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Author Details

Aimee M Deaton
2006
27
19
PMIDPaper TitleJournal TitlePublished Year
37492105Human gain-of-function variants in HNF1A confer protection from diabetes but independently increase hepatic secretion of atherogenic lipoproteins.Cell Genom2023
36261593Using human genetics to improve safety assessment of therapeutics.Nature Reviews Drug Discovery2023
37808681Activin E is a TGFβ ligand that signals specifically through activin receptor-like kinase 7.2023
35493704Rare coding variants in DNA damage repair genes associated with timing of natural menopause.Human Genetics and Genomics Advances2022
35896531Rare loss of function variants in the hepatokine gene INHBE protect from abdominal obesity.Nature Communications2022
34079032Association of the transthyretin variant V122I with polyneuropathy among individuals of African ancestry.Sci Rep2021
32590049Nonclinical cardiovascular safety evaluation of romosozumab, an inhibitor of sclerostin for the treatment of osteoporosis in postmenopausal women at high risk of fracture.Regulatory Toxicology and Pharmacology2020
30952858Phenotypes associated with genes encoding drug targets are predictive of clinical trial side effects.Nature Communications2019
30346593Rationalizing Secondary Pharmacology Screening Using Human Genetic and Pharmacological Evidence.Toxicological Sciences2019
30476138Sequence variants associating with urinary biomarkers.Hum Mol Genet2019
30643255A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis.Nat Genet2019
31068582Author Correction: Phenotypes associated with genes encoding drug targets are predictive of clinical trial side effects.Nature Communications2019
30504769Genome-wide association meta-analysis yields 20 loci associated with gallstone disease.Nat Commun2018
30271901A rare missense variant in <i>NR1H4</i> associates with lower cholesterol levels.Commun Biol2018
27151365MNase titration reveals differences between nucleosome occupancy and chromatin accessibility.Nat Commun2016
27304074Enhancer regions show high histone H3.3 turnover that changes during differentiation.Elife2016
25908537A dominant role for the methyl-CpG-binding protein Mbd2 in controlling Th2 induction by dendritic cells.Nat Commun2015
25082344H3K27 modifications define segmental regulatory domains in the Drosophila bithorax complex.eLife2014
24578067A unique DNA methylation signature defines a population of IFN-γ/IL-4 double-positive T cells during helminth infection.European Journal of Immunology2014
25158628Nucleosomal occupancy changes locally over key regulatory regions during cell differentiation and reprogramming.Nat Commun2014
23837789Multiplexed Illumina sequencing libraries from picogram quantities of DNA.BMC Genomics2013
21576262CpG islands and the regulation of transcription.Genes and Development2011
21628449Cell type-specific DNA methylation at intragenic CpG islands in the immune system.Genome Research2011
20393567CpG islands influence chromatin structure via the CpG-binding protein Cfp1.Nature2010
19247482A temporal threshold for formaldehyde crosslinking and fixation.PLoS ONE2009
18681894Specificity of Atonal and Scute bHLH factors: analysis of cognate E box binding sites and the influence of Senseless.Genes to Cells2008
16507360A transient heterochromatic state in Xist preempts X inactivation choice without RNA stabilization.Mol Cell2006
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deCODE genetics/Amgen Inc.
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University of Iceland
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Harvard Medical School
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University of California San Diego
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Gladstone Institute of Data Science and Biotechnology, Gladstone Institutes
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University of Washington School of Medicine
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