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(16)
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Reconstructing evolutionary trajectories of mutation signature activities in cancer using TrackSig.
Not available
S-EPMC7002414
|
biostudies-literature
Cite
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use.
Not available
S-EPMC6534468
|
biostudies-literature
Cite
Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.
Not available
S-EPMC4321900
|
biostudies-literature
Cite
Polygenic and developmental profiles of autism differ by age at diagnosis.
Not available
S-EPMC12571882
|
biostudies-literature
Cite
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
Not available
S-EPMC5945951
|
biostudies-literature
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Rare and low-frequency coding variants alter human adult height.
Not available
S-EPMC5302847
|
biostudies-literature
Cite
Colorectal-cancer incidence and mortality with screening flexible sigmoidoscopy.
Not available
S-EPMC3641846
|
biostudies-literature
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The landscape of viral associations in human cancers.
Not available
S-EPMC8076016
|
biostudies-literature
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Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples.
Not available
S-EPMC7505971
|
biostudies-literature
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Combined burden and functional impact tests for cancer driver discovery using DriverPower.
Not available
S-EPMC7002750
|
biostudies-literature
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