statistiche per BONORA, ELENA

Distribuzione geografica

Continente	#
NA - Nord America	3377
EU - Europa	2092
AS - Asia	748
AF - Africa	75
Continente sconosciuto - Info sul continente non disponibili	17
SA - Sud America	5
OC - Oceania	2
Totale	6316

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Nazione	#
US - Stati Uniti d'America	3374
GB - Regno Unito	761
IT - Italia	493
CN - Cina	375
SE - Svezia	245
VN - Vietnam	177
IN - India	165
UA - Ucraina	147
RU - Federazione Russa	123
FR - Francia	106
DE - Germania	73
ZA - Sudafrica	66
EE - Estonia	64
BG - Bulgaria	36
EU - Europa	16
HR - Croazia	11
JP - Giappone	10
SC - Seychelles	9
CH - Svizzera	7
GR - Grecia	7
TR - Turchia	6
CL - Cile	5
NL - Olanda	5
UZ - Uzbekistan	5
RO - Romania	4
CA - Canada	3
ES - Italia	3
IR - Iran	3
SK - Slovacchia (Repubblica Slovacca)	3
AU - Australia	2
LB - Libano	2
A2 - ???statistics.table.value.countryCode.A2???	1
AE - Emirati Arabi Uniti	1
AT - Austria	1
BD - Bangladesh	1
CY - Cipro	1
FI - Finlandia	1
IE - Irlanda	1
PK - Pakistan	1
PL - Polonia	1
SA - Arabia Saudita	1
Totale	6316

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Città	#
Southend	694
Fairfield	612
Ann Arbor	356
Seattle	282
Woodbridge	275
Houston	262
Ashburn	252
Wilmington	237
Cambridge	228
Bologna	176
Dong Ket	123
Redmond	118
Jacksonville	83
Nanjing	78
Westminster	78
Padova	65
Saint Petersburg	38
Sofia	36
Shenyang	35
San Diego	34
Jinan	30
Dearborn	28
Tianjin	26
Changsha	25
Falls Church	24
Nanchang	24
Hebei	22
Haikou	20
Redwood City	20
Beijing	18
Abano Terme	17
Zhengzhou	14
Kuban	13
Guangzhou	12
Jiaxing	12
Milan	12
Phoenix	12
Costa Mesa	9
Fuzhou	9
Mahé	9
Taizhou	8
Frankfurt Am Main	6
Hangzhou	6
Tokyo	6
Verona	6
Chengdu	5
Gallo	4
Istanbul	4
Lausanne	4
Portici	4
San Jose	4
Selargius	4
Taiyuan	4
Ascoli Piceno	3
Bratislava	3
Castel Maggiore	3
Formigine	3
Leawood	3
Muizenberg	3
Napoli	3
Ningbo	3
Radcliffe	3
Ravenna	3
Rome	3
San Venanzo	3
Serra	3
Shanghai	3
Udine	3
Ardabil	2
Bovolone	2
Caserta	2
Chicago	2
Chongqing	2
Dallas	2
Darfo	2
Den Haag	2
Ferrara	2
Frattamaggiore	2
Fremont	2
Grafing	2
Granarolo	2
Hernani	2
Jesi	2
Köln	2
Lanzhou	2
Norwalk	2
Pieve Di Cadore	2
Provo	2
Reghin	2
Rochester	2
San Pietro In Casale	2
Shenzhen	2
Torino	2
Toronto	2
Trieste	2
Zelarino	2
Albany	1
Amsterdam	1
Arconate	1
Atlanta	1
Totale	4588

