Wang H - Search Results

1

Identification of pathways for atherosclerosis in mice: integration of quantitative trait locus analysis and global gene expression data.

Wang SS, Schadt EE, Wang H, Wang X, Ingram-Drake L, Shi W, Drake TA, Lusis AJ. Wang SS, et al. Among authors: wang h, wang x. Circ Res. 2007 Aug 3;101(3):e11-30. doi: 10.1161/CIRCRESAHA.107.152975. Epub 2007 Jul 19. Circ Res. 2007. PMID: 17641228

2

Genetic and genomic analysis of a fat mass trait with complex inheritance reveals marked sex specificity.

Wang S, Yehya N, Schadt EE, Wang H, Drake TA, Lusis AJ. Wang S, et al. Among authors: wang h. PLoS Genet. 2006 Feb;2(2):e15. doi: 10.1371/journal.pgen.0020015. Epub 2006 Feb 3. PLoS Genet. 2006. PMID: 16462940 Free PMC article.

3

Tissue-specific expression and regulation of sexually dimorphic genes in mice.

Yang X, Schadt EE, Wang S, Wang H, Arnold AP, Ingram-Drake L, Drake TA, Lusis AJ. Yang X, et al. Among authors: wang h, wang s. Genome Res. 2006 Aug;16(8):995-1004. doi: 10.1101/gr.5217506. Epub 2006 Jul 6. Genome Res. 2006. PMID: 16825664 Free PMC article.

4

A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity.

Lee H, Jen JC, Wang H, Chen Z, Mamsa H, Sabatti C, Baloh RW, Nelson SF. Lee H, et al. Among authors: wang h. Hum Mol Genet. 2006 Jan 15;15(2):251-8. doi: 10.1093/hmg/ddi441. Epub 2005 Dec 5. Hum Mol Genet. 2006. PMID: 16330481

5

Suggestive linkage to chromosome 6q in families with bilateral vestibulopathy.

Jen JC, Wang H, Lee H, Sabatti C, Trent R, Hannigan I, Brantberg K, Halmagyi GM, Nelson SF, Baloh RW. Jen JC, et al. Among authors: wang h. Neurology. 2004 Dec 28;63(12):2376-9. doi: 10.1212/01.wnl.0000149498.79541.49. Neurology. 2004. PMID: 15623703

6

Linkage disequilibrium and haplotype homozygosity in population samples genotyped at a high marker density.

Wang H, Lin CH, Service S, Chen Y, Freimer N, Sabatti C; International Collaborative Group on Isolated Populations. Wang H, et al. Hum Hered. 2006;62(4):175-89. doi: 10.1159/000096599. Epub 2006 Oct 30. Hum Hered. 2006. PMID: 17077642

7

Markov Models for inferring copy number variations from genotype data on Illumina platforms.

Wang H, Veldink JH, Blauw H, van den Berg LH, Ophoff RA, Sabatti C. Wang H, et al. Hum Hered. 2009;68(1):1-22. doi: 10.1159/000210445. Epub 2009 Apr 1. Hum Hered. 2009. PMID: 19339782 Free PMC article.

8

A novel mutation in KCNA1 causes episodic ataxia without myokymia.

Lee H, Wang H, Jen JC, Sabatti C, Baloh RW, Nelson SF. Lee H, et al. Among authors: wang h. Hum Mutat. 2004 Dec;24(6):536. doi: 10.1002/humu.9295. Hum Mutat. 2004. PMID: 15532032

9

Backward genotype-trait association (BGTA)-based dissection of complex traits in case-control designs.

Zheng T, Wang H, Lo SH. Zheng T, et al. Among authors: wang h. Hum Hered. 2006;62(4):196-212. doi: 10.1159/000096995. Epub 2006 Nov 15. Hum Hered. 2006. PMID: 17114886 Free PMC article.

10

Structure of the trypanosome paraflagellar rod and insights into non-planar motility of eukaryotic cells.

Zhang J, Wang H, Imhof S, Zhou X, Liao S, Atanasov I, Hui WH, Hill KL, Zhou ZH. Zhang J, et al. Among authors: wang h. Cell Discov. 2021 Jul 13;7(1):51. doi: 10.1038/s41421-021-00281-2. Cell Discov. 2021. PMID: 34257277 Free PMC article.

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