IRIS
CALABRESE, Giuseppe
 Distribuzione geografica
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Continente #
EU - Europa 3.647
NA - Nord America 3.284
AS - Asia 1.851
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 3
SA - Sud America 2
AF - Africa 1
Totale 8.794
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Nazione #
US - Stati Uniti d'America 3.274
CN - Cina 907
UA - Ucraina 765
IT - Italia 567
GB - Regno Unito 510
SE - Svezia 500
TR - Turchia 466
FR - Francia 376
IN - India 370
DE - Germania 366
IE - Irlanda 281
FI - Finlandia 136
VN - Vietnam 75
BE - Belgio 38
AT - Austria 35
RU - Federazione Russa 22
RO - Romania 15
IL - Israele 11
CA - Canada 10
GR - Grecia 10
IR - Iran 10
NL - Olanda 9
EU - Europa 6
PL - Polonia 6
AU - Australia 3
MD - Moldavia 3
MY - Malesia 3
TW - Taiwan 3
BR - Brasile 2
CZ - Repubblica Ceca 2
ES - Italia 2
KR - Corea 2
CH - Svizzera 1
JP - Giappone 1
LT - Lituania 1
NO - Norvegia 1
OM - Oman 1
SC - Seychelles 1
SG - Singapore 1
SK - Slovacchia (Repubblica Slovacca) 1
TH - Thailandia 1
Totale 8.794
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Città #
Jacksonville 814
Chandler 698
Southend 449
Princeton 293
Dublin 281
Izmir 262
Nanjing 243
Dearborn 174
Beijing 169
Wilmington 158
Cambridge 134
Chieti 122
Nanchang 99
Grafing 93
Dong Ket 75
Ann Arbor 72
Altamura 70
Boardman 63
Kunming 50
Woodbridge 50
Hebei 49
Shenyang 49
Tianjin 47
Brussels 36
Vienna 34
Washington 32
Jiaxing 30
Jinan 28
Hangzhou 26
Grevenbroich 24
Pescara 24
Rome 21
Augusta 18
Düsseldorf 18
Kocaeli 18
Guangzhou 16
Ningbo 16
Norwalk 16
Changsha 15
San Mateo 15
Zhengzhou 14
Auburn Hills 13
Lanzhou 13
Bangalore 9
Helsinki 9
Leawood 9
Changchun 8
Orange 8
Ardabil 7
Atessa 7
Hefei 7
Los Angeles 7
Montesilvano Marina 7
Toronto 7
Kraków 6
Milan 6
Bucharest 5
Houston 5
Mumbai 5
Termoli 5
Campobasso 4
Caserta 4
Cluj-napoca 4
L'aquila 4
Teramo 4
Agnone 3
Alingsås 3
Bari 3
Bologna 3
Castelraimondo 3
Chicago 3
Chisinau 3
Fairfield 3
Kuala Lumpur 3
Melegnano 3
Moscow 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
Edinburgh 2
Fuzhou 2
Haikou 2
Isernia 2
Kfar Saba 2
Madrid 2
Melendugno 2
Monmouth Junction 2
Montréal 2
Newcastle 2
North Palm Beach 2
Ranipet 2
Totale 5.167
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Nome #
Zinc sulfate supplementation improves thyroid function in hypozincemic Down children 138
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 134
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 119
16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer. 113
Detection of chromosomal aneuploidies in fetal cells isolated from maternal blood using single-chromosome dual-probe FISH analysis. 110
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 102
Discovering a familial Xp11.4 microduplication: Does the mother matter? 99
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 96
Therapeutic potential of hAECs for early Achilles tendon defect repair through regeneration 94
X/Y translocation in a family with Leri-Weill dyschondrosteosis 91
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 91
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis 91
Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence? 90
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 89
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 85
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs 83
I nuovi orizzonti della diagnosi prenatale 83
Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders 83
Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly. 82
A new case of pure partial 7q duplication 80
SHOX mutations detected by FISH and direct sequencing in patients with short stature 80
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 79
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 79
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 77
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 76
Characterization of novel genes in AZF regions 75
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 75
Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures 75
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 74
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 74
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 74
Concerns about using Zn supplementation in Down's syndrome (DS) children. 73
[Chromosome anomalies and Waldenström's macroglobulinemia]. 73
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 72
Comparison of methods for the detection of in situ restriction enzyme - nick translation using fluorochromes and confocal microscopy 71
Prenatal diagnosis using the triple test 71
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 69
The methylenetethrahydrofolate reductase (MTHFR) C677T polymorphism and male infertility in Italy. 69
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 69
AluI and HaeIII restriction enzyme banding patterns of Macaca fuscata and Cercopithecus aethiops sabaeus chromosomes. 69
Human homologue sequences to the drosophila dishevelled segment-polarity gene are deleted in the Di George Syndrome 68
Cytogenetic survey of benign prostate hyperplasia 68
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 67
[Cytogenetic study of 201 subjects with altered reproductive fitness]. 67
