Systems Genetics in Human Endothelial Cells Identifies Non-coding Variants Modifying Enhancers, Expression, and Complex Disease Traits

The identification of causal variants and mechanisms underlying complex disease traits in humans is important for the progress of human disease genetics; this requires finding strategies to detect functional regulatory variants in disease-relevant cell types. To achieve this, we collected genetic an...

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Bibliografiset tiedot
Julkaisussa:Am J Hum Genet
Päätekijät: Stolze, Lindsey K., Conklin, Austin C., Whalen, Michael B., López Rodríguez, Maykel, Õunap, Kadri, Selvarajan, Ilakya, Toropainen, Anu, Örd, Tiit, Li, Jin, Eshghi, Anna, Solomon, Alice E., Fang, Yun, Kaikkonen, Minna U., Romanoski, Casey E.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Elsevier 2020
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7273528/
https://ncbi.nlm.nih.gov/pubmed/32442411
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2020.04.008
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