IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

SCUVERA, GIULIETTA
 Distribuzione geografica
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Continente #
NA - Nord America 253
EU - Europa 71
AS - Asia 13
OC - Oceania 1
SA - Sud America 1
Totale 339
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Nazione #
US - Stati Uniti d'America 247
IT - Italia 38
DE - Germania 15
CN - Cina 7
CA - Canada 6
GB - Regno Unito 5
FR - Francia 4
AE - Emirati Arabi Uniti 3
IE - Irlanda 3
NL - Olanda 3
TW - Taiwan 2
UA - Ucraina 2
AU - Australia 1
CL - Cile 1
FI - Finlandia 1
TR - Turchia 1
Totale 339
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Città #
Fairfield 37
Milan 31
Seattle 24
Houston 18
Woodbridge 18
Ashburn 17
Buffalo 12
Cambridge 12
Santa Cruz 12
Wilmington 8
Ann Arbor 5
Chicago 3
Clearwater 3
Dublin 3
Nürnberg 3
Phoenix 3
Southend 3
Wuhan 3
Beijing 2
Las Vegas 2
Los Angeles 2
Mountain View 2
Ottawa 2
San Jose 2
Taipei 2
University Park 2
Antalya 1
Arkadelphia 1
Berlin 1
Brisbane 1
Carson City 1
Dallas 1
Easton 1
Fremont 1
Hamilton 1
Helsinki 1
Jacksonville 1
Leeds 1
Milpitas 1
Nijmegen 1
Palo Alto 1
Portland 1
Reston 1
Riva 1
Rotterdam 1
San Francisco 1
Yellow Springs 1
Totale 252
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Nome #
MIR137 is the key gene mediator of the syndromic obesity phenotype of patients with 1p21.3 microdeletions, file dfa8b998-3bfe-748b-e053-3a05fe0a3a96 140
Autoimmunity and cytokine imbalance in inherited epidermolysis bullosa, file dfa8b997-5e27-748b-e053-3a05fe0a3a96 119
Olfactory Malformations in Mendelian Disorders of the Epigenetic Machinery, file dfa8b9a3-dec0-748b-e053-3a05fe0a3a96 72
Identification of an atypical microdeletion generating the RNF135-SUZ12 chimeric gene and causing a position effect in an NF1 patient with overgrowth, file dfa8b999-31b7-748b-e053-3a05fe0a3a96 8
16p13 microduplication without CREBBP involvement : moving toward a phenotype delineation, file dfa8b998-7e25-748b-e053-3a05fe0a3a96 4
16p13 microduplication without CREBBP involvement : moving toward a phenotype delineation, file dfa8b997-f928-748b-e053-3a05fe0a3a96 3
The absence that makes the difference: choroidal abnormalities in Legius syndrome, file dfa8b99a-932e-748b-e053-3a05fe0a3a96 2
New Insights into Kleefstra Syndrome : Report of Two Novel Cases with Previously Unreported Features and Literature Review, file dfa8b99d-c5ce-748b-e053-3a05fe0a3a96 2
Response to "Characteristics of 2p15-p16.1 microdeletion syndrome : review and description of two additional patients", file dfa8b993-60ef-748b-e053-3a05fe0a3a96 1
Is cutis verticis Gyrata-Intellectual Disability syndrome an underdiagnosed condition? : A case report and review of 62 cases, file dfa8b997-f292-748b-e053-3a05fe0a3a96 1
Perthes disease : A new finding in Floating-Harbor syndrome, file dfa8b99a-3f34-748b-e053-3a05fe0a3a96 1
A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome, file dfa8b99b-7fae-748b-e053-3a05fe0a3a96 1
Progressive bone impairment with age and pubertal development in neurofibromatosis type I, file dfa8b99d-6ef1-748b-e053-3a05fe0a3a96 1
Totale 355
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Categoria #
all - tutte 755
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 755
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201914 0 0 0 0 0 0 0 0 0 0 8 6
2019/202087 4 1 4 16 8 10 8 10 13 4 4 5
2020/202182 4 2 3 5 15 5 14 6 6 8 4 10
2021/202269 6 3 1 5 5 3 7 4 4 4 18 9
2022/202345 0 0 20 11 2 7 0 0 0 1 4 0
2023/202414 0 1 2 0 2 4 0 0 3 2 0 0
Totale 355