DEIANA, MANILA
 Distribuzione geografica
Continente #
EU - Europa 172
NA - Nord America 139
AS - Asia 92
SA - Sud America 2
OC - Oceania 1
Totale 406
Nazione #
IT - Italia 144
US - Stati Uniti d'America 139
SG - Singapore 75
FI - Finlandia 11
KR - Corea 9
AZ - Azerbaigian 2
CN - Cina 2
DE - Germania 2
IE - Irlanda 2
NL - Olanda 2
RO - Romania 2
BG - Bulgaria 1
BO - Bolivia 1
CZ - Repubblica Ceca 1
EC - Ecuador 1
FR - Francia 1
HK - Hong Kong 1
JO - Giordania 1
LV - Lettonia 1
NZ - Nuova Zelanda 1
PK - Pakistan 1
PL - Polonia 1
PT - Portogallo 1
RU - Federazione Russa 1
SK - Slovacchia (Repubblica Slovacca) 1
TR - Turchia 1
UA - Ucraina 1
Totale 406
Città #
Santa Clara 90
Assemini 68
Singapore 34
Cagliari 29
Helsinki 11
Los Angeles 9
Seoul 9
Baku 2
Dublin 2
Falkenstein 2
Guangzhou 2
Milan 2
Rome 2
Amman 1
Amsterdam 1
Auckland 1
Benevento 1
Bologna 1
Bratislava 1
Buffalo 1
Catania 1
Florence 1
Forest City 1
Friesland 1
Hong Kong 1
Islamabad 1
La Paz 1
Lauterbourg 1
Prague 1
Quito 1
Reggio Emilia 1
Riga 1
San Marcellino 1
Sassari 1
Sofia 1
Warsaw 1
Totale 285
Nome #
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome. 52
Identification of ten loci associated with height highlights new biological pathways in human growth 40
Overexpression of the Cytokine BAFF and Autoimmunity Risk 32
Dissection of the BAFF pathway in Multiple Sclerosis with a view toward more specific and effective therapies 25
Heritability of cardiovascular and personality traits in 6,148 Sardinians. 21
Clinical relevance of immune microenvironment and gene-expression-based biomarkers in colorectal cancer 16
Novel action of FOXL2 as mediator of Col1a2 gene autoregulation 15
beta-thalassemia in the Italian population 14
Differential secretion of the mutated protein is a major component affecting phenotypic severity in CRLF1-associated disorders 14
Sindrome di Crisponi e Sindrome della sudorazione indotta dal freddo tipo I: due sindromi un entità genetica 14
Improvement of prenatal diagnosis of Wilson disease using microsatellite markers. 13
FOXL2: Forkhead transcription factor and Blepharophimosis/Ptosis/Epicanthus inversus syndrome (BPES) 12
BCL11A is associated with persistent HbF and ameliorates the ²-thalassemia phenotype. 12
Microarray and functional analyses of primordial follicles formation and the etiology of premature ovarian failure. 12
Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa 12
Wilson disease mutations associated with uncommon haplotypes in Mediterranean patients 12
Role of the Blepharophimosis/Ptosis/Epicanthus Inversus syndrome (BPES) gene FOXL2 in ovarian and eye development. 11
The forkhead transcription factor Foxl2 is sumoylated in both human and mouse: sumoylation affects its stability, localization, and activity. 11
Crisponi Syndrome and Cold-Induced Sweating Type 1: Two Syndromes - One Genetic Entity 11
Erratum: Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa (The American Journal of Human Genetics (2016) 99(1) (236-245) (S0002929716301616) (10.1016/j.ajhg.2016.05.026)) 11
Crisponi Syndrome and Cold-induced Sweating Type 1: two syndromes, but one genetic entity 11
Sindrome di Crisponi e Sindrome della sudorazione indotta dal freddo tipo I: due sindromi un entità genetica. 11
FOXL2 inactivation by a translocation 171 kb away: Analysis of 500 kb of chromosome 3 for candidate long-range regulatory sequences 9
FOXL2 modulates cartilage, skeletal development and IGF1-dependent growth in mice 9
Studio delle basi genetiche delle tireopatie autoimmuni nella popolazione sarda 9
Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development. 8
Molecular pathology and haplotype analysis of Wilson disease in Mediterranean populations 8
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 8
Intratumoral transcriptomic heterogeneity correlates with tumor location in colorectal cancer 6
Overgrowth of a mouse model of the Simpson - Golabi - Behmel syndrome is independent of IGF signaling 5
Totale 444
Categoria #
all - tutte 1.404
article - articoli 907
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 2.311


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202419 0 0 0 0 0 0 0 0 0 0 11 8
2024/2025425 4 1 42 17 173 51 53 36 48 0 0 0
Totale 444