The autosomal genetic control of sexually dimorphic traits in humans is largely the same across the sexes

por Kassam, Irfahan, McRae, Allan F.
Publicado 2016

Case-Control Association Testing of Common Variants from Sequencing of DNA Pools

por McRae, Allan F., Richter, Melinda M., Lind, Penelope A.
Publicado 2013

The role of critical immune genes in brain disorders: insights from neuroimaging immunogenetics

por Bian, Beilei, Couvy-Duchesne, Baptiste, Wray, Naomi R., McRae, Allan F.
Publicado 2022

Genome-wide DNA methylation profiling in whole blood reveals epigenetic signatures associated with migraine

por Gerring, Zachary F., McRae, Allan F., Montgomery, Grant W., Nyholt, Dale R.
Publicado 2018

Seasonal Effects on Gene Expression

por Goldinger, Anita, Shakhbazov, Konstantin, Henders, Anjali K., McRae, Allan F., Montgomery, Grant W., Powell, Joseph E.
Publicado 2015

Predicting gene targets from integrative analyses of summary data from GWAS and eQTL studies for 28 human complex traits

por Pavlides, Jennifer M. Whitehead, Zhu, Zhihong, Gratten, Jacob, McRae, Allan F., Wray, Naomi R., Yang, Jian
Publicado 2016

An overview of DNA methylation-derived trait score methods and applications

por Nabais, Marta F., Gadd, Danni A., Hannon, Eilis, Mill, Jonathan, McRae, Allan F., Wray, Naomi R.
Publicado 2023

Congenital Sensorineural Deafness in Australian Stumpy-Tail Cattle Dogs Is an Autosomal Recessive Trait That Maps to CFA10

por Sommerlad, Susan, McRae, Allan F., McDonald, Brenda, Johnstone, Isobel, Cuttell, Leigh, Seddon, Jennifer M., O'Leary, Caroline A.
Publicado 2010

Fast set-based association analysis using summary data from GWAS identifies novel gene loci for human complex traits

por Bakshi, Andrew, Zhu, Zhihong, Vinkhuyzen, Anna A. E., Hill, W. David, McRae, Allan F., Visscher, Peter M., Yang, Jian
Publicado 2016

Shared genetic control of expression and methylation in peripheral blood

por Shakhbazov, Konstantin, Powell, Joseph E., Hemani, Gibran, Henders, Anjali K., Martin, Nicholas G., Visscher, Peter M., Montgomery, Grant W., McRae, Allan F.
Publicado 2016

Inflammation-driven bone formation in a mouse model of ankylosing spondylitis: sequential not parallel processes

por Tseng, Hsu-Wen, Pitt, Miranda E., Glant, Tibor T., McRae, Allan F., Kenna, Tony J., Brown, Matthew A., Pettit, Allison R., Thomas, Gethin P.
Publicado 2016

Genotype effects contribute to variation in longitudinal methylome patterns in older people

por Zhang, Qian, Marioni, Riccardo E, Robinson, Matthew R, Higham, Jon, Sproul, Duncan, Wray, Naomi R, Deary, Ian J, McRae, Allan F, Visscher, Peter M
Publicado 2018

Congruence of Additive and Non-Additive Effects on Gene Expression Estimated from Pedigree and SNP Data

por Powell, Joseph E., Henders, Anjali K., McRae, Allan F., Kim, Jinhee, Hemani, Gibran, Martin, Nicholas G., Dermitzakis, Emmanouil T., Gibson, Greg, Montgomery, Grant W., Visscher, Peter M.
Publicado 2013

The epigenetic clock and telomere length are independently associated with chronological age and mortality

por Marioni, Riccardo E, Harris, Sarah E, Shah, Sonia, McRae, Allan F, von Zglinicki, Thomas, Martin-Ruiz, Carmen, Wray, Naomi R, Visscher, Peter M, Deary, Ian J
Publicado 2016

The epigenetic clock and telomere length are independently associated with chronological age and mortality

por Marioni, Riccardo E, Harris, Sarah E, Shah, Sonia, McRae, Allan F, von Zglinicki, Thomas, Martin-Ruiz, Carmen, Wray, Naomi R, Visscher, Peter M, Deary, Ian J
Publicado 2018

Association between DNA methylation variability and self-reported exposure to heavy metals

por Freydenzon, Anna, Nabais, Marta F., Lin, Tian, Williams, Kelly L., Wallace, Leanne, Henders, Anjali K., Blair, Ian P., Wray, Naomi R., Pamphlett, Roger, McRae, Allan F.
Publicado 2022

Contribution of genetic variation to transgenerational inheritance of DNA methylation

por McRae, Allan F, Powell, Joseph E, Henders, Anjali K, Bowdler, Lisa, Hemani, Gibran, Shah, Sonia, Painter, Jodie N, Martin, Nicholas G, Visscher, Peter M, Montgomery, Grant W
Publicado 2014

Role of DNA Methylation in Type 2 Diabetes Etiology: Using Genotype as a Causal Anchor

por Elliott, Hannah R., Shihab, Hashem A., Lockett, Gabrielle A., Holloway, John W., McRae, Allan F., Smith, George Davey, Ring, Susan M., Gaunt, Tom R., Relton, Caroline L.
Publicado 2017

OSCA: a tool for omic-data-based complex trait analysis

por Zhang, Futao, Chen, Wenhan, Zhu, Zhihong, Zhang, Qian, Nabais, Marta F., Qi, Ting, Deary, Ian J., Wray, Naomi R., Visscher, Peter M., McRae, Allan F., Yang, Jian
Publicado 2019

Promoter-anchored chromatin interactions predicted from genetic analysis of epigenomic data

por Wu, Yang, Qi, Ting, Wang, Huanwei, Zhang, Futao, Zheng, Zhili, Phillips-Cremins, Jennifer E., Deary, Ian J., McRae, Allan F., Wray, Naomi R., Zeng, Jian, Yang, Jian
Publicado 2020