IRIS
NERI, Tauro Maria
 Distribuzione geografica
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Continente #
NA - Nord America 4.197
EU - Europa 3.629
AS - Asia 1.579
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 2
AF - Africa 1
Totale 9.414
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Nazione #
US - Stati Uniti d'America 4.098
CN - Cina 1.363
IE - Irlanda 771
SE - Svezia 690
UA - Ucraina 672
FI - Finlandia 580
DE - Germania 417
IT - Italia 315
TR - Turchia 137
CA - Canada 99
GB - Regno Unito 90
BE - Belgio 33
IN - India 32
NL - Olanda 21
SG - Singapore 16
VN - Vietnam 14
FR - Francia 13
AT - Austria 7
KR - Corea 7
EU - Europa 6
JP - Giappone 5
IR - Iran 3
LT - Lituania 3
LU - Lussemburgo 3
RO - Romania 2
SI - Slovenia 2
AU - Australia 1
CM - Camerun 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
ES - Italia 1
GR - Grecia 1
HR - Croazia 1
IL - Israele 1
MD - Moldavia 1
MK - Macedonia 1
NZ - Nuova Zelanda 1
PK - Pakistan 1
PL - Polonia 1
PT - Portogallo 1
RU - Federazione Russa 1
Totale 9.414
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Città #
Jacksonville 800
Dublin 770
Chandler 673
Dearborn 448
Beijing 355
Nanjing 225
Ashburn 222
San Mateo 176
Princeton 174
Ann Arbor 150
Izmir 125
Wilmington 105
Toronto 93
Shenyang 85
Boardman 84
Nanchang 74
Kunming 68
Helsinki 67
Jinan 63
New York 62
Hebei 52
Hefei 52
Jiaxing 49
Des Moines 39
Parma 38
Shanghai 38
Bremen 36
Woodbridge 31
Changsha 30
Tianjin 30
Brussels 23
Norwalk 23
Guangzhou 22
Seattle 21
Grafing 20
Rome 19
Haikou 18
Los Angeles 17
Zhengzhou 17
Chengdu 15
Ningbo 15
Dong Ket 14
Fremont 14
Taizhou 14
Fuzhou 12
Kocaeli 12
Milan 12
Auburn Hills 11
Leawood 11
Monmouth Junction 11
Hangzhou 10
Chongqing 9
Waanrode 9
Houston 8
Napoli 8
Rockville 8
Taiyuan 8
Vienna 7
Augusta 6
Falls Church 6
Pune 6
Shaoxing 6
Wellesley 6
Wenzhou 6
Naples 5
Rio Saliceto 5
Seongnam 5
Wuhan 5
Ardea 4
Baotou 4
Bologna 4
Borås 4
Genova 4
Mestre 4
Mumbai 4
Quzhou 4
Tappahannock 4
Aversa 3
Düsseldorf 3
Florence 3
Huizen 3
Lanzhou 3
Luxembourg 3
Mountain View 3
Pavia 3
Regensburg 3
Vilnius 3
Abbiategrasso 2
Amantea 2
Ambes 2
Andretta 2
Ardabil 2
Bacoli 2
Bastiglia 2
Chaoyang 2
Chicago 2
Cutrofiano 2
Edinburgh 2
Fairfield 2
Focsani 2
Totale 5.750
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Nome #
Role of immunoglobulin G fragment C receptor polymorphism-mediatedantibody-dependant1. cellular cytotoxicity in colorectal cancer treated withcetuximab therapy. Pharmacogenomics J. 150
Analisi dello spettro mutazionale del gene NF1 mediate Protein Truncation Test (PTT) 118
Oligonucleotide Ligation Assay (OLA) e mutazioni silenti del gene CFTR: una rara causa di parziale fallimento del test 117
Evidence fo Epigenetic Abnormalities of the Androgen Receptor Gene in Foreskin from Children with Hypospadias 112
Associations between two single nucleotide polymorphisms of the adiponectin gene, its circulating concentrations and cardiometabolic risk factors in prepubertal children with and without abdominal obesity. 101
Analysis of HLA-DR and –C in 141 multiple sclerosis patients from Emilia, Northern Italy 81
Alterations of type IV collagen alpha chains in patients with chronic acquired glomerulopathies: analogies with Alport’s syndrome 79
5 OP Keratin 8 gene mutation in patients with chronic pancreatitis 79
Urinary excretion of brush-border antigen revealed by monoclonal antibody: early indicator of toxic nephropathy. 77
Rapporti fra citochine infiammatorie e fattori di crescita: meccanismi noti ed ipotizzabili negli IUGR 76
Influence of APOE status on lexical-semantic skills in Mild Cognitive Impairment 76
Fluorescent in situ hybridisation on tissue sections: a quantitative approach with confocal laser scanning microscopy 75
HLA-DRB4 as a genetic risk factor for Churg-Strauss syndrome 75
Alterations of type IV collagen alpha chains in patients with chronic acquired glomerulopathies: mRNA levels, protein expression and urinary loss 75
Street ME, Seghini P, Fieni S, Viveri MA, Viani I, Martorana D, Volta C, Neri T M, Granellini D, Bernasconi S 74
Febbre Mediterranea Familiare (FMF) e sindrome associata a mutazioni del recettore del TNF-alfa (TRAPS): nuove varianti e cross-talk fra i 2 geni 73
BRCA-1 status, molecular markers and clinical viariables in breast cancer (BC) patients with high probability of having an inherited cancer predisposing genetic mutation 73
Association of keratin 8 gene mutation with chronic pancreatitis 73
Diagnosi di maschio XX nel corso di screening di candidati alla fecondazione assistita mediante ICSI (Intracytoplasmatic Sperm Injection) 72
