IRIS
MORIZIO, Elisena
 Distribuzione geografica
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Continente #
NA - Nord America 1.649
EU - Europa 1.633
AS - Asia 795
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 2
AF - Africa 1
SA - Sud America 1
Totale 4.083
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Nazione #
US - Stati Uniti d'America 1.646
CN - Cina 393
UA - Ucraina 289
IT - Italia 237
SE - Svezia 228
IE - Irlanda 227
GB - Regno Unito 197
DE - Germania 177
IN - India 168
TR - Turchia 149
FR - Francia 136
FI - Finlandia 55
RU - Federazione Russa 45
VN - Vietnam 42
SG - Singapore 24
BE - Belgio 12
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 4.083
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Città #
Chandler 376
Jacksonville 315
Dublin 224
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
Hebei 28
Altamura 27
Kunming 22
Woodbridge 21
Tianjin 19
Washington 18
Los Angeles 17
Shenyang 17
Jiaxing 15
Munich 14
Singapore 14
Hangzhou 13
Jinan 13
Brno 12
Ningbo 11
Pescara 11
Brussels 10
Augusta 8
Helsinki 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
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
Fuzhou 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
Greater Sudbury 1
Guiyang 1
Haikou 1
Harbin 1
Isernia 1
Killorglin 1
La Canada Flintridge 1
Totale 2.543
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Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 142
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 111
Discovering a familial Xp11.4 microduplication: Does the mother matter? 107
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis 101
Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence? 99
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 93
A new case of pure partial 7q duplication 92
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 90
Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly. 88
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 87
I nuovi orizzonti della diagnosi prenatale 86
SHOX mutations detected by FISH and direct sequencing in patients with short stature 86
Characterization of novel genes in AZF regions 86
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 85
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 84
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 81
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 80
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 80
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 78
A case of triploidy detected by crosstrimester test. 78
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 77
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 77
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 76
A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man. 76
Cytogenetic survey of benign prostate hyperplasia 75
Prenatal diagnosis using the triple test 73
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 72
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 71
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 71
Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus 71
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 71
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping 69
Molecular studies in three patients with isodicentric Y chromosome 69
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 68
P53 loss and point mutation are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis 68
FISH analysis in detecting 9p duplication (p22p24) 67
Non-invasive prenatal screening: a 20-year experience in Italy 67
Rhombencephalosynapsis in a severely polymalformed fetus with non-mosaic tetrasomy 9p, in intracytoplasmic-sperm-injection pregnancy. 67
Molecular characterization of two extra marker chromosomes detected at prenatal diagnosis 66
Comparison of combined, stepwise sequential, contingent, and integrated screening in 7292 high-risk pregnant women 65
Genomic organization, physical mapping, and involvement in Yq microdeletions of the VCY2 (BPY 2) gene 65
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 65
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb 62
Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male 62
Effectiveness of crosstrimester test in selecting high-risk pregnant women to undergo invasive prenatal diagnosis 62
De novo complex chromosome rearrangement detected by fluorescence in situ hybridization on amniotic fluid cells 60
Chromosome 11 rearrangements and specific MLL amplification revealed by spectral karyotyping in a patient with refractory anaemia with excess of blasts(RAEB)”. 60
Molecular characterization of an unusual variant t(15;17) detected in an APL patient 59
FISH detection of mixed chimerism in 33 patients submitted to bone marrow transplantation 59
Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay 57
Retrospective investigation of hematopoietic chimerism after BMT by PCR amplification hypervariable DNA regions 56
Detection of an insertion deletion of region 8q13-q21.2 in a patient with Duane syndrome: implications for mapping and cloning a Duane gene 52
Complex chromosome translocation of standard t(8;21) and t(15;17) arise from a two-step mechanism by fluorescence in situ hybridization analysis 50
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? 46
A 343 Italian cohort of patients analysed with array-comparative genomic hybridization: unsolved problems and genetic counselling difficulties 35
null 31
Assignment of the β-arrestin 1 gene (ARRB1) to human chromosome 11q13 25
Totale 4.156
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Categoria #
all - tutte 13.286
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 13.286
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020613 0 52 6 23 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
2024/202561 54 7 0 0 0 0 0 0 0 0 0 0
Totale 4.156