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Evolution of Genetic Techniques: Past, Present, and Beyond

BioMed research international, 2015-01, Vol.2015, p.461524-7

2015

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Propolis Extract Regulates microRNA Expression in Glioblastoma and Brain Cancer Stem Cells

Anti-cancer agents in medicinal chemistry, 2022, Vol.22 (2), p.378-389

2022

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A Case of Myosin Heavy Chain 9-Related Disorder Following Splenectomy Due to Misdiagnosis of Idiopathic Thrombocytopenic Purpura

Curēus (Palo Alto, CA), 2024-02

2024

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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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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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A hypofunctional PAX1 mutation causes autosomal recessively inherited otofaciocervical syndrome

Human genetics, 2013-11, Vol.132 (11), p.1311-1320

2013

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G-1639A but Not C1173T VKORC1 Gene Polymorphism Is Related to Ischemic Stroke and Its Various Risk Factors in Ukrainian Population

BioMed research international, 2016-01, Vol.2016, p.1298198-10

2016

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Functional consequences and structural interpretation of mutations of human choline acetyltransferase

Human mutation, 2011-11, Vol.32 (11), p.1259-1267

2011

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Epidemiological analysis of Leishmania tropica strains and giemsa-stained smears from Syrian and Turkish leishmaniasis patients using multilocus microsatellite typing (MLMT)

PLoS neglected tropical diseases, 2017-04, Vol.11 (4), p.e0005538

2017

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The importance of fluorescence in situ hybridization analysis in myelodysplastic syndromes

Journal of biotechnology, 2014-09, Vol.185, p.S13-S13

Karaca, Emin

2014

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Molecular Testing for Fragile X: Analysis of 5062 Tests from 1105 Fragile X Families—Performed in 12 Clinical Laboratories in Spain

BioMed research international, 2014-01, Vol.2014, p.195793-8

2014

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Whole Exome Sequencing Reveals Genetic Predisposition in a Large Family with Retinitis Pigmentosa

BioMed research international, 2014-01, Vol.2014, p.302487-6

2014

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Cytogenetic as an Important Tool for Diagnosis and Prognosis for Patients with Hypocellular Primary Myelodysplastic Syndrome

BioMed research international, 2014-01, Vol.2014, p.542395-10

2014

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MicroRNA Expression Profile in the Prenatal Amniotic Fluid Samples of Pregnant Women with Down Syndrome

Balkan medical journal, 2018-03, Vol.35 (2), p.163-166

2018

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Association between bronchopulmonary dysplasia and MBL2 and IL1-RN polymorphisms

Pediatrics international, 2012-12, Vol.54 (6), p.863-868

2012

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Clinical, Neuroimaging, and Genetic Features of the Patients with L-2-Hydroxyglutaric Aciduria

The journal of pediatric research, 2018-03, Vol.5 (1), p.39-43

2018

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Diagnostic Role of MicroRNA Expression Profile in the Prenatal Amniotic Fluid Samples of Pregnant Women with Down Syndrome

Balkan medical journal, 2018-03, Vol.35 (2), p.163-166

2018

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Micronucleus evaluation for determining the chromosomal breakages after radionuclide synovectomy in patients with hemophilia

Annals of nuclear medicine, 2012, Vol.26 (1), p.41-46

2012

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Eight years of follow-up experience in children with mendelian susceptibility to mycobacterial disease and review of the literature

Asian Pacific journal of allergy and immunology, 2023-12, Vol.41 (4), p.372-378

2023

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Two Newly Discovered Variations of the Plasminogen Activator Inhibitor 1 Gene in 3 Turkish Cases

Clinical and applied thrombosis/hemostasis, 2012-06, Vol.18 (3), p.327-330

2012

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The effect of interleukin-10 gene promoter polymorphisms on early-onset coronary artery disease

Anadolu kardiyoloji dergisi : AKD, 2011-06, Vol.11 (4), p.285-289

2011

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Diverse phenotypic and genotypic presentation of RAG1 mutations in two cases with SCID

Clinical and experimental medicine, 2009-12, Vol.9 (4), p.339-342, Article 339

2009

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Association between clinical variations and copy number variations in cases with Turner syndrome

Journal of Pediatric Endocrinology and Metabolism, 2022-09, Vol.35 (9), p.1161-1168

2022

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The evaluation of hTERT mRNA expression in acute leukemia children and 2 years follow-up of 40 cases

International journal of hematology, 2008-04, Vol.87 (3), p.276-283

2008

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Evolution of Genetic Techniques: Past, Present, and Beyond

Propolis Extract Regulates microRNA Expression in Glioblastoma and Brain Cancer Stem Cells

A Case of Myosin Heavy Chain 9-Related Disorder Following Splenectomy Due to Misdiagnosis of Idiopathic Thrombocytopenic Purpura

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

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

A hypofunctional PAX1 mutation causes autosomal recessively inherited otofaciocervical syndrome

G-1639A but Not C1173T VKORC1 Gene Polymorphism Is Related to Ischemic Stroke and Its Various Risk Factors in Ukrainian Population

Functional consequences and structural interpretation of mutations of human choline acetyltransferase

Epidemiological analysis of Leishmania tropica strains and giemsa-stained smears from Syrian and Turkish leishmaniasis patients using multilocus microsatellite typing (MLMT)

The importance of fluorescence in situ hybridization analysis in myelodysplastic syndromes

Molecular Testing for Fragile X: Analysis of 5062 Tests from 1105 Fragile X Families—Performed in 12 Clinical Laboratories in Spain

Whole Exome Sequencing Reveals Genetic Predisposition in a Large Family with Retinitis Pigmentosa

Cytogenetic as an Important Tool for Diagnosis and Prognosis for Patients with Hypocellular Primary Myelodysplastic Syndrome

MicroRNA Expression Profile in the Prenatal Amniotic Fluid Samples of Pregnant Women with Down Syndrome

Association between bronchopulmonary dysplasia and MBL2 and IL1-RN polymorphisms

Clinical, Neuroimaging, and Genetic Features of the Patients with L-2-Hydroxyglutaric Aciduria

Diagnostic Role of MicroRNA Expression Profile in the Prenatal Amniotic Fluid Samples of Pregnant Women with Down Syndrome

Micronucleus evaluation for determining the chromosomal breakages after radionuclide synovectomy in patients with hemophilia

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

Eight years of follow-up experience in children with mendelian susceptibility to mycobacterial disease and review of the literature

Two Newly Discovered Variations of the Plasminogen Activator Inhibitor 1 Gene in 3 Turkish Cases

The effect of interleukin-10 gene promoter polymorphisms on early-onset coronary artery disease

Diverse phenotypic and genotypic presentation of RAG1 mutations in two cases with SCID

Association between clinical variations and copy number variations in cases with Turner syndrome

The evaluation of hTERT mRNA expression in acute leukemia children and 2 years follow-up of 40 cases

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