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Author Details

Michael D Linderman
Middlebury College
2006
43
23
PMIDPaper TitleJournal TitlePublished Year
34195837NPSV: A simulation-driven approach to genotyping structural variants in whole-genome sequencing data.Gigascience2021
34058740Development and Validation of a Comprehensive Genomics Knowledge Scale.Public Health Genomics2021
34195837NPSV: A simulation-driven approach to genotyping structural variants in whole-genome sequencing data.Gigascience2021
34058740Development and Validation of a Comprehensive Genomics Knowledge Scale.Public Health Genomics2021
30808425Predispositional genome sequencing in healthy adults: design, participant characteristics, and early outcomes of the PeopleSeq Consortium.Genome Med2019
31775760MySeq: privacy-protecting browser-based personal Genome analysis for genomics education and exploration.BMC Med Genomics2019
31604420DECA: scalable XHMM exome copy-number variant calling with ADAM and Apache Spark.BMC Bioinformatics2019
30808425Predispositional genome sequencing in healthy adults: design, participant characteristics, and early outcomes of the PeopleSeq Consortium.Genome Med2019
31775760MySeq: privacy-protecting browser-based personal Genome analysis for genomics education and exploration.BMC Med Genomics2019
31604420DECA: scalable XHMM exome copy-number variant calling with ADAM and Apache Spark.BMC Bioinformatics2019
29382336Impacts of incorporating personal genome sequencing into graduate genomics education: a longitudinal study over three course years.BMC Med Genomics2018
29382336Impacts of incorporating personal genome sequencing into graduate genomics education: a longitudinal study over three course years.BMC Med Genomics2018
28051073Psychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project.Eur J Hum Genet2017
28469811Factors associated with success of telaprevir- and boceprevir-based triple therapy for hepatitis C virus infection.World J Hepatol2017
28502727Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx Study.J Mol Diagn2017
28895531Genetic identification of a common collagen disease in puerto ricans via identity-by-descent mapping in a health system.Elife2017
28051073Psychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project.Eur J Hum Genet2017
28502727Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx Study.J Mol Diagn2017
28469811Factors associated with success of telaprevir- and boceprevir-based triple therapy for hepatitis C virus infection.World J Hepatol2017
28895531Genetic identification of a common collagen disease in puerto ricans via identity-by-descent mapping in a health system.Elife2017
26036856Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project.Eur J Hum Genet2016
27023617Personal Genome Sequencing in Ostensibly Healthy Individuals and the PeopleSeq Consortium.J Pers Med2016
26810587Toward clinical genomics in everyday medicine: perspectives and recommendations.Expert Rev Mol Diagn2016
27245685Development and clinical application of an integrative genomic approach to personalized cancer therapy.Genome Med2016
27213804Exome sequencing of extreme clopidogrel response phenotypes identifies B4GALT2 as a determinant of on-treatment platelet reactivity.Clin Pharmacol Ther2016
27310265Visualization and cellular hierarchy inference of single-cell data using SPADE.Nat Protoc2016
26898680Impact of Genomic Counseling on Informed Decision-Making among ostensibly Healthy Individuals Seeking Personal Genome Sequencing: the HealthSeq Project.J Genet Couns2016
26508568Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project.Eur J Hum Genet2016
26036856Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project.Eur J Hum Genet2016
26508568Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project.Eur J Hum Genet2016
27213804Exome sequencing of extreme clopidogrel response phenotypes identifies B4GALT2 as a determinant of on-treatment platelet reactivity.Clin Pharmacol Ther2016
27310265Visualization and cellular hierarchy inference of single-cell data using SPADE.Nat Protoc2016
27245685Development and clinical application of an integrative genomic approach to personalized cancer therapy.Genome Med2016
26898680Impact of Genomic Counseling on Informed Decision-Making among ostensibly Healthy Individuals Seeking Personal Genome Sequencing: the HealthSeq Project.J Genet Couns2016
27023617Personal Genome Sequencing in Ostensibly Healthy Individuals and the PeopleSeq Consortium.J Pers Med2016
26810587Toward clinical genomics in everyday medicine: perspectives and recommendations.Expert Rev Mol Diagn2016
25754315Novel, compound heterozygous, single-nucleotide variants in MARS2 associated with developmental delay, poor growth, and sensorineural hearing loss.Hum Mutat2015
25754315Novel, compound heterozygous, single-nucleotide variants in MARS2 associated with developmental delay, poor growth, and sensorineural hearing loss.Hum Mutat2015
25634025How do students react to analyzing their own genomes in a whole-genome sequencing course?: outcomes of a longitudinal cohort study.Genet Med2015
26264128Preparing the next generation of genomicists: a laboratory-style course in medical genomics.BMC Med Genomics2015
26551672Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.Nat Genet2015
26578856A dynamical model improves reconstruction of handwriting from multichannel electromyographic recordings.Front Neurosci2015
26264128Preparing the next generation of genomicists: a laboratory-style course in medical genomics.BMC Med Genomics2015
26578856A dynamical model improves reconstruction of handwriting from multichannel electromyographic recordings.Front Neurosci2015
26551672Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.Nat Genet2015
25634025How do students react to analyzing their own genomes in a whole-genome sequencing course?: outcomes of a longitudinal cohort study.Genet Med2015
23927549A founder mutation in COL4A3 causes autosomal recessive Alport syndrome in the Ashkenazi Jewish population.Clin Genet2014
23927549A founder mutation in COL4A3 causes autosomal recessive Alport syndrome in the Ashkenazi Jewish population.Clin Genet2014
24758382Analytical validation of whole exome and whole genome sequencing for clinical applications.BMC Med Genomics2014
25085501Integrated genome-wide association, coexpression network, and expression single nucleotide polymorphism analysis identifies novel pathway in allergic rhinitis.BMC Med Genomics2014
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Co-authored papers 15
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Co-authored papers 9
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Stanford University School of Medicine
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Brigham and Women's Hospital, Broad Institute Ariadne Labs and Harvard Medical School
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Hasso Plattner Institute for Digital Health at Mount Sinai
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Vanderbilt University Medical Center
Co-authored papers 3
Hasso Plattner Institute for Digital Health, Icahn School of Medicine at Mount Sinai
Co-authored papers 2
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The Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 2
Icahn School of Medicine at Mount Sinai, University of Wisconsin-Madison
Co-authored papers 2
Johns Hopkins Berman Institute of Bioethics.
Co-authored papers 2
Northwestern University, Center for Genetic Medicine
Co-authored papers 2
Stanford University
Co-authored papers 2
Institute for Next Generation Healthcare
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Icahn School of Medicine at Mount Sinai
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Institute of Neuroscience and Medicine (INM-1), Research Center Juelich
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William Harvey Research Institute, Queen Mary University of London
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