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Human genetics branches out in Barcelona.
Rabionet R, Espinosa-Parrilla Y, Estivill X. Rabionet R, et al. Among authors: estivill x. Genome Biol. 2008;9(8):318. doi: 10.1186/gb-2008-9-8-318. Epub 2008 Aug 13. Genome Biol. 2008. PMID: 18710599 Free PMC article.
Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients.
Wattenhofer M, Di Iorio MV, Rabionet R, Dougherty L, Pampanos A, Schwede T, Montserrat-Sentis B, Arbones ML, Iliades T, Pasquadibisceglie A, D'Amelio M, Alwan S, Rossier C, Dahl HH, Petersen MB, Estivill X, Gasparini P, Scott HS, Antonarakis SE. Wattenhofer M, et al. Among authors: estivill x. J Mol Med (Berl). 2002 Feb;80(2):124-31. doi: 10.1007/s00109-001-0310-6. Epub 2001 Dec 18. J Mol Med (Berl). 2002. PMID: 11907649
Are MYO1C and MYO1F associated with hearing loss?
Zadro C, Alemanno MS, Bellacchio E, Ficarella R, Donaudy F, Melchionda S, Zelante L, Rabionet R, Hilgert N, Estivill X, Van Camp G, Gasparini P, Carella M. Zadro C, et al. Among authors: estivill x. Biochim Biophys Acta. 2009 Jan;1792(1):27-32. doi: 10.1016/j.bbadis.2008.10.017. Epub 2008 Nov 5. Biochim Biophys Acta. 2009. PMID: 19027848 Free article.
Variants at APOE influence risk of deep and lobar intracerebral hemorrhage.
Biffi A, Sonni A, Anderson CD, Kissela B, Jagiella JM, Schmidt H, Jimenez-Conde J, Hansen BM, Fernandez-Cadenas I, Cortellini L, Ayres A, Schwab K, Juchniewicz K, Urbanik A, Rost NS, Viswanathan A, Seifert-Held T, Stoegerer EM, Tomás M, Rabionet R, Estivill X, Brown DL, Silliman SL, Selim M, Worrall BB, Meschia JF, Montaner J, Lindgren A, Roquer J, Schmidt R, Greenberg SM, Slowik A, Broderick JP, Woo D, Rosand J; International Stroke Genetics Consortium. Biffi A, et al. Among authors: estivill x. Ann Neurol. 2010 Dec;68(6):934-43. doi: 10.1002/ana.22134. Ann Neurol. 2010. PMID: 21061402 Free PMC article.
713 results