Found: 25
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HPCA confirmed as a genetic cause of DYT2-like dystonia phenotype.
- Published in:
- 2018
- By:
- Publication type:
- journal article
ADORA1 mutations are not a common cause of Parkinson's disease and dementia with Lewy bodies.
- Published in:
- 2017
- By:
- Publication type:
- letter
Parkinson's disease due to the R1441G mutation in Dardarin: a founder effect in the Basques.
- Published in:
- 2006
- By:
- Publication type:
- journal article
Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms.
- Published in:
- 2019
- By:
- Publication type:
- journal article
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 2, p. 562
- By:
- Publication type:
- Article
Using genome-wide complex trait analysis to quantify ‘missing heritability’ in Parkinson's disease.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 14, p. 2973
- By:
- Publication type:
- Article
Using genome-wide complex trait analysis to quantify ‘missing heritability’ in Parkinson's disease.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 8, p. 1696
- By:
- Publication type:
- Article
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 5, p. 1039
- By:
- Publication type:
- Article
Using genome-wide complex trait analysis to quantify ‘missing heritability’ in Parkinson's disease.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 22, p. 4996
- By:
- Publication type:
- Article
Lack of replication of association between GIGYF2 variants and Parkinson disease.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 2, p. 341
- By:
- Publication type:
- Article
Sequencing analysis of OMI/HTRA2 shows previously reported pathogenic mutations in neurologically normal controls.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 13, p. 1988, doi. 10.1093/hmg/ddn096
- By:
- Publication type:
- Article
Accurate prediction of a minimal region around a genetic association signal that contains the causal variant.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 2, p. 238, doi. 10.1038/ejhg.2013.115
- By:
- Publication type:
- Article
Profiling transcription initiation in human aged brain using deep-CAGE.
- Published in:
- 2011
- By:
- Publication type:
- Abstract
C9orf72 is differentially expressed in the central nervous system and myeloid cells and consistently reduced in C9orf72, MAPT and GRN mutation carriers.
- Published in:
- Acta Neuropathologica Communications, 2016, v. 4, p. 1, doi. 10.1186/s40478-016-0306-7
- By:
- Publication type:
- Article
Genome-wide association study confirms extant PD risk loci among the Dutch.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 6, p. 655, doi. 10.1038/ejhg.2010.254
- By:
- Publication type:
- Article
Genome-wide association study reveals genetic risk underlying Parkinson's disease.
- Published in:
- Nature Genetics, 2009, v. 41, n. 12, p. 1308, doi. 10.1038/ng.487
- By:
- Publication type:
- Article
Cooperative Genome-Wide Analysis Shows Increased Homozygosity in Early Onset Parkinson's Disease.
- Published in:
- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0028787
- By:
- Publication type:
- Article
Variation at GRN 3'-UTR rs5848 Is Not Associated with a Risk of Frontotemporal Lobar Degeneration in Dutch Population.
- Published in:
- PLoS ONE, 2009, v. 4, n. 10, p. 1, doi. 10.1371/journal.pone.0007494
- By:
- Publication type:
- Article
Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobe.
- Published in:
- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0320-1
- By:
- Publication type:
- Article
LRRK2 is expressed in areas affected by Parkinson's disease in the adult mouse brain.
- Published in:
- European Journal of Neuroscience, 2006, v. 23, n. 3, p. 659, doi. 10.1111/j.1460-9568.2006.04616.x
- By:
- Publication type:
- Article
Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease.
- Published in:
- Brain: A Journal of Neurology, 2012, v. 135, n. 9, p. 2875, doi. 10.1093/brain/aws161
- By:
- Publication type:
- Article
The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions.
- Published in:
- Brain: A Journal of Neurology, 2012, v. 135, n. 3, p. 723
- By:
- Publication type:
- Article
Use of support vector machines for disease risk prediction in genome-wide association studies: Concerns and opportunities.
- Published in:
- Human Mutation, 2012, v. 33, n. 12, p. 1708, doi. 10.1002/humu.22161
- By:
- Publication type:
- Article
Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk.
- Published in:
- JAMA Neurology, 2013, v. 70, n. 10, p. 1268, doi. 10.1001/jamaneurol.2013.448
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- Publication type:
- Article
Assessment of the impact of a personalised nutrition intervention in impaired glucose regulation over 26 weeks: a randomised controlled trial.
- Published in:
- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-55105-6
- By:
- Publication type:
- Article