BRCA mutations, molecular markers, and clinical variables in early-onset breast cancer: A population-based study. 72
BRCA1 and BRCA2 status in a sample of italian women with early onset breast cancer (EOBC) 72
Ruolo dei geni del collagene di tipo IV e dei loro prodotti proteici nelle glomerulopatie umane acquisite 71
Valutazione del gene COL4A5 e del suo prodotto proteico nelle nefropatie glomerulari acquisite 69
Association of HLA-DRB1 *0401 Allele with chronic pancreatitis 68
PTPN22 R620W polymorphism in the ANCA-associated vasculitides. 68
Screening mutazionale nel gene BRCA1 in pazienti con tumori al seno e all’ovaio 68
Interazioni tra IL-6 e sistema IGF/IGFBP nella placenta e nel siero cordonale di nati IUGR 68
Androgen receptor CAG repeats and gene methylation in children with premature pubarche 67
Oligonucleotide Ligation Assay (OLA) e mutazioni silenti del gene CFTR: una rara causa di parziale fallimento del test 66
Polimorfismi dei geni delle citochine e dei loro recettori nella sindrome di Churg-Strauss 66
Pili canaliculi: a familial study 66
Tipizzazione dei polimorfismi dei geni del locus HLA, delle citochine e dei loro recettori nella Fibrosi Retroperitoneale Idiopatica (FRI) 66
Aromatase is differentially expressed in peripheral blood leukocytes from children, and adult female and male subjects. 66
Characterization of a novel mutation in the F8 promoter region associated with mild hemophilia A and resistance to DDAVP therapy. 66
Molecular profile and clinical variables in BRCA1-positive breast cancers. A population-based study 65
Studio delle triplette CAG e della metilazione del gene per il recettore degli androgeni in bambini prepuberi, donne e pazienti con pubarca prematuro 65
A novel mutation of the NR0B1 (DAX-1)gene in a family with two monozygotic twin sisters and a congenital adrenal ipoplasia affected child 65
Clinico-pathological and biomolecular findings in Italian patients with multiple cutaneous neurofibromas. 64
Correlazione fra HLA-DRB1*03 e periaortite cronica: una ipotesi di origine autoimmune 64
BRCA1 and BRCA2 status in a sample of italian women with early onset breast cancer (EOBC) 64
IL-6, IGFBP-1, IGFBP-2 (mRNA and proteins) and IGF-II are significantly increased in the placenta and correlate with neonatal size in IUGR with altered placental doppler velocimetry 64
Chronic periaortitis and HLA–DRB1*03: Another clue to an autoimmune origin 63
Crescita e disordini puberali nella Neurofibromatosi di tipo 1 62
Chronic periaortitis and HLA-DRB1*03: another clue to an autoimmune origin 61
Modulazione della riespressione del gene FHIT in cellule di carcinoma polmonare 61
Serological and molecular study on the HLA phenotype of female breast cancer patients. 61
DUPLICAZIONE DELL DELL’ESONE 13 DEL GENE F8 NEI P ’ESONE PAZIENTI EMOFILICI CON AZIENTI FENO FENOTIPO LIEVE: TIPO LA CASISTICA DELLA REGIONE EMILIA ROMA ROMAGNA GNA 61
A breast cancer patient from Italy with germline mutations in both the BRCA1 and BRCA2 genes 61
Novel association of HLA-haplotypes with primary sclerosing cholangitis (PSC) in a southern European population 61
Alport syndrome in Italy. A multicenter screening for COL4A5 gene mutations 61
Febbre Mediterranea Familiare e Sindrome Associata a mutazioni nel recettore TNF-alfa: nuove varianti ed interazioni fra i due geni 60
Keratin 8 mutations in patients with chronic pancreatitis 60
Human T-cell receptor alpha chain gene during ontogeny 60
BRCA mutations, molecular markers, and clinical variables in early-onset breast cancer: A population-based study 60
T-cell receptor beta-chain gene rearrangement and expression during human thymic ontogenesis. 59
T-cell receptor beta-chain gene rearrangement and expression during human thymic ontogenesis. 59
The new tumor suppressor gene inhibitor of growth family member 4 (ING4) regulates the production of pro-angiogenic molecules by myeloma cells and suppresses hypoxia inducible factor (HIF)-1{alpha} activity being involved in myeloma-induced angiogenesis. 59
CORRELAZIONE FRA HLA-DRB1*03 E PERIAORTITE CRONICA: UNA IPOTESI DI ORIGINE AUTOIMMUNE 58
Riconoscimento in situ di RNA messaggeri umani specifici mediante microscopia confocale in fluorescenza 58
Malattia di Fabry e linfedema familiare. Descrizione di due casi 58
[Genetic markers in insulin-dependent juvenile diabetes]. 58
BRCA1 status. Molecular markers and clinical variables in breast cancer (BC) patients with high probability of having an inherited, cancer-predisposing genetic mutation 58
