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- 2022
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Mark
Multiple sclerosis diagnosis and phenotype identification by multivariate classification of in vivo frontal cortex metabolite profiles
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- Contribution to journal › Article
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Mark
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
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- Contribution to journal › Article
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Mark
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
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- Contribution to journal › Article
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Mark
International stroke genetics consortium recommendations for studies of genetics of stroke outcome and recovery
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- Contribution to journal › Article
- 2021
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Mark
Congenital stationary night blindness : an update and review of the disease spectrum in Saudi Arabia
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- Contribution to journal › Scientific review
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Mark
Treatment outcomes in persons with severe haemophilia B in the Nordic region : The B-NORD study
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- Contribution to journal › Article
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Mark
Synovial fluid neutrophils in oligoarticular juvenile idiopathic arthritis have an altered phenotype and impaired effector functions
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- Contribution to journal › Article
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Mark
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes
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- Contribution to journal › Article
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Mark
AXL Knock-Out in SNU475 Hepatocellular Carcinoma Cells Provides Evidence for Lethal Effect Associated with G2 Arrest and Polyploidization
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- Contribution to journal › Article
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Mark
The European/International Fibromuscular Dysplasia Registry and Initiative (FEIRI)-clinical phenotypes and their predictors based on a cohort of 1000 patients
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- Contribution to journal › Article