IRIS
CALABRESE, Giuseppe
 Distribuzione geografica
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Continente #
NA - Nord America 7.802
EU - Europa 5.014
AS - Asia 4.836
SA - Sud America 464
Continente sconosciuto - Info sul continente non disponibili 230
AF - Africa 68
OC - Oceania 7
Totale 18.421
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Nazione #
US - Stati Uniti d'America 7.552
SG - Singapore 1.745
CN - Cina 1.425
IT - Italia 775
UA - Ucraina 774
GB - Regno Unito 579
IE - Irlanda 570
RU - Federazione Russa 518
SE - Svezia 510
DE - Germania 491
TR - Turchia 485
VN - Vietnam 427
FR - Francia 415
IN - India 414
BR - Brasile 371
FI - Finlandia 177
CA - Canada 116
BD - Bangladesh 78
HK - Hong Kong 46
AT - Austria 40
MX - Messico 39
JP - Giappone 32
AR - Argentina 30
IQ - Iraq 30
ZA - Sudafrica 28
PL - Polonia 27
NL - Olanda 24
CR - Costa Rica 20
CZ - Repubblica Ceca 20
IL - Israele 19
BE - Belgio 18
VE - Venezuela 17
KR - Corea 16
RO - Romania 16
EC - Ecuador 15
ES - Italia 14
LT - Lituania 14
PH - Filippine 14
PK - Pakistan 14
HN - Honduras 12
MY - Malesia 12
SA - Arabia Saudita 11
GR - Grecia 10
IR - Iran 10
SV - El Salvador 10
CO - Colombia 9
ID - Indonesia 9
PR - Porto Rico 9
TT - Trinidad e Tobago 9
CL - Cile 8
AU - Australia 7
GT - Guatemala 7
JM - Giamaica 7
KE - Kenya 7
UZ - Uzbekistan 7
CW - ???statistics.table.value.countryCode.CW??? 6
DZ - Algeria 6
EU - Europa 6
GP - Guadalupe 6
OM - Oman 6
PE - Perù 6
AZ - Azerbaigian 5
NI - Nicaragua 5
DO - Repubblica Dominicana 4
EG - Egitto 4
JO - Giordania 4
LB - Libano 4
PY - Paraguay 4
SC - Seychelles 4
SY - Repubblica araba siriana 4
TN - Tunisia 4
TW - Taiwan 4
CH - Svizzera 3
DK - Danimarca 3
EE - Estonia 3
MA - Marocco 3
MD - Moldavia 3
NP - Nepal 3
TH - Thailandia 3
UY - Uruguay 3
AE - Emirati Arabi Uniti 2
AL - Albania 2
BB - Barbados 2
ET - Etiopia 2
GD - Grenada 2
MU - Mauritius 2
NO - Norvegia 2
RS - Serbia 2
SN - Senegal 2
XK - ???statistics.table.value.countryCode.XK??? 2
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
BQ - ???statistics.table.value.countryCode.BQ??? 1
BW - Botswana 1
CG - Congo 1
CI - Costa d'Avorio 1
GE - Georgia 1
GY - Guiana 1
KG - Kirghizistan 1
KW - Kuwait 1
Totale 18.195
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Città #
Singapore 1.131
San Jose 927
Jacksonville 815
Chandler 692
Dublin 565
Ashburn 488
Southend 449
Beijing 371
Princeton 292
Council Bluffs 287
Dallas 274
Izmir 263
Nanjing 243
Los Angeles 214
Dearborn 179
Wilmington 158
Santa Clara 137
The Dalles 137
Cambridge 135
Chieti 125
Buffalo 123
Ho Chi Minh City 120
Tongling 109
Munich 103
Nanchang 99
Boardman 92
Grafing 92
New York 85
Hanoi 79
Dong Ket 75
Ann Arbor 72
Altamura 71
Moscow 54
Pescara 53
Woodbridge 50
Hebei 49
Kunming 49
Shenyang 48
Tianjin 47
Rome 45
Columbus 42
Orem 41
Hong Kong 38
Phoenix 37
São Paulo 37
Washington 37
Helsinki 36
Vienna 36
Chicago 34
Brooklyn 31
Jiaxing 31
Montreal 30
Tokyo 30
Atlanta 28
Jinan 28
Redondo Beach 27
Hangzhou 26
Milan 26
Grevenbroich 25
Toronto 24
Denver 21
Houston 21
Johannesburg 21
Augusta 20
Hefei 20
San Francisco 20
Stockholm 20
London 19
Warsaw 19
Düsseldorf 18
Kocaeli 18
Norwalk 18
Brno 17
Haiphong 17
Boston 16
Chennai 16
Guangzhou 16
Kimball 16
Ningbo 16
North Bergen 16
San José 16
Seoul 16
Mexico City 15
San Mateo 15
Zhengzhou 15
Changsha 14
Poplar 14
Seattle 14
Auburn Hills 13
Brussels 13
Charlotte 13
Lanzhou 13
Rio de Janeiro 13
Baghdad 12
Brasília 11
Campinas 11
Manchester 11
Las Vegas 10
Mumbai 10
Philadelphia 10
Totale 10.665
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Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 226
16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer. 212
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis 197
Zinc sulfate supplementation improves thyroid function in hypozincemic Down children 191
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 190
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 185
Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence? 184
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 181
Discovering a familial Xp11.4 microduplication: Does the mother matter? 178
Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly. 174
A new case of pure partial 7q duplication 169
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 168
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 165
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 164
[Chromosome anomalies and Waldenström's macroglobulinemia]. 162
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 161
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 157
Non-invasive prenatal screening: a 20-year experience in Italy 157
Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA). 155
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 155
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 155
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 154
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 154
X/Y translocation in a family with Leri-Weill dyschondrosteosis 153
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs 153
[Cytogenetic study of 201 subjects with altered reproductive fitness]. 153
Identification of multiple transcribed sequences from the spinal muscular atrophy region on human chromosome 151
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 151
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome 149
Therapeutic potential of hAECs for early Achilles tendon defect repair through regeneration 149
Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures 148
Human homologue sequences to the drosophila dishevelled segment-polarity gene are deleted in the Di George Syndrome 147
AluI and HaeIII restriction enzyme banding patterns of Macaca fuscata and Cercopithecus aethiops sabaeus chromosomes. 147
A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man. 146
I nuovi orizzonti della diagnosi prenatale 145
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 145
