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Mersin Üniversitesi

  Professor Mehmet Emin Erdal
users.ozgecmis
:
Department
:
Faculty of Medicine .
BIRTH DATE
:
02 January 1960 .
Business Address
:
Mersin Üniversitesi Tıp Fakültesi Tıbbi Biyoloji Ad. Çiftlikköy Kampüsü 33343 Yenişehir/ Mersin .
Mobile Phone
:
+90-532-5209131 .
Phone
:
+90-324-3610684 .
Internal
:
29088 .
Fax
:
+90-324-3412400 .
Alternative e-mail
:
Alternative e-mail
:
Created
:
2015-06-01 08:24:44 .
Last Modification
:
2019-10-30 08:57:56 .
Researcher ID :
Scopus ID :
Orcid ID :
Scholar ID :
h-index :
25
Publons ID :
Point :

Degree Department/Program Institute Year
1980
1987
1998
Doctorate Thesis

1. Investigate the levels of serum proteins in patients with cancer and some types of haptoglobin frequency with polyacrylamide gel disc electrophoresis method, Supervisor: Dr. DOÇ.DR. TURGAY BUDAK, Dicle University, Graduate School of Health Sciences, Medical Biology Department, Diyarbakır, Turkey, .

Title Dutie Institution/Other Year
2014-07-08 - 2017-07-08
2014-07-08 - 2017-07-08
International - SCI/SCI-Expanded category 74150
2019
131. Zeybek, A.; öz, N.; Kalemci, S.; Edgünlü, T.; Kızıltuğ, M.; Tosun, K.; Tunç, M.; Tekin, L.; Erdal, M. Diagnostic Value of MiR-125b as a Potential Biomarker for Stage I Lung Adenocarcinoma. CURRENT MOLECULAR MEDICINE , 2019, 19, 216-227. 100 + 0
http://dx.doi.org/10.2174/1566524019666190314113800

130. Ay, M.; Ay, .; çayan, F.; Tekin, S.; Karakaş, .; Derici yildirim, D.; Erdal, M. Genetic Predisposition to Unexplained Recurrent Pregnancy Loss: Killer Cell Immunoglobulin-Like Receptor Gene Polymorphisms as Potential Biomarkers. GENETIC TESTING AND MOLECULAR BIOMARKERS, 2019, 23, 57-65. 200 + 0
http://dx.doi.org/10.1089/gtmb.2018.0082

2018
129. Erdal, M.; Görücü yılmaz, .; Gürgül, S.; Uzun, C.; Derici yıldırım, D.; Erdal, N. . PROGRESS IN BIOPHYSICS AND MOLECULAR BIOLOGY, 2018, 132, 35-42. 850 + 0
10.1016/j.pbiomolbio.2017.08.001

2017
128. Söylemez, F.; Izci ay, .; Ay, M.; Altıntaş, E.; Türkseven, .; Erdal, M. . BRATISLAVA MEDICAL JOURNAL, 2017, 118, 695-701. 400 + 0
10.4149/BLL_2017_131

127. Dogru, G.; Ay, O.; Erdal, M.; Ay, M.; Tombak, A.; Karakas, U. The role of certain gene polymorphisms involved in the apoptotic pathways in polycythemia vera and essential thrombocytosis. ADVANCES IN CLINICAL AND EXPERIMENTAL MEDICINE, 2017, 26, 761-765. 650 + 0
http://dx.doi.org/10.17219/acem/63087

126. Ay, O.; Balkan, M.; Erdal, M.; Rustemoğlu, A.; Atar, M.; Hatipoğlu, N.; Bodakçi, M.; Yıldız, .; Akbas, H.; Karakaş, . Association of microRNA-related gene polymorphisms and idiopathic azoospermia in a south-east Turkey population. BIOTECHNOLOGY & BIOTECHNOLOGICAL EQUIPMENT, 2017, 31, 356-362. 450 + 0
http://dx.doi.org/10.1080/13102818.2017.1281759

2016
125. Kenar, A.; Unal, G.; Guler, H.; Albuz, B.; Kiroglu, Y.; Erdal, M.; Herken, H. Relationship between the DAT1 gene and the effects of methylphenidate administration in adult attention deficit hyperactivity disorder: a magnetic resonance spectroscopy study. EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES, 2016, 20, 1373-1378. 300 + 0
http://www.europeanreview.org/wp/wp-content/uploads/1373-1378-1.pdf

124. Görücü yilmaz, S.; Erdal, M.; Avci özge, A.; Sungur, M. SNP Variation in MicroRNA Biogenesis Pathway Genes as a New Innovation Strategy for Alzheimer Disease Diagnostics. ALZHEIMER DISEASE AND ASSOCIATED DISORDERS, 2016, 30, 203-209. 850 + 0
http://dx.doi.org/10.1097/WAD.0000000000000135

