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Author Details

Kenneth B Beckman
University of Minnesota Genomics Center (UMNGC)
1996
89
41
PMIDPaper TitleJournal TitlePublished Year
36180068Admixture mapping of severe asthma exacerbations in Hispanic/Latino children and youth.Thorax2023
37802634Novel insights into the whole-blood DNA methylome of asthma in ethnically diverse children and youth.Eur Respir J2023
37784136Epigenomic response to albuterol treatment in asthma-relevant airway epithelial cells.Clin Epigenetics2023
37467337More than bad luck: Cancer and aging are linked to replication-driven changes to the epigenome.Sci Adv2023
37302406Outpatient treatment of COVID-19 and incidence of post-COVID-19 condition over 10 months (COVID-OUT): a multicentre, randomised, quadruple-blind, parallel-group, phase 3 trial.Lancet Infect Dis2023
36796456Multi-omic approach associates blood methylome with bronchodilator drug response in pediatric asthma.J Allergy Clin Immunol2023
36598240Mycobacterium tuberculosis Requires the Outer Membrane Lipid Phthiocerol Dimycocerosate for Starvation-Induced Antibiotic Tolerance.mSystems2023
33127576Comparative analysis of genome-wide DNA methylation identifies patterns that associate with conserved transcriptional programs in osteosarcoma.Bone2022
36962725Health inequities in SARS-CoV-2 infection, seroprevalence, and COVID-19 vaccination: Results from the East Bay COVID-19 study.PLOS Glob Public Health2022
35033200Epigenome-wide association study of lung function in Latino children and youth with asthma.Clin Epigenetics2022
34897429The genome of the zebra mussel, Dreissena polymorpha: a resource for comparative genomics, invasion genetics, and biocontrol.G3 (Bethesda)2022
33459354Leukocyte telomere length, cancer incidence and all-cause mortality among Chinese adults: Singapore Chinese Health Study.Int J Cancer2021
33684206Biological Aging Predicts Vulnerability to COVID-19 Severity in UK Biobank Participants.J Gerontol A Biol Sci Med Sci2021
33941849Low frequency variants associated with leukocyte telomere length in the Singapore Chinese population.Commun Biol2021
34125893Dissecting and tuning primer editing by proofreading polymerases.Nucleic Acids Res2021
34174468Neither Donor nor Recipient Mitochondrial Haplotypes Are Associated with Unrelated Donor Transplant Outcomes: A Validation Study from the CIBMTR.Transplant Cell Ther2021
34116245Prediction of False-Positive Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Molecular Results in a High-Throughput Open-Platform System.J Mol Diagn2021
34259552Saliva Testing Is Accurate for Early-Stage and Presymptomatic COVID-19.Microbiol Spectr2021
34195577A multi-center phase II randomized clinical trial of losartan on symptomatic outpatients with COVID-19.EClinicalMedicine2021
32676624COVID-19 severity is predicted by earlier evidence of accelerated aging.medRxiv2020
33276717A rapid, cost-effective tailed amplicon method for sequencing SARS-CoV-2.BMC Genomics2020
31171785Loci for human leukocyte telomere length in the Singaporean Chinese population and trans-ethnic genetic studies.Nat Commun2019
31577800Association between mitochondrial genetic variation and breast cancer risk: The Multiethnic Cohort.PLoS One2019
30891420Next generation sequencing for clinical diagnostics: Five year experience of an academic laboratory.Mol Genet Metab Rep2019
31036053Measuring sequencer size bias using REcount: a novel method for highly accurate Illumina sequencing-based quantification.Genome Biol2019
31034279Resequencing Study Confirms That Host Defense and Cell Senescence Gene Variants Contribute to the Risk of Idiopathic Pulmonary Fibrosis.Am J Respir Crit Care Med2019
29318605Leukocyte telomere length in relation to risk of lung adenocarcinoma incidence: Findings from the Singapore Chinese Health Study.Int J Cancer2018
29911110Optimization of a microfluidics-based next generation sequencing assay for clinical oncology diagnostics.Ann Transl Med2018
30097329Corrigendum to "Single cell sequencing reveals heterogeneity within ovarian cancer epithelium and cancer associated stromal cells" [Gyncol. Oncol. 144 (2017) 598-606].Gynecol Oncol2018
