Eleftheria Zeggini-Van Elburg

Hinxton, ENG, United Kingdom

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 10 publications

Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits.

Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits.

Journal: Nature communications

Published: December 21, 2018

Correction: Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa.

Correction: Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa.

Journal: Molecular psychiatry

Published: November 14, 2018

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

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

Journal: Nature communications

Published: March 16, 2018

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

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

Journal: Nature genetics

Published: June 09, 2017

Statistical methods to detect pleiotropy in human complex traits.

Statistical methods to detect pleiotropy in human complex traits.

Journal: Open biology

Published: May 22, 2017

Integrative epigenomics, transcriptomics and proteomics of patient chondrocytes reveal genes and pathways involved in osteoarthritis.

Integrative epigenomics, transcriptomics and proteomics of patient chondrocytes reveal genes and pathways involved in osteoarthritis.

Journal: Scientific reports

Published: April 20, 2017

Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.

Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.

Journal: American journal of human genetics

Published: November 28, 2016

Insights into metabolic disease from studying genetics in isolated populations: stories from Greece to Greenland.

Insights into metabolic disease from studying genetics in isolated populations: stories from Greece to Greenland.

Journal: Diabetologia

Published: January 22, 2016

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

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

Journal: Human molecular genetics

Published: December 23, 2015

Next-generation association studies for complex traits.

Next-generation association studies for complex traits.

Journal: Nature genetics

Published: March 30, 2011

Showing 1-10 of 10

Last Updated: 09/26/2026