Bicocca Open Archive

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ROVERSI, GAIA
 Distribuzione geografica
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Continente #
NA - Nord America 6.331
AS - Asia 3.390
EU - Europa 3.123
SA - Sud America 563
AF - Africa 94
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 2
Totale 13.507
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Nazione #
US - Stati Uniti d'America 6.049
SG - Singapore 1.040
IT - Italia 783
CN - Cina 761
VN - Vietnam 640
DE - Germania 473
BR - Brasile 432
HK - Hong Kong 417
RU - Federazione Russa 395
SE - Svezia 346
IE - Irlanda 291
CA - Canada 222
UA - Ucraina 195
FR - Francia 129
GB - Regno Unito 128
IN - India 103
AT - Austria 92
FI - Finlandia 78
BD - Bangladesh 77
ID - Indonesia 60
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 14
CH - Svizzera 13
VE - Venezuela 13
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
JM - Giamaica 7
UY - Uruguay 7
BO - Bolivia 6
DZ - Algeria 6
KZ - Kazakistan 6
MY - Malesia 6
CR - Costa Rica 5
GR - Grecia 5
JO - Giordania 5
LB - Libano 5
LT - Lituania 5
IR - Iran 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
GP - Guadalupe 1
HN - Honduras 1
HR - Croazia 1
HU - Ungheria 1
KE - Kenya 1
KH - Cambogia 1
LA - Repubblica Popolare Democratica del Laos 1
LC - Santa Lucia 1
MD - Moldavia 1
Totale 13.495
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Città #
Ann Arbor 1.055
Singapore 581
Ashburn 498
Woodbridge 449
Hong Kong 407
San Jose 363
Fairfield 331
Frankfurt am Main 308
Chandler 302
Dublin 284
Milan 266
Houston 251
Wilmington 235
Ho Chi Minh City 205
Jacksonville 190
Dearborn 174
Seattle 160
Hanoi 157
New York 139
Toronto 125
Beijing 119
Cambridge 118
Santa Clara 105
Los Angeles 104
Princeton 86
Vienna 86
The Dalles 76
Chicago 75
Nanjing 75
Dallas 63
Altamura 55
Shanghai 52
Hefei 51
Jakarta 49
Lauterbourg 43
São Paulo 42
Lawrence 40
Moscow 40
Council Bluffs 37
Buffalo 35
Boardman 33
Munich 33
Lachine 32
Rome 31
Seoul 29
Shenyang 29
Helsinki 28
London 25
Warsaw 25
Tokyo 24
Da Nang 23
Jinan 22
Nanchang 22
Guangzhou 20
Montreal 20
Nuremberg 20
Andover 19
Atlanta 19
Fremont 19
San Diego 18
Brussels 16
Turin 16
Chennai 15
Hải Dương 15
Tianjin 15
Changsha 14
Hebei 14
Phoenix 14
Quận Bình Thạnh 14
Jiaxing 13
Johannesburg 13
Lissone 13
Rio de Janeiro 13
Salt Lake City 13
Denver 12
Ningbo 12
Orem 12
Waterloo 12
Baghdad 11
Mexico City 11
Ottawa 11
Stockholm 11
Taizhou 11
Turku 11
Ankara 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
Bologna 8
Boston 8
Totale 8.782
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Nome #
Olfactory receptor genes and chromosome 11 structural aberrations: Players or spectators? 616
Molecular signatures of medullary thyroid carcinoma by matrix-assisted laser desorption/ionisation mass spectrometry imaging 593
Interphase FISH: A Helpful Assay in Prenatal Cytogenetics Diagnosis 559
Refining the Phenotype of Recurrent Rearrangements of Chromosome 16 545
Familiar unbalanced complex rearrangements involving 13 p-arm: Description of two cases 466
Instability of short arm of acrocentric chromosomes: Lesson from non-acrocentric satellited chromosomes. report of 24 unrelated cases 434
Genomic and epigenomic profile of uterine smooth muscle tumors of uncertain malignant potential (Stumps) revealed similarities and differences with leiomyomas and leiomyosarcomas 417
The effect of culture on human bone marrow mesenchymal stem cells: Focus on DNA methylation profiles 414
Parent-of-origin effect of hypomorphic pathogenic variants and somatic mosaicism impact on phenotypic expression of retinoblastoma 402
Characterization of Chromosomal Breakpoints in 12 Cases with 8p Rearrangements Defines a Continuum of Fragility of the Region 354
Human chromosome 18 and acrocentrics: A dangerous liaison 334
Proteome analysis in thyroid pathology 326
Insights into the Peritumoural Brain Zone of Glioblastoma: CDK4 and EXT2 May Be Potential Drivers of Malignancy 320
Tubal histopathological abnormalities in BRCA1/2 mutation carriers undergoing prophylactic salpingo-oophorectomy: a case-control study 296
An Alternative Approach in Endocrine Pathology Research: MALDI-IMS in Papillary Thyroid Carcinoma 291
