IRIS
NERI, Tauro Maria
 Distribuzione geografica
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Continente #
NA - Nord America 4.242
EU - Europa 3.674
AS - Asia 1.804
AF - Africa 23
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 2
Totale 9.751
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Nazione #
US - Stati Uniti d'America 4.143
CN - Cina 1.455
IE - Irlanda 771
SE - Svezia 690
UA - Ucraina 672
FI - Finlandia 580
DE - Germania 418
IT - Italia 354
SG - Singapore 149
TR - Turchia 137
CA - Canada 99
GB - Regno Unito 90
BE - Belgio 33
IN - India 32
CI - Costa d'Avorio 22
NL - Olanda 21
VN - Vietnam 14
FR - Francia 13
AT - Austria 7
KR - Corea 7
CZ - Repubblica Ceca 6
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
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 9.751
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Città #
Jacksonville 800
Dublin 770
Chandler 673
Dearborn 448
Beijing 355
Nanjing 225
Ashburn 224
San Mateo 176
Princeton 174
Ann Arbor 150
Izmir 125
Wilmington 105
Toronto 93
Boardman 87
Shenyang 85
Singapore 79
Nanchang 74
Kunming 68
Helsinki 67
Jinan 63
New York 62
Shanghai 62
Hebei 52
Hefei 52
Jiaxing 49
Los Angeles 43
Des Moines 39
Parma 39
Bremen 36
Woodbridge 31
Changsha 30
Tianjin 30
Guangzhou 24
Brussels 23
Norwalk 23
Abidjan 22
Rome 22
Seattle 21
Grafing 20
Milan 20
Haikou 18
Zhengzhou 17
Chengdu 15
Ningbo 15
Dong Ket 14
Fremont 14
Taizhou 14
Fuzhou 12
Kocaeli 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
Dallas 6
Falls Church 6
Naples 6
Pune 6
Shaoxing 6
Wellesley 6
Wenzhou 6
Brno 5
Rio Saliceto 5
Seongnam 5
Wuhan 5
Ardea 4
Baotou 4
Bologna 4
Borås 4
Genova 4
Mestre 4
Mumbai 4
Quzhou 4
Reggio Emilia 4
Tappahannock 4
Aversa 3
Briosco 3
Düsseldorf 3
Florence 3
Huizen 3
Lanzhou 3
Luxembourg 3
Mountain View 3
Palermo 3
Pavia 3
Regensburg 3
Vilnius 3
Abbiategrasso 2
Amantea 2
Ambes 2
Andretta 2
Angri 2
Ardabil 2
Totale 5.928
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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. 156
Oligonucleotide Ligation Assay (OLA) e mutazioni silenti del gene CFTR: una rara causa di parziale fallimento del test 130
Analisi dello spettro mutazionale del gene NF1 mediate Protein Truncation Test (PTT) 120
Evidence fo Epigenetic Abnormalities of the Androgen Receptor Gene in Foreskin from Children with Hypospadias 115
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. 103
5 OP Keratin 8 gene mutation in patients with chronic pancreatitis 85
Analysis of HLA-DR and –C in 141 multiple sclerosis patients from Emilia, Northern Italy 82
Alterations of type IV collagen alpha chains in patients with chronic acquired glomerulopathies: analogies with Alport’s syndrome 81
Alterations of type IV collagen alpha chains in patients with chronic acquired glomerulopathies: mRNA levels, protein expression and urinary loss 80
Fluorescent in situ hybridisation on tissue sections: a quantitative approach with confocal laser scanning microscopy 78
Urinary excretion of brush-border antigen revealed by monoclonal antibody: early indicator of toxic nephropathy. 78
Rapporti fra citochine infiammatorie e fattori di crescita: meccanismi noti ed ipotizzabili negli IUGR 77
Influence of APOE status on lexical-semantic skills in Mild Cognitive Impairment 77
Ruolo dei geni del collagene di tipo IV e dei loro prodotti proteici nelle glomerulopatie umane acquisite 76
BRCA mutations, molecular markers, and clinical variables in early-onset breast cancer: A population-based study. 76
Association of keratin 8 gene mutation with chronic pancreatitis 76
HLA-DRB4 as a genetic risk factor for Churg-Strauss syndrome 76
BRCA-1 status, molecular markers and clinical viariables in breast cancer (BC) patients with high probability of having an inherited cancer predisposing genetic mutation 75
Street ME, Seghini P, Fieni S, Viveri MA, Viani I, Martorana D, Volta C, Neri T M, Granellini D, Bernasconi S 75
Febbre Mediterranea Familiare (FMF) e sindrome associata a mutazioni del recettore del TNF-alfa (TRAPS): nuove varianti e cross-talk fra i 2 geni 74
