IRIS
CONTI, ANNA
 Distribuzione geografica
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Continente #
NA - Nord America 568
EU - Europa 313
AS - Asia 104
AF - Africa 8
OC - Oceania 3
Totale 996
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Nazione #
US - Stati Uniti d'America 563
IT - Italia 173
CN - Cina 72
NL - Olanda 45
IE - Irlanda 28
FI - Finlandia 21
UA - Ucraina 19
IN - India 12
VN - Vietnam 12
CI - Costa d'Avorio 8
DE - Germania 7
FR - Francia 6
GB - Regno Unito 6
CA - Canada 5
SG - Singapore 5
NZ - Nuova Zelanda 3
BE - Belgio 2
PL - Polonia 2
ES - Italia 1
IL - Israele 1
JP - Giappone 1
KR - Corea 1
RO - Romania 1
SE - Svezia 1
SI - Slovenia 1
Totale 996
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Città #
Chandler 140
Amsterdam 38
Ashburn 38
Napoli 30
Beijing 28
Jacksonville 24
Millbury 23
Princeton 22
Nanjing 21
Woodbridge 20
Boston 16
Naples 16
Des Moines 12
Dong Ket 12
Wilmington 12
Seattle 11
Lawrence 7
Genova 6
Pune 6
Ottawa 5
Caserta 4
Changsha 4
Falls Church 4
Milan 4
Nanchang 4
Singapore 4
Brest 3
Dearborn 3
Dunedin 3
Hebei 3
Jiaxing 3
Montesarchio 3
Boardman 2
Caivano 2
Castellammare di Stabia 2
Dublin 2
Eboli 2
Fairfield 2
Indiana 2
New Delhi 2
Pomigliano D'arco 2
Pozzuoli 2
Redmond 2
Rosignano Marittimo 2
Salerno 2
Shanghai 2
Shenyang 2
Tianjin 2
Waanrode 2
Acerra 1
Augusta 1
Baranzate 1
Cambridge 1
Campagna 1
Changchun 1
Cormeilles-en-Parisis 1
Ercolano 1
Formia 1
Godiasco 1
Hangzhou 1
Harrisonburg 1
Houston 1
Kitamachi 1
Kunming 1
Misterbianco 1
Mountain View 1
New York 1
Nola 1
Norwalk 1
Palermo 1
Parma 1
Phoenix 1
Quarto 1
Redwood City 1
Rome 1
San Giovanni Rotondo 1
San Mango 1
Sant'antimo 1
Shefa-'Amr 1
Valladolid 1
Warsaw 1
Washington 1
Yeoncheon-gun 1
Totale 597
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Nome #
Metformin restores the mitochondrial network and reverses mitochondrial dysfunction in Down syndrome cells 75
Inverted duplication of 15q with terminal deletion in a multiple malformed newborn with intrauterine growth failure and lethal phenotype 57
Mitochondrial dysfunction in down syndrome: molecular mechanisms and therapeutic targets 51
First trimester ultrasound features of X-linked Opitz syndrome and early molecular diagnosis: case report and review of the literature 50
Prenatal diagnosis of 22q11 microdeletion in a fetus with a conotruncal heart defect 45
Constitutional chromothripsis involving the critical region of 9q21.13 microdeletion syndrome 43
Human trisomic ipscs from down syndrome fibroblasts manifest mitochondrial alterations early during neuronal differentiation 42
40 Mb duplication in chromosome band 5p13.1p15.33 with 800 kb terminal deletion in a foetus with mild phenotypic features 41
Chromosomal Microarray Analysis versus Karyotyping in Fetuses with Increased Nuchal Translucency 40
Overexpression of Chromosome 21 miRNAs May Affect Mitochondrial Function in the Hearts of Down Syndrome Fetuses 38
Human miRNAs on chromosome 21 are differentially expressed in Down syndrome fetal hearts 37
Mild Wolf-Hirschhorn phenotype and partial GH deficiency in a patient with a 4p terminal deletion. 36
Short stature and primary ovarian insufficiency possibly due to chromosomal position effect in a balanced X;1 translocation 36
Gene Expression Profile in Liver Transplantation and the Influence of Gene Dysregulation Occurring in Deceased Donor Grafts 35
Targeting mitochondrial network architecture in down syndrome and aging 35
Selective cognitive impairment and tall stature due to chromosome 19 supernumerary ring. 34
Chronic pro-oxidative state and mitochondrial dysfunctions are more pronounced in fibroblasts from Down syndrome foeti with congenital heart defects 33
Pioglitazone improves mitochondrial organization and bioenergetics in down syndrome cells 32
Differential expression of human chromosome 21 miRNAs in Down syndrome fetal hearts 30
Clinical Description of a Patient Carrying the Smallest Reported Deletion Involving 10p14 Region 30
Prenatally diagnosed distal 16p11.2 microdeletion with a novel association with congenital diaphragmatic hernia: a case report 30
Variegated silencing of a large Xq region causes hypomelanosis of Ito phenotype in a case of balanced X;2 translocation. 29
Variegated silencing throughepigenetic modifications of a large Xq region in a case of balanced X;2translocation with Incontinentia Pigmenti-like phenotype 28
NRIP1/RIP140 siRNA-mediated attenuation counteracts mitochondrial dysfunction in Down syndrome 28
Human miRNAs on chromosome 21 are differentially expressed in Down syndrome fetal hearts. 27
Trascriptome alterations and functional profiling of the heart of human fetuses with chromosome 21 trisomy. 24
Identification of Novel Pax8 Targets in FRTL-5 Thyroid Cells by Gene Silencing and Expression Microarray Analysis 22
Overexpression of the Hsa21 Transcription Factor RUNX1 Modulates the Extracellular Matrix in Trisomy 21 Cells 20
Down Syndrome Fetal Fibroblasts Display Alterations of Endosomal Trafficking Possibly due to SYNJ1 Overexpression 17
Pure 16q21q22.1 deletion in a complex rearrangement possibly caused by a chromothripsis event. 16
Short 9q interstitial deletion in a neonate with lethal non-immune hydrops. 13
Totale 1.074
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Categoria #
all - tutte 3.904
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 3.904
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20192 0 0 0 0 0 0 0 0 0 1 1 0
2019/2020126 36 2 7 9 16 2 2 1 5 21 17 8
2020/202190 1 3 7 5 13 11 6 0 19 4 9 12
2021/2022214 1 4 0 2 4 6 2 12 42 24 56 61
2022/2023324 33 17 20 27 41 30 6 41 53 39 13 4
2023/2024142 8 39 9 14 8 28 7 24 3 2 0 0
Totale 1.074