Li L - Search Results

1

LRRK2 P755L variant in sporadic Parkinson's disease.

Tomiyama H, Mizuta I, Li Y, Funayama M, Yoshino H, Li L, Murata M, Yamamoto M, Kubo SI, Mizuno Y, Toda T, Hattori N. Tomiyama H, et al. Among authors: li y, li l. J Hum Genet. 2008;53(11-12):1012-1015. doi: 10.1007/s10038-008-0336-5. Epub 2008 Oct 16. J Hum Genet. 2008. PMID: 18923807

2

No evidence for pathogenic role of GIGYF2 mutation in Parkinson disease in Japanese patients.

Li L, Funayama M, Tomiyama H, Li Y, Yoshino H, Sasaki R, Kokubo Y, Kuzuhara S, Mizuno Y, Hattori N. Li L, et al. Among authors: li y. Neurosci Lett. 2010 Aug 2;479(3):245-8. doi: 10.1016/j.neulet.2010.05.071. Neurosci Lett. 2010. PMID: 20641165

3

PLA2G6 variant in Parkinson's disease.

Tomiyama H, Yoshino H, Ogaki K, Li L, Yamashita C, Li Y, Funayama M, Sasaki R, Kokubo Y, Kuzuhara S, Hattori N. Tomiyama H, et al. Among authors: li y, li l. J Hum Genet. 2011 May;56(5):401-3. doi: 10.1038/jhg.2011.22. Epub 2011 Mar 3. J Hum Genet. 2011. PMID: 21368765

4

Clinicogenetic study of GBA mutations in patients with familial Parkinson's disease.

Li Y, Sekine T, Funayama M, Li L, Yoshino H, Nishioka K, Tomiyama H, Hattori N. Li Y, et al. Among authors: li l. Neurobiol Aging. 2014 Apr;35(4):935.e3-8. doi: 10.1016/j.neurobiolaging.2013.09.019. Epub 2013 Oct 12. Neurobiol Aging. 2014. PMID: 24126159

5

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.

6

Four SNPS on chromosome 9p21 confer risk to premature, familial CAD and MI in an American Caucasian population (GeneQuest).

Abdullah KG, Li L, Shen GQ, Hu Y, Yang Y, MacKinlay KG, Topol EJ, Wang QK. Abdullah KG, et al. Among authors: li l. Ann Hum Genet. 2008 Sep;72(Pt 5):654-7. doi: 10.1111/j.1469-1809.2008.00454.x. Epub 2008 May 26. Ann Hum Genet. 2008. PMID: 18505420 Free PMC article.

7

Genetic variant R952Q in LRP8 is associated with increased plasma triglyceride levels in patients with early-onset CAD and MI.

Shen GQ, Li L, Wang QK. Shen GQ, et al. Among authors: li l. Ann Hum Genet. 2012 May;76(3):193-9. doi: 10.1111/j.1469-1809.2012.00705.x. Epub 2012 Mar 8. Ann Hum Genet. 2012. PMID: 22404453

8

Association of SNP rs17465637 on chromosome 1q41 and rs599839 on 1p13.3 with myocardial infarction in an American caucasian population.

Wang AZ, Li L, Zhang B, Shen GQ, Wang QK. Wang AZ, et al. Among authors: li l. Ann Hum Genet. 2011 Jul;75(4):475-82. doi: 10.1111/j.1469-1809.2011.00646.x. Epub 2011 Apr 4. Ann Hum Genet. 2011. PMID: 21463265 Free PMC article.

9

Identification of association of common AGGF1 variants with susceptibility for Klippel-Trenaunay syndrome using the structure association program.

Hu Y, Li L, Seidelmann SB, Timur AA, Shen PH, Driscoll DJ, Wang QK. Hu Y, et al. Among authors: li l. Ann Hum Genet. 2008 Sep;72(Pt 5):636-43. doi: 10.1111/j.1469-1809.2008.00458.x. Epub 2008 Jun 16. Ann Hum Genet. 2008. PMID: 18564129 Free PMC article.

10

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.

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