SCOLARI, FRANCESCO
 Distribuzione geografica
Continente #
NA - Nord America 6.108
EU - Europa 2.509
AS - Asia 1.866
AF - Africa 121
SA - Sud America 90
OC - Oceania 81
Continente sconosciuto - Info sul continente non disponibili 2
Totale 10.777
Nazione #
US - Stati Uniti d'America 5.961
CN - Cina 869
DE - Germania 791
IT - Italia 270
FR - Francia 254
JP - Giappone 224
GB - Regno Unito 210
IN - India 188
PL - Polonia 164
VN - Vietnam 141
CA - Canada 128
IE - Irlanda 104
SE - Svezia 83
RU - Federazione Russa 78
NL - Olanda 73
AU - Australia 72
ES - Italia 72
KR - Corea 68
ZA - Sudafrica 65
CZ - Repubblica Ceca 54
FI - Finlandia 49
CH - Svizzera 46
HK - Hong Kong 43
BE - Belgio 38
TR - Turchia 38
ID - Indonesia 36
UA - Ucraina 36
TW - Taiwan 34
NO - Norvegia 31
IR - Iran 30
BR - Brasile 28
RO - Romania 27
CL - Cile 24
PH - Filippine 24
SG - Singapore 23
HR - Croazia 22
PK - Pakistan 20
SA - Arabia Saudita 20
GR - Grecia 19
TH - Thailandia 18
CO - Colombia 16
IQ - Iraq 16
AT - Austria 15
IL - Israele 13
MX - Messico 13
DK - Danimarca 12
LT - Lituania 12
MY - Malesia 12
AR - Argentina 11
BG - Bulgaria 11
AE - Emirati Arabi Uniti 10
EG - Egitto 10
PT - Portogallo 10
NZ - Nuova Zelanda 9
NG - Nigeria 8
DZ - Algeria 7
HU - Ungheria 7
TN - Tunisia 7
MA - Marocco 6
NP - Nepal 6
PE - Perù 6
BA - Bosnia-Erzegovina 5
BD - Bangladesh 5
EC - Ecuador 5
SI - Slovenia 5
JO - Giordania 4
CY - Cipro 3
ET - Etiopia 3
GE - Georgia 3
MK - Macedonia 3
MQ - Martinica 3
QA - Qatar 3
AZ - Azerbaigian 2
BT - Bhutan 2
CM - Camerun 2
LK - Sri Lanka 2
LU - Lussemburgo 2
MG - Madagascar 2
MO - Macao, regione amministrativa speciale della Cina 2
PS - Palestinian Territory 2
RE - Reunion 2
RS - Serbia 2
SN - Senegal 2
TZ - Tanzania 2
UG - Uganda 2
AM - Armenia 1
AP - ???statistics.table.value.countryCode.AP??? 1
BY - Bielorussia 1
EU - Europa 1
GN - Guinea 1
IS - Islanda 1
KE - Kenya 1
KY - Cayman, isole 1
LV - Lettonia 1
MV - Maldive 1
NA - Namibia 1
PR - Porto Rico 1
SK - Slovacchia (Repubblica Slovacca) 1
SY - Repubblica araba siriana 1
TT - Trinidad e Tobago 1
Totale 10.775
Città #
Fairfield 643
Woodbridge 486
Houston 421
Buffalo 375
Ashburn 343
Seattle 337
Ann Arbor 253
Cambridge 213
Beijing 204
Columbus 177
Wilmington 159
Warsaw 139
Dong Ket 126
Frankfurt am Main 120
Dublin 96
Shanghai 86
Wuhan 76
Stockholm 68
Las Vegas 60
New York 59
Chicago 55
Hangzhou 54
Los Angeles 54
Nürnberg 54
Tokyo 54
Phoenix 53
Muizenberg 49
Guangzhou 44
Ottawa 44
Centre Hall 43
Clearwater 41
Paris 40
Nuremberg 35
San Francisco 34
San Diego 33
Helsinki 32
Milan 32
Chappaqua 27
Bengaluru 26
Seoul 26
Shenyang 26
Riva 25
Chengdu 23
Dallas 23
Toronto 23
Changsha 21
Leawood 21
Selden 20
Madison 19
Dearborn 18
Boardman 17
Jakarta 16
San Jose 16
Taipei 16
Atlanta 15
Zurich 15
Delhi 14
London 14
Nanjing 14
Rome 14
Denver 13
Henderson 13
Kolkata 13
Milpitas 13
Rochester 13
Split 13
Sydney 13
Tianjin 13
Barcelona 12
Central 12
Hyderabad 12
Lappeenranta 12
Mumbai 12
Wakayama 12
Council Bluffs 11
Provo 11
Scranton 11
Singapore 11
Zhengzhou 11
Bethesda 10
Philadelphia 10
Santander 10
Austin 9
Büdelsdorf 9
Chennai 9
Frankfurt Am Main 9
Hanoi 9
Madrid 9
Moscow 9
Nashville 9
Suri 9
Amsterdam 8
Bangkok 8
Berlin 8
Bologna 8
Boston 8
Boulder 8
Brisbane 8
