Interrogation of human hematopoiesis at single-cell and single-variant resolution-Reference-Cited by-同舟云学术

Interrogation of human hematopoiesis at single-cell and single-variant resolution

Published:2019-03-11 Issue:4 Volume:51 Page:683-693
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Ulirsch Jacob C.^ORCID,Lareau Caleb A.^ORCID,Bao Erik L.^ORCID,Ludwig Leif S.,Guo Michael H.,Benner Christian,Satpathy Ansuman T.^ORCID,Kartha Vinay K.,Salem Rany M.^ORCID,Hirschhorn Joel N.,Finucane Hilary K.^ORCID,Aryee Martin J.^ORCID,Buenrostro Jason D.^ORCID,Sankaran Vijay G.^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/s41588-019-0362-6.pdf

Reference73 articles.

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2. Sankaran, V. G. & Orkin, S. H. Genome-wide association studies of hematologic phenotypes: a window into human hematopoiesis. Curr. Opin. Genet. Dev. 23, 339–344 (2013).

3. Astle, W. J. et al. The allelic landscape of human blood cell trait variation and links to common complex disease. Cell 167, 1415–1429 (2016).

4. Boyle, E. A., Li, Y. I. & Pritchard, J. K. An expanded view of complex traits: from polygenic to omnigenic. Cell 169, 1177–1186 (2017).

5. Farh, K. K. et al. Genetic and epigenetic fine mapping of causal autoimmune disease variants. Nature 518, 337–343 (2015).

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