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Investigation of the genetic aetiology of Lewy body diseases with and without dementia.
- Published in:
- Brain Communications, 2024, v. 6, n. 4, p. 1, doi. 10.1093/braincomms/fcae190
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- Publication type:
- Article
The genetic and clinico-pathological profile of early-onset progressive supranuclear palsy.
- Published in:
- 2019
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- Publication type:
- journal article
Vascular disease and vascular risk factors in relation to motor features and cognition in early Parkinson's disease.
- Published in:
- 2016
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- Publication type:
- journal article
Genetic risk and age in Parkinson's disease: Continuum not stratum.
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- Movement Disorders, 2015, v. 30, n. 6, p. 850, doi. 10.1002/mds.26192
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- Publication type:
- Article
C9ORF72 expansion in amyotrophic lateral sclerosis/frontotemporal dementia also causes parkinsonism.
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- Movement Disorders, 2012, v. 27, n. 8, p. 1072, doi. 10.1002/mds.25022
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- Publication type:
- Article
Parkin-related disease clinically diagnosed as a pallido-pyramidal syndrome.
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- Movement Disorders, 2009, v. 24, n. 1, p. 138, doi. 10.1002/mds.22181
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- Publication type:
- Article
Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools.
- Published in:
- Human Genetics, 2002, v. 110, n. 5, p. 471, doi. 10.1007/s00439-002-0706-6
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- Article
GENES AND SCHIZOPHRENIA: A REVIEW OF DYSBINDIN-1 AND NEUREGULIN-1.
- Published in:
- Current Medical Literature: Neurology, 2005, v. 21, n. 3, p. 41
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- Publication type:
- Article
Cis- and trans- loci influence expression of the schizophrenia susceptibility gene DTNBP1.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 8, p. 1169, doi. 10.1093/hmg/ddn006
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- Publication type:
- Article
Strong evidence that GNB1L is associated with schizophrenia.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 4, p. 555, doi. 10.1093/hmg/ddm330
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- Publication type:
- Article
Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 14, p. 1947, doi. 10.1093/hmg/ddi199
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- Publication type:
- Article
Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease study.
- Published in:
- 2019
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- Publication type:
- journal article
Is the MC1R variant p.R160W associated with Parkinson's?
- Published in:
- 2016
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- Publication type:
- letter
Polygenic risk of Parkinson disease is correlated with disease age at onset.
- Published in:
- Annals of Neurology, 2015, v. 77, n. 4, p. 582, doi. 10.1002/ana.24335
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- Publication type:
- Article
Autonomic Dysfunction in Early Parkinson's Disease: Results from the United Kingdom Tracking Parkinson's Study.
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- Movement Disorders Clinical Practice, 2017, v. 4, n. 4, p. 509, doi. 10.1002/mdc3.12454
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- Publication type:
- Article
P3-265: Testing for association between Alzheimer's disease with psychosis and variants identified as influencing risk of schizophrenia
- Published in:
- 2008
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- Publication type:
- Abstract
Association of Genetic Risk for Rheumatoid Arthritis With Cognitive and Psychiatric Phenotypes Across Childhood and Adolescence.
- Published in:
- JAMA Network Open, 2019, v. 2, n. 6, p. e196118, doi. 10.1001/jamanetworkopen.2019.6118
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- Publication type:
- Article
Association analysis of NOTCH4 loci in schizophrenia using family and population-based controls.
- Published in:
- Nature Genetics, 2001, v. 28, n. 2, p. 126, doi. 10.1038/88836
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- Publication type:
- Article
No evidence for association between polymorphisms in GRM3 and schizophrenia.
- Published in:
- BMC Psychiatry, 2005, v. 5, p. 1, doi. 10.1186/1471-244X-5-23
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- Publication type:
- Article
Dysbindin-1 and schizophrenia: from genetics to neuropathology.
