Special issue on ‘Genetic epidemiology of complex diseases: impact of population history and modelling assumptions’

[1]  K. Van Steen,et al.  A different view on fine-scale population structure in Western African populations , 2019, Human Genetics.

[2]  S. Djurovic,et al.  Discovery of shared genomic loci using the conditional false discovery rate approach , 2019, Human Genetics.

[3]  S. Montgomery,et al.  Identifying causal variants and genes using functional genomics in specialized cell types and contexts , 2019, Human Genetics.

[4]  Lawrence H. Uricchio.  Evolutionary perspectives on polygenic selection, missing heritability, and GWAS , 2019, Human Genetics.

[5]  E. Génin.  Missing heritability of complex diseases: case solved? , 2019, Human Genetics.

[6]  N. Sheehan,et al.  Epidemiology, genetic epidemiology and Mendelian randomisation: more need than ever to attend to detail , 2019, Human Genetics.

[7]  Marvin N. Wright,et al.  Statistical learning approaches in the genetic epidemiology of complex diseases , 2019, Human Genetics.

[8]  N. Timpson,et al.  Is population structure in the genetic biobank era irrelevant, a challenge, or an opportunity? , 2019, Human Genetics.

[9]  The Four Horsemen of the ‘Omicsalypse’: ontology, replicability, probability and epistemology , 2019, Human Genetics.

[10]  Kevin L. Keys,et al.  OpenMendel: a cooperative programming project for statistical genetics , 2019, Human Genetics.

[11]  J. Ioannidis,et al.  Assessment of systematic effects of methodological characteristics on candidate genetic associations , 2012, Human Genetics.