Works matching AU Morgan, Anna

Results: 80
    1
    2

    Normal hearing function genetics: have you heard all about it? An integrated approach of genome-wide association studies and transcriptome-wide association studies in three Italian cohorts.

    Published in:
    Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1522338
    By:
    • Santin, Aurora;
    • Pianigiani, Giulia;
    • Gialluisi, Alessandro;
    • Pecori, Alessandro;
    • Spedicati, Beatrice;
    • Costanzo, Simona;
    • Persichillo, Mariarosaria;
    • Bracone, Francesca;
    • Nardone, Giuseppe Giovanni;
    • Tesolin, Paola;
    • Lenarduzzi, Stefania;
    • Morgan, Anna;
    • De Curtis, Amalia;
    • van der Valk, Wouter;
    • Rousset, Francis;
    • Roccio, Marta;
    • Locher, Heiko;
    • Iacoviello, Licia;
    • Concas, Maria Pina;
    • Girotto, Giorgia
    Publication type:
    Article
    3
    4

    Mutations in PLS1, encoding fimbrin, cause autosomal dominant nonsyndromic hearing loss.

    Published in:
    Human Mutation, 2019, v. 40, n. 12, p. 2286, doi. 10.1002/humu.23891
    By:
    • Morgan, Anna;
    • Koboldt, Daniel C.;
    • Barrie, Elizabeth S.;
    • Crist, Erin R.;
    • García García, Gema;
    • Mezzavilla, Massimo;
    • Faletra, Flavio;
    • Mihalic Mosher, Theresa;
    • Wilson, Richard K.;
    • Blanchet, Catherine;
    • Manickam, Kandamurugu;
    • Roux, Anne‐Francoise;
    • Gasparini, Paolo;
    • Dell'Orco, Daniele;
    • Girotto, Giorgia
    Publication type:
    Article
    5
    6
    7
    8
    9
    10
    11

    Pendred Syndrome, or Not Pendred Syndrome? That Is the Question.

    Published in:
    Genes, 2021, v. 12, n. 10, p. 1569, doi. 10.3390/genes12101569
    By:
    • Tesolin, Paola;
    • Fiorino, Sofia;
    • Lenarduzzi, Stefania;
    • Rubinato, Elisa;
    • Cattaruzzi, Elisabetta;
    • Ammar, Lydie;
    • Castro, Veronica;
    • Orzan, Eva;
    • Granata, Claudio;
    • Dell'Orco, Daniele;
    • Morgan, Anna;
    • Girotto, Giorgia
    Publication type:
    Article
    12
    13
    14

    The Role of Knockout Olfactory Receptor Genes in Odor Discrimination.

    Published in:
    Genes, 2021, v. 12, n. 5, p. 631, doi. 10.3390/genes12050631
    By:
    • Concas, Maria Pina;
    • Cocca, Massimiliano;
    • Francescatto, Margherita;
    • Battistuzzi, Thomas;
    • Spedicati, Beatrice;
    • Feresin, Agnese;
    • Morgan, Anna;
    • Gasparini, Paolo;
    • Girotto, Giorgia;
    • Crisponi, Laura
    Publication type:
    Article
    15
    16
    17
    18
    19
    20
    21

    Uncovering a Novel Pathogenic Mechanism of BCS1L in Mitochondrial Disorders: Insights from Functional Studies on the c.38A>G Variant.

    Published in:
    International Journal of Molecular Sciences, 2025, v. 26, n. 8, p. 3670, doi. 10.3390/ijms26083670
    By:
    • Capaci, Valeria;
    • Zupin, Luisa;
    • Magistrati, Martina;
    • Bonati, Maria Teresa;
    • Celsi, Fulvio;
    • Marrone, Irene;
    • Baldo, Francesco;
    • Ura, Blendi;
    • Spedicati, Beatrice;
    • Morgan, Anna;
    • Bruno, Irene;
    • Zeviani, Massimo;
    • Dallabona, Cristina;
    • Girotto, Giorgia;
    • Magnolato, Andrea
    Publication type:
    Article
    22
    23
    24
    25
    26
    27
    28
    29

    Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss.

    Published in:
    Human Molecular Genetics, 2021, v. 30, n. 19, p. 1785, doi. 10.1093/hmg/ddab145
    By:
    • Bassani, Sissy;
    • Beelen, Edward van;
    • Rossel, Mireille;
    • Voisin, Norine;
    • Morgan, Anna;
    • Arribat, Yoan;
    • Chatron, Nicolas;
    • Chrast, Jacqueline;
    • Cocca, Massimiliano;
    • Delprat, Benjamin;
    • Faletra, Flavio;
    • Giannuzzi, Giuliana;
    • Guex, Nicolas;
    • Machavoine, Roxane;
    • Pradervand, Sylvain;
    • Smits, Jeroen J;
    • Kamp, Jiddeke M van de;
    • Ziegler, Alban;
    • Amati, Francesca;
    • Marlin, Sandrine
    Publication type:
    Article
    30

    Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss.

    Published in:
    Human Molecular Genetics, 2015, v. 24, n. 19, p. 5655, doi. 10.1093/hmg/ddv279
    By:
    • Vuckovic, Dragana;
    • Dawson, Sally;
    • Scheffer, Deborah I.;
    • Rantanen, Taina;
    • Morgan, Anna;
    • Di Stazio, Mariateresa;
    • Vozzi, Diego;
    • Nutile, Teresa;
    • Concas, Maria P.;
    • Biino, Ginevra;
    • Nolan, Lisa;
    • Bahl, Aileen;
    • Loukola, Anu;
    • Viljanen, Anne;
    • Davis, Adrian;
    • Ciullo, Marina;
    • Corey, David P.;
    • Pirastu, Mario;
    • Gasparini, Paolo;
    • Girotto, Giorgia
    Publication type:
    Article
    31

    The p.Cys169Tyr variant of connexin 26 is not a polymorphism.

    Published in:
    Human Molecular Genetics, 2015, v. 24, n. 9, p. 2641, doi. 10.1093/hmg/ddv026
    By:
    • Zonta, Francesco;
    • Girotto, Giorgia;
    • Buratto, Damiano;
    • Crispino, Giulia;
    • Morgan, Anna;
    • Abdulhadi, Khalid;
    • Alkowari, Moza;
    • Badii, Ramin;
    • Gasparini, Paolo;
    • Mammano, Fabio
    Publication type:
    Article
    32
    33
    34
    35
    36
    37
    38
    39

    Comparative Effectiveness of an Automated Text Messaging Service for Monitoring COVID-19 at Home.

    Published in:
    2022
    By:
    • Delgado, M. Kit;
    • Morgan, Anna U.;
    • Asch, David A.;
    • Xiong, Ruiying;
    • Kilaru, Austin S.;
    • Lee, Kathleen C.;
    • Do, David;
    • Friedman, Ari B.;
    • Meisel, Zachary F.;
    • Snider, Christopher K.;
    • Lam, Doreen;
    • Parambath, Andrew;
    • Wood, Christian;
    • Wilson, Chidinma M.;
    • Perez, Michael;
    • Chisholm, Deena L.;
    • Kelly, Sheila;
    • O'Malley, Christina J.;
    • Mannion, Nancy;
    • Huffenberger, Ann Marie
    Publication type:
    Journal Article
    40
    41
    42
    43
    44
    45
    46
    47
    48
    49
    50