Li C - Search Results

1

A prevalence-based association test for case-control studies.

Ryckman KK, Jiang L, Li C, Bartlett J, Haines JL, Williams SM. Ryckman KK, et al. Among authors: li c. Genet Epidemiol. 2008 Nov;32(7):600-5. doi: 10.1002/gepi.20342. Genet Epidemiol. 2008. PMID: 18473366

2

Leveraging Identity-by-Descent for Accurate Genotype Inference in Family Sequencing Data.

Li B, Wei Q, Zhan X, Zhong X, Chen W, Li C, Haines J. Li B, et al. Among authors: li c. PLoS Genet. 2015 Jun 4;11(6):e1005271. doi: 10.1371/journal.pgen.1005271. eCollection 2015 Jun. PLoS Genet. 2015. PMID: 26043085 Free PMC article.

3

Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1.

Zheng W, Long J, Gao YT, Li C, Zheng Y, Xiang YB, Wen W, Levy S, Deming SL, Haines JL, Gu K, Fair AM, Cai Q, Lu W, Shu XO. Zheng W, et al. Among authors: li c. Nat Genet. 2009 Mar;41(3):324-8. doi: 10.1038/ng.318. Epub 2009 Feb 15. Nat Genet. 2009. PMID: 19219042 Free PMC article.

4

Genetic Association Analysis of Drusen Progression.

Hoffman JD, van Grinsven MJ, Li C, Brantley M Jr, McGrath J, Agarwal A, Scott WK, Schwartz SG, Kovach J, Pericak-Vance M, Sanchez CI, Haines JL. Hoffman JD, et al. Among authors: li c. Invest Ophthalmol Vis Sci. 2016 Apr 1;57(4):2225-31. doi: 10.1167/iovs.15-18571. Invest Ophthalmol Vis Sci. 2016. PMID: 27116550 Free PMC article.

5

Variations in the alpha2A-adrenergic receptor gene and their functional effects.

Kurnik D, Muszkat M, Li C, Sofowora GG, Solus J, Xie HG, Harris PA, Jiang L, McMunn C, Ihrie P, Dawson EP, Williams SM, Wood AJ, Stein CM. Kurnik D, et al. Among authors: li c. Clin Pharmacol Ther. 2006 Mar;79(3):173-85. doi: 10.1016/j.clpt.2005.10.006. Epub 2006 Feb 7. Clin Pharmacol Ther. 2006. PMID: 16513442

6

Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates.

McCauley JL, Li C, Jiang L, Olson LM, Crockett G, Gainer K, Folstein SE, Haines JL, Sutcliffe JS. McCauley JL, et al. Among authors: li c. BMC Med Genet. 2005 Jan 12;6:1. doi: 10.1186/1471-2350-6-1. BMC Med Genet. 2005. PMID: 15647115 Free PMC article.

7

Recurrent tissue-specific mtDNA mutations are common in humans.

Samuels DC, Li C, Li B, Song Z, Torstenson E, Boyd Clay H, Rokas A, Thornton-Wells TA, Moore JH, Hughes TM, Hoffman RD, Haines JL, Murdock DG, Mortlock DP, Williams SM. Samuels DC, et al. Among authors: li c, li b. PLoS Genet. 2013 Nov;9(11):e1003929. doi: 10.1371/journal.pgen.1003929. Epub 2013 Nov 7. PLoS Genet. 2013. PMID: 24244193 Free PMC article.

8

Beta-1-adrenoceptor genetic variants and ethnicity independently affect response to beta-blockade.

Kurnik D, Li C, Sofowora GG, Friedman EA, Muszkat M, Xie HG, Harris PA, Williams SM, Nair UB, Wood AJ, Stein CM. Kurnik D, et al. Among authors: li c. Pharmacogenet Genomics. 2008 Oct;18(10):895-902. doi: 10.1097/FPC.0b013e328309733f. Pharmacogenet Genomics. 2008. PMID: 18794726 Free PMC article.

9

Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors.

Sutcliffe JS, Delahanty RJ, Prasad HC, McCauley JL, Han Q, Jiang L, Li C, Folstein SE, Blakely RD. Sutcliffe JS, et al. Among authors: li c. Am J Hum Genet. 2005 Aug;77(2):265-79. doi: 10.1086/432648. Epub 2005 Jul 1. Am J Hum Genet. 2005. PMID: 15995945 Free PMC article.

10

Haplotype association analysis for late onset diseases using nuclear family data.

Li C, Boehnke M. Li C, et al. Genet Epidemiol. 2006 Apr;30(3):220-30. doi: 10.1002/gepi.20139. Genet Epidemiol. 2006. PMID: 16470533 Free article.

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