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Re-evaluation of Genetic Variants in Parkinson’s Disease Using Targeted Panel and Next-Generation Sequencing

Twin research and human genetics, 2023-04, Vol.26 (2), p.164-170

2023

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The high frequency of chromosomal copy number variations and candidate genes in epilepsy patients

Clinical neurology and neurosurgery, 2021-03, Vol.202, p.106487-106487, Article 106487

2021

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Design of a new balun bandpass filter with single‐band balance and dual‐band filtering characteristics

Microwave and optical technology letters, 2019-11, Vol.61 (11), p.2586-2590

2019

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Evaluating of colchicine use patterns and attack frequency of familial Mediterranean fever patients in the COVID‐19 pandemic

International journal of rheumatic diseases, 2023-05, Vol.26 (5), p.988-991

2023

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Maximum lift/drag ratio improvement of TUAVs via small aerodynamic modifications

Aircraft engineering and aerospace technology, 2018-11, Vol.90 (9), p.1438-1444

2018

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An alternative coupling matrix arrangement for capacitively loaded multi-mode microstrip diplexers having close channel bands

International journal of electronics and communications, 2023-03, Vol.161, p.154540, Article 154540

2023

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Blau syndrome with a rare mutation in exon 9 of NOD2 gene

Autoimmunity (Chur, Switzerland), 2019-11, Vol.52 (7-8), p.256-263

2019

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Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in Central Anatolia

Annals of Saudi medicine, 2019-11, Vol.39 (6), p.382-387

2019

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Aerodynamic Optimization of a UAV Wing subject to Weight, Geometric, Root Bending Moment, and Performance Constraints

International journal of aerospace engineering, 2019, Vol.2019, p.1-14

2019

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The clinical, cytogenetics and molecular characterization of inverted duplication/deletion of chromosome 8p in a boy with mental and motor retardation: Genotype-phenotype correlation in a case report

The Egyptian journal of medical human genetics, 2018-10, Vol.19 (4), p.437-441

2018

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Design of fourth order microstrip filter using the open loop resonator with a novel interdigital loading element

2017 IEEE MTT-S International Microwave Symposium (IMS), 2017, p.1819-1822

2017

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Germ-line MTHFR C677T, FV H1299R and PAI-1 5G/4G variations in breast carcinoma

Asian Pacific journal of cancer prevention : APJCP, 2013-01, Vol.14 (5), p.2903-2908

2013

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CCR2 Polymorphism in Chronic Renal Failure Patients Requiring Long-Term Hemodialysis

Internal Medicine, 2011, Vol.50(21), pp.2457-2461

2011

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Association of endothelial nitric oxide synthase Glu298Asp gene polymorphism in psoriasis cases with hypertension

Annals of Saudi medicine, 2014-07, Vol.34 (4), p.340-345

2014

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association between methylene-tetrahydrofolate reductase gene polymorphism and lung cancer risk

Molecular biology reports, 2011-02, Vol.38 (2), p.991-996

2011

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A novel microstrip diplexer design with tunable bandwidths and switchable channels for 4.5G applications

Elektrik : Turkish journal of electrical engineering & computer sciences, 2017, Vol.25, p.4445-4456

2017

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A Frame-Shift Mutation in the SLC34A2 Gene in Three Patients with Pulmonary Alveolar Microlithiasis in an Inbred Family

Internal Medicine, 2010, Vol.49(1), pp.45-49

2010

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Two candidate genes for recurrent pregnancy loss and infertility: Could ZP3 and UPK3B give us new diagnostic and therapeutic approach?