123. Basay, O.; Basay, B.; Alacam, H.; Ozturk, O.; Buber, A.; Yilmaz, S.; Kiroglu, Y.; Erdal, M.; Herken, H. The impact of synapsin III gene on the neurometabolite level alterations after single-dose methylphenidate in attention-deficit hyperactivity disorder patients. NEUROPSYCHIATRIC DISEASE AND TREATMENT, 2016, 12, 1141-1149. 100 + 0
https://dx.doi.org/10.2147/NDT.S106076

122. Ozturk, O.; Basay, B.; Buber, A.; Basay, O.; Alacam, H.; Bacanlı, A.; Yılmaz, .; Erdal, M.; Herken, H.; Ercan, E. Brain-Derived Neurotrophic Factor Gene Val66Met Polymorphism Is a Risk Factor for Attention-Deficit Hyperactivity Disorder in a Turkish Sample. PSYCHIATRY INVESTIGATION, 2016, 13, 518-525. 100 + 0
http://dx.doi.org/10.4306/pi.2016.13.5.518

121. Sengul, C.; Erdal, M.; Sengul, C.; Ay, O.; Buber, A.; Alacam, H.; Ay, M.; Herken, H. Association of the Neuropeptide Y LEU7PRO rs16139 and NEUREXIN 3 rs760288 Polymorphisms with Alcohol Dependence. KLINIK PSIKOFARMAKOLOJI BULTENI-BULLETIN OF CLINICAL PSYCHOPHARMACOLOGY, 2016, 26, 15-20. 650 + 0
https://dx.doi.org/10.5455/bcp.20151016123639

120. Buber, A.; Basay, B.; Basay, O.; Ozturk, O.; Alacam, H.; Yazici, K.; Bacanli, A.; Ay, M.; Erdal, M.; Herken, H. Synapsin Polymorphisms Could Be Correlated with Stroop Simple Reaction Time Scores. AMERICAN JOURNAL OF MOLECULAR BIOLOGY, 2016, 06, 25-32. 100 + 0
http://dx.doi.org/10.4236/ajmb.2016.61003

119. Yılmaz, .; Erdal, M.; özge, A.; Sungur, M. Can Peripheral MicroRNA Expression Data Serve as Epigenomic (Upstream) Biomarkers of Alzheimer's Disease?. OMICS: A JOURNAL OF INTEGRATIVE BIOLOGY, 2016, 20, 456-461. 850 + 0
http://dx.doi.org/10.1089/omi.2016.0099

118. Ozturk, O.; Alacam, H.; Basay, B.; Basay, O.; Buber, A.; Ay, O.; Agladioglu, K.; Erdal, M.; Herken, H. The Effect of Single Dose Methylphenidate on Neurometabolites according to COMT Gene Val158Met Polymorphism in the Patient with Attention Deficit Hyperactivity Disorder: A Study Using Magnetic Resonance Spectroscopy. CLINICAL PSYCHOPHARMACOLOGY AND NEUROSCIENCE, 2016, 14, 184-193. 100 + 0
https://dx.doi.org/10.9758/cpn.2016.14.2.184

117. Basay, B.; Buber, A.; Basay, O.; Alacam, H.; Ozturk, O.; Suren, S.; Ay, O.; Acikel, C.; Agladioglu, K.; Erdal, M. White matter alterations related to attention-deficit hyperactivity disorder and COMT val(158)met polymorphism: children with valine homozygote attention-deficit hyperactivity disorder have altered white matter connectivity in the right cingulum (cingulate gyrus). NEUROPSYCHIATRIC DISEASE AND TREATMENT, 2016, 12, 969-981. 100 + 0
https://dx.doi.org/10.2147/NDT.S104450

116. Savaşoğlu, K.; Erdal, M. Association of MMP-2 (-1306 C>T), MMP-9 (-1562 C>T) Gene Polymorphism and the Formation of the Hematological Malignancies. . IRANIAN JOURNAL OF PUBLIC HEALTH, 2016, 45, 392-393. 500 + 0
http://ijph.tums.ac.ir/index.php/ijph/article/view/6275/4653

115. Camkurt, M.; Karababa, F.; Erdal, M.; Bayazıt, H.; Kandemir, S.; Ay, M.; Kandemir, H.; Ay, .; çiçek, E.; Selek, S. Investigation of Dysregulation of Several MicroRNAs in Peripheral Blood of Schizophrenia Patients. CLINICAL PSYCHOPHARMACOLOGY AND NEUROSCIENCE, 2016, 14, 256-260. 450 + 0
http://dx.doi.org/10.9758/cpn.2016.14.3.256