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Nome	#
Syndromic intellectual disability: A new phenotype caused by an aromatic amino acid decarboxylase gene (DDC) variant.	132
A Greek Family with a Follicular Variant of Familial Papillary Thyroid Carcinoma: TCO, MNG1, fPTC/PRN, and NMTC1 Excluded as Susceptibility Loci	128
BRAF exon 15 mutations in papillary carcinoma and adjacent thyroid parenchyma: A search for the early molecular events associated with tumor development	115
A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder.	114
Apolipoprotein B is a new target of the GDNF/RET and ET-3/EDNRB signalling pathways	111
Analysis of a Sardinian Multiplex Family with Autism Spectrum Disorder Points to Post-Synaptic Density Gene Variants and Identifies CAPG as a Functionally Relevant Candidate Gene	110
Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma	109
An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells.	108
The RET51/FKBP52 complex and its involvement in Parkinson disease.	107
Neuroactive Steroids in First-Episode Psychosis: A Role for Progesterone?	105
null	105
Mutant MYO1F alters the mitochondrial network and induces tumor proliferation in thyroid cancer	105
Gut epithelial and vascular barrier abnormalities in patients with chronic intestinal pseudo-obstruction	105
TOM: a web-based integrated approach for identification of candidate disease genes	105
Expression of the Bitter taste receptor, T2R38, in enteroendocrine cells of the colonic mucosa of overweight/obese vs. Lean subjects	103
TOM: enhancement and extension of a tool suite for in silico approaches to multigenic complex disorders.	103
Definition of miRNAs expression profile in glioblastoma samples: the relevance of non-neoplastic brain reference.	101
Expression of 19 microRNAs in glioblastoma and comparison with other brain neoplasia of grades I–III	99
Enteric neuropathies: Yesterday, Today and Tomorrow	98
Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients.	96
INPP4B overexpression and c-KIT downregulation in human achalasia.	95
miRNAs expression analysis in paired fresh/frozen and dissected formalin fixed and paraffin embedded glioblastoma using real-time pCR.	93
Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III	92
Novel Mutations in Neurogenic Chronic Intestinal Pseudo-Obstruction Identified by High-Throughput Sequencing	92
null	91
Somatic APC mosaicism and oligogenic inheritance in genetically unsolved colorectal adenomatous polyposis patients	88
Integrated web-based approach to multigenic diseases	88
Mutations in RAD21 Disrupt Regulation of APOB in Patients With Chronic Intestinal Pseudo-Obstruction.	87
Incidence of neuroepithelial primary brain tumors among adult population of Emilia-Romagna Region, Italy	86
GSTT1 and M1 polymorphisms in Hurthle thyroid cancer patients	86
The FAGenomicH project: Towards a whole candidate gene approach to identify markers associated with fatness and production traits in pigs and investigate the pig as a model for human obesity	85
null	85
Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.	85
The tyrosine kinase receptor RET interacts in vivo with aryl hydrocarbon receptor-interacting protein to alter survivin availability.	84
Molecular features of thyroid oncocytic tumors	83
Expression of RAD21 immunoreactivity in myenteric neurons of the human and mouse small intestine	83
Genetic Predisposition to Familial Nonmedullary Thyroid Cancer: An Update of Molecular Findings and State-of-the-Art Studies	82
C620R mutation of the murine ret proto-oncogene: loss of function effect in homozygotes and possible gain of function effect in heterozygotes.	82
Oncocytic glioblastoma: a glioblastoma showing oncocytic changes and increased mitochondrial DNA copy number	81
Which elderly newly diagnosed glioblastoma patients can benefit from radiotherapy and temozolomide? A PERNO prospective study	80
Protective Actions of Epithelial 5-Hydroxytryptamine 4 Receptors in Normal and Inflamed Colon	79
A mutation screening of oncogenes, tumor suppressor gene TP53 and nuclear encoded mitochondrial complex I genes in oncocytic thyroid tumors	78
Su1852 The 5-HT4 Selective Agonist Prucalopride Exerts Neural and Epithelial Protective Effects In Vitro	77
null	76
Familial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family	75
Genomic profiles of primary and metastatic esophageal adenocarcinoma identified via digital sorting of pure cell populations: Results from a case report	75
Pattern of care and effectiveness of treatment for glioblastoma patients in the real world: Results from a prospective population-based registry. Could survival differ in a high-volume center?	74
