Emmanouil Tsafantakis

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

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

Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

Inês Barroso, Jiyoung Heo, Beverley Balkau, 2015, Nature communications.

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.

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.

A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

Claude Bouchard, Christian Gieger, Joel Eriksson, 2016, Nature communications.