IRIS
CALABRESE, Giuseppe
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 6.922
EU - Europa 4.905
AS - Asia 4.818
SA - Sud America 455
Continente sconosciuto - Info sul continente non disponibili 224
AF - Africa 65
OC - Oceania 7
Totale 17.396
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 6.773
SG - Singapore 1.744
CN - Cina 1.423
UA - Ucraina 774
IT - Italia 696
GB - Regno Unito 570
IE - Irlanda 568
RU - Federazione Russa 513
SE - Svezia 510
DE - Germania 486
TR - Turchia 484
VN - Vietnam 426
IN - India 414
FR - Francia 412
BR - Brasile 362
FI - Finlandia 177
BD - Bangladesh 78
CA - Canada 77
HK - Hong Kong 46
AT - Austria 40
MX - Messico 39
JP - Giappone 31
AR - Argentina 30
IQ - Iraq 30
ZA - Sudafrica 28
PL - Polonia 26
NL - Olanda 23
CZ - Repubblica Ceca 20
BE - Belgio 18
VE - Venezuela 17
KR - Corea 16
RO - Romania 16
EC - Ecuador 15
ES - Italia 14
IL - Israele 14
PK - Pakistan 14
LT - Lituania 13
MY - Malesia 12
SA - Arabia Saudita 11
GR - Grecia 10
IR - Iran 10
CO - Colombia 9
CR - Costa Rica 9
ID - Indonesia 9
CL - Cile 8
PH - Filippine 8
AU - Australia 7
KE - Kenya 7
UZ - Uzbekistan 7
DZ - Algeria 6
EU - Europa 6
JM - Giamaica 6
OM - Oman 6
PE - Perù 6
AZ - Azerbaigian 5
DO - Repubblica Dominicana 4
EG - Egitto 4
JO - Giordania 4
LB - Libano 4
PY - Paraguay 4
SY - Repubblica araba siriana 4
TN - Tunisia 4
TW - Taiwan 4
CH - Svizzera 3
DK - Danimarca 3
GT - Guatemala 3
HN - Honduras 3
MA - Marocco 3
MD - Moldavia 3
NP - Nepal 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
TH - Thailandia 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
EE - Estonia 1
GE - Georgia 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
PR - Porto Rico 1
Totale 17.175
Salva come PNG Salva come JPEG
Città #
Singapore 1.131
San Jose 824
Jacksonville 812
Chandler 692
Dublin 565
Ashburn 472
Southend 449
Beijing 371
Princeton 291
Council Bluffs 284
Dallas 265
Izmir 263
Nanjing 243
Los Angeles 203
Dearborn 179
Wilmington 157
The Dalles 137
Cambridge 135
Santa Clara 134
Chieti 125
Ho Chi Minh City 120
Tongling 109
Munich 103
Nanchang 99
Boardman 92
Grafing 92
Buffalo 88
New York 81
Hanoi 79
Dong Ket 75
Ann Arbor 72
Altamura 71
Moscow 54
Pescara 52
Woodbridge 50
Hebei 49
Kunming 49
Shenyang 48
Tianjin 47
Columbus 40
Rome 40
Orem 39
Hong Kong 38
São Paulo 37
Helsinki 36
Vienna 36
Washington 34
Jiaxing 31
Tokyo 29
Jinan 28
Phoenix 28
Montreal 27
Redondo Beach 27
Brooklyn 26
Hangzhou 26
Grevenbroich 25
Chicago 24
Atlanta 23
Johannesburg 21
Augusta 20
Hefei 20
Stockholm 20
Düsseldorf 18
Kocaeli 18
San Francisco 18
Toronto 18
Warsaw 18
Brno 17
Denver 17
Haiphong 17
Norwalk 17
Chennai 16
Guangzhou 16
London 16
Ningbo 16
Seoul 16
Mexico City 15
San Mateo 15
Zhengzhou 15
Changsha 14
Houston 14
Poplar 14
Auburn Hills 13
Boston 13
Brussels 13
Lanzhou 13
Milan 13
Rio de Janeiro 13
Baghdad 12
Charlotte 12
Campinas 11
Manchester 11
Seattle 11
Brasília 10
Mumbai 10
Bangalore 9
Leawood 9
Querétaro 9
Amsterdam 8
Biên Hòa 8
Totale 10.360
Salva come PNG Salva come JPEG
Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 217
16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer. 204
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis 186
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 183
Zinc sulfate supplementation improves thyroid function in hypozincemic Down children 181
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 178
Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence? 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 172
Discovering a familial Xp11.4 microduplication: Does the mother matter? 166
A new case of pure partial 7q duplication 162
Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly. 160
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 160
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 158
[Chromosome anomalies and Waldenström's macroglobulinemia]. 157
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 157
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 153
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 151
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 149
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 149
Identification of multiple transcribed sequences from the spinal muscular atrophy region on human chromosome 148
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 148
X/Y translocation in a family with Leri-Weill dyschondrosteosis 147
Non-invasive prenatal screening: a 20-year experience in Italy 147
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs 145
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 145
AluI and HaeIII restriction enzyme banding patterns of Macaca fuscata and Cercopithecus aethiops sabaeus chromosomes. 144
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 143
[Cytogenetic study of 201 subjects with altered reproductive fitness]. 143
Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA). 142
Human homologue sequences to the drosophila dishevelled segment-polarity gene are deleted in the Di George Syndrome 141
Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures 141
Therapeutic potential of hAECs for early Achilles tendon defect repair through regeneration 141
I nuovi orizzonti della diagnosi prenatale 140
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome 139
Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders 139
A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man. 139
Concerns about using Zn supplementation in Down's syndrome (DS) children. 138
