IRIS
CALABRESE, Giuseppe
 Distribuzione geografica
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Continente #
EU - Europa 4.338
NA - Nord America 4.270
AS - Asia 3.335
SA - Sud America 231
AF - Africa 22
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 5
Totale 12.207
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Nazione #
US - Stati Uniti d'America 4.219
CN - Cina 1.157
SG - Singapore 1.119
UA - Ucraina 766
IT - Italia 629
IE - Irlanda 567
GB - Regno Unito 534
SE - Svezia 498
DE - Germania 483
TR - Turchia 476
FR - Francia 402
IN - India 384
BR - Brasile 207
FI - Finlandia 175
RU - Federazione Russa 130
VN - Vietnam 105
AT - Austria 40
CA - Canada 34
CZ - Repubblica Ceca 19
BE - Belgio 17
NL - Olanda 15
RO - Romania 15
BD - Bangladesh 14
HK - Hong Kong 13
PL - Polonia 13
ZA - Sudafrica 12
IL - Israele 11
MX - Messico 11
GR - Grecia 10
IR - Iran 10
JP - Giappone 8
AR - Argentina 7
ES - Italia 7
IQ - Iraq 7
LT - Lituania 7
EU - Europa 6
VE - Venezuela 6
AU - Australia 5
UZ - Uzbekistan 5
CL - Cile 4
MD - Moldavia 3
MY - Malesia 3
PK - Pakistan 3
SA - Arabia Saudita 3
TW - Taiwan 3
DK - Danimarca 2
EC - Ecuador 2
EG - Egitto 2
KE - Kenya 2
KR - Corea 2
NO - Norvegia 2
OM - Oman 2
PE - Perù 2
AE - Emirati Arabi Uniti 1
AZ - Azerbaigian 1
BB - Barbados 1
BH - Bahrain 1
CH - Svizzera 1
CR - Costa Rica 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
ET - Etiopia 1
GD - Grenada 1
GE - Georgia 1
GY - Guiana 1
HN - Honduras 1
ID - Indonesia 1
JO - Giordania 1
KZ - Kazakistan 1
MK - Macedonia 1
NP - Nepal 1
PY - Paraguay 1
RS - Serbia 1
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
SY - Repubblica araba siriana 1
TG - Togo 1
TH - Thailandia 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
UY - Uruguay 1
Totale 12.207
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Città #
Jacksonville 811
Singapore 721
Chandler 692
Dublin 564
Southend 449
Princeton 291
Izmir 263
Beijing 250
Nanjing 243
Ashburn 196
Dearborn 179
Wilmington 157
The Dalles 137
Cambridge 135
Chieti 123
Tongling 109
Munich 103
Nanchang 99
Grafing 92
Boardman 91
Santa Clara 86
Dong Ket 75
Los Angeles 75
Ann Arbor 72
Altamura 71
Woodbridge 50
Hebei 49
Kunming 49
Shenyang 48
Pescara 46
Tianjin 46
Helsinki 36
Vienna 36
Washington 33
Jiaxing 31
Rome 29
Jinan 28
Hangzhou 26
Grevenbroich 25
New York 23
Brooklyn 21
Council Bluffs 20
Hefei 20
Augusta 18
Düsseldorf 18
Kocaeli 18
Brno 17
Norwalk 17
Guangzhou 16
Ningbo 16
San Francisco 15
San Mateo 15
Zhengzhou 15
Changsha 14
Auburn Hills 13
Brussels 13
Lanzhou 13
Chicago 12
Hong Kong 12
Toronto 12
Dallas 11
São Paulo 11
Bangalore 9
Ho Chi Minh City 9
Leawood 9
Seattle 9
Stockholm 9
Boston 8
Changchun 8
Hanoi 8
Johannesburg 8
London 8
Milan 8
Montesilvano Marina 8
Mumbai 8
Orange 8
Tokyo 8
Ardabil 7
Atessa 7
Campinas 7
Charlotte 7
Mexico City 7
Moscow 7
Rio de Janeiro 7
Teramo 7
Atlanta 6
Brasília 6
Contagem 6
Kraków 6
Belo Horizonte 5
Bucharest 5
Chennai 5
Dhaka 5
Espoo 5
Frankfurt am Main 5
Houston 5
Porto Alegre 5
Tashkent 5
Turku 5
Vasto 5
Totale 7.236
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Nome #
16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer. 163
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 161
Zinc sulfate supplementation improves thyroid function in hypozincemic Down children 154
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 147
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 146
Discovering a familial Xp11.4 microduplication: Does the mother matter? 128
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 127
Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly. 119
Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence? 118
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 117
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis 117
[Chromosome anomalies and Waldenström's macroglobulinemia]. 116
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 116
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 115
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 114
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 114
X/Y translocation in a family with Leri-Weill dyschondrosteosis 112
A new case of pure partial 7q duplication 112
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 112
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 111
Therapeutic potential of hAECs for early Achilles tendon defect repair through regeneration 110
A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man. 110
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 109
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 108
Concerns about using Zn supplementation in Down's syndrome (DS) children. 106
Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders 106
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome 105
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs 105
Characterization of novel genes in AZF regions 105
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 104
Identification of multiple transcribed sequences from the spinal muscular atrophy region on human chromosome 102
I nuovi orizzonti della diagnosi prenatale 102
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 102
SHOX mutations detected by FISH and direct sequencing in patients with short stature 99
AluI and HaeIII restriction enzyme banding patterns of Macaca fuscata and Cercopithecus aethiops sabaeus chromosomes. 98
Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures 98
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 97
Array-CGH characterization of a de novo t(X;Y)(p22;q11) in a female with short stature and mental retardation. 97
