Halil Gürhan Karabulut

WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome

Janson J. White, Juliana F. Mazzeu, Zeynep Coban‐Akdemir et al. · The American Journal of Human Genetics · 2017 · 115 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Factor V Leiden and prothrombin gene G20210A mutations in ocular Behçet disease

Figen Batıoğlu, Leyla S. Atmaca, Halil Gürhan Karabulut et al. · Acta Ophthalmologica Scandinavica · 2003 · 35 citations

Medicine, Genetics, Ophthalmology +13

The impact of vitamin D receptor genotype on the management of anemia in hemodialysis patients

Şehsuvar Ertürk, Sim Kutlay, Halil Gürhan Karabulut et al. · American Journal of Kidney Diseases · 2002 · 30 citations

Medicine, Hematology, Nephrology +14

Glu298Asp polymorphism of the eNOS gene is associated with coronary collateral development

Sadi Güleç, Halil Gürhan Karabulut, Aydan Ongun et al. · Atherosclerosis · 2007 · 30 citations

Medicine, Cardiology, Genetics +13

Association Between N363S and BclI Polymorphisms of the Glucocorticoid Receptor Gene (NR3C1) and Glucocorticoid Side Effects During Childhood Acute Lymphoblastic Leukemia Treatment

Meriç Kaymak Cihan, Halil Gürhan Karabulut, Nüket Yürür Kutlay et al. · Turkish Journal of Hematology · 2017 · 29 citations · Full text

Medicine, Genetics, Pediatrics +16