Publications by authors named "Sarenur Yilmaz"

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Heterozygous Pyrin (MEFV) E148Q allele carriers indicate a reduced glaucoma risk for Turkish population: a prospective clinical analysis.
Orkun Muhsinoglu, Ibrahim Akalin, Remzi Karadag, Sarenur Yilmaz, Huseyin Bayramlar

Ophthalmic Genet· August 2024

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Bi-allelic Pathogenic Variants in TUBGCP2 Cause Microcephaly and Lissencephaly Spectrum Disorders.
Tadahiro Mitani, Jaya Punetha, Ibrahim Akalin, Davut Pehlivan, Mateusz Dawidziuk, Sarenur Yilmaz

Am J Hum Genet· November 2019

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Novel Gene Mutation in a Patient with Gorlin-Goltz Syndrome.
Emin Ozlu, Ayse Serap Karadag, Ibrahim Akalın, Gozde Yesil, Sarenur Yılmaz

Ann Dermatol· August 2019

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Ear atresia: Is there a role of apoptosis-regulating miRNAs?
Ezgi Aslan, Emre Akbas, Sena Yilmaz, Ahmet Salih Karaoglu, Ubeyde Telli, Sarenur Yilmaz

North Clin Istanb· September 2018

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Cilioretinal artery: Vasculogenesis might be promoted by plasminogen activator inhibitor-1 5G allele.
Sarenur Yilmaz, Aylin Ardagil, Ibrahim Akalin, Meltem Guzin Altinel, Yasar Dag

Ophthalmic Genet· December 2017

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Laparoscopic cholecystectomy in an adult with agenesis of right hemidiaphragm and limb reduction defects: First report in literature.
Julide Sagiroglu, Ercument Tombalak, Sarenur Basaran Yilmaz, Fikret Balyemez, Tunc Eren

North Clin Istanb· November 2015

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Lentiginoses in polycythemia vera patient: Is there a role for JAK2 (V617F) mutation?
Tugba Kevser Uzuncakmak, Sarenur Yilmaz, Ayse Serap Karadag, Necmettin Akdeniz, Ibrahim Akalin

JAKSTAT· September 2015

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Relation of stem cell markers ALDH1 and CD44 with clinicopathological factors in urothelial carcinomas of urinary bladder.
Serkan Senol, Asif Yildırım, Ibrahim Akalin, Fatih Uruç, Bengü Çobanoğlu, Sarenur Yilmaz

Int J Clin Exp Med· June 2015

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Human CLP1 mutations alter tRNA biogenesis, affecting both peripheral and central nervous system function.
Ender Karaca, Stefan Weitzer, Davut Pehlivan, Hiroshi Shiraishi, Tasos Gogakos, Sarenur Yilmaz

Cell· April 2014

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