Morgan A - Search Results

1

Which Came First? When Usher Syndrome Type 1 Couples with Neuropsychiatric Disorders.

Tesolin P, Santin A, Morgan A, Lenarduzzi S, Rubinato E, Girotto G, Spedicati B. Tesolin P, et al. Among authors: morgan a. Audiol Res. 2023 Dec 11;13(6):989-995. doi: 10.3390/audiolres13060086. Audiol Res. 2023. PMID: 38131811 Free PMC article.

2

Usher syndrome: an effective sequencing approach to establish a genetic and clinical diagnosis.

Lenarduzzi S, Vozzi D, Morgan A, Rubinato E, D'Eustacchio A, Osland TM, Rossi C, Graziano C, Castorina P, Ambrosetti U, Morgutti M, Girotto G. Lenarduzzi S, et al. Among authors: morgan a. Hear Res. 2015 Feb;320:18-23. doi: 10.1016/j.heares.2014.12.006. Epub 2015 Jan 6. Hear Res. 2015. PMID: 25575603 Free article.

3

Lights and Shadows in the Genetics of Syndromic and Non-Syndromic Hearing Loss in the Italian Population.

Morgan A, Lenarduzzi S, Spedicati B, Cattaruzzi E, Murru FM, Pelliccione G, Mazzà D, Zollino M, Graziano C, Ambrosetti U, Seri M, Faletra F, Girotto G. Morgan A, et al. Genes (Basel). 2020 Oct 22;11(11):1237. doi: 10.3390/genes11111237. Genes (Basel). 2020. PMID: 33105617 Free PMC article.

4

Non-Syndromic Autosomal Dominant Hearing Loss: The First Italian Family Carrying a Mutation in the NCOA3 Gene.

Tesolin P, Morgan A, Notarangelo M, Ortore RP, Concas MP, Notarangelo A, Girotto G. Tesolin P, et al. Among authors: morgan a. Genes (Basel). 2021 Jul 6;12(7):1043. doi: 10.3390/genes12071043. Genes (Basel). 2021. PMID: 34356059 Free PMC article.

5

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

Tesolin P, Fiorino S, Lenarduzzi S, Rubinato E, Cattaruzzi E, Ammar L, Castro V, Orzan E, Granata C, Dell'Orco D, Morgan A, Girotto G. Tesolin P, et al. Among authors: morgan a. Genes (Basel). 2021 Oct 1;12(10):1569. doi: 10.3390/genes12101569. Genes (Basel). 2021. PMID: 34680964 Free PMC article.

6

Challenging Occam's Razor: Dual Molecular Diagnoses Explain Entangled Clinical Pictures.

Spedicati B, Morgan A, Pianigiani G, Musante L, Rubinato E, Santin A, Nardone GG, Faletra F, Girotto G. Spedicati B, et al. Among authors: morgan a. Genes (Basel). 2022 Nov 3;13(11):2023. doi: 10.3390/genes13112023. Genes (Basel). 2022. PMID: 36360260 Free PMC article.

7

The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian Population.

Spedicati B, Santin A, Nardone GG, Rubinato E, Lenarduzzi S, Graziano C, Garavelli L, Miccoli S, Bigoni S, Morgan A, Girotto G. Spedicati B, et al. Among authors: morgan a. Biomedicines. 2023 Feb 24;11(3):703. doi: 10.3390/biomedicines11030703. Biomedicines. 2023. PMID: 36979683 Free PMC article.

8

Puzzling Out the Genetic Architecture of Endometriosis: Whole-Exome Sequencing and Novel Candidate Gene Identification in a Deeply Clinically Characterised Cohort.

Santin A, Spedicati B, Morgan A, Lenarduzzi S, Tesolin P, Nardone GG, Mazzà D, Di Lorenzo G, Romano F, Buonomo F, Mangogna A, Concas MP, Zito G, Ricci G, Girotto G. Santin A, et al. Among authors: morgan a. Biomedicines. 2023 Jul 27;11(8):2122. doi: 10.3390/biomedicines11082122. Biomedicines. 2023. PMID: 37626618 Free PMC article.

9

Natural human knockouts and Mendelian disorders: deep phenotyping in Italian isolates.

Spedicati B, Cocca M, Palmisano R, Faletra F, Barbieri C, Francescatto M, Mezzavilla M, Morgan A, Pelliccione G, Gasparini P, Girotto G. Spedicati B, et al. Among authors: morgan a. Eur J Hum Genet. 2021 Aug;29(8):1272-1281. doi: 10.1038/s41431-021-00850-9. Epub 2021 Mar 16. Eur J Hum Genet. 2021. PMID: 33727708 Free PMC article.

10

PSIP1/LEDGF: a new gene likely involved in sensorineural progressive hearing loss.

Girotto G, Scheffer DI, Morgan A, Vozzi D, Rubinato E, Di Stazio M, Muzzi E, Pensiero S, Giersch AB, Corey DP, Gasparini P. Girotto G, et al. Among authors: morgan a. Sci Rep. 2015 Dec 22;5:18568. doi: 10.1038/srep18568. Sci Rep. 2015. PMID: 26689366 Free PMC article.

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