IRIS
CALABRESE, Giuseppe
 Distribuzione geografica
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Continente #
EU - Europa 4.127
NA - Nord America 3.775
AS - Asia 2.300
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 4
SA - Sud America 3
AF - Africa 2
Totale 10.217
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Nazione #
US - Stati Uniti d'America 3.761
CN - Cina 912
UA - Ucraina 762
IT - Italia 602
IE - Irlanda 566
GB - Regno Unito 514
SE - Svezia 492
TR - Turchia 466
SG - Singapore 445
DE - Germania 397
FR - Francia 384
IN - India 368
FI - Finlandia 164
RU - Federazione Russa 126
VN - Vietnam 77
AT - Austria 35
CZ - Repubblica Ceca 18
BE - Belgio 16
RO - Romania 15
CA - Canada 14
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
ZA - Sudafrica 1
Totale 10.217
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Città #
Jacksonville 810
Chandler 691
Dublin 563
Southend 449
Singapore 379
Princeton 291
Izmir 262
Nanjing 243
Ashburn 179
Dearborn 179
Beijing 169
Wilmington 156
Cambridge 134
Chieti 122
Nanchang 99
Grafing 92
Boardman 91
Dong Ket 75
Ann Arbor 72
Santa Clara 72
Altamura 71
Woodbridge 50
Hebei 49
Kunming 49
Los Angeles 49
Shenyang 48
Tianjin 46
Pescara 34
Vienna 34
Helsinki 31
Jiaxing 31
Munich 31
Washington 31
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
Lanzhou 13
Brussels 12
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
Espoo 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
Fuzhou 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
Totale 6.220
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Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 147
Zinc sulfate supplementation improves thyroid function in hypozincemic Down children 144
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 133
16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer. 130
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 125
Discovering a familial Xp11.4 microduplication: Does the mother matter? 116
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 109
Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence? 109
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis 105
Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly. 104
Therapeutic potential of hAECs for early Achilles tendon defect repair through regeneration 104
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 102
X/Y translocation in a family with Leri-Weill dyschondrosteosis 101
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 100
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 99
[Chromosome anomalies and Waldenström's macroglobulinemia]. 99
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 97
A new case of pure partial 7q duplication 96
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 95
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 94
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs 93
Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders 93
Characterization of novel genes in AZF regions 92
A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man. 92
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 91
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 90
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 90
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome 89
SHOX mutations detected by FISH and direct sequencing in patients with short stature 89
Concerns about using Zn supplementation in Down's syndrome (DS) children. 87
I nuovi orizzonti della diagnosi prenatale 87
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 87
Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures 86
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 84
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 84
AluI and HaeIII restriction enzyme banding patterns of Macaca fuscata and Cercopithecus aethiops sabaeus chromosomes. 83
Array-CGH characterization of a de novo t(X;Y)(p22;q11) in a female with short stature and mental retardation. 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 82
Human homologue sequences to the drosophila dishevelled segment-polarity gene are deleted in the Di George Syndrome 81
[Cytogenetic study of 201 subjects with altered reproductive fitness]. 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
Cytogenetic survey of benign prostate hyperplasia 80
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 80
A case of triploidy detected by crosstrimester test. 79
Sensitivity of cutaneous chronic myelomonocytic leukaemia lesions to hypomethylating treatment 79
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 77
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 77
Identification of multiple transcribed sequences from the spinal muscular atrophy region on human chromosome 76
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
Molecular studies in three patients with isodicentric Y chromosome 76
Growth delay in Down syndrome and zinc sulphate supplementation 74
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping 74
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature. 74
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization 74
Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay 74
Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri-Weill dyschondrosteosis. 73
Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus 73
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 73
[Cytogenetic study of 140 patients with changes in sexual features]. 73
Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells. 73
Acquisition of i(8q) as an early event in malignant triton tumors 72
P53 loss and point mutation are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis 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
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 72
Screening biochimici prenatali: l’esperienza del tri-test in 17.869 gravidanze della regione Abruzzo. 71
FISH analysis in detecting 9p duplication (p22p24) 71
Non-invasive prenatal screening: a 20-year experience in Italy 71
Rhombencephalosynapsis in a severely polymalformed fetus with non-mosaic tetrasomy 9p, in intracytoplasmic-sperm-injection pregnancy. 71
Fetal Translocation between chromosomes 2, 18, and 21 resolved by fish 70
Correlation between apoptosis and TP53 status in osteosarcoma 70
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. 70
Molecular characterization of two extra marker chromosomes detected at prenatal diagnosis 70
Genomic organization, physical mapping, and involvement in Yq microdeletions of the VCY2 (BPY 2) gene 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
Two newborns with chromosome 4 imbalances: deletion 4q33-->q35 and ring r(4)(pterq35.2-qter). 66
Philadelphia (Ph), 14q+ and 1q+ chromosomes in immunoblastic phase (Richter's syndrome) in a patient with T chronic lymphocytic leukaemia. 66
Prognostic value of atypical chromosomal changes during chronic myeloid leukemia. 66
The polymorphic polyglutamine repeat in the mitochondrial DNA polymerase γ gene is not associated with oligozoospermia 66
Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male 65
Detection of chromosomal aneuploidies in fetal cells isolated from maternal blood using single-chromosome dual-probe FISH analysis 65
A Mosaic Ring Chromosome 21 in a Patient with Mild Intellectual Disability not Evidenced by Array-Cgh 65
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb 64
Effectiveness of crosstrimester test in selecting high-risk pregnant women to undergo invasive prenatal diagnosis 64
Effect of HpaII and MspI restriction endonucleases on chronic myelogenous leukemia chromosomes. Detection of CpG dinucleotide demethylation in situ. 64
Karyotype refinement by multicolor fluorescence in situ hybridization analysis in 18 patients with acute lymphoblastic leukemia. 63
De novo complex chromosome rearrangement detected by fluorescence in situ hybridization on amniotic fluid cells 63
Molecular characterization of an unusual variant t(15;17) detected in an APL patient 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
Cytogenetics and acute non lymphocytic leukemia. 62
Heterochromatic polymorphisms of chromosome 16 evidenced by Alu I endonuclease digestion in chronic myelogenous leukemia. 62
Totale 8.197
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Categoria #
all - tutte 36.380
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 36.380
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.118 0 0 0 0 164 148 269 176 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
2024/2025861 172 325 268 83 13 0 0 0 0 0 0 0
Totale 10.404