Ege Sackey
5PUBLICATIONS
37CO-AUTHORS
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Publications (5)
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|Nov 17, 2022
Genome-wide association study of a lipedema phenotype among women in the UK Biobank identifies multiple genetic risk factors.Yann C Klimentidis, Zhao Chen, Manuel L Gonzalez-Garay
|May 27, 2021
Correction: Janus-faced EPHB4-associated disorders: novel pathogenic variants and unreported intrafamilial overlapping phenotypes.Silvia Martin-Almedina, Kazim Ogmen, Ege Sackey
|Apr 17, 2021
Janus-faced EPHB4-associated disorders: novel pathogenic variants and unreported intrafamilial overlapping phenotypes.Silvia Martin-Almedina, Kazim Ogmen, Ege Sackey
|Apr 28, 2020
Mutations in SPATA13/ASEF2 cause primary angle closure glaucoma.Naushin H Waseem, Sancy Low, Amna Z Shah
|Oct 23, 2019
Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia.Matias Wagner, Daniel P S Osborn, Ina Gehweiler
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Frequent Collaborators
4 joint publications
Pia Ostergaard
2 joint publications
Christina Karapouliou
2 joint publications
Rhiannon Mellis
2 joint publications
Cathrine Ebbing
2 joint publications
Alexandra Robinson
2 joint publications
Dionysios Grigoriadis
2 joint publications
Mary Beth Dinulos
2 joint publications
Jenny Lord
2 joint publications
Kazim Ogmen
2 joint publications
Silvia Martin-Almedina
