IRIS
MORIZIO, Elisena
 Distribuzione geografica
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Continente #
NA - Nord America 2.901
AS - Asia 2.034
EU - Europa 1.981
SA - Sud America 143
AF - Africa 24
OC - Oceania 4
Continente sconosciuto - Info sul continente non disponibili 2
Totale 7.089
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Nazione #
US - Stati Uniti d'America 2.850
SG - Singapore 765
CN - Cina 586
UA - Ucraina 292
IT - Italia 274
SE - Svezia 234
IE - Irlanda 229
DE - Germania 225
GB - Regno Unito 219
RU - Federazione Russa 204
IN - India 189
VN - Vietnam 183
TR - Turchia 158
FR - Francia 151
BR - Brasile 117
FI - Finlandia 75
BD - Bangladesh 38
CA - Canada 28
HK - Hong Kong 28
JP - Giappone 19
MX - Messico 17
BE - Belgio 15
IQ - Iraq 14
CZ - Repubblica Ceca 12
RO - Romania 12
KR - Corea 11
ZA - Sudafrica 11
AR - Argentina 10
NL - Olanda 10
IL - Israele 9
PL - Polonia 8
ES - Italia 7
VE - Venezuela 6
LT - Lituania 5
AU - Australia 4
ID - Indonesia 4
IR - Iran 4
UZ - Uzbekistan 4
CL - Cile 3
EC - Ecuador 3
KE - Kenya 3
MY - Malesia 3
PH - Filippine 3
PK - Pakistan 3
AT - Austria 2
AZ - Azerbaigian 2
CO - Colombia 2
EG - Egitto 2
EU - Europa 2
GR - Grecia 2
JO - Giordania 2
MA - Marocco 2
TW - Taiwan 2
AE - Emirati Arabi Uniti 1
AL - Albania 1
CH - Svizzera 1
CR - Costa Rica 1
DZ - Algeria 1
GD - Grenada 1
GT - Guatemala 1
HN - Honduras 1
JM - Giamaica 1
KG - Kirghizistan 1
MK - Macedonia 1
NG - Nigeria 1
NO - Norvegia 1
NP - Nepal 1
OM - Oman 1
PA - Panama 1
PE - Perù 1
PY - Paraguay 1
QA - Qatar 1
RS - Serbia 1
SC - Seychelles 1
SN - Senegal 1
SY - Repubblica araba siriana 1
TG - Togo 1
TH - Thailandia 1
TN - Tunisia 1
Totale 7.089
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Città #
Singapore 525
Chandler 376
San Jose 347
Jacksonville 315
Dublin 226
Ashburn 216
Southend 169
Beijing 161
Princeton 113
Dearborn 101
Dallas 97
Izmir 95
Los Angeles 94
Nanjing 93
Chieti 75
Boardman 57
Ann Arbor 55
Ho Chi Minh City 54
Santa Clara 53
Cambridge 52
Grafing 52
Wilmington 51
Munich 49
Tongling 44
Nanchang 43
Dong Ket 40
The Dalles 35
Council Bluffs 33
New York 32
Hanoi 30
Hebei 28
Altamura 27
Buffalo 27
Hong Kong 26
Kunming 22
Helsinki 21
Woodbridge 21
Tianjin 20
Washington 20
Shenyang 17
Tokyo 17
Jiaxing 15
Montreal 15
São Paulo 15
Moscow 14
Orem 14
Hangzhou 13
Jinan 13
Atlanta 12
Brno 12
Brussels 12
Redondo Beach 12
Brooklyn 11
Chennai 11
Ningbo 11
Pescara 11
Augusta 10
Johannesburg 10
Seoul 10
Denver 9
Stockholm 9
Kocaeli 8
Phoenix 8
Bangalore 7
Chicago 7
Düsseldorf 7
Frankfurt am Main 7
Grevenbroich 7
Hefei 7
Norwalk 7
San Mateo 7
Warsaw 7
Baghdad 6
Boston 6
Haiphong 6
Manchester 6
Mumbai 6
San Francisco 6
Auburn Hills 5
Charlotte 5
Guangzhou 5
Houston 5
Hải Dương 5
Lanzhou 5
London 5
Memphis 5
Mexico City 5
New Delhi 5
Poplar 5
Rome 5
Toronto 5
Amsterdam 4
Atessa 4
Bucharest 4
Cluj-napoca 4
Milan 4
Querétaro 4
Tashkent 4
Ardabil 3
Bắc Giang 3
Totale 4.382
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Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 212
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 181
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis 179
Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence? 167
Discovering a familial Xp11.4 microduplication: Does the mother matter? 164
Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly. 158
A new case of pure partial 7q duplication 158
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 156
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 154
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 148
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 147
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 146
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 145
Non-invasive prenatal screening: a 20-year experience in Italy 143
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 141
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 141
