statistiche ricercatore

MASERATI, EMANUELA

Distribuzione geografica

Continente	#
EU - Europa	2.997
NA - Nord America	2.121
AS - Asia	585
SA - Sud America	44
AF - Africa	33
OC - Oceania	32
Totale	5.812

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Nazione	#
US - Stati Uniti d'America	2.044
FR - Francia	1.529
DE - Germania	676
IT - Italia	315
CN - Cina	146
VN - Vietnam	96
GB - Regno Unito	89
JP - Giappone	75
IN - India	69
CA - Canada	61
ES - Italia	45
IE - Irlanda	42
RU - Federazione Russa	41
TR - Turchia	38
AU - Australia	31
TW - Taiwan	30
FI - Finlandia	26
HK - Hong Kong	25
CZ - Repubblica Ceca	22
PL - Polonia	21
RO - Romania	21
KR - Corea	20
NL - Olanda	18
GR - Grecia	17
PT - Portogallo	16
ZA - Sudafrica	16
BR - Brasile	15
TH - Thailandia	15
HR - Croazia	14
CL - Cile	13
RS - Serbia	12
BE - Belgio	10
ID - Indonesia	10
IR - Iran	10
MX - Messico	10
UA - Ucraina	10
CH - Svizzera	9
DK - Danimarca	8
EE - Estonia	8
HU - Ungheria	7
IL - Israele	7
BG - Bulgaria	6
PK - Pakistan	6
AE - Emirati Arabi Uniti	5
AR - Argentina	5
AT - Austria	5
EC - Ecuador	5
LB - Libano	5
LT - Lituania	5
ML - Mali	5
NG - Nigeria	5
SE - Svezia	5
SG - Singapore	5
SK - Slovacchia (Repubblica Slovacca)	5
NI - Nicaragua	4
NO - Norvegia	4
PH - Filippine	4
CO - Colombia	3
EG - Egitto	3
JO - Giordania	3
KW - Kuwait	3
MY - Malesia	3
SI - Slovenia	3
CY - Cipro	2
DZ - Algeria	2
IS - Islanda	2
KZ - Kazakistan	2
MK - Macedonia	2
NP - Nepal	2
PE - Perù	2
SA - Arabia Saudita	2
BA - Bosnia-Erzegovina	1
CR - Costa Rica	1
DM - Dominica	1
KE - Kenya	1
LU - Lussemburgo	1
LV - Lettonia	1
MT - Malta	1
NZ - Nuova Zelanda	1
OM - Oman	1
SY - Repubblica araba siriana	1
TN - Tunisia	1
VE - Venezuela	1
Totale	5.812

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Città	#
Fairfield	259
Houston	231
Ann Arbor	127
Woodbridge	126
Ashburn	124
Seattle	109
Buffalo	88
Santa Cruz	84
Cambridge	81
Paris	78
Dong Ket	55
Wilmington	53
Nürnberg	46
Beijing	42
Bologna	42
Chicago	39
Como	38
Dublin	37
Wuhan	30
Boardman	25
Taipei	24
Bengaluru	23
Istanbul	18
Ottawa	18
Rome	18
San Diego	18
Leawood	16
Los Angeles	16
New York	16
Phoenix	16
Hangzhou	15
Muizenberg	14
Shanghai	14
Dallas	13
Las Vegas	13
Belgrade	12
Helsinki	12
Tokyo	12
Hanoi	11
Milan	11
Palermo	11
Ankara	10
Clearwater	10
Montpellier	10
Zagreb	9
Boulder	8
Castenaso	8
Central	8
Santiago	8
Seoul	8
Tallinn	8
Bangkok	7
Madrid	7
Moscow	7
Toronto	7
Valencia	7
Akron	6
Barcelona	6
Guangzhou	6
Jakarta	6
Kurokami	6
Laval	6
Mountain View	6
Mumbai	6
Riva	6
Saint Petersburg	6
Scranton	6
University Park	6
Athens	5
Buenos Aires	5
Cincinnati	5
Costa Mesa	5
Council Bluffs	5
Hong Kong	5
Provo	5
Rochester	5
San Francisco	5
Turin	5
Vancouver	5
Yamashitacho	5
Adelaide	4
Bangalore	4
Brisbane	4
Cercola	4
Chengdu	4
Coimbra	4
Easton	4
Hamburg	4
Hamilton	4
Henderson	4
Hyderabad	4
Lake Forest	4
London	4
Managua	4
Manchester	4
Naples	4
New Orleans	4
Oslo	4
Padova	4
Providence	4
Totale	2.369

