POLIMANTI, RENATO
 Distribuzione geografica
Continente #
NA - Nord America 2.596
EU - Europa 199
AS - Asia 128
SA - Sud America 3
Continente sconosciuto - Info sul continente non disponibili 1
Totale 2.927
Nazione #
US - Stati Uniti d'America 2.596
SG - Singapore 82
IT - Italia 43
CN - Cina 39
DE - Germania 38
IE - Irlanda 34
RU - Federazione Russa 21
UA - Ucraina 21
FI - Finlandia 9
GB - Regno Unito 9
CZ - Repubblica Ceca 7
SE - Svezia 5
FR - Francia 4
BE - Belgio 2
CL - Cile 2
ID - Indonesia 2
KR - Corea 2
BR - Brasile 1
DK - Danimarca 1
ES - Italia 1
EU - Europa 1
GR - Grecia 1
HK - Hong Kong 1
IN - India 1
MD - Moldavia 1
NL - Olanda 1
PL - Polonia 1
SA - Arabia Saudita 1
Totale 2.927
Città #
Wilmington 892
Houston 725
Woodbridge 415
Chandler 112
Fairfield 99
Singapore 72
Cambridge 37
Seattle 36
Ashburn 34
Dublin 34
Ann Arbor 29
Medford 27
Rome 19
Munich 17
Dearborn 13
Lawrence 12
New York 12
Beijing 11
Santa Clara 11
Helsinki 9
Jacksonville 8
Brno 7
Nanjing 7
San Diego 5
Kunming 4
Florence 3
London 3
Moscow 3
Brussels 2
Engelhard 2
Guangzhou 2
Hefei 2
Jakarta 2
Locate di Triulzi 2
Milan 2
Mountain View 2
Nanchang 2
Norwalk 2
Redwood City 2
Roccagorga 2
Roseto degli Abruzzi 2
Saint Petersburg 2
San Mateo 2
Scicli 2
Verona 2
Anzio 1
Athens 1
Changsha 1
Chisinau 1
Falls Church 1
Frankfurt am Main 1
Ganzhou 1
Hangzhou 1
Hanover 1
Irving 1
Kilburn 1
Kraków 1
Paris 1
Redmond 1
Rotterdam 1
San Francisco 1
Seoul 1
Shanghai 1
Shenzhen 1
São Paulo 1
Taizhou 1
Turin 1
Tübingen 1
Wuhan 1
Totale 2.714
Nome #
Explorative genetic association study of GSTT2B copy number variant in complex disease risks 344
Effect of the GSTM1 gene deletion on glycemic variability, sympatho-vagal balance and arterial stiffness in patients with metabolic syndrome, but without diabetes 331
GSTA1 gene variation associated with gestational hypertension and its involvement in pregnancy-related pathogenic conditions 316
GPX1*Pro198Leu AND GPX3 rs2070593 as genetic risk markers for Italian asthmatic patients 309
Non-coding variants contribute to the clinical heterogeneity of TTR amyloidosis 305
Haplotype differences for copy number variants in the 22q11.23 region among human populations: A pigmentation-based model for selective pressure 294
Population diversity of the genetically determined TTR expression in human tissues and its implications in TTR amyloidosis 292
Most recent common ancestor of TTR Val30Met mutation in Italian population and its potential role in genotype-phenotype correlation 271
Deletion polymorphism of GSTT1 gene as protective marker for allergic rhinitis 254
From adaptive licensing to adaptive pathways: Delivering a flexible life-span approach to bring new drugs to patients 105
Phenome-wide association study of TTR and RBP4 genes in 361,194 individuals reveals novel insights in the genetics of hereditary and wildtype transthyretin amyloidoses 71
Epigenetic profiling of Italian patients identified methylation sites associated with hereditary transthyretin amyloidosis 50
Epigenomic Profiles of African-American Transthyretin Val122Ile Carriers Reveals Putatively Dysregulated Amyloid Mechanisms 19
Cross-ancestry genome-wide association studies identified heterogeneous loci associated with differences of allele frequency and regulome tagging between participants of European descent and other ancestry groups from the UK Biobank. 13
Totale 2.974
Categoria #
all - tutte 7.329
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 7.329


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020550 0 0 0 0 0 100 86 74 91 62 74 63
2020/2021512 56 62 60 64 50 50 59 48 13 21 23 6
2021/2022125 6 11 5 1 3 15 6 8 6 15 9 40
2022/2023228 15 27 10 41 13 50 20 14 27 0 7 4
2023/202459 12 5 4 3 3 13 1 8 0 0 0 10
2024/2025178 24 70 53 17 9 5 0 0 0 0 0 0
Totale 2.974