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The effects of IGF-1 and erythropoietin on apoptosis and telomerase activity in necrotizing enterocolitis model

Pediatric research, 2021-09, Vol.90 (3), p.559-564

2021

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Prenatal diagnosis of a case with tetrasomy 9p confirmed by cytogenetics, FISH, microarray analysis and review

Taiwanese journal of obstetrics & gynecology, 2022-01, Vol.61 (1), p.122-126

2022

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Co-occurrences of polymorphic heterochromatin regions of chromosomes and effect on reproductive failure

Reproductive biology, 2020-03, Vol.20 (1), p.42-47

2020

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Association between Ala–9Val polymorphism of Mn-SOD gene and schizophrenia

Progress in neuro-psychopharmacology & biological psychiatry, 2005, Vol.29 (1), p.123-131

2005

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Comparison of indications and results of prenatal invasive diagnostic tests before and after the implementation of the use of cell-free fetal DNA: a tertiary referral center experience

Journal of assisted reproduction and genetics, 2020-08, Vol.37 (8), p.2019-2024

2020

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DRD4 genotyping may differentiate symptoms of attention-deficit/hyperactivity disorder and sluggish cognitive tempo

Revista brasileira de psiquiatria, 2020-11, Vol.42 (6), p.630-637

2020

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Long-term clinical outcomes and management of hypertriglyceridemia in children with Apo-CII deficiency

Nutrition, metabolism, and cardiovascular diseases, 2024-07, Vol.34 (7), p.1798-1806

2024

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Effectiveness of Mesenchymal Stem Cell Therapy for COVID-19 Patients in the Intensive Care Unit: A Case-Control Study

Turkish journal of haematology, 2022-12, Vol.39 (4), p.222-229

2022

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Bilateral Familial Elastofibroma Dorsi: Is Genetic Abnormality Essential?

The Annals of thoracic surgery, 2014-08, Vol.98 (2), p.e31-e32

2014

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Elective Termination Decision in Sex Chromosomal Abnormalities-Current Situation in Decision Making Process

Reproductive system & sexual disorders current research, 2012, Vol.1 (4)

Akin, Haluk

2012

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Association of arms2 gene rs10490924 and htra1 gene rs11200638 polymorphisms with exudative age-related macular degeneration in western aegean population of turkey

Journal of Retina-Vitreous, 2021, Vol.30 (2), p.182

2021

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MEFV mutations in patients with familial Mediterranean fever from the Aegean region of Turkey

Molecular biology reports, 2010, Vol.37 (1), p.93-98

2010

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Primary male infertility in Izmir/Turkey: a cytogenetic and molecular study of 187 infertile Turkish patients

Journal of assisted reproduction and genetics, 2011-05, Vol.28 (5), p.419-423

2011

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Investigation of miRNA and cytokine expressions in latent tuberculosis infection and active tuberculosis

Turkish journal of medical sciences, 2022-01, Vol.52 (3), p.649-657

2022

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20-year experience on prenatal diagnosis in a reference university medical genetics center in Turkey

TURKISH JOURNAL OF MEDICAL SCIENCES, 2021-08, Vol.51 (4), p.1775-1780

2021

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Uniparental Disomy of Chromosome 4: A Case of Whole Chromosome UPD Presenting with LRBA Deficiency

Journal of clinical immunology, 2025-12, Vol.45 (1), p.10, Article 10

2025

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DRD4 genotyping may differentiate symptoms of attention-deficit/hyperactivity disorder and sluggish cognitive tempo

Revista brasileira de psiquiatria, 2020

2020

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Clinicopathological characteristics, genetics and prognosis of patients with myeloid sarcoma: a single-center study

Journal of clinical pathology, 2023-04, Vol.76 (4), p.244-251

2023

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Investigation of genotype–phenotype correlation in patients with AZF microdeletion in a single‐reference centre

Andrologia, 2021-11, Vol.53 (10), p.e14188-n/a

2021

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Molecular analysis and clinical findings of Griscelli syndrome patients

