IRIS Institutional Research Information System - OPENBS Open Archive UniBS

BERTINI, Valeria
 Distribuzione geografica
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Continente #
EU - Europa 748
NA - Nord America 552
AS - Asia 148
OC - Oceania 3
SA - Sud America 1
Totale 1.452
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Nazione #
US - Stati Uniti d'America 549
PL - Polonia 524
CN - Cina 93
UA - Ucraina 67
IT - Italia 42
FI - Finlandia 33
DE - Germania 28
HK - Hong Kong 24
FR - Francia 21
VN - Vietnam 20
GB - Regno Unito 12
IE - Irlanda 10
BE - Belgio 4
AU - Australia 3
CA - Canada 3
IN - India 3
SE - Svezia 3
TR - Turchia 3
NL - Olanda 2
RU - Federazione Russa 2
SG - Singapore 2
EC - Ecuador 1
IL - Israele 1
JP - Giappone 1
KR - Corea 1
Totale 1.452
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Città #
Warsaw 524
Fairfield 92
Jacksonville 48
Woodbridge 48
Ashburn 40
Chandler 38
Houston 34
Cambridge 30
Seattle 27
Wilmington 27
Helsinki 26
Hong Kong 24
Beijing 23
Princeton 22
New York 21
Ann Arbor 20
Dong Ket 20
Nanjing 19
Brescia 18
Dearborn 13
Dublin 10
San Diego 9
Shenyang 6
Des Moines 5
Nanchang 5
Rome 5
Brussels 4
Hebei 4
Jinan 4
Los Angeles 4
Phoenix 4
Shanghai 4
Changsha 3
Haikou 3
Jiaxing 3
Verona 3
Zhengzhou 3
Boardman 2
Kunming 2
Lanzhou 2
London 2
Melbourne 2
Milan 2
Munich 2
San Francisco 2
Tianjin 2
Toronto 2
Travagliato 2
Ankara 1
Augusta 1
Baotou 1
Camden 1
Canberra 1
Cankaya 1
Como 1
Denver 1
Fuzhou 1
Guayaquil 1
Hangzhou 1
Islington 1
Izhevsk 1
Markham 1
Nuoro 1
Orange 1
Saint Louis 1
San Mateo 1
Seoul 1
Singapore 1
Sundbyberg 1
Taizhou 1
Tel Aviv 1
Tokyo 1
Umeå 1
Varano de' Melegari 1
Vieste 1
Washington 1
Totale 1.243
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Nome #
SNP array and FISH analysis of a proband with a 22q13.2- 22qter duplication shed light on the molecular origin of the rearrangement 259
ITGB2 mutation combined with deleted ring 21 chromosome in a child with leukocyte adhesion deficiency 248
Generation of induced pluripotent stem cells (iPSC) from an atrial fibrillation patient carrying a KCNA5 p.D322H mutation 238
Generation of induced pluripotent stem cells (iPSC) from an atrial fibrillation patient carrying a PITX2 p.M200V mutation 210
Cytogenetic and molecular characterization of a de-novo t(2p;7p) translocation involving TNS3 and EXOC6B genes in a boy with a complex syndromic phenotype 117
Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype 97
Human iPSC modeling of a familial form of atrial fibrillation reveals a gain of function of If and ICaL in patient-derived cardiomyocytes 76
SNP array and FISH analysis of a proband with a 22q13.2- 22qter duplication shades light on the molecular origin of the rearrangement. 66
Application of SNP-Arrays, FISH and GenotypeColour in Molecular Diagnosis of Mental Retardation 59
Application of SNP-arrays, FISH and genotypecolour in molecular diagnosis of mental retardation 54
Inherited duplication of the pseudoautosomal region Xq28 in a subject with Gilles de la Tourette syndrome and intellectual disability: A case report 54
RNA-Seq of Dermal Fibroblasts from Patients with Hypermobile Ehlers-Danlos Syndrome and Hypermobility Spectrum Disorders Supports Their Categorization as a Single Entity with Involvement of Extracellular Matrix Degrading and Proinflammatory Pathomechanisms 13
Deciphering disease signatures and molecular targets in vascular Ehlers-Danlos syndrome through transcriptome and miRNome sequencing of dermal fibroblasts 11
Totale 1.502
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Categoria #
all - tutte 4.654
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 4.654
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201952 0 0 0 0 0 0 0 0 0 0 30 22
2019/2020449 39 24 22 38 36 56 34 47 40 52 37 24
2020/2021286 12 24 11 32 21 33 21 36 29 27 13 27
2021/202299 4 17 0 2 1 4 5 8 5 19 9 25
2022/2023112 11 1 4 11 14 24 2 14 18 1 5 7
2023/2024116 8 2 13 14 15 27 2 4 25 5 1 0
Totale 1.502