CARRIERO, MIRIAM LUCIA
 Distribuzione geografica
Continente #
AS - Asia 152
NA - Nord America 73
EU - Europa 58
SA - Sud America 32
AF - Africa 2
Totale 317
Nazione #
SG - Singapore 71
US - Stati Uniti d'America 69
HK - Hong Kong 42
IT - Italia 24
BR - Brasile 23
CN - Cina 20
VN - Vietnam 10
DE - Germania 7
NL - Olanda 6
AT - Austria 5
FI - Finlandia 4
VE - Venezuela 4
IN - India 3
MX - Messico 3
RU - Federazione Russa 3
GB - Regno Unito 2
ID - Indonesia 2
PL - Polonia 2
AE - Emirati Arabi Uniti 1
AO - Angola 1
AR - Argentina 1
BG - Bulgaria 1
CA - Canada 1
CO - Colombia 1
EC - Ecuador 1
ES - Italia 1
FR - Francia 1
KG - Kirghizistan 1
PT - Portogallo 1
PY - Paraguay 1
SE - Svezia 1
TR - Turchia 1
UY - Uruguay 1
UZ - Uzbekistan 1
ZA - Sudafrica 1
Totale 317
Città #
Hong Kong 42
Singapore 38
Beijing 10
Ashburn 8
Los Angeles 6
Caracas 4
Hanoi 4
Ho Chi Minh City 4
Rome 4
Amsterdam 3
Bologna 3
Council Bluffs 3
Frankfurt am Main 3
Rio de Janeiro 3
The Dalles 3
Vienna 3
Buffalo 2
Curitiba 2
Helsinki 2
Lappeenranta 2
Mexico City 2
Modena 2
New York 2
Nuremberg 2
Potenza 2
Redondo Beach 2
Santa Clara 2
Zhengzhou 2
Ankara 1
Annapolis 1
Asunción 1
Bishkek 1
Boise 1
Campinas 1
Chennai 1
Chicago 1
Fitzgerald 1
Franca 1
Frascati 1
Frederico Westphalen 1
Guayaquil 1
Hampton Bays 1
Houston 1
Hyderabad 1
Jakarta 1
Jundiaí 1
Klerksdorp 1
Lombard 1
Londrina 1
Luanda 1
Milan 1
Mogi das Cruzes 1
Montevideo 1
Montreal 1
Mumbai 1
Munich 1
North Bergen 1
Nova Iguaçu 1
Orem 1
Passo Fundo 1
Pelotas 1
Ponta Porã 1
Popayán 1
Poplar 1
Porto 1
Porto Alegre 1
Resistencia 1
Rio Grande 1
Rio Negro 1
Sofia 1
South Tangerang 1
Stockholm 1
São Carlos 1
São José dos Pinhais 1
São João de Meriti 1
São Roque do Canaã 1
Tashkent 1
Teresópolis 1
Thái Nguyên 1
Warsaw 1
Weifang 1
Wroclaw 1
Wuxi 1
Totale 220
Nome #
Genetic Variability of SOX10-Related Disorders within an Italian Family: Straddling the Line between Kallmann and Waardenburg Syndrome 66
WDFY3 Haploinsufficiency Is Associated With Autosomal Dominant Neurodevelopmental Disorders and Macrocephaly 66
Implementing the risk stratification and clinical management of breast cancer families using polygenic risk score evaluation: A pilot study 50
A Novel COL4A5 Pathogenic Variant Joins the Dots in a Family with a Synchronous Diagnosis of Alport Syndrome and Polycystic Kidney Disease 47
Co-Inheritance of Pathogenic Variants in PKD1 and PKD2 Genes Determined by Parental Segregation and De Novo Origin: A Case Report 43
Integrated AI medical emergency diagnostics advising system 34
Prenatal identification of a pathogenic maternal FGFR1 variant in two consecutive pregnancies with fetal forebrain malformations 33
Totale 339
Categoria #
all - tutte 1.368
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 1.368


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2024/2025203 0 53 9 3 6 14 22 7 23 44 15 7
2025/2026136 30 24 25 18 31 8 0 0 0 0 0 0
Totale 339