30225373Comprehensive Functional Analysis of the Enterococcus faecalis Core Genome Using an Ordered, Sequence-Defined Collection of Insertional Mutations in Strain OG1RF.mSystems2018
30443602Evaluating the Information Content of Shallow Shotgun Metagenomics.mSystems2018
28502791Single-Strand Consensus Sequencing Reveals that HIV Type but not Subtype Significantly Impacts Viral Mutation Frequencies and Spectra.J Mol Biol2017
28111004Single cell sequencing reveals heterogeneity within ovarian cancer epithelium and cancer associated stromal cells.Gynecol Oncol2017
26810587Toward clinical genomics in everyday medicine: perspectives and recommendations.Expert Rev Mol Diagn2016
27454739Systematic improvement of amplicon marker gene methods for increased accuracy in microbiome studies.Nat Biotechnol2016
27266705Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia.BMC Genet2016
27021046No Association between the Mitochondrial Genome and Prostate Cancer Risk: The Multiethnic Cohort.Cancer Epidemiol Biomarkers Prev2016
25611102Clinical validation of targeted next-generation sequencing for inherited disorders.Arch Pathol Lab Med2015
26644969Persistent microbial dysbiosis in preterm premature rupture of membranes from onset until delivery.PeerJ2015
26340450Association of Genes, Pathways, and Haplogroups of the Mitochondrial Genome with the Risk of Colorectal Cancer: The Multiethnic Cohort.PLoS One2015
26074333mRNA 3'-UTR shortening is a molecular signature of mTORC1 activation.Nat Commun2015
25958132Next generation sequencing in endocrine practice.Mol Genet Metab2015
24092820Characterizing the genetic basis of transcriptome diversity through RNA-sequencing of 922 individuals.Genome Res2014
25327703Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25.Nat Commun2014
24885806Implementation of Cloud based next generation sequencing data analysis in a clinical laboratory.BMC Res Notes2014
24296977Type I interferon signaling genes in recurrent major depression: increased expression detected by whole-blood RNA sequencing.Mol Psychiatry2014
22583563Genetic and environmental predictors of serum 25-hydroxyvitamin D concentrations among middle-aged and elderly Chinese in Singapore.Br J Nutr2013
23658746Associations of PON1 and genetic ancestry with obesity in early childhood.PLoS One2013
23416278Association between celiac disease and iron deficiency in Caucasians, but not non-Caucasians.Clin Gastroenterol Hepatol2013
23583980Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.Nat Genet2013
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Collaborators

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Co-authored papers 22
Institute for Human Genetics, University of California San Francisco (UCSF)
Co-authored papers 9
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Co-authored papers 5
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Co-authored papers 4
Department of Surgery University of Minnesota Minneapolis Minnesota USA.
Co-authored papers 4
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University of Pittsburgh
Co-authored papers 3
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Massachusetts General Hospital and Harvard Medical School
Co-authored papers 3
Co-authored papers 3
University of Washington
Co-authored papers 3
University of Minnesota
Co-authored papers 3
Co-authored papers 3
Macalester College
Co-authored papers 3
Buck Institute for Research on Aging
Co-authored papers 3
Division of Epidemiology and Clinical Research, University of Minnesota
Co-authored papers 2
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University of Minnesota
Co-authored papers 2
Center for Molecular Medicine, University Medical Center Utrecht
Co-authored papers 2
University of British Columbia and BC Children's Hospital
Co-authored papers 2
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University of California san francisco
Co-authored papers 2
Western University
Co-authored papers 2
Mayo Clinic
Co-authored papers 2