MORGAN, ANNA

MORGAN, ANNA  

Dipartimento Universitario Clinico di Scienze mediche, chirurgiche e della salute  

Settore MED/03 - Genetica Medica  

Mostra records
Risultati 1 - 20 di 56 (tempo di esecuzione: 0.052 secondi).
Titolo Data di pubblicazione Autori File
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids 1-gen-2022 Morgan, AnnaConcas, Maria PinaGirotto, Giorgia +
A new case of TAR syndrome confirms the importance of noncoding variants in the etiopathogenesis of the disease 1-gen-2021 Morgan A.La Bianca M.Faletra F.Girotto G. +
A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta 1-gen-2014 MORGAN, ANNAGASPARINI, PAOLO +
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss 1-gen-2013 GIROTTO, GIORGIAD'ADAMO, ADAMO PIOVOZZI, DIEGOMORGAN, ANNAGASPARINI, PAOLO +
A saturated map of common genetic variants associated with human height 1-gen-2022; 1-gen-2022 Catamo, EulaliaCocca, MassimilianoConcas, Maria PinaFrancescatto, MargheritaMorgan, AnnaTesolin, PaolaGasparini, PaoloGirotto, Giorgia +
A Wars2 Mutant Mouse Model Displays OXPHOS Deficiencies and Activation of Tissue-Specific Stress Response Pathways 1-gen-2018 Morgan, Anna +
Assessment of the olfactory function in Italian patients with type 3 von Willebrand disease caused by a homozygous 253 Kb deletion involving VWF and TMEM16B/ANO2 1-gen-2015 CENEDESE, VALENTINAMEZZAVILLA, MASSIMOMORGAN, ANNAGASPARINI, PAOLOMENINI, ANNA MARIA +
Challenging Occam's Razor: Dual Molecular Diagnoses Explain Entangled Clinical Pictures 1-gen-2022 Spedicati, BeatriceMorgan, AnnaRubinato, ElisaSantin, AuroraFaletra, FlavioGirotto, Giorgia +
Congenital hyperinsulinism: clinical and molecular analysis of a large Italian cohort. 1-gen-2013 ATHANASAKIS, EMMANOUILMORGAN, ANNAVENTURA, ALESSANDROGASPARINI, PAOLO +
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals 1-gen-2022 Cocca, MassimilianoFeresin, AgneseMorgan, AnnaSpedicati, BeatriceCatamo, EulaliaRizzi, FedericaGirotto, GiorgiaPistis, GiorgioFrancescatto, MargheritaConcas, Maria PinaBianca, Martina LaPirastu, NicolaGasparini, Paolo +
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits 1-gen-2018 Barbieri, Caterina MBrumat, MarcoCocca, MassimilianoGandin, IlariaGasparini, PaoloGirotto, GiorgiaMorgan, AnnaRobino, AntoniettaTraglia, MichelaVuckovic, Dragana +
Genetic dissection of temperament personality traits in Italian isolates 1-gen-2022 Concas M. P.Minelli A.Aere S.Morgan A.Tesolin P.Gasparini P.Girotto G. +
Genetics, odor perception and food liking: The intriguing role of cinnamon 1-gen-2021 Concas M. P.Morgan A.Gasparini P.Girotto G. +
Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus 1-gen-2023 Marco BrumatMassimiliano CoccaMaria Pina ConcasGiorgia GirottoAnna Morgan +
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk 1-gen-2017 VUCKOVIC, DRAGANAGandin, IlariaBRUMAT, MARCOCOCCA, MASSIMILIANOMORGAN, ANNAROBINO, ANTONIETTAGIROTTO, GIORGIAGASPARINI, PAOLO +
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss 1-gen-2015 VUCKOVIC, DRAGANAMORGAN, ANNADI STAZIO, MARIATERESAVOZZI, DiegoCONCAS, MARIA PINAGASPARINI, PAOLOGIROTTO, GIORGIA +
Genomic Studies in a Large Cohort of Hearing Impaired Italian Patients Revealed Several New Alleles, a Rare Case of Uniparental Disomy (UPD) and the Importance to Search for Copy Number Variations 1-gen-2018 Morgan, AnnaLenarduzzi, StefaniaCappellani, StefaniaPecile, VannaMorgutti, MarcelloBrumat, MarcoLa Bianca, MartinaFaletra, FlavioGasparini, PaoloGirotto, Giorgia +
Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B-Associated Disorders 1-gen-2023 Di Stazio, MariateresaFaletra, FlavioMorgan, AnnaGirotto, GiorgiaCosta, PaolaCarrozzi, Marcod’Adamo, Adamo P. +
Hearing Function: Identification of New Candidate Genes Further Explaining the Complexity of This Sensory Ability 1-gen-2021 Concas, Maria PinaMorgan, AnnaFrancescatto, MargheritaGasparini, PaoloGirotto, Giorgia +
Hearing loss and brain abnormalities due to pathogenic mutations in ADGRV1 gene: a case report 1-gen-2020 Faletra F.Morgan A.Girotto G. +