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- 2020
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Mark
13q12.2 deletions in acute lymphoblastic leukemia lead to upregulation of FLT3 through enhancer hijacking
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- Contribution to journal › Article
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De novo variants in CAMTA1 cause a syndrome variably associated with spasticity, ataxia, and intellectual disability
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- Contribution to journal › Article
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Global RNA expression and DNA methylation patterns in primary anaplastic thyroid cancer
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- Contribution to journal › Article
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Mark
Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia
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- Contribution to journal › Article
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Mark
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
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- Contribution to journal › Article
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Mark
New generation genetic testing entering the clinic
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- Contribution to journal › Article
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Mark
Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke
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- Contribution to journal › Article
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Mark
BMD-Related Genetic Risk Scores Predict Site-Specific Fractures as Well as Trabecular and Cortical Bone Microstructure
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- Contribution to journal › Article
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Mark
Loci associated with genomic damage levels in chronic kidney disease patients and controls
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- Contribution to journal › Article
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The CCND1 c.870G risk allele is enriched in individuals of African ancestry with plasma cell dyscrasias
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- Contribution to journal › Letter