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

Waggoner DJ, et al. NSD1 analysis for Sotos syndrome: insights and perspectives from the clinical laboratory. Genet Med. 2005 Oct;7(8):524-33.

Wagner KD et al. RNA induction and inheritance of epigenetic cardiac hypertrophy in the mouse. Dev Cell. 2008 Jun;14(6):962-9.

Wai T et al. The mitochondrial DNA genetic bottleneck results from replication of a subpopulation of genomes. 2008 Nat Genet. Dec;40(12):1484-8

Wall JD et al. Assessing the performance of the haplotype block model of linkage disequilibrium. Am J Hum Genet. 2003 Sep; 73(3): 502-15. Epub 2003 Aug 11.

Walker AP et al.Results communication and patient education after screening for possible hemochromatosis and iron overload: experience from the HEIRS Study of a large ethnically and linguistically diverse group. Genet Med. 2007 Nov;9(11):778-91.

Wang WY et al. Genome-wide association studies: theoretical and practical concerns. Nat Rev Genet. 2005 Feb;6(2):109-18.

Wang X et al. Dynamic tracking of human hematopoietic stem cell engraftment using in vivo bioluminescence imaging. Blood. 2003 Nov 15;102(10):3478-82.Epub 2003 Aug 28.

Wang Y et al. Accelerated Evolution of the PACAP Precursor Gene During Human Origin. Genetics. 2005 Apr 16; [Epub ahead of print]

Wapner R et al. First-trimester screening for trisomies 21 and 18. N Engl J Med. 2003 Oct 9;349(15):1405-13.

Ware SM et al. Identification and functional analysis of ZIC3 mutations in heterotaxy and related congenital heart defects. Am J Hum Genet. 2004 Jan;74(1):93-105. Epub 2003 Dec 16.

Waring SC et al. Genome-wide association studies in Alzheimer disease. Arch Neurol. 2008 Mar;65(3):329-34.

Wassarman K., (2002) Small RNAs in bacteria: diverse regulators of gene expression in response to environmental changes. Cell 109:141-144.

Weaver IC et al. Epigenetic programming by maternal behavior. Nat Neurosci. 2004 Aug;7(8):847-54. Epub 2004 Jun 27.

Weaving LS et al. Mutations of CDKL5 Cause a Severe Neurodevelopmental Disorder with Infantile Spasms and Mental Retardation. Am J Hum Genet. 2004 Oct 18; 75 (6) [Epub ahead of print]

Weil D et al. Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin. Hum Mol Genet 2003;12(5):463-471.

Weiss LA, et al Association between microdeletion and microduplication at 16p11.2 and autism. N Engl J Med. 2008 Feb 14;358(7):667-75. Epub 2008 Jan 9.

Wellcome Trust Case Control Consortium. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature. 2007 Jun 7;447(7145):661-78.

Wenzel LB et al. Health-related quality of life in a racially diverse population screened for hemochromatosis: results from the Hemochromatosis and Iron Overload Screening (HEIRS) study. Genet Med. 2007 Oct;9(10):705-12.

Wersinger C et al. Mutations in the lipid-binding domain of alpha-synuclein confer overlapping, yet distinct, functional properties in the regulation of dopamine transporter activity. Mol Cell Neurosci. 2003 Sep;24(1):91-105.

Wijsman EM et al. Evidence for a novel late-onset Alzheimer disease locus on chromosome 19p13.2. Am J Hum Genet. 2004 Sep;75 (3): 398-409. Epub 2004 Jul 08.

Wilkie AO et al. FGFs, their receptors, and human limb malformations: clinical and molecular correlations. Am J Med Genet. 2002 Oct 15;112(3):266-78.

Williams RS. Another surprise from the mitochondrial genome.  N Engl J Med. 2002 Aug 22;347(8):609-12.

Wilson FH et al. A cluster of metabolic defects caused by mutation in a mitochondrial tRNA. Science. 2004 Nov 12; 306 (5699): 1190-4. Epub 2004 Oct 21.

Winn MP, et al. Unexpected role of TRPC6 channel in familial nephrotic syndrome: does it have clinical implications? J Am Soc Nephrol. 2006 Feb;17(2):378-87.

Wolf SM et al. Using Preimplantation Genetic Diagnosis to Create a Stem Cell Donor: Issues, Guidelines & Limits, Journal ofLaw, Medicine & Ethics 31:327-336 (2003)

Wolfberg AJ: Genes on the Web - Direct-to-Consumer Marketing of Genetic Testing. New Engl. J. Med 355: 543-545 (Aug. 16, 2006)

Wong KK et al. A comprehensive analysis of common copy-number variations in the human genome. Am J Hum Genet. 2007 Jan;80(1):91-104. Epub 2006 Dec 5.

Wood A et al. The Paf1 complex is essential for histone monoubiquitination by the Rad6-Bre1 complex, which signals for histone methylation by COMPASS and Dot1p. J Biol Chem. 2003 Sep 12;278(37):34739-42. Epub 2003 Jul 21.

Worgan LC et al. Spectrum of mutations in mut methylmalonic acidemia and identification of a common Hispanic mutation and haplotype. Hum Mutat. 2006 Jan;27(1):31-43.