Central District 8
Easton 8
Totale 6.055
Nome #
Genome-wide association study identifies susceptibility loci for IgA nephropathy, file ddc633e2-affc-4e2e-e053-3705fe0a4c80 744
Genomic Mismatch at LIMS1 Locus and Kidney Allograft Rejection., file ddc633e3-c884-4e2e-e053-3705fe0a4c80 548
IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22–23, file ddc633e2-a7b2-4e2e-e053-3705fe0a4c80 541
CHOLESTEROL CRYSTAL EMBOLISM: A RECOGNIZABLE CAUSE OF RENAL DISEASE, file ddc633e2-a7b3-4e2e-e053-3705fe0a4c80 541
IgA nephropathy: the presence of familial disease does not confer an increased risk for progression, file ddc633e2-a7ae-4e2e-e053-3705fe0a4c80 415
Uromodulin storage diseases: clinical aspects and mechanisms., file ddc633e2-a7b4-4e2e-e053-3705fe0a4c80 384
Cyclosporine in patients with steroid-resistant nephrotic syndrome: an open-label, nonrandomized, retrospective study, file ddc633e2-a991-4e2e-e053-3705fe0a4c80 357
Genetic drivers of kidney defects in the digeorge syndrome, file ddc633e3-560f-4e2e-e053-3705fe0a4c80 329
Infertility and hypergonadotropic hypogonadism as first evidence of hereditary apolipoprotein A-I amyloidosis, file ddc633e2-a86b-4e2e-e053-3705fe0a4c80 320
Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics., file ddc633e2-a7b5-4e2e-e053-3705fe0a4c80 266
Defective intracellular trafficking of uromodulin mutant isoforms, file ddc633e2-a87e-4e2e-e053-3705fe0a4c80 262
Renal outcome in patients with congenital anomalies of the kidney and urinary tract., file ddc633e2-b09c-4e2e-e053-3705fe0a4c80 254
Atheroembolic renal disease, file ddc633e2-b05e-4e2e-e053-3705fe0a4c80 252
Low cerebrovascular event rate in subjects with patent foramen ovale and different clinical presentations: results from a prospective non randomized study on a population including patients with and without patent foramen ovale closure., file ddc633e3-f03f-4e2e-e053-3705fe0a4c80 233
Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome., file ddc633e2-aff9-4e2e-e053-3705fe0a4c80 214
The importance of skin biopsy in the diverse clinical manifestations of cholesterol embolism., file ddc633e2-aa51-4e2e-e053-3705fe0a4c80 193
Rituximab in Children with Steroid-Dependent Nephrotic Syndrome: A Multicenter, Open-Label, Noninferiority, Randomized Controlled Trial., file ddc633e3-cf0e-4e2e-e053-3705fe0a4c80 181
Repetitive fragmentation products of albumin and alpha1-antitrypsin in glomerular diseases associated with nephrotic syndrome., file ddc633e2-a86c-4e2e-e053-3705fe0a4c80 180
Clinical features and long-term outcome of nephrotic syndrome associated with heterozygous NPHS1 and NPHS2 mutations., file ddc633e2-b060-4e2e-e053-3705fe0a4c80 175
Search for genetic association between IgA nephropathy and candidate genes selected by function or by gene mapping at loci IGAN2 and IGAN3, file ddc633e2-bb7c-4e2e-e053-3705fe0a4c80 175
Suprarenal aortic cross-clamping in the elective surgery of abdominal aortic aneurysms. Lessons from 68 cases out of consecutive survey of 746 abdominal aortic substitutions., file ddc633e3-33de-4e2e-e053-3705fe0a4c80 172
Active focal segmental glomerulosclerosis is associated with massive oxidation of plasma albumin, file ddc633e2-a87f-4e2e-e053-3705fe0a4c80 170
