Cihan Öner

RAPID COMMUNICATION: A Novel Melanocortin 4 Receptor (MC4R) Gene Mutation Associated with Morbid Obesity

Mehmet Mergen, Hatice Mergen, Metin Özata et al. · The Journal of Clinical Endocrinology & Metabolism · 2001 · 129 citations

Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene

Stephan M. Tanner, Zhongyuan Li, James D. Perko et al. · Proceedings of the National Academy of Sciences · 2005 · 106 citations · Full text

Genetically heterogeneous selective intestinal malabsorption of vitamin B₁₂: Founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East

Stephan M. Tanner, Zhong-Yuan Li, Ryan Bisson et al. · Human Mutation · 2004 · 87 citations

The molecular basis of familial hypercholesterolaemia in Turkish patients

Mert Sozen, Ros Whittall, Cihan Öner et al. · Atherosclerosis · 2005 · 43 citations

Metabolic Syndrome, Lipid Disorder, Turkish Patients +6

Mitochondrial DNA sequence variation in the Anatolian peninsula (Turkey)

Hatice Mergen, R. Öner, Cihan Öner · Journal of Genetics · 2004 · 34 citations

Anatolian Peninsula, Dna, Phylogenetics +7