Association of HLA-DRB1 *0401 Allele with chronic pancreatitis 74
Oligonucleotide Ligation Assay (OLA) e mutazioni silenti del gene CFTR: una rara causa di parziale fallimento del test 73
Diagnosi di maschio XX nel corso di screening di candidati alla fecondazione assistita mediante ICSI (Intracytoplasmatic Sperm Injection) 73
Valutazione del gene COL4A5 e del suo prodotto proteico nelle nefropatie glomerulari acquisite 73
PTPN22 R620W polymorphism in the ANCA-associated vasculitides. 73
BRCA1 and BRCA2 status in a sample of italian women with early onset breast cancer (EOBC) 73
Androgen receptor CAG repeats and gene methylation in children with premature pubarche 69
Screening mutazionale nel gene BRCA1 in pazienti con tumori al seno e all’ovaio 69
Pili canaliculi: a familial study 69
Aromatase is differentially expressed in peripheral blood leukocytes from children, and adult female and male subjects. 69
A novel mutation of the NR0B1 (DAX-1)gene in a family with two monozygotic twin sisters and a congenital adrenal ipoplasia affected child 69
Correlazione fra HLA-DRB1*03 e periaortite cronica: una ipotesi di origine autoimmune 68
Tipizzazione dei polimorfismi dei geni del locus HLA, delle citochine e dei loro recettori nella Fibrosi Retroperitoneale Idiopatica (FRI) 68
Interazioni tra IL-6 e sistema IGF/IGFBP nella placenta e nel siero cordonale di nati IUGR 68
Polimorfismi dei geni delle citochine e dei loro recettori nella sindrome di Churg-Strauss 67
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 67
Characterization of a novel mutation in the F8 promoter region associated with mild hemophilia A and resistance to DDAVP therapy. 67
Molecular profile and clinical variables in BRCA1-positive breast cancers. A population-based study 66
Studio delle triplette CAG e della metilazione del gene per il recettore degli androgeni in bambini prepuberi, donne e pazienti con pubarca prematuro 66
Chronic periaortitis and HLA–DRB1*03: Another clue to an autoimmune origin 66
Clinico-pathological and biomolecular findings in Italian patients with multiple cutaneous neurofibromas. 65
BRCA1 and BRCA2 status in a sample of italian women with early onset breast cancer (EOBC) 65
Chronic periaortitis and HLA-DRB1*03: another clue to an autoimmune origin 64
Crescita e disordini puberali nella Neurofibromatosi di tipo 1 63
Modulazione della riespressione del gene FHIT in cellule di carcinoma polmonare 63
A breast cancer patient from Italy with germline mutations in both the BRCA1 and BRCA2 genes 63
Febbre Mediterranea Familiare e Sindrome Associata a mutazioni nel recettore TNF-alfa: nuove varianti ed interazioni fra i due geni 62
Keratin 8 mutations in patients with chronic pancreatitis 62
Human T-cell receptor alpha chain gene during ontogeny 62
Serological and molecular study on the HLA phenotype of female breast cancer patients. 62
T-cell receptor beta-chain gene rearrangement and expression during human thymic ontogenesis. 62
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 62
Novel association of HLA-haplotypes with primary sclerosing cholangitis (PSC) in a southern European population 62
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. 62
Alport syndrome in Italy. A multicenter screening for COL4A5 gene mutations 62
Riconoscimento in situ di RNA messaggeri umani specifici mediante microscopia confocale in fluorescenza 61
T-cell receptor beta-chain gene rearrangement and expression during human thymic ontogenesis. 61
BRCA mutations, molecular markers, and clinical variables in early-onset breast cancer: A population-based study 61
BRCA1 status. Molecular markers and clinical variables in breast cancer (BC) patients with high probability of having an inherited, cancer-predisposing genetic mutation 60
Clinical, histopathological and biochemical findings in Fabry's disease. A case report 60
CORRELAZIONE FRA HLA-DRB1*03 E PERIAORTITE CRONICA: UNA IPOTESI DI ORIGINE AUTOIMMUNE 59
Malattia di Fabry e linfedema familiare. Descrizione di due casi 59