Human homologue sequences to the drosophila dishevelled segment-polarity gene are deleted in the Di George Syndrome 96
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 96
A case of triploidy detected by crosstrimester test. 96
[Cytogenetic study of 201 subjects with altered reproductive fitness]. 96
Comparison of methods for the detection of in situ restriction enzyme - nick translation using fluorochromes and confocal microscopy 94
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 94
Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA). 92
A genetic assessment of trisomy 21 in a patient with persistent truncus arteriosus who died 38 years ago. 91
Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay 91
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 90
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 90
[Cytogenetic study of 140 patients with changes in sexual features]. 90
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature. 90
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 88
Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus 88
Cytogenetic survey of benign prostate hyperplasia 88
A Mosaic Ring Chromosome 21 in a Patient with Mild Intellectual Disability not Evidenced by Array-Cgh 88
Chromosome changes in 19 patients with Waldenström's macroglobulinemia. 87
Sensitivity of cutaneous chronic myelomonocytic leukaemia lesions to hypomethylating treatment 87
Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri-Weill dyschondrosteosis. 86
Growth delay in Down syndrome and zinc sulphate supplementation 86
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization 86
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 86
The methylenetethrahydrofolate reductase (MTHFR) C677T polymorphism and male infertility in Italy. 85
Prenatal diagnosis using the triple test 84
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping 84
Chromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genes. 84
Delayed Diagnosis of Potocki-Shaffer Syndrome in a Woman with Multiple Exostoses and Mental Retardation 84
Non-invasive prenatal screening: a 20-year experience in Italy 84
Correlation between apoptosis and TP53 status in osteosarcoma 83
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 83
Molecular studies in three patients with isodicentric Y chromosome 83
Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells. 83
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. 82
Two newborns with chromosome 4 imbalances: deletion 4q33-->q35 and ring r(4)(pterq35.2-qter). 82
Philadelphia (Ph), 14q+ and 1q+ chromosomes in immunoblastic phase (Richter's syndrome) in a patient with T chronic lymphocytic leukaemia. 82
Clinical-Grade Expanded Regulatory T Cells Are Enriched with Highly Suppressive Cells Producing IL-10, Granzyme B, and IL-35 82
Fetal Translocation between chromosomes 2, 18, and 21 resolved by fish 81
Acquisition of i(8q) as an early event in malignant triton tumors 81
FISH analysis in detecting 9p duplication (p22p24) 81
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 81
P53 loss and point mutation are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis 81
Genomic organization, physical mapping, and involvement in Yq microdeletions of the VCY2 (BPY 2) gene 80
Molecular characterization of two extra marker chromosomes detected at prenatal diagnosis 80
Effect of HpaII and MspI restriction endonucleases on chronic myelogenous leukemia chromosomes. Detection of CpG dinucleotide demethylation in situ. 80
Comparison of combined, stepwise sequential, contingent, and integrated screening in 7292 high-risk pregnant women 79
Cytogenetics and acute non lymphocytic leukemia. 79
Screening biochimici prenatali: l’esperienza del tri-test in 17.869 gravidanze della regione Abruzzo. 78
Prognostic value of atypical chromosomal changes during chronic myeloid leukemia. 78
[Clinical and cytogenetic staging of chronic myeloid leukemia. Philadelphia positive]. 78
Characterization of a new TSPY gene family member in Yq (TSPYq1). 77
Effectiveness of crosstrimester test in selecting high-risk pregnant women to undergo invasive prenatal diagnosis 77
Rhombencephalosynapsis in a severely polymalformed fetus with non-mosaic tetrasomy 9p, in intracytoplasmic-sperm-injection pregnancy. 77
Karyotype refinement by multicolor fluorescence in situ hybridization analysis in 18 patients with acute lymphoblastic leukemia. 76
On chromosomal DNA modifications by chemical and physical treatment of C-bands. 76
Heterochromatic polymorphisms of chromosome 16 evidenced by Alu I endonuclease digestion in chronic myelogenous leukemia. 75
Cytogenetic study of the heterochromatic polymorphisms in 100 subjects with Down syndrome and their parents. 75
Detection of chromosomal aneuploidies in fetal cells isolated from maternal blood using single-chromosome dual-probe FISH analysis 75
Chromosome mapping of the rat phospholipase C b1 gene. 73
Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male 73
Chromosome 11 rearrangements and specific MLL amplification revealed by spectral karyotyping in a patient with refractory anaemia with excess of blasts(RAEB)”. 73
Cytogenetics and bone marrow transplantation. 73
Totale 9.560
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Categoria #
all - tutte 49.079
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 49.079
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021962 0 3 149 4 53 176 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
2025/2026577 464 113 0 0 0 0 0 0 0 0 0 0
Totale 12.401