Novel germline variants identified in the inner mitochondrial membrane transporter TIMM44 and their role in predisposition to oncocytic thyroid carcinomas.	74
Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumours.	73
The FOXE1 locus is a major genetic determinant for familial nonmedullary thyroid carcinoma	72
Distribution and Characterization of RAD21 Immunoreactivity in Mouse and Human Enteric Neurons	72
DICER1 mutations in familial multinodular goiter with and without ovarian sertoli-leydig cell tumors	70
Association of the interleukin-4/interleukin-4 receptor genetic variants with hand osteoathrtitis.	68
Dealing With BRCA1/2 unclassified variants in a cancer genetics clinic: Does cosegregation analysis help?	68
Aryl hydrocarbon receptor interacting protein mutations seem not to associate with familial non-medullary thyroid cancer.	67
L’encefalomiopatia Mitocondriale Neurogastrointestinale (MNGIE): Il Fegato Come Nuova Fonte Di Timidina Fosforilasi	67
HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain	67
EXCAVATOR: detecting copy number variants from whole-exome sequencing data.	65
Interleukin-4/interleukin-4 receptor gene polymorphisms in hand osteoarthritis	64
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits	64
Identification of BRCA1/2 p.Ser1613Gly, p.Pro871Leu, p.Lys1183Arg, p.Glu1038Gly, p.Ser1140Gly, p.Ala2466Val, p.His2440Arg variants in women under 45 years old with breast nodules suspected of having breast cancer in Burkina Faso	64
Su2019 Functional Characterization of a Novel RAD21 Mutation in Familial Chronic Intestinal Pseudo-Obstruction (CIPO)	62
null	62
Mitochondrial Neurogastrointestinal Encephalomyopathy: The Liver As a Tissue Source to Restore Thymidine Phosphorylase Activity	60
Mutation screening and association analysis of six candidate genes for autism on chromosome 7q.	58
null	57
null	56
Mast cell-nerve interactions correlate with bloating and abdominal pain severity in patients with non-celiac gluten / wheat sensitivity	53
Rasal1 and ros1 gene variants in hereditary breast cancer	52
Whole Genome Sequencing Prioritizes CHEK2, EWSR1, and TIAM1 as Possible Predisposition Genes for Familial Non-Medullary Thyroid Cancer	52
Novel mutations in mitochondrial respiratory complexes and their functional relevance in thyroid oncocytoma.	51
Identifying Gene-Environment Interactions in Schizophrenia: Contemporary Challenges for Integrated, Large-scale Investigations	51
Whole genome sequencing of familial non-medullary thyroid cancer identifies germline alterations in MAPK/ERK and PI3K/AKT signaling pathways	50
The FAGenomicH project: a whole candidate gene approach to identify markers associated with fatness traits in pigs and investigate the pig as a model for human obesity	48
A germline mutation in the POT1 gene is a candidate for familial non-medullary thyroid cancer	47
Intestinal epithelial barrier disfunction in patients with chronic intestinal pseudo-obstruction	43
Evidence of RET/GDNF-related apolipoprotein B (APOB) activation and altered expression in patients with chronic intestinal pseudo-obstruction (CIPO)	42
Targeted Sequencing of Sorted Esophageal Adenocarcinoma Cells Unveils Known and Novel Mutations in the Separated Subpopulations	42
The Liver as a New Tissue Source of Thymidine Phosphorylase for Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE)	38
mtDNA inherited and somatic variability in Alzheimer Disease	37
Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): The liver as a new source of thymidine phosphorylase	37
Liver tissue as new source to replace thymidine phosphorylase activity in mitochondrial neurogastrointestinal encephalomyopathy	36
The Liver As a Tissue Source to Restore Thymidine Phosphorylase Activity	36
mtDNA inherited and somatic variability in Alzheimer’s disease	33
Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy	32
null	30
null	20
Genetics of familial non-medullary thyroid carcinoma (FNMTC)	19
null	12
null	10
Totale	6602

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Categoria	#
all - tutte	6602
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	6602

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2016/2017	33	0	0	0	0	0	0	0	0	0	0	32	1
2017/2018	179	0	0	0	1	5	8	3	2	1	0	149	10
2018/2019	577	35	65	16	52	8	67	27	45	44	93	47	78
2019/2020	2480	323	59	27	136	265	243	311	346	386	160	104	120
2020/2021	1522	273	98	51	91	91	78	100	92	161	99	81	307
2021/2022	1750	118	69	112	136	195	138	52	171	92	220	447	0
Totale													6602

CRIS Current Research Information System

statistiche per BONORA, ELENA