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Molecular etiology of arthrogryposis in multiple families of mostly Turkish origin

The Journal of clinical investigation, 2016-02, Vol.126 (2), p.762-778

2016

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Carbonic anhydrase VA deficiency: a very rare case of hyperammonemic encephalopathy

Journal of Pediatric Endocrinology and Metabolism, 2020-10, Vol.33 (10), p.1349-1352

2020

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Gene expression changes in bioceramic paste-treated human dental pulp cells

Journal of Oral Science, 2016, Vol.58(3), pp.307-315

2016

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Effects of triethylene glycol dimethacrylate (TEGDMA) on the odontoclastic differentiation ability of human dental pulp cells

Journal of applied oral science, 2017-11, Vol.25 (6), p.631-640

2017

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Genotype–phenotype characteristics of 57 patients with Prader–Willi syndrome: a single-center experience from Turkey

Clinical dysmorphology, 2024-10, Vol.33 (4), p.145-151

2024

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The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey

International journal of human genetics, 2015-01, Vol.60 (1), p.1-9

2015

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Increased Endothelial Dysfunction and Insulin Resistance in Patients with Klinefelter Syndrome

Endocrine, metabolic & immune disorders drug targets, 2018-01, Vol.18 (4), p.401-406

2018

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Coexistence of severe developmental delay, epilepsy, and hemangioma in Snijders Blok‐Fisher syndrome suggests the presence of a POU3F3‐related SNIBFIS endophenotype: A case report

American journal of medical genetics. Part A, 2021-05, Vol.185 (5), p.1554-1560

2021

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The presence of MEFV gene mutations in patients with primary osteoarthritis who require surgery

The Korean Journal of Internal Medicine, 2013, 28(5), , pp.594-598

2013

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Three Afghani siblings with a novel homozygous variant and further delineation of the clinical features of METTL5 related intellectual disability syndrome

Turkish journal of pediatrics, 2022-09, Vol.64 (5), p.956-963

2022

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Methylation of SOCS3 in Myeloproliferative Neoplasms and Secondary Erythrocytosis/Thrombocythemia

Turkish journal of haematology, 2013-03, Vol.30 (1), p.13-18

2013

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Mitochondrial complex I and III mRNA levels in bipolar disorder

Journal of affective disorders, 2015-09, Vol.184, p.160-163

2015

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Hypoxia inhibits mineralization ability of human dental pulp cells treated with TEGDMA but increases cell survival in accordance with the culture time

Archives of oral biology, 2016-11, Vol.71, p.59-64

2016

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POU3F3‐related disorder: Defining the phenotype and expanding the molecular spectrum

Clinical genetics, 2023-08, Vol.104 (2), p.186-197

2023

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Association of retinal vein occlusion, homocysteine, and the thrombophilic mutations in a Turkish population: A case-control study

Ophthalmic genetics, 2017-07, Vol.38 (4), p.352-356

2017

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Gorlin-chaudhry-moss syndrome revisited: Expanding the phenotype

American journal of medical genetics. Part A, 2013-07, Vol.161A (7), p.1737-1742

2013

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Mitochondrial complex I and III gene mRNA levels in schizophrenia, and their relationship with clinical features

Journal of Molecular Psychiatry, 2014-12, Vol.2 (1), p.6-6, Article 6

2014

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Karyotype Analysis Results in Girls Followed with Short Stature

Gülhane tıp dergisi, 2017, p.1

2017

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Prenatal diagnosis of Cri-du chat syndrome following high maternal serum human chorionic gonodotrophin and choroid plexus cysts

Prenatal diagnosis, 2009-05, Vol.29 (5), p.536-537

2009

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FMF hastalarındaki MEFV gen mutasyon sıklığı ve mutasyonların dağılımı: Tek bir merkezden geniş bir hasta grubunun analizi

Gülhane tıp dergisi, 2017-03, Vol.59 (1), p.24

2017

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MEFV gene mutation frequency and distribution of mutations in FMF patients: Analysis of a large group of patients from a single center

Gülhane tıp dergisi, 2017, p.1

2017

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Is Turkey a prothrombin gene mutation region similar to the Mediterranean countries?

Anatolian journal of cardiology, 2016-03, Vol.16 (3), p.228-228

2016

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The investigation of angiotensin converting enzyme I/D and plasminogen activator inhibitor-1 4G/5G polymorphisms in venous thromboembolism patients

Tüberküloz ve toraks, 2013-01, Vol.61 (2), p.88-95

2013

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Molecular etiology of arthrogryposis in multiple families of mostly Turkish origin

Carbonic anhydrase VA deficiency: a very rare case of hyperammonemic encephalopathy

Gene expression changes in bioceramic paste-treated human dental pulp cells

Effects of triethylene glycol dimethacrylate (TEGDMA) on the odontoclastic differentiation ability of human dental pulp cells

Genotype–phenotype characteristics of 57 patients with Prader–Willi syndrome: a single-center experience from Turkey

The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey

Increased Endothelial Dysfunction and Insulin Resistance in Patients with Klinefelter Syndrome

Coexistence of severe developmental delay, epilepsy, and hemangioma in Snijders Blok‐Fisher syndrome suggests the presence of a POU3F3‐related SNIBFIS endophenotype: A case report

Erratum: The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey

The presence of MEFV gene mutations in patients with primary osteoarthritis who require surgery

Three Afghani siblings with a novel homozygous variant and further delineation of the clinical features of METTL5 related intellectual disability syndrome

Methylation of SOCS3 in Myeloproliferative Neoplasms and Secondary Erythrocytosis/Thrombocythemia

Mitochondrial complex I and III mRNA levels in bipolar disorder

Hypoxia inhibits mineralization ability of human dental pulp cells treated with TEGDMA but increases cell survival in accordance with the culture time

POU3F3‐related disorder: Defining the phenotype and expanding the molecular spectrum

Association of retinal vein occlusion, homocysteine, and the thrombophilic mutations in a Turkish population: A case-control study

Gorlin-chaudhry-moss syndrome revisited: Expanding the phenotype

Mitochondrial complex I and III gene mRNA levels in schizophrenia, and their relationship with clinical features

Karyotype Analysis Results in Girls Followed with Short Stature

Prenatal diagnosis of Cri-du chat syndrome following high maternal serum human chorionic gonodotrophin and choroid plexus cysts

FMF hastalarındaki MEFV gen mutasyon sıklığı ve mutasyonların dağılımı: Tek bir merkezden geniş bir hasta grubunun analizi

MEFV gene mutation frequency and distribution of mutations in FMF patients: Analysis of a large group of patients from a single center

Is Turkey a prothrombin gene mutation region similar to the Mediterranean countries?

The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey

The investigation of angiotensin converting enzyme I/D and plasminogen activator inhibitor-1 4G/5G polymorphisms in venous thromboembolism patients

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