Publication Types:

Etiopathogenesis of Sheehan's Syndrome: Roles of Coagulation Factors and TNF-Alpha

Özgün Makale
Halit Diri, Elif Funda Sener, Fahri Bayram, Nazife Tascioglu, Yasin Simsek, Munis Dundar
International Journal of Endocrinology. 12: 37.
Publication year: 2014

The role of TNF-alpha and PAI-1 gene polymorphisms in familial Mediterranean fever

Özgün Makale
Munis Dundar, Aslihan Kiraz, Burhan Balta, Elif Funda Emirogullari, Gokmen Zararsiz, Alper Yurci, Duran Aslan, Mevlut Baskol
Modern Rheumatology. 23: 140-145.
Publication year: 2013

A molecular analysis of familial Mediterranean fever disease in a cohort of Turkish patients

Özgün Makale
Munis Dundar, Aslihan Kiraz, Elif Funda Emirogullari, Cetin Saatci, Serpi Taheri, Mevlut Baskol, Seher Polat, Yusuf Ozkul
Annals of Saudi Medicine. 32: 343-348.
Publication year: 2012

Common Familial Mediterranean Fever gene mutations in a Turkish cohort

Özgün Makale
Munis Dundar, Elif Funda Emirogullari, Aslihan Kiraz, Serpil Taheri, Mevlut Baskol
Molecular Biology Reports. 38: 5065-5069.
Publication year: 2011

Loss of Dermatan-4-Sulfotransferase 1 Function Results in Adducted Thumb-Clubfoot Syndrome

Özgün Makale
Munis Dundar, Thomas Mueller, Qi Zhang, Jing Pan, Beat Steinmann, Julia Vodopiutz, Robert Gruber, Tohru Sonoda, Birgit Krabichler, Gerd Utermann, Jacques U. Baenziger, Lijuan Zhang, Andreas R. Janecke
American Journal of Human Genetics. 85: 873-882.
Publication year: 2009

How the I1307K adenomatous polyposis coli gene variant contributes in the assessment of risk of colorectal cancer, but not stomach cancer, in a Turkish population

Özgün Makale
Munis Dundar, Ahmet Okay Caglayan, Cetin Saatci, Hatice Karaca, Mevlut Baskol, Serpil Tahiri, Yusuf Ozkul
Cancer Genetics and Cytogenetics. 177: 95-97.
Publication year: 2007

A novel acropectoral syndrome maps to chromosome 7q36

Özgün Makale
Munis Dundar, Tilda M Gordon, Irfan Ozyazgan, Fahri Oguzkaya, Yusuf Ozkul, Alexander Cooke, A Graham Wilkinson, Susan Holloway, Frances R Goodman, John L Tolmie
J Med Genet 2001;38:304-309
Publication year: 2000