IRIS
GENESIO, RITA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 470
EU - Europa 234
AS - Asia 144
AF - Africa 13
Totale 861
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 468
IT - Italia 146
SG - Singapore 75
CN - Cina 49
NL - Olanda 49
CI - Costa d'Avorio 13
VN - Vietnam 12
FR - Francia 11
IE - Irlanda 9
IN - India 7
FI - Finlandia 6
DE - Germania 4
UA - Ucraina 4
ES - Italia 3
CA - Canada 2
PL - Polonia 2
IL - Israele 1
Totale 861
Salva come PNG Salva come JPEG
Città #
Chandler 114
Singapore 67
Amsterdam 46
Ashburn 40
Santa Clara 24
Beijing 23
Napoli 22
Naples 19
Millbury 17
Des Moines 16
Boston 15
Lawrence 14
Dong Ket 12
Seattle 9
Princeton 8
Wilmington 8
Formia 7
Milan 6
Nanjing 6
Genova 5
Dearborn 4
Jiaxing 4
Montesarchio 4
Woodbridge 4
Brest 3
Fairfield 3
Hebei 3
Jacksonville 3
Barakaldo 2
Caserta 2
Dallas 2
Nanchang 2
New Delhi 2
New York 2
Ottawa 2
Pomigliano D'arco 2
Pozzuoli 2
San Cesareo 2
Shanghai 2
Avellino 1
Boardman 1
Cambridge 1
Campagna 1
Changsha 1
Dublin 1
Ercolano 1
Fort Worth 1
Frankfurt am Main 1
Godiasco 1
Guangzhou 1
Hangzhou 1
Harrisonburg 1
Helsinki 1
Kronberg 1
Misterbianco 1
Munich 1
Nola 1
Palermo 1
Parma 1
Phoenix 1
Redmond 1
Redwood City 1
Rome 1
Salerno 1
San Giovanni Rotondo 1
San Mango 1
Sant'antimo 1
Shefa-'Amr 1
Shenyang 1
Strasbourg 1
Utrecht 1
Valladolid 1
Warsaw 1
Washington 1
Totale 563
Salva come PNG Salva come JPEG
Nome #
Metformin restores the mitochondrial network and reverses mitochondrial dysfunction in Down syndrome cells 79
First trimester ultrasound features of X-linked Opitz syndrome and early molecular diagnosis: case report and review of the literature 58
Mitochondrial dysfunction in down syndrome: molecular mechanisms and therapeutic targets 56
40 Mb duplication in chromosome band 5p13.1p15.33 with 800 kb terminal deletion in a foetus with mild phenotypic features 49
A small 7q11.23 microduplication involving GTF2I in a family with intellectual disability 49
Targeting mitochondrial network architecture in down syndrome and aging 49
Overexpression of Chromosome 21 miRNAs May Affect Mitochondrial Function in the Hearts of Down Syndrome Fetuses 48
Chromosomal Microarray Analysis versus Karyotyping in Fetuses with Increased Nuchal Translucency 48
Human trisomic ipscs from down syndrome fibroblasts manifest mitochondrial alterations early during neuronal differentiation 47
Complex chromosomal rearrangements causing Langer-Giedion syndrome atypical phenotype: Genotype-phenotype correlation and literature review. 45
Alterations in metabolic patterns have a key role in diagnosis and progression of primrose syndrome 43
Short stature and primary ovarian insufficiency possibly due to chromosomal position effect in a balanced X;1 translocation 41
Pioglitazone improves mitochondrial organization and bioenergetics in down syndrome cells 39
M170. GENETIC CHARACTERIZATION OF A COHORT OF PATIENTS AFFECTED BY SCHIZOPHRENIA. THE ROLE FOR RARE STRUCTURAL VARIANTS IN MODULATING TREATMENT RESISTANT ENDOPHENOTYPES: PRELIMINARY DATA 38
A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2 34
Prenatally diagnosed distal 16p11.2 microdeletion with a novel association with congenital diaphragmatic hernia: a case report 33
Apparent recessive inheritance of sideroblastic anemia type 2 due to uniparental isodisomy at the SLC25A38 locus 33
Dual diagnosis in a child with familial SCN8A-related encephalopathy complicated by a 1p13.2 deletion involving NRAS gene 30
Germline mutations and new copy number variants among 40 pediatric cancer patients suspected for genetic predisposition 26
Sensorineural Hearing Loss in a Patient Affected by Congenital Cytomegalovirus Infection: Is It Useful to Identify Comorbid Pathologies? 25
Two cases of 16q12.1q21 deletions and refinement of the critical region 23
Clinical Phenotype, Immunological Abnormalities, and Genomic Findings in Patients with DiGeorge Spectrum Phenotype without 22q11.2 Deletion 20
Case Report: Ophthalmologic Evaluation Over a Long Follow-Up Time in a Patient With Wolfram Syndrome Type 2: Slowly Progressive Optic Neuropathy as a Possible Clinical Finding 14
Totale 927
Salva come PNG Salva come JPEG
Categoria #
all - tutte 4.268
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 4.268
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202061 0 0 0 0 13 5 2 1 8 13 17 2
2020/202168 1 0 9 2 12 0 9 0 15 4 3 13
2021/2022168 1 4 0 7 5 4 0 11 23 15 48 50
2022/2023258 27 19 13 15 34 28 4 30 37 44 7 0
2023/2024151 3 29 9 13 8 13 4 34 6 1 26 5
2024/2025117 44 28 8 7 30 0 0 0 0 0 0 0
Totale 927