Coexistence of Different Circulating Anti-PodocyteAntibodies in Membranous Nephropathy, file ddc633e2-b2d1-4e2e-e053-3705fe0a4c80 170
The pathophysiology of IgA nephropathy, file ddc633e2-bb0f-4e2e-e053-3705fe0a4c80 167
The Case | Cystic renal disease, nephrogenic diabetes insipidus, and polycytemia., file ddc633e3-ce66-4e2e-e053-3705fe0a4c80 164
PREDICTORS OF RENAL AND PATIENT OUTCOMES IN ATHEROEMBOLIC RENAL DISEASE: A PROSPECTIVE STUDY., file ddc633e2-a7bd-4e2e-e053-3705fe0a4c80 158
Renal apolipoprotein A-I amyloidosis: a rare and usually ignored cause of hereditary tubulointerstitial nephritis, file ddc633e2-b0a3-4e2e-e053-3705fe0a4c80 143
Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33., file ddc633e2-a86a-4e2e-e053-3705fe0a4c80 142
The rediscovery of uromodulin (Tamm-Horsfall protein): from tubulointerstitial nephropathy to chronic kidney disease., file ddc633e2-affa-4e2e-e053-3705fe0a4c80 141
IgA nephropathy--the case for a genetic basis becomes stronger., file ddc633e2-b09b-4e2e-e053-3705fe0a4c80 137
Phenotypic expansion of DGKE-associated diseases., file ddc633e3-ce5c-4e2e-e053-3705fe0a4c80 133
Cis and trans regulatory elements in NPHS2 promoter: implications in proteinuria and progression of renal diseases, file ddc633e2-a880-4e2e-e053-3705fe0a4c80 131
Deciphering Variability of PKD1 and PKD2 in an Italian Cohort of 643 Patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD), file ddc633e3-5611-4e2e-e053-3705fe0a4c80 131
Autosomal Dominant tubulointerstitial Kidney Disease with Adult onset due to a novel Renin Mutation Mapping in the Mature protein, file ddc633e3-f2d9-4e2e-e053-3705fe0a4c80 131
Mutations in DSTYK and dominant urinary tract malformations., file ddc633e2-b7e6-4e2e-e053-3705fe0a4c80 128
GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway, file ddc633e3-55c9-4e2e-e053-3705fe0a4c80 128
Genetic approaches to human renal agenesis/hypoplasia and dysplasia., file ddc633e2-a7ac-4e2e-e053-3705fe0a4c80 126
A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13., file ddc633e2-b05f-4e2e-e053-3705fe0a4c80 122
Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci., file ddc633e2-a87d-4e2e-e053-3705fe0a4c80 115
Genetic studies of IgA nephropathy: past, present, and future., file ddc633e2-b05c-4e2e-e053-3705fe0a4c80 114
Lack of association between dialysis modality and outcomes in atheroembolic renal disease, file ddc633e2-b09a-4e2e-e053-3705fe0a4c80 113
Urinary secretion and extracellular aggregation of mutant uromodulin isoforms, file ddc633e2-b111-4e2e-e053-3705fe0a4c80 111
Familial aggregation of primary glomerulonephritis in an Italian population isolate: Valtrompia study, file ddc633e2-a7ad-4e2e-e053-3705fe0a4c80 109
Copy number disorders are a Common Cause of Congenital Kidney Malformations, file ddc633e3-cf0f-4e2e-e053-3705fe0a4c80 109
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens, file ddc633e3-cf0d-4e2e-e053-3705fe0a4c80 102
The progression from obesity to type 2 diabetes in Alström syndrome., file ddc633e3-f252-4e2e-e053-3705fe0a4c80 102
Non-collagen genes role in digenic Alport syndrome, file ddc633e3-d25d-4e2e-e053-3705fe0a4c80 101
The Case ∣ Familial occurrence of retinitis pigmentosa, deafness, and nephropathy., file ddc633e2-b00d-4e2e-e053-3705fe0a4c80 100
