Bicocca Open Archive

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ROVERSI, GAIA
 Distribuzione geografica
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Continente #
NA - Nord America 5.352
EU - Europa 2.800
AS - Asia 2.703
SA - Sud America 451
AF - Africa 48
Continente sconosciuto - Info sul continente non disponibili 4
Totale 11.358
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Nazione #
US - Stati Uniti d'America 5.209
SG - Singapore 877
CN - Cina 711
IT - Italia 613
VN - Vietnam 475
DE - Germania 458
RU - Federazione Russa 390
BR - Brasile 377
HK - Hong Kong 357
SE - Svezia 345
IE - Irlanda 290
UA - Ucraina 190
GB - Regno Unito 117
CA - Canada 100
AT - Austria 91
FI - Finlandia 71
FR - Francia 67
ID - Indonesia 54
IN - India 48
BE - Belgio 34
KR - Corea 34
AR - Argentina 33
DK - Danimarca 32
MX - Messico 31
JP - Giappone 28
TR - Turchia 27
BD - Bangladesh 26
PL - Polonia 25
ZA - Sudafrica 21
NL - Olanda 20
ES - Italia 19
IQ - Iraq 12
CZ - Repubblica Ceca 11
MA - Marocco 10
EC - Ecuador 9
PK - Pakistan 8
CO - Colombia 7
CH - Svizzera 6
PE - Perù 6
PH - Filippine 6
VE - Venezuela 6
LT - Lituania 5
TH - Thailandia 5
CL - Cile 4
GR - Grecia 4
IR - Iran 4
SA - Arabia Saudita 4
UY - Uruguay 4
BO - Bolivia 3
BY - Bielorussia 3
DZ - Algeria 3
EU - Europa 3
IL - Israele 3
LK - Sri Lanka 3
TN - Tunisia 3
AE - Emirati Arabi Uniti 2
AZ - Azerbaigian 2
CR - Costa Rica 2
DO - Repubblica Dominicana 2
EG - Egitto 2
ET - Etiopia 2
JM - Giamaica 2
JO - Giordania 2
KZ - Kazakistan 2
LB - Libano 2
LY - Libia 2
MY - Malesia 2
PY - Paraguay 2
QA - Qatar 2
RO - Romania 2
RS - Serbia 2
SN - Senegal 2
SV - El Salvador 2
UZ - Uzbekistan 2
VG - Isole Vergini Britanniche 2
AM - Armenia 1
AO - Angola 1
GA - Gabon 1
HN - Honduras 1
HR - Croazia 1
KG - Kirghizistan 1
MU - Mauritius 1
NO - Norvegia 1
NP - Nepal 1
PA - Panama 1
PT - Portogallo 1
SI - Slovenia 1
SK - Slovacchia (Repubblica Slovacca) 1
TM - Turkmenistan 1
TW - Taiwan 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 11.358
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Città #
Ann Arbor 1.055
Singapore 493
Woodbridge 449
Ashburn 407
Hong Kong 356
Fairfield 331
Chandler 302
Frankfurt am Main 294
Dublin 283
Houston 250
Wilmington 235
Milan 212
Jacksonville 188
Dearborn 174
Seattle 160
Ho Chi Minh City 159
New York 120
Cambridge 118
Beijing 116
Hanoi 104
Santa Clara 94
Princeton 86
Vienna 85
Los Angeles 76
Nanjing 75
Altamura 55
Dallas 55
Shanghai 52
Hefei 50
Jakarta 49
Lawrence 40
Moscow 39
São Paulo 36
Munich 33
Lachine 32
Shenyang 29
The Dalles 29
Seoul 28
Buffalo 27
Chicago 26
London 23
Jinan 22
Nanchang 22
Helsinki 21
Warsaw 21
Guangzhou 20
Nuremberg 20
Tokyo 20
Andover 19
Fremont 19
Toronto 19
Council Bluffs 17
San Diego 17
Atlanta 16
Montreal 16
San Jose 16
Brussels 15
Tianjin 15
Changsha 14
Hebei 14
Quận Bình Thạnh 14
Jiaxing 13
Lissone 13
Salt Lake City 13
Turin 13
Johannesburg 12
Ningbo 12
Phoenix 12
Rio de Janeiro 12
Waterloo 12
Chennai 11
Da Nang 11
Mexico City 11
Ottawa 11
Taizhou 11
Turku 11
Ankara 10
Boardman 10
Denver 10
Falls Church 10
Kent 10
Kunming 10
Norwalk 10
Stockholm 10
Dong Ket 9
Ha Long 9
Hải Dương 9
Rome 9
Zhengzhou 9
Boston 8
Columbus 8
Düsseldorf 8
Loreto 8
Monza 8
Biên Hòa 7
Curitiba 7
Hangzhou 7
Pune 7
St Louis 7
Tampa 7
Totale 7.567
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Nome #
Molecular signatures of medullary thyroid carcinoma by matrix-assisted laser desorption/ionisation mass spectrometry imaging 544
Olfactory receptor genes and chromosome 11 structural aberrations: Players or spectators? 539
Interphase FISH: A Helpful Assay in Prenatal Cytogenetics Diagnosis 504
Refining the Phenotype of Recurrent Rearrangements of Chromosome 16 480
Familiar unbalanced complex rearrangements involving 13 p-arm: Description of two cases 408
The effect of culture on human bone marrow mesenchymal stem cells: Focus on DNA methylation profiles 366
Instability of short arm of acrocentric chromosomes: Lesson from non-acrocentric satellited chromosomes. report of 24 unrelated cases 365
Genomic and epigenomic profile of uterine smooth muscle tumors of uncertain malignant potential (Stumps) revealed similarities and differences with leiomyomas and leiomyosarcomas 355
Parent-of-origin effect of hypomorphic pathogenic variants and somatic mosaicism impact on phenotypic expression of retinoblastoma 340
Characterization of Chromosomal Breakpoints in 12 Cases with 8p Rearrangements Defines a Continuum of Fragility of the Region 282
Human chromosome 18 and acrocentrics: A dangerous liaison 275
Proteome analysis in thyroid pathology 268
Insights into the Peritumoural Brain Zone of Glioblastoma: CDK4 and EXT2 May Be Potential Drivers of Malignancy 256
