Found: 8
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Association of Schizophrenia Risk With Disordered Niacin Metabolism in an Indian Genome-wide Association Study.
- Published in:
- 2019
- By:
- Publication type:
- journal article
A genome-wide association study of essential hypertension in an Australian population using a DNA pooling approach.
- Published in:
- Molecular Genetics & Genomics, 2017, v. 292, n. 2, p. 307, doi. 10.1007/s00438-016-1274-0
- By:
- Publication type:
- Article
Evidence of a Recessively Inherited CCN3 Mutation as a Rare Cause of Early-Onset Parkinsonism.
- Published in:
- Frontiers in Neurology, 2020, v. 11, p. 1, doi. 10.3389/fneur.2020.00331
- By:
- Publication type:
- Article
Hunting for Familial Parkinson's Disease Mutations in the Post Genome Era.
- Published in:
- Genes, 2021, v. 12, n. 3, p. 430, doi. 10.3390/genes12030430
- By:
- Publication type:
- Article
Analysis of DNA methylation associates the cystine–glutamate antiporter SLC7A11 with risk of Parkinson's disease.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-15065-7
- By:
- Publication type:
- Article
Investigation of Homocysteine-Pathway-Related Variants in Essential Hypertension.
- Published in:
- 2012
- By:
- Publication type:
- Journal Article
Investigation of Homocysteine-Pathway-Related Variants in Essential Hypertension.
- Published in:
- International Journal of Hypertension, 2012, p. 1, doi. 10.1155/2012/190923
- By:
- Publication type:
- Article
Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing.
- Published in:
- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0667-1
- By:
- Publication type:
- Article