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Nome	#
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula, file e2188be5-ffdd-4564-e053-6605fe0a49d6	663
BUSULFAN, CYCLOPHOSPHAMIDE AND MELPHALAN AS CONDITIONING REGIMEN FOR BONE MARROW TRANSPLANTATION IN CHILDREN WITH MYELODYSPLASTIC SYNDROMES., file e2188be5-f817-4564-e053-6605fe0a49d6	544
Graft-versus-leukemia effects after allogeneic bone marrow transplantation are active also in the presence of clones with chromosomal anomalies in addition to the Ph chromosome., file e2188be5-fb74-4564-e053-6605fe0a49d6	424
Transposition of c–abl oncogene in a case of masked Ph chromosome duplicated in blastic phase, file e2188be5-fb72-4564-e053-6605fe0a49d6	418
Constitutional trisomy 8 as first mutation in multistep carcinogenesis: clinical, cytogenetic, and molecular data on three cases., file e2188be5-fb7a-4564-e053-6605fe0a49d6	393
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes, file e2188be6-0103-4564-e053-6605fe0a49d6	321
MLL-MLLT10 fusion in acute monoblastic leukemia: variant complex rearrangements and 11q proximal breakpoint heterogeneity, file e2188be5-fcce-4564-e053-6605fe0a49d6	320
A 45, X male with a Yp/18 translocation., file e2188be5-fb9d-4564-e053-6605fe0a49d6	286
Different breakpoints in Philadelphia chromosome variant translocations and in constitutional and sporadic translocations., file e2188be5-fb9e-4564-e053-6605fe0a49d6	260
A homozygous contiguous gene deletion in chromosome 16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patient, file e2188be6-015f-4564-e053-6605fe0a49d6	255
Roberts Syndrome: phenotypic variation, cytogenetic definition and heterozygote detection, file e2188be5-fb73-4564-e053-6605fe0a49d6	230
Clonal Chromosome Anomalies Affecting Fli1 Mimic Inherited Thrombocytopenia Of The Paris-Trousseau Type, file e2188be6-0163-4564-e053-6605fe0a49d6	208
Novel recurrent chromosome anomalies in Shwachman Diamond syndrome, file e2188be6-d768-4564-e053-6605fe0a49d6	195
A new recurrent chromosome change in pediatric therapy-related myelodysplastic syndrome: unbalanced translocation 1/6 with cryptic duplication of the short arms of chromosome 6, file e2188be6-0053-4564-e053-6605fe0a49d6	167
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis, file e2188be5-ff8f-4564-e053-6605fe0a49d6	150
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498), file e2188be5-fd07-4564-e053-6605fe0a49d6	142
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms, file e2188be6-0456-4564-e053-6605fe0a49d6	138
Cadmium Impairs p53 Activity in HepG2 Cells, file e2188be6-042c-4564-e053-6605fe0a49d6	124
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells, file e2188be5-ffde-4564-e053-6605fe0a49d6	121
Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases, file e2188be7-ab50-4564-e053-6605fe0a49d6	112
Ph-positive CML in blastic phase with monosomy 7 in a Down syndrome patient. Monitoring by interphase cytogenetics and demonstration of maternal allelic loss, file e2188be5-fb7d-4564-e053-6605fe0a49d6	107
Establishment and characterization of a B-cell line derived from a patient with a myelodysplastic syndrome which expresses myelomonocytic and lymphoid markers, file e2188be6-018c-4564-e053-6605fe0a49d6	103
Centralized cytogenetic analysis of pediatric acute leukemia: results of an italian collaborative experience, file e2188be5-fb7c-4564-e053-6605fe0a49d6	73
Myelodysplastic syndromes: the pediatric point of view., file e2188be5-f818-4564-e053-6605fe0a49d6	54
Patau sindrome with long survival in a case of unusual mosaic trisomy 13, file e2188be5-f816-4564-e053-6605fe0a49d6	44
Mesenchymal stem cells from Shwachman–Diamond syndromepatients display normal functions and do not contribute tohematological defects, file e2188be6-0180-4564-e053-6605fe0a49d6	41
MEIOTIC ORIGIN OF TRISOMY IN NEOPLASM: EVIDENCE IN A CASE OF ERYTROLEUKAEMIA, file e2188be5-f9e2-4564-e053-6605fe0a49d6	31
Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome., file e2188be6-bbaf-4564-e053-6605fe0a49d6	13
Novel evidence of karyotype instability in Shwachman Diamond Syndrome, file e2188be7-40f8-4564-e053-6605fe0a49d6	13
Parental Origin of the Deletion Del(20q) in Shwachman-Diamond Patients and Loss of the Paternally Derived Allele of the Imprinted L3MBTL1 Gene, file e2188be6-86e8-4564-e053-6605fe0a49d6	10
DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimation, file e2188be6-e4b2-4564-e053-6605fe0a49d6	5
Microarray expression studies on bone marrow of patients with Shwachman-Diamond syndrome in relation to deletion of the long arm of chromosome 20, other chromosome anomalies or normal karyotype, file e2188be7-596f-4564-e053-6605fe0a49d6	5
Comprehensive characterization of mesenchymal stromal cells from patients with Fanconi anaemia., file e2188be6-2f63-4564-e053-6605fe0a49d6	3
gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML, file e2188be7-11c3-4564-e053-6605fe0a49d6	3
Expression studies in patients with Shwachman Diamond syndrome in relation to clonal chromosome anomalies in bone marrow, file e2188be7-40f6-4564-e053-6605fe0a49d6	3
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning, file e2188be6-1e31-4564-e053-6605fe0a49d6	2
Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases, file e2188be6-5940-4564-e053-6605fe0a49d6	2
Molecular Mechanisms Generating and Stabilizing Terminal 22q13 Deletions in 44 Subjects with Phelan/McDermid Syndrome, file e2188be6-a81e-4564-e053-6605fe0a49d6	1
Totale	5.984

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Categoria	#
all - tutte	11.017
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	11.017

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2018/2019	285	0	0	0	0	0	0	0	0	0	83	111	91
2019/2020	806	83	84	66	120	67	60	61	54	73	45	42	51
2020/2021	633	27	65	31	48	58	62	44	35	63	55	60	85
2021/2022	882	68	86	50	137	124	26	57	42	47	32	152	61
2022/2023	727	35	53	141	94	45	67	47	59	30	33	76	47
2023/2024	1.721	34	47	44	23	238	36	609	283	375	32	0	0
Totale													5.984