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Author Details
Full Name
Alice L Mann
Affiliation
Wellcome Sanger Institute
ORCID
Career Start Year
2016
Papers
10
H Index
10
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35288711
Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseases.
Nat Genet
2022
35072136
GA4GH: International policies and standards for data sharing across genomic research and healthcare.
Cell Genom
2021
33863903
Genetic perturbation of PU.1 binding and chromatin looping at neutrophil enhancers associates with autoimmune disease.
Nat Commun
2021
29379200
Shared genetic effects on chromatin and gene expression indicate a role for enhancer priming in immune response.
Nat Genet
2018
28614302
Corrigendum: Common genetic variation drives molecular heterogeneity in human iPSCs.
Nature
2017
28489815
Common genetic variation drives molecular heterogeneity in human iPSCs.
Nature
2017
28126036
Genome-wide analysis of differential transcriptional and epigenetic variability across human immune cell types.
Genome Biol
2017
27347004
From GWAS to function: lessons from blood cells.
ISBT Sci Ser
2016
27863251
Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells.
Cell
2016
27863252
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
Cell
2016
1 - 10 of 10
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