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Author Details
Full Name
Lu Chen
Affiliation
ORCID
Career Start Year
2014
Papers
16
H Index
12
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
33863903
Genetic perturbation of PU.1 binding and chromatin looping at neutrophil enhancers associates with autoimmune disease.
Nat Commun
2021
31064398
Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome.
Genome Biol
2019
30390057
Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.
Nat Genet
2018
28126036
Genome-wide analysis of differential transcriptional and epigenetic variability across human immune cell types.
Genome Biol
2017
28283040
Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome.
Genome Biol
2017
27751981
Changing Treatment May Affect the Predictive Ability of European Treatment Outcome Study Scoring for the Prognosis of Patients with Chronic Myeloid Leukemia.
Turkish Journal of Haematology
2017
27863251
Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells.
Cell
2016
27347004
From GWAS to function: lessons from blood cells.
ISBT Sci Ser
2016
27486782
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.
Am J Hum Genet
2016
27588453
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.
Am J Hum Genet
2016
27668658
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.
Nat Genet
2016
27863252
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
Cell
2016
25962519
Erratum: A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans.
Nat Commun
2015
25225788
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans.
Nat Commun
2014
24816252
An atlas of genetic influences on human blood metabolites.
Nat Genet
2014
25258084
Transcriptional diversity during lineage commitment of human blood progenitors.
Science
2014
1 - 16 of 16
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