Ege Sackey
St. George's University Of London
London, ENG, United Kingdom
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 9 publications
Genetic association analysis of 77,539 genomes reveals rare disease etiologies.
Journal: Nature medicine
Published: October 21, 2022
Genome-wide association study of a lipedema phenotype among women in the UK Biobank identifies multiple genetic risk factors.
Journal: European journal of human genetics : EJHG
Published: June 22, 2021
Investigation of clinical characteristics and genome associations in the 'UK Lipoedema' cohort.
Journal: PloS one
Published: June 10, 2021
Correction: Janus-faced EPHB4-associated disorders: novel pathogenic variants and unreported intrafamilial overlapping phenotypes.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: May 27, 2021
Redefining WILD syndrome: a primary lymphatic dysplasia with congenital multisegmental lymphoedema, cutaneous lymphovascular malformation, CD4 lymphopaenia and warts.
Journal: Journal of medical genetics
Published: April 05, 2021
Janus-faced EPHB4-associated disorders: novel pathogenic variants and unreported intrafamilial overlapping phenotypes.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: December 18, 2020
Mutations in SPATA13/ASEF2 cause primary angle closure glaucoma.
Journal: PLoS genetics
Published: September 02, 2019
Showing 1-9 of 9
Last Updated: 09/26/2026