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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2011 | 2 |
2012 | 1 |
2013 | 3 |
2014 | 3 |
2024 | 0 |
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7 results
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Page 1
Estrogen-related receptor gamma and hearing function: evidence of a role in humans and mice.
Neurobiol Aging. 2013 Aug;34(8):2077.e1-9. doi: 10.1016/j.neurobiolaging.2013.02.009. Epub 2013 Mar 26.
Neurobiol Aging. 2013.
PMID: 23540940
Free PMC article.
Expression and replication studies to identify new candidate genes involved in normal hearing function.
Girotto G, Vuckovic D, Buniello A, Lorente-Cánovas B, Lewis M, Gasparini P, Steel KP.
Girotto G, et al.
PLoS One. 2014 Jan 14;9(1):e85352. doi: 10.1371/journal.pone.0085352. eCollection 2014.
PLoS One. 2014.
PMID: 24454846
Free PMC article.
Item in Clipboard
Linkage study and exome sequencing identify a BDP1 mutation associated with hereditary hearing loss.
Girotto G, Abdulhadi K, Buniello A, Vozzi D, Licastro D, d'Eustacchio A, Vuckovic D, Alkowari MK, Steel KP, Badii R, Gasparini P.
Girotto G, et al.
PLoS One. 2013 Dec 2;8(12):e80323. doi: 10.1371/journal.pone.0080323. eCollection 2013.
PLoS One. 2013.
PMID: 24312468
Free PMC article.
Clinical Trial.
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Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients.
Vozzi D, Morgan A, Vuckovic D, D'Eustacchio A, Abdulhadi K, Rubinato E, Badii R, Gasparini P, Girotto G.
Vozzi D, et al.
Gene. 2014 Jun 1;542(2):209-16. doi: 10.1016/j.gene.2014.03.033. Epub 2014 Mar 20.
Gene. 2014.
PMID: 24657061
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GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari population.
Khalifa Alkowari M, Girotto G, Abdulhadi K, Dipresa S, Siam R, Najjar N, Badii R, Gasparini P.
Khalifa Alkowari M, et al.
Int J Audiol. 2012 Mar;51(3):181-5. doi: 10.3109/14992027.2011.625983. Epub 2011 Nov 21.
Int J Audiol. 2012.
PMID: 22103400
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Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways.
Girotto G, Pirastu N, Sorice R, Biino G, Campbell H, d'Adamo AP, Hastie ND, Nutile T, Polasek O, Portas L, Rudan I, Ulivi S, Zemunik T, Wright AF, Ciullo M, Hayward C, Pirastu M, Gasparini P.
Girotto G, et al.
J Med Genet. 2011 Jun;48(6):369-74. doi: 10.1136/jmg.2010.088310. Epub 2011 Apr 14.
J Med Genet. 2011.
PMID: 21493956
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A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss.
Faletra F, Girotto G, D'Adamo AP, Vozzi D, Morgan A, Gasparini P.
Faletra F, et al.
Gene. 2014 Jan 25;534(2):236-9. doi: 10.1016/j.gene.2013.10.052. Epub 2013 Nov 6.
Gene. 2014.
PMID: 24211385
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