Doç. Dr. Serbülent Yiğit

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Evaluation of the 18-bp deletion/insertion variant of the VEGF gene in athletes

Ünver Ş., Nursal A. F., Yiğit S., Atan T.

NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS , 2024 (SCI-Expanded) Sürdürülebilir Kalkınma

Evaluation of a circadian rhythm gene (PER3) VNTR variant in Turkish athletes

Ünver Ş., Yiğit S., Tural E., Yigit E., Atan T.

Nucleosides, Nucleotides and Nucleic Acids , cilt.43, sa.2, ss.173-183, 2024 (SCI-Expanded)

Association of MIF-173G/C, IL-4 VNTR, and IL-1RA VNTR variants with FMF-related amyloidosis in a Turkish cohort

Yiğit S., Nursal A. F., Keskin A., Kaya S., Kuruca N., Sezer O.

JOURNAL OF INVESTIGATIVE MEDICINE , cilt.72, sa.1, ss.17-25, 2024 (SCI-Expanded)

Evaluating interleukin-6 levels and the rs1800795 variant in Turkish patients with COVID-19: a prospective cohort study

SEZER Ö., NURSAL A. F., Gunal O., Gorgun S., Tekcan A., Unluguzel Ustun G., et al.

NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS , cilt.43, sa.4, ss.377-390, 2024 (SCI-Expanded)

Effect of vitamin D receptor gene BsmI polymorphism on hospitalization of SARS-CoV-2 positive patients

Aci R., Keskin A., Yigit S., Sezer O., Kaya M. T.

NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS , cilt.43, sa.3, ss.264-275, 2024 (SCI-Expanded) Sürdürülebilir Kalkınma

MEFV gene pathogenic variants: a risk factor for dysmenorrhea in the Turkish population

Nacar M. C., Yiğit S., Ozsoy A. Z., Demirturk F., Nursal A. F., Karakus N.

NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS , 2023 (SCI-Expanded) Sürdürülebilir Kalkınma

Lack of association between VNTR variant of the circadian gene (PER3) and major depressive disorder in a sample of a Turkish population

Yiğit S., Nursal A. F., Ozsoy F., DUMAN E., Ustaoglu M. S.

NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS , 2023 (SCI-Expanded)

Association of eNOS gene 4a/4b VNTR and T786C polymorphism with Crimean-Congo hemorrhagic fever

Coskun U. S. S., YİĞİT S., Ozmen Z. C., DEVECİ K., Tekcan A., Barut H. S., et al.

NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS , cilt.42, sa.7, ss.507-515, 2023 (SCI-Expanded)

Clock 3111 T/C and Period3 VNTR gene polymorphisms and proteins, and melatonin levels in women with infertility

Aci R., Çiftci G., YİĞİT S., Sezer O., Keskin A.

JOURNAL OF ASSISTED REPRODUCTION AND GENETICS , cilt.40, sa.5, ss.1109-1116, 2023 (SCI-Expanded)

The effect of a 18 bp deletion/insertion variant of VEGF gene on the FMF development

Sezer O., NURSAL A. F., Kuruca Şahbazoğlu N., YİĞİT S.

NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS , cilt.42, sa.4, ss.296-307, 2023 (SCI-Expanded)

Role of VEGF I/D variant in suspectibility to odontogenic cyst formation

Yildiz S., NURSAL A. F., YİĞİT S., Tumer M. K.

NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS , cilt.42, sa.4, ss.308-316, 2023 (SCI-Expanded)

Dual effect of methylene-tetrahydrofolate reductase and angiotensin-converting enzyme gene polymorphisms on the risk of acute ischemic stroke

KARAKUŞ N., YİĞİT S., Basol N., Incealtin O.

JOURNAL OF GENETICS , cilt.102, sa.1, 2023 (SCI-Expanded)

Association of ACE ID, MTHFR C677T, and MIF-173GC variants with the clinical course of COVID-19 patients

Tekcan A., Cihangiroglu M., Capraz M., Capraz A., Yigit S., NURSAL A. F., et al.

NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS , cilt.42, sa.10, ss.782-796, 2023 (SCI-Expanded) Sürdürülebilir Kalkınma

The evaluation of superoxide dismutase 1 gene insertion/deletion variant in athletes

Nursal A. F., Ünver Ş., Yiğit S., Orhan O. M., Atan T.

REVISTA DA ASSOCIACAO MEDICA BRASILEIRA , cilt.69, sa.12, 2023 (SCI-Expanded)

Lack of association of superoxide dismutase I/D variant with osteopenia/osteoporosis in Turkish postmenopausal women

NACAR M. C., YİĞİT S.

NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS , cilt.42, sa.9, ss.671-682, 2023 (SCI-Expanded)

Effect of IL-6-174G/C and-572G/C variants on susceptibility to osteoarthritis in Turkish population

Yiğit S., Tekcan A., Inanir A., Nursal A. F., Akkanat S., Tural E.

NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS , cilt.42, ss.65-76, 2023 (SCI-Expanded)

Impact of methylene-tetrahydrofolate reductase gene C677T and A1298C polymorphisms as a risk factor for hepatitis B virus infection

KARAKUŞ N., YİĞİT S., Kocak M., BOZKURT N., Duygu F.

NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS , cilt.42, sa.9, ss.683-695, 2023 (SCI-Expanded)

Vascular endothelial growth factor gene insertion/deletion polymorphism is associated with Vitamin D level in Turkish patients with coronavirus disease 2019

Yigit S., Tural Ş., Aci R., Sezer O.

REVISTA DA ASSOCIACAO MEDICA BRASILEIRA , cilt.69, sa.7, 2023 (SCI-Expanded)

VEGF and eNOS variants may influence intervertebral disc degeneration

Aydın H. E., Yiğit S., Kaya I., Tural E., Tuncer S., Nursal A. F.

NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS , cilt.41, sa.10, ss.982-993, 2022 (SCI-Expanded)

A circadian rhythm gene (PER3) VNTR variant as possible risk factor in cohort of Turkish females with primary dysmenorrhea

NACAR M. C., NURSAL A. F., Kuruca Şahbazoğlu N., YİĞİT S.

NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS , cilt.41, sa.9, ss.900-909, 2022 (SCI-Expanded)

Methylene-tetrahydrofolate reductase gene C677T and A1298C polymorphisms as a risk factor for Crimean-Congo hemorrhagic fever

KARAKUŞ N., Duygu F., Rustemoglu A., YİĞİT S.

NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS , cilt.41, sa.9, ss.878-890, 2022 (SCI-Expanded)

ACTN3 R577X variant: could it be a determinant of sports performance in elite athletes in a Turkish population?

Canikli A., Nursal A. F., Ünver Ş., YİĞİT S.

JOURNAL OF GENETICS , cilt.101, sa.1, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium

DÜNDAR M., FAHRİOGLU U., Yildiz S. H., Bakir-Gungor B., TEMEL Ş. G., AKIN H., et al.

FUNCTIONAL & INTEGRATIVE GENOMICS , cilt.22, sa.3, ss.291-315, 2022 (SCI-Expanded)

Relation of vitamin D and BsmI variant with temporomandibular diseases in the Turkish population

Yildiz S., Tumer M. K., YİĞİT S., Nursal A. F., Rustemoglu A., Balel Y.

BRITISH JOURNAL OF ORAL & MAXILLOFACIAL SURGERY , cilt.59, sa.5, ss.555-560, 2021 (SCI-Expanded)

Angiotensin-converting enzyme-1 gene insertion/deletion polymorphism may be associated with COVID-19 clinical severity: a prospective cohort study

Gunal O., Sezer O., Ustun G. U., Ozturk C. E., Sen A., YİĞİT S., et al.

ANNALS OF SAUDI MEDICINE , cilt.41, sa.3, ss.141-146, 2021 (SCI-Expanded)

eNOS and VEGF Variants Might Increase the Risk of Pancreatic Cancer

Hasan Dagmura H. D., YİĞİT S., GÜMÜŞAY Ö., NURSAL A. F., DALDAL E., KARAKUŞ N.

CYTOLOGY AND GENETICS , cilt.55, sa.2, ss.177-182, 2021 (SCI-Expanded)

The Impact of PER3 VNTR Polymorphism on the Development of Schizophrenia in a Turkish Population

Ozsoy F., YİĞİT S., NURSAL A. F., Kulu M., KARAKUŞ N.

CYTOLOGY AND GENETICS , cilt.55, sa.2, ss.188-193, 2021 (SCI-Expanded)

Possible Association of PER2/PER3 Variable Number Tandem Repeat Polymorphism Variants with Susceptibility and Clinical Characteristics in Pancreatic Cancer

DAGMURA H., YİĞİT S., NURSAL A. F., Duman E., GÜMÜŞAY Ö.

