ASSELTA, ROSANNA

ASSELTA, ROSANNA  

Dipartimento di Biotecnologie Mediche e Medicina Traslazionale  

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Risultati 1 - 20 di 175 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Gynecologic and obstetric complications in women with congenital fibrinogen disorders: insights from the Prospective Rare Bleeding Disorders Database 2025 Mohsenian, SaminPalla, RobertaMenegatti, MarziaSiboni, Simona MariaAsselta, RosannaPeyvandi, Flora + Article (author) -
P25.045.A A genome-wide association study for survival from a multi-center European study identified variants associated with the risk of death due to COVID-19 2024 Francesca MinnaiRosanna Asselta + Article (author) -
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database 2024 Mohsenian, SaminPalla, RobertaMenegatti, MarziaAsselta, RosannaSiboni, Simona MariaPeyvandi, Flora + Article (author) -
Lewy pathology formation in patient-derived GBA1 Parkinson's disease midbrain organoids 2024 Frattini, EmanueleLopez, GianlucaCarsana, Emma VTosi, MattiaTrezzi, IlariaMagni, ManuelaStraniero, LetiziaSamarani, MauraVezzoli, ElenaPittaro, AlessandraSilipigni, RosamariaModa, FabioCorti, StefaniaComi, Giacomo PFerrero, StefanoAsselta, RosannaAureli, Massimo + Article (author) -
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease 2024 Straniero L.Asselta R.Isaias I. U.Ticozzi N. + Article (author) -
A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death 2024 Minnai, FrancescaAsselta, RosannaMonforte, Antonella D. 'ArminioRusconi, StefanoGabrieli, AriannaRiva, AgostinoColaneri, Marta + Article (author) -
In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear 2023 Robusto, MichelaMassa, ValentinaAmbrosetti, UmbertoDuga, StefanoAsselta, Rosanna + Article (author) -
Corrigendum to ‘An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs’ [J Hepatol 2021;75(3):572–581] (Journal of Hepatology (2021) 75(3) (572–581), (S0168827821003342), (10.1016/j.jhep.2021.04.055)) 2022 Asselta R.Zhang J.Battezzati P. M.Casella G.Colli A.Cristoferi L.Lampertico P.Malinverno F.Mancuso C.Marra F.Massironi S.Miele L.O'Donnell S.Ronca V.Valenti L.Zuin M.Tanaka T.Lotta L. A.Levi S.Bell A. + Article (author) -
β-Glucocerebrosidase Deficiency Activates an Aberrant Lysosome-Plasma Membrane Axis Responsible for the Onset of Neurodegeneration 2022 Lunghi, GiuliaCarsana, Emma VeronicaLoberto, NicolettaPrioni, SimonaMauri, LauraBassi, RosariaDuga, StefanoStraniero, LetiziaAsselta, RosannaFrattini, EmanueleFerrari, ElenaAureli, Massimo + Article (author) -
Detailed stratified GWAS analysis for severe COVID-19 in four European populations 2022 Mantovani, AlbertoZanella, AlbertoBandera, AlessandraCherubini, AlessandroProtti, AlessandroAghemo, AlessioLleo, AnaGori, AndreaFracanzani, Anna LudovicaRuello, AntonellaPesenti, AntonioHu, CinziaPaccapelo, CinziaCappadona, ClaudioGalimberti, DanielaScarpini, ElioParaboschi, Elvezia MariaMartinelli-Boneschi, FilippoPeyvandi, FloraBlasi, FrancescoMalvestiti, FrancescoGrasselli, GiacomoCostantino, GiorgioBaselli, GuidoTerranova, LeonardoCarrabba, MariaMiozzo, MonicaMontano, NicolaPreatoni, PaolettaBonfanti, PaoloGualtierotti, RobertaPelusi, SerenaBosari, SilvanoAliberti, StefanoRimoldi, ValeriaDuga, StefanoAsselta, RosannaValenti, Luca + Article (author) -
Novel genes and sex differences in COVID-19 severity 2022 Duga, StefanoAsselta, RosannaValenti, Luca + Article (author) -
Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease Risk 2022 Straniero L.Rimoldi V.Monfrini E.Aureli M.Duga S.Asselta R. + Article (author) -
An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs 2021 Asselta R.Battezzati P. M.Cristoferi L.Lampertico P.Malinverno F.Mancuso C.Marra F.Massironi S.O'Donnell S.Ronca V.Valenti L.Zuin M. + Article (author) -
SLC22A4 Gene in Hereditary Non-syndromic Hearing Loss: Recurrence and Incomplete Penetrance of the p.C113Y Mutation in Northwest Africa 2021 M. RobustoL. MauriU. AmbrosettiS. DugaR. Asselta + Article (author) -
Clinical relevance of clonal hematopoiesis in persons aged ≥80 years [Clinical relevance of clonal hematopoiesis in persons aged >= 80 years] 2021 Asselta R.Duga S.Selmi C.Bicchieri M.Passamonti F.Bolli N. + Article (author) -
Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality 2021 Duga S.Asselta R.Valenti L. + Article (author) -
Rare variants lowering the levels of coagulation factor X are protective against ischemic heart disease 2020 Paraboschi, Elvezia MariaPeyvandi, FloraMenegatti, MarziaAsselta, RosannaDuga, Stefano + Article (author) -
Profiling the mutational landscape of coagulation factor V deficiency 2020 Paraboschi, Elvezia MariaRimoldi, ValeriaPeyvandi, FloraDuga, StefanoAsselta, Rosanna + Article (author) -
Genomewide Association Study of Severe Covid-19 with Respiratory Failure 2020 Baselli, GuidoAsselta, RosannaZanella, AlbertoBandera, AlessandraProtti, AlessandroAghemo, AlessioLleo, AnaGori, AndreaFracanzani, Anna LudovicaPesenti, AntonioPaccapelo, CinziaParaboschi, Elvezia M.Martinelli-Boneschi, FilippoPeyvandi, FloraBlasi, FrancescoGrasselli, GiacomoCostantino, GiorgioTerranova, LeonardoCarrabba, MariaMiozzo, MonicaMontano, NicolaSacchi, NicolettaPreatoni, PaolettaBonfanti, PaoloGualtierotti, RobertaPelusi, SerenaAliberti, StefanoRimoldi, ValeriaBosari, SilvanoDuga, StefanoValenti, Luca + Article (author) -
The SPID-GBA study: Sex distribution, penetrance, incidence, and dementia in GBA-PD 2020 Straniero L.Asselta R.Rimoldi V.Aureli M.Duga S. + Article (author) -