193 related articles for article (PubMed ID: 31085086)
21. Inferring the Nature of Missing Heritability in Human Traits Using Data from the GWAS Catalog.
López-Cortegano E; Caballero A
Genetics; 2019 Jul; 212(3):891-904. PubMed ID: 31123044
[TBL] [Abstract][Full Text] [Related]
22. Histamine N-methyltransferase Thr105Ile is not associated with Parkinson's disease or essential tremor.
Keeling BH; Vilariño-Güell C; Soto-Ortolaza AI; Ross OA; Uitti RJ; Rajput A; Wszolek ZK; Farrer MJ
Parkinsonism Relat Disord; 2010 Feb; 16(2):112-4. PubMed ID: 19773194
[TBL] [Abstract][Full Text] [Related]
23. Dominant Genetic Variation and Missing Heritability for Human Complex Traits: Insights from Twin versus Genome-wide Common SNP Models.
Chen X; Kuja-Halkola R; Rahman I; Arpegård J; Viktorin A; Karlsson R; Hägg S; Svensson P; Pedersen NL; Magnusson PK
Am J Hum Genet; 2015 Nov; 97(5):708-14. PubMed ID: 26544805
[TBL] [Abstract][Full Text] [Related]
24. [Genetics of movement disorders].
Lohmann K; Brockmann K
Nervenarzt; 2013 Feb; 84(2):143-50. PubMed ID: 23354823
[TBL] [Abstract][Full Text] [Related]
25. Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.
Winkelmann J; Lichtner P; Pütz B; Trenkwalder C; Hauk S; Meitinger T; Strom T; Muller-Myhsok B
Mov Disord; 2006 Jan; 21(1):28-33. PubMed ID: 16124010
[TBL] [Abstract][Full Text] [Related]
26. Essential tremor in Parkinson's disease kindreds from a population of similar genetic background.
Spanaki C; Plaitakis A
Mov Disord; 2009 Aug; 24(11):1662-8. PubMed ID: 19514058
[TBL] [Abstract][Full Text] [Related]
27. Association between restless legs syndrome and essential tremor.
Ondo WG; Lai D
Mov Disord; 2006 Apr; 21(4):515-8. PubMed ID: 16250022
[TBL] [Abstract][Full Text] [Related]
28. Prediction of depression and anxiety via patient-assessed tremor severity, not physician-reported motor symptom severity, in patients with Parkinson's disease or essential tremor who have undergone deep brain stimulation.
Achey RL; Yamamoto E; Sexton D; Hammer C; Lee BS; Butler RS; Thompson NR; Nagel SJ; Machado AG; Lobel DA
J Neurosurg; 2018 Dec; 129(6):1562-1571. PubMed ID: 29473781
[TBL] [Abstract][Full Text] [Related]
29. Lack of Causal Effects or Genetic Correlation between Restless Legs Syndrome and Parkinson's Disease.
Estiar MA; Senkevich K; Yu E; Varghaei P; Krohn L; Bandres-Ciga S; Noyce AJ; Rouleau GA; Gan-Or Z
Mov Disord; 2021 Aug; 36(8):1967-1972. PubMed ID: 33974305
[TBL] [Abstract][Full Text] [Related]
30. Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors.
Liu H; Dehestani M; Blauwendraat C; Makarious MB; Leonard H; Kim JJ; Schulte C; Noyce A; Jacobs BM; Foote I; Sharma M; ; Nalls M; Singleton A; Gasser T; Bandres-Ciga S
Ann Neurol; 2022 Aug; 92(2):270-278. PubMed ID: 35599344
[TBL] [Abstract][Full Text] [Related]
