Li L - Search Results

1

Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population.

Shen GQ, Rao S, Martinelli N, Li L, Olivieri O, Corrocher R, Abdullah KG, Hazen SL, Smith J, Barnard J, Plow EF, Girelli D, Wang QK. Shen GQ, et al. Among authors: li l. J Hum Genet. 2008;53(2):144-150. doi: 10.1007/s10038-007-0230-6. Epub 2007 Dec 8. J Hum Genet. 2008. PMID: 18066490

2

Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis.

Wang Q, Rao S, Shen GQ, Li L, Moliterno DJ, Newby LK, Rogers WJ, Cannata R, Zirzow E, Elston RC, Topol EJ. Wang Q, et al. Among authors: li l. Am J Hum Genet. 2004 Feb;74(2):262-71. doi: 10.1086/381560. Epub 2004 Jan 19. Am J Hum Genet. 2004. PMID: 14732905 Free PMC article.

3

Genetic linkage analysis of longitudinal hypertension phenotypes using three summary measures.

Rao S, Li L, Li X, Moser KL, Guo Z, Shen G, Cannata R, Zirzow E, Topol EJ, Wang Q. Rao S, et al. Among authors: li x, li l. BMC Genet. 2003 Dec 31;4 Suppl 1(Suppl 1):S24. doi: 10.1186/1471-2156-4-S1-S24. BMC Genet. 2003. PMID: 14975092 Free PMC article.

4

Multivariate sib-pair linkage analysis of longitudinal phenotypes by three step-wise analysis approaches.

Guo Z, Li X, Rao S, Moser KL, Zhang T, Gong B, Shen G, Li L, Cannata R, Zirzow E, Topol EJ, Wang Q. Guo Z, et al. Among authors: li x, li l. BMC Genet. 2003 Dec 31;4 Suppl 1(Suppl 1):S68. doi: 10.1186/1471-2156-4-S1-S68. BMC Genet. 2003. PMID: 14975136 Free PMC article.

5

Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p.

Chen S, Ondo WG, Rao S, Li L, Chen Q, Wang Q. Chen S, et al. Among authors: li l. Am J Hum Genet. 2004 May;74(5):876-85. doi: 10.1086/420772. Epub 2004 Apr 7. Am J Hum Genet. 2004. PMID: 15077200 Free PMC article.

6

Genome-wide linkage scan identifies a novel genetic locus on chromosome 5p13 for neonatal atrial fibrillation associated with sudden death and variable cardiomyopathy.

Oberti C, Wang L, Li L, Dong J, Rao S, Du W, Wang Q. Oberti C, et al. Among authors: li l. Circulation. 2004 Dec 21;110(25):3753-9. doi: 10.1161/01.CIR.0000150333.87176.C7. Epub 2004 Dec 13. Circulation. 2004. PMID: 15596564 Free PMC article.

7

Mapping a new genetic locus for X linked retinitis pigmentosa to Xq28.

Melamud A, Shen GQ, Chung D, Xi Q, Simpson E, Li L, Peachey NS, Zegarra H, Hagstrom SA, Wang QK, Traboulsi EI. Melamud A, et al. Among authors: li l. J Med Genet. 2006 Jun;43(6):e27. doi: 10.1136/jmg.2005.031518. J Med Genet. 2006. PMID: 16740911 Free PMC article.

8

LINKAGE programs: linkage analysis for monogenic cardiovascular diseases.

Li L, Wang QK, Rao S. Li L, et al. Methods Mol Med. 2006;128:41-60. doi: 10.1385/1-59745-159-2:41. Methods Mol Med. 2006. PMID: 17071989

9

Identification of a novel GPR143 mutation in a large Chinese family with congenital nystagmus as the most prominent and consistent manifestation.

Liu JY, Ren X, Yang X, Guo T, Yao Q, Li L, Dai X, Zhang M, Wang L, Liu M, Wang QK. Liu JY, et al. Among authors: li l. J Hum Genet. 2007;52(6):565-570. doi: 10.1007/s10038-007-0152-3. Epub 2007 May 22. J Hum Genet. 2007. PMID: 17516023

10

An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction.

Shen GQ, Li L, Girelli D, Seidelmann SB, Rao S, Fan C, Park JE, Xi Q, Li J, Hu Y, Olivieri O, Marchant K, Barnard J, Corrocher R, Elston R, Cassano J, Henderson S, Hazen SL, Plow EF, Topol EJ, Wang QK. Shen GQ, et al. Among authors: li j, li l. Am J Hum Genet. 2007 Oct;81(4):780-91. doi: 10.1086/521581. Epub 2007 Aug 31. Am J Hum Genet. 2007. PMID: 17847002 Free PMC article.

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