Biodiscovery, 2017-08, Vol.20, p.e20113-2

2017

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Association Between Inherited Thrombophilia and Impaired Right Ventricular Function in Deep Vein Thrombosis Without Symptomatic Pulmonary Embolism

Clinical and applied thrombosis/hemostasis, 2014-04, Vol.20 (3), p.270-277

2014

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A New Mutation, Hb A2-Canakkale [δ10(A7)Ala→Val; HBD: c.32C>T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A2 Levels

Hemoglobin, 2022-03, Vol.46 (2), p.87-90

2022

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A New Mutation, Hb A 2 -Canakkale [δ10(A7)Ala→Val; HBD : c.32C>T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A 2 Levels

Hemoglobin, 2022-03, Vol.46 (2), p.87-90

2022

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The comparison of telomeric DNA length in different biological materials in various cancers by real-time PCR amplification of circulating tumour DNA

Journal of biotechnology, 2017-08, Vol.256, p.S79-S79

2017

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Evaluation of the cell death pathway and apoptosis-stunning effect relationship after low- and high-dose I-131 administrations in rat thyroid tissue

Cancer biotherapy & radiopharmaceuticals, 2006-08, Vol.21 (4), p.342

2006

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Clinical characteristics and cytogenetic abnormalities of chromosome 22q11.2 syndrome: Results from thirteen patients with variable phenotypes

Journal of biotechnology, 2016-08, Vol.231, p.S82-S82

2016

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Association Between ApoE4 Allele and Deep Venous Thrombosis: A Pilot Study

Clinical and applied thrombosis/hemostasis, 2011-04, Vol.17 (2), p.225-228

2011

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Re-evaluation of Genetic Variants in Parkinson’s Disease Using Targeted Panel and Next-Generation Sequencing

The high frequency of chromosomal copy number variations and candidate genes in epilepsy patients

Design of a new balun bandpass filter with single‐band balance and dual‐band filtering characteristics

Evaluating of colchicine use patterns and attack frequency of familial Mediterranean fever patients in the COVID‐19 pandemic

Maximum lift/drag ratio improvement of TUAVs via small aerodynamic modifications

An alternative coupling matrix arrangement for capacitively loaded multi-mode microstrip diplexers having close channel bands

Blau syndrome with a rare mutation in exon 9 of NOD2 gene

Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in Central Anatolia

Aerodynamic Optimization of a UAV Wing subject to Weight, Geometric, Root Bending Moment, and Performance Constraints

The clinical, cytogenetics and molecular characterization of inverted duplication/deletion of chromosome 8p in a boy with mental and motor retardation: Genotype-phenotype correlation in a case report

Design of fourth order microstrip filter using the open loop resonator with a novel interdigital loading element

Germ-line MTHFR C677T, FV H1299R and PAI-1 5G/4G variations in breast carcinoma

CCR2 Polymorphism in Chronic Renal Failure Patients Requiring Long-Term Hemodialysis

Association of endothelial nitric oxide synthase Glu298Asp gene polymorphism in psoriasis cases with hypertension

association between methylene-tetrahydrofolate reductase gene polymorphism and lung cancer risk

A novel microstrip diplexer design with tunable bandwidths and switchable channels for 4.5G applications

A Frame-Shift Mutation in the SLC34A2 Gene in Three Patients with Pulmonary Alveolar Microlithiasis in an Inbred Family

Two candidate genes for recurrent pregnancy loss and infertility: Could ZP3 and UPK3B give us new diagnostic and therapeutic approach?

Association Between Inherited Thrombophilia and Impaired Right Ventricular Function in Deep Vein Thrombosis Without Symptomatic Pulmonary Embolism

A New Mutation, Hb A2-Canakkale [δ10(A7)Ala→Val; HBD: c.32C>T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A2 Levels

A New Mutation, Hb A 2 -Canakkale [δ10(A7)Ala→Val; HBD : c.32C>T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A 2 Levels

The comparison of telomeric DNA length in different biological materials in various cancers by real-time PCR amplification of circulating tumour DNA

Evaluation of the cell death pathway and apoptosis-stunning effect relationship after low- and high-dose I-131 administrations in rat thyroid tissue

Clinical characteristics and cytogenetic abnormalities of chromosome 22q11.2 syndrome: Results from thirteen patients with variable phenotypes

Association Between ApoE4 Allele and Deep Venous Thrombosis: A Pilot Study

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