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Leukocyte telomere length as a compensatory mechanism in vitamin D metabolism

PloS one, 2022-02, Vol.17 (2), p.e0264337-e0264337

2022

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Radiation exposure in pregnancy: outcomes, perceptions and teratological counseling in Turkish women

Annals of Saudi medicine, 2022-05, Vol.42 (3), p.214-221

2022

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SHBG gene polymorphism (rs1799941) associates with metabolic syndrome in children and adolescents

PloS one, 2015-02, Vol.10 (2), p.e0116915-e0116915

2015

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A Planetary Health Lens for Rare Diseases in Refugee Populations and Innovating Systems Medicine Education

Omics (Larchmont, N.Y.), 2019-07, Vol.23 (7), p.338-339

2019

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The S447X variant of lipoprotein lipase gene is inversely associated with severity of coronary artery disease

Heart and vessels, 2011-07, Vol.26 (4), p.457-463

2011

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Levan based fibrous scaffolds electrospun via co-axial and single-needle techniques for tissue engineering applications

Carbohydrate polymers, 2018-08, Vol.193, p.316-325

2018

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Evaluation of Clinical Findings and Molecular Genetic Results of the Patients with CACNA1A Variants: Single Center Experience (P13-9.007)

Neurology, 2023-04, Vol.100 (17_supplement_2)

2023

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Bilateral plaque like macular atrophy and pigmentary retinopathy in an infant with a missense mutation in the MFF gene

Ophthalmic genetics, 2023-09, Vol.44 (5), p.1-495

2023

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Familial hypercholesterolemia with extensive coronary artery disease and tuberous and tendinous xanthomas: A case report and mutation analysis

Journal of clinical lipidology, 2018-07, Vol.12 (4), p.863-867

2018

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Novel Variants and Phenotypic Heterogeneity in Congenital Insensitivity to Pain (S23.002)

Neurology, 2023-04, Vol.100 (17_supplement_2)

2023

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Effects of lecithin: Cholesterol acyltransferase genotypes, enzyme levels, and activity on high-density lipoprotein levels

Journal of clinical lipidology, 2011-05, Vol.5 (3), p.152-158

2011

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Pigmentary retinopathy with perivascular sparing in a SOFT syndrome patient with a novel homozygous splicing variant in POC1A gene

Ophthalmic genetics, 2023-02, Vol.44 (1), p.70-73

2023

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Association of Celiac Disease and Plasminogen Activator Inhibitor-1 Polymorphism

Genel tip dergisi, 2022-10, Vol.32 (5), p.601-604

2022

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Frequency of Y chromosome Microdeletions in Turkish Infertile Men: Single Center Experience

Genel tip dergisi, 2022-12, Vol.32 (6), p.737-739

2022

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Co-existing bipolar disease and 17q12 deletion: a rare case report

Psychiatric genetics, 2022-02, Vol.32 (1), p.30-33

2022

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Leukocyte telomere length as a compensatory mechanism in vitamin D metabolism

PloS one, 2022-01, Vol.17 (2), p.e0264337

2022

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The investigation of the amounts and expressions of epidermal growth factor, epidermal growth factor receptor, and epidermal growth factor receptor gene polymorphisms in acne vulgaris

Journal of cosmetic dermatology, 2021-01, Vol.20 (1), p.346-351

2021

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A systems genetics approach to dyslipidemia in children and adolescents

Omics (Larchmont, N.Y.), 2015-04, Vol.19 (4), p.248-259

2015

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Multi-locus candidate gene analyses of lipid levels in a pediatric Turkish cohort: lessons learned on LPL, CETP, LIPC, ABCA1, and SHBG

Omics (Larchmont, N.Y.), 2013-12, Vol.17 (12), p.636-645

2013

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Coronary artery disease from a perspective of genomic risk score, ethical approaches and suggestions

Anadolu kardiyoloji dergisi : AKD, 2012-03, Vol.12 (2), p.171-177

2012

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SHBG Gene Polymorphism (rs1799941) Associates with Metabolic Syndrome in Children and Adolescents: e0116915