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene. 59
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene. 59
[Genetic markers in insulin-dependent juvenile diabetes]. 58
Mesangio-proliferative glomerulonephritis with prevalent deposits of IgA and histocompatibility antigens 58
Ruolo dei geni del collageno di tipo 4 nelle glomerulopatie acquisite 58
Fabry's Disease with Familial Lymphedema of the Lower Limbs. Case Report and Family Study 58
Interleukin-6 and Insulin-like growth factor system relationships and differences in the human placenta and fetus from the 35th week of gestation 57
Role of the 4A5 collagen gene and its product in human acquired glomerulopathies 57
Expression of TCR beta chain gene N-diversity is not an early event in human thymic ontogeny 57
Febbre Mediterranea Familiare (FMF) e sindrome associata a mutazioni del recettore del TNF-alfa (TRAPS): nuove varianti e cross-talk fra i 2 geni. 57
Genetica della Febbre Mediterranea Familiare in Italia 56
BRCA mutations, molecular markers, and clinical variables in early-onset breastcancer: a population-based study. 56
La tecnica multiplex ligation probe amplification (MLPA) per la determinazione dello stato di portatrice in emofilia. 56
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 56
HLA ANTIGENS AND INSULIN DEPENDENT DIABETES MELLITUS. A FAMILY STUDY 56
Ulteriori nuove mutazioni sul gene COL4A5 mediante PCR e sequenziamento diretto 56
HLA-DRB1 e TNF, ma non CFTR, sono fattori di rischio per la colangite sclerosante 56
Premature pubarche as epiphenomenon of non-random androgen receptor gene methylation 55
Coagulation factor genes polymorphisms in primary sporadic focal segmental glomerulosclerosis 55
HLA-DR antigens and cardiolipin antibodies in northen Italian systemic erythematosus patients. 55
Sospetta eterogeneità genetica nella Febbre Mediterranea Familiare 55
Rapid and sensitive MLPA approach for identification of deletion carriers in haemophilia 55
Selective sensitization of peripheral blood T lymphocytes to hepatitis B core antigen in patients with chronic active hepatitis type B. 55
Gastrointestinal stromal tumor and other primary metachronous or synchronous neoplasms as a suspicion criterion for syndromic setting 54
Different expression of BRCA1 status and clinical variables in a sample of Italian women with early onset breast cancer (EOBC) 54
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
Inversione dell’introne 1 nel gene del fattore VIII della coagulazione 53
Missense mutations in the COL4A5 gene in patients with X-linked Alport syndrome 53
Immunoglobulin G Fragment C Receptor Polymorphisms and Clinical Efficacy of Trastuzumab-Based Therapy in Patients With HER-2/neu-Positive Metastatic Breast Cancer. 53
Association beetween fetal Doppler velocimetry abnormalities and confined placental trisomy 22: a case report 53
Sospetta eterogeneità genetica nella Febbre Mediterranea Familiare 52
L’analisi mutazionale del gene COL4A5 mediante sequenziamento diretto rende possibile la diagnosi nella quasi totalità dei casi 52
Male breast cancer (MBC) in Parma province: descriptive epidemiology, molecular markers and clinical variables. 52
Comparison of human and porcine insulin therapies in children with newly diagnosed diabetes mellitus. 52
L'ANALISI MUTAZIONALE DEL GENE COL4A5 MEDIANTE SEQUENZIAMENTO DIRETTO RENDE POSSIBILE LA DIAGNOSI NELLA QUASI TOTALITA'DEI CASI 52
TAP genes, coding for the transporters associated with antigen processing, contribute to the genetic predisposition to primary sclerosing cholangitis (PSC) 52
The contribution of MHC region genes in the genetic predisposition to primary sclerosing cholangitis (PSC) 52
Totale 6.629
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Categoria #
all - tutte 32.673
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 32.673
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.210 0 445 176 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
2023/2024823 36 118 21 18 78 222 34 40 15 54 67 120
2024/2025112 101 11 0 0 0 0 0 0 0 0 0 0
Totale 9.777