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Association of copy number variation across the genome with neuropsychiatric traits in the general population.
Guyatt AL, Stergiakouli E, Martin J, Walters J, O'Donovan M, Owen M, Thapar A, Kirov G, Rodriguez S, Rai D, Zammit S, Gaunt TR. Guyatt AL, et al. Among authors: rodriguez s. Am J Med Genet B Neuropsychiatr Genet. 2018 Jul;177(5):489-502. doi: 10.1002/ajmg.b.32637. Epub 2018 Apr 24. Am J Med Genet B Neuropsychiatr Genet. 2018. PMID: 29687944 Free PMC article.
Amplification ratio control system for copy number variation genotyping.
Guthrie PA, Gaunt TR, Abdollahi MR, Rodriguez S, Lawlor DA, Smith GD, Day IN. Guthrie PA, et al. Among authors: rodriguez s. Nucleic Acids Res. 2011 Apr;39(8):e54. doi: 10.1093/nar/gkr046. Epub 2011 Feb 7. Nucleic Acids Res. 2011. PMID: 21300641 Free PMC article.
Collapsed methylation quantitative trait loci analysis for low frequency and rare variants.
Richardson TG, Shihab HA, Hemani G, Zheng J, Hannon E, Mill J, Carnero-Montoro E, Bell JT, Lyttleton O, McArdle WL, Ring SM, Rodriguez S, Campbell C, Smith GD, Relton CL, Timpson NJ, Gaunt TR. Richardson TG, et al. Among authors: rodriguez s. Hum Mol Genet. 2016 Oct 1;25(19):4339-4349. doi: 10.1093/hmg/ddw283. Epub 2016 Aug 24. Hum Mol Genet. 2016. PMID: 27559110 Free PMC article.
2,201 results