Wang J - Search Results

1

Ankyrin G overexpression in Hutchinson-Gilford progeria syndrome fibroblasts identified through biological filtering of expression profiles.

Wang J, Robinson JF, O'Neil CH, Edwards JY, Williams CM, Huff MW, Pickering JG, Hegele RA. Wang J, et al. J Hum Genet. 2006;51(11):934-942. doi: 10.1007/s10038-006-0042-0. Epub 2006 Oct 11. J Hum Genet. 2006. PMID: 17033732

2

Genomic basis of cystathioninuria (MIM 219500) revealed by multiple mutations in cystathionine gamma-lyase (CTH).

Wang J, Hegele RA. Wang J, et al. Hum Genet. 2003 Apr;112(4):404-8. doi: 10.1007/s00439-003-0906-8. Epub 2003 Feb 6. Hum Genet. 2003. PMID: 12574942

3

Polymorphisms in the gene encoding phosphatidylserine-specific phospholipase A1 ( PSPLA1).

Wang J, Wen XY, Stewart AK, Hegele RA. Wang J, et al. J Hum Genet. 2002;47(11):611-3. doi: 10.1007/s100380200093. J Hum Genet. 2002. PMID: 12436198

4

Optimizing RNA extraction yield from whole blood for microarray gene expression analysis.

Wang J, Robinson JF, Khan HM, Carter DE, McKinney J, Miskie BA, Hegele RA. Wang J, et al. Clin Biochem. 2004 Sep;37(9):741-4. doi: 10.1016/j.clinbiochem.2004.03.013. Clin Biochem. 2004. PMID: 15329310

5

Multiplex ligation-dependent probe amplification of LDLR enhances molecular diagnosis of familial hypercholesterolemia.

Wang J, Ban MR, Hegele RA. Wang J, et al. J Lipid Res. 2005 Feb;46(2):366-72. doi: 10.1194/jlr.D400030-JLR200. Epub 2004 Dec 1. J Lipid Res. 2005. PMID: 15576851 Free article.

6

Homozygous missense mutation (G56R) in glycosylphosphatidylinositol-anchored high-density lipoprotein-binding protein 1 (GPI-HBP1) in two siblings with fasting chylomicronemia (MIM 144650).

Wang J, Hegele RA. Wang J, et al. Lipids Health Dis. 2007 Sep 20;6:23. doi: 10.1186/1476-511X-6-23. Lipids Health Dis. 2007. PMID: 17883852 Free PMC article.

7

Polygenic determinants of severe hypertriglyceridemia.

Wang J, Ban MR, Zou GY, Cao H, Lin T, Kennedy BA, Anand S, Yusuf S, Huff MW, Pollex RL, Hegele RA. Wang J, et al. Hum Mol Genet. 2008 Sep 15;17(18):2894-9. doi: 10.1093/hmg/ddn188. Epub 2008 Jul 1. Hum Mol Genet. 2008. PMID: 18596051

8

A multiplex human syndrome implicates a key role for intestinal cell kinase in development of central nervous, skeletal, and endocrine systems.

Lahiry P, Wang J, Robinson JF, Turowec JP, Litchfield DW, Lanktree MB, Gloor GB, Puffenberger EG, Strauss KA, Martens MB, Ramsay DA, Rupar CA, Siu V, Hegele RA. Lahiry P, et al. Among authors: wang j. Am J Hum Genet. 2009 Feb;84(2):134-47. doi: 10.1016/j.ajhg.2008.12.017. Epub 2009 Jan 29. Am J Hum Genet. 2009. PMID: 19185282 Free PMC article.

9

A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia.

Hegele RA, Ban MR, Hsueh N, Kennedy BA, Cao H, Zou GY, Anand S, Yusuf S, Huff MW, Wang J. Hegele RA, et al. Among authors: wang j. Hum Mol Genet. 2009 Nov 1;18(21):4189-94. doi: 10.1093/hmg/ddp361. Epub 2009 Aug 5. Hum Mol Genet. 2009. PMID: 19656773 Free PMC article.

10

Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.

Johansen CT, Wang J, Lanktree MB, Cao H, McIntyre AD, Ban MR, Martins RA, Kennedy BA, Hassell RG, Visser ME, Schwartz SM, Voight BF, Elosua R, Salomaa V, O'Donnell CJ, Dallinga-Thie GM, Anand SS, Yusuf S, Huff MW, Kathiresan S, Hegele RA. Johansen CT, et al. Among authors: wang j. Nat Genet. 2010 Aug;42(8):684-7. doi: 10.1038/ng.628. Epub 2010 Jul 25. Nat Genet. 2010. PMID: 20657596 Free PMC article.

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