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2007, Neurological disease and therapy, ISBN 084933697X, Volume 83., ix, 386
An authoritative collection of recent breakthroughs in Parkinson's Disease (PD) research, Parkinson's Disease: Genetics and Pathogenesis spans key findings on... 
Parkinson Disease | physiopathology | Genetic aspects | Parkinson's disease | genetics | Pathophysiology | Medical Genetics | Neurology | Neuroscience | Parkinson Disease - genetics
Book
PLoS Genetics, ISSN 1553-7390, 2012, Volume 8, Issue 3, pp. e1002548 - e1002548
Journal Article
2007, Neurological disease and therapy, ISBN 084933697X, Volume 83.
Web Resource
Journal of Neurology, ISSN 0340-5354, 2014, Volume 261, Issue 2, pp. 259 - 266
The last 5 years have seen rapid progress in Parkinson's disease (PD) genetics, with the publication of a series of large-scale genome wide association studies... 
Genetics | Genome wide-association study | Parkinson's disease | LRRK2 | GBA | Parkin | RISK-FACTORS | ALPHA-SYNUCLEIN | IDENTIFICATION | GLUCOCEREBROSIDASE MUTATIONS | CLINICAL NEUROLOGY | GAUCHER-DISEASE | KINASE 2 LRRK2 | HEREDITARY PARKINSONISM | PINK1 | VPS35 MUTATIONS | GENOME-WIDE ASSOCIATION | Genetic aspects | Research | Genetic susceptibility | Risk factors
Journal Article
Neurology, ISSN 0028-3878, 08/2012, Volume 79, Issue 7, pp. 659 - 667
Journal Article
Handbook of Behavioral Neuroscience, ISSN 1569-7339, 2017, Volume 24, pp. 839 - 855
Since the mid-1990s, genetic studies have advanced our understanding of Parkinson's disease (PD) etiology, showing it to be a polygenic disorder with a... 
PRKN | PINK1 | synuclein | genetics | GWAS | Parkinson's disease | LRRK2
Journal Article
Bioinformatics, ISSN 1367-4803, 04/2017, Volume 33, Issue 7, pp. 1031 - 1039
Journal Article
CURRENT MOLECULAR MEDICINE, ISSN 1566-5240, 2014, Volume 14, Issue 8, pp. 1079 - 1088
Parkinson Disease (PD) is a common neurodegenerative disorder of intricate etiology, caused by progressive loss of aminergic neurons and accumulation of Lewy... 
RESPONSIVE PARKINSONISM | MEDICINE, RESEARCH & EXPERIMENTAL | parkinsonism | Parkinson disease | multifactorial | CLINICAL-FEATURES | risk factor | GLUCOCEREBROSIDASE MUTATIONS | INTRAFAMILIAL VARIABILITY | SUBSTANTIA-NIGRA | GAUCHER-DISEASE | RARE VARIANTS | SNCA DUPLICATION | Genetics | ALPHA-SYNUCLEIN GENE | PATHOLOGICAL FEATURES | monogenic
Journal Article
Current Molecular Medicine, ISSN 1566-5240, 03/2014, Volume 14, Issue 8, pp. 1079 - 1088
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 07/2011, Volume 89, Issue 1, pp. 162 - 167
Journal Article
by Nalls, Michael A and Plagnol, Vincent and Hernandez, Dena G and Sharma, Manu and Sheerin, Una-Marie and Saad, Mohamad and Simon-Sanchez, Javier and Schulte, Claudia and Lesage, Suzanne and Sveinbjornsdottir, Sigurlaug and Arepalli, Sampath and Barker, Roger and Ben-Shlomo, Yoav and Berendse, Henk W and Berg, Daniela and Bhatia, Kailash and de Bie, Rob M. A and Biffi, Alessano and Bloem, Bas and Bochdanovits, Zoltan and Bonin, Michael and Bras, Jose M and Brockmann, Kathrin and Brooks, Janet and Burn, David J and Charlesworth, Gavin and Chen, Honglei and Chinnery, Patrick F and Chong, Sean and Clarke, Carl E and Cookson, Mark R and Cooper, J. Mark and Corvol, Jean Christophe and Counsell, Carl and Damier, Philippe and Dartigues, Jean-Francois and Deloukas, Panos and Deuschl, Guenther and Dexter, David T and van Dijk, Karin D and Dillman, Allissa and Durif, Frank and Duerr, Alexana and Edkins, Sarah and Evans, Jonathan R and Foltynie, Thomas and Gao, Jianjun and Gardner, Michelle and Gibbs, J. Raphael and Goate, Alison and Gray, Emma and Guerreiro, Rita and Gustafsson, Omar and Harris, Clare and van Hilten, Jacobus J and Hofman, Albert and Hollenbeck, Albert and Holton, Janice and Hu, Michele and Huang, Xuemei and Huber, Heiko and Hudson, Gavin and Hunt, Sarah E and Huttenlocher, Johanna and Illig, Thomas and Jonsson, Palmi V and Lambert, Jean-Charles and Langford, Cordelia and Lees, Anew and Lichtner, Peter and Limousin, Patricia and Lopez, Grisel and Lorenz, Delia and McNeill, Alisdair and Moorby, Catriona and Moore, Matthew and Morris, Huw R and Morrison, Karen E and Mudanohwo, Ese and O'Sullivan, Sean S and Pearson, Justin and Perlmutter, Joel S and Petursson, Hjoervar and Pollak, Pierre and Post, Bart and Potter, Simon and Ravina, Bernard and Revesz, Tamas and Riess, Olaf and Rivadeneira, Fernando and Rizzu, Patrizia and Ryten, Mina and Sawcer, Stephen and Schapira, Anthony and Scheffer, Hans and Shaw, Karen and Shoulson, Ira and Siansky, Ellen and Smith, Colin and Spencer, Chris C. A and ... and Wellcome Trust Case-Control Consor and Int Parkinson Dis Genomics Consort and International Parkinson Disease Genomics Consortium
Lancet, The, ISSN 0140-6736, 2011, Volume 377, Issue 9766, pp. 641 - 649
Journal Article