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- 2020
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Mark
Prostate cancer risk SNP rs10993994 is a trans-eQTL for SNHG11 mediated through MSMB
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- Contribution to journal › Article
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Genomic imprinting analyses identify maternal effects as a cause of phenotypic variability in type 1 diabetes and rheumatoid arthritis
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- Contribution to journal › Article
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Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk
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- Contribution to journal › Article
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Search for multiple myeloma risk factors using Mendelian randomization
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- Contribution to journal › Article
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Mark
C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts
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- Contribution to journal › Article
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Mark
Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals
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- Contribution to journal › Article
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Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes
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- Contribution to journal › Article
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Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length
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- Contribution to journal › Article
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Sex differences in oncogenic mutational processes
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- Contribution to journal › Article
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Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples
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- Contribution to journal › Article