Glomerular Autoimmune Multicomponents of Human Lupus Nephritis In Vivo (2): Planted Antigens., file ddc633e3-cf0c-4e2e-e053-3705fe0a4c80 98
Glomerular autoimmune multicomponents of human lupus nephritis in vivo: α-enolase and annexin AI, file ddc633e3-d57c-4e2e-e053-3705fe0a4c80 92
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis, file ddc633e4-26c3-4e2e-e053-3705fe0a4c80 80
Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindreds, file ddc633e2-b0a0-4e2e-e053-3705fe0a4c80 67
The copy number variation landscape of congenital anomalies of the kidney and urinary tract., file ddc633e3-c886-4e2e-e053-3705fe0a4c80 66
Liver biopsy discloses a new apolipoprotein A-I hereditary amyloidosis in several unrelated Italian families, file ddc633e2-b0a1-4e2e-e053-3705fe0a4c80 63
Multi-Autoantibody Signature and Clinical Outcome in Membranous Nephropathy, file ddc633e4-26c6-4e2e-e053-3705fe0a4c80 59
Type IV Collagen Mutations in Familial IgA Nephropathy, file ddc633e4-26c8-4e2e-e053-3705fe0a4c80 51
Autoimmunity in membranous nephropathy targets aldose reductase and SOD2, file ddc633e2-b099-4e2e-e053-3705fe0a4c80 49
Uromodulin: from monogenic to multifactorial diseases., file ddc633e3-d120-4e2e-e053-3705fe0a4c80 43
Rituximab is a safe and effective long-term treatment for children with steroid and calcineurin inhibitor-dependent idiopathic nephrotic syndrome., file ddc633e3-04ef-4e2e-e053-3705fe0a4c80 38
Berger's Disease, file ddc633e2-bcea-4e2e-e053-3705fe0a4c80 35
Glomerular clusterin is associated with PKC-alpha/beta regulation and good outcome of membranous glomerulonephritis in humans, file ddc633e2-a7b1-4e2e-e053-3705fe0a4c80 34
A model to predict disease progression in patients with autosomal dominant polycystic kidney disease (ADPKD): the ADPKD Outcomes Model, file ddc633e3-ce51-4e2e-e053-3705fe0a4c80 33
IDENTIFICATION OF A NEW LOCUS FOR MEDULLARY CYSTIC DISEASE ON CHROMOSOME 16, file ddc633e3-d749-4e2e-e053-3705fe0a4c80 32
ORO-FACIO-DIGITAL SYNDROME, file ddc633e2-bce8-4e2e-e053-3705fe0a4c80 30
AUTOSOMAL DOMINANT MEDULLARY CYSTIC KIDNEY DISEASE, file ddc633e2-bce9-4e2e-e053-3705fe0a4c80 26
LES FORMES FAMILIALES DE NÉPHROPATHIE À IgA ÉTUDES CLINIQUE ET GÉNÉTIQUE, file ddc633e2-b3c6-4e2e-e053-3705fe0a4c80 24
Rituximab versus steroids and cyclophosphamide for the treatment of primary membranous nephropathy: Protocol of a pilot randomised controlled trial, file ddc633e4-200c-4e2e-e053-3705fe0a4c80 14
Geographic Differences in Genetic Susceptibility to IgA Nephropathy: GWAS Replication Study and Geospatial Risk Analysis, file ddc633e2-b273-4e2e-e053-3705fe0a4c80 2
Rituximab in children with resistant idiopathic nephrotic syndrome, file ddc633e2-bb0e-4e2e-e053-3705fe0a4c80 1
Totale 11.171
Categoria #
all - tutte 26.367
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 26.367


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019434 0 0 0 0 0 0 0 0 0 0 238 196
2019/20202.412 243 231 213 266 235 206 201 175 205 143 147 147
2020/20212.027 99 187 126 155 129 235 212 182 144 130 167 261
2021/20221.953 152 184 84 209 219 66 164 74 101 83 416 201
2022/20231.633 68 108 384 212 71 210 122 95 63 95 115 90
2023/20241.440 109 144 104 83 155 89 139 172 67 126 252 0
Totale 11.171