IRIS
MORIZIO, Elisena
 Distribuzione geografica
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Continente #
NA - Nord America 1.652
EU - Europa 1.596
AS - Asia 777
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 2
AF - Africa 1
SA - Sud America 1
Totale 4.031
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Nazione #
US - Stati Uniti d'America 1.649
CN - Cina 397
UA - Ucraina 292
IT - Italia 246
IE - Irlanda 237
SE - Svezia 234
GB - Regno Unito 198
IN - India 170
DE - Germania 164
TR - Turchia 149
FR - Francia 136
FI - Finlandia 53
VN - Vietnam 42
BE - Belgio 12
RO - Romania 12
IL - Israele 8
RU - Federazione Russa 5
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
CZ - Repubblica Ceca 1
EC - Ecuador 1
JP - Giappone 1
SC - Seychelles 1
Totale 4.031
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Città #
Chandler 385
Jacksonville 319
Dublin 233
Southend 169
Princeton 116
Dearborn 101
Izmir 94
Nanjing 94
Ashburn 86
Chieti 82
Beijing 81
Ann Arbor 55
Grafing 52
Cambridge 51
Wilmington 51
Nanchang 43
Dong Ket 40
Boardman 39
Hebei 28
Altamura 27
Kunming 22
Woodbridge 21
Tianjin 19
Washington 19
Shenyang 18
Jiaxing 15
Hangzhou 13
Jinan 13
Ningbo 11
Brussels 10
Pescara 9
Augusta 8
Kocaeli 8
Bangalore 7
Düsseldorf 7
Grevenbroich 7
Norwalk 7
San Mateo 7
Helsinki 6
Auburn Hills 5
Guangzhou 5
Hefei 5
Lanzhou 5
New York 5
Termoli 5
Atessa 4
Bucharest 4
Cluj-napoca 4
Los Angeles 4
Montesilvano Marina 4
Mumbai 4
Ardabil 3
Changchun 3
Changsha 3
Kuala Lumpur 3
Melegnano 3
Milan 3
Stockholm 3
Teramo 3
Zhengzhou 3
Abu Sinan 2
Bologna 2
Edinburgh 2
Fuzhou 2
Hanoi 2
Kfar Saba 2
Leawood 2
Melendugno 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
Chicago 1
Collecorvino 1
Cuenca 1
Delhi 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
L’Aquila 1
Macerata 1
Monmouth Junction 1
Moscow 1
Totale 2.513
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Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 137
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 107
Discovering a familial Xp11.4 microduplication: Does the mother matter? 102
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 101
Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence? 96
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis 92
A new case of pure partial 7q duplication 89
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 89
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 86
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 85
Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly. 85
I nuovi orizzonti della diagnosi prenatale 85
SHOX mutations detected by FISH and direct sequencing in patients with short stature 85
Characterization of novel genes in AZF regions 84
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 83
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 82
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 79
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 77
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 77
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 76
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 76
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 75
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 75
A case of triploidy detected by crosstrimester test. 75
Prenatal diagnosis using the triple test 72
A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man. 72
Cytogenetic survey of benign prostate hyperplasia 71
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 71
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 69
Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus 69
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 67
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 67
Molecular studies in three patients with isodicentric Y chromosome 67
P53 loss and point mutation are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis 67
Rhombencephalosynapsis in a severely polymalformed fetus with non-mosaic tetrasomy 9p, in intracytoplasmic-sperm-injection pregnancy. 67
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 66
Genomic organization, physical mapping, and involvement in Yq microdeletions of the VCY2 (BPY 2) gene 65
Molecular characterization of two extra marker chromosomes detected at prenatal diagnosis 65
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping 64
FISH analysis in detecting 9p duplication (p22p24) 63
Non-invasive prenatal screening: a 20-year experience in Italy 63
Comparison of combined, stepwise sequential, contingent, and integrated screening in 7292 high-risk pregnant women 62
Effectiveness of crosstrimester test in selecting high-risk pregnant women to undergo invasive prenatal diagnosis 61
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 61
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb 60
Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male 60
De novo complex chromosome rearrangement detected by fluorescence in situ hybridization on amniotic fluid cells 59
Chromosome 11 rearrangements and specific MLL amplification revealed by spectral karyotyping in a patient with refractory anaemia with excess of blasts(RAEB)”. 59
Molecular characterization of an unusual variant t(15;17) detected in an APL patient 58
FISH detection of mixed chimerism in 33 patients submitted to bone marrow transplantation 58
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 54
Detection of an insertion deletion of region 8q13-q21.2 in a patient with Duane syndrome: implications for mapping and cloning a Duane gene 51
Complex chromosome translocation of standard t(8;21) and t(15;17) arise from a two-step mechanism by fluorescence in situ hybridization analysis 48
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? 44
Isolation and enrichment of circulating fetal cells for nipd: An overview 32
null 31
A 343 Italian cohort of patients analysed with array-comparative genomic hybridization: unsolved problems and genetic counselling difficulties 30
Assignment of the β-arrestin 1 gene (ARRB1) to human chromosome 11q13 23
Totale 4.151
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Categoria #
all - tutte 11.955
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 11.955
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019145 0 0 0 0 0 0 0 0 0 3 1 141
2019/2020865 227 52 6 23 94 80 125 78 26 73 77 4
2020/2021484 59 2 60 5 19 78 13 4 95 66 29 54
2021/2022321 13 5 4 54 40 56 4 24 13 3 28 77
2022/20231.081 72 139 67 125 101 211 58 96 152 11 28 21
2023/2024344 34 12 42 11 29 135 62 16 1 2 0 0
Totale 4.151