IRIS
MORIZIO, Elisena
 Distribuzione geografica
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Continente #
NA - Nord America 1.756
EU - Europa 1.660
AS - Asia 986
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 2
AF - Africa 1
SA - Sud America 1
Totale 4.408
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Nazione #
US - Stati Uniti d'America 1.753
CN - Cina 395
UA - Ucraina 289
IT - Italia 240
SE - Svezia 228
IE - Irlanda 227
SG - Singapore 212
GB - Regno Unito 197
DE - Germania 184
IN - India 168
TR - Turchia 150
FR - Francia 138
FI - Finlandia 69
RU - Federazione Russa 45
VN - Vietnam 42
BE - Belgio 13
CZ - Repubblica Ceca 12
RO - Romania 12
IL - Israele 8
NL - Olanda 4
CA - Canada 3
IR - Iran 3
MY - Malesia 3
AU - Australia 2
EU - Europa 2
GR - Grecia 2
KR - Corea 2
TW - Taiwan 2
EC - Ecuador 1
JP - Giappone 1
SC - Seychelles 1
Totale 4.408
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Città #
Chandler 376
Jacksonville 315
Dublin 224
Singapore 185
Southend 169
Princeton 113
Dearborn 101
Izmir 94
Nanjing 93
Ashburn 84
Beijing 80
Chieti 74
Boardman 57
Ann Arbor 55
Grafing 52
Cambridge 51
Wilmington 50
Nanchang 43
Dong Ket 40
Santa Clara 35
Hebei 28
Altamura 27
Los Angeles 23
Kunming 22
Woodbridge 21
Helsinki 20
Munich 20
Tianjin 19
Washington 18
Shenyang 17
Jiaxing 15
Hangzhou 13
Jinan 13
Brno 12
Brussels 11
Ningbo 11
Pescara 11
Augusta 8
Kocaeli 8
Bangalore 7
Düsseldorf 7
Grevenbroich 7
Norwalk 7
San Mateo 7
Auburn Hills 5
Guangzhou 5
Hefei 5
Lanzhou 5
New York 5
Atessa 4
Bucharest 4
Cluj-napoca 4
Mumbai 4
Ardabil 3
Changchun 3
Clifton 3
Fuzhou 3
Kuala Lumpur 3
Melegnano 3
Milan 3
Montesilvano Marina 3
Parma 3
Stockholm 3
Teramo 3
Zhengzhou 3
Abu Sinan 2
Bologna 2
Changsha 2
Espoo 2
Hanoi 2
Kfar Saba 2
Leawood 2
Melendugno 2
Moscow 2
Newcastle 2
Pavia 2
Roseto Degli Abruzzi 2
San Vito Chietino 2
Seoul 2
Taipei 2
Taizhou 2
Toronto 2
Vasto 2
Waanrode 2
Ürümqi 2
Atlanta 1
Avezzano 1
Collecorvino 1
Cuenca 1
Delhi 1
Edinburgh 1
Ely 1
Fairfield 1
Fano 1
Farnborough 1
Frankfurt am Main 1
Greater Sudbury 1
Guiyang 1
Haikou 1
Harbin 1
Totale 2.775
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Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 147
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
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
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
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
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
SHOX mutations detected by FISH and direct sequencing in patients with short stature 89
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
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
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
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
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
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
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping 74
Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay 74
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
P53 loss and point mutation are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis 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
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
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
Comparison of combined, stepwise sequential, contingent, and integrated screening in 7292 high-risk pregnant women 68
Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male 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
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
Chromosome 11 rearrangements and specific MLL amplification revealed by spectral karyotyping in a patient with refractory anaemia with excess of blasts(RAEB)”. 61
Retrospective investigation of hematopoietic chimerism after BMT by PCR amplification hypervariable DNA regions 56
Complex chromosome translocation of standard t(8;21) and t(15;17) arise from a two-step mechanism by fluorescence in situ hybridization analysis 55
Detection of an insertion deletion of region 8q13-q21.2 in a patient with Duane syndrome: implications for mapping and cloning a Duane gene 54
Comparative study of FISH, PCR and cytogenetics on 25 patients submitted to bone marrow transplantation (BMT) for chronic myelogenous leukemia (CML); which tests can we use in routine analysis post BMT? 47
A 343 Italian cohort of patients analysed with array-comparative genomic hybridization: unsolved problems and genetic counselling difficulties 41
Assignment of the β-arrestin 1 gene (ARRB1) to human chromosome 11q13 37
null 31
Totale 4.481
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Categoria #
all - tutte 15.265
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 15.265
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020532 0 0 0 0 88 80 124 77 25 60 74 4
2020/2021458 56 0 59 3 16 75 9 2 95 62 29 52
2021/2022305 13 2 2 52 38 56 4 22 13 2 28 73
2022/20231.032 68 135 65 124 99 201 50 89 145 11 26 19
2023/2024409 33 11 41 11 29 130 59 15 1 17 3 59
2024/2025386 54 170 126 31 5 0 0 0 0 0 0 0
Totale 4.481