FORZAN, MONICA

FORZAN, MONICA  

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Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease 2020 Cassina M.Clementi M.Degortes D.Favaro A.Forzan M.Santonastaso P.Tenconi E. + NATURE GENETICS - -
Setup and Validation of a Targeted Next-Generation Sequencing Approach for the Diagnosis of Lysosomal Storage Disorders 2020 Zanetti A.D'Avanzo F.Bertoldi L.Zampieri G.Feltrin E.De Pascale F.Rampazzo A.Forzan M.Valle G.Tomanin R. THE JOURNAL OF MOLECULAR DIAGNOSTICS - -
Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies 2020 Cassina, MClementi, MDegortes, DFavaro, AForzan, MSantonastaso, PTenconi, E + ADDICTION BIOLOGY - -
Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders: A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches 2019 Cassina M.Clementi M.Degortes D.Favaro A.Forzan M.Tenconi E. + BIOLOGICAL PSYCHIATRY - -
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders 2019 Cassina M.Clementi M.Degortes D.Forzan M. + CELL - -
The Arg1038Gly missense variant in the NF1 gene causes a mild phenotype without neurofibromas 2019 Trevisson, EvaMorbidoni, ValeriaForzan, MonicaFUMINI, VALENTINAParrozzani, RaffaeleCassina, MatteoMidena, EdoardoSalviati, LeonardoClementi, Maurizio + MOLECULAR GENETICS & GENOMIC MEDICINE - -
Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa 2018 Tenconi, ECassina, MClementi, MDegortes, DFavaro, AngelaForzan, MSantonastaso, P. + MOLECULAR PSYCHIATRY - -
A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling 2017 Favaro, AngelaSantonastaso, PaoloMonteleone, PalmieroBruson, AliceClementi, MaurizioDegortes, DanielaForzan, MonicaTenconi, ElenaGambaro, Giovanni + SCIENTIFIC REPORTS - -
Catechol-O-Methyltransferase (COMT) Val158Met Polymorphism and Eating Disorders: Data From a New Biobank and Meta-Analysis of Previously Published Studies 2017 Collantoni, EnricoSolmi, MarcoGallicchio, DavideSantonastaso, PaoloMENEGUZZO, PAOLOClementi, MaurizioPINATO, CLAUDIAForzan, MonicaCassina, MatteoSiani, RobertaTenconi, ElenaVeronese, NicolaFavaro, Angela + EUROPEAN EATING DISORDERS REVIEW - -
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index 2017 FAVARO, ANGELASANTONASTASO, PAOLOBRUSON, ALICECLEMENTI, MAURIZIODEGORTES, DANIELAFORZAN, MONICATENCONI, ELENA + MOLECULAR PSYCHIATRY - -
Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa 2017 CASSINA, MATTEOCLEMENTI, MAURIZIODEGORTES, DANIELAFAVARO, ANGELAFORZAN, MONICASANTONASTASO, PAOLOTENCONI, ELENA + THE AMERICAN JOURNAL OF PSYCHIATRY - -
A genome-wide association study of anorexia nervosa 2014 FAVARO, ANGELASANTONASTASO, PAOLOBRUSON, ALICECLEMENTI, MAURIZIODEGORTES, DANIELAFORZAN, MONICATENCONI, ELENA + MOLECULAR PSYCHIATRY - -
p.Arg1809Cys substitution in neurofibromin is associated with a distinctive NF1 phenotype without neurofibromas. 2014 TREVISSON, EVAFORZAN, MONICACLEMENTI, MAURIZIO + EUROPEAN JOURNAL OF HUMAN GENETICS - -
Using ancestry-informative markers to identify fine structure across 15 populations of European origin 2014 FAVARO, ANGELASANTONASTASO, PAOLOBRUSON, ALICECLEMENTI, MAURIZIODEGORTES, DANIELAFORZAN, MONICATENCONI, ELENA + EUROPEAN JOURNAL OF HUMAN GENETICS - -
CATECHOL-O-METHYLTRANSFERASE GENOTYPE MODIFIES EXECUTIVE FUNCTIONING AND PREFRONTAL FUNCTIONAL CONNECTIVITY IN WOMEN WITH ANOREXIA NERVOSA. 2012 FAVARO, ANGELACLEMENTI, MAURIZIOManara RBOSELLO, ROMINAFORZAN, MONICABRUSON, ALICETENCONI, ELENADEGORTES, DANIELASANTONASTASO, PAOLO + JOURNAL OF PSYCHIATRY & NEUROSCIENCE - -
Functional Splicing Assay mediante l'utilizzo di minigeni plasmidici nel gene NF1 2010 Forzan, Monica - - -
Is CFTR 621+3 A > G a cystic fibrosis causing mutation? 2010 FORZAN, MONICASALVIATI, LEONARDOCASARIN, ALBERTOBRUSON, ALICETREVISSON, EVACLEMENTI, MAURIZIO + JOURNAL OF HUMAN GENETICS - -