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UnknownCNValidatron: accurate and efficient validation of PennCNV calls using computer vision.
Not available
S-EPMC12910869 | biostudies-literature
UnknownWorking memory and reaction time variability mediate the relationship between polygenic risk and ADHD traits in a general population sample.
Not available
S-EPMC9763105 | biostudies-literature
UnknownCommon and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase.
Not available
S-EPMC4742860 | biostudies-literature
UnknownGermline variants at SOHLH2 influence multiple myeloma risk.
Not available
S-EPMC8055668 | biostudies-literature
UnknownDepression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses.
Not available
S-EPMC10839245 | biostudies-literature
UnknownRare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology.
Not available
S-EPMC8810832 | biostudies-literature
UnknownHundreds of variants clustered in genomic loci and biological pathways affect human height.
Not available
S-EPMC2955183 | biostudies-literature
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