statistiche ricercatore

FANTASIA, DONATELLA

Distribuzione geografica

Continente	#
NA - Nord America	424
EU - Europa	420
AS - Asia	188
AF - Africa	1
SA - Sud America	1
Totale	1.034

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Nazione	#
US - Stati Uniti d'America	424
CN - Cina	99
IT - Italia	90
UA - Ucraina	69
GB - Regno Unito	56
IE - Irlanda	54
SE - Svezia	53
IN - India	44
DE - Germania	42
TR - Turchia	37
FR - Francia	34
FI - Finlandia	14
BE - Belgio	4
VN - Vietnam	4
RU - Federazione Russa	3
IL - Israele	2
EC - Ecuador	1
IR - Iran	1
RO - Romania	1
SC - Seychelles	1
TW - Taiwan	1
Totale	1.034

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Città	#
Chandler	107
Jacksonville	81
Dublin	54
Southend	50
Princeton	29
Nanjing	25
Izmir	24
Dearborn	20
Beijing	17
Grafing	17
Cambridge	13
Wilmington	12
Ann Arbor	11
Nanchang	11
Altamura	10
Ashburn	9
Boardman	9
Chieti	9
Tianjin	8
Hebei	7
Kunming	7
Shenyang	7
Pescara	6
Los Angeles	5
Woodbridge	5
Brussels	4
Dong Ket	4
Hangzhou	4
New York	4
Grevenbroich	3
Norwalk	3
Auburn Hills	2
Changsha	2
Düsseldorf	2
Hefei	2
Jiaxing	2
Kfar Saba	2
Melendugno	2
Ningbo	2
Teramo	2
Washington	2
Ürümqi	2
Ancona	1
Ardabil	1
Augusta	1
Bologna	1
Bucharest	1
Changchun	1
Cuenca	1
Edinburgh	1
Fucecchio	1
Harbin	1
Helsinki	1
Isernia	1
Jinan	1
L'aquila	1
Lappeenranta	1
Milan	1
Monmouth Junction	1
Moscow	1
Mumbai	1
Narni	1
Orange	1
Roseto Degli Abruzzi	1
Sambuceto	1
Stockholm	1
Taipei	1
Totale	622

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Nome	#
Detection of chromosomal aneuploidies in fetal cells isolated from maternal blood using single-chromosome dual-probe FISH analysis.	112
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis	93
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
SHOX mutations detected by FISH and direct sequencing in patients with short stature	85
Characterization of novel genes in AZF regions	84
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
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA	69
Fluorescence in situ hybridization analysis of minimal residual disease and the relevance of the der(9) deletion in imatinib-treated patients with chronic myeloid leukemia.	65
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping	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	61
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb	60
Chromosome 11 rearrangements and specific MLL amplification revealed by spectral karyotyping in a patient with refractory anaemia with excess of blasts(RAEB)”.	59
Detection of chromosomal aneuploidies in fetal cells isolated from maternal blood using single-chromosome dual-probe FISH analysis	59
Totale	1.058

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Categoria	#
all - tutte	3.056
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	3.056

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2018/2019	37	0	0	0	0	0	0	0	0	0	0	0	37
2019/2020	212	54	14	1	9	23	16	26	22	5	21	20	1
2020/2021	89	15	0	16	0	4	18	0	0	11	14	4	7
2021/2022	80	0	2	2	12	3	18	0	7	7	0	8	21
2022/2023	292	18	45	24	30	26	52	11	22	40	5	8	11
2023/2024	71	7	3	3	4	6	28	14	0	1	4	1	0
Totale													1.058