Search Filters
Format Format
Subjects Subjects
Subjects Subjects
Sort by Item Count (A-Z)
Filter by Count
genetic predisposition to disease (3) 3
genome-wide association study (3) 3
humans (3) 3
parkinson's disease (3) 3
risk factors (3) 3
alleles (2) 2
alpha-synuclein (2) 2
brain - metabolism (2) 2
expression (2) 2
frontotemporal dementia (2) 2
gene expression (2) 2
gene loci (2) 2
genes (2) 2
genome-wide association (2) 2
genomes (2) 2
genomics (2) 2
index medicus (2) 2
neurology. diseases of the nervous system (2) 2
polymorphism, single nucleotide (2) 2
studies (2) 2
age (1) 1
age at onset (1) 1
alzheimer disease (1) 1
alzheimers-disease (1) 1
animals (1) 1
apoe (1) 1
biology (1) 1
brain research (1) 1
chemokine receptor cxcr4 (1) 1
clinical genetics, medical genetics, molecular neuroscience, predictive markers (1) 1
clinical neurology (1) 1
diagnosis (1) 1
disease (1) 1
dna methylation (1) 1
efficient (1) 1
fibroblast-growth-factor (1) 1
gba (1) 1
gba mutations (1) 1
gene (1) 1
gene expression profiling (1) 1
gene expression regulation (1) 1
gene regulatory networks (1) 1
genetic aspects (1) 1
genetic diversity (1) 1
genetic loci - genetics (1) 1
genetics & heredity (1) 1
genotype (1) 1
glucocerebrosidase (1) 1
haplotypes (1) 1
health risk assessment (1) 1
heritability (1) 1
international ftd-genomics consortium (1) 1
international genomics of alzheimer's project (1) 1
international parkinson's disease genomics consortium (1) 1
longevity (1) 1
medical genetics (1) 1
medical research (1) 1
metaanalysis (1) 1
mice, transgenic (1) 1
microglia - metabolism (1) 1
movement disorders (1) 1
mutations (1) 1
network integration (1) 1
neurodegeneration (1) 1
neurodegenerative diseases (1) 1
neurodegenerative diseases - genetics (1) 1
neuroscience (1) 1
neurosciences. biological psychiatry. neuropsychiatry (1) 1
parkinson disease (1) 1
parkinson disease - genetics (1) 1
parkinsons disease (1) 1
parkinsons-disease (1) 1
pathogenesis (1) 1
penetrance (1) 1
physiological aspects (1) 1
polymorphism, single nucleotide - genetics (1) 1
population (1) 1
predicting gene-function (1) 1
progressive supranuclear palsy (1) 1
progressive supranuclear palsy; chemokine receptor cxcr4; predicting gene-function; genome-wide association; parkinsons-disease; frontotemporal dementia; alzheimers-disease; network integration; alpha-syneclein; expression (1) 1
psychiatry (1) 1
psychiatry and mental health; cellular and molecular neuroscience; biological psychiatry (1) 1
receptors, cxcr4 - genetics (1) 1
receptors, cxcr4 - metabolism (1) 1
research (1) 1
risk (1) 1
risk assessment (1) 1
risk loci (1) 1
schizophrenia (1) 1
sequence (1) 1
settore bio/13 - biologia applicata (1) 1
settore med/26 - neurologia (1) 1
single nucleotide polymorphisms (1) 1
snca (1) 1
statistical power (1) 1
synuclein (1) 1
tmem175 (1) 1
variants (1) 1
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range

by Plagnol, Vincent and Nalls, Michael A and Bras, Jose M 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 Amouyel, Philippe and Arepalli, Sampath and Band, Gavin and Barker, Roger A and Bellinguez, Celine 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 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 Freeman, Colin 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 Hellenthal, Garrett 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 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 and Morrison, Karen E and Mudanohwo, Ese and O'Sullivan, Sean S and Pearson, Justin and Pearson, Richard and Perlmutter, Joel S and Petursson, Hjoervar and Pirinen, Matti 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 ... and WTCCC2 and Wellcome Trust Case Control Consortium 2 (WTCCC2) and International Parkinson's Disease Genomics Consortium (IPDGC)
PLoS genetics, ISSN 1553-7390, 2011, Volume 7, Issue 6, p. e1002142
Journal Article
Movement Disorders, ISSN 0885-3185, 06/2019, Volume 34, Issue 6, pp. 866 - 875
Increasing evidence supports an extensive and complex genetic contribution to PD. Previous genome-wide association studies (GWAS) have shed light on the... 
