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Author Details
Full Name
M Ryan Corces
Affiliation
Gladstone Institute of Neurological Disease
ORCID
Career Start Year
2010
Papers
39
H Index
29
Expertise
CM4AI Collaborator
Nathan Sheffield (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37587197
Whole genome deconvolution unveils Alzheimer's resilient epigenetic signature.
Nat Commun
2023
35093191
Epigenomic priming of immune genes implicates oligodendroglia in multiple sclerosis susceptibility.
Neuron
2022
35478247
Chromatin accessibility profiling by ATAC-seq.
Nat Protoc
2022
35532363
The Cell Type-Specific 5hmC Landscape and Dynamics of Healthy Human Hematopoiesis and TET2-Mutant Preleukemia.
Blood Cancer Discov
2022
36466610
Deep learning approaches for noncoding variant prioritization in neurodegenerative diseases.
Front Aging Neurosci
2022
36333818
Single-cell spatial proteomic imaging for human neuropathology.
Acta Neuropathol Commun
2022
34341533
LKB1 inactivation modulates chromatin accessibility to drive metastatic progression.
Nat Cell Biol
2021
33790476
Author Correction: ArchR is a scalable software package for integrative single-cell chromatin accessibility analysis.
Nat Genet
2021
33633365
ArchR is a scalable software package for integrative single-cell chromatin accessibility analysis.
Nat Genet
2021
34859208
PEPATAC: an optimized pipeline for ATAC-seq data analysis with serial alignments.
NAR Genom Bioinform
2021
34819668
ecDNA hubs drive cooperative intermolecular oncogene expression.
Nature
2021
34516796
Complement factor C1q mediates sleep spindle loss and epileptic spikes after mild brain injury.
Science
2021
34568834
Monocytic differentiation and AHR signaling as Primary Nodes of BET Inhibitor Response in Acute Myeloid Leukemia.
Blood Cancer Discov
2021
34418357
GATM and GAMT synthesize creatine locally throughout the mammalian body and within oligodendrocytes of the brain.
Brain Res
2021
32150611
Single-cell mutational profiling enhances the clinical evaluation of AML MRD.
Blood Adv
2020
33106633
Single-cell epigenomic analyses implicate candidate causal variants at inherited risk loci for Alzheimer's and Parkinson's diseases.
Nat Genet
2020
30958261
Single-cell lineage tracing by endogenous mutations enriched in transposase accessible mitochondrial DNA.
Elife
2019
31375813
Massively parallel single-cell chromatin landscapes of human immune cell development and intratumoral T cell exhaustion.
Nat Biotechnol
2019
31133759
HiChIRP reveals RNA-associated chromosome conformation.
Nat Methods
2019
29706549
Integrated Single-Cell Analysis Maps the Continuous Regulatory Landscape of Human Hematopoietic Differentiation.
Cell
2018
30361341
The chromatin accessibility landscape of primary human cancers.
Science
2018
29686426
Transcript-indexed ATAC-seq for precision immune profiling.
Nat Med
2018
28846090
An improved ATAC-seq protocol reduces background and enables interrogation of frozen tissues.
Nat Methods
2017
28089908
Human AML-iPSCs Reacquire Leukemic Properties after Differentiation and Model Clonal Variation of Disease.
Cell Stem Cell
2017
28954238
Rapid Chromatin Switch in the Direct Reprogramming of Fibroblasts to Neurons.
Cell Rep
2017
29164062
Preleukemic Hematopoietic Stem Cells in Human Acute Myeloid Leukemia.
Front Oncol
2017
28945252
Enhancer connectome in primary human cells identifies target genes of disease-associated DNA elements.
Nat Genet
2017
28729405
Superenhancer Analysis Defines Novel Epigenomic Subtypes of Non-APL AML, Including an RARα Dependency Targetable by SY-1425, a Potent and Selective RARα Agonist.
Cancer Discov
2017
26855137
The three-dimensional cancer genome.
Curr Opin Genet Dev
2016
27526324
Lineage-specific and single-cell chromatin accessibility charts human hematopoiesis and leukemia evolution.
Nat Genet
2016
27213817
A humanized bone marrow ossicle xenotransplantation model enables improved engraftment of healthy and leukemic human hematopoietic cells.
Nat Med
2016
25398938
Mutant WT1 is associated with DNA hypermethylation of PRC2 targets in AML and responds to EZH2 inhibition.
Blood
2015
26607380
Leukemia-Associated Cohesin Mutants Dominantly Enforce Stem Cell Programs and Impair Human Hematopoietic Progenitor Differentiation.
Cell Stem Cell
2015
25599133
Isocitrate dehydrogenase 1 and 2 mutations induce BCL-2 dependence in acute myeloid leukemia.
Nat Med
2015
24550281
Preleukemic mutations in human acute myeloid leukemia affect epigenetic regulators and persist in remission.
Proc Natl Acad Sci U S A
2014
25005245
Pre-leukemic evolution of hematopoietic stem cells: the importance of early mutations in leukemogenesis.
Leukemia
2014
22932223
Clonal evolution of preleukemic hematopoietic stem cells precedes human acute myeloid leukemia.
Sci Transl Med
2012
21423168
A long noncoding RNA maintains active chromatin to coordinate homeotic gene expression.
Nature
2011
20502519
Insulin signaling and dietary restriction differentially influence the decline of learning and memory with age.
PLoS Biol
2010
1 - 39 of 39
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