano in Campania 1
Houston 1
Kronberg 1
Lagos 1
Lappeenranta 1
Limatola 1
Marano di Napoli 1
Mugnano di Napoli 1
Padula 1
Pescara 1
Pignataro Maggiore 1
Pozza di Fassa 1
Redwood City 1
San Cesareo 1
San Tammaro 1
Seattle 1
Trento 1
Vigodarzere 1
Woodbridge 1
Totale 251
Nome #
A first update on mapping the human genetic architecture of COVID-19 52
ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population 52
C9orf72 intermediate repeats confer genetic risk for severe covid-19 pneumonia independently of age 30
Employing a systematic approach to biobanking and analyzing clinical and genetic data for advancing COVID-19 research 27
Association of toll-like receptor 7 variants with life-threatening COVID-19 disease in males: Findings from a nested case-control study 25
Protective role of a tmprss2 variant on severe covid-19 outcome in young males and elderly women 24
Rare variants in Toll-like receptor 7 results in functional impairment and downregulation of cytokine-mediated signaling in COVID-19 patients 23
Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in European males 22
Inherited rare variants in homologous recombination and neurodevelopmental genes are associated with increased risk of neuroblastoma 22
Role of Colchicine Treatment in Tumor Necrosis Factor Receptor Associated Periodic Syndrome (TRAPS): Real-Life Data from the AIDA Network 19
Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality 19
The polymorphism L412F in TLR3 inhibits autophagy and is a marker of severe COVID-19 in males 14
Solving unsolved rare neurological diseases—a Solve-RD viewpoint 13
A case report: bone marrow mesenchymal stem cells from a Rett syndrome patient are prone to senescence and show a lower degree of apoptosis 12
Frequency of the LRRK2 G2019S mutation in Italian patients affected by Parkinson's disease 11
Carriers of ADAMTS13 Rare Variants Are at High Risk of Life-Threatening COVID-19 10
Ultra-rare RTEL1 gene variants associate with acute severity of COVID-19 and evolution to pulmonary fibrosis as a specific long COVID disorder 8
Reduced expression of MECP2 affects cell commitment and maintenance in neurons by triggering senescence: new perspective for Rett syndrome 8
Gain- and Loss-of-Function CFTR Alleles Are Associated with COVID-19 Clinical Outcomes 7
A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death 5
Twist exome capture allows for lower average sequence coverage in clinical exome sequencing 5
Totale 408
Categoria #
all - tutte 2.367
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 2.367


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202121 2 0 0 0 0 0 2 0 8 1 6 2
2021/202266 1 0 2 0 0 0 5 12 2 4 19 21
2022/2023143 9 6 9 2 15 12 2 5 31 35 11 6
2023/2024178 9 25 46 14 14 10 10 19 1 7 23 0
Totale 408