IRIS
CALABRESE, Giuseppe
 Distribuzione geografica
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Continente #
NA - Nord America 5.203
EU - Europa 4.423
AS - Asia 4.049
SA - Sud America 395
AF - Africa 46
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 5
Totale 14.127
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Nazione #
US - Stati Uniti d'America 5.108
SG - Singapore 1.442
CN - Cina 1.346
UA - Ucraina 771
IT - Italia 635
IE - Irlanda 567
GB - Regno Unito 563
SE - Svezia 510
DE - Germania 483
TR - Turchia 479
FR - Francia 404
IN - India 394
BR - Brasile 336
VN - Vietnam 223
FI - Finlandia 177
RU - Federazione Russa 135
CA - Canada 57
AT - Austria 40
MX - Messico 27
JP - Giappone 25
PL - Polonia 25
ZA - Sudafrica 25
AR - Argentina 20
BD - Bangladesh 20
CZ - Repubblica Ceca 19
HK - Hong Kong 19
BE - Belgio 17
KR - Corea 16
NL - Olanda 16
IQ - Iraq 15
RO - Romania 15
LT - Lituania 13
IL - Israele 12
ES - Italia 11
EC - Ecuador 10
GR - Grecia 10
IR - Iran 10
VE - Venezuela 10
EU - Europa 6
AU - Australia 5
CL - Cile 5
ID - Indonesia 5
KE - Kenya 5
MY - Malesia 5
PE - Perù 5
PK - Pakistan 5
UZ - Uzbekistan 5
EG - Egitto 4
OM - Oman 4
PY - Paraguay 4
TW - Taiwan 4
DO - Repubblica Dominicana 3
DZ - Algeria 3
JO - Giordania 3
MD - Moldavia 3
SA - Arabia Saudita 3
AE - Emirati Arabi Uniti 2
AZ - Azerbaigian 2
CO - Colombia 2
CR - Costa Rica 2
DK - Danimarca 2
ET - Etiopia 2
GD - Grenada 2
NO - Norvegia 2
NP - Nepal 2
RS - Serbia 2
TN - Tunisia 2
UY - Uruguay 2
BB - Barbados 1
BH - Bahrain 1
CH - Svizzera 1
CI - Costa d'Avorio 1
GE - Georgia 1
GT - Guatemala 1
GY - Guiana 1
HN - Honduras 1
KW - Kuwait 1
KZ - Kazakistan 1
LB - Libano 1
MA - Marocco 1
MK - Macedonia 1
QA - Qatar 1
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
SY - Repubblica araba siriana 1
TG - Togo 1
TH - Thailandia 1
TT - Trinidad e Tobago 1
Totale 14.127
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Città #
Singapore 950
Jacksonville 811
Chandler 692
Dublin 564
Southend 449
Beijing 360
Ashburn 352
Princeton 291
Izmir 263
Dallas 256
Nanjing 243
Los Angeles 186
Dearborn 179
Wilmington 157
The Dalles 137
Cambridge 135
Chieti 123
Tongling 109
Munich 103
Nanchang 99
Santa Clara 99
Grafing 92
Boardman 91
Buffalo 87
Dong Ket 75
Ann Arbor 72
Altamura 71
New York 63
Ho Chi Minh City 50
Woodbridge 50
Hebei 49
Kunming 49
Shenyang 48
Tianjin 47
Pescara 46
Helsinki 36
Vienna 36
Hanoi 34
São Paulo 33
Washington 33
Jiaxing 31
Rome 31
Jinan 28
Redondo Beach 27
Brooklyn 26
Hangzhou 26
Grevenbroich 25
Tokyo 25
Montreal 21
Augusta 20
Chicago 20
Council Bluffs 20
Hefei 20
Johannesburg 20
Stockholm 20
Düsseldorf 18
Hong Kong 18
Kocaeli 18
Brno 17
Norwalk 17
Warsaw 17
Denver 16
Guangzhou 16
Ningbo 16
San Francisco 16
Seoul 16
San Mateo 15
Toronto 15
Zhengzhou 15
Changsha 14
Atlanta 13
Auburn Hills 13
Boston 13
Brussels 13
Lanzhou 13
Phoenix 13
Poplar 13
Houston 12
London 12
Mexico City 12
Campinas 11
Chennai 11
Orem 11
Rio de Janeiro 11
Brasília 10
Seattle 10
Bangalore 9
Leawood 9
Manchester 9
Changchun 8
Milan 8
Montesilvano Marina 8
Mumbai 8
Orange 8
Querétaro 8
Ardabil 7
Atessa 7
Charlotte 7
Haiphong 7
Moscow 7
Totale 8.525
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Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 181
16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer. 177
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 166
Zinc sulfate supplementation improves thyroid function in hypozincemic Down children 161
Widening of a Y-chromosome interval 6 deletion transmitted from a father to his infertile son accounts for an oligozoospermia critical region distal to RBM1 and DAZ genes 155
Discovering a familial Xp11.4 microduplication: Does the mother matter? 146
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 145
Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly. 138
Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence? 138
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis 137
A new case of pure partial 7q duplication 134
