A-Z Articles Index by First Author's Last Name A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Ebert BL et al. Identification of RPS14 as a 5q- syndrome gene by RNA interference screen. Nature. 2008 Jan 17;451(7176):335-9.

Eddy S. (2002) Computational genomics of noncoding RNA genes. Cell 109:137-140.

Elstner M et al. Single-cell expression profiling of dopaminergic neurons combined with association analysis identifies pyridoxal kinase as Parkinson's disease gene. Ann Neurol. 2009 Dec;66(6):792-8

Enard W et al. Molecular evolution of FOXP2, a gene involved in speech and language. Nature advance online publication DOI:10.1038/nature01025 Letters to Nature.

Enard W et al. Molecular evolution of FOXP2, a gene involved in speech and language. Nature. 2002 Aug 22;418(6900):869-72 DOI:10.1038/nature01025 Letters to Nature.

Eng C et al. A role for mitochondrial enzymes in inherited neoplasia and beyond. Nat Rev Cancer. 2003 Mar;3(3):193-202.

Erbe CB et al. Connexin 26 and connexin 30 mutations in children with nonsyndromic hearing loss. Laryngoscope. 2004 Apr;114(4):607-11.

Erdogan F et al. High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease. J Med Genet. 2008 Nov;45(11):704-9. Epub 2008 Aug 19.

Eriksson M et al. Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome. Nature. 2003 May 15;423(6937):293-8

Erkko H et al. A recurrent mutation in PALB2 in Finnish cancer families. Nature. 2007 Mar 15;446(7133):316-9. Epub 2007 Feb 7.

Estep AL et al. HRAS mutations in Costello syndrome: Detection of constitutional activating mutations in codon 12 and 13 and loss of wild-type allele in malignancy. Am J Med Genet A. 2006 Jan 1;140(1):8-16.