GENETIC TESTING AND MOLECULAR BIOMARKERS , sa.2, ss.124-130, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma

VNTR Variant of the eNOS Gene and its Relationship with Osteoporosis in Postmenopausal Turkish Women

NURSAL A. F., YİĞİT S., Tekcan A., ÖZSOY A. Z., ATEŞ H. Ö.

ENDOCRINE METABOLIC & IMMUNE DISORDERS-DRUG TARGETS , cilt.21, sa.9, ss.1691-1695, 2021 (SCI-Expanded)

Analysis of Interleukin-1 Receptor Antagonist Variable Number Tandem Repeat Variant in Recurrent Aphthous Stomatitis

Tekcan A., YİĞİT S., NURSAL A. F., TÜMER M. K., YERLİYURT K., Kuruca Şahbazoğlu N.

ENDOCRINE METABOLIC & IMMUNE DISORDERS-DRUG TARGETS , cilt.21, sa.1, ss.139-144, 2021 (SCI-Expanded)

Influence of ESR1 Variants on Clinical Characteristics and Fibromyalgia Syndrome in Turkish Women

Arslan H. S., NURSAL A. F., Inanir A., KARAKUŞ N., YİĞİT S.

ENDOCRINE METABOLIC & IMMUNE DISORDERS-DRUG TARGETS , cilt.21, sa.7, ss.1326-1332, 2021 (SCI-Expanded)

Impact of Endothelial NOS VNTR Variant on Susceptibility to Diabetic Neuropathy and Type 2 Diabetes Mellitus

YİĞİT S., NURSAL A. F., UZUN S., Rustemoglu H., Dashatan P. A., Soylu H., et al.

CURRENT NEUROVASCULAR RESEARCH , sa.5, ss.700-705, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma

Estrogen Receptor 1 Gene rs22346939 and rs9340799 Variants are Associated with Major Depressive Disorder and its Clinical Features

Ozsoy F., NURSAL A. F., KARAKUŞ N., Demir M. O., YİĞİT S.

CURRENT NEUROVASCULAR RESEARCH , cilt.18, sa.1, ss.12-19, 2021 (SCI-Expanded)

A Case-Control Study Investigating the Effect of MTHFR C677T Variant on Performance of Elite Athletes

NURSAL A. F., YİĞİT S., Rustemoglu H., Cenikli A.

ENDOCRINE METABOLIC & IMMUNE DISORDERS-DRUG TARGETS , cilt.21, sa.9, ss.1685-1690, 2021 (SCI-Expanded)

Effect of AUTS2 gene rs6943555 variant in male patients with schizophrenia in a Turkish population

Ozsoy F., KARAKUŞ N., YİĞİT S., Kulu M.

GENE , cilt.756, 2020 (SCI-Expanded)

Effects of Paraoxonase-1 variants on course of severity and mortality of Crimean-Congo hemorrhagic fever

Karakus N., YİĞİT S., Duygu F., Barut S., Rustemoglu A., Basol N.

Gene , cilt.687, ss.188-192, 2019 (SCI-Expanded)

Significance of IL-1Ra and IL-6 gene variants in Turkish patients with Crimean-Congo hemorrhagic fever

Coskun U. S. S., Nursal A. F., Gunes F., Rustemoglu A., Yayli A., Karakus N., et al.

Asian Pacific Journal of Tropical Biomedicine , cilt.9, sa.2, ss.85-90, 2019 (SCI-Expanded)

Effect of a functional variant of tumor necrosis factor-β gene in temporomandibular disorders: A pilot study

Yerliyurt K., Nursal A. F., Tekcan A., Karakus N., Tumer M. K., YİĞİT S.

Journal of Clinical Laboratory Analysis , cilt.33, sa.1, 2019 (SCI-Expanded)

Il-1β and IL-1Ra variant profiles in Turkish patients with diabetic peripheral neuropathy

Nursal A. F., Inanir A., Rustemoglu A., Uzun S., Sahin K., YİĞİT S.

Endocrine, Metabolic and Immune Disorders - Drug Targets , cilt.19, sa.2, ss.150-158, 2019 (SCI-Expanded)

Influence of the MIF polymorphism-173G > C on Turkish postmenopausal women with osteoporosis

Ozsoy A. Z., Karakus N., Tural Ş., YİĞİT S., Kara N., Alayli G., et al.

ZEITSCHRIFT FUR RHEUMATOLOGIE , cilt.77, sa.7, ss.629-632, 2018 (SCI-Expanded)

The evaluation of two genetic polymorphisms of paraoxonase 1 in patients with pulmonary embolism

Basol N., Karakus N., Savas A. Y., Karakus K., Kaya İ., Karaman S., et al.

Journal of Clinical Laboratory Analysis , cilt.32, sa.7, 2018 (SCI-Expanded)

Angiotensin converting enzyme gene insertion/deletion variant and familial Mediterranean fever-related amyloidosis

Nursal A. F., Turkmen E., Kaya S. U., Tekcan A., Sezer O., Celik S. D., et al.

Iranian Journal of Kidney Diseases , cilt.12, sa.3, ss.150-155, 2018 (SCI-Expanded)

Association between vitamin k epoxide reductase (VKORC1)-1639g>a polymorphism and osteoporosis in postmenopausal women

Kutluturk F., Inanir A., Rustemoglu A., Kaya S. U., Demir A. K., Dursun G., et al.

Endocrine, Metabolic and Immune Disorders - Drug Targets , cilt.18, sa.3, ss.281-286, 2018 (SCI-Expanded)

The IL-1Ra gene variable number tandem repeat variant is associated with susceptibility to temporomandibular disorders in Turkish population

Tumer M. K., Nursal A. F., Tekcan A., Yerliyurt K., Geyko A., YİĞİT S.

Journal of Clinical Laboratory Analysis , cilt.32, sa.2, 2018 (SCI-Expanded)

MTHFR gene C677T and A1298C variants are associated with FMF risk in a Turkish cohort

Nursal A. F., Kaya S., Sezer O., Karakus N., YİĞİT S.

Journal of Clinical Laboratory Analysis , cilt.32, sa.2, 2018 (SCI-Expanded)

Macrophage Migration Inhibitory Factor-173GC Variant Might Increase the Risk of Behcet's Disease

NURSAL A. F., YİĞİT S., Tural E., KALKAN G., TÜMER M. K., TEKCAN A.

MEDICAL PRINCIPLES AND PRACTICE , cilt.27, sa.3, ss.285-289, 2018 (SCI-Expanded)

The investigation of association between IL-1Ra and ACE I/D polymorphisms in carpal tunnel syndrome

Cevik B., Tekcan A., Inanir A., Kurt S. G., YİĞİT S.

Journal of Clinical Laboratory Analysis , cilt.32, sa.1, 2018 (SCI-Expanded)

Investigation of CD40 gene rs4810485 and rs1883832 mutations in patients with recurrent aphthous stomatitis

YİĞİT S., Tekcan A., Rustemoglu A., Tumer M. K., KALKAN G., Yerliyurt K.

Archives of Oral Biology , cilt.74, ss.51-54, 2017 (SCI-Expanded)

CLINICAL SIGNIFICANCE OF NCOA5 GENE RS2903908 POLYMORPHISM IN BEHCET'S DISEASE

Rustemoglu A., Inal E., Inanır A., Ekinci D., Gul U., YİĞİT S., et al.

EXCLI JOURNAL , ss.609-617, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma

The IL4-VNTR P1 Allele, IL4-VNTR P2P2 Genotype, and IL4-VNTR_IL6-174CG P2P1-GG genotype are associated with an increased risk of brucellosis

Gunal O., YİĞİT S., Yalcın A. D., Celik B., Barut S., Demir O., et al.

Japanese Journal of Infectious Diseases , cilt.70, sa.1, ss.61-64, 2017 (SCI-Expanded)

Evaluation of MIF -173 G/C polymorphism in Turkish patients with ankylosing spondylitis

Gürel Ç., İnanır A., Nursal A. F., Tekcan A., Rüstemoğlu A., YİĞİT S.

Balkan Medical Journal , cilt.33, sa.6, ss.614-619, 2016 (SCI-Expanded)

Association of Genetic Polymorphisms in TNF and MIF Gene with the Risk of Primary Dysmenorrhea

Dogru H. Y., Ozsoy A. Z., Karakus N., Delibas I. B., Isguder C. K., YİĞİT S.

