CALABRESE, Giuseppe
 Distribuzione geografica
Continente #
EU - Europa 4.190
NA - Nord America 3.935
AS - Asia 2.689
SA - Sud America 94
AF - Africa 6
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 4
Totale 10.924
Nazione #
US - Stati Uniti d'America 3.918
CN - Cina 916
SG - Singapore 804
UA - Ucraina 763
IT - Italia 623
IE - Irlanda 566
GB - Regno Unito 515
SE - Svezia 492
TR - Turchia 469
DE - Germania 407
FR - Francia 394
IN - India 368
FI - Finlandia 170
RU - Federazione Russa 129
BR - Brasile 88
VN - Vietnam 77
AT - Austria 39
CZ - Repubblica Ceca 18
BE - Belgio 17
RO - Romania 15
CA - Canada 14
NL - Olanda 13
IL - Israele 11
GR - Grecia 10
IR - Iran 10
HK - Hong Kong 8
PL - Polonia 7
EU - Europa 6
AU - Australia 4
UZ - Uzbekistan 4
BD - Bangladesh 3
MD - Moldavia 3
MX - Messico 3
MY - Malesia 3
TW - Taiwan 3
ZA - Sudafrica 3
ES - Italia 2
KR - Corea 2
LT - Lituania 2
NO - Norvegia 2
OM - Oman 2
VE - Venezuela 2
AR - Argentina 1
AZ - Azerbaigian 1
CH - Svizzera 1
CL - Cile 1
EC - Ecuador 1
GE - Georgia 1
GY - Guiana 1
ID - Indonesia 1
IQ - Iraq 1
JP - Giappone 1
KZ - Kazakistan 1
PK - Pakistan 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
Totale 10.924
Città #
Jacksonville 810
Chandler 691
Dublin 563
Singapore 449
Southend 449
Princeton 291
Izmir 262
Nanjing 243
Ashburn 181
Dearborn 179
Beijing 169
Wilmington 156
The Dalles 135
Cambridge 134
Chieti 123
Nanchang 99
Grafing 92
Boardman 91
Dong Ket 75
Ann Arbor 72
Santa Clara 72
Altamura 71
Los Angeles 50
Woodbridge 50
Hebei 49
Kunming 49
Shenyang 48
Pescara 46
Tianjin 46
Helsinki 36
Vienna 36
Jiaxing 31
Munich 31
Washington 31
Jinan 28
Rome 28
Hangzhou 26
Grevenbroich 25
Augusta 18
Düsseldorf 18
Kocaeli 18
Brno 17
Norwalk 17
Guangzhou 16
Ningbo 16
San Mateo 15
Zhengzhou 15
Changsha 14
Auburn Hills 13
Brussels 13
Lanzhou 13
New York 11
Bangalore 9
Leawood 9
Changchun 8
Milan 8
Montesilvano Marina 8
Orange 8
Toronto 8
Ardabil 7
Atessa 7
Hefei 7
Hong Kong 7
Moscow 7
Teramo 7
Kraków 6
São Paulo 6
Bucharest 5
Espoo 5
Houston 5
Mumbai 5
Vasto 5
Bari 4
Campobasso 4
Caserta 4
Clifton 4
Cluj-napoca 4
Parma 4
Porto Alegre 4
Rio de Janeiro 4
Seattle 4
Tashkent 4
Waanrode 4
Agnone 3
Alingsås 3
Bologna 3
Cagliari 3
Campinas 3
Castelraimondo 3
Chisinau 3
Contagem 3
Fairfield 3
Fuzhou 3
Kuala Lumpur 3
L'aquila 3
London 3
Melegnano 3
Mexico City 3
Nuremberg 3
Pavia 3
Totale 6.463
Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 157
Zinc sulfate supplementation improves thyroid function in hypozincemic Down children 146
16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer. 146
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 138
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 131
Discovering a familial Xp11.4 microduplication: Does the mother matter? 123
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 114
Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence? 112
Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly. 109
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis 108
Therapeutic potential of hAECs for early Achilles tendon defect repair through regeneration 107
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 106
A new case of pure partial 7q duplication 105
[Chromosome anomalies and Waldenström's macroglobulinemia]. 105
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 105
X/Y translocation in a family with Leri-Weill dyschondrosteosis 104
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 104
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 103
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 102
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 102
A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man. 102
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 100
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 98
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs 97
Characterization of novel genes in AZF regions 96
Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders 96
Concerns about using Zn supplementation in Down's syndrome (DS) children. 95
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 95
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 92
I nuovi orizzonti della diagnosi prenatale 92
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 92
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome 91
SHOX mutations detected by FISH and direct sequencing in patients with short stature 91
Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures 91
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 87
AluI and HaeIII restriction enzyme banding patterns of Macaca fuscata and Cercopithecus aethiops sabaeus chromosomes. 87
Array-CGH characterization of a de novo t(X;Y)(p22;q11) in a female with short stature and mental retardation. 87
[Cytogenetic study of 201 subjects with altered reproductive fitness]. 86
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 85
A case of triploidy detected by crosstrimester test. 85
Comparison of methods for the detection of in situ restriction enzyme - nick translation using fluorochromes and confocal microscopy 84
Human homologue sequences to the drosophila dishevelled segment-polarity gene are deleted in the Di George Syndrome 84