An Alternative Approach in Endocrine Pathology Research: MALDI-IMS in Papillary Thyroid Carcinoma 246
A targeted approach to genetic counseling in breast cancer patients: The experience of an Italian local project 241
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor 234
Tubal histopathological abnormalities in BRCA1/2 mutation carriers undergoing prophylactic salpingo-oophorectomy: a case-control study 230
Solid cell nests of the thyroid gland: Morphological, immunohistochemical and genetic features 214
Rothmund-Thomson syndrome 214
Identification of two novel RECQL4 exonic SNPs and genomic characterization of the IVS12 minisatellite 208
The neural progenitor-restricted isoform of the MARK4 gene in 19q13.2 is upregulated in human gliomas and overexpressed in a subset of glioblastoma cell lines 204
RNA hyperediting and alternative splicing of hematopoietic cell phosphatase (PTPN6) gene in acute myeloid leukemia 203
Exploring the link between MORF4L1 and risk of breast cancer 199
Evidence for a link between TNFRSF11A and risk of breast cancer 197
Germline mutation in the juxtamembrane domain of the kit gene in a family with gastrointestinal stromal tumors and urticaria pigmentosa 196
RNA processing defects of the helicase gene RECQL4 in a compound heterozygous Rothmund-Thomson patient 191
Rothmund-Thomson syndrome and RECQL4 defect: splitting and lumping 187
The CASP8 rs3834129 polymorphism and breast cancer risk in BRCA1 mutation carriers 185
Differential cytogenomics and miRNA signature of the Acute Myeloid Leukaemia Kasumi-1 cell line CD34+38- compartment 181
Multiple localization of endogenous MARK4L protein in human glioma 180
Targeted next-generation sequencing appoints c16orf57 as clericuzio-type poikiloderma with neutropenia gene 179
Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers 178
Genomic Complexity and Complex Chromosomal Rearrangements in Genetic Diagnosis: Two Illustrative Cases on Chromosome 7 177
Clinical utility gene card for: Rothmund-Thomson syndrome 175
Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers 174
Piebald trait: implication of kit mutation on in vitro melanocyte survival and on the clinical application of cultured epidermal autografts 169
Two new CHEK2 germ-line variants detected in breast cancer/sarcoma families negative for BRCA1, BRCA2, and TP53 gene mutations 169
Impact and Reproducibility of In-House Targeted Next-Generation Sequencing Biomarker Testing in Non–Small-Cell Lung Cancer: An Italian Multi-Institutional Experience 164
Clericuzio-type poikiloderma with neutropenia syndrome in three sibs with mutations in the C16orf57 gene: delineation of the phenotype 161
Cytogenetically Balanced Reciprocal Translocation Could Hide Molecular Genomic Unbalances: Implications for Foetal Phenotype Correlation 159
Constitutional de novo deletion of the FBXW7 gene in a patient with focal segmental glomerulosclerosis and multiple primitive tumors 157
Atypical Rothmund-Thomson syndrome in a patient with compound Heterozygous Mutations in RECQL4 Gene and phenotypic features in RECQL4 syndromes 155
Uptake of Risk-Reducing Salpingo-Oophorectomy and Gynaecologic Surveillance Among Germline BRCA Pathogenic Variants Carriers 154
Novel physiological RECQL4 alternative transcript disclosed by molecular characterisation of Rothmund–Thomson Syndrome sibs with mild phenotype 154
Evaluation of family history in individuals with heterozygous BRCA pathogenic variants diagnosed with breast or ovarian cancer in a single center in Italy 153
Identification of novel genomic markers related to progression to glioblastoma through genomic profiling of 25 primary glioma cell lines 145
Sindrome di Rothmund-Thomson: caratterizzazione clinico-molecolare di tre nuovi pazienti 145
Spontaneous chromosomal instability in peripheral blood lymphocytes from two molecularly confirmed italian patients with hereditary fibrosis poikiloderma: Insights into cancer predisposition 139
Search for genomic imbalances in a cohort of 24 Cornelia de Lange patients negative for mutations in the NIPBL and SMC1L1 genes 138
Identification of oligodendroglioma specific chromosomal copy number changes in the glioblastoma MI-4 cell line by array-CGH and FISH analyses 136
Totale 11.673
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Categoria #
all - tutte 37.173
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 37.173
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021630 0 0 0 0 0 0 100 122 103 117 79 109
2021/2022761 67 69 81 65 72 69 12 45 53 32 65 131
2022/20231.244 154 347 121 114 80 179 16 65 101 17 29 21
2023/2024823 26 28 27 34 94 205 195 27 71 11 14 91
2024/20251.987 102 180 88 109 209 138 128 83 207 300 167 276
2025/20262.670 688 347 365 509 494 244 23 0 0 0 0 0
Totale 11.673