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Page 1
The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population.
Stapleton CP, Heinzel A, Guan W, van der Most PJ, van Setten J, Lord GM, Keating BJ, Israni AK, de Borst MH, Bakker SJL, Snieder H, Weale ME, Delaney F, Hernandez-Fuentes MP, Reindl-Schwaighofer R, Oberbauer R, Jacobson PA, Mark PB, Chapman FA, Phelan PJ, Kennedy C, Sexton D, Murray S, Jardine A, Traynor JP, McKnight AJ, Maxwell AP, Smyth LJ, Oetting WS, Matas AJ, Mannon RB, Schladt DP, Iklé DN, Cavalleri GL, Conlon PJ; UK Ireland Renal Transplant Consortium; DeKAF Genomics and GEN03 Studies; International Genetics and Translational Research in Transplantation Network. Stapleton CP, et al. Among authors: cavalleri gl. Am J Transplant. 2019 Aug;19(8):2262-2273. doi: 10.1111/ajt.15326. Epub 2019 Mar 28. Am J Transplant. 2019. PMID: 30920136 Free PMC article.
An assessment of the Irish population for large-scale genetic mapping studies involving epilepsy and other complex diseases.
O'Dushlaine CT, Dolan C, Weale ME, Stanton A, Croke DT, Kalviainen R, Eriksson K, Kantanen AM, Gibson RA, Hosford D, Sisodiya SM, Gill M, Corvin AP, Morris DW, Delanty N, Cavalleri GL. O'Dushlaine CT, et al. Among authors: cavalleri gl. Eur J Hum Genet. 2008 Feb;16(2):176-83. doi: 10.1038/sj.ejhg.5201938. Epub 2007 Oct 31. Eur J Hum Genet. 2008. PMID: 17971835
A genome-wide association study of recipient genotype and medium-term kidney allograft function.
O'Brien RP, Phelan PJ, Conroy J, O'Kelly P, Green A, Keogan M, O'Neill D, Jennings S, Traynor C, Casey J, McCormack M, Conroy R, Chubb A, Ennis S, Shields DC, Cavalleri GL, Conlon PJ. O'Brien RP, et al. Among authors: cavalleri gl. Clin Transplant. 2013 May-Jun;27(3):379-87. doi: 10.1111/ctr.12093. Epub 2013 Feb 21. Clin Transplant. 2013. PMID: 23432519
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.
Kasperaviciute D, Catarino CB, Matarin M, Leu C, Novy J, Tostevin A, Leal B, Hessel EV, Hallmann K, Hildebrand MS, Dahl HH, Ryten M, Trabzuni D, Ramasamy A, Alhusaini S, Doherty CP, Dorn T, Hansen J, Krämer G, Steinhoff BJ, Zumsteg D, Duncan S, Kälviäinen RK, Eriksson KJ, Kantanen AM, Pandolfo M, Gruber-Sedlmayr U, Schlachter K, Reinthaler EM, Stogmann E, Zimprich F, Théâtre E, Smith C, O'Brien TJ, Meng Tan K, Petrovski S, Robbiano A, Paravidino R, Zara F, Striano P, Sperling MR, Buono RJ, Hakonarson H, Chaves J, Costa PP, Silva BM, da Silva AM, de Graan PN, Koeleman BP, Becker A, Schoch S, von Lehe M, Reif PS, Rosenow F, Becker F, Weber Y, Lerche H, Rössler K, Buchfelder M, Hamer HM, Kobow K, Coras R, Blumcke I, Scheffer IE, Berkovic SF, Weale ME; UK Brain Expression Consortium; Delanty N, Depondt C, Cavalleri GL, Kunz WS, Sisodiya SM. Kasperaviciute D, et al. Among authors: cavalleri gl. Brain. 2013 Oct;136(Pt 10):3140-50. doi: 10.1093/brain/awt233. Epub 2013 Sep 6. Brain. 2013. PMID: 24014518 Free PMC article.
Personalized medicine and human genetic diversity.
Lu YF, Goldstein DB, Angrist M, Cavalleri G. Lu YF, et al. Cold Spring Harb Perspect Med. 2014 Jul 24;4(9):a008581. doi: 10.1101/cshperspect.a008581. Cold Spring Harb Perspect Med. 2014. PMID: 25059740 Free PMC article. Review.
Association of CYP3A variants with kidney transplant outcomes.
Traynor C, Conlon P Jr, Phelan PJ, O'Kelly P, Elens L, McCormack M, Cavalleri G, Comber H, van Schaik RH, Conlon PJ. Traynor C, et al. Ren Fail. 2015 May;37(4):562-6. doi: 10.3109/0886022X.2015.1007013. Epub 2015 Feb 3. Ren Fail. 2015. PMID: 25644970 Free article.
Clinical manifestations of prune belly syndrome.
Chhabra R, Awan A, Stapleton C, Cavalleri G, Conlon P. Chhabra R, et al. Clin Med (Lond). 2016 Jun 1;16 Suppl 3(Suppl 3):s5. doi: 10.7861/clinmedicine.16-3-s5. Clin Med (Lond). 2016. PMID: 27252342 Free PMC article. No abstract available.
184 results