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 84
Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay 84
A genetic assessment of trisomy 21 in a patient with persistent truncus arteriosus who died 38 years ago. 83
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 83
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 83
Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA). 82
Identification of multiple transcribed sequences from the spinal muscular atrophy region on human chromosome 81
Cytogenetic survey of benign prostate hyperplasia 81
Sensitivity of cutaneous chronic myelomonocytic leukaemia lesions to hypomethylating treatment 80
Prenatal diagnosis using the triple test 79
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature. 79
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 78
The methylenetethrahydrofolate reductase (MTHFR) C677T polymorphism and male infertility in Italy. 78
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization 78
Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells. 78
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 78
Growth delay in Down syndrome and zinc sulphate supplementation 77
Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus 77
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 77
Molecular studies in three patients with isodicentric Y chromosome 77
[Cytogenetic study of 140 patients with changes in sexual features]. 77
Chromosome changes in 19 patients with Waldenström's macroglobulinemia. 77
Non-invasive prenatal screening: a 20-year experience in Italy 77
Fetal Translocation between chromosomes 2, 18, and 21 resolved by fish 76
Chromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genes. 76
A Mosaic Ring Chromosome 21 in a Patient with Mild Intellectual Disability not Evidenced by Array-Cgh 76
Acquisition of i(8q) as an early event in malignant triton tumors 75
Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri-Weill dyschondrosteosis. 75
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping 75
Clinical-Grade Expanded Regulatory T Cells Are Enriched with Highly Suppressive Cells Producing IL-10, Granzyme B, and IL-35 75
Rhombencephalosynapsis in a severely polymalformed fetus with non-mosaic tetrasomy 9p, in intracytoplasmic-sperm-injection pregnancy. 75
Correlation between apoptosis and TP53 status in osteosarcoma 74
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. 74
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 74
Philadelphia (Ph), 14q+ and 1q+ chromosomes in immunoblastic phase (Richter's syndrome) in a patient with T chronic lymphocytic leukaemia. 74
FISH analysis in detecting 9p duplication (p22p24) 73
Comparison of combined, stepwise sequential, contingent, and integrated screening in 7292 high-risk pregnant women 73
P53 loss and point mutation are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis 73
Screening biochimici prenatali: l’esperienza del tri-test in 17.869 gravidanze della regione Abruzzo. 72
Molecular characterization of two extra marker chromosomes detected at prenatal diagnosis 72
On chromosomal DNA modifications by chemical and physical treatment of C-bands. 72
Prognostic value of atypical chromosomal changes during chronic myeloid leukemia. 72
Delayed Diagnosis of Potocki-Shaffer Syndrome in a Woman with Multiple Exostoses and Mental Retardation 72
Genomic organization, physical mapping, and involvement in Yq microdeletions of the VCY2 (BPY 2) gene 71
Characterization of a new TSPY gene family member in Yq (TSPYq1). 70
Two newborns with chromosome 4 imbalances: deletion 4q33-->q35 and ring r(4)(pterq35.2-qter). 70
Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male 68
Effectiveness of crosstrimester test in selecting high-risk pregnant women to undergo invasive prenatal diagnosis 68
Effect of HpaII and MspI restriction endonucleases on chronic myelogenous leukemia chromosomes. Detection of CpG dinucleotide demethylation in situ. 68
Cytogenetic study of the heterochromatic polymorphisms in 100 subjects with Down syndrome and their parents. 68
The polymorphic polyglutamine repeat in the mitochondrial DNA polymerase γ gene is not associated with oligozoospermia 68
Karyotype refinement by multicolor fluorescence in situ hybridization analysis in 18 patients with acute lymphoblastic leukemia. 67
Heterochromatic polymorphisms of chromosome 16 evidenced by Alu I endonuclease digestion in chronic myelogenous leukemia. 67
Detection of chromosomal aneuploidies in fetal cells isolated from maternal blood using single-chromosome dual-probe FISH analysis 67
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb 66
Cytogenetics and bone marrow transplantation. 66
SHOX point mutations and deletions in Leri-Weill dyschondrosteosis. 66
Chromosome 11 rearrangements and specific MLL amplification revealed by spectral karyotyping in a patient with refractory anaemia with excess of blasts(RAEB)”. 65
Totale 8.661
Categoria #
all - tutte 43.981
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 43.981


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020188 0 0 0 0 0 0 0 0 0 0 182 6
2020/20211.100 138 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
2024/20251.572 172 325 268 83 53 29 74 83 307 121 57 0
Totale 11.115