SALVI, ERIKA

SALVI, ERIKA  

Dipartimento di Scienze della Salute  

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Risultati 1 - 20 di 55 (tempo di esecuzione: 0.006 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
A "Candidate-Interactome" Aggregate Analysis of Genome-Wide Association Data in Multiple Sclerosis 1-gen-2013 V.A..G. RiciglianoB. Filippo MartinelliG. ComiD. CusiD. GalimbertiF.R. GueriniS. LupoliF. MacciardiE. Salvi + Article (author) -
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia 1-ott-2015 E. SalviD. GalimbertiE. ScarpiniM. Serpente + Article (author) -
A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility 1-ago-2022 Lupoli, SaraSalvi, ErikaBarlassina, CristinaCusi, DanieleComi, GiancarloMartinelli Boneschi, Filippo + Article (author) -
A novel network analysis approach reveals DNA damage, oxidative stress and calcium/cAMP homeostasis-associated biomarkers in frontotemporal dementia 1-gen-2017 Galimberti, DanielaCusi, DanieleSalvi, Erika + Article (author) -
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape 23-nov-2016 E. SalviC. BarlassinaF. D'AvilaD. Cusi + Article (author) -
A regulatory variant in CCR6 is associated with susceptibility to antitopoisomerase-positive systemic sclerosis 1-dic-2013 D. CusiE. Salvi + Article (author) -
A standard based approach for biomedical knowledge representation 1-gen-2011 C. ContiF. RizziE. SalviD.M. Cusi + Book Part (author) -
Adducin- and ouabain-related gene variants predict the antihypertensive activity of rostafuroxin, part 2 : clinical studies 24-nov-2010 C. LanzaniE. SalviD.M. CusiF. MacciardiP. Ferrari + Article (author) -
Association analysis of noncoding variants in neuroligins 3 and 4X genes with autism spectrum disorder in an Italian cohort 22-ott-2016 E. SalviD. Cusi + Article (author) -
Blood pressure loci identified with a gene-centric array 9-dic-2011 E. SalviA. StucchiD. Cusi + Article (author) -
Comparison of different methods to estimate genetic ancestry and control for stratification in genome-wide association studies 3-giu-2008 E. SalviG. GuffantiF. TorriS. LupoliC. BarlassinaD. CusiF. Macciardi + Conference Object -
Copy number variations and cognitive phenotypes in unselected populations 1-gen-2015 E. SalviD. Cusi + Article (author) -
Coronary risk in relation to genetic variation in MEOX2 and TCF15 in a Flemish population 1-ott-2015 E. SalviM. BarcellaC. Barlassina + Article (author) -
Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette's Syndrome and OCD 1-gen-2015 C. BarlassinaD. CusiS. LupoliF. MacciardiE. Salvi + Article (author) -
Dietary Salt Intake, Blood Pressure, and Genes 1-set-2013 S. LupoliE. SalviC. Barlassina Article (author) -
Directional dominance on stature and cognition in diverse human populations 1-gen-2015 E. SalviD. Cusi + Article (author) -
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens 1-nov-2014 C. BarlassinaE. SalviD. Cusi + Article (author) -
Effect of intravenous l-carnitine in Chinese patients with chronic heart failure 1-gen-2016 E. Salvi + Article (author) -
Evidence for the contribution of the X chromosome to Systemic Sclerosis susceptibility : association with the functional IRAK1 196Phe/532Ser haplotype 1-gen-2011 D.M. CusiE. Salvi + Article (author) -
Fine mapping of AHI1 as a schizophrenia susceptibility gene: from association to evolutionary evidence 1-gen-2010 F. TorriS. LupoliE. SalviF. Macciardi + Article (author) -