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome 66
Correlation between apoptosis and TP53 status in osteosarcoma 66
Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri-Weill dyschondrosteosis. 66
Growth delay in Down syndrome and zinc sulphate supplementation 66
Rhombencephalosynapsis in a severely polymalformed fetus with non-mosaic tetrasomy 9p, in intracytoplasmic-sperm-injection pregnancy. 66
A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man. 66
Genomic organization, physical mapping, and involvement in Yq microdeletions of the VCY2 (BPY 2) gene 65
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 65
Molecular studies in three patients with isodicentric Y chromosome 65
P53 loss and point mutation are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis 65
A case of triploidy detected by crosstrimester test. 65
Identification of multiple transcribed sequences from the spinal muscular atrophy region on human chromosome 64
Sensitivity of cutaneous chronic myelomonocytic leukaemia lesions to hypomethylating treatment 64
Screening biochimici prenatali: l’esperienza del tri-test in 17.869 gravidanze della regione Abruzzo. 63
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. 63
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping 63
Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus 63
Chromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genes. 63
Fetal Translocation between chromosomes 2, 18, and 21 resolved by fish 62
Acquisition of i(8q) as an early event in malignant triton tumors 62
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 62
Molecular characterization of two extra marker chromosomes detected at prenatal diagnosis 62
Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells. 62
FISH analysis in detecting 9p duplication (p22p24) 61
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 61
Chromosome changes in 19 patients with Waldenström's macroglobulinemia. 61
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 61
Characterization of a new TSPY gene family member in Yq (TSPYq1). 60
Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA). 60
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 60
Prognostic value of atypical chromosomal changes during chronic myeloid leukemia. 60
A genetic assessment of trisomy 21 in a patient with persistent truncus arteriosus who died 38 years ago. 59
Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male 59
Comparison of combined, stepwise sequential, contingent, and integrated screening in 7292 high-risk pregnant women 59
Effectiveness of crosstrimester test in selecting high-risk pregnant women to undergo invasive prenatal diagnosis 59
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization 59
Two newborns with chromosome 4 imbalances: deletion 4q33-->q35 and ring r(4)(pterq35.2-qter). 58
Molecular characterization of an unusual variant t(15;17) detected in an APL patient 58
On chromosomal DNA modifications by chemical and physical treatment of C-bands. 58
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature. 58
De novo complex chromosome rearrangement detected by fluorescence in situ hybridization on amniotic fluid cells 57
FISH detection of mixed chimerism in 33 patients submitted to bone marrow transplantation 57
Non-invasive prenatal screening: a 20-year experience in Italy 57
Karyotype refinement by multicolor fluorescence in situ hybridization analysis in 18 patients with acute lymphoblastic leukemia. 56
SHOX point mutations and deletions in Leri-Weill dyschondrosteosis. 56
Detection of chromosomal aneuploidies in fetal cells isolated from maternal blood using single-chromosome dual-probe FISH analysis 56
Delayed Diagnosis of Potocki-Shaffer Syndrome in a Woman with Multiple Exostoses and Mental Retardation 56
The polymorphic polyglutamine repeat in the mitochondrial DNA polymerase γ gene is not associated with oligozoospermia 56
Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay 56
Microdeletions in interval 6 of the Y chromosome detected by STS-PCR in 6 of 33 patients with idiopathic oligo- or azoospermia. 55
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb 55
Chromosome 11 rearrangements and specific MLL amplification revealed by spectral karyotyping in a patient with refractory anaemia with excess of blasts(RAEB)”. 55
Cytogenetics and bone marrow transplantation. 55
Philadelphia (Ph), 14q+ and 1q+ chromosomes in immunoblastic phase (Richter's syndrome) in a patient with T chronic lymphocytic leukaemia. 55
Cytogenetic study of the heterochromatic polymorphisms in 100 subjects with Down syndrome and their parents. 55
Heterochromatic polymorphisms of chromosome 16 evidenced by Alu I endonuclease digestion in chronic myelogenous leukemia. 54
Totale 7.073
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Categoria #
all - tutte 20.512
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 20.512
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019940 0 0 0 19 350 15 144 18 11 9 5 369
2019/20201.916 573 134 11 55 170 145 268 178 52 139 185 6
2020/20211.123 142 5 150 6 56 179 18 12 247 160 43 105
2021/2022644 24 12 6 87 64 97 5 58 37 6 68 180
2022/20232.225 165 283 146 223 210 444 159 189 278 22 54 52
2023/2024169 60 36 73 0 0 0 0 0 0 0 0 0
Totale 9.007