BIOCHEMICAL GENETICS , sa.4, ss.457-466, 2016 (SCI-Expanded)

Interleukin-1Ra rs2234663 and Interleukin-4 rs79071878 Polymorphisms in Familial Mediterranean Fever

Nursal A. F., Tekcan A., Kaya S. U., Sezer O., YİĞİT S.

Gene , cilt.582, sa.2, ss.173-177, 2016 (SCI-Expanded)

Mutational Spectrum of the MEFV Gene in AA Amyloidosis Associated With Familial Mediterranean Fever

Nursal A. F., Tekcan A., Kaya S. U., Turkmen E., YİĞİT S.

IRANIAN JOURNAL OF KIDNEY DISEASES , sa.3, ss.107-112, 2016 (SCI-Expanded)

Relationship between major depressive disorder and ACE gene I/D polymorphism in a Turkish population

Inanir S., YİĞİT S., Çelikel F. Ç., Ates O., Taycan S. E., Nursal A. F., et al.

Revista de Psiquiatria Clinica , cilt.43, sa.2, ss.27-30, 2016 (SCI-Expanded)

The Evaluation of IL6 and ESR1 Gene Polymorphisms in Primary Dysmenorrhea

Ozsoy A. Z., Karakus N., YİĞİT S., Cakmak B., Nacar M. C., Yilmaz Dogru H.

IMMUNOLOGICAL INVESTIGATIONS , sa.1, ss.75-86, 2016 (SCI-Expanded) Sürdürülebilir Kalkınma

The importance of MTHFR C677T/A1298C combined polymorphisms in pulmonary embolism in Turkish population

Basol N., Karakus N., Savas A. Y., Kaya I., Karakus K., YİĞİT S.

MEDICINA-LITHUANIA , sa.1, ss.35-40, 2016 (SCI-Expanded) Sürdürülebilir Kalkınma

Angiotensin converting enzyme and methylenetetrahydrofolate reductase gene variations in fibromyalgia syndrome

Inanir A., YİĞİT S., Tekcan A., Pinarli F. A., Inanir S., Karakus N.

GENE , sa.2, ss.188-192, 2015 (SCI-Expanded)

Mthfr and IL-4 gene polymorphisms are not associated with primary dysmenorrhea in young adults

Ozsoy A. Z., Cakmak B., Nacar M. C., Cetin A., Demirturk F., Dogru H. Y., et al.

International Journal of Human Genetics , cilt.15, sa.2, ss.73-79, 2015 (SCI-Expanded)

Associations of rs4810485 and rs1883832 polymorphisms of CD40 gene with susceptibility and clinical findings of Beh‡et's disease

İnal E. E., Rüstemoğlu A., İnanır A., Ekinci D., Gül Ü., YİĞİT S., et al.

RHEUMATOLOGY INTERNATIONAL , sa.5, ss.837-843, 2015 (SCI-Expanded)

Association between the ACE gene I/D polymorphism and osteoporosis in a Turkish population

Cakmak B., Inanir A., Karakus N., Ates O., YİĞİT S.

ZEITSCHRIFT FUR RHEUMATOLOGIE , sa.4, ss.346-350, 2015 (SCI-Expanded) Sürdürülebilir Kalkınma

The effect of IL-4 and MTHFR gene variants in ankylosing spondylitis

YİĞİT S., Inanir A., Tural Ş., Filiz B., Tekcan A.

ZEITSCHRIFT FUR RHEUMATOLOGIE , cilt.74, sa.1, ss.60-66, 2015 (SCI-Expanded)

Lack of Association Between MIF Gene-173G>C Polymorphism with Multiple Sclerosis

Cevik B., Yiğit S., Karakus N., Aksoy D., Ates O., Kurt S.

IN VIVO , sa.1, ss.71-76, 2015 (SCI-Expanded) Sürdürülebilir Kalkınma

Association of Methylenetetrahydrofolate Reductase Gene C677T Polymorphism With Multiple Sclerosis in Turkish Patients

Cevik B., YİĞİT S., Karakus N., Aksoy D., Kurt S., Ates O.

JOURNAL OF INVESTIGATIVE MEDICINE , sa.8, ss.980-984, 2014 (SCI-Expanded) Sürdürülebilir Kalkınma

Association analysis of three ABCB1 (MDR1) gene variants (C1236T, G2677A/T and C3435T) and their genotype/haplotype combinations with the familial Mediterranean fever

Rustemoglu A., GÜMÜŞ AKAY G., Karakus N., YİĞİT S., Sahin S., Tasliyurt T.

Xenobiotica , cilt.44, sa.10, ss.933-940, 2014 (SCI-Expanded)

Clinical symptoms in fibromyalgia are associated to catechol-O-methyltransferase (COMT) gene Val158Met polymorphism

Inanir A., Karakus N., Ates O., Sezer S., Bozkurt N., Inanir S., et al.

XENOBIOTICA , sa.10, ss.952-956, 2014 (SCI-Expanded) Sürdürülebilir Kalkınma

The Evaluation of Angiotensin-converting Enzyme (ACE) Gene I/D and IL-4 Gene Intron 3 VNTR Polymorphisms in Coronary Artery Disease

Basol N., Celik A., Karakus N., Ozsoy S. D., Yiğit S.

IN VIVO , cilt.28, sa.5, ss.983-988, 2014 (SCI-Expanded) Sürdürülebilir Kalkınma

Capsaicin inhibits cell proliferation by cytochrome c release in gastric cancer cells

MERAL Ö., Alpay M., KISMALI G., Kosova F., Cakir D. U., PEKCAN M., et al.

TUMOR BIOLOGY , sa.7, ss.6485-6492, 2014 (SCI-Expanded)

Molecular Analysis of Genetic Variation in Angiotensin I-Converting Enzyme Gene in Turkish Athletes

İNANIR A., Cenikli A., Tural E., Tekcan A., Tural Ş., Cakil D., et al.

INTERNATIONAL JOURNAL OF HUMAN GENETICS , cilt.14, sa.2, ss.101-105, 2014 (SCI-Expanded)

The role of IL-4 gene 70 bp VNTR and ACE gene I/D variants in Familial Mediterranean fever

YİĞİT S., Tural Ş., Tekcan A., TAŞLIYURT T., İNANIR A., Uzunkaya S., et al.

CYTOKINE , cilt.67, sa.1, ss.1-6, 2014 (SCI-Expanded)

Effects of interleukin (IL)-6 gene polymorphisms on recurrent aphthous stomatitis

Karakus N., YİĞİT S., Rustemoglu A., Kalkan G., Bozkurt N.

ARCHIVES OF DERMATOLOGICAL RESEARCH , sa.2, ss.173-180, 2014 (SCI-Expanded)

Significant association of interleukin-4 gene intron 3 VNTR polymorphism with susceptibility to knee osteoarthritis

YİĞİT S., İNANIR A., Tekcan A., Tural E., ÖZTÜRK G., KISMALI G., et al.

GENE , cilt.537, sa.1, ss.6-9, 2014 (SCI-Expanded)

Association of MTHFR gene C677T mutation with recurrent aphthous stomatitis and number of oral ulcers

Kalkan G., Karakus N., YİĞİT S.

CLINICAL ORAL INVESTIGATIONS , sa.2, ss.437-441, 2014 (SCI-Expanded) Sürdürülebilir Kalkınma

The Investigation of Obesity Susceptibility with IL-4 Gene Intron 3 VNTR and IL-6 Gene-597G/A Polymorphisms in a Turkish Population

Tekcan A., YİĞİT S., RÜSTEMOĞLU A., GÜREL Ç., Sahin S., TAŞLIYURT T.

INTERNATIONAL JOURNAL OF HUMAN GENETICS , cilt.13, sa.4, ss.209-213, 2013 (SCI-Expanded)

Common MEFV gene mutations in Turkish patients with Behcet's disease

Tasliyurt T., YİĞİT S., Rustemoglu A., Gul U., Ates O.

GENE , sa.1, ss.100-103, 2013 (SCI-Expanded) Sürdürülebilir Kalkınma

The importance of association between angiotensin-converting enzyme (ACE) Gene I/D polymorphism and diabetic peripheral neuropathy

Inanir A., Basol N., Karakus N., YİĞİT S.

GENE , sa.2, ss.253-256, 2013 (SCI-Expanded)

Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population

Kalkan G., YİĞİT S., Karakuş N., Ateş Ö., Bozkurt N., Özdemir A., et al.

Gene , cilt.530, sa.1, ss.109-112, 2013 (SCI-Expanded)

High Association of IL-4 Gene Intron 3 VNTR Polymorphism with Diabetic Peripheral Neuropathy

Basol N., Inanir A., YİĞİT S., Karakus N., Kaya S. U.