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene. 57
Clinical, histopathological and biochemical findings in Fabry's disease. A case report 57
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene. 57
Interleukin-6 and Insulin-like growth factor system relationships and differences in the human placenta and fetus from the 35th week of gestation 56
Expression of TCR beta chain gene N-diversity is not an early event in human thymic ontogeny 56
Mesangio-proliferative glomerulonephritis with prevalent deposits of IgA and histocompatibility antigens 56
Fabry's Disease with Familial Lymphedema of the Lower Limbs. Case Report and Family Study 56
Premature pubarche as epiphenomenon of non-random androgen receptor gene methylation 55
Studio del numero delle triplette CAG e della metilazione del gene per il recettore degli androgeni in bambine prepuberi, donne e pazienti con pubarca prematuro 55
Ruolo dei geni del collageno di tipo 4 nelle glomerulopatie acquisite 55
HLA-DRB1 e TNF, ma non CFTR, sono fattori di rischio per la colangite sclerosante 55
Febbre Mediterranea Familiare (FMF) e sindrome associata a mutazioni del recettore del TNF-alfa (TRAPS): nuove varianti e cross-talk fra i 2 geni. 55
BRCA mutations, molecular markers, and clinical variables in early-onset breastcancer: a population-based study. 54
HLA ANTIGENS AND INSULIN DEPENDENT DIABETES MELLITUS. A FAMILY STUDY 54
Ulteriori nuove mutazioni sul gene COL4A5 mediante PCR e sequenziamento diretto 54
Selective sensitization of peripheral blood T lymphocytes to hepatitis B core antigen in patients with chronic active hepatitis type B. 54
Coagulation factor genes polymorphisms in primary sporadic focal segmental glomerulosclerosis 53
Identification of anchovy (Engraulis encrasicholus L.) and gilt sardine (Sardinella aurita) by polymerase chain reaction, sequence of their mitochondrial cytochrome b gene, and restriction analysis of polymerase chain reaction products in semipreserves 53
Familial giant cell arteritis and polymyalgia rheumatica: aggregation in 2 families 53
Genetica della Febbre Mediterranea Familiare in Italia 53
HLA-DR antigens and cardiolipin antibodies in northen Italian systemic erythematosus patients. 53
Role of the 4A5 collagen gene and its product in human acquired glomerulopathies 53
Sospetta eterogeneità genetica nella Febbre Mediterranea Familiare 53
Rapid and sensitive MLPA approach for identification of deletion carriers in haemophilia 53
Inversione dell’introne 1 nel gene del fattore VIII della coagulazione 52
Gastrointestinal stromal tumor and other primary metachronous or synchronous neoplasms as a suspicion criterion for syndromic setting 52
Different expression of BRCA1 status and clinical variables in a sample of Italian women with early onset breast cancer (EOBC) 52
The contribution of MHC region genes in the genetic predisposition to primary sclerosing cholangitis (PSC) 52
Immunoglobulin G Fragment C Receptor Polymorphisms and Clinical Efficacy of Trastuzumab-Based Therapy in Patients With HER-2/neu-Positive Metastatic Breast Cancer. 52
Sospetta eterogeneità genetica nella Febbre Mediterranea Familiare 51
L’analisi mutazionale del gene COL4A5 mediante sequenziamento diretto rende possibile la diagnosi nella quasi totalità dei casi 51
Missense mutations in the COL4A5 gene in patients with X-linked Alport syndrome 51
Comparison of human and porcine insulin therapies in children with newly diagnosed diabetes mellitus. 51
TAP genes, coding for the transporters associated with antigen processing, contribute to the genetic predisposition to primary sclerosing cholangitis (PSC) 51
Cavallini G. Keratin 8 mutations in patients with chronic pancreatitis 50
Sospetta eterogeneità genetica nella Febbre Mediterranea Familiare 50
La tecnica multiplex ligation probe amplification (MLPA) per la determinazione dello stato di portatrice in emofilia. 50
Male breast cancer (MBC) in Parma province: descriptive epidemiology, molecular markers and clinical variables. 50
Totale 6.410
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Categoria #
all - tutte 28.050
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 28.050
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019235 0 0 0 0 0 0 0 0 0 20 185 30
2019/20202.593 383 445 176 55 230 300 339 47 180 217 49 172
2020/20211.264 16 174 118 11 167 13 137 17 318 24 247 22
2021/2022798 9 6 12 29 21 25 106 154 32 69 83 252
2022/20232.770 338 264 175 178 250 317 20 144 958 13 88 25
2023/2024598 36 118 21 18 78 222 34 40 15 16 0 0
Totale 9.440