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Relationship between Glutathione S-transferase gene polymorphisms and clinical features of psoriasis: A case-control study in the Turkish population

Türkderm, 2024-10, Vol.58 (3), p.75-82

2024

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Comparison of MicroRNA Levels of 18-60-month-old Autistic Children with Those of Their Siblings and Controls

Clinical Psychopharmacology and Neuroscience, 2024, 22(2), , pp.322-332

2024

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Evaluation of immunological abnormalities in patients with rare syndromes

Central-European journal of immunology, 2022-01, Vol.47 (4), p.299-307

2022

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Novel findings, mini‐review and dysmorphological characterization of 16p13.11 microduplication syndrome

International journal of developmental neuroscience, 2022-06, Vol.82 (4), p.289-294

2022

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Interchromosomal effect: Report of a father and son, bearing different translocations of the same chromosome, and a review of the current literature

Andrologia, 2021-02, Vol.53 (1), p.e13805-n/a

2021

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A new approach to chromosomal abnormalities in sperm from patients with oligoasthenoteratozoospermia: detection of double aneuploidy in addition to single aneuploidy and diploidy by five-color fluorescence in situ hybridization using one probe set

Fertility and sterility, 2008-06, Vol.89 (6), p.1709-1717

2008

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X Chromosome Pericentric Inversion: Report of a Case with 46,X,inv(X)(p11.2q26) and a Mini-Review of the Literature

Gazi tıp dergisi, 2024-10, Vol.35 (3), p.338-341

2024

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A rare case in literature: Isochromosome Xq in Klinefelter syndrome

Andrologia, 2019-06, Vol.51 (5), p.e13253-n/a

2019

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Cerebral creatine deficiency syndrome with a novel missense variant in SLC6A8 gene

Neurology and clinical neuroscience, 2023-09, Vol.11 (5), p.286-288

2023

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An Unusual Diagnostic Journey Through MLPA: From Spinal Muscular Atrophy to a Severe Case of Prader-Willi Syndrome

Journal of Clinical Practice & Research, 2023-09, Vol.45 (5), p.528-533

Göktaş, Emine

2023

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NAT2 Gene Polymorphisms in Turkish Patients with Psoriasis Vulgaris

BioMed research international, 2018-01, Vol.2018 (2018), p.1-14

2018

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A Novel Pathogenic Variant of the CFTR Gene in a Patient with Cystic Fibrosis Phenotype—c.4096A > T

Journal of pediatric genetics (Birmingham, Ala.), 2020-03, Vol.9 (1), p.040-043

2020

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A Turkish Family with Loeys-dietz Syndrome and a Report of a Homozygous Patient with SMAD3 Pathogenic Variation

Haseki tıp bülteni, 2022-01, Vol.60 (1), p.84-88

2022

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Male infertility associated with de novo pericentric inversion of chromosome 1

Turkish journal of urology, 2017-12, Vol.43 (4), p.560-562

2017

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Investigation of the relationship between ischemic stroke and endothelial nitric oxide synthase gene polymorphisms [G894T, intron 4 VNTR and T786C]

TURKISH JOURNAL OF MEDICAL SCIENCES, 2019-04, Vol.49 (2), p.589-594

2019

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Localized Placental Mesenchymal Dysplasia in Monochorionic Diamniotic Twin Placenta with Beckwith-Wiedemann Syndrome

Fetal and pediatric pathology, 2022-07, Vol.41 (4), p.1-664

2022

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MicroRNAs and lung cancer

Tüberküloz ve toraks, 2013-01, Vol.61 (1), p.57-62

2013

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Differentiated Thyroid Papillary Carcinoma with Cerebellar Metastasis: A Case Report

Turkish Journal of Endocrinology and Metabolism, 2017-03, Vol.21 (1), p.22-25

2017

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Early Morphokinetic Monitoring of Embryos after Intracytoplasmic Sperm Injection with Fresh Ejaculate Sperm in Nonmosaic Klinefelter Syndrome: A Different Presentation

Case reports in genetics, 2015-01, Vol.2015 (2015), p.1-4

2015

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The Genetic Analysis of Cystic Fibrosis Patients With Seven Novel Mutations in the CFTR Gene in the Central Anatolian Region of Turkey

