70 related articles for article (PubMed ID: 18280617)
1. Further delineation of the association signal on chromosome 5 from the first whole genome association study in Parkinson's disease.
Sharma M; Lichtner P; Kruger R; Berg D; Schulte C; Illig T; Riess O; Gasser T
Neurobiol Aging; 2009 Oct; 30(10):1706-9. PubMed ID: 18280617
[TBL] [Abstract][Full Text] [Related]
2. Toward identification of susceptibility genes for sporadic Parkinson's disease.
Toda T; Momose Y; Murata M; Tamiya G; Yamamoto M; Hattori N; Inoko H
J Neurol; 2003 Oct; 250 Suppl 3():III40-3. PubMed ID: 14579123
[TBL] [Abstract][Full Text] [Related]
3. Multiple candidate gene analysis identifies alpha-synuclein as a susceptibility gene for sporadic Parkinson's disease.
Mizuta I; Satake W; Nakabayashi Y; Ito C; Suzuki S; Momose Y; Nagai Y; Oka A; Inoko H; Fukae J; Saito Y; Sawabe M; Murayama S; Yamamoto M; Hattori N; Murata M; Toda T
Hum Mol Genet; 2006 Apr; 15(7):1151-8. PubMed ID: 16500997
[TBL] [Abstract][Full Text] [Related]
4. Identification of a risk haplotype of the alpha-synuclein gene in Japanese with sporadic Parkinson's disease.
Kobayashi H; Ujike H; Hasegawa J; Yamamoto M; Kanzaki A; Sora I
Mov Disord; 2006 Dec; 21(12):2157-64. PubMed ID: 17078049
[TBL] [Abstract][Full Text] [Related]
5. Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population.
Saad M; Lesage S; Saint-Pierre A; Corvol JC; Zelenika D; Lambert JC; Vidailhet M; Mellick GD; Lohmann E; Durif F; Pollak P; Damier P; Tison F; Silburn PA; Tzourio C; Forlani S; Loriot MA; Giroud M; Helmer C; Portet F; Amouyel P; Lathrop M; Elbaz A; Durr A; Martinez M; Brice A;
Hum Mol Genet; 2011 Feb; 20(3):615-27. PubMed ID: 21084426
[TBL] [Abstract][Full Text] [Related]
6. Microtubule-associated protein tau (MAPT) influences the risk of Parkinson's disease among Indians.
Das G; Misra AK; Das SK; Ray K; Ray J
Neurosci Lett; 2009 Aug; 460(1):16-20. PubMed ID: 19450659
[TBL] [Abstract][Full Text] [Related]
7. Association study of GATA-2 transcription factor gene (GATA2) polymorphism and Parkinson's disease.
Kurzawski M; Białecka M; Sławek J; Kłodowska-Duda G; Droździk M
Parkinsonism Relat Disord; 2010 May; 16(4):284-7. PubMed ID: 19864173
[TBL] [Abstract][Full Text] [Related]
8. Fibroblast growth factor 20 gene and Parkinson's disease in the Japanese population.
Satake W; Mizuta I; Suzuki S; Nakabayashi Y; Ito C; Watanabe M; Takeda A; Hasegawa K; Sakoda S; Yamamoto M; Hattori N; Murata M; Toda T
Neuroreport; 2007 Jun; 18(9):937-40. PubMed ID: 17515805
[TBL] [Abstract][Full Text] [Related]
9. The transcription factor PITX3 is associated with sporadic Parkinson's disease.
Fuchs J; Mueller JC; Lichtner P; Schulte C; Munz M; Berg D; Wüllner U; Illig T; Sharma M; Gasser T
Neurobiol Aging; 2009 May; 30(5):731-8. PubMed ID: 17905480
[TBL] [Abstract][Full Text] [Related]
10. Role of ethnicity on the association of MAPT H1 haplotypes and subhaplotypes in Parkinson's disease.
Winkler S; König IR; Lohmann-Hedrich K; Vieregge P; Kostic V; Klein C
Eur J Hum Genet; 2007 Nov; 15(11):1163-8. PubMed ID: 17637803
[TBL] [Abstract][Full Text] [Related]
11. Meta-analysis in genome-wide association datasets: strategies and application in Parkinson disease.
Evangelou E; Maraganore DM; Ioannidis JP
PLoS One; 2007 Feb; 2(2):e196. PubMed ID: 17332845
[TBL] [Abstract][Full Text] [Related]
12. LINGO1 gene analysis in Parkinson's disease phenotypes.
Lorenzo-Betancor O; Samaranch L; García-Martín E; Cervantes S; Agúndez JA; Jiménez-Jiménez FJ; Alonso-Navarro H; Luengo A; Coria F; Lorenzo E; Irigoyen J; Pastor P;
Mov Disord; 2011 Mar; 26(4):722-7. PubMed ID: 21506150
[TBL] [Abstract][Full Text] [Related]
13. Replication of the Wellcome Trust genome-wide association study on essential hypertension in a Korean population.
Hong KW; Jin HS; Cho YS; Lee JY; Lee JE; Cho NH; Shin C; Lee SH; Park HK; Oh B
Hypertens Res; 2009 Jul; 32(7):570-4. PubMed ID: 19424278
[TBL] [Abstract][Full Text] [Related]
14. Association study of sporadic Parkinson's disease genetic risk factors in patients from Russia by APEX technology.
Shadrina M; Nikopensius T; Slominsky P; Illarioshkin S; Bagyeva G; Markova E; Ivanova-Smolenskaia I; Kurg A; Limborska S; Metspalu A
Neurosci Lett; 2006 Sep; 405(3):212-6. PubMed ID: 16876316
[TBL] [Abstract][Full Text] [Related]
15. A genome-wide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosis.
Mushiroda T; Wattanapokayakit S; Takahashi A; Nukiwa T; Kudoh S; Ogura T; Taniguchi H; Kubo M; Kamatani N; Nakamura Y;
J Med Genet; 2008 Oct; 45(10):654-6. PubMed ID: 18835860
[TBL] [Abstract][Full Text] [Related]
16. A genetic association study of the FXYD domain containing ion transport regulator 6 (FXYD6) gene, encoding phosphohippolin, in susceptibility to schizophrenia in a Japanese population.
Ito Y; Nakamura Y; Takahashi N; Saito S; Aleksic B; Iwata N; Inada T; Ozaki N
Neurosci Lett; 2008 Jun; 438(1):70-5. PubMed ID: 18455306
[TBL] [Abstract][Full Text] [Related]
17. Multiple alpha-synuclein gene polymorphisms are associated with Parkinson's disease in a Norwegian population.
Myhre R; Toft M; Kachergus J; Hulihan MM; Aasly JO; Klungland H; Farrer MJ
Acta Neurol Scand; 2008 Nov; 118(5):320-7. PubMed ID: 18485051
[TBL] [Abstract][Full Text] [Related]
18. Association study between the LINGO1 gene and Parkinson's disease in the Italian population.
Annesi F; De Marco EV; Rocca FE; Nicoletti A; Pugliese P; Nicoletti G; Arabia G; Tarantino P; De Mari M; Lamberti P; Gallerini S; Marconi R; Epifanio A; Morgante L; Cozzolino A; Barone P; Torchia G; Zappia M; Annesi G; Quattrone A
Parkinsonism Relat Disord; 2011 Sep; 17(8):638-41. PubMed ID: 21752692
[TBL] [Abstract][Full Text] [Related]
19. Genome-wide association study identifies ANXA11 as a new susceptibility locus for sarcoidosis.
Hofmann S; Franke A; Fischer A; Jacobs G; Nothnagel M; Gaede KI; Schürmann M; Müller-Quernheim J; Krawczak M; Rosenstiel P; Schreiber S
Nat Genet; 2008 Sep; 40(9):1103-6. PubMed ID: 19165924
[TBL] [Abstract][Full Text] [Related]
20. rs224136 on chromosome 10q21.1 and variants in PHOX2B, NCF4, and FAM92B are not major genetic risk factors for susceptibility to Crohn's disease in the German population.
Glas J; Seiderer J; Pasciuto G; Tillack C; Diegelmann J; Pfennig S; Konrad A; Schmechel S; Wetzke M; Török HP; Stallhofer J; Jürgens M; Griga T; Klein W; Epplen JT; Schiemann U; Mussack T; Lohse P; Göke B; Ochsenkühn T; Folwaczny M; Müller-Myhsok B; Brand S
Am J Gastroenterol; 2009 Mar; 104(3):665-72. PubMed ID: 19262523
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
