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8. Type 2 diabetes mellitus disease risk genes identified by genome wide copy number variation scan in normal populations. Prabhanjan M; Suresh RV; Murthy MN; Ramachandra NB Diabetes Res Clin Pract; 2016 Mar; 113():160-70. PubMed ID: 26830856 [TBL] [Abstract][Full Text] [Related]
9. Do polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic Parkinson's disease? Sutherland GT; Halliday GM; Silburn PA; Mastaglia FL; Rowe DB; Boyle RS; O'Sullivan JD; Ly T; Wilton SD; Mellick GD Mov Disord; 2009 Apr; 24(6):833-8. PubMed ID: 19224617 [TBL] [Abstract][Full Text] [Related]
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12. Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder. Yin CL; Chen HI; Li LH; Chien YL; Liao HM; Chou MC; Chou WJ; Tsai WC; Chiu YN; Wu YY; Lo CZ; Wu JY; Chen YT; Gau SS Mol Autism; 2016; 7():23. PubMed ID: 27042285 [TBL] [Abstract][Full Text] [Related]
13. Resequencing analysis of five Mendelian genes and the top genes from genome-wide association studies in Parkinson's Disease. Benitez BA; Davis AA; Jin SC; Ibanez L; Ortega-Cubero S; Pastor P; Choi J; Cooper B; Perlmutter JS; Cruchaga C Mol Neurodegener; 2016 Apr; 11():29. PubMed ID: 27094865 [TBL] [Abstract][Full Text] [Related]
14. Molecular pathogenesis of Parkinson's disease: update. Saiki S; Sato S; Hattori N J Neurol Neurosurg Psychiatry; 2012 Apr; 83(4):430-6. PubMed ID: 22138181 [TBL] [Abstract][Full Text] [Related]
15. Analysis of Leucine-rich repeat kinase 2 (LRRK2) and Parkinson protein 2 (parkin, PARK2) genes mutations in Slovak Parkinson disease patients. Bognar C; Baldovic M; Benetin J; Kadasi L; Zatkova A Gen Physiol Biophys; 2013 Mar; 32(1):55-66. PubMed ID: 23531835 [TBL] [Abstract][Full Text] [Related]
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17. A DNA resequencing array for genes involved in Parkinson's disease. Wilkins EJ; Rubio JP; Kotschet KE; Cowie TF; Boon WC; O'Hely M; Burfoot R; Wang W; Sue CM; Speed TP; Stankovitch J; Horne MK Parkinsonism Relat Disord; 2012 May; 18(4):386-90. PubMed ID: 22243833 [TBL] [Abstract][Full Text] [Related]
18. Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population. Nuytemans K; Meeus B; Crosiers D; Brouwers N; Goossens D; Engelborghs S; Pals P; Pickut B; Van den Broeck M; Corsmit E; Cras P; De Deyn PP; Del-Favero J; Van Broeckhoven C; Theuns J Hum Mutat; 2009 Jul; 30(7):1054-61. PubMed ID: 19405094 [TBL] [Abstract][Full Text] [Related]
19. Exonic rearrangements in the known Parkinson's disease-causing genes are a rare cause of the disease in South African patients. van der Merwe C; Carr J; Glanzmann B; Bardien S Neurosci Lett; 2016 Apr; 619():168-71. PubMed ID: 27001088 [TBL] [Abstract][Full Text] [Related]
20. Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans. Haraksingh RR; Abyzov A; Urban AE BMC Genomics; 2017 Apr; 18(1):321. PubMed ID: 28438122 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]