Ege Ozkan (Ege Sackey)

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 4

Top Topics

Genome Wide Association Study

Top Venues

European journal of human genetics : EJHG

Genetics in medicine : official journal of the American College of Medical Genetics

Nature communications

This page only lists publications with an associated author ORCID identifier.

Publications

Yann C Klimentidis, Zhao Chen, Manuel L Gonzalez-Garay, Dionysios Grigoriadis, Ege Ozkan, Alan M Pittman, Pia Ostergaard, Karen L Herbst
Genome-wide association study of a lipedema phenotype among women in the UK Biobank identifies multiple genetic risk factors. European journal of human genetics : EJHG (2022)
Silvia Martin-Almedina, Kazim Ogmen, Ege Ozkan, Dionysios Grigoriadis, Christina Karapouliou, Noeline Nadarajah, Cathrine Ebbing, Jenny Lord, Rhiannon Mellis, Fanny Kortuem, Mary Beth Dinulos, Cassandra Polun, Sherri Bale, Giles Atton, Alexandra Robinson, Hallvard Reigstad, Gunnar Houge, Axel von der Wense, Wolf-Henning Becker, Steve Jeffery, Peter S Mortimer, Kristiana Gordon, Katherine S Josephs, Sarah Robart, Mark David Kilby, Stephanie Vallee, Jerome L Gorski, Maja Hempel, Siren Berland, Shehla Mohammed, Pia Ostergaard
Janus-faced EPHB4-associated disorders: novel pathogenic variants and unreported intrafamilial overlapping phenotypes. Genetics in medicine : official journal of the American College of Medical Genetics 23 (7) (2021)
Naushin H Waseem, Sancy Low, Amna Z Shah, Deepa Avisetti, Pia Ostergaard, Michael Simpson, Katarzyna A Niemiec, Belen Martin-Martin, Hebah Aldehlawi, Saima Usman, Pak Sang Lee, Anthony P Khawaja, Jonathan B Ruddle, Ameet Shah, Ege Ozkan, Alexander C Day, Yuzhen Jiang, Geoff Swinfield, Ananth Viswanathan, Giovanna Alfano, Christina Chakarova, Heather J Cordell, David F Garway-Heath, Peng T Khaw, Shomi S Bhattacharya, Ahmad Waseem, Paul J Foster
Mutations in SPATA13/ASEF2 cause primary angle closure glaucoma. PLoS genetics 16 (4) (2020)
Matias Wagner, Daniel P S Osborn, Ina Gehweiler, Maike Nagel, Ulrike Ulmer, Somayeh Bakhtiari, Rim Amouri, Reza Boostani, Faycal Hentati, Maryam M Hockley, Benedikt Hölbling, Thomas Schwarzmayr, Ehsan Ghayoor Karimiani, Christoph Kernstock, Reza Maroofian, Wolfgang Müller-Felber, Ege Ozkan, Sergio Padilla-Lopez, Selina Reich, Jennifer Reichbauer, Hossein Darvish, Neda Shahmohammadibeni, Abbas Tafakhori, Katharina Vill, Stephan Zuchner, Michael C Kruer, Juliane Winkelmann, Yalda Jamshidi, Rebecca Schüle
Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia. Nature communications 10 (1) (2019)