JOURNAL OF MOLECULAR NEUROSCIENCE , sa.2, ss.437-441, 2013 (SCI-Expanded)

The association between Interleukin (IL)-4 gene intron 3 VNTR polymorphism and alopecia areata (AA) in Turkish population

Kalkan G., Karakus N., Baş Y., Takçi Z., Özuǧuz P., Ateş Ö., et al.

GENE , sa.2, ss.565-569, 2013 (SCI-Expanded)

Association of interleukin (IL)-4 gene intron 3 VNTR polymorphism with multiple sclerosis in Turkish population

Karakus N., YİĞİT S., Kurt G. S., Cevik B., Demir O., Ates O.

HUMAN IMMUNOLOGY , sa.9, ss.1157-1160, 2013 (SCI-Expanded) Sürdürülebilir Kalkınma

Association between interleukin 4 gene intron 3 VNTR polymorphism and recurrent aphthous stomatitis in a cohort of Turkish patients

Kalkan G., YİĞİT S., Karakus N., Baş Y., Seçkin H. Y.

GENE , sa.1, ss.207-210, 2013 (SCI-Expanded)

Association between fibromyalgia syndrome and polymorphism of the IL-4 gene in a Turkish population

YİĞİT S., İNANIR A., Tekcan A., Inanir S., Tural Ş., Ates O.

GENE , cilt.527, sa.1, ss.62-64, 2013 (SCI-Expanded)

High association of angiotensin-converting enzyme (ACE) gene insertion/deletion (I/D) polymorphism with recurrent aphthous stomatitis

Karakus N., YİĞİT S., Kalkan G., Sezer S.

ARCHIVES OF DERMATOLOGICAL RESEARCH , sa.6, ss.513-517, 2013 (SCI-Expanded) Sürdürülebilir Kalkınma

Association between MEFV gene mutations and recurrent aphthous stomatitis in a cohort of Turkish patients

Kalkan G., YİĞİT S., Karakus N., Baş Y., Pancar G. Ş., Balta I.

JOURNAL OF DERMATOLOGY , sa.7, ss.516-521, 2013 (SCI-Expanded) Sürdürülebilir Kalkınma

Association of MTHFR gene C677T mutation with diabetic peripheral neuropathy and diabetic retinopathy

YİĞİT S., Karakus N., Inanir A.

MOLECULAR VISION , ss.1626-1630, 2013 (SCI-Expanded)

Association of Missense Mutations of Mediterranean Fever (MEFV) Gene with Multiple Sclerosis in Turkish Population

YİĞİT S., Karakus N., Kurt S. G., Ates O.

JOURNAL OF MOLECULAR NEUROSCIENCE , sa.2, ss.275-279, 2013 (SCI-Expanded) Sürdürülebilir Kalkınma

IL-4 and MTHFR gene polymorphism in rheumatoid arthritis and their effects

İNANIR A., YİĞİT S., Tekcan A., Tural Ş., Kismali G.

IMMUNOLOGY LETTERS , cilt.152, sa.2, ss.104-108, 2013 (SCI-Expanded)

Association of MEFV Gene Mutations With Rheumatoid Factor Levels in Patients With Rheumatoid Arthritis

İNANIR A., YİĞİT S., KARAKUŞ N., Tekin S., RÜSTEMOĞLU A.

JOURNAL OF INVESTIGATIVE MEDICINE , cilt.61, sa.3, ss.593-596, 2013 (SCI-Expanded)

Association of IL-4 gene VNTR variant with deep venous thrombosis in Behcet's disease and its effect on ocular involvement

İNANIR A., Tural Ş., YİĞİT S., Kalkan G., Pancar G. S., Demir H. D., et al.

MOLECULAR VISION , cilt.19, ss.675-683, 2013 (SCI-Expanded)

MTHFR gene C677T mutation and ACE gene I/D polymorphism in Turkish patients with osteoarthritis

İNANIR A., YİĞİT S., Tural Ş., Cecen O., Yildirim E.

DISEASE MARKERS , cilt.34, sa.1, ss.17-22, 2013 (SCI-Expanded)

Investigation of Associations between Obesity and LEP G2548A and LEPR 668A/G Polymorphisms in a Turkish Population

Sahin S., RÜSTEMOĞLU A., Tekcan A., TAŞLIYURT T., Guven H., YİĞİT S.

DISEASE MARKERS , cilt.2013, ss.673-677, 2013 (SCI-Expanded)

DD genotype of ACE gene I/D polymorphism is associated with Behcet disease in a Turkish population

YİĞİT S., Tural Ş., RÜSTEMOĞLU A., İNANIR A., Gul U., Kalkan G., et al.

MOLECULAR BIOLOGY REPORTS , cilt.40, sa.1, ss.365-368, 2013 (SCI-Expanded)

Association between sequence variations of the Mediterranean fever gene and fibromyalgia syndrome in a cohort of Turkish patients

KARAKUŞ N., YİĞİT S., İNANIR A., Inanir S., Toprak H., Okan S.

CLINICA CHIMICA ACTA , cilt.414, ss.36-40, 2012 (SCI-Expanded)

Association of angiotensin converting enzyme (ACE) gene I/D polymorphism and rheumatoid arthritis

YİĞİT S., İNANIR A., Tural Ş., Ates O.

GENE , cilt.511, sa.1, ss.106-108, 2012 (SCI-Expanded)

Significance of MEFV gene R202Q polymorphism in Turkish familial Mediterranean fever patients

YİĞİT S., KARAKUŞ N., TAŞLIYURT T., Kaya S. U., BOZKURT N., Kisacik B.

GENE , cilt.506, sa.1, ss.43-45, 2012 (SCI-Expanded)

MDR1 gene polymorphisms may be associated with Behcet's disease and its colchicum treatment response

Rustemoglu A., Gül Ü., GÜMÜŞ AKAY G., Gönül M., YİĞİT S., Bozkurt N., et al.

GENE , sa.2, ss.333-339, 2012 (SCI-Expanded)

Significant association between insertion/deletion polymorphism of the angiotensin-convertig enzyme gene and ankylosing spondylitis

İNANIR A., YİĞİT S., Tural Ş., Ozturk S. D., Akkanet S., Habiboglu A.

MOLECULAR VISION , cilt.18, sa.220-25, ss.2107-2113, 2012 (SCI-Expanded) Sürdürülebilir Kalkınma

Association between the methylene tetrahydrofolate reductase gene C677T mutation and colchicine unresponsiveness in Behcet's disease

KARAKUŞ N., YİĞİT S., Kalkan G., RÜSTEMOĞLU A., Inanir A., Gul U., et al.

MOLECULAR VISION , cilt.18, sa.174, ss.1696-1700, 2012 (SCI-Expanded)

Common Mediterranean fever (MEFV) gene mutations associated with ankylosing spondylitis in Turkish population

YİĞİT S., İNANIR A., KARAKUŞ N., Kesici E., BOZKURT N.

DISEASE MARKERS , cilt.33, sa.3, ss.113-118, 2012 (SCI-Expanded)

Analysis of common MDR1 (ABCB1) gene C1236T and C3435T polymorphisms in Turkish patients with familial Mediterranean fever

Rüstemoglu A., GÜMÜŞ AKAY G., YİĞİT S., Tasliyurt T.

GENETICS AND MOLECULAR RESEARCH , sa.4, ss.3411-3420, 2011 (SCI-Expanded) Sürdürülebilir Kalkınma

Periodontal disease in patients with familial Mediterranean fever: from inflammation to amyloidosis

Cengiz M. I., Bagci H., Cengiz S., YİĞİT S., Cengiz K.

JOURNAL OF PERIODONTAL RESEARCH , cilt.44, sa.3, ss.354-361, 2009 (SCI-Expanded)

A Retrospective Study in Cases with Sex Chromosome Anomaly in Samsun and Around

Okten G., Kara N., Güneş S., Tural S. B., YİĞİT S., Pinarli F. A.

TURKIYE KLINIKLERI TIP BILIMLERI DERGISI , cilt.29, sa.3, ss.643-647, 2009 (SCI-Expanded) Sürdürülebilir Kalkınma

Clinical significance of MEFV mutations in ankylosing spondylitis

Durmuş D., Alaylı G., Cengiz K., YİĞİT S., Canturk F., Bagci H.

JOINT BONE SPINE , cilt.76, sa.3, ss.260-264, 2009 (SCI-Expanded)

Two turner syndrome patients with the mosaic 45,X/46,X,i(Xq) karyotype: Case report

Güneş S., Kara N., Surucu B., Okten G., Yiğit S., Sezer O.

