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- 2020
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Mark
Clonal competition within complex evolutionary hierarchies shapes AML over time
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- Contribution to journal › Article
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Mark
PHF1 fusions cause distinct gene expression and chromatin accessibility profiles in ossifying fibromyxoid tumors and mesenchymal cells
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- Contribution to journal › Article
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Mark
Absence of GP130 cytokine receptor signaling causes extended Stüve-Wiedemann syndrome
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- Contribution to journal › Article
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Mark
Human Physiology of Genetic Defects Causing Beta-cell Dysfunction
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- Contribution to journal › Scientific review
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Mark
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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Mark
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
Hydroxysteroid 17-β dehydrogenase 13 variant increases phospholipids and protects against fibrosis in nonalcoholic fatty liver disease
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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