Richardson TG - Search Results

1

Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases.

Zheng J, Haberland V, Baird D, Walker V, Haycock PC, Hurle MR, Gutteridge A, Erola P, Liu Y, Luo S, Robinson J, Richardson TG, Staley JR, Elsworth B, Burgess S, Sun BB, Danesh J, Runz H, Maranville JC, Martin HM, Yarmolinsky J, Laurin C, Holmes MV, Liu JZ, Estrada K, Santos R, McCarthy L, Waterworth D, Nelson MR, Smith GD, Butterworth AS, Hemani G, Scott RA, Gaunt TR. Zheng J, et al. Among authors: richardson tg. Nat Genet. 2020 Oct;52(10):1122-1131. doi: 10.1038/s41588-020-0682-6. Epub 2020 Sep 7. Nat Genet. 2020. PMID: 32895551 Free PMC article.

2

Influence of adiposity-related genetic markers in a population of saudi arabians where other variables influencing obesity may be reduced.

Alharbi KK, Richardson TG, Khan IA, Syed R, Mohammed AK, Boustred CR, Gaunt TR, Tamimi W, Al-Daghri NM, Day IN. Alharbi KK, et al. Among authors: richardson tg. Dis Markers. 2014;2014:758232. doi: 10.1155/2014/758232. Epub 2014 Nov 17. Dis Markers. 2014. PMID: 25484485 Free PMC article.

3

Identifying Highly Penetrant Disease Causal Mutations Using Next Generation Sequencing: Guide to Whole Process.

Erzurumluoglu AM, Rodriguez S, Shihab HA, Baird D, Richardson TG, Day IN, Gaunt TR. Erzurumluoglu AM, et al. Among authors: richardson tg. Biomed Res Int. 2015;2015:923491. doi: 10.1155/2015/923491. Epub 2015 Apr 6. Biomed Res Int. 2015. PMID: 26106619 Free PMC article. Review.

4

A Protein Domain and Family Based Approach to Rare Variant Association Analysis.

Richardson TG, Shihab HA, Rivas MA, McCarthy MI, Campbell C, Timpson NJ, Gaunt TR. Richardson TG, et al. PLoS One. 2016 Apr 29;11(4):e0153803. doi: 10.1371/journal.pone.0153803. eCollection 2016. PLoS One. 2016. PMID: 27128313 Free PMC article.

5

Incorporating Non-Coding Annotations into Rare Variant Analysis.

Richardson TG, Campbell C, Timpson NJ, Gaunt TR. Richardson TG, et al. PLoS One. 2016 Apr 29;11(4):e0154181. doi: 10.1371/journal.pone.0154181. eCollection 2016. PLoS One. 2016. PMID: 27128317 Free PMC article.

6

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. 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.

7

A pathway-centric approach to rare variant association analysis.

Richardson TG, Timpson NJ, Campbell C, Gaunt TR. Richardson TG, et al. Eur J Hum Genet. 2016 Jan;25(1):123-129. doi: 10.1038/ejhg.2016.113. Epub 2016 Aug 31. Eur J Hum Genet. 2016. PMID: 27577545 Free PMC article.

8

Mendelian Randomization Analysis Identifies CpG Sites as Putative Mediators for Genetic Influences on Cardiovascular Disease Risk.

Richardson TG, Zheng J, Davey Smith G, Timpson NJ, Gaunt TR, Relton CL, Hemani G. Richardson TG, et al. Am J Hum Genet. 2017 Oct 5;101(4):590-602. doi: 10.1016/j.ajhg.2017.09.003. Am J Hum Genet. 2017. PMID: 28985495 Free PMC article.

9

Using Y-Chromosomal Haplogroups in Genetic Association Studies and Suggested Implications.

Erzurumluoglu AM, Baird D, Richardson TG, Timpson NJ, Rodriguez S. Erzurumluoglu AM, et al. Among authors: richardson tg. Genes (Basel). 2018 Jan 22;9(1):45. doi: 10.3390/genes9010045. Genes (Basel). 2018. PMID: 29361760 Free PMC article.

10

Systematic Mendelian randomization framework elucidates hundreds of CpG sites which may mediate the influence of genetic variants on disease.

Richardson TG, Haycock PC, Zheng J, Timpson NJ, Gaunt TR, Davey Smith G, Relton CL, Hemani G. Richardson TG, et al. Hum Mol Genet. 2018 Sep 15;27(18):3293-3304. doi: 10.1093/hmg/ddy210. Hum Mol Genet. 2018. PMID: 29893838 Free PMC article.

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