Xiong L - Search Results

1

Genetic association studies of neurotensin gene and restless legs syndrome in French Canadians.

Xiong L, Levchenko A, Montplaisir J, Rivière JB, Thibodeau P, St-Onge J, Gaspar C, Desautels A, Lespérance P, Chouinard S, Turecki G, Rouleau GA. Xiong L, et al. Sleep Med. 2008 Mar;9(3):273-82. doi: 10.1016/j.sleep.2007.03.020. Epub 2007 Jul 17. Sleep Med. 2008. PMID: 17644423

2

Mutational analysis of neurotensin in familial restless legs syndrome.

Desautels A, Turecki G, Xiong L, Rochefort D, Montplaisir J, Rouleau GA. Desautels A, et al. Among authors: xiong l. Mov Disord. 2004 Jan;19(1):90-4. doi: 10.1002/mds.10617. Mov Disord. 2004. PMID: 14743366

3

The 14q restless legs syndrome locus in the French Canadian population.

Levchenko A, Montplaisir JY, Dubé MP, Riviere JB, St-Onge J, Turecki G, Xiong L, Thibodeau P, Desautels A, Verlaan DJ, Rouleau GA. Levchenko A, et al. Among authors: xiong l. Ann Neurol. 2004 Jun;55(6):887-91. doi: 10.1002/ana.20140. Ann Neurol. 2004. PMID: 15174026

4

CAA insertion polymorphism in the 3'UTR of Nogo gene on 2p14 is not associated with schizophrenia.

Xiong L, Rouleau GA, Delisi LE, St-Onge J, Najafee R, Rivière JB, Benkelfat C, Tabbane K, Fathalli F, Danics Z, Labelle A, Lal S, Joober R. Xiong L, et al. Brain Res Mol Brain Res. 2005 Jan 5;133(1):153-6. doi: 10.1016/j.molbrainres.2004.08.024. Brain Res Mol Brain Res. 2005. PMID: 15661375

5

Restless legs syndrome: confirmation of linkage to chromosome 12q, genetic heterogeneity, and evidence of complexity.

Desautels A, Turecki G, Montplaisir J, Xiong L, Walters AS, Ehrenberg BL, Brisebois K, Desautels AK, Gingras Y, Johnson WG, Lugaresi E, Coccagna G, Picchietti DL, Lazzarini A, Rouleau GA. Desautels A, et al. Among authors: xiong l. Arch Neurol. 2005 Apr;62(4):591-6. doi: 10.1001/archneur.62.4.591. Arch Neurol. 2005. PMID: 15824258

6

Association study of the trinucleotide repeat polymorphism within SMARCA2 and schizophrenia.

Sengupta S, Xiong L, Fathalli F, Benkelfat C, Tabbane K, Danics Z, Labelle A, Lal S, Krebs MO, Rouleau G, Joober R. Sengupta S, et al. Among authors: xiong l. BMC Genet. 2006 Jun 3;7:34. doi: 10.1186/1471-2156-7-34. BMC Genet. 2006. PMID: 16749937 Free PMC article.

7

A novel autosomal dominant restless legs syndrome locus maps to chromosome 20p13.

Levchenko A, Provost S, Montplaisir JY, Xiong L, St-Onge J, Thibodeau P, Rivière JB, Desautels A, Turecki G, Dubé MP, Rouleau GA. Levchenko A, et al. Among authors: xiong l. Neurology. 2006 Sep 12;67(5):900-1. doi: 10.1212/01.wnl.0000233991.20410.b6. Neurology. 2006. PMID: 16966564

8

Canadian restless legs syndrome twin study.

Xiong L, Jang K, Montplaisir J, Levchenko A, Thibodeau P, Gaspar C, Turecki G, Rouleau GA. Xiong L, et al. Neurology. 2007 May 8;68(19):1631-3. doi: 10.1212/01.wnl.0000261016.90374.fd. Neurology. 2007. PMID: 17485653 No abstract available.

9

Molecular genetic studies of DMT1 on 12q in French-Canadian restless legs syndrome patients and families.

Xiong L, Dion P, Montplaisir J, Levchenko A, Thibodeau P, Karemera L, Rivière JB, St-Onge J, Gaspar C, Dubé MP, Desautels A, Turecki G, Rouleau GA. Xiong L, et al. Am J Med Genet B Neuropsychiatr Genet. 2007 Oct 5;144B(7):911-7. doi: 10.1002/ajmg.b.30528. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17510944

10

Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions.

Winkelmann J, Schormair B, Lichtner P, Ripke S, Xiong L, Jalilzadeh S, Fulda S, Pütz B, Eckstein G, Hauk S, Trenkwalder C, Zimprich A, Stiasny-Kolster K, Oertel W, Bachmann CG, Paulus W, Peglau I, Eisensehr I, Montplaisir J, Turecki G, Rouleau G, Gieger C, Illig T, Wichmann HE, Holsboer F, Müller-Myhsok B, Meitinger T. Winkelmann J, et al. Among authors: xiong l. Nat Genet. 2007 Aug;39(8):1000-6. doi: 10.1038/ng2099. Epub 2007 Jul 18. Nat Genet. 2007. PMID: 17637780

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