ROSSI, Rachele
 Distribuzione geografica
Continente #
NA - Nord America 147
EU - Europa 122
AS - Asia 24
AF - Africa 1
SA - Sud America 1
Totale 295
Nazione #
US - Stati Uniti d'America 140
IT - Italia 55
FR - Francia 30
DE - Germania 14
CN - Cina 10
FI - Finlandia 10
CA - Canada 7
SE - Svezia 6
GB - Regno Unito 4
HK - Hong Kong 3
IN - India 3
AE - Emirati Arabi Uniti 2
RU - Federazione Russa 2
VN - Vietnam 2
CL - Cile 1
IQ - Iraq 1
JP - Giappone 1
LT - Lituania 1
SG - Singapore 1
TW - Taiwan 1
ZA - Sudafrica 1
Totale 295
Città #
Ferrara 29
Santa Cruz 26
Ashburn 11
Lappeenranta 10
Fairfield 8
Bremen 7
Seattle 7
Shanghai 7
Bologna 6
Stockholm 6
Chicago 5
Des Moines 5
Grand Valley 5
London 4
San Diego 4
Trebaseleghe 4
Unterschleissheim 4
Cambridge 3
Houston 3
Las Vegas 3
Los Angeles 3
New York 3
Avon 2
Boardman 2
Central 2
Delhi 2
Dong Ket 2
Montreal 2
Rome 2
Saint Petersburg 2
San Francisco 2
San Jose 2
Solagna 2
Wilmington 2
Albignasego 1
Boulder 1
Brockport 1
Clearwater 1
Crugers 1
Dallas 1
Dehradun 1
Evanston 1
Ferrara di Monte Baldo 1
Genoa 1
Hangzhou 1
Henderson 1
Herndon 1
Lake Forest 1
Lexington 1
Milan 1
Muizenberg 1
Nantes 1
New Orleans 1
Omaha 1
Padova 1
Paris 1
Pasadena 1
Provo 1
Reston 1
Rüsselsheim am Main 1
Taipei 1
Tokyo 1
Tübingen 1
Vilnius 1
Washington 1
Woodbridge 1
Yuen Long San Hui 1
Totale 220
Nome #
Ethnicity-related DMD Genotype Landscapes in European and Non-European Countries, file e309ade3-3b50-3969-e053-3a05fe0a2c94 58
Physical and transcriptional characterization of human urinary stem cell populations, file e309ade2-5afd-3969-e053-3a05fe0a2c94 53
Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family, file e309ade2-1ad6-3969-e053-3a05fe0a2c94 40
RNA-seq in DMD urinary stem cells recognized muscle-related transcription signatures and addressed the identification of atypical mutations by whole-genome sequencing, file e309ade5-88ed-3969-e053-3a05fe0a2c94 30
Solving unsolved rare neurological diseases—a Solve-RD viewpoint, file e309ade4-dee0-3969-e053-3a05fe0a2c94 18
Tumor Necrosis Factor Receptor SF10A (TNFRSF10A) SNPs Correlate With Corticosteroid Response in Duchenne Muscular Dystrophy, file e309ade2-c7c0-3969-e053-3a05fe0a2c94 16
Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype, file e309ade1-3a17-3969-e053-3a05fe0a2c94 14
Solving patients with rare diseases through programmatic reanalysis of genome-phenome data, file e309ade4-e7f2-3969-e053-3a05fe0a2c94 14
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases, file e309ade4-f9a4-3969-e053-3a05fe0a2c94 12
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study, file e309ade2-c0a5-3969-e053-3a05fe0a2c94 10
Should aip gene screening be recommended in family members of FIPA patients with R16H variant?, file e309ade0-37b1-3969-e053-3a05fe0a2c94 9
RNAseq in urine-derived stem cells identified the expression of 308 neuromuscular gene transcripts [NEXT GENERATION SEQUENCING AND EXPERIMENTAL MYOLOGY: P.384], file e309ade1-fbb5-3969-e053-3a05fe0a2c94 5
International-DMD (IDMD): a PTC Therapeutics-supported diagnostic project to widely identify Dystrophin mutations by NGS technologies, file e309ade2-5900-3969-e053-3a05fe0a2c94 4
Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia, file e309ade1-6d4b-3969-e053-3a05fe0a2c94 3
Urine-Derived Stem Cells Express 571 Neuromuscular Disorders Causing Genes, Making Them a Potential in vitro Model for Rare Genetic Diseases, file e309ade5-2daf-3969-e053-3a05fe0a2c94 3
THE PRESENT AND THE FUTURE OF COLLAGEN VI GENES ANALYSIS: OVERVIEW OF CELLULAR MODELS, GENOME AND TRANSCRIPTOME STUDIES, file e309ade5-6a52-3969-e053-3a05fe0a2c94 3
THE PRESENT AND THE FUTURE OF COLLAGEN VI GENES ANALYSIS: OVERVIEW OF CELLULAR MODELS, GENOME AND TRANSCRIPTOME STUDIES, file e309ade5-6a51-3969-e053-3a05fe0a2c94 2
Transcriptomics analysis in collagen VI myopathy: Role of circadian genes using novel fluidic card tools, file e309ade0-f00f-3969-e053-3a05fe0a2c94 1
International-DMD (IDMD): a PTC Therapeutics-supported diagnostic project to widely identify Dystrophin mutations by NGS technologies, file e309ade2-c1b3-3969-e053-3a05fe0a2c94 1
Totale 296
Categoria #
all - tutte 1.687
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 1.687


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20209 0 2 1 0 0 1 5 0 0 0 0 0
2020/202113 0 0 0 1 0 0 0 0 3 0 2 7
2021/202275 0 5 1 10 4 4 1 4 3 3 30 10
2022/2023109 2 6 17 19 17 16 7 6 2 3 12 2
2023/202488 2 2 6 2 3 26 2 13 8 24 0 0
Totale 296