IRIS
ASSELTA, ROSANNA
 Distribuzione geografica
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Continente #
EU - Europa 42
AS - Asia 14
NA - Nord America 14
SA - Sud America 4
AF - Africa 1
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
Totale 77
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Nazione #
IT - Italia 32
US - Stati Uniti d'America 14
CN - Cina 6
EC - Ecuador 4
ID - Indonesia 3
CZ - Repubblica Ceca 2
DE - Germania 2
GB - Regno Unito 2
IE - Irlanda 2
IN - India 2
PH - Filippine 2
AU - Australia 1
CY - Cipro 1
FR - Francia 1
GH - Ghana 1
GR - Grecia 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 77
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Città #
Abbiategrasso 15
Ashburn 6
Shanghai 6
Lecco 5
Quito 4
Council Bluffs 2
Dublin 2
Genoa 2
Marikina City 2
Mumbai 2
Tegal 2
Trieste 2
Triggiano 2
Accra 1
Adelaide 1
Athens 1
Brent 1
Coventry 1
Denver 1
Essen 1
Frankfurt am Main 1
Limassol 1
Pristina 1
Saint Albans 1
San Giovanni Rotondo 1
Srengseng 1
Totale 65
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Nome #
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction., file de164a8f-2a6f-73f5-e053-d805fe0a7be4 18
Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease, file de164a8f-2a6e-73f5-e053-d805fe0a7be4 13
Prospective evaluation of the role of imaging techniques and TMPRSS2:ERG mutation for the diagnosis of clinically significant prostate cancer, file f487e2ed-a086-4be4-abdb-5e777dbbb7f0 10
Clinical relevance of clonal hematopoiesis in persons aged ≥80 years, file de164a8f-24e4-73f5-e053-d805fe0a7be4 7
DNAJC12 and dopa-responsive nonprogressive parkinsonism, file 35b4e136-8121-422f-a0b3-c7d14c5ba0b0 5
Survival and dementia in GBA-associated Parkinson's disease: The mutation matters, file 89a56edd-34ad-4fdd-9c2d-eed22468295a 5
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease, file de164a8f-2a6c-73f5-e053-d805fe0a7be4 4
The expanding spectrum of PRPS1-associated phenotypes: three novel mutations segregating with X-linked hearing loss and mild peripheral neuropathy, file d0f34f0b-cd37-4b1b-8e56-6991a13f644a 3
Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease, file de164a8f-3196-73f5-e053-d805fe0a7be4 3
null, file 1e1a0469-1128-4b2c-bbb2-bc718a8f5749 2
Role of Cytoskeletal Diaphanous-Related Formins in Hearing Loss, file a838fde1-c768-4cd0-b021-f7d85f86ba5c 2
Phenotypic Characterization of Genetically Lowered Human Lipoprotein(a) Levels, file de164a8f-2e79-73f5-e053-d805fe0a7be4 2
Radiomics and gene expression profile to characterise the disease and predict outcome in patients with lung cancer, file de164a8f-34ff-73f5-e053-d805fe0a7be4 2
SLC22A4 Gene in Hereditary Non-syndromic Hearing Loss: Recurrence and Incomplete Penetrance of the p.C113Y Mutation in Northwest Africa, file de164a8f-1b0c-73f5-e053-d805fe0a7be4 1
Totale 77
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Categoria #
all - tutte 559
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 559
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211 0 0 0 0 0 0 0 0 0 1 0 0
2021/202221 0 0 0 0 0 0 0 1 0 0 0 20
2022/202340 2 0 0 0 2 2 8 5 6 2 6 7
2023/202415 0 0 3 0 1 0 3 2 6 0 0 0
Totale 77