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Author Details
Full Name
Matthew E Johnson
Affiliation
Center for Spatial and Functional Genomics, Children's Hospital of Philadelphia
ORCID
Career Start Year
2001
Papers
31
H Index
15
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37689782
Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms.
Nat Commun
2023
37584517
Integrative Genomic Analyses Identify LncRNA Regulatory Networks across Pediatric Leukemias and Solid Tumors.
Cancer Res
2023
35659055
Implicating effector genes at COVID-19 GWAS loci using promoter-focused Capture-C in disease-relevant immune cell types.
Genome Biol
2022
35537191
Variant-to-gene-mapping analyses reveal a role for pancreatic islet cells in conferring genetic susceptibility to sleep-related traits.
Sleep
2022
33069917
Variant-to-Gene-Mapping Analyses Reveal a Role for the Hypothalamus in Genetic Susceptibility to Inflammatory Bowel Disease.
Cell Mol Gastroenterol Hepatol
2021
33545232
3D promoter architecture re-organization during iPSC-derived neuronal cell differentiation implicates target genes for neurodevelopmental disorders.
Prog Neurobiol
2021
34799566
Cis-regulatory architecture of human ESC-derived hypothalamic neuron differentiation aids in variant-to-gene mapping of relevant complex traits.
Nat Commun
2021
34532616
CRISPR-Cas9-Mediated Genome Editing Confirms <i>EPDR1</i> as an Effector Gene at the BMD GWAS-Implicated '<i>STARD3NL</i>' Locus.
JBMR Plus
2021
34343493
A UVB-responsive common variant at chromosome band 7p21.1 confers tanning response and melanoma risk via regulation of the aryl hydrocarbon receptor, AHR.
Am J Hum Genet
2021
33459256
Biological constraints on GWAS SNPs at suggestive significance thresholds reveal additional BMI loci.
Elife
2021
33397451
Genome-wide association study implicates novel loci and reveals candidate effector genes for longitudinal pediatric bone accrual.
Genome Biol
2021
32535942
Canonical Notch signaling is required for bone morphogenetic protein-mediated human osteoblast differentiation.
Stem Cells
2020
32778141
An evolutionary driver of interspersed segmental duplications in primates.
Genome Biol
2020
32620744
Mapping effector genes at lupus GWAS loci using promoter Capture-C in follicular helper T cells.
Nat Commun
2020
30890710
Genome-scale Capture C promoter interactions implicate effector genes at GWAS loci for bone mineral density.
Nat Commun
2019
31264971
T follicular helper cells in human efferent lymph retain lymphoid characteristics.
J Clin Invest
2019
29150566
The Loss of TET2 Promotes CD8<sup>+</sup> T Cell Memory Differentiation.
J Immunol
2018
30392958
Distinct Regulation of Th17 and Th1 Cell Differentiation by Glutaminase-Dependent Metabolism.
Cell
2018
29797095
Leveraging epigenomics and contactomics data to investigate SNP pairs in GWAS.
Hum Genet
2018
27539148
The type 2 diabetes presumed causal variant within TCF7L2 resides in an element that controls the expression of ACSL5.
Diabetologia
2016
24667787
Characterization of the transcriptional machinery bound across the widely presumed type 2 diabetes causal variant, rs7903146, within TCF7L2.
Eur J Hum Genet
2015
25567984
DNA binding by FOXP3 domain-swapped dimer suggests mechanisms of long-range chromosomal interactions.
Nucleic Acids Res
2015
24337390
A ChIP-seq-defined genome-wide map of MEF2C binding reveals inflammatory pathways associated with its role in bone density determination.
Calcif Tissue Int
2014
25469308
Two novel type 2 diabetes loci revealed through integration of TCF7L2 DNA occupancy and SNP association data.
BMJ Open Diabetes Res Care
2014
24878043
Genome-wide analyses of ChIP-Seq derived FOXA2 DNA occupancy in liver points to genetic networks underpinning multiple complex traits.
J Clin Endocrinol Metab
2014
24719615
Genetic susceptibility to type 2 diabetes and obesity: follow-up of findings from genome-wide association studies.
Int J Endocrinol
2014
23276256
A specific family of interspersed repeats (SINEs) facilitates meiotic synapsis in mammals.
Mol Cytogenet
2013
17101969
Recurrent duplication-driven transposition of DNA during hominoid evolution.
Proc Natl Acad Sci U S A
2006
15737067
Lineage-specific expansions of retroviral insertions within the genomes of African great apes but not humans and orangutans.
PLoS Biol
2005
11586358
Positive selection of a gene family during the emergence of humans and African apes.
Nature
2001
11948212
Divergent origins and concerted expansion of two segmental duplications on chromosome 16.
J Hered
2001
1 - 31 of 31
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row(s) 1 - 30 of 30
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Andrew D Wells
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6
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University of Michigan School of Medicine ann arbor
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University of Washington
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Diana L Cousminer
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Yadav Wagley
Department of Orthopedic Surgery University of Michigan Medical School Ann Arbor
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Benjamin F Voight
Perelman School of Medicine, University of Pennsylvania
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Klaus H Kaestner
Department of Genetics and Institute for Diabetes, University of Pennsylvania
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Casey S Greene
Dartmouth College Geisel School of Medicine, Princeton University, University of Colorado Anschutz Medical Campus, University of Pennsylvania Perelman School of Medicine
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