المؤلفون: Simon-Sanchez, J., Hilten, J.J. van, Warrenburg, B. van de, Post, B., Berendse, H.W., Arepalli, S., Hernandez, D.G., Bie, R.M.A. de, Velseboer, D., Scheffer, H., Bloem, B., Dijk, K.D. van, Rivadeneira, F., Hofman, A., Uitterlinden, A.G., Rizzu, P., Bochdanovits, Z., Singleton, A.B., Heutink, P.

المصدر: European Journal of Human Genetics

مصطلحات موضوعية: SNCA, BST1, GAK/DGKQ, HLA, MAPT, PD

العلاقة: lumc-id: 4431386; https://hdl.handle.net/1887/108594Test

الإتاحة: https://doi.org/10.1038/ejhg.2010.254Test
https://hdl.handle.net/1887/108594Test

المؤلفون: Sampath Arepalli, Zoltán Bochdanovits, Rob M.A. de Bie, Bart P.C. van de Warrenburg, Albert Hofman, Bart Post, Peter Heutink, Fernando Rivadeneira, Andrew B. Singleton, Dena G. Hernandez, Hans Scheffer, Jacobus J. van Hilten, Karin van Dijk, B.R. Bloem, Daan C. Velseboer, Henk W. Berendse, Patrizia Rizzu, André G. Uitterlinden, Javier Simón-Sánchez

المساهمون: Erasmus MC other, Internal Medicine, Epidemiology, Clinical Genetics, Human genetics, Neurology, Anatomy and neurosciences, NCA - Neurodegeneration, Neuroscience Campus Amsterdam - Neurodegeneration, ANS - Amsterdam Neuroscience, ACS - Amsterdam Cardiovascular Sciences, Graduate School

المصدر: Simon-Sanchez, J, van Hilten, J J, van de Warrenburg, B, Post, B, Berendse, H W, Arepalli, S, Hernandez, D G, de Bie, R M A, Velseboer, D, Scheffer, H, Bloem, B, van Dijk, K D, Rivadeneira, F, Hofman, A, Uitterlinden, A G, Rizzu, P, Bochdanovits, Z, Singleton, A B & Heutink, P 2011, ' Genome-wide association study confirms extant PD risk loci among the Dutch ', European Journal of Human Genetics, vol. 19, no. 6, pp. 655-661 . https://doi.org/10.1038/ejhg.2010.254Test
European Journal of Human Genetics, 19, 655-61
European Journal of Human Genetics, 19(6), 655-661. Nature Publishing Group
European Journal of Human Genetics, 19(6), 655-661
European journal of human genetics, 19(6), 655-661. Nature Publishing Group
European Journal of Human Genetics, 19, 6, pp. 655-61

مصطلحات موضوعية: Male, Linkage disequilibrium, Genome-wide association study, Genomic disorders and inherited multi-system disorders Functional Neurogenomics [IGMD 3], 0302 clinical medicine, Gene Frequency, Risk Factors, Genotype, MAPT, Age of Onset, Genetics (clinical), Netherlands, Aged, 80 and over, Genetics, 0303 health sciences, Intracellular Signaling Peptides and Proteins, Parkinson Disease, Middle Aged, HLA, alpha-Synuclein, PD, Female, Functional Neurogenomics [DCN 2], Adult, Adolescent, BST1, tau Proteins, Single-nucleotide polymorphism, Locus (genetics), Human leukocyte antigen, Protein Serine-Threonine Kinases, Biology, GPI-Linked Proteins, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, SDG 3 - Good Health and Well-being, Antigens, CD, Humans, Genetic Predisposition to Disease, GAK/DGKQ, ADP-ribosyl Cyclase, Allele frequency, Aged, 030304 developmental biology, Case-control study, DNA Fingerprinting, Genetic Loci, Case-Control Studies, SNCA, 030217 neurology & neurosurgery, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31aeaba6e660fbed1a1d0b0fc4b049e2Test
https://research.vu.nl/en/publications/d9194a9e-7750-462b-b3a1-37034d688dabTest