By Dr Angli Xue

Preprints

Xue A; Yazar S; Alquicira-Hernández J; Cuomo ASE; Senabouth A; Gordon G; Kathail P; Ye CJ; Hewitt AW; Powell JE, 2024, Genetic variants associated with cell-type-specific intra-individual gene expression variability reveal new mechanisms of genome regulation, , http://dx.doi.org/10.1101/2024.05.05.592598

Xue A; Zhu Z; Wang H; Jiang L; Visscher PM; Zeng J; Yang J, 2023, Unravelling the complex causal effects of substance use behaviours on common diseases, , http://dx.doi.org/10.21203/rs.3.rs-3465061/v1

Xue A; Yazar S; Neavin D; Powell JE, 2022, Pitfalls and opportunities for applying PEER factors in single-cell eQTL analyses, , http://dx.doi.org/10.1101/2022.08.02.502566

Zhang H; Xiu X; Xue A; Yang Y; Yang Y; Zhao H, 2021, The putative causal effect of type 2 diabetes in risk of cataract: a Mendelian randomization study in East Asian, , http://dx.doi.org/10.1101/2021.02.08.430342

Xue A; Jiang L; Zhu Z; Wray NR; Visscher PM; Zeng J; Yang J, 2020, Genome-wide analyses of behavioural traits biased by misreports and longitudinal changes, , http://dx.doi.org/10.1101/2020.06.15.20131284

Revez JA; Lin T; Qiao Z; Xue A; Holtz Y; Zhu Z; Zeng J; Wang H; Sidorenko J; Kemper KE; Vinkhuyzen AAE; Frater J; Eyles D; Burne THJ; Mitchell B; Martin NG; Zhu G; Visscher PM; Yang J; Wray NR; McGrath JJ, 2019, Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration, , http://dx.doi.org/10.1101/860767

Cheng F-F; Zhuang Y-Y; Wen X-R; Xue A; Yang J; Jin Z-B, 2019, Towards the identification of causal genes for age-related macular degeneration, , http://dx.doi.org/10.1101/778613

Zeng J; Xue A; Jiang L; Lloyd-Jones LR; Wu Y; Wang H; Zheng Z; Yengo L; Kemper KE; Goddard ME; Wray NR; Visscher PM; Yang J, 2019, Bayesian analysis of GWAS summary data reveals differential signatures of natural selection across human complex traits and functional genomic categories, , http://dx.doi.org/10.1101/752527

Noyce AJ; Bandres-Ciga S; Kim J; Heilbron K; Kia D; Hemani G; Xue A; Lawlor DA; Smith GD; Duran R; Gan-Or Z; Blauwendraat C; Gibbs JR; Hinds DA; Yang J; Visscher P; Cuzick J; Morris H; Hardy J; Wood NW; Nalls MA; Singleton AB, 2019, The Parkinson’s Disease Mendelian Randomization Research Portal, , http://dx.doi.org/10.1101/604033

Wang H; Zhang F; Zeng J; Wu Y; Kemper KE; Xue A; Zhang M; Powell JE; Goddard ME; Wray NR; Visscher PM; McRae AF; Yang J, 2019, Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank, , http://dx.doi.org/10.1101/519538

Nalls MA; Blauwendraat C; Vallerga CL; Heilbron K; Bandres-Ciga S; Chang D; Tan M; Kia DA; Noyce AJ; Xue A; Bras J; Young E; von Coelln R; Simón-Sánchez J; Schulte C; Sharma M; Krohn L; Pihlstrom L; Siitonen A; Iwaki H; Leonard H; Faghri F; Raphael Gibbs J; Hernandez DG; Scholz SW; Botia JA; Martinez M; Corvol J-C; Lesage S; Jankovic J; Shulman LM; Sutherland M; Tienari P; Majamaa K; Toft M; Andreassen OA; Bangale T; Brice A; Yang J; Gan-Or Z; Gasser T; Heutink P; Shulman JM; Wood N; Hinds DA; Hardy JA; Morris HR; Gratten J; Visscher PM; Graham RR; Singleton AB, 2018, Expanding Parkinson’s disease genetics: novel risk loci, genomic context, causal insights and heritable risk, , http://dx.doi.org/10.1101/388165

Xue A; Wu Y; Zhu Z; Zhang F; Kemper KE; Zheng Z; Yengo L; Lloyd-Jones LR; Sidorenko J; Wu Y; McRae AF; Visscher PM; Zeng J; Yang J, 2018, Novel susceptibility loci and genetic regulation mechanisms for type 2 diabetes, , http://dx.doi.org/10.1101/284570

Qi T; Wu Y; Zeng J; Zhang F; Xue A; Jiang L; Zhu Z; Kemper K; Yengo L; Zheng Z; Marioni RE; Montgomery GW; Deary IJ; Wray NR; Visscher PM; McRae AF; Yang J, 2018, Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood, , http://dx.doi.org/10.1101/274472

Zeng J; de Vlaming R; Wu Y; Robinson MR; Lloyd-Jones L; Yengo L; Yap C; Xue A; Sidorenko J; McRae AF; Powell JE; Montgomery GW; Metspalu A; Esko T; Gibson G; Wray NR; Visscher PM; Yang J, 2017, Widespread signatures of negative selection in the genetic architecture of human complex traits, , http://dx.doi.org/10.1101/145755

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