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 134
[Chromosome anomalies and Waldenström's macroglobulinemia]. 131
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 130
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 129
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 127
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 127
Identification of multiple transcribed sequences from the spinal muscular atrophy region on human chromosome 126
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 126
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs 125
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 125
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 124
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 124
X/Y translocation in a family with Leri-Weill dyschondrosteosis 123
Concerns about using Zn supplementation in Down's syndrome (DS) children. 120
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 120
A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man. 120
AluI and HaeIII restriction enzyme banding patterns of Macaca fuscata and Cercopithecus aethiops sabaeus chromosomes. 119
Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures 119
Therapeutic potential of hAECs for early Achilles tendon defect repair through regeneration 119
I nuovi orizzonti della diagnosi prenatale 118
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 118
Characterization of novel genes in AZF regions 116
A case of triploidy detected by crosstrimester test. 115
Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders 115
SHOX mutations detected by FISH and direct sequencing in patients with short stature 114
[Cytogenetic study of 201 subjects with altered reproductive fitness]. 114
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome 113
Comparison of methods for the detection of in situ restriction enzyme - nick translation using fluorochromes and confocal microscopy 112
Human homologue sequences to the drosophila dishevelled segment-polarity gene are deleted in the Di George Syndrome 112
Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA). 112
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 112
Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay 112
Cytogenetic survey of benign prostate hyperplasia 110
Non-invasive prenatal screening: a 20-year experience in Italy 108
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 107
Spectral karyotyping (SKY) refinement of a complex karyotype with t(20;21) in a Ph-positive CML patient submitted to peripheral blood stem cell transplantation 107
Array-CGH characterization of a de novo t(X;Y)(p22;q11) in a female with short stature and mental retardation. 107
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature. 106
A Mosaic Ring Chromosome 21 in a Patient with Mild Intellectual Disability not Evidenced by Array-Cgh 106
Assignment of TACSTD1 (alias TROP1, M4S1) to human chromosome 2p21 and refinement of mapping of TACSTD2 (alias TROP2, M1S1) to human chromosome 1p32 by in situ hybridization 105
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 104
Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus 102
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 102
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization 102
Aneuploidy screening using circulating fetal cells in maternal blood by dual-probe FISH protocol: A prospective feasibility study on a series of 172 pregnant women 102
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 101
Fluorescence in situ hybridization analysis of minimal residual disease and the relevance of the der(9) deletion in imatinib-treated patients with chronic myeloid leukemia. 100
A genetic assessment of trisomy 21 in a patient with persistent truncus arteriosus who died 38 years ago. 99
[Cytogenetic study of 140 patients with changes in sexual features]. 99
Fetal Translocation between chromosomes 2, 18, and 21 resolved by fish 98
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping 98
