IRIS
CALABRESE, Giuseppe
 Distribuzione geografica
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Continente #
EU - Europa 4.088
NA - Nord America 3.757
AS - Asia 2.224
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 4
SA - Sud America 3
AF - Africa 1
Totale 10.083
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Nazione #
US - Stati Uniti d'America 3.744
CN - Cina 905
UA - Ucraina 762
IT - Italia 594
IE - Irlanda 566
GB - Regno Unito 514
SE - Svezia 492
TR - Turchia 466
DE - Germania 395
FR - Francia 380
SG - Singapore 376
IN - India 368
FI - Finlandia 140
RU - Federazione Russa 126
VN - Vietnam 77
AT - Austria 35
CZ - Repubblica Ceca 18
BE - Belgio 15
RO - Romania 15
CA - Canada 13
IL - Israele 11
NL - Olanda 11
GR - Grecia 10
IR - Iran 10
EU - Europa 6
PL - Polonia 6
AU - Australia 4
MD - Moldavia 3
MY - Malesia 3
TW - Taiwan 3
BR - Brasile 2
ES - Italia 2
KR - Corea 2
CH - Svizzera 1
EC - Ecuador 1
JP - Giappone 1
LT - Lituania 1
NO - Norvegia 1
OM - Oman 1
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
TH - Thailandia 1
Totale 10.083
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Città #
Jacksonville 810
Chandler 691
Dublin 563
Southend 449
Singapore 331
Princeton 291
Izmir 262
Nanjing 243
Ashburn 179
Dearborn 179
Beijing 168
Wilmington 156
Cambridge 134
Chieti 122
Nanchang 99
Grafing 92
Boardman 91
Dong Ket 75
Ann Arbor 72
Altamura 71
Santa Clara 71
Woodbridge 50
Hebei 49
Kunming 49
Los Angeles 48
Shenyang 48
Tianjin 46
Pescara 34
Vienna 34
Jiaxing 31
Washington 31
Munich 30
Jinan 28
Hangzhou 26
Rome 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
Helsinki 13
Lanzhou 13
Brussels 11
New York 11
Bangalore 9
Leawood 9
Changchun 8
Milan 8
Montesilvano Marina 8
Orange 8
Toronto 8
Ardabil 7
Atessa 7
Hefei 7
Moscow 7
Teramo 7
Kraków 6
Bucharest 5
Houston 5
Mumbai 5
Vasto 5
Bari 4
Campobasso 4
Caserta 4
Clifton 4
Cluj-napoca 4
Parma 4
Seattle 4
Waanrode 4
Agnone 3
Alingsås 3
Bologna 3
Castelraimondo 3
Chisinau 3
Fairfield 3
Kuala Lumpur 3
L'aquila 3
Melegnano 3
Pavia 3
Redwood City 3
Roseto Degli Abruzzi 3
Stockholm 3
Taipei 3
Taizhou 3
Tehran 3
Voronezh 3
Abu Sinan 2
Atri 2
Caselle Torinese 2
Cerano 2
Chicago 2
Fuzhou 2
Haikou 2
Totale 6.145
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Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 146
Zinc sulfate supplementation improves thyroid function in hypozincemic Down children 143
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 132
16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer. 125
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 122
Discovering a familial Xp11.4 microduplication: Does the mother matter? 116
Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence? 107
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 106
Therapeutic potential of hAECs for early Achilles tendon defect repair through regeneration 103
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis 103
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 102
Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly. 101
X/Y translocation in a family with Leri-Weill dyschondrosteosis 99
[Chromosome anomalies and Waldenström's macroglobulinemia]. 99
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 98
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 95
A new case of pure partial 7q duplication 94
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 94
Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders 93
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 93
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs 92
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 92
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 90
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 89
Characterization of novel genes in AZF regions 89
SHOX mutations detected by FISH and direct sequencing in patients with short stature 88
A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man. 88
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome 87
Concerns about using Zn supplementation in Down's syndrome (DS) children. 87
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 87
I nuovi orizzonti della diagnosi prenatale 86
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 86
Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures 85
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 83
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 83
Array-CGH characterization of a de novo t(X;Y)(p22;q11) in a female with short stature and mental retardation. 83
Human homologue sequences to the drosophila dishevelled segment-polarity gene are deleted in the Di George Syndrome 81
Comparison of methods for the detection of in situ restriction enzyme - nick translation using fluorochromes and confocal microscopy 80
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 80
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 80
Cytogenetic survey of benign prostate hyperplasia 80
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 80
[Cytogenetic study of 201 subjects with altered reproductive fitness]. 80
AluI and HaeIII restriction enzyme banding patterns of Macaca fuscata and Cercopithecus aethiops sabaeus chromosomes. 79