TURKIYE KLINIKLERI TIP BILIMLERI DERGISI , cilt.28, sa.2, ss.236-238, 2008 (SCI-Expanded)

Familial t(1;17)(p34;q25) balanced translocation carrier with mental retardation and epilepsy cases: Scientific letter

Guenes S. O., Kara N., Oekten G., Tasdemir H. A., Sezer O. T., YİĞİT S., et al.

TURKIYE KLINIKLERI TIP BILIMLERI DERGISI , cilt.28, sa.1, ss.83-86, 2008 (SCI-Expanded)

MEFV mutations in patients with familial Mediterranean fever in the Black Sea region of Turkey

YİĞİT S., Bagci H., Ozkaya O., Ozdamar K., Cengiz K., Akpolat T.

JOURNAL OF RHEUMATOLOGY , cilt.35, sa.1, ss.106-113, 2008 (SCI-Expanded)

Triploidy syndrome with 69,XXX karyotype: Case report

Güneş S., Acikgoez Y., Kara N., Oekten G., Sezer O., YİĞİT S.

TURKIYE KLINIKLERI TIP BILIMLERI DERGISI , cilt.27, sa.2, ss.276-278, 2007 (SCI-Expanded)

69 XXX karyotipli Triploidi Sendromu

Güneş S., Açıkgöz Y., Kara N., Gülsen Ö., Özlem S., Yiğit S.

Türkiye Klinikleri Journal of Medical Science , cilt.27, ss.276-278, 2007 (SCI-Expanded)

Lack of evidence for association between endothelial nitric oxide synthase gene polymorphism (glu298asp) with Behcet's disease in the Turkish population

Kara N., Senturk N., Güneş S., Bagci H., Yiğit S., Turanli A.

ARCHIVES OF DERMATOLOGICAL RESEARCH , cilt.297, sa.10, ss.468-471, 2006 (SCI-Expanded)

Diğer Dergilerde Yayınlanan Makaleler

The Role Of Rora (Rar-Related Orphan Receptor Alpha) Receptors, One Of The Candidate Genes Identified For Sheep Reproductive Traits, In Sheep Reproduction

USTAOĞLU M. S., ACİ R., YİĞİT S.

Caucasian Journal of Science , cilt.2023, sa.10, ss.38-48, 2023 (Hakemli Dergi)

Distribution of the prion protein gene 23-bp indel polymorphism in Jersey cattle in Turkey

Ustaoğlu M. S., Yiğit S.

Journal of Experimental and Molecular Biology , cilt.2223, sa.91, ss.6-9, 2023 (Hakemli Dergi)

The effect of RORA (RAR-Related Orphan Receptor Alpha) receptors on litter size in Akkaraman sheep breed

Yiğit S., Kul S., Aci R., Keskin A., Tuygun T., DUMAN E.

MOLECULAR BIOLOGY RESEARCH COMMUNICATIONS , cilt.12, sa.3, ss.109-115, 2023 (ESCI) Sürdürülebilir Kalkınma

Analysis of Endotheal Nitric Oxide Synthase Gene VNTR Variant in Turkish FMF Patients

Turkeli O. S., NURSAL A. F., YİĞİT S., Tekcan A.

MEDICAL JOURNAL OF BAKIRKOY , cilt.18, sa.4, ss.433-439, 2022 (ESCI)

Role of Interleukin-6 Gene Variants in the Development of Oral Squamous Cell Carcinoma

GÜMÜŞAY Ö., YİĞİT S., NURSAL A. F., Tekcan A., DAGMURA H., Kuruca Şahbazoğlu N.

TURK ONKOLOJI DERGISI-TURKISH JOURNAL OF ONCOLOGY , cilt.37, sa.4, ss.371-378, 2022 (ESCI)

Association between NOS3 intron 4 VNTR variant and sports performance

Ünver Ş., Atan T., NURSAL A. F., YİĞİT S.

ANNALS OF CLINICAL AND ANALYTICAL MEDICINE , cilt.13, sa.2, ss.225-229, 2022 (ESCI)

Circadian clock gene variants may affect circadian fluctuations of anaerobic performance

ATAN T., ÜNVER Ş., NURSAL A. F., YİĞİT S., TEKCAN A.

ANNALS OF CLINICAL AND ANALYTICAL MEDICINE , cilt.12, sa.3, ss.264-268, 2021 (ESCI)

Kırım-Kongo Kanamalı Ateşi Laboratuvar Tanı Yöntemlerine Genel Bakış

Bahrıkarehmı L., Yiğit S.

Black Sea Journal of Health Science , cilt.4, sa.1, ss.48-51, 2021 (Hakemli Dergi) Sürdürülebilir Kalkınma

ACAN Gene VNTR Polymorphism and Intervertebral Disc Degeneration in a Turkish Population

Oz T., Kaya I., NURSAL A. F., AYDIN H. E., DEMİR O., YİĞİT S.

HASEKI TIP BULTENI-MEDICAL BULLETIN OF HASEKI , cilt.58, sa.4, ss.309-314, 2020 (ESCI)

SARS-COV-2'NİN GELİŞİMİ

Bahrıkarehmı L., Fallah A., Yiğit S.

Black Sea Journal of Health Science , cilt.3, sa.3, ss.94-101, 2020 (Hakemli Dergi)

The Role of Interleukin-4 VNTR Polymorphism in Dysmenorrhea Development

ESEN M., NURSAL A. F., Duman E., YİĞİT S.

HASEKI TIP BULTENI-MEDICAL BULLETIN OF HASEKI , cilt.58, sa.4, ss.364-369, 2020 (ESCI)

Genetic Variations of miRNAs and the Risk of Oral Squamous Cell Carcinoma: A Case-control Study

Yilmaz K., GÜMÜŞAY Ö., NURSAL A. F., KARAKUŞ N., YİĞİT S.

HASEKI TIP BULTENI-MEDICAL BULLETIN OF HASEKI , cilt.58, sa.3, ss.268-273, 2020 (ESCI)

Influence of PON1 gene polymorphisms (rs662 and rs854560) on the chronicity of HBV infection

KARAKUŞ N., Duygu F., Coskun U. S., Atay A., YİĞİT S.

META GENE , cilt.23, 2020 (ESCI)

C Deletion in Exon 4 Codon 63 of p53 Gene in Turkish Patients with Oral Squamous Cell Carcinoma

Tekcan A., Gümüşay Ö., Nursal A. F., YİĞİT S., Yildiz S., Tümer M. K.

TURK ONKOLOJI DERGISI-TURKISH JOURNAL OF ONCOLOGY , sa.2, ss.163-166, 2020 (ESCI) Sürdürülebilir Kalkınma

Importance of Genetic Polymorphisms (Rs662 and Rs854560) of the Paraoxonase-1 Gene as Risk Factor for Acute Ischemic Stroke in Turkish Population

KARAKUŞ N., BAŞOL KAYA N., YİĞİT S., Cogas P., Ceviz T., Kablan A., et al.

International Journal of Critical Care and Emergency Medicine , cilt.5, sa.6, 2019 (Hakemli Dergi)

Impact of the Functional VNTR Variants of the Interleukin-1 Receptor Antagonist and Interleukin-4 Genes on Oral Squamous Cell Carcinoma

Gümüşay Ö., Yiğit S., Nursal A. F., Tekcan A.

ISTANBUL MEDICAL JOURNAL , cilt.20, sa.3, ss.202-207, 2019 (Hakemli Dergi)

Investigation of the role of interleukin-1 receptor antagonist VNTR variant on the Behçet’s disease

Dursun G., NURSAL A. F., DENİZ DEMİR H., KARAKUŞ N., DEMİR O., YİĞİT S.

EUROPEAN JOURNAL OF RHEUMATOLOGY , cilt.5, sa.1, ss.27-31, 2018 (Hakemli Dergi)

Dental Manifestations in a Female Patient with Apert’xxs Syndrome

NURSAL A. F., TÜMER M. K., YİĞİT S., TEKCAN A.

Black Sea Journal of Health Science , cilt.1, sa.1, ss.9-12, 2018 (Hakemli Dergi)

Impact of glucocorticoid receptor gene Bcl-1 variant on temporomandibular disorders.

TÜMER M. K., YERLİYURT K., NURSAL A. F., KARAKUŞ N., TEKCAN A., YİĞİT S.

Biomedical Research , cilt.28, sa.(20), ss.8795-8800, 2017 (Scopus)

PSÖDOEKSFOLİASYON SENDROM/GLOKOMHASTALIĞININ CLUSTERİN rs11136000 GENPOLİMORFİZMİYLE İLİŞKİSİNİN ARAŞTIRILMASI

Kılıçarslan S., TEKCAN A., DENİZ DEMİR H., YİĞİT S.