Balkan Medical Journal, 2021-11, Vol.38 (6), p.357-364

2021

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Impact of Simultaneous Presence of Multiple PML-RARA Isoforms on Phenotype in Patients with Acute Promyelocytic Leukaemia

Journal of the College of Physicians and Surgeons--Pakistan, 2024-11, Vol.34 (11), p.1552-1556

2024

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Association of Apolipoprotein E Polymorphism with Intravitreal Ranibizumab Treatment Outcomes in Age-Related Macular Degeneration

Current eye research, 2016-06, Vol.41 (6), p.862-866

2016

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Genetic Analysis of MEFV Gene Pyrin Domain in Patients With Behcet’s Disease

Mediators of Inflammation, 2006-01, Vol.2006 (3), p.229-232

2006

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Analysis of genetic polymorphisms associated with intervertebral disc degeneration

Cellular and Molecular Biology, 2018-07, Vol.64 (10), p.61-65

2018

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A Special Chromosome Imbalance “Jumping translocation of 1q” in Burkitt Lymphoma

Gazi tıp dergisi, 2022-07, Vol.33 (3)

2022

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Relationship between Glutathione S-transferase gene polymorphisms and clinical features of psoriasis: A case-control study in the Turkish population

Comparison of MicroRNA Levels of 18-60-month-old Autistic Children with Those of Their Siblings and Controls

Evaluation of immunological abnormalities in patients with rare syndromes

Novel findings, mini‐review and dysmorphological characterization of 16p13.11 microduplication syndrome

Interchromosomal effect: Report of a father and son, bearing different translocations of the same chromosome, and a review of the current literature

A new approach to chromosomal abnormalities in sperm from patients with oligoasthenoteratozoospermia: detection of double aneuploidy in addition to single aneuploidy and diploidy by five-color fluorescence in situ hybridization using one probe set

X Chromosome Pericentric Inversion: Report of a Case with 46,X,inv(X)(p11.2q26) and a Mini-Review of the Literature

A rare case in literature: Isochromosome Xq in Klinefelter syndrome

Cerebral creatine deficiency syndrome with a novel missense variant in SLC6A8 gene

An Unusual Diagnostic Journey Through MLPA: From Spinal Muscular Atrophy to a Severe Case of Prader-Willi Syndrome

NAT2 Gene Polymorphisms in Turkish Patients with Psoriasis Vulgaris

A Novel Pathogenic Variant of the CFTR Gene in a Patient with Cystic Fibrosis Phenotype—c.4096A > T

A Turkish Family with Loeys-dietz Syndrome and a Report of a Homozygous Patient with SMAD3 Pathogenic Variation

Male infertility associated with de novo pericentric inversion of chromosome 1

Investigation of the relationship between ischemic stroke and endothelial nitric oxide synthase gene polymorphisms [G894T, intron 4 VNTR and T786C]

Localized Placental Mesenchymal Dysplasia in Monochorionic Diamniotic Twin Placenta with Beckwith-Wiedemann Syndrome

MicroRNAs and lung cancer

Differentiated Thyroid Papillary Carcinoma with Cerebellar Metastasis: A Case Report

Early Morphokinetic Monitoring of Embryos after Intracytoplasmic Sperm Injection with Fresh Ejaculate Sperm in Nonmosaic Klinefelter Syndrome: A Different Presentation

The Genetic Analysis of Cystic Fibrosis Patients With Seven Novel Mutations in the CFTR Gene in the Central Anatolian Region of Turkey

Impact of Simultaneous Presence of Multiple PML-RARA Isoforms on Phenotype in Patients with Acute Promyelocytic Leukaemia

Association of Apolipoprotein E Polymorphism with Intravitreal Ranibizumab Treatment Outcomes in Age-Related Macular Degeneration

Genetic Analysis of MEFV Gene Pyrin Domain in Patients With Behcet’s Disease

Analysis of genetic polymorphisms associated with intervertebral disc degeneration

A Special Chromosome Imbalance “Jumping translocation of 1q” in Burkitt Lymphoma

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