Bicocca Open Archive

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ROVERSI, GAIA
 Distribuzione geografica
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Continente #
NA - Nord America 6.126
AS - Asia 3.352
EU - Europa 2.971
SA - Sud America 563
AF - Africa 94
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 2
Totale 13.112
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Nazione #
US - Stati Uniti d'America 5.916
SG - Singapore 1.040
CN - Cina 752
VN - Vietnam 636
IT - Italia 633
DE - Germania 473
BR - Brasile 432
HK - Hong Kong 417
RU - Federazione Russa 395
SE - Svezia 346
IE - Irlanda 291
UA - Ucraina 194
CA - Canada 154
FR - Francia 129
GB - Regno Unito 128
IN - India 102
AT - Austria 92
FI - Finlandia 78
ID - Indonesia 60
BD - Bangladesh 56
AR - Argentina 43
ES - Italia 40
TR - Turchia 40
KR - Corea 36
BE - Belgio 35
JP - Giappone 34
MX - Messico 34
DK - Danimarca 32
IQ - Iraq 29
PL - Polonia 29
ZA - Sudafrica 28
PH - Filippine 25
CO - Colombia 22
NL - Olanda 22
PK - Pakistan 20
MA - Marocco 18
EC - Ecuador 15
SA - Arabia Saudita 14
TH - Thailandia 13
VE - Venezuela 13
CH - Svizzera 12
CZ - Repubblica Ceca 12
TN - Tunisia 10
UZ - Uzbekistan 10
CL - Cile 9
IL - Israele 9
EG - Egitto 8
ET - Etiopia 8
PE - Perù 8
PY - Paraguay 8
UY - Uruguay 7
BO - Bolivia 6
DZ - Algeria 6
JM - Giamaica 6
KZ - Kazakistan 6
GR - Grecia 5
JO - Giordania 5
LB - Libano 5
LT - Lituania 5
CR - Costa Rica 4
IR - Iran 4
MY - Malesia 4
NP - Nepal 4
AE - Emirati Arabi Uniti 3
AO - Angola 3
AZ - Azerbaigian 3
BY - Bielorussia 3
DO - Repubblica Dominicana 3
EU - Europa 3
KG - Kirghizistan 3
LK - Sri Lanka 3
OM - Oman 3
PA - Panama 3
QA - Qatar 3
RS - Serbia 3
SN - Senegal 3
TW - Taiwan 3
AL - Albania 2
AU - Australia 2
BG - Bulgaria 2
BH - Bahrain 2
CI - Costa d'Avorio 2
CY - Cipro 2
LY - Libia 2
RO - Romania 2
SV - El Salvador 2
VG - Isole Vergini Britanniche 2
AM - Armenia 1
BA - Bosnia-Erzegovina 1
GA - Gabon 1
GN - Guinea 1
HN - Honduras 1
HR - Croazia 1
HU - Ungheria 1
KE - Kenya 1
KH - Cambogia 1
LA - Repubblica Popolare Democratica del Laos 1
MD - Moldavia 1
MU - Mauritius 1
MV - Maldive 1
Totale 13.102
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Città #
Ann Arbor 1.055
Singapore 581
Ashburn 475
Woodbridge 449
Hong Kong 407
San Jose 361
Fairfield 331
Frankfurt am Main 308
Chandler 302
Dublin 284
Houston 250
Wilmington 235
Milan 213
Ho Chi Minh City 205
Jacksonville 190
Dearborn 174
Seattle 160
Hanoi 155
New York 135
Beijing 119
Cambridge 118
Los Angeles 102
Santa Clara 101
Princeton 86
Vienna 86
Chicago 75
Nanjing 75
The Dalles 75
Toronto 65
Dallas 60
Altamura 55
Shanghai 52
Hefei 51
Jakarta 49
Lauterbourg 43
São Paulo 42
Lawrence 40
Moscow 40
Council Bluffs 37
Munich 33
Lachine 32
Buffalo 31
Seoul 29
Shenyang 29
Helsinki 28
London 25
Warsaw 25
Tokyo 24
Da Nang 23
Jinan 22
Nanchang 22
Guangzhou 20
Nuremberg 20
Andover 19
Fremont 19
Montreal 19
Atlanta 18
San Diego 18
Brussels 16
Chennai 15
Hải Dương 15
Tianjin 15
Changsha 14
Hebei 14
Quận Bình Thạnh 14
Jiaxing 13
Johannesburg 13
Lissone 13
Phoenix 13
Rio de Janeiro 13
Salt Lake City 13
Turin 13
Ningbo 12
Orem 12
Rome 12
Waterloo 12
Baghdad 11
Mexico City 11
Ottawa 11
Stockholm 11
Taizhou 11
Turku 11
Ankara 10
Boardman 10
Denver 10
Falls Church 10
Istanbul 10
Kent 10
Kunming 10
Norwalk 10
Zhengzhou 10
Curitiba 9
Dong Ket 9
Ha Long 9
Haiphong 9
St Louis 9
Zurich 9
Addis Ababa 8
Boston 8
Columbus 8
Totale 8.573
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Nome #
Olfactory receptor genes and chromosome 11 structural aberrations: Players or spectators? 603
Molecular signatures of medullary thyroid carcinoma by matrix-assisted laser desorption/ionisation mass spectrometry imaging 581
Interphase FISH: A Helpful Assay in Prenatal Cytogenetics Diagnosis 551
Refining the Phenotype of Recurrent Rearrangements of Chromosome 16 535
Familiar unbalanced complex rearrangements involving 13 p-arm: Description of two cases 460
Instability of short arm of acrocentric chromosomes: Lesson from non-acrocentric satellited chromosomes. report of 24 unrelated cases 420
The effect of culture on human bone marrow mesenchymal stem cells: Focus on DNA methylation profiles 402
Genomic and epigenomic profile of uterine smooth muscle tumors of uncertain malignant potential (Stumps) revealed similarities and differences with leiomyomas and leiomyosarcomas 401
Parent-of-origin effect of hypomorphic pathogenic variants and somatic mosaicism impact on phenotypic expression of retinoblastoma 388
Characterization of Chromosomal Breakpoints in 12 Cases with 8p Rearrangements Defines a Continuum of Fragility of the Region 341
Human chromosome 18 and acrocentrics: A dangerous liaison 328
