IRIS
CALABRESE, Giuseppe
 Distribuzione geografica
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Continente #
NA - Nord America 6.501
EU - Europa 4.872
AS - Asia 4.771
SA - Sud America 436
AF - Africa 65
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 6
Totale 16.657
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Nazione #
US - Stati Uniti d'America 6.379
SG - Singapore 1.730
CN - Cina 1.412
UA - Ucraina 774
IT - Italia 673
GB - Regno Unito 569
IE - Irlanda 568
RU - Federazione Russa 513
SE - Svezia 510
DE - Germania 486
TR - Turchia 482
VN - Vietnam 423
IN - India 414
FR - Francia 409
BR - Brasile 356
FI - Finlandia 177
BD - Bangladesh 71
CA - Canada 68
HK - Hong Kong 44
AT - Austria 40
MX - Messico 34
JP - Giappone 31
IQ - Iraq 30
ZA - Sudafrica 28
PL - Polonia 26
AR - Argentina 25
NL - Olanda 23
CZ - Repubblica Ceca 20
BE - Belgio 18
KR - Corea 16
RO - Romania 16
VE - Venezuela 16
IL - Israele 14
PK - Pakistan 14
LT - Lituania 13
EC - Ecuador 12
ES - Italia 12
GR - Grecia 10
IR - Iran 10
ID - Indonesia 9
SA - Arabia Saudita 9
MY - Malesia 8
CL - Cile 7
CO - Colombia 7
KE - Kenya 7
UZ - Uzbekistan 7
AU - Australia 6
DZ - Algeria 6
EU - Europa 6
OM - Oman 6
PH - Filippine 6
AZ - Azerbaigian 5
PE - Perù 5
DO - Repubblica Dominicana 4
EG - Egitto 4
JM - Giamaica 4
JO - Giordania 4
LB - Libano 4
PY - Paraguay 4
SY - Repubblica araba siriana 4
TN - Tunisia 4
TW - Taiwan 4
CH - Svizzera 3
MA - Marocco 3
MD - Moldavia 3
NP - Nepal 3
UY - Uruguay 3
AE - Emirati Arabi Uniti 2
BB - Barbados 2
CR - Costa Rica 2
DK - Danimarca 2
ET - Etiopia 2
GD - Grenada 2
HN - Honduras 2
MU - Mauritius 2
NO - Norvegia 2
RS - Serbia 2
SN - Senegal 2
TH - Thailandia 2
AL - Albania 1
BH - Bahrain 1
BW - Botswana 1
CG - Congo 1
CI - Costa d'Avorio 1
GE - Georgia 1
GT - Guatemala 1
GY - Guiana 1
KG - Kirghizistan 1
KW - Kuwait 1
KZ - Kazakistan 1
LK - Sri Lanka 1
LY - Libia 1
MK - Macedonia 1
NG - Nigeria 1
PA - Panama 1
QA - Qatar 1
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
SV - El Salvador 1
TG - Togo 1
Totale 16.656
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Città #
Singapore 1.123
San Jose 823
Jacksonville 811
Chandler 692
Dublin 565
Ashburn 455
Southend 449
Beijing 365
Princeton 291
Dallas 265
Izmir 263
Nanjing 243
Los Angeles 202
Dearborn 179
Wilmington 157
The Dalles 137
Cambridge 135
Chieti 125
Ho Chi Minh City 119
Council Bluffs 112
Tongling 109
Santa Clara 108
Munich 103
Nanchang 99
Boardman 92
Grafing 92
Buffalo 87
Hanoi 78
New York 77
Dong Ket 75
Ann Arbor 72
Altamura 71
Moscow 54
Pescara 51
Woodbridge 50
Hebei 49
Kunming 49
Shenyang 48
Tianjin 47
Orem 37
São Paulo 37
Helsinki 36
Hong Kong 36
Vienna 36
Rome 35
Washington 34
Jiaxing 31
Tokyo 29
Jinan 28
Redondo Beach 27
Brooklyn 26
Hangzhou 26
Grevenbroich 25
Montreal 25
Atlanta 23
Chicago 21
Johannesburg 21
Augusta 20
Hefei 20
Stockholm 20
Düsseldorf 18
Kocaeli 18
Warsaw 18
Brno 17
Haiphong 17
Norwalk 17
Toronto 17
Chennai 16
Denver 16
Guangzhou 16
Ningbo 16
San Francisco 16
Seoul 16
London 15
San Mateo 15
Zhengzhou 15
Changsha 14
Mexico City 14
Phoenix 14
Poplar 14
Auburn Hills 13
Boston 13
Brussels 13
Lanzhou 13
Baghdad 12
Houston 12
Milan 12
Rio de Janeiro 12
Campinas 11
Manchester 11
Seattle 11
Brasília 10
Mumbai 10
Bangalore 9
Leawood 9
Amsterdam 8
Biên Hòa 8
Can Tho 8
Changchun 8
Da Nang 8
Totale 10.045
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Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 212
16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer. 199
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 181
Zinc sulfate supplementation improves thyroid function in hypozincemic Down children 179
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis 179
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 175
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 170
Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence? 167
Discovering a familial Xp11.4 microduplication: Does the mother matter? 164
Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly. 158
A new case of pure partial 7q duplication 158
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 156
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 154
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 154
[Chromosome anomalies and Waldenström's macroglobulinemia]. 153
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 148
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 147
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 146
Identification of multiple transcribed sequences from the spinal muscular atrophy region on human chromosome 145
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 145
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 144
Non-invasive prenatal screening: a 20-year experience in Italy 143
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs 142
X/Y translocation in a family with Leri-Weill dyschondrosteosis 141
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 141
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 141
AluI and HaeIII restriction enzyme banding patterns of Macaca fuscata and Cercopithecus aethiops sabaeus chromosomes. 140
Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures 140
[Cytogenetic study of 201 subjects with altered reproductive fitness]. 140
I nuovi orizzonti della diagnosi prenatale 138
Human homologue sequences to the drosophila dishevelled segment-polarity gene are deleted in the Di George Syndrome 137
Therapeutic potential of hAECs for early Achilles tendon defect repair through regeneration 137
Comparison of methods for the detection of in situ restriction enzyme - nick translation using fluorochromes and confocal microscopy 136
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome 136
A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man. 136
Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA). 135
Concerns about using Zn supplementation in Down's syndrome (DS) children. 135
Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders 135
A case of triploidy detected by crosstrimester test. 133
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 133
Characterization of novel genes in AZF regions 131
Array-CGH characterization of a de novo t(X;Y)(p22;q11) in a female with short stature and mental retardation. 131
A Mosaic Ring Chromosome 21 in a Patient with Mild Intellectual Disability not Evidenced by Array-Cgh 129
Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay 129
Fetal Translocation between chromosomes 2, 18, and 21 resolved by fish 128
Cytogenetic survey of benign prostate hyperplasia 128
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature. 128
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 126
SHOX mutations detected by FISH and direct sequencing in patients with short stature 125
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 124
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 124
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 124
Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus 123
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 122
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 120
Chromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genes. 119
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 118
A genetic assessment of trisomy 21 in a patient with persistent truncus arteriosus who died 38 years ago. 118
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization 118
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. 117
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 117
[Cytogenetic study of 140 patients with changes in sexual features]. 117
Clinical-Grade Expanded Regulatory T Cells Are Enriched with Highly Suppressive Cells Producing IL-10, Granzyme B, and IL-35 117
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 116
Delayed Diagnosis of Potocki-Shaffer Syndrome in a Woman with Multiple Exostoses and Mental Retardation 115
[Clinical and cytogenetic staging of chronic myeloid leukemia. Philadelphia positive]. 114
Chromosome changes in 19 patients with Waldenström's macroglobulinemia. 113
Sensitivity of cutaneous chronic myelomonocytic leukaemia lesions to hypomethylating treatment 111
Growth delay in Down syndrome and zinc sulphate supplementation 110
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping 109
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 107
Two newborns with chromosome 4 imbalances: deletion 4q33-->q35 and ring r(4)(pterq35.2-qter). 106
Comparison of combined, stepwise sequential, contingent, and integrated screening in 7292 high-risk pregnant women 106
Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri-Weill dyschondrosteosis. 105
Prognostic value of atypical chromosomal changes during chronic myeloid leukemia. 105
Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells. 105
Genomic organization, physical mapping, and involvement in Yq microdeletions of the VCY2 (BPY 2) gene 104
Molecular studies in three patients with isodicentric Y chromosome 104
Correlation between apoptosis and TP53 status in osteosarcoma 103
The methylenetethrahydrofolate reductase (MTHFR) C677T polymorphism and male infertility in Italy. 103
Philadelphia (Ph), 14q+ and 1q+ chromosomes in immunoblastic phase (Richter's syndrome) in a patient with T chronic lymphocytic leukaemia. 103
Rhombencephalosynapsis in a severely polymalformed fetus with non-mosaic tetrasomy 9p, in intracytoplasmic-sperm-injection pregnancy. 102
Prenatal diagnosis using the triple test 101
Cytogenetics and acute non lymphocytic leukemia. 101
Effect of HpaII and MspI restriction endonucleases on chronic myelogenous leukemia chromosomes. Detection of CpG dinucleotide demethylation in situ. 101
Detection of chromosomal aneuploidies in fetal cells isolated from maternal blood using single-chromosome dual-probe FISH analysis 101
Acquisition of i(8q) as an early event in malignant triton tumors 100
Screening biochimici prenatali: l’esperienza del tri-test in 17.869 gravidanze della regione Abruzzo. 100
FISH analysis in detecting 9p duplication (p22p24) 100
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb 99
Karyotype refinement by multicolor fluorescence in situ hybridization analysis in 18 patients with acute lymphoblastic leukemia. 98
Cytogenetic survey of sixty-one patients with preleukemic syndrome including myeloproliferative and myelodysplastic diseases. 98
Chromosome 11 rearrangements and specific MLL amplification revealed by spectral karyotyping in a patient with refractory anaemia with excess of blasts(RAEB)”. 97
Molecular characterization of two extra marker chromosomes detected at prenatal diagnosis 97
P53 loss and point mutation are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis 97
On chromosomal DNA modifications by chemical and physical treatment of C-bands. 97
Heterochromatic polymorphisms of chromosome 16 evidenced by Alu I endonuclease digestion in chronic myelogenous leukemia. 97
Cytogenetics in patients with chronic myelogenous leukemia treated with bone marrow transplantation. 97
Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male 96
De novo complex chromosome rearrangement detected by fluorescence in situ hybridization on amniotic fluid cells 96
Totale 12.700
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Categoria #
all - tutte 64.551
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 64.551
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021103 0 0 0 0 0 0 0 0 0 0 0 103
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
2025/20265.048 464 223 468 606 504 332 883 337 518 415 221 77
Totale 16.872