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المؤلفون: Angharad M. Roberts, Alexander Ing, Helen Sage, Paul J.R. Barton, Daniel G. MacArthur, Birgit Funke, Steven M. Harrison, Eric Vallabh Minikel, Konrad J. Karczewski, Nicola Whiffin, Roddy Walsh, Stuart A. Cook, James S. Ware, K Thomson, Anne H. O’Donnell-Luria, Zach Zappala
المساهمون: Fondation Leducq, British Heart Foundation, Wellcome Trust, Department of Health, Royal Brompton & Harefield NHS Foundation Trust
المصدر: The American Journal of Human Genetics. 104:187-190
مصطلحات موضوعية: Genetics & Heredity, Science & Technology, Genome, Genetic Variation, High resolution, 11 Medical And Health Sciences, Computational biology, 06 Biological Sciences, Biology, Genetic architecture, Interpretation (model theory), Genetic variation, Prevalence, Genetics, Letters to the Editor, Life Sciences & Biomedicine, Genetics (clinical)
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd31f6b8efd6e5d42a11df5ec4030234
https://doi.org/10.1016/j.ajhg.2018.11.012 -
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المؤلفون: K Thomson, Eric Vallabh Minikel, Angharad M. Roberts, Nicola Whiffin, Stuart A. Cook, Helen Sage, Roddy Walsh, Daniel G. MacArthur, Alexander Ing, Zach Zappala, Konrad J. Karczewski, Paul J.R. Barton, Steven M. Harrison, James S. Ware, Anne H. O’Donnell-Luria
مصطلحات موضوعية: 0303 health sciences, education.field_of_study, Interpretation (logic), Computer science, 030305 genetics & heredity, Population, High resolution, Genomics, Computational biology, Genome, Genetic architecture, 03 medical and health sciences, Allele, education, Allele frequency, 030304 developmental biology
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23cfa337ce7b9e79c3904a85ab634267
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المؤلفون: Eric Wu, David A. Knowles, Konrad J. Karczewski, Kimberly R. Kukurba, Kevin S. Smith, Stephen B. Montgomery, Alexis Battle, Xin Li, Zach Zappala, Noah Simon
المصدر: The American Journal of Human Genetics. 95(3):245-256
مصطلحات موضوعية: RNA, Untranslated, Quantitative Trait Loci, Biology, Quantitative trait locus, Genome, Polymorphism, Single Nucleotide, DNA sequencing, White People, Article, Genetics, Humans, Family, Genetics(clinical), Lymphocytes, Gene, Genetics (clinical), Genome, Human, Sequence Analysis, RNA, Haplotype, High-Throughput Nucleotide Sequencing, Minor allele frequency, Haplotypes, Expression quantitative trait loci, Human genome, Transcriptome