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- 2023
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Mark
Rare-variant collapsing and bioinformatic analyses for amyloidosis, dementia and Parkinson’s disease in the UK biobank reveal novel susceptibility loci
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- Contribution to journal › Letter
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Mark
Deficiency of the Heterogeneous Nuclear Ribonucleoprotein U locus leads to delayed hindbrain neurogenesis
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- Contribution to journal › Article
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Mark
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis
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- Contribution to journal › Article
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Mark
Contribution of rare genetic variants to heart failure and cardiomyopathy in the UK Biobank
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- Contribution to journal › Letter
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Mark
Genetic variants associated with weight loss and metabolic outcomes after bariatric surgery : A systematic review
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- Contribution to journal › Scientific review
- 2022
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Mark
Four Swedish cases of CSF1R-related leukoencephalopathy : Visualization of clinical phenotypes
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- Contribution to journal › Article
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Mark
Thrombotic Risk Determined by Protein C Receptor (PROCR) Variants among Middle-Aged and Older Adults : A Population-Based Cohort Study
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- Contribution to journal › Article
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Mark
N-terminus DUX4-immunohistochemistry is a reliable methodology for the diagnosis of DUX4-fused B-lymphoblastic leukemia/lymphoma (N-terminus DUX4 IHC for DUX4-fused B-ALL)
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- Contribution to journal › Article
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Mark
Genome-wide meta-analysis of monoclonal gammopathy of undetermined significance (MGUS) identifies risk loci impacting IRF-6
(
- Contribution to journal › Letter
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Mark
The diagnostic utility of DNA copy number analysis of core needle biopsies from soft tissue and bone tumors
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- Contribution to journal › Article