I nuovi orizzonti della diagnosi prenatale 138
A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man. 136
A case of triploidy detected by crosstrimester test. 133
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 133
Characterization of novel genes in AZF regions 131
Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay 129
Cytogenetic survey of benign prostate hyperplasia 128
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 126
SHOX mutations detected by FISH and direct sequencing in patients with short stature 125
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 124
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 124
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 124
Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus 123
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 122
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 120
A 343 Italian cohort of patients analysed with array-comparative genomic hybridization: unsolved problems and genetic counselling difficulties 119
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 118
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 117
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 116
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping 109
Comparison of combined, stepwise sequential, contingent, and integrated screening in 7292 high-risk pregnant women 106
Genomic organization, physical mapping, and involvement in Yq microdeletions of the VCY2 (BPY 2) gene 104
Molecular studies in three patients with isodicentric Y chromosome 104
Rhombencephalosynapsis in a severely polymalformed fetus with non-mosaic tetrasomy 9p, in intracytoplasmic-sperm-injection pregnancy. 102
Prenatal diagnosis using the triple test 101
FISH analysis in detecting 9p duplication (p22p24) 100
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb 99
Chromosome 11 rearrangements and specific MLL amplification revealed by spectral karyotyping in a patient with refractory anaemia with excess of blasts(RAEB)”. 97
Molecular characterization of two extra marker chromosomes detected at prenatal diagnosis 97
P53 loss and point mutation are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis 97
Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male 96
De novo complex chromosome rearrangement detected by fluorescence in situ hybridization on amniotic fluid cells 96
Molecular characterization of an unusual variant t(15;17) detected in an APL patient 95
Effectiveness of crosstrimester test in selecting high-risk pregnant women to undergo invasive prenatal diagnosis 94
Retrospective investigation of hematopoietic chimerism after BMT by PCR amplification hypervariable DNA regions 84
FISH detection of mixed chimerism in 33 patients submitted to bone marrow transplantation 84
Assignment of the β-arrestin 1 gene (ARRB1) to human chromosome 11q13 84
Complex chromosome translocation of standard t(8;21) and t(15;17) arise from a two-step mechanism by fluorescence in situ hybridization analysis 83
1q21.1 Duplication Syndrome and Anorectal Malformations: A Literature Review and a New Case 81
The Role of Lifestyle Intervention in Female Fertility: A Modifiable Factor for Preconception Health 78
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? 78
Detection of an insertion deletion of region 8q13-q21.2 in a patient with Duane syndrome: implications for mapping and cloning a Duane gene 75
First case of two supernumerary markers derived from chromosome 5 and chromosome 8 71
null 31
Totale 7.172
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Categoria #
all - tutte 26.554
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 26.554
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202152 0 0 0 0 0 0 0 0 0 0 0 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
2024/2025905 54 170 126 31 29 10 29 29 120 14 114 179
2025/20262.172 186 62 174 260 242 162 399 148 233 168 104 34
Totale 7.172