Browsing by Author Ennis, Sean


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Showing results 2 to 8 of 8 < previous 
Published DateTitleAuthor(s)
Dec-2011First implication of STRA6 mutations in isolated anophthalmia, microphthalmia and coloboma: a new dimension to the STRA6 phenotypeCasey, JillianKawaguchi, RikiMorrissey, MariaMcGettigan, Paul A.Nielsen, Jens ErikConroy, JudithRegan, ReginaKennedy, BreandánLynch, SallyGreen, AndrewEnnis, Seanet al.
15-Jul-2010Functional impact of global rare copy number variation in autism spectrum disordersPinto, DalilaPagnamenta, Alistair T.Klei, LambertusRegan, ReginaConroy, JudithCasey, JillianGreen, AndrewSegurado, RicardoShah, NaishaEnnis, Seanet al.
27-Jul-2010A genome-wide scan for common alleles affecting risk for autismAnney, RichardKlei, LambertusPinto, DalilaRegan, ReginaCasey, JillianSegurado, RicardoShah, NaishaEnnis, Seanet al.
Jul-2012Identification of a mutation in LARS as a novel cause of infantile hepatopathyCasey, JillianMcGettigan, Paul A.Lynam-Lennon, NiamhRegan, ReginaConroy, JudithBourke, BillyLynch, SallyEnnis, Seanet al.
Apr-2012A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorderCasey, JillianMagalhaes, TiagoConroy, Judith M.Regan, ReginaShah, NaishaShields, Denis C.Green, AndrewEnnis, Seanet al.
Apr-2012Recessive mutations in MCM4/PRKDC cause a novel syndrome involving a primary immunodeficiency and a disorder of DNA repairCasey, JillianNobbs, MichaelMcGettigan, Paul A.Ennis, Seanet al.
May-2014Unexpected genetic heterogeneity for primary ciliary dyskinesia in the Irish Traveller populationCasey, JillianMcGettigan, Paul A.Healy, FionaReynolds, AlisonKennedy, BreandánEnnis, SeanSlattery, DubhfeasaLynch, SallyHogg, Claire