Bozok Tıp Dergisi , cilt.7, sa.2, ss.1-6, 2017 (Hakemli Dergi)

Evaluation of Protein C Gene Polymorphism in Patientswith Diagnosis of Pulmonary embolism in Turkish Population

Ceviz T., KARAKUŞ N., BAŞOL N., YİĞİT S.

JOURNAL OF CLINICAL AND R E S E A R C H A R T I C L EEXPERIMENTAL INVESTIGATIONS , cilt.8, sa.1, ss.6-11, 2017 (Hakemli Dergi)

MEME KANSERLİ HASTALARDA BRCA1 VE BRCA2 GEN MUTASYONLARININ DEĞERLENDİRİLMESİ

KARAKUŞ N., KARA N., YİĞİT S., OKAN İ.

Cumhuriyet Tıp Dergisi (ELEKTRONİK) , cilt.39, sa.1, ss.374-379, 2017 (Hakemli Dergi)

The Correlation between Rs1800795 Variant of IL 6 and Sports Performance among Turkish Elite Athletes

CENİKLİ A., NURSAL A. F., TURAL E., POLAT Y., TAŞMEKTEPLİGİL M. Y., YİĞİT S.

International Journal of Humanities, Social Sciences and Education , cilt.3, sa.11, ss.1-5, 2016 (Hakemli Dergi)

Epigenetik ve Kanser

GÜREL Ç., NURSAL A. F., YİĞİT S.

Turkiye Klinikleri J Radiat Oncol , cilt.2, sa.1, ss.45-51, 2016 (Hakemli Dergi)

The Endothelial Nitric Oxide Synthase Gene Variant rs2070744 in Turkish Elite Athletes

CENİKLİ A., NURSAL A. F., TEKCAN A., DEMİRTÜRK F., YİĞİT S.

The Annals of Eurasian Medicine , cilt.4, sa.2, ss.31-34, 2016 (Hakemli Dergi)

Adenosine Deaminase Gene G22a Polymorphism as a Risk Factor for Schizophreniain Turkish Population

RÜSTEMOĞLU A., CUMURCU H. B., NURSAL A. F., BALKAN M., Uzun M., YİĞİT S.

Dicle Tıp Dergisi , cilt.43, sa.2, ss.218-223, 2016 (Hakemli Dergi)

The Effect of IL 4 Gene Polymorphism in Carpal Tunnel SyndromeKarpal Tünel Sendromunda IL 4 Gen Polimorfizminin Etkisi

TEKCAN A., ÇEVİK B., İNANIR A., YİĞİT S.

JOURNAL OF CLINICAL AND ANALYTICAL MEDICINE , cilt.7, sa.4, ss.475-478, 2016 (Scopus)

Outcomes of Turkish ankylosing spondylitis patients Türk ankilozan spondilit hastalarinin sonuçlari

Inanir A., YİĞİT S., Akif Sariyildiz M., Sogut E.

European Journal of General Medicine , cilt.10, sa.3, ss.145-149, 2013 (Scopus)

Chromosomal abnormalities in couples with recurrent pregnancyloss Tekrarlayan düşükleri olan çiftlerde kromozom anomalileri

Ökten G., Güneş S., Kara N., Tural Ş., YİĞİT S., Taşkin E.

Ondokuz Mayis Universitesi Tip Dergisi , cilt.24, sa.3, ss.90-94, 2007 (Scopus)

Lack of evidence for association between endothelial nitric oxide synthase gene polymorphisms (T-786C AND G894T) and early-onset coronary artery disease

Kara N., Yesildag O., YİĞİT S., Yüksel S., Bagci H., Bek Y.

Journal of Biological Sciences , cilt.7, sa.8, ss.1442-1447, 2007 (Scopus)

Tekrarlayan Düşükleri Olan 46,XX, t(3;7) (p21;q36) Dengeli Translokasyon Taşıyıcısı Anne ve Kız İki Olgu

Kara N., Koçak İ., Güneş S., Ökten G., Sezer Ö., Yiğit S.

TURKIYE KLINIKLERI JINEKOLOJI OBSTETRIK , cilt.17, sa.1, ss.65-68, 2007 (Scopus)

Konjenital Malformasyonlu Olgularda Kromozomal Anomaliler

Güneş S., Ökten G., Kara N., Yiğit S., Tural Ş.

Ondokuz Mayıs Üniversitesi Tıp Dergisi (. Journal of Experimental and Clinical Medicine) , cilt.22, sa.3, 2007 (Hakemli Dergi)

Chromosomal abnormalities in cases with congenital malformations Konjenital malformasyonlu olgularda kromozomal anomaliler

Güneş S., Ökten G., Kara N., Yiğit S., Tural Ş., Taşkin E., et al.

Ondokuz Mayis Universitesi Tip Dergisi , cilt.22, sa.3, ss.113-118, 2005 (Scopus)

Results of amniocentesis cytogenetic analysis between 2000 and 2005 years at Samsun and around Samsun ve çevresinde 2000-2005 yillari arasinda amniyosentez sitogenetik analiz sonuçlari

Kara N., Ökten G., Güneş S., Koçak İ., Yiğit S., Tural Ş., et al.

Ondokuz Mayis Universitesi Tip Dergisi , cilt.22, sa.3, ss.119-122, 2005 (Scopus)

Samsun ve Çevresinde 2000-2005 Yılları Arasında Amniosentez Sitogenetik Analiz Sonuçlar

Kara N., Ökten G., Güneş S., Koçak İ., Yiğit S., Bekar Tural Ş., et al.

JOURNAL OF EXPERIMENTAL AND CLINICAL MEDICINE , cilt.22, sa.3, ss.119-122, 2005 (Scopus)

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

EXAMINATION OF BRUXISM AWARENESS AMONG ATHLETES

Ünver Ş., Yiğit S.

EGE 10th INTERNATIONAL CONFERENCE ON SOCIAL SCIENCES, İzmir, Türkiye, 22 - 24 Aralık 2023, ss.1926-1930

"SHEEP FARMING AND THE IMPACT OF THE RORA GENE ON GROWTH TRAITS: GENETIC SELECTION POTENTIAL IN RED MEAT PRODUCTION"

Ustaoğlu M. S., Yiğit S.

10th International Başkent" Congress on Medicine, Nursing, and Health Sciences, Ankara, Türkiye, 28 - 30 Ekim 2023, ss.73-80

APAF1, SMC2 ,GART Gen Mutasyonlarının Holstein Sığırlarda Fertilizasyon Üzerine Etkilerinin İncelenmesi

Ustaoğlu M. S., Yiğit S.

ULUSLARARASI AKADEMİK VE BİLİMSEL ÇALIŞMALAR VE ARAŞTIRMALAR Kongresi, Ankara, Türkiye, 21 - 23 Şubat 2022, ss.18-20

CWC15 GEN MUTASYONUNUN JERSEYLERDE FERTİLİZASYON ETKİSİ

USTAOĞLU M. S., YİĞİT S.

MIDDLE EAST INTERNATIONAL CONFERENCE ON CONTEMPORARY SCIENTIFIC STUDIES-VII, BEİRUT, Lübnan, 01 Aralık 2022, ss.537-548

Türkiye’de Varroazisde Voltaj Kapılı Sodyum Kanalı Geninde L925 Mutasyonun Araştırılması

Tuygun T., YİĞİT S., GÜRLER A. T., AKPINAR R., Nursal A. F., KURUCA ŞAHBAZOĞLU N., et al.

22. Ulusal Parazitoloji Kongresi, Aydın, Türkiye, 11 Ekim 2021, ss.222

ACAN GENE VNTR VARIANT AND SUSPECTIBILITY TO INTERVERTEBRAL DISC DEGENERATION IN A TURKISH POPULATION

ÖZ T., NURSAL A. F., YİĞİT S., KAYA İ., AYDIN H. E.

3.Uluslararası GAP Matematı̇k - Mühendı̇slı̇k - Fen ve Sağlık Bı̇lı̇mleri Kongresi, Şanlıurfa, Türkiye, 29 Kasım 2019

ENOS and VEGF variants might increase risk of pancreatic cancer

DAGMURA H., YİĞİT S., GÜMÜŞAY Ö., NURSAL A. F., DALDAL E., KARAKUŞ N., et al.

2. Uluslararası 19 Mayıs Yenilikçi Bilimsel Yaklaşımlar Kongresi, Samsun, Türkiye, 14 Kasım 2019

C-DELETION IN EXON 4 CODON 63 OF P53 GENE IN TURKISH PATIENTS WITH ORAL SQUAMOUS CELL CARCINOMA

TEKCAN A., YİĞİT S., NURSAL A. F., YILDIZ S., GÜMÜŞAY Ö.

