IRIS
MORIZIO, Elisena
 Distribuzione geografica
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Continente #
NA - Nord America 1.858
EU - Europa 1.697
AS - Asia 1.159
SA - Sud America 51
AF - Africa 7
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 2
Totale 4.777
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Nazione #
US - Stati Uniti d'America 1.849
CN - Cina 395
SG - Singapore 368
UA - Ucraina 289
IT - Italia 243
SE - Svezia 229
IE - Irlanda 227
DE - Germania 199
GB - Regno Unito 198
IN - India 170
TR - Turchia 152
FR - Francia 143
FI - Finlandia 71
BR - Brasile 48
RU - Federazione Russa 47
VN - Vietnam 42
BE - Belgio 13
CZ - Repubblica Ceca 12
RO - Romania 12
IL - Israele 8
CA - Canada 7
NL - Olanda 6
HK - Hong Kong 4
AU - Australia 3
BD - Bangladesh 3
IR - Iran 3
MY - Malesia 3
ZA - Sudafrica 3
EU - Europa 2
GR - Grecia 2
JP - Giappone 2
KR - Corea 2
LT - Lituania 2
MA - Marocco 2
TW - Taiwan 2
AR - Argentina 1
AT - Austria 1
AZ - Azerbaigian 1
EC - Ecuador 1
HN - Honduras 1
ID - Indonesia 1
IQ - Iraq 1
MK - Macedonia 1
MX - Messico 1
NO - Norvegia 1
OM - Oman 1
PL - Polonia 1
SC - Seychelles 1
TG - Togo 1
UZ - Uzbekistan 1
VE - Venezuela 1
Totale 4.777
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Città #
Chandler 376
Jacksonville 315
Singapore 227
Dublin 224
Southend 169
Princeton 113
Dearborn 101
Izmir 94
Nanjing 93
Ashburn 85
Beijing 80
Chieti 74
Boardman 57
Ann Arbor 55
Cambridge 52
Grafing 52
Wilmington 51
Nanchang 43
Dong Ket 40
Santa Clara 37
The Dalles 35
Munich 29
Hebei 28
Los Angeles 28
Altamura 27
Kunming 22
Woodbridge 21
Helsinki 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
New York 7
Norwalk 7
San Mateo 7
Auburn Hills 5
Guangzhou 5
Hefei 5
Lanzhou 5
Atessa 4
Bucharest 4
Cluj-napoca 4
Mumbai 4
Stockholm 4
Ardabil 3
Atlanta 3
Boston 3
Changchun 3
Clifton 3
Frankfurt am Main 3
Fuzhou 3
Guarulhos 3
Hong Kong 3
Johannesburg 3
Kuala Lumpur 3
Melegnano 3
Milan 3
Montesilvano Marina 3
Parma 3
Teramo 3
Zhengzhou 3
Abu Sinan 2
Bologna 2
Brooklyn 2
Cagliari 2
Changsha 2
Charlotte 2
Chicago 2
Contagem 2
Dallas 2
Espoo 2
Hanoi 2
Kfar Saba 2
Leawood 2
Melendugno 2
Moscow 2
Newcastle 2
Nuremberg 2
Pavia 2
Porto Alegre 2
Roseto Degli Abruzzi 2
San Francisco 2
San Vito Chietino 2
Seoul 2
Taipei 2
Taizhou 2
Tokyo 2
Toronto 2
Vasto 2
Totale 2.893
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Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 158
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 134
Discovering a familial Xp11.4 microduplication: Does the mother matter? 125
Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence? 114
Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly. 110
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis 110
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 110
A new case of pure partial 7q duplication 107
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 106
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 106
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 105
A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man. 105
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 103
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 99
Characterization of novel genes in AZF regions 98
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 96
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 95
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 95
I nuovi orizzonti della diagnosi prenatale 94
SHOX mutations detected by FISH and direct sequencing in patients with short stature 92
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 90
A case of triploidy detected by crosstrimester test. 88
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 87
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 87
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 85
Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay 85
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 84
Cytogenetic survey of benign prostate hyperplasia 83
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 81
Prenatal diagnosis using the triple test 80
Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus 80
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 79
Molecular studies in three patients with isodicentric Y chromosome 79
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 78
Non-invasive prenatal screening: a 20-year experience in Italy 78
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping 77
Rhombencephalosynapsis in a severely polymalformed fetus with non-mosaic tetrasomy 9p, in intracytoplasmic-sperm-injection pregnancy. 76
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 75
P53 loss and point mutation are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis 75
FISH analysis in detecting 9p duplication (p22p24) 74
Comparison of combined, stepwise sequential, contingent, and integrated screening in 7292 high-risk pregnant women 74
Genomic organization, physical mapping, and involvement in Yq microdeletions of the VCY2 (BPY 2) gene 73
Molecular characterization of two extra marker chromosomes detected at prenatal diagnosis 73
Effectiveness of crosstrimester test in selecting high-risk pregnant women to undergo invasive prenatal diagnosis 71
Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male 70
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb 68
De novo complex chromosome rearrangement detected by fluorescence in situ hybridization on amniotic fluid cells 68
Chromosome 11 rearrangements and specific MLL amplification revealed by spectral karyotyping in a patient with refractory anaemia with excess of blasts(RAEB)”. 68
Molecular characterization of an unusual variant t(15;17) detected in an APL patient 66
FISH detection of mixed chimerism in 33 patients submitted to bone marrow transplantation 65
Retrospective investigation of hematopoietic chimerism after BMT by PCR amplification hypervariable DNA regions 58
Complex chromosome translocation of standard t(8;21) and t(15;17) arise from a two-step mechanism by fluorescence in situ hybridization analysis 57
Detection of an insertion deletion of region 8q13-q21.2 in a patient with Duane syndrome: implications for mapping and cloning a Duane gene 56
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? 56
A 343 Italian cohort of patients analysed with array-comparative genomic hybridization: unsolved problems and genetic counselling difficulties 55
Assignment of the β-arrestin 1 gene (ARRB1) to human chromosome 11q13 47
null 31
1q21.1 Duplication Syndrome and Anorectal Malformations: A Literature Review and a New Case 15
Totale 4.854
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Categoria #
all - tutte 18.960
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 18.960
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20204 0 0 0 0 0 0 0 0 0 0 0 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
2024/2025759 54 170 126 31 29 10 29 29 120 14 114 33
Totale 4.854