A case of triploidy detected by crosstrimester test. 78
Sensitivity of cutaneous chronic myelomonocytic leukaemia lesions to hypomethylating treatment 78
A genetic assessment of trisomy 21 in a patient with persistent truncus arteriosus who died 38 years ago. 76
The methylenetethrahydrofolate reductase (MTHFR) C677T polymorphism and male infertility in Italy. 76
Prenatal diagnosis using the triple test 76
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 76
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 75
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 75
Molecular studies in three patients with isodicentric Y chromosome 75
Identification of multiple transcribed sequences from the spinal muscular atrophy region on human chromosome 73
Growth delay in Down syndrome and zinc sulphate supplementation 73
Acquisition of i(8q) as an early event in malignant triton tumors 72
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping 72
Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus 72
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 72
Chromosome changes in 19 patients with Waldenström's macroglobulinemia. 72
Chromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genes. 72
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization 72
Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay 72
Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri-Weill dyschondrosteosis. 71
P53 loss and point mutation are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis 71
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature. 71
Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells. 71
Screening biochimici prenatali: l’esperienza del tri-test in 17.869 gravidanze della regione Abruzzo. 70
Correlation between apoptosis and TP53 status in osteosarcoma 70
FISH analysis in detecting 9p duplication (p22p24) 70
[Cytogenetic study of 140 patients with changes in sexual features]. 70
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 70
Rhombencephalosynapsis in a severely polymalformed fetus with non-mosaic tetrasomy 9p, in intracytoplasmic-sperm-injection pregnancy. 70
Fetal Translocation between chromosomes 2, 18, and 21 resolved by fish 69
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. 69
Genomic organization, physical mapping, and involvement in Yq microdeletions of the VCY2 (BPY 2) gene 69
Molecular characterization of two extra marker chromosomes detected at prenatal diagnosis 69
Non-invasive prenatal screening: a 20-year experience in Italy 69
Characterization of a new TSPY gene family member in Yq (TSPYq1). 68
Comparison of combined, stepwise sequential, contingent, and integrated screening in 7292 high-risk pregnant women 68
On chromosomal DNA modifications by chemical and physical treatment of C-bands. 68
Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA). 67
Delayed Diagnosis of Potocki-Shaffer Syndrome in a Woman with Multiple Exostoses and Mental Retardation 67
Prognostic value of atypical chromosomal changes during chronic myeloid leukemia. 66
Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male 65
Philadelphia (Ph), 14q+ and 1q+ chromosomes in immunoblastic phase (Richter's syndrome) in a patient with T chronic lymphocytic leukaemia. 65
Detection of chromosomal aneuploidies in fetal cells isolated from maternal blood using single-chromosome dual-probe FISH analysis 65
The polymorphic polyglutamine repeat in the mitochondrial DNA polymerase γ gene is not associated with oligozoospermia 65
Two newborns with chromosome 4 imbalances: deletion 4q33-->q35 and ring r(4)(pterq35.2-qter). 64
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb 64
Effect of HpaII and MspI restriction endonucleases on chronic myelogenous leukemia chromosomes. Detection of CpG dinucleotide demethylation in situ. 64
A Mosaic Ring Chromosome 21 in a Patient with Mild Intellectual Disability not Evidenced by Array-Cgh 64
Effectiveness of crosstrimester test in selecting high-risk pregnant women to undergo invasive prenatal diagnosis 63
FISH detection of mixed chimerism in 33 patients submitted to bone marrow transplantation 63
Cytogenetic study of the heterochromatic polymorphisms in 100 subjects with Down syndrome and their parents. 63
Karyotype refinement by multicolor fluorescence in situ hybridization analysis in 18 patients with acute lymphoblastic leukemia. 62
De novo complex chromosome rearrangement detected by fluorescence in situ hybridization on amniotic fluid cells 62
Molecular characterization of an unusual variant t(15;17) detected in an APL patient 62
Cytogenetics and acute non lymphocytic leukemia. 62
Heterochromatic polymorphisms of chromosome 16 evidenced by Alu I endonuclease digestion in chronic myelogenous leukemia. 62
Totale 8.081
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Categoria #
all - tutte 33.483
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 33.483
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.184 0 0 11 55 164 148 269 176 51 122 182 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
2024/2025709 172 325 212 0 0 0 0 0 0 0 0 0
Totale 10.252