Weedon Mn, Jackson L, Harrison Jw, Ruth Ks, Tyrrell J, Hattersley At, Wright Cf. BMJ 2021
Times Cited: 9
Times Cited: 9
Times Cited
Times Co-cited
Similarity
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Massively parallel characterization of CYP2C9 variant enzyme activity and abundance.
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Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study.
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Variation in the glucose transporter gene SLC2A2 is associated with glycemic response to metformin.
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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.
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A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose.
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A scientometric review of genome-wide association studies.
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The mutational constraint spectrum quantified from variation in 141,456 humans.
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Very low-depth whole-genome sequencing in complex trait association studies.
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Exome Sequencing-Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants.
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Analysis of protein-coding genetic variation in 60,706 humans.
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The "All of Us" Research Program.
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Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.
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Human Gain-of-Function MC4R Variants Show Signaling Bias and Protect against Obesity.
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Unreliability of genotyping arrays for detecting very rare variants in human genetic studies: Example from a recent study of MC4R.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.