PloS one, 2015-02, Vol.10 (2)

2015

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Interaction among 5,10 methylenetetrahydrofolate reductase, plasminogen activator inhibitor and endothelial nitric oxide synthase gene polymorphisms predicts the severity of coronary artery disease in Turkish patients

Coronary artery disease, 2006-08, Vol.17 (5), p.413-417

2006

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Coronary artery disease from a perspective of genomic risk score, ethical approaches and suggestions/Genomik risk skorlamasi perspektifinden koroner arter hastaligi, etik yaklasim ve oneriler

Anadolu kardiyoloji dergisi : AKD, 2012-03, Vol.12 (2), p.171

2012

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Türk Toplumunda Düşük Yüksek Dansiteli Lipoprotein-Kolesterol düzeyi Ve Lesitin Kolesterol Asiltransferaz Ilişkisinin Gen Ve Protein Düzeyinde Araştırılması

Ağırbaşlı, Deniz

2009

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Plasminogen Activator Inhibitor-1

Encyclopedia of Signaling Molecules, p.4055-4063

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Leukocyte telomere length as a compensatory mechanism in vitamin D metabolism

Radiation exposure in pregnancy: outcomes, perceptions and teratological counseling in Turkish women

SHBG gene polymorphism (rs1799941) associates with metabolic syndrome in children and adolescents

A Planetary Health Lens for Rare Diseases in Refugee Populations and Innovating Systems Medicine Education

The S447X variant of lipoprotein lipase gene is inversely associated with severity of coronary artery disease

Levan based fibrous scaffolds electrospun via co-axial and single-needle techniques for tissue engineering applications

Evaluation of Clinical Findings and Molecular Genetic Results of the Patients with CACNA1A Variants: Single Center Experience (P13-9.007)

Bilateral plaque like macular atrophy and pigmentary retinopathy in an infant with a missense mutation in the MFF gene

Familial hypercholesterolemia with extensive coronary artery disease and tuberous and tendinous xanthomas: A case report and mutation analysis

Novel Variants and Phenotypic Heterogeneity in Congenital Insensitivity to Pain (S23.002)

Effects of lecithin: Cholesterol acyltransferase genotypes, enzyme levels, and activity on high-density lipoprotein levels

Pigmentary retinopathy with perivascular sparing in a SOFT syndrome patient with a novel homozygous splicing variant in POC1A gene

Association of Celiac Disease and Plasminogen Activator Inhibitor-1 Polymorphism

Frequency of Y chromosome Microdeletions in Turkish Infertile Men: Single Center Experience

Co-existing bipolar disease and 17q12 deletion: a rare case report

Leukocyte telomere length as a compensatory mechanism in vitamin D metabolism

The investigation of the amounts and expressions of epidermal growth factor, epidermal growth factor receptor, and epidermal growth factor receptor gene polymorphisms in acne vulgaris

A systems genetics approach to dyslipidemia in children and adolescents

Multi-locus candidate gene analyses of lipid levels in a pediatric Turkish cohort: lessons learned on LPL, CETP, LIPC, ABCA1, and SHBG

Coronary artery disease from a perspective of genomic risk score, ethical approaches and suggestions

SHBG Gene Polymorphism (rs1799941) Associates with Metabolic Syndrome in Children and Adolescents: e0116915

Interaction among 5,10 methylenetetrahydrofolate reductase, plasminogen activator inhibitor and endothelial nitric oxide synthase gene polymorphisms predicts the severity of coronary artery disease in Turkish patients

Coronary artery disease from a perspective of genomic risk score, ethical approaches and suggestions/Genomik risk skorlamasi perspektifinden koroner arter hastaligi, etik yaklasim ve oneriler

Türk Toplumunda Düşük Yüksek Dansiteli Lipoprotein-Kolesterol düzeyi Ve Lesitin Kolesterol Asiltransferaz Ilişkisinin Gen Ve Protein Düzeyinde Araştırılması

Plasminogen Activator Inhibitor-1

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