Concerns about using Zn supplementation in Down's syndrome (DS) children. 144
Comparison of methods for the detection of in situ restriction enzyme - nick translation using fluorochromes and confocal microscopy 143
Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders 143
Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay 142
A case of triploidy detected by crosstrimester test. 141
Characterization of novel genes in AZF regions 140
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 140
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature. 139
Array-CGH characterization of a de novo t(X;Y)(p22;q11) in a female with short stature and mental retardation. 139
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 136
Fetal Translocation between chromosomes 2, 18, and 21 resolved by fish 135
Cytogenetic survey of benign prostate hyperplasia 135
A Mosaic Ring Chromosome 21 in a Patient with Mild Intellectual Disability not Evidenced by Array-Cgh 135
SHOX mutations detected by FISH and direct sequencing in patients with short stature 134
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 134
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 133
Clinical-Grade Expanded Regulatory T Cells Are Enriched with Highly Suppressive Cells Producing IL-10, Granzyme B, and IL-35 133
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 132
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 132
Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus 132
[Cytogenetic study of 140 patients with changes in sexual features]. 130
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 129
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. 129
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 129
Chromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genes. 129
Correlation between apoptosis and TP53 status in osteosarcoma 128
A genetic assessment of trisomy 21 in a patient with persistent truncus arteriosus who died 38 years ago. 127
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 127
Chromosome changes in 19 patients with Waldenström's macroglobulinemia. 126
[Clinical and cytogenetic staging of chronic myeloid leukemia. Philadelphia positive]. 124
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization 124
Comparison of combined, stepwise sequential, contingent, and integrated screening in 7292 high-risk pregnant women 122
Delayed Diagnosis of Potocki-Shaffer Syndrome in a Woman with Multiple Exostoses and Mental Retardation 122
Growth delay in Down syndrome and zinc sulphate supplementation 121
Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells. 121
The Crucial Role of Hereditary Cancer Panel Testing in Unaffected Individuals with a Strong Family History of Cancer: A Retrospective Study of a Cohort of 103 Healthy Subjects 120
Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri-Weill dyschondrosteosis. 118
Sensitivity of cutaneous chronic myelomonocytic leukaemia lesions to hypomethylating treatment 118
Rhombencephalosynapsis in a severely polymalformed fetus with non-mosaic tetrasomy 9p, in intracytoplasmic-sperm-injection pregnancy. 118
Two newborns with chromosome 4 imbalances: deletion 4q33-->q35 and ring r(4)(pterq35.2-qter). 117
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping 117
Molecular studies in three patients with isodicentric Y chromosome 116
P53 loss and point mutation are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis 115
Detection of chromosomal aneuploidies in fetal cells isolated from maternal blood using single-chromosome dual-probe FISH analysis 115
Genomic organization, physical mapping, and involvement in Yq microdeletions of the VCY2 (BPY 2) gene 113
Prognostic value of atypical chromosomal changes during chronic myeloid leukemia. 113
The methylenetethrahydrofolate reductase (MTHFR) C677T polymorphism and male infertility in Italy. 111
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb 111
Philadelphia (Ph), 14q+ and 1q+ chromosomes in immunoblastic phase (Richter's syndrome) in a patient with T chronic lymphocytic leukaemia. 111
Screening biochimici prenatali: l’esperienza del tri-test in 17.869 gravidanze della regione Abruzzo. 109
Effect of HpaII and MspI restriction endonucleases on chronic myelogenous leukemia chromosomes. Detection of CpG dinucleotide demethylation in situ. 109
Clinical usefulness of NGS multi-gene panel testing in hereditary cancer analysis 108
Cytogenetic survey of sixty-one patients with preleukemic syndrome including myeloproliferative and myelodysplastic diseases. 108
Karyotype refinement by multicolor fluorescence in situ hybridization analysis in 18 patients with acute lymphoblastic leukemia. 107
Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male 107
Cytogenetics and acute non lymphocytic leukemia. 107
Acquisition of i(8q) as an early event in malignant triton tumors 106
FISH analysis in detecting 9p duplication (p22p24) 106
Prenatal diagnosis using the triple test 106
Chromosome 11 rearrangements and specific MLL amplification revealed by spectral karyotyping in a patient with refractory anaemia with excess of blasts(RAEB)”. 106
On chromosomal DNA modifications by chemical and physical treatment of C-bands. 106
Heterochromatic polymorphisms of chromosome 16 evidenced by Alu I endonuclease digestion in chronic myelogenous leukemia. 106
Molecular characterization of two extra marker chromosomes detected at prenatal diagnosis 105
Cytogenetics in patients with chronic myelogenous leukemia treated with bone marrow transplantation. 105
Totale 13.775
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Categoria #
all - tutte 72.541
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 72.541
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022500 0 0 0 0 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
2025/20265.062 464 223 468 606 504 332 883 337 518 415 221 91
2026/20271.535 102 299 271 674 189 0 0 0 0 0 0 0
Totale 18.421