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

Iafrate AJ et al. Detection of large-scale variation in the human genome. Nat Genet. 2004 Sep;36(9):949-51. Epub 2004 Aug 01.

Ibrahimi OA et al. Proline to arginine mutations in FGF receptors 1 and 3 result in Pfeiffer and Muenke craniosynostosis syndromes through enhancement of FGF binding affinity.Hum Mol Genet. 2004 Jan 1;13(1):69-78. Epub 2003 Nov 12.

Ibrahimi OA et al. Structural basis for fibroblast growth factor receptor 2 activation in Apert syndrome. Proc Natl Acad Sci U S A. 2001 Jun 19;98(13):7182-7. Epub 2001 Jun 05.

Iles MM. What Can Genome-Wide Association Studies Tell Us about the Genetics of Common Disease. PLoS Genet 2008; 4(2): e33. doi: 10.1371/journal.pgen.0040033

International Schizophrenia Consortium. Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature. 2008 Sep 11;455(7210):237-41.

Irwin WA et al. Mitochondrial dysfunction and apoptosis in myopathic mice with collagen VI deficiency. Nat Genet. 2003 Dec;35(4):367-71.

Ishkanian AS et al. A tiling resolution DNA microarray with complete coverage of the human genome. Nat Genet. 2004 Mar;36(3):299-303. Epub 2004 Feb 15.