نتائج البحث - Daniel G. MacArthur
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Face up to false positives حسب Daniel G. MacArthur
منشور في 2012Artigo -
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UDP-N-Acetylglucosamine 2-Epimerase/N-Acetylmannosamine Kinase (GNE) Binds to Alpha-Actinin 1: Novel Pathways in Skeletal Muscle? حسب Shira Amsili, Hagit Zer, Stephan Hinderlich, Sabine Krause, Michal Becker‐Cohen, Daniel G. MacArthur, Kathryn N. North, Stella Mitrani‐Rosenbaum
منشور في 2008Artigo -
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Using ALoFT to determine the impact of putative loss-of-function variants in protein-coding genes حسب Suganthi Balasubramanian, Yao Fu, Mayur Pawashe, Patrick D. McGillivray, Mike Jin, Jeremy Liu, Konrad J. Karczewski, Daniel G. MacArthur, Mark Gerstein
منشور في 2017Artigo -
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Human genetic variation alters CRISPR-Cas9 on- and off-targeting specificity at therapeutically implicated loci حسب Samuel Lessard, Laurent C. Francioli, Jessica Alföldi, Jean‐Claude Tardif, Patrick T. Ellinor, Daniel G. MacArthur, Guillaume Lettre, Stuart H. Orkin, Matthew C. Canver
منشور في 2017Artigo -
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Association analysis of the ACTN3 R577X polymorphism and complex quantitative body composition and performance phenotypes in adolescent Greeks حسب Colin N. Moran, Nan Yang, Mark E.S. Bailey, Αθανάσιος Τσιόκανος, Athanasios Z. Jamurtas, Daniel G. MacArthur, Kathryn N. North, Yannis Pitsiladis, Richard H. Wilson
منشور في 2006Artigo -
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Quantifying unobserved protein-coding variants in human populations provides a roadmap for large-scale sequencing projects حسب James Zou, Gregory Valiant, Paul Valiant, Konrad J. Karczewski, Siu On Chan, Kaitlin E. Samocha, Monkol Lek, Shamil Sunyaev, Mark J. Daly, Daniel G. MacArthur
منشور في 2016Artigo -
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Base-specific mutational intolerance near splice sites clarifies the role of nonessential splice nucleotides حسب Sidi Zhang, Kaitlin E. Samocha, Manuel A. Rivas, Konrad J. Karczewski, Emma Daly, Ben Schmandt, Benjamin M. Neale, Daniel G. MacArthur, Mark J. Daly
منشور في 2018Artigo -
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Patterns of genic intolerance of rare copy number variation in 59,898 human exomes حسب Douglas M. Ruderfer, Tymor Hamamsy, Monkol Lek, Konrad J. Karczewski, David Kavanagh, Kaitlin E. Samocha, Mark J. Daly, Daniel G. MacArthur, Menachem Fromer, Shaun Purcell
منشور في 2016Artigo -
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Pathogenic <i>ASXL1</i> somatic variants in reference databases complicate germline variant interpretation for Bohring-Opitz Syndrome حسب Colleen M. Carlston, Anne O’Donnell‐Luria, Hunter R. Underhill, Beryl B. Cummings, Ben Weisburd, Eric Vallabh Minikel, Daniel P. Birnbaum, Tatiana Tvrdik, Daniel G. MacArthur, Rong Mao
منشور في 2017Revisão -
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STRetch: detecting and discovering pathogenic short tandem repeat expansions حسب Harriet Dashnow, Monkol Lek, Belinda Phipson, Andreas Halman, Simon Sadedin, Andrew Lonsdale, Mark R. Davis, Phillipa J. Lamont, Joshua S. Clayton, Nigel G. Laing, Daniel G. MacArthur, Alicia Oshlack
منشور في 2018Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Genetics
Gene
Medicine
Computational biology
Phenotype
Genome
Exome sequencing
Genotype
Mutation
Exome
Population
Internal medicine
Pathology
Single-nucleotide polymorphism
Gene expression
Allele
Bioinformatics
Computer science
Disease
Environmental health
Genomics
Human genome
Endocrinology
Transcriptome
Genome-wide association study
Mendelian inheritance
Sociology
Genetic variation
Demography