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 98
Delayed Diagnosis of Potocki-Shaffer Syndrome in a Woman with Multiple Exostoses and Mental Retardation 98
Chromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genes. 97
Sensitivity of cutaneous chronic myelomonocytic leukaemia lesions to hypomethylating treatment 97
Chromosome changes in 19 patients with Waldenström's macroglobulinemia. 96
[Clinical and cytogenetic staging of chronic myeloid leukemia. Philadelphia positive]. 96
Clinical-Grade Expanded Regulatory T Cells Are Enriched with Highly Suppressive Cells Producing IL-10, Granzyme B, and IL-35 96
Comparison of combined, stepwise sequential, contingent, and integrated screening in 7292 high-risk pregnant women 95
Growth delay in Down syndrome and zinc sulphate supplementation 93
The methylenetethrahydrofolate reductase (MTHFR) C677T polymorphism and male infertility in Italy. 91
Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri-Weill dyschondrosteosis. 91
Molecular studies in three patients with isodicentric Y chromosome 91
Philadelphia (Ph), 14q+ and 1q+ chromosomes in immunoblastic phase (Richter's syndrome) in a patient with T chronic lymphocytic leukaemia. 91
Acquisition of i(8q) as an early event in malignant triton tumors 90
Correlation between apoptosis and TP53 status in osteosarcoma 90
Prenatal diagnosis using the triple test 90
Genomic organization, physical mapping, and involvement in Yq microdeletions of the VCY2 (BPY 2) gene 90
Effect of HpaII and MspI restriction endonucleases on chronic myelogenous leukemia chromosomes. Detection of CpG dinucleotide demethylation in situ. 90
Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells. 90
Chromosome abnormalities in breast fibroadenomas 89
Two newborns with chromosome 4 imbalances: deletion 4q33-->q35 and ring r(4)(pterq35.2-qter). 88
P53 loss and point mutation are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis 87
Prognostic value of atypical chromosomal changes during chronic myeloid leukemia. 87
Complex translocation involving Ph chromosome in a patient with typical chronic myelogenous leukemia. 87
Rhombencephalosynapsis in a severely polymalformed fetus with non-mosaic tetrasomy 9p, in intracytoplasmic-sperm-injection pregnancy. 87
FISH analysis in detecting 9p duplication (p22p24) 86
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb 86
Cytogenetics and acute non lymphocytic leukemia. 86
Cytogenetic survey of sixty-one patients with preleukemic syndrome including myeloproliferative and myelodysplastic diseases. 86
Detection of chromosomal aneuploidies in fetal cells isolated from maternal blood using single-chromosome dual-probe FISH analysis 86
Screening biochimici prenatali: l’esperienza del tri-test in 17.869 gravidanze della regione Abruzzo. 85
Effectiveness of crosstrimester test in selecting high-risk pregnant women to undergo invasive prenatal diagnosis 85
Molecular characterization of two extra marker chromosomes detected at prenatal diagnosis 85
Molecular characterization of an unusual variant t(15;17) detected in an APL patient 85
Heterochromatic polymorphisms of chromosome 16 evidenced by Alu I endonuclease digestion in chronic myelogenous leukemia. 84
Cytogenetics in patients with chronic myelogenous leukemia treated with bone marrow transplantation. 84
On chromosomal DNA modifications by chemical and physical treatment of C-bands. 83
Hinf I restriction endonuclease digestion on human fixed metaphase chromosomes. 83
Totale 10.891
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Categoria #
all - tutte 55.774
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 55.774
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021753 0 0 0 0 0 176 14 10 249 158 43 103
2021/2022618 24 8 3 83 61 96 5 55 32 6 68 177
2022/20232.120 160 281 144 223 210 433 121 176 262 18 48 44
2023/2024908 56 32 71 27 56 286 171 45 6 38 5 115
2024/20252.281 172 325 268 83 53 29 74 83 307 121 284 482
2025/20262.500 464 223 468 606 504 235 0 0 0 0 0 0
Totale 14.324