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Author Details
Full Name
Leah C Kottyan
Affiliation
Cincinnati Children's Hospital Medical Center
ORCID
Career Start Year
2009
Papers
93
H Index
28
Expertise
CM4AI Collaborator
Nevan J Krogan (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36383166
Utilization of electronic health record data to evaluate the association of urban environment with systemic lupus erythematosus symptoms.
Rheumatology (Oxford)
2023
37758692
Proteomic and genetic analyses of influenza A viruses identify pan-viral host targets.
Nat Commun
2023
37660987
Breakthroughs in understanding and treating eosinophilic gastrointestinal diseases presented at the CEGIR/TIGERs Symposium at the 2022 American Academy of Allergy, Asthma & Immunology Meeting.
J Allergy Clin Immunol
2023
37794597
Effector memory TÂ cells induce innate inflammation by triggering DNA damage and a non-canonical STING pathway in dendritic cells.
Cell Rep
2023
37745430
After the Infection: A Survey of Pathogens and Non-communicable Human Disease.
medRxiv
2023
37455310
A functional mechanism for a non-coding variant near AGTR2 associated with risk for preterm birth.
BMC Med
2023
36949074
A DNA tumor virus globally reprograms host 3D genome architecture to achieve immortal growth.
Nat Commun
2023
36945549
An atlas of gene regulatory networks for memory CD4 <sup>+</sup> T cells in youth and old age.
bioRxiv
2023
37337107
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy.
Nat Genet
2023
36621880
Returning integrated genomic risk and clinical recommendations: The eMERGE study.
Genet Med
2023
36719906
maxATAC: Genome-scale transcription-factor binding prediction from ATAC-seq with deep neural networks.
PLoS Comput Biol
2023
36585519
Gene-environment interactions and their impact on human health.
Genes Immun
2023
36400179
Genome-wide admixture and association analysis identifies African ancestry-specific risk loci of eosinophilic esophagitis in African Americans.
J Allergy Clin Immunol
2023
36846987
Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female-Specific Health Conditions.
J Am Heart Assoc
2023
36746961
Author Correction: Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits.
Nat Commun
2023
36778284
B cell repertoire in children with skin barrier dysfunction supports altered IgE maturation associated with allergic food sensitization.
bioRxiv
2023
36540998
Quantifying factors that affect polygenic risk score performance across diverse ancestries and age groups for body mass index.
Pac Symp Biocomput
2023
36824978
Macrophage epigenetic memories of early life injury drive neonatal nociceptive priming.
bioRxiv
2023
35252945
CASCADE: high-throughput characterization of regulatory complex binding altered by non-coding variants.
Cell Genom
2022
35765100
Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations.
Genome Med
2022
35576187
Epigenetic and transcriptional dysregulation in CD4+ T cells in patients with atopic dermatitis.
PLoS Genet
2022
35595084
Multiancestral polygenic risk score for pediatric asthma.
J Allergy Clin Immunol
2022
35388006
Lupus enhancer risk variant causes dysregulation of IRF8 through cooperative lncRNA and DNA methylation machinery.
Nat Commun
2022
36253972
Frontotemporal degeneration genetic risk loci and transcription regulation as a possible mechanistic link to disease risk.
Medicine (Baltimore)
2022
36376295
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure.
Nat Commun
2022
33446329
Very early onset eosinophilic esophagitis is common, responds to standard therapy, and demonstrates enrichment for CAPN14 genetic variants.
J Allergy Clin Immunol
2021
33712590
Global discovery of lupus genetic risk variant allelic enhancer activity.
Nat Commun
2021
33761354
IRF1 governs the differential interferon-stimulated gene responses in human monocytes and macrophages by regulating chromatin accessibility.
Cell Rep
2021
34473385
Whole blood transcriptomics identifies gene expression associated with peanut allergy in infants at high risk.
Clin Exp Allergy
2021
34815391
Desmoplakin and periplakin genetically and functionally contribute to eosinophilic esophagitis.
Nat Commun
2021
34799401
Epstein-Barr virus nuclear antigen 2 extensively rewires the human chromatin landscape at autoimmune risk loci.
Genome Res
2021
33941608
Medical Records-Based Genetic Studies of the Complement System.
J Am Soc Nephrol
2021
34176557
Epigenetics of obstructive sleep apnea syndrome: a systematic review.
J Clin Sleep Med
2021
34111109
Runx1 shapes the chromatin landscape via a cascade of direct and indirect targets.
PLoS Genet
2021
33272962
Meta-analysis of 208370 East Asians identifies 113 susceptibility loci for systemic lupus erythematosus.
Ann Rheum Dis
2021
33446330
Replication and meta-analyses nominate numerous eosinophilic esophagitis risk genes.
J Allergy Clin Immunol
2021
32375053
Suppression of Inflammasome Activation by IRF8 and IRF4 in cDCs Is Critical for T Cell Priming.
Cell Rep
2020
32017227
IL-33 promotes type 1 cytokine expression via p38 MAPK in human NK cells.
J Leukoc Biol
2020
31980060
Noncoding Variants as Genetic Contributors to Autoimmune Disease Pathogenesis.
J Invest Dermatol
2020
31910986
The genetic etiology of eosinophilic esophagitis.
J Allergy Clin Immunol
2020
33426398
Comprehensive Review of Steroid-Sensitive Nephrotic Syndrome Genetic Risk Loci and Transcriptional Regulation as a Possible Mechanistic Link to Disease Risk.
Kidney Int Rep
2020
33205070
Erratum: Therapeutic Targeting of Follicular T Cells with Chimeric Antigen Receptor-Expressing Natural Killer Cells.
Cell Rep Med
2020
32864635
Therapeutic Targeting of Follicular T Cells with Chimeric Antigen Receptor-Expressing Natural Killer Cells.
Cell Rep Med
2020
32405233
The Promise and Peril of Natural Killer Cell Therapies in Pulmonary Infection.
Immunity
2020
30414468
Immunology of the ancestral differences in eosinophilic esophagitis.
Ann Allergy Asthma Immunol
2019
29904099
Genetic variants at the 16p13 locus confer risk for eosinophilic esophagitis.
Genes Immun
2019
30578870
17β-Estradiol protects the esophageal epithelium from IL-13-induced barrier dysfunction and remodeling.
J Allergy Clin Immunol
2019
30423114
Genetic influences on susceptibility to rheumatoid arthritis in African-Americans.
Hum Mol Genet
2019
30626591
Genetic, Inflammatory, and Epithelial Cell Differentiation Factors Control Expression of Human Calpain-14.
G3 (Bethesda)
2019
29129581
Eosinophilic esophagitis (EoE) genetic susceptibility is mediated by synergistic interactions between EoE-specific and general atopic disease loci.
J Allergy Clin Immunol
2018
1 - 50 of 93
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row(s) 1 - 30 of 30
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Co-authored papers
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Carl D Langefeld
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Co-authored papers
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University of Washington Medical Center
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Krzysztof Kiryluk
Columbia University
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Barry I Freedman
Co-authored papers
5
Deborah S Cunninghame Graham
Co-authored papers
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Marylyn D Ritchie
Center for Systems Genomics, Pennsylvania State University, University Park
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Michelle Petri
Co-authored papers
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Wei-Qi Wei
Vanderbilt University Medical Center
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Gurjit K Khurana Hershey
Cincinnati Children's Hospital Medical Center
Co-authored papers
5
John D Reveille
University of Texas
Co-authored papers
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Joshua C Denny
Vanderbilt University
Co-authored papers
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