Proteome analysis in thyroid pathology 309
Insights into the Peritumoural Brain Zone of Glioblastoma: CDK4 and EXT2 May Be Potential Drivers of Malignancy 307
Tubal histopathological abnormalities in BRCA1/2 mutation carriers undergoing prophylactic salpingo-oophorectomy: a case-control study 287
A targeted approach to genetic counseling in breast cancer patients: The experience of an Italian local project 283
An Alternative Approach in Endocrine Pathology Research: MALDI-IMS in Papillary Thyroid Carcinoma 279
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor 258
Solid cell nests of the thyroid gland: Morphological, immunohistochemical and genetic features 247
Rothmund-Thomson syndrome 244
Identification of two novel RECQL4 exonic SNPs and genomic characterization of the IVS12 minisatellite 237
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 233
Exploring the link between MORF4L1 and risk of breast cancer 231
RNA processing defects of the helicase gene RECQL4 in a compound heterozygous Rothmund-Thomson patient 231
RNA hyperediting and alternative splicing of hematopoietic cell phosphatase (PTPN6) gene in acute myeloid leukemia 226
Impact and Reproducibility of In-House Targeted Next-Generation Sequencing Biomarker Testing in Non–Small-Cell Lung Cancer: An Italian Multi-Institutional Experience 225
Germline mutation in the juxtamembrane domain of the kit gene in a family with gastrointestinal stromal tumors and urticaria pigmentosa 222
Evidence for a link between TNFRSF11A and risk of breast cancer 221
Genomic Complexity and Complex Chromosomal Rearrangements in Genetic Diagnosis: Two Illustrative Cases on Chromosome 7 220
Rothmund-Thomson syndrome and RECQL4 defect: splitting and lumping 216
The CASP8 rs3834129 polymorphism and breast cancer risk in BRCA1 mutation carriers 210
Cytogenetically Balanced Reciprocal Translocation Could Hide Molecular Genomic Unbalances: Implications for Foetal Phenotype Correlation 205
Multiple localization of endogenous MARK4L protein in human glioma 203
Differential cytogenomics and miRNA signature of the Acute Myeloid Leukaemia Kasumi-1 cell line CD34+38- compartment 203
Uptake of Risk-Reducing Salpingo-Oophorectomy and Gynaecologic Surveillance Among Germline BRCA Pathogenic Variants Carriers 202
Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers 201
Targeted next-generation sequencing appoints c16orf57 as clericuzio-type poikiloderma with neutropenia gene 201
Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers 199
Evaluation of family history in individuals with heterozygous BRCA pathogenic variants diagnosed with breast or ovarian cancer in a single center in Italy 196
Piebald trait: implication of kit mutation on in vitro melanocyte survival and on the clinical application of cultured epidermal autografts 196
Clinical utility gene card for: Rothmund-Thomson syndrome 194
Two new CHEK2 germ-line variants detected in breast cancer/sarcoma families negative for BRCA1, BRCA2, and TP53 gene mutations 192
Atypical Rothmund-Thomson syndrome in a patient with compound Heterozygous Mutations in RECQL4 Gene and phenotypic features in RECQL4 syndromes 186
Clericuzio-type poikiloderma with neutropenia syndrome in three sibs with mutations in the C16orf57 gene: delineation of the phenotype 183
Constitutional de novo deletion of the FBXW7 gene in a patient with focal segmental glomerulosclerosis and multiple primitive tumors 177
Novel physiological RECQL4 alternative transcript disclosed by molecular characterisation of Rothmund–Thomson Syndrome sibs with mild phenotype 175
Sindrome di Rothmund-Thomson: caratterizzazione clinico-molecolare di tre nuovi pazienti 169
Spontaneous chromosomal instability in peripheral blood lymphocytes from two molecularly confirmed italian patients with hereditary fibrosis poikiloderma: Insights into cancer predisposition 167
Identification of novel genomic markers related to progression to glioblastoma through genomic profiling of 25 primary glioma cell lines 165
Identification of oligodendroglioma specific chromosomal copy number changes in the glioblastoma MI-4 cell line by array-CGH and FISH analyses 159
Search for genomic imbalances in a cohort of 24 Cornelia de Lange patients negative for mutations in the NIPBL and SMC1L1 genes 158
Totale 13.427
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Categoria #
all - tutte 40.409
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 40.409
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021188 0 0 0 0 0 0 0 0 0 0 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
2025/20264.424 688 347 365 509 494 244 738 209 355 367 108 0
Totale 13.427