III. ULUSLARARASI BATTALGAZİ BİLİMSEL ÇALIŞMALAR KONGRESİ, Malatya, Türkiye, 21 Eylül 2019

ENOS GENİ VNTR VARYANTININ ORAL SKUAMOZ HÜCRELİ KARSİNOMLU HASTALARDA DEĞERLENDİRİLMESİ

YİĞİT S., GÜMÜŞAY Ö., NURSAL A. F., TEKCAN A., YILDIZ S.

III. ULUSLARARASI BATTALGAZİ BİLİMSEL ÇALIŞMALAR KONGRESİ, Malatya, Türkiye, 21 Eylül 2019

CORRELATION BETWEEN PERIOD3 VNTR POLYMORPHISM AND SCHIZOPHRENIA

ÖZSOY F., YİĞİT S., NURSAL A. F.

2nd International Health Sciences and Life Congress, Burdur, Türkiye, 24 Nisan 2019

GENETIC ASSOCIATION OF THE ESR1 GENE VARIANTS WITH MAJOR DEPRESSIVE DISORDER

YİĞİT S., NURSAL A. F., ÖZSOY F., KARAKUŞ N.

2nd International Health Sciences and Life Congress 24-27 April 2019 Burdur/TURKEY, Burdur, Türkiye, 24 Nisan 2019

Physical activity in disease prevention: Do epigenetic modifications have an impact?

NURSAL A. F., YİĞİT S., TEKCAN A.

10. Uluslararası Sosyal Bilimler ve Spor Kongresi, Hatay, Türkiye, 23 - 25 Kasım 2018

Sarcopenia and Exercise in the Elderly

NURSAL A. F., YİĞİT S., TEKCAN A.

10. Uluslararası Sosyal Bilimler ve Spor Kongresi, Hatay, Türkiye, 23 - 25 Kasım 2018

Effect of IL-6 rs1800795 and rs1800796 Variants on Susceptibility to Knee Osteoarthritis in Turkish Population

YİĞİT S., TEKCAN A., NURSAL A. F., İNANIR A.

WITAM-2018: International Congress on the World of Technology and Advanced Materials, Kırşehir, Türkiye, 21 - 23 Eylül 2018

Associations of Between IL-6 Gene Variation and Oral Squamous Cell Carcinoma (OSCC)

NURSAL A. F., YİĞİT S., TEKCAN A., GÜMÜŞAY Ö.

WITAM-2018: International Congress on the World of Technology and Advanced Materials, Kırşehir, Türkiye, 21 - 23 Eylül 2018

Analysis of Interleukin-1 Receptor Antagonist VNTR variant in Recurrent Aphthous Stomatitis

TEKCAN A., NURSAL A. F., YİĞİT S., TÜMER M. K.

WITAM-2018: International Congress on the World of Technology and Advanced Materials, Kırşehir, Türkiye, 21 - 23 Eylül 2018

Obezite, Bariatrik Cerrahi ve Genetik

NURSAL A. F., YİĞİT S., ÖZSOY Z.

I. Uluslararası Sağlık Bilimleri ve Yaşam Kongresi, Burdur, Türkiye, 2 - 05 Mayıs 2018

Elit Sporcularda Metilentetrahidrofolat Redüktaz (MTHFR) Geni rs1801133 Varyantı

YİĞİT S., CANİKLİ A., NURSAL A. F., RÜSTEMOĞLU A., Rüstemoğlu H., TAŞMEKTEPLİGİL M. Y.

International Eurasian Conferance on Biological and Chemical Sciences, 26 - 27 Nisan 2018

Oral kanserli hastalarda Interlökin- 6 (IL-6) gen polimorfizmleri

YİĞİT S., NURSAL A. F., GÜMÜŞAY Ö., KARAKUŞ N., Yılmaz E., Öz T.

INTERNATIONAL EURASIAN CONFERENCE ONBIOLOGICAL AND CHEMICAL SCIENCES, 26 - 27 Nisan 2018

The MEFV gene variant is associated with suspectibility to temporomandibular disorders in Turkish population

YİĞİT S., TÜMER M. K., NURSAL A. F., TEKCAN A.

INTERNATIONAL EURASIAN CONFERENCE ON BIOLOGICAL AND CHEMICAL SCIENCES, Ankara, Türkiye, 26 - 27 Nisan 2018

Multipl Skleroz Hastalarında Anjiotensin Dönüştürücü Enzim Geni I/D Polimorfizminin Değerlendirilmesi

ÇEVİK B., KARAKUŞ N., KURT S. G., AKSOY D., SÜMBÜL O., ATEŞ H. Ö., et al.

53. Ulusal Nöroloji Kongresi, Antalya, Türkiye, 24 - 30 Kasım 2017, ss.25

The Investigation of Association Between Clusterin Gene rs11136000 Polymorphism in Pseudoexophylosis Syndrome/Glaucoma

YİĞİT S., TEKCAN A., DENİZ DEMİR H., NURSAL A. F., kılıçarslan s.

VI. International Congress of Molecular Medicine, 22 - 25 Mayıs 2017

The Investigation of MDR1 Gene C1236T and C3435T Polymorphisms on the Epilepsy Patients

Şahin K., TEKCAN A., ÇEVİK B., RÜSTEMOĞLU A., YİĞİT S.

VI. International Congress of Molecular Medicine, 22 - 25 Mayıs 2017

The IL-1Ra Gene VNTR Variant is Associatedwith Susceptibility to Temporomandibular Disorders in Turkish Population

YİĞİT S., TÜMER M. K., NURSAL A. F., TEKCAN A.

Uluslararası Moleküler Tıp Kongresi, 22 - 25 Mayıs 2017

miRNA’xxlar ve Kanser İlaç Direncinde Rolü

NURSAL A. F., YİĞİT S., PEHLİVAN S.

3. Uluslararası İlaç ve Eczacılık Kongresi, Türkiye, 26 - 29 Nisan 2017

Assciation Between TNF-Beta Variant (rs909253) And Risk of Temporomandibular Disorders

YİĞİT S., NURSAL A. F., TÜMER M. K., TEKCAN A.

International DNA Day and Genome Congress, 24 - 28 Nisan 2017, ss.96

Significance of Macrophage Migration Inhibition Factor rs755622 Variant in Predicting Behçet’xxs Disease

YİĞİT S., NURSAL A. F., TEKCAN A., KALKAN G., RÜSTEMOĞLU H.

INTERNATIONAL DNA DAY AND GENOME CONGRESS, 24 - 28 Nisan 2017

The Investigation of ACE I/D Variant of FMF-Related Amyloidosis Susceptibity in Turkish patients

YİĞİT S., NURSAL A. F., TEKCAN A.

International DNA Day and Genome Congress April 24-28, 2017, 24 - 28 Nisan 2017

The Use of Bioinformatics Applications in the Analysis of Diseases Related Homocysteine Metabolism Protein Pathway

TEKCAN A., YİĞİT S.

INTERNATIONAL DNA DAY AND GENOME CONGRESS, 24 - 28 Nisan 2017

Nanotıp ve Kanserde İlaç Direnci

YİĞİT S., NURSAL A. F., Öz T., Yılmaz K.

3.Uluslararası İlaç ve Eczcılık Kongresi, 26 - 29 Nisan 2017

Romatoid artrit tedavisinde JAK inhibitörleri

NURSAL A. F., YİĞİT S., PEHLİVAN S.

3.Uluslarası İlaç ve Eczacılık Kongresi, 26 - 29 Nisan 2017

Probiyotikler ve Epigenom

YİĞİT S., NURSAL A. F.

3.Uluslararası İlaç ve Eczacılık Kongresi, 26 - 29 Nisan 2017

miRNA’lar ve Kanser İlaç Direncinde Rolü

NURSAL A. F., YİĞİT S., PEHLİVAN S.

3.Uluslararası İlaç ve Eczacılık Kongresi, 26 - 29 Nisan 2017

Lomber Dejeneratif Disk Hastalıklarında Multipotent Mezenkimal Kök Hücre Tedavisi

NURSAL A. F., YİĞİT S.

3.Uluslararası İlaç ve Eczacılık Kongresi, 26 - 29 Nisan 2017

Significance of Macrophage Migration Inhibitory Factor rs755622 variant in predicting Behçet’xxs disease

YİĞİT S., NURSAL A. F., TEKCAN A., KALKAN G., Rüstemoğlu H.