- Published in:
- 2004
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- Publication type:
- journal article
CSF-resident CD4<sup>+</sup> T-cells display a distinct gene expression profile with relevance to immune surveillance and multiple sclerosis.
- Published in:
- Brain Communications, 2021, v. 3, n. 3, p. 1, doi. 10.1093/braincomms/fcab155
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- Publication type:
- Article
Huntington's disease age at motor onset is modified by the tandem hexamer repeat in TCERG1.
- Published in:
- NPJ Genomic Medicine, 2022, v. 7, n. 1, p. 1, doi. 10.1038/s41525-022-00317-w
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- Publication type:
- Article
Molecular mechanisms in 22q11 deletion syndrome.
- Published in:
- 2011
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- Publication type:
- Journal Article
Molecular Mechanisms in 22q11 Deletion Syndrome.
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- Schizophrenia Bulletin, 2011, v. 37, n. 5, p. 882, doi. 10.1093/schbul/sbr095
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- Publication type:
- Article
Is the Dysbindin Gene (DTNBP1) a Susceptibility Gene for Schizophrenia?
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- Schizophrenia Bulletin, 2005, v. 31, n. 4, p. 800, doi. 10.1093/schbul/sbi061
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- Publication type:
- Article
Whole Genome Association Study in a Homogenous Population in Shandong Peninsula of China Reveals JARID2 as a Susceptibility Gene for Schizophrenia.
- Published in:
- Journal of Biomedicine & Biotechnology, 2009, p. 1, doi. 10.1155/2009/536918
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- Publication type:
- Article
Analysis of copy number variation using quantitative interspecies competitive PCR.
- Published in:
- Nucleic Acids Research, 2008, v. 36, n. 17, p. e112, doi. 10.1093/nar/gkn495
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- Publication type:
- Article
Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p.
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- Journal of Neurology, 2011, v. 258, n. 4, p. 647, doi. 10.1007/s00415-010-5815-x
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- Publication type:
- Article
The genetic aetiology of late-onset chronic progressive cerebellar ataxia.
- Published in:
- Journal of Neurology, 2009, v. 256, n. 3, p. 343, doi. 10.1007/s00415-009-0015-2
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- Publication type:
- Article
Genome-Wide Association Study of Pain in Parkinson's Disease Implicates TRPM8 as a Risk Factor.
- Published in:
- 2020
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- Publication type:
- letter
Genome‐Wide Association Study of Pain in Parkinson's Disease Implicates TRPM8 as a Risk Factor.
- Published in:
- Movement Disorders, 2020, v. 35, n. 4, p. 705, doi. 10.1002/mds.28001
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- Publication type:
- Article
Genetic meta-analysis of levodopa induced dyskinesia in Parkinson's disease.
- Published in:
- NPJ Parkinson's Disease, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41531-023-00573-2
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- Publication type:
- Article
Assessing the relationship between monoallelic PRKN mutations and Parkinson's risk.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 1, p. 78, doi. 10.1093/hmg/ddaa273
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- Publication type:
- Article
An InDel in Phospholipase-C-B-1 Is Linked with Euthyroid Multinodular Goiter.
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- Thyroid, 2018, v. 28, n. 7, p. 891, doi. 10.1089/thy.2017.0312
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- Publication type:
- Article
Further evidence for the association of MMP9 with nephropathy in type 2 diabetes and application of DNA pooling technology to candidate gene screening.
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- Journal of Nephrology (JNonline), 2008, v. 21, n. 3, p. 400
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- Publication type:
- Article
Recent advances in the genetics of schizophrenia.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 2, p. 125, doi. 10.1093/hmg/ddg302
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- Publication type:
- Article
Recent advances in the genetics of schizophrenia.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. suppl_2, p. R125, doi. 10.1093/hmg/ddg302
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- Publication type:
- Article
DNA pooling identifies QTLs on chromosome 4 for general cognitive ability in children.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 5, p. 915, doi. 10.1093/hmg/8.5.915
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- Publication type:
- Article