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- 2018
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Mark
Genome-wide meta-analysis identifies novel determinants of circulating serum progranulin
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- Contribution to journal › Article
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Mark
A genome-wide association study of IgM antibody against phosphorylcholine : Shared genetics and phenotypic relationship to chronic lymphocytic leukemia
(
- Contribution to journal › Article
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Mark
Functional analyses of rare genetic variants in complement component C9 identified in patients with age-related macular degeneration
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- Contribution to journal › Article
- 2017
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Mark
Early microgliosis precedes neuronal loss and behavioural impairment in mice with a frontotemporal dementia-causing CHMP2B mutation
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- Contribution to journal › Article
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Mark
Proteomics insights into infantile neuronal ceroid lipofuscinosis (CLN1) point to the involvement of cilia pathology in the disease
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- Contribution to journal › Article
- 2016
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Mark
Genome wide association study identifies two loci associated with cadmium in erythrocytes among never-smokers
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- Contribution to journal › Article
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Mark
Analysis with the exome array identifies multiple new independent variants in lipid loci
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- Contribution to journal › Article
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Mark
Mutations in the polyglutamylase gene TTLL5, expressed in photoreceptor cells and spermatozoa, are associated with cone-rod degeneration and reduced male fertility
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- Contribution to journal › Article
- 2015
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Mark
Low dietary protein content alleviates motor symptoms in mice with mutant dynactin/dynein-mediated neurodegeneration.
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- Contribution to journal › Article
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Mark
Identification of novel genes for glucose metabolism based upon expression pattern in human islets and effect on insulin secretion and glycemia.
(
- Contribution to journal › Article