Comparison of methods for the detection of in situ restriction enzyme - nick translation using fluorochromes and confocal microscopy 137
A case of triploidy detected by crosstrimester test. 136
Characterization of novel genes in AZF regions 134
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature. 134
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 134
Array-CGH characterization of a de novo t(X;Y)(p22;q11) in a female with short stature and mental retardation. 134
Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay 132
Fetal Translocation between chromosomes 2, 18, and 21 resolved by fish 131
Cytogenetic survey of benign prostate hyperplasia 131
A Mosaic Ring Chromosome 21 in a Patient with Mild Intellectual Disability not Evidenced by Array-Cgh 131
SHOX mutations detected by FISH and direct sequencing in patients with short stature 130
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 130
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 129
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 128
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 127
Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus 125
[Cytogenetic study of 140 patients with changes in sexual features]. 125
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 124
Chromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genes. 123
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 122
A genetic assessment of trisomy 21 in a patient with persistent truncus arteriosus who died 38 years ago. 121
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 121
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization 121
Clinical-Grade Expanded Regulatory T Cells Are Enriched with Highly Suppressive Cells Producing IL-10, Granzyme B, and IL-35 121
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 120
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. 120
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 120
Chromosome changes in 19 patients with Waldenström's macroglobulinemia. 119
[Clinical and cytogenetic staging of chronic myeloid leukemia. Philadelphia positive]. 118
Delayed Diagnosis of Potocki-Shaffer Syndrome in a Woman with Multiple Exostoses and Mental Retardation 116
Growth delay in Down syndrome and zinc sulphate supplementation 114
Sensitivity of cutaneous chronic myelomonocytic leukaemia lesions to hypomethylating treatment 114
Two newborns with chromosome 4 imbalances: deletion 4q33-->q35 and ring r(4)(pterq35.2-qter). 111
Comparison of combined, stepwise sequential, contingent, and integrated screening in 7292 high-risk pregnant women 111
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping 110
Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells. 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 108
Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri-Weill dyschondrosteosis. 108
Molecular studies in three patients with isodicentric Y chromosome 108
Prognostic value of atypical chromosomal changes during chronic myeloid leukemia. 108
Correlation between apoptosis and TP53 status in osteosarcoma 107
Genomic organization, physical mapping, and involvement in Yq microdeletions of the VCY2 (BPY 2) gene 107
The methylenetethrahydrofolate reductase (MTHFR) C677T polymorphism and male infertility in Italy. 106
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb 106
Philadelphia (Ph), 14q+ and 1q+ chromosomes in immunoblastic phase (Richter's syndrome) in a patient with T chronic lymphocytic leukaemia. 106
Effect of HpaII and MspI restriction endonucleases on chronic myelogenous leukemia chromosomes. Detection of CpG dinucleotide demethylation in situ. 105
Detection of chromosomal aneuploidies in fetal cells isolated from maternal blood using single-chromosome dual-probe FISH analysis 105
Rhombencephalosynapsis in a severely polymalformed fetus with non-mosaic tetrasomy 9p, in intracytoplasmic-sperm-injection pregnancy. 105
Cytogenetics and acute non lymphocytic leukemia. 103
Karyotype refinement by multicolor fluorescence in situ hybridization analysis in 18 patients with acute lymphoblastic leukemia. 102
Acquisition of i(8q) as an early event in malignant triton tumors 102
Screening biochimici prenatali: l’esperienza del tri-test in 17.869 gravidanze della regione Abruzzo. 102
Prenatal diagnosis using the triple test 102
P53 loss and point mutation are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis 102
Heterochromatic polymorphisms of chromosome 16 evidenced by Alu I endonuclease digestion in chronic myelogenous leukemia. 102
Cytogenetic survey of sixty-one patients with preleukemic syndrome including myeloproliferative and myelodysplastic diseases. 102
FISH analysis in detecting 9p duplication (p22p24) 101
Molecular characterization of two extra marker chromosomes detected at prenatal diagnosis 101
Cytogenetics in patients with chronic myelogenous leukemia treated with bone marrow transplantation. 101
Chromosome abnormalities in breast fibroadenomas 101
On chromosomal DNA modifications by chemical and physical treatment of C-bands. 100
Clinical usefulness of NGS multi-gene panel testing in hereditary cancer analysis 99
Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male 99
Totale 13.049
Salva come PNG Salva come JPEG
Categoria #
all - tutte 68.708
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 68.708
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022586 0 0 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
2025/20265.062 464 223 468 606 504 332 883 337 518 415 221 91
2026/2027510 102 299 109 0 0 0 0 0 0 0 0 0
Totale 17.396