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Molecular analysis of cluster headache.
Zarrilli F, Tomaiuolo R, Ceglia C, Lombardo B, Izzo B, Castaldo G, Pastore L, De Simone R. Zarrilli F, et al. Among authors: ceglia c. Clin J Pain. 2015 Jan;31(1):52-7. doi: 10.1097/AJP.0000000000000075. Clin J Pain. 2015. PMID: 24469609
Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss.
Iossa S, Costa V, Corvino V, Auletta G, Barruffo L, Cappellani S, Ceglia C, Cennamo G, D'Adamo AP, D'Amico A, Di Paolo N, Forte R, Gasparini P, Laria C, Lombardo B, Malesci R, Vitale A, Marciano E, Franzè A. Iossa S, et al. Among authors: ceglia c. Mol Cytogenet. 2015 Mar 20;8:18. doi: 10.1186/s13039-015-0120-0. eCollection 2015. Mol Cytogenet. 2015. PMID: 25821518 Free PMC article.
Two novel genomic rearrangements identified in suicide subjects using a-CGH array.
Lombardo B, Zarrilli F, Ceglia C, Vitale A, Keller S, Sarchiapone M, Carli V, Stuppia L, Chiariotti L, Castaldo G, Pastore L. Lombardo B, et al. Among authors: ceglia c. Clin Chem Lab Med. 2015 Sep 1;53(10):e245-8. doi: 10.1515/cclm-2014-1255. Clin Chem Lab Med. 2015. PMID: 25719327 Free article. No abstract available.
Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array-based detection rate.
Catusi I, Recalcati MP, Bestetti I, Garzo M, Valtorta C, Alfonsi M, Alghisi A, Cappellani S, Casalone R, Caselli R, Ceccarini C, Ceglia C, Ciaschini AM, Coviello D, Crosti F, D'Aprile A, Fabretto A, Genesio R, Giagnacovo M, Granata P, Longo I, Malacarne M, Marseglia G, Montaldi A, Nardone AM, Palka C, Pecile V, Pessina C, Postorivo D, Redaelli S, Renieri A, Rigon C, Tiberi F, Tonelli M, Villa N, Zilio A, Zuccarello D, Novelli A, Larizza L, Giardino D. Catusi I, et al. Among authors: ceglia c. Mol Genet Genomic Med. 2020 Jan;8(1):e1056. doi: 10.1002/mgg3.1056. Epub 2019 Dec 18. Mol Genet Genomic Med. 2020. PMID: 31851782 Free PMC article.