A targeted approach to genetic counseling in breast cancer patients: The experience of an Italian local project 291
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor 261
Solid cell nests of the thyroid gland: Morphological, immunohistochemical and genetic features 257
Rothmund-Thomson syndrome 252
Identification of two novel RECQL4 exonic SNPs and genomic characterization of the IVS12 minisatellite 244
RNA processing defects of the helicase gene RECQL4 in a compound heterozygous Rothmund-Thomson patient 244
Impact and Reproducibility of In-House Targeted Next-Generation Sequencing Biomarker Testing in Non–Small-Cell Lung Cancer: An Italian Multi-Institutional Experience 243
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 240
Exploring the link between MORF4L1 and risk of breast cancer 233
RNA hyperediting and alternative splicing of hematopoietic cell phosphatase (PTPN6) gene in acute myeloid leukemia 231
Germline mutation in the juxtamembrane domain of the kit gene in a family with gastrointestinal stromal tumors and urticaria pigmentosa 230
Genomic Complexity and Complex Chromosomal Rearrangements in Genetic Diagnosis: Two Illustrative Cases on Chromosome 7 229
Evidence for a link between TNFRSF11A and risk of breast cancer 225
Uptake of Risk-Reducing Salpingo-Oophorectomy and Gynaecologic Surveillance Among Germline BRCA Pathogenic Variants Carriers 220
Rothmund-Thomson syndrome and RECQL4 defect: splitting and lumping 217
Cytogenetically Balanced Reciprocal Translocation Could Hide Molecular Genomic Unbalances: Implications for Foetal Phenotype Correlation 212
The CASP8 rs3834129 polymorphism and breast cancer risk in BRCA1 mutation carriers 211
Multiple localization of endogenous MARK4L protein in human glioma 205
Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers 205
Differential cytogenomics and miRNA signature of the Acute Myeloid Leukaemia Kasumi-1 cell line CD34+38- compartment 205
Targeted next-generation sequencing appoints c16orf57 as clericuzio-type poikiloderma with neutropenia gene 205
Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers 204
Evaluation of family history in individuals with heterozygous BRCA pathogenic variants diagnosed with breast or ovarian cancer in a single center in Italy 203
Clinical utility gene card for: Rothmund-Thomson syndrome 200
Piebald trait: implication of kit mutation on in vitro melanocyte survival and on the clinical application of cultured epidermal autografts 197
Two new CHEK2 germ-line variants detected in breast cancer/sarcoma families negative for BRCA1, BRCA2, and TP53 gene mutations 196
Atypical Rothmund-Thomson syndrome in a patient with compound Heterozygous Mutations in RECQL4 Gene and phenotypic features in RECQL4 syndromes 190
Clericuzio-type poikiloderma with neutropenia syndrome in three sibs with mutations in the C16orf57 gene: delineation of the phenotype 188
Sindrome di Rothmund-Thomson: caratterizzazione clinico-molecolare di tre nuovi pazienti 183
Novel physiological RECQL4 alternative transcript disclosed by molecular characterisation of Rothmund–Thomson Syndrome sibs with mild phenotype 182
Constitutional de novo deletion of the FBXW7 gene in a patient with focal segmental glomerulosclerosis and multiple primitive tumors 180
Identification of oligodendroglioma specific chromosomal copy number changes in the glioblastoma MI-4 cell line by array-CGH and FISH analyses 173
Spontaneous chromosomal instability in peripheral blood lymphocytes from two molecularly confirmed italian patients with hereditary fibrosis poikiloderma: Insights into cancer predisposition 171
Identification of novel genomic markers related to progression to glioblastoma through genomic profiling of 25 primary glioma cell lines 169
Search for genomic imbalances in a cohort of 24 Cornelia de Lange patients negative for mutations in the NIPBL and SMC1L1 genes 159
Totale 13.822
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Categoria #
all - tutte 42.405
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 42.405
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/20264.796 688 347 365 509 494 244 738 209 355 367 206 274
2026/202723 23 0 0 0 0 0 0 0 0 0 0 0
Totale 13.822