Zheng, Jie;Erzurumluoglu, A. Mesut;Elsworth, Benjamin L.;Kemp, John P.;Howe, Laurence;Haycock, Philip C.;Hemani, Gibran;Tansey, Katherine;Laurin, Charles;St Pourcain, Beate;Warrington, Nicole M.;Finucane, Hilary K.;Price, Alkes L.;Bulik-Sullivan, Brendan K.;Anttila, Verneri;Paternoster, Lavinia;Gaunt, Tom R.;Evans, David M.;Neale, Benjamin M. Motivation: LD score regression is a reliable and efficient method of using genome-wide association study (GWAS) summary-level results data to estimate the SNP heritability of complex traits and diseases, partition this heritability into functional c...

Zheng, Jie;Erzurumluoglu, A. Mesut;Elsworth, Benjamin L.;Kemp, John P.;Howe, Laurence;Haycock, Philip C.;Hemani, Gibran;Tansey, Katherine;Laurin, Charles;St Pourcain, Beate;Warrington, Nicole M.;Finucane, Hilary K.;Price, Alkes L.;Bulik-Sullivan, Brendan K.;Anttila, Verneri;Paternoster, Lavinia;Gaunt, Tom R.;Evans, David M.;Neale, Benjamin M. Motivation: LD score regression is a reliable and efficient method of using genome-wide association study (GWAS) summary-level results data to estimate the SNP heritability of complex traits and diseases, partition this heritability into functional c...

For a complete, stable theory $T$ we construct, in a reasonably canonical way, a related stable theory $T^*$ which has higher independent amalgamation properties over the algebraic closure of the empty-set. The theory $T^*$ is an algebraic cover of $...

Zheng, Jie;Erzurumluoglu, A. Mesut;Elsworth, Benjamin L.;Kemp, John P.;Howe, Laurence;Haycock, Philip C.;Hemani, Gibran;Tansey, Katherine;Laurin, Charles;St Pourcain, Beate;Warrington, Nicole M.;Finucane, Hilary K.;Price, Alkes L.;Bulik-Sullivan, Brendan K.;Anttila, Verneri;Paternoster, Lavinia;Gaunt, Tom R.;Evans, David M.;Neale, Benjamin M. Motivation: LD score regression is a reliable and efficient method of using genome-wide association study (GWAS) summary-level results data to estimate the SNP heritability of complex traits and diseases, partition this heritability into functional c...

Zheng, Jie;Erzurumluoglu, A. Mesut;Elsworth, Benjamin L.;Kemp, John P.;Howe, Laurence;Haycock, Philip C.;Hemani, Gibran;Tansey, Katherine;Laurin, Charles;St Pourcain, Beate;Warrington, Nicole M.;Finucane, Hilary K.;Price, Alkes L.;Bulik-Sullivan, Brendan K.;Anttila, Verneri;Paternoster, Lavinia;Gaunt, Tom R.;Evans, David M.;Neale, Benjamin M. Motivation: LD score regression is a reliable and efficient method of using genome-wide association study (GWAS) summary-level results data to estimate the SNP heritability of complex traits and diseases, partition this heritability into functional c...

Zheng, Jie;Erzurumluoglu, A. Mesut;Elsworth, Benjamin L.;Kemp, John P.;Howe, Laurence;Haycock, Philip C.;Hemani, Gibran;Tansey, Katherine;Laurin, Charles;St Pourcain, Beate;Warrington, Nicole M.;Finucane, Hilary K.;Price, Alkes L.;Bulik-Sullivan, Brendan K.;Anttila, Verneri;Paternoster, Lavinia;Gaunt, Tom R.;Evans, David M.;Neale, Benjamin M. Motivation: LD score regression is a reliable and efficient method of using genome-wide association study (GWAS) summary-level results data to estimate the SNP heritability of complex traits and diseases, partition this heritability into functional c...

Zheng, Jie;Erzurumluoglu, A. Mesut;Elsworth, Benjamin L.;Kemp, John P.;Howe, Laurence;Haycock, Philip C.;Hemani, Gibran;Tansey, Katherine;Laurin, Charles;St Pourcain, Beate;Warrington, Nicole M.;Finucane, Hilary K.;Price, Alkes L.;Bulik-Sullivan, Brendan K.;Anttila, Verneri;Paternoster, Lavinia;Gaunt, Tom R.;Evans, David M.;Neale, Benjamin M. Motivation: LD score regression is a reliable and efficient method of using genome-wide association study (GWAS) summary-level results data to estimate the SNP heritability of complex traits and diseases, partition this heritability into functional c...

We study automorphism groups of sparse graphs from the viewpoint of topological dynamics and the Kechris, Pestov, Todor\v{c}evi\'c correspondence. We investigate amenable and extremely amenable subgroups of these groups using the space of orientation...

Zheng, Jie;Rodriguez, Santiago;Laurin, Charles;Baird, Denis;Trela-Larsen, Lea;Erzurumluoglu, Mesut A.;Zheng, Yi;White, Jon;Giambartolomei, Claudia;Zabaneh, Delilah;Morris, Richard;Kumari, Meena;Casas, Juan P.;Hingorani, Aroon D.;Evans, David M.;Gaunt, Tom R.;Day, Ian N. M. Motivation: Fine mapping is a widely used approach for identifying the causal variant(s) at disease-associated loci. Standard methods (e.g. multiple regression) require individual level genotypes. Recent fine mapping methods using summary-level data ...