Publications by authors named "Mahmut Akyol"

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A novel mutation of sgk-1 gene in central serous chorioretinopathy.
Mahmut Akyol, Muhammet Kazım Erol, Ozdemir Ozdemir, Deniz Turgut Coban, Ahmet Burak Bilgin

Int J Ophthalmol· February 2015

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Investigation of the serum glucocorticoid kinase 1 gene in patients with transient tachypnea of the newborn.
Osman Oztekin, Mahmut Akyol, Salih Kalay, Gonul Tezel, Mustafa Akcakus

J Matern Fetal Neonatal Med· July 2013

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Keratoconus presenting with bilateral simultaneous acute corneal hydrops.
Burak Bilgin, Betül Unal, Mustafa Unal, Erkan Doğan, Aslı Cetinkaya, Mahmut Akyol

Cont Lens Anterior Eye· April 2013

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CLOCK gene variants associate with sleep duration in two independent populations.
Karla V Allebrandt, Maris Teder-Laving, Mahmut Akyol, Irene Pichler, Bertram Müller-Myhsok

Biol Psychiatry· June 2010

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The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG).
Moritz F Sinner, Arne Pfeufer, Mahmut Akyol, Britt-Maria Beckmann, Martin Hinterseer

Eur Heart J· April 2008

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The common non-synonymous variant G38S of the KCNE1-(minK)-gene is not associated to QT interval in Central European Caucasians: results from the KORA study.
Mahmut Akyol, Shapour Jalilzadeh, Moritz F Sinner, Siegfried Perz, Britt M Beckmann

Eur Heart J· February 2007

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A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization.
Dan E Arking, Arne Pfeufer, Wendy Post, W H Linda Kao, Christopher Newton-Cheh, Mahmut Akyol

Nat Genet· June 2006

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Common variants in myocardial ion channel genes modify the QT interval in the general population: results from the KORA study.
Arne Pfeufer, Shapour Jalilzadeh, Siegfried Perz, Jakob C Mueller, Martin Hinterseer, Mahmut Akyol

Circ Res· April 2005

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