31. The endocytic membrane trafficking pathway plays a major role in the risk of Parkinson's disease.
Bandres-Ciga S; Saez-Atienzar S; Bonet-Ponce L; Billingsley K; Vitale D; Blauwendraat C; Gibbs JR; Pihlstrøm L; Gan-Or Z; ; Cookson MR; Nalls MA; Singleton AB
Mov Disord; 2019 Apr; 34(4):460-468. PubMed ID: 30675927
[TBL] [Abstract][Full Text] [Related]
32. Polymorphisms in the glial glutamate transporter SLC1A2 are associated with essential tremor.
Thier S; Lorenz D; Nothnagel M; Poremba C; Papengut F; Appenzeller S; Paschen S; Hofschulte F; Hussl AC; Hering S; Poewe W; Asmus F; Gasser T; Schöls L; Christensen K; Nebel A; Schreiber S; Klebe S; Deuschl G; Kuhlenbäumer G
Neurology; 2012 Jul; 79(3):243-8. PubMed ID: 22764253
[TBL] [Abstract][Full Text] [Related]
33. Association of candidate genetic variants with restless legs syndrome in end stage renal disease: a multicenter case-control study in Taiwan.
Lin CH; Chen ML; Wu VC; Li WY; Sy HN; Wu SL; Chang CC; Chiu PF; Liou HH; Lin CY; Chang HW; Lin SY; Wu KD; Chen YM; Wu RM
Eur J Neurol; 2014 Mar; 21(3):492-8. PubMed ID: 24433515
[TBL] [Abstract][Full Text] [Related]
34. Missing heritability in Parkinson's disease: the emerging role of non-coding genetic variation.
Ohnmacht J; May P; Sinkkonen L; Krüger R
J Neural Transm (Vienna); 2020 May; 127(5):729-748. PubMed ID: 32248367
[TBL] [Abstract][Full Text] [Related]
35. Familial Aggregation and Co-Aggregation of Essential Tremor and Parkinson's Disease.
Louis ED; Clark L; Ottman R
Neuroepidemiology; 2016; 46(1):31-6. PubMed ID: 26606512
[TBL] [Abstract][Full Text] [Related]
36. Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.
Do CB; Tung JY; Dorfman E; Kiefer AK; Drabant EM; Francke U; Mountain JL; Goldman SM; Tanner CM; Langston JW; Wojcicki A; Eriksson N
PLoS Genet; 2011 Jun; 7(6):e1002141. PubMed ID: 21738487
[TBL] [Abstract][Full Text] [Related]
37. IL1B polymorphism is associated with essential tremor in Chinese population.
Chen J; Huang P; He Y; Shen J; Du J; Cui S; Chen S; Ma J
BMC Neurol; 2019 May; 19(1):99. PubMed ID: 31092216
[TBL] [Abstract][Full Text] [Related]
38. Lrrk2 R1628P variant is a risk factor for essential tremor.
Chao YX; Ng EY; Tan L; Prakash KM; Au WL; Zhao Y; Tan EK
Sci Rep; 2015 Mar; 5():9029. PubMed ID: 25761573
[TBL] [Abstract][Full Text] [Related]
39. Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease.
Blauwendraat C; Iwaki H; Makarious MB; Bandres-Ciga S; Leonard HL; Grenn FP; Lake J; Krohn L; Tan M; Kim JJ; Gibbs JR; Hernandez DG; Ruskey JA; Pihlstrøm L; Toft M; van Hilten JJ; Marinus J; Schulte C; Brockmann K; Sharma M; Siitonen A; Majamaa K; Eerola-Rautio J; Tienari PJ; Grosset DG; Lesage S; Corvol JC; Brice A; Wood N; Hardy J; Gan-Or Z; Heutink P; Gasser T; Morris HR; Noyce AJ; Nalls MA; Singleton AB;
Ann Neurol; 2021 Jul; 90(1):35-42. PubMed ID: 33901317
[TBL] [Abstract][Full Text] [Related]
40. Lingo2 variants associated with essential tremor and Parkinson's disease.
Wu YW; Prakash KM; Rong TY; Li HH; Xiao Q; Tan LC; Au WL; Ding JQ; Chen SD; Tan EK
Hum Genet; 2011 Jun; 129(6):611-5. PubMed ID: 21287203
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]