Journal of pediatric hematology/oncology, 2012-10, Vol.34 (7), p.541-544

2012

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Investigation of possible associations of the BDNF, SNAP-25 and SYN III genes with the neurocognitive measures: BDNF and SNAP-25 genes might be involved in attention domain, SYN III gene in executive function

Nordic journal of psychiatry, 2022-11, Vol.76 (8), p.610-615

2022

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Kısmi ve Tam Dönümlü Spektral Metotların Karşılaştırması

Mühendislik bilimleri dergisi, 2012-02, Vol.18 (2), p.95-103

2012

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A Severe α Thalassemia Case Compound Heterozygous for Hb Adana in α1 Gene and 20.5 kb Double Gene Deletion

Journal of pediatric hematology/oncology, 2009-08, Vol.31 (8), p.592-594

2009

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A complex t(15;22;17)(q22;q11.2;q21) variant of APL

Cancer genetics, 2024-08, Vol.286-287, p.48-51

2024

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Complex karyotype with double Philadelphia chromosome and T315I mutation results in blastic phase and extensive extramedullary infiltration in a chronic myeloid leukemia patient

Cancer genetics, 2022-08, Vol.266-267, p.74-80

2022

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The effects of IGF-1 and erythropoietin on apoptosis and telomerase activity in necrotizing enterocolitis model

Prenatal diagnosis of a case with tetrasomy 9p confirmed by cytogenetics, FISH, microarray analysis and review

Co-occurrences of polymorphic heterochromatin regions of chromosomes and effect on reproductive failure

Association between Ala–9Val polymorphism of Mn-SOD gene and schizophrenia

Comparison of indications and results of prenatal invasive diagnostic tests before and after the implementation of the use of cell-free fetal DNA: a tertiary referral center experience

DRD4 genotyping may differentiate symptoms of attention-deficit/hyperactivity disorder and sluggish cognitive tempo

Long-term clinical outcomes and management of hypertriglyceridemia in children with Apo-CII deficiency

Effectiveness of Mesenchymal Stem Cell Therapy for COVID-19 Patients in the Intensive Care Unit: A Case-Control Study

Bilateral Familial Elastofibroma Dorsi: Is Genetic Abnormality Essential?

Elective Termination Decision in Sex Chromosomal Abnormalities-Current Situation in Decision Making Process

Association of arms2 gene rs10490924 and htra1 gene rs11200638 polymorphisms with exudative age-related macular degeneration in western aegean population of turkey

MEFV mutations in patients with familial Mediterranean fever from the Aegean region of Turkey

Primary male infertility in Izmir/Turkey: a cytogenetic and molecular study of 187 infertile Turkish patients

Investigation of miRNA and cytokine expressions in latent tuberculosis infection and active tuberculosis

20-year experience on prenatal diagnosis in a reference university medical genetics center in Turkey

Uniparental Disomy of Chromosome 4: A Case of Whole Chromosome UPD Presenting with LRBA Deficiency

DRD4 genotyping may differentiate symptoms of attention-deficit/hyperactivity disorder and sluggish cognitive tempo

Clinicopathological characteristics, genetics and prognosis of patients with myeloid sarcoma: a single-center study

Investigation of genotype–phenotype correlation in patients with AZF microdeletion in a single‐reference centre

Molecular analysis and clinical findings of Griscelli syndrome patients

Investigation of possible associations of the BDNF, SNAP-25 and SYN III genes with the neurocognitive measures: BDNF and SNAP-25 genes might be involved in attention domain, SYN III gene in executive function

Kısmi ve Tam Dönümlü Spektral Metotların Karşılaştırması

A Severe α Thalassemia Case Compound Heterozygous for Hb Adana in α1 Gene and 20.5 kb Double Gene Deletion

A complex t(15;22;17)(q22;q11.2;q21) variant of APL

Complex karyotype with double Philadelphia chromosome and T315I mutation results in blastic phase and extensive extramedullary infiltration in a chronic myeloid leukemia patient

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