IRIS
MORIZIO, Elisena
 Distribuzione geografica
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Continente #
NA - Nord America 2.762
AS - Asia 2.012
EU - Europa 1.972
SA - Sud America 143
AF - Africa 24
OC - Oceania 4
Continente sconosciuto - Info sul continente non disponibili 2
Totale 6.919
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Nazione #
US - Stati Uniti d'America 2.717
SG - Singapore 762
CN - Cina 585
UA - Ucraina 292
IT - Italia 266
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
HK - Hong Kong 28
CA - Canada 22
BD - Bangladesh 20
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
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 6.919
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Città #
Singapore 524
Chandler 376
Jacksonville 315
San Jose 289
Dublin 226
Ashburn 209
Southend 169
Beijing 161
Princeton 113
Dearborn 101
Izmir 95
Dallas 93
Nanjing 93
Los Angeles 90
Chieti 75
Boardman 57
Ann Arbor 55
Ho Chi Minh City 54
Cambridge 52
Grafing 52
Wilmington 51
Munich 49
Santa Clara 49
Tongling 44
Nanchang 43
Dong Ket 40
The Dalles 35
Hanoi 30
New York 30
Hebei 28
Altamura 27
Hong Kong 26
Buffalo 25
Kunming 22
Helsinki 21
Woodbridge 21
Tianjin 20
Washington 19
Shenyang 17
Tokyo 17
Jiaxing 15
São Paulo 15
Moscow 14
Orem 14
Hangzhou 13
Jinan 13
Atlanta 12
Brno 12
Brussels 12
Montreal 12
Redondo Beach 12
Brooklyn 11
Chennai 11
Ningbo 11
Pescara 11
Johannesburg 10
Seoul 10
Augusta 9
Denver 9
Stockholm 9
Kocaeli 8
Phoenix 8
Bangalore 7
Chicago 7
Council Bluffs 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
Auburn Hills 5
Charlotte 5
Guangzhou 5
Houston 5
Hải Dương 5
Lanzhou 5
London 5
Mexico City 5
New Delhi 5
Poplar 5
San Francisco 5
Toronto 5
Amsterdam 4
Atessa 4
Bucharest 4
Cluj-napoca 4
Milan 4
Querétaro 4
Rome 4
Tashkent 4
Ardabil 3
Bắc Giang 3
Changchun 3
Totale 4.265
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Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 210
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 179
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis 169
Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence? 165
Discovering a familial Xp11.4 microduplication: Does the mother matter? 162
A new case of pure partial 7q duplication 156
Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly. 155
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 153
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 152
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 146
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 144
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 142
Non-invasive prenatal screening: a 20-year experience in Italy 142
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 141
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 137
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 136
A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man. 136
I nuovi orizzonti della diagnosi prenatale 135
A case of triploidy detected by crosstrimester test. 131
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 130
Characterization of novel genes in AZF regions 129
Cytogenetic survey of benign prostate hyperplasia 128
Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay 128
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
SHOX mutations detected by FISH and direct sequencing in patients with short stature 124
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 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 123
Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus 121
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 120
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 120
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 119
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 118
A 343 Italian cohort of patients analysed with array-comparative genomic hybridization: unsolved problems and genetic counselling difficulties 116
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 115
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 115
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 103
Molecular studies in three patients with isodicentric Y chromosome 103
Prenatal diagnosis using the triple test 101
FISH analysis in detecting 9p duplication (p22p24) 100
Rhombencephalosynapsis in a severely polymalformed fetus with non-mosaic tetrasomy 9p, in intracytoplasmic-sperm-injection pregnancy. 100
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb 98
Chromosome 11 rearrangements and specific MLL amplification revealed by spectral karyotyping in a patient with refractory anaemia with excess of blasts(RAEB)”. 96
P53 loss and point mutation are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis 96
Molecular characterization of two extra marker chromosomes detected at prenatal diagnosis 94
De novo complex chromosome rearrangement detected by fluorescence in situ hybridization on amniotic fluid cells 93
Effectiveness of crosstrimester test in selecting high-risk pregnant women to undergo invasive prenatal diagnosis 93
Molecular characterization of an unusual variant t(15;17) detected in an APL patient 93
Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male 91
FISH detection of mixed chimerism in 33 patients submitted to bone marrow transplantation 84
Retrospective investigation of hematopoietic chimerism after BMT by PCR amplification hypervariable DNA regions 83
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
Assignment of the β-arrestin 1 gene (ARRB1) to human chromosome 11q13 82
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? 77
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
1q21.1 Duplication Syndrome and Anorectal Malformations: A Literature Review and a New Case 66
The Role of Lifestyle Intervention in Female Fertility: A Modifiable Factor for Preconception Health 58
First case of two supernumerary markers derived from chromosome 5 and chromosome 8 42
null 31
Totale 7.002
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Categoria #
all - tutte 24.806
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 24.806
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021143 0 0 0 0 0 0 0 0 0 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
2024/2025905 54 170 126 31 29 10 29 29 120 14 114 179
2025/20262.002 186 62 174 260 242 162 399 148 233 136 0 0
Totale 7.002