Parkinson's disease | age at onset | TMEM175 | GBA | SNCA | METAANALYSIS | GBA MUTATIONS | CLINICAL NEUROLOGY | PENETRANCE | LONGEVITY | RISK LOCI | GLUCOCEREBROSIDASE | STATISTICAL POWER | APOE | EXPRESSION | EFFICIENT | Neurodegenerative diseases | Alleles | Genomes | Heritability | Gene loci | Genetic diversity | Synuclein | Age | Movement disorders
Journal Article
npj Parkinson's Disease, ISSN 2373-8057, 12/2019, Volume 5, Issue 1, pp. 1 - 14
Parkinson’s disease (PD), with its characteristic loss of nigrostriatal dopaminergic neurons and deposition of α-synuclein in neurons, is often considered a... 
Studies | Brain research | Disease | Pathogenesis | Genomics | Schizophrenia | Genomes | Gene loci | Gene expression
Journal Article
npj Parkinson's Disease, ISSN 2373-8057, 12/2019, Volume 5, Issue 1, pp. 1 - 9
Mitochondrial dysfunction has been implicated in the etiology of monogenic Parkinson’s disease (PD). Yet the role that mitochondrial processes play in the most... 
Journal Article
by Bonham, Luke W and Karch, Celeste M and Fan, Chun C and Tan, Chin and Geier, Ethan G and Wang, Yunpeng and Wen, Natalie and Broce, Iris J and Li, Yi and Barkovich, Matthew J and Ferrari, Raffaele and Hardy, John and Momeni, Parastoo and Höglinger, Günter and Müller, Ulrich and Hess, Christopher P and Sugrue, Leo P and Dillon, William P and Schellenberg, Gerard D and Miller, Bruce L and Andreassen, Ole A and Dale, Anders M and Barkovich, A. James and Yokoyama, Jennifer S and Desikan, Rahul S and Hernandez, D.G and Nalls, M.A and Rohrer, J.D and Ramasamy, A and Kwok, J.B.J and Dobson-Stone, C and Schofield, P.R and Halliday, G.M and Hodges, J.R and Piguet, O and Bartley, L and Thompson, E and Haan, E and Hernández, I and Ruiz, A and Boada, M and Borroni, B and Padovani, A and Cruchaga, C and Cairns, N.J and Benussi, L and Binetti, G and Ghidoni, R and Forloni, G and Albani, D and Galimberti, D and Fenoglio, C and Serpente, M and Scarpini, E and Clarimón, J and Lleó, A and Blesa, R and Waldö, M. Landqvist and Nilsson, K and Nilsson, C and MacKenzie, I.R.A and Hsiung, G.-Y.R and Mann, D.M.A and Grafman, J and Morris, C.M and Attems, J and Griffiths, T.D and McKeith, I.G and Thomas, A.J and Pietrini, P and Huey, E.D and Wassermann, E.M and Baborie, A and Jaros, E and Tierney, M.C and Pastor, P and Razquin, C and Ortega-Cubero, S and Alonso, E and Perneczky, R and Diehl-Schmid, J and Alexopoulos, P and Kurz, A and Rainero, I and Rubino, E and Pinessi, L and Rogaeva, E and George-Hyslop, P. St and Rossi, G and Tagliavini, F and Giaccone, G and Rowe, J.B and Schlachetzki, J.C.M and Uphill, J and Collinge, J and Mead, S and Danek, A and Van Deerlin, V.M and Grossman, M and Trojanowski, J.Q and ... and IPDGC and IFGC and IGAP and International Parkinson’s Disease Genetics Consortium (IPDGC) and International Genomics of Alzheimer’s Project (IGAP) and International FTD-Genomics Consortium (IFGC)
Translational Psychiatry, ISSN 2158-3188, 12/2018, Volume 8, Issue 1, pp. 73 - 10
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.