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Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes.
Lohmueller KE, Sparsø T, Li Q, Andersson E, Korneliussen T, Albrechtsen A, Banasik K, Grarup N, Hallgrimsdottir I, Kiil K, Kilpeläinen TO, Krarup NT, Pers TH, Sanchez G, Hu Y, Degiorgio M, Jørgensen T, Sandbæk A, Lauritzen T, Brunak S, Kristiansen K, Li Y, Hansen T, Wang J, Nielsen R, Pedersen O. Lohmueller KE, et al. Am J Hum Genet. 2013 Dec 5;93(6):1072-86. doi: 10.1016/j.ajhg.2013.11.005. Epub 2013 Nov 27. Am J Hum Genet. 2013. PMID: 24290377 Free PMC article.
Inferring the mode and strength of ongoing selection.
Barroso GV, Lohmueller KE. Barroso GV, et al. Among authors: lohmueller ke. Genome Res. 2023 Apr;33(4):632-643. doi: 10.1101/gr.276386.121. Epub 2023 Apr 13. Genome Res. 2023. PMID: 37055196 Free PMC article.
Remembering distinguished professor Robert K. Wayne.
Leonard JA, von Holdt B, Smith TB, Sork VL, Shapiro B, Ostrander EA, Rieseberg LH, Van Valkenburgh B, Lohmueller KE. Leonard JA, et al. Among authors: lohmueller ke. Mol Ecol. 2023 May;32(9):2364-2368. doi: 10.1111/mec.16926. Epub 2023 Mar 29. Mol Ecol. 2023. PMID: 36991555 No abstract available.
Assessing the evolutionary impact of amino acid mutations in the human genome.
Boyko AR, Williamson SH, Indap AR, Degenhardt JD, Hernandez RD, Lohmueller KE, Adams MD, Schmidt S, Sninsky JJ, Sunyaev SR, White TJ, Nielsen R, Clark AG, Bustamante CD. Boyko AR, et al. Among authors: lohmueller ke. PLoS Genet. 2008 May 30;4(5):e1000083. doi: 10.1371/journal.pgen.1000083. PLoS Genet. 2008. PMID: 18516229 Free PMC article.
93 results