Arthur Gilly

Very low-depth whole-genome sequencing in complex trait association studies

Xiangyu Ge, Jeremy Schwartzentruber, Eleftheria Zeggini, 2017, bioRxiv.

Very low-depth sequencing in a founder population identifies a cardioprotective APOC3 signal missed by genome-wide imputation

Eleftheria Zeggini, Aliki-Eleni Farmaki, Arthur Gilly, 2016, Human molecular genetics.

Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants

Gil McVean, Rebecca N. Nsubuga, Vasiliki Mamakou, 2014, Nature Communications.

Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis

Kari Stefansson, Sophie Hackinger, Eleftheria Zeggini, 2018, Nature Genetics.

A reference panel of 64,976 haplotypes for genotype imputation

Laura J. Scott, He Zhang, Gonçalo Abecasis, 2015, bioRxiv.

Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits

Jeremy Schwartzentruber, Eleftheria Zeggini, Ioanna Tachmazidou, 2017, Nature Communications.

Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits

Inês Barroso, Klaudia Walter, Ioanna Ntalla, 2018, Nature Communications.