IRIS
MORIZIO, Elisena
 Distribuzione geografica
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Continente #
NA - Nord America 2.309
EU - Europa 1.780
AS - Asia 1.678
SA - Sud America 114
AF - Africa 17
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 2
Totale 5.903
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Nazione #
US - Stati Uniti d'America 2.272
SG - Singapore 610
CN - Cina 566
UA - Ucraina 291
IT - Italia 248
SE - Svezia 233
IE - Irlanda 228
DE - Germania 223
GB - Regno Unito 216
IN - India 182
TR - Turchia 155
FR - Francia 150
BR - Brasile 99
VN - Vietnam 92
FI - Finlandia 74
RU - Federazione Russa 49
CA - Canada 19
MX - Messico 15
BE - Belgio 13
JP - Giappone 13
BD - Bangladesh 12
CZ - Repubblica Ceca 12
RO - Romania 12
KR - Corea 10
ZA - Sudafrica 10
IL - Israele 9
AR - Argentina 8
NL - Olanda 7
PL - Polonia 7
ES - Italia 6
HK - Hong Kong 5
IQ - Iraq 4
IR - Iran 4
LT - Lituania 4
AU - Australia 3
ID - Indonesia 3
MY - Malesia 3
VE - Venezuela 3
AT - Austria 2
AZ - Azerbaigian 2
EU - Europa 2
GR - Grecia 2
KE - Kenya 2
MA - Marocco 2
PK - Pakistan 2
TW - Taiwan 2
AE - Emirati Arabi Uniti 1
CL - Cile 1
CR - Costa Rica 1
DZ - Algeria 1
EC - Ecuador 1
GD - Grenada 1
HN - Honduras 1
MK - Macedonia 1
NO - Norvegia 1
OM - Oman 1
PE - Perù 1
PY - Paraguay 1
QA - Qatar 1
RS - Serbia 1
SC - Seychelles 1
TG - Togo 1
UZ - Uzbekistan 1
Totale 5.903
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Città #
Singapore 414
Chandler 376
Jacksonville 315
Dublin 225
Southend 169
Ashburn 163
Beijing 158
Princeton 113
Dearborn 101
Izmir 95
Dallas 93
Nanjing 93
Los Angeles 82
Chieti 74
Boardman 57
Ann Arbor 55
Cambridge 52
Grafing 52
Wilmington 51
Munich 49
Santa Clara 44
Tongling 44
Nanchang 43
Dong Ket 40
The Dalles 35
Hebei 28
Altamura 27
New York 27
Buffalo 25
Ho Chi Minh City 22
Kunming 22
Helsinki 21
Woodbridge 21
Tianjin 20
Washington 19
Shenyang 17
Jiaxing 15
Hangzhou 13
Jinan 13
Tokyo 13
Brno 12
Redondo Beach 12
Brooklyn 11
Brussels 11
Ningbo 11
Pescara 11
São Paulo 11
Seoul 10
Augusta 9
Johannesburg 9
Montreal 9
Hanoi 8
Kocaeli 8
Stockholm 8
Atlanta 7
Bangalore 7
Chicago 7
Denver 7
Düsseldorf 7
Grevenbroich 7
Hefei 7
Norwalk 7
San Mateo 7
Boston 6
Chennai 6
Mumbai 6
Phoenix 6
Warsaw 6
Auburn Hills 5
Charlotte 5
Frankfurt am Main 5
Guangzhou 5
Lanzhou 5
London 5
Manchester 5
Mexico City 5
Toronto 5
Atessa 4
Bucharest 4
Cluj-napoca 4
Hong Kong 4
Houston 4
New Delhi 4
Poplar 4
Querétaro 4
San Francisco 4
Ardabil 3
Changchun 3
Clifton 3
Dhaka 3
Fuzhou 3
Guarulhos 3
Haiphong 3
Kuala Lumpur 3
Melegnano 3
Milan 3
Montesilvano Marina 3
Nuremberg 3
Parma 3
São José dos Campos 3
Totale 3.652
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Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 181
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 166
Discovering a familial Xp11.4 microduplication: Does the mother matter? 144
Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly. 137
Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence? 136
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis 135
A new case of pure partial 7q duplication 134
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 129
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 128
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 125
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 124
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 124
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 124
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 123
A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man. 120
I nuovi orizzonti della diagnosi prenatale 117
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 117
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 117
Characterization of novel genes in AZF regions 116
A case of triploidy detected by crosstrimester test. 114
SHOX mutations detected by FISH and direct sequencing in patients with short stature 113
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 111
Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay 110
Cytogenetic survey of benign prostate hyperplasia 109
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 107
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 105
Non-invasive prenatal screening: a 20-year experience in Italy 105
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 104
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 103
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 102
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 101
Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus 100
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 99
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping 97
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 95
Comparison of combined, stepwise sequential, contingent, and integrated screening in 7292 high-risk pregnant women 94
Molecular studies in three patients with isodicentric Y chromosome 91
Genomic organization, physical mapping, and involvement in Yq microdeletions of the VCY2 (BPY 2) gene 90
Prenatal diagnosis using the triple test 89
P53 loss and point mutation are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis 87
Rhombencephalosynapsis in a severely polymalformed fetus with non-mosaic tetrasomy 9p, in intracytoplasmic-sperm-injection pregnancy. 87
FISH analysis in detecting 9p duplication (p22p24) 85
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb 85
Effectiveness of crosstrimester test in selecting high-risk pregnant women to undergo invasive prenatal diagnosis 85
Molecular characterization of two extra marker chromosomes detected at prenatal diagnosis 85
A 343 Italian cohort of patients analysed with array-comparative genomic hybridization: unsolved problems and genetic counselling difficulties 85
Molecular characterization of an unusual variant t(15;17) detected in an APL patient 84
De novo complex chromosome rearrangement detected by fluorescence in situ hybridization on amniotic fluid cells 80
Chromosome 11 rearrangements and specific MLL amplification revealed by spectral karyotyping in a patient with refractory anaemia with excess of blasts(RAEB)”. 80
Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male 78
FISH detection of mixed chimerism in 33 patients submitted to bone marrow transplantation 74
Retrospective investigation of hematopoietic chimerism after BMT by PCR amplification hypervariable DNA regions 70
Complex chromosome translocation of standard t(8;21) and t(15;17) arise from a two-step mechanism by fluorescence in situ hybridization analysis 70
Assignment of the β-arrestin 1 gene (ARRB1) to human chromosome 11q13 67
Detection of an insertion deletion of region 8q13-q21.2 in a patient with Duane syndrome: implications for mapping and cloning a Duane gene 66
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? 66
1q21.1 Duplication Syndrome and Anorectal Malformations: A Literature Review and a New Case 41
The Role of Lifestyle Intervention in Female Fertility: A Modifiable Factor for Preconception Health 31
null 31
First case of two supernumerary markers derived from chromosome 5 and chromosome 8 13
Totale 5.986
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Categoria #
all - tutte 22.828
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 22.828
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021324 0 0 0 0 0 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
2024/2025905 54 170 126 31 29 10 29 29 120 14 114 179
2025/2026986 186 62 174 260 242 62 0 0 0 0 0 0
Totale 5.986