Uluslarası DNA Günleri ve Genom Kongresi, 24 - 28 Nisan 2017

INVESTIGATION OF SPESIFIC IL-1β RS16944 AND IL-1RA VNTR POLYMORPHISMS: THE SUSCEPTIBILITY CANDITATES FOR DIABETİC PERIPHERAL NEUROPATHY IN TURKİSH POPULATION

RÜSTEMOĞLU A., NURSAL A. F., YİĞİT S., KAYA S.

Uluslararası DNA Günü ve Genom Kongresi, 24 - 28 Nisan 2017

KADINLARDA MENOPOZ SONRASI OSTEOPOOZ GELİŞİMİNDE MIF GENİ 173G CPOLİMORFİZMİNİN ETKİSİ

TURAL Ş., ÖZSOY A. Z., KARAKUŞ N., YİĞİT S., KARA N., TÜMER M. K., et al.

1. ULUSLARARASI KADIN ÇOCUK SAĞLIĞI VE EĞİTİMİ KONGRESİ, 14 - 15 Mayıs 2016

Türk Populasyonunda Majör Depresyonun Genetik Temeli

TEKCAN A., YİĞİT S.

VI. Uluslararası Canik Sempozyumu Hedefe Doğru İnsan Psikolojik Danışma ve Rehberlik, 5 - 07 Mayıs 2016

Temporomandibular Düzensizlikler Psikososyal Sorunlara Yol Açar Mı

TÜMER M. K., YİĞİT S.

VI. Uluslararası Canik Sempozyumu Hedefe Doğru İnsan Psikolojik Danışma ve Rehberlik, 5 - 07 Mayıs 2016

Association Between Osteoporosis and Polymorphisms of the MIF Gene 173G C Polimorphism in Turkish Postmenopausal Women

TURAL Ş., ÖZSOY A. Z., KARAKUŞ N., YİĞİT S., KARA N., TÜMER M. K., et al.

1. uluslararası kadın ve çocuk sağlığı kongresi, 14 - 15 Nisan 2016

Kadınlarda Menopoz Sonrası Osteopooz Gelişiminde MIF Geni 173g C Polimorfizminin Etkisi

TURAL Ş., ÖZSOY A. Z., KARAKUŞ N., YİĞİT S., KARA N., ALAYLI G., et al.

21 Uluslararası Kadın Çocuk Sağlığı ve Eğitimi Kongresi, 14 - 15 Nisan 2016

Association of NCOA5 gene rs2903908 variant with the Behcet sdisease

RÜSTEMOĞLU A., ERKOL İNAL E., İNANIR A., EKİNCİ D., GÜL Ü., YİĞİT S., et al.

ESHG 2015, 6 - 09 Haziran 2015

Angiotensin converting enzyme and methylenetetrahydrofolate reductase gene variations in fibromyalgia syndrome

İNANIR A., TEKCAN A., YİĞİT S., ALPASLAN PINARLI F., SEMA İ., KARAKUŞ N.

5th International Congress of Molecular Medicine, 20 - 22 Mayıs 2015

The Importance of NPC1 gene polymorphism in coronary artery disease

DEMİR ÖZTÜRK S., YİĞİT S., ÇELİK A., NURSAL A. F., TEKCAN A., RÜSTEMOĞLU A., et al.

5th International Congress of Molecular Medicine, Türkiye, 20 - 22 Mayıs 2015

FMF Genetiği

Yiğit S.

Ailesel Akdeniz Ateşi (FMF) Sempozyumu, 6 Aralık 2013, Tokat, Türkiye, 06 Aralık 2013

Catechol O methyltransferase Val158Met polymorphism and uterineleiomyoma

ATEŞ H. Ö., DEMİRTÜRK F., SEZER S., YİĞİT S.

ESHG2012, 23 - 26 Haziran 2012

MEFV gene mutations are associated with Behçet s Disease

RÜSTEMOĞLU A., YİĞİT S., GÜL Ü., TAŞLIYURT T., ATEŞ H. Ö.

ESHG2012, 23 - 26 Haziran 2012

Determining MEFV Gene Alterations in FMF Patients

YİĞİT S., TAŞLIYURT T., UZUN S., KISMALI G.

lV. INTERNATIONAL CONGRESS OF MOLECULER MEDICINE 2011., 27 - 30 Haziran 2011

The presence of MEFV mutations in ankylosing spondylitis and their clinical significance more options

DURMUŞ D., ALAYLI G., CENGİZ K., CENGİZ K., YİĞİT S., CANTÜRK F., et al.

ANNALS OF THE RHEUMATIC DISEASES, 13 - 16 Haziran 2007

Ailesel t(1;17)(p34;q25) dengeli translokasyon taşıyıcısı üç mental retardasyon ve epilepsy olgusu.

GÜNEŞ S., KARA N., ÖKTEN G., TAŞDEMİR H. A., SEZER Ö., YİĞİT S., et al.

VII. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi. Kayseri., Kayseri, Türkiye, 17 - 20 Mayıs 2006, ss.1-185

Tekrarlayan Düşükleri Olan Çiftlerde Sitogenetik Analiz Sonuçları VII Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi 99 Kayseri 2006

ÖKTEN G., KARA N., YİĞİT S., TURAL Ş., TAŞKIN E.

VII. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Türkiye, 17 - 20 Mayıs 2006

Homolog Kromozom Çiftinin Her İkisinde inv 9 P11q13 Kromozom Yapısı Görülen 46 XX inv 9 P11q13 X2 Karyotipine Sahip Habituel Abortuslu Bir Olgu 97 Kayseri 2006

TURAL Ş., GÜNEŞ S., KARA N., YİĞİT S., KOÇAK İ., ÖKTEN G.

VII. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Türkiye, 17 - 20 Mayıs 2006

Konjenital Anomalili Olgularda Sitogenetik Analiz Sonuçları Kayseri 2006

GÜNEŞ S., ÖKTEN G., KARA N., YİĞİT S., TURAL Ş., TAŞKIN E., et al.

VII. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, 95, Türkiye, 17 - 20 Mayıs 2006

Samsun ve Çevresinde 2000 2005 Yılları Arasında Amniyosentez Örneklerinde Sitogenetik Analiz Sonuçları Kongresi 133 Kayseri 2006

KARA N., ÖKTEN G., KOÇAK İ., YİĞİT S., TURAL Ş., TAŞKIN E., et al.

VII. Ulusal Prenatal Tanı ve Tıbbi Genetik, Türkiye, 17 - 20 Mayıs 2006

46,X,del(Xp)(p11.21→pter)/45,X Gözlenen Turner Sendromlu bir Olgu.

KARA N., GÜVEN A., GÜNEŞ S., ÖKTEN G., ÖZGEN T., YİĞİT S., et al.

IX. Ulusal Tıbbi Biyoloji Kongresi. Manisa., Manisa, Türkiye, 24 - 27 Kasım 2005

45,X/46,X,i(Xq) Karyotipe Sahip iki Mozaik Turner Sendromlu Olgu

GÜNEŞ S., KARA N., SÜRÜCÜ B., ÖKTEN G., YİĞİT S., SEZER Ö.

IX. Ulusal Tıbbi Biyoloji Kongresi. Manisa., Manisa, Türkiye, 24 - 27 Kasım 2005

Tekrarlayan Düşükleri olan 46,XX,t(3;7)(p21;q36) Dengeli Translokasyon Taşıyıcısı Anne ve Kız iki Olgu.

KARA N., KOÇAK İ., GÜNEŞ S., ÖKTEN G., SEZER Ö., YİĞİT S.

IX. Ulusal Tıbbi Biyoloji Kongresi. Manisa., Manisa, Türkiye, 24 - 27 Kasım 2005

69,XXX Karyotipe Sahip Bir Triploidi Olgusu.

GÜNEŞ S., AÇIKGÖZ Y., KARA N., ÖKTEN G., SEZER Ö., YİĞİT S.

IX. Ulusal Tıbbi Biyoloji Kongresi. Manisa., Manisa, Türkiye, 24 - 27 Kasım 2005

Cytogenetic study of cases with sex anomaly

Ökten G., KARA N., GÜNEŞ S., TURAL Ş., YİĞİT S., Alparslan Pınarlı F.

Fifth International Symposium on genetics, Health and Disease, 4 - 07 Mayıs 2005

Metrikler

Yayın

209

Atıf (WoS)

895

H-İndeks (WoS)

Atıf (Scopus)

959

H-İndeks (Scopus)

Proje

Tez Danışmanlığı

Açık Erişim

BM Sürdürülebilir Kalkınma Amaçları

Yayınlar & Eserler

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Diğer Dergilerde Yayınlanan Makaleler

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar