83 related articles for article (PubMed ID: 11977177)
1. Segregation analysis of Parkinson disease revealing evidence for a major causative gene.
Maher NE; Currie LJ; Lazzarini AM; Wilk JB; Taylor CA; Saint-Hilaire MH; Feldman RG; Golbe LI; Wooten GF; Myers RH
Am J Med Genet; 2002 May; 109(3):191-7. PubMed ID: 11977177
[TBL] [Abstract][Full Text] [Related]
2. Environmental, medical, and family history risk factors for Parkinson's disease: a New England-based case control study.
Taylor CA; Saint-Hilaire MH; Cupples LA; Thomas CA; Burchard AE; Feldman RG; Myers RH
Am J Med Genet; 1999 Dec; 88(6):742-9. PubMed ID: 10581500
[TBL] [Abstract][Full Text] [Related]
3. Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families.
Pankratz N; Nichols WC; Uniacke SK; Halter C; Murrell J; Rudolph A; Shults CW; Conneally PM; Foroud T;
Hum Mol Genet; 2003 Oct; 12(20):2599-608. PubMed ID: 12925570
[TBL] [Abstract][Full Text] [Related]
4. Complex segregation analysis of Parkinson's disease: The Mayo Clinic Family Study.
McDonnell SK; Schaid DJ; Elbaz A; Strain KJ; Bower JH; Ahlskog JE; Maraganore DM; Rocca WA
Ann Neurol; 2006 May; 59(5):788-95. PubMed ID: 16634030
[TBL] [Abstract][Full Text] [Related]
5. Evidence for a major gene influencing risk of pancreatic cancer.
Klein AP; Beaty TH; Bailey-Wilson JE; Brune KA; Hruban RH; Petersen GM
Genet Epidemiol; 2002 Aug; 23(2):133-49. PubMed ID: 12214307
[TBL] [Abstract][Full Text] [Related]
6. Genetic susceptibility to Parkinson's disease.
Johnson WG
Geriatrics; 1991 Aug; 46 Suppl 1():52-9. PubMed ID: 1894147
[TBL] [Abstract][Full Text] [Related]
7. Clinical genetic analysis of Parkinson's disease in the Contursi kindred.
Golbe LI; Di Iorio G; Sanges G; Lazzarini AM; La Sala S; Bonavita V; Duvoisin RC
Ann Neurol; 1996 Nov; 40(5):767-75. PubMed ID: 8957018
[TBL] [Abstract][Full Text] [Related]
8. Environmental factors can confound identification of a major gene effect: results from a segregation analysis of a simulated population of lung cancer families.
Sellers TA; Weaver TW; Phillips B; Altmann M; Rich SS
Genet Epidemiol; 1998; 15(3):251-62. PubMed ID: 9593112
[TBL] [Abstract][Full Text] [Related]
9. Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset families.
Winkelmann J; Muller-Myhsok B; Wittchen HU; Hock B; Prager M; Pfister H; Strohle A; Eisensehr I; Dichgans M; Gasser T; Trenkwalder C
Ann Neurol; 2002 Sep; 52(3):297-302. PubMed ID: 12205641
[TBL] [Abstract][Full Text] [Related]
10. alpha-Synuclein and Parkinson disease susceptibility.
Winkler S; Hagenah J; Lincoln S; Heckman M; Haugarvoll K; Lohmann-Hedrich K; Kostic V; Farrer M; Klein C
Neurology; 2007 Oct; 69(18):1745-50. PubMed ID: 17872362
[TBL] [Abstract][Full Text] [Related]
11. [The alpha-synuclein gene microsatellite polymorphism and late-onset sporadic Parkinson's disease susceptibility].
Zhao XP; Zheng HM; Xie HJ; Ding SJ; Ren DM
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Aug; 21(4):339-41. PubMed ID: 15300629
[TBL] [Abstract][Full Text] [Related]
12. A clinical and genetic study of familial Parkinson's disease.
Maraganore DM; Harding AE; Marsden CD
Mov Disord; 1991; 6(3):205-11. PubMed ID: 1922124
[TBL] [Abstract][Full Text] [Related]
13. Genetic basis of common diseases: the general theory of Mendelian recessive genetics.
Hutchinson M; Spanaki C; Lebedev S; Plaitakis A
Med Hypotheses; 2005; 65(2):282-6. PubMed ID: 15922101
[TBL] [Abstract][Full Text] [Related]
14. Potential role of an additive genetic component in the cause of amyotrophic lateral sclerosis and parkinsonism-dementia in the western Pacific.
Bailey-Wilson JE; Plato CC; Elston RC; Garruto RM
Am J Med Genet; 1993 Jan; 45(1):68-76. PubMed ID: 8418664
[TBL] [Abstract][Full Text] [Related]
15. Familial aggregation of early- and late-onset Parkinson's disease.
Marder K; Levy G; Louis ED; Mejia-Santana H; Cote L; Andrews H; Harris J; Waters C; Ford B; Frucht S; Fahn S; Ottman R
Ann Neurol; 2003 Oct; 54(4):507-13. PubMed ID: 14520664
[TBL] [Abstract][Full Text] [Related]
16. Clinical features of familial Parkinson's disease in Thai patients.
Prueksaritanond S; Boongird P; Pulkes T; Prueksaritanond S
Qual Prim Care; 2009; 17(2):115-22. PubMed ID: 19416604
[TBL] [Abstract][Full Text] [Related]
17. A clinical-genetic study of Parkinson's disease in a genetically isolated community.
Dekker MC; van Swieten JC; Houwing-Duistermaat JJ; Snijders PJ; Boeren E; Hofman A; Breteler MM; Heutink P; Oostra BA; van Duijn CM
J Neurol; 2003 Sep; 250(9):1056-62. PubMed ID: 14504966
[TBL] [Abstract][Full Text] [Related]
18. 5,10-methylenetetrahydrofolate reductase C677T gene polymorphism can influence age at onset of Parkinson's disease.
Lin JJ; Yueh KC; Liu CS; Liu JT; Lin SZ
Acta Neurol Taiwan; 2007 Sep; 16(3):150-7. PubMed ID: 17966954
[TBL] [Abstract][Full Text] [Related]
19. Segregation analysis of 231 Ashkenazi Jewish families for evidence of additional breast cancer susceptibility genes.
Kaufman DJ; Beaty TH; Struewing JP
Cancer Epidemiol Biomarkers Prev; 2003 Oct; 12(10):1045-52. PubMed ID: 14578141
[TBL] [Abstract][Full Text] [Related]
20. Phenotypic commonalities in familial and sporadic Parkinson disease.
Baba Y; Markopoulou K; Putzke JD; Whaley NR; Farrer MJ; Wszolek ZK; Uitti RJ
Arch Neurol; 2006 Apr; 63(4):579-83. PubMed ID: 16606772
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