2015
114. Sen, A.; Arslan, M.; Erdal, M.; Ay, O.; Yilmaz, S.; Kurt, E.; Arpaci, B. LACK OF ASSOCIATIONS BETWEEN CLU AND PICALM GENE POLYMORPHISMS AND ALZHEIMER'S DISEASE IN A TURKISH POPULATION. IDEGGYOGYASZATI SZEMLE-CLINICAL NEUROSCIENCE, 2015, 68, 113-120. 600 + 0
Publications_024.pdf

113. Altintas, Z.; Ucbilek, E.; Erdal, M.; Sezgin, O.; Altintas, E. Methylation and Expression of the Genes That Have a Role in the Wnt Signaling Pathway in Ulcerative Colitis. GASTROENTEROLOGY, 2015, 148, S694-S694. 700 + 0
112. Dasdag, S.; Akdag, M.; Erdal, M.; Erdal, N.; Ay, O.; Ay, M.; Yilmaz, S.; Tasdelen, B.; Yegin, K. Long term and excessive use of 900 MHz radiofrequency radiation alter microRNA expression in brain. INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 2015, 91, 306-311. 500 + 0
https://dx.doi.org/10.3109/09553002.2015.997896

111. Terzi, E.; Bulut, B.; Tursen, U.; Kaya, T.; Tursen, B.; Erdal, M.; Yilmaz, S. Microchimerism in alopecia areata. INTERNATIONAL JOURNAL OF DERMATOLOGY, 2015, 54, E448-E452. 300 + 0
https://dx.doi.org/10.1111/ijd.12795

110. Kayar, N.; Alptekin, N.; Erdal, M. Interleukin-1 receptor antagonist gene polymorphism, adverse pregnancy outcome and periodontitis in Turkish women. ARCHIVES OF ORAL BIOLOGY, 2015, 60, 1777-1783. 1000 + 0
https://dx.doi.org/10.1016/j.archoralbio.2015.09.013

109. Ay, O.; Ay, M.; Erdal, M.; Cayan, F.; Tekin, S.; Soylemez, F.; Sungur, M.; Yildirim, D. Folate Metabolism Gene Polymorphisms and Risk for Down Syndrome Offspring in Turkish Women. GENETIC TESTING AND MOLECULAR BIOMARKERS, 2015, 19, 191-197. 550 + 0
https://dx.doi.org/10.1089/gtmb.2014.0262

108. Zamani, A.; Erdal, M.; Dursun, H.; Ay, O.; Ural, O.; Edgunlu, T.; Tuncez, E.; Yildirim, M. Evaluation of TLR2 and TLR4 Polymorphisms in Chronic HBV Infection. BRITISH JOURNAL OF MEDICINE AND MEDICAL RESEARCH, 2015, 7, 195-202. 650 + 0
http://dx.doi.org/10.9734/BJMMR/2015/10648

107. Dasdag, S.; Akdag, M.; Erdal, M.; Erdal, N.; Ay, O.; Ay, M.; Yilmaz, S.; Tasdelen, B.; Yegin, K. Effects of 2.4 GHz radiofrequency radiation emitted from Wi-Fi equipment on microRNA expression in brain tissue. INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 2015, 91, 555-561. 500 + 5
https://dx.doi.org/10.3109/09553002.2015.1028599


Times Cited: 1
106. Gedik, H.; Erdal, M.; Yilmaz, S.; Sengul, C.; Sengul, C.; Herken, H. Association of microRNA Biogenesis Pathway Gene Variants and Alcohol Dependence Risk. DNA AND CELL BIOLOGY, 2015, 34, 220-226. 750 + 0
https://dx.doi.org/10.1089/dna.2014.2549

105. Tombak, A.; Ay, O.; Erdal, M.; Sungur, M.; Ucar, M.; Akdeniz, A.; Tiftik, E. MicroRNA Expression Analysis in Patients with Primary Myelofibrosis, Polycythemia vera and Essential Thrombocythemia. INDIAN JOURNAL OF HEMATOLOGY AND BLOOD TRANSFUSION, 2015, 31, 416-425. 600 + 5
https://dx.doi.org/10.1007/s12288-014-0492-z


Times Cited: 1
104. Kandemir, H.; Erdal, M.; Selek, S.; Ay, O.; Karababa, I.; Ay, M.; Kandemir, S.; Yilmaz, S.; Ekinci, S.; Tasdelen, B. Microribonucleic acid dysregulations in children and adolescents with obsessive-compulsive disorder. NEUROPSYCHIATRIC DISEASE AND TREATMENT, 2015, 11, 1695-1701. 550 + 0
https://dx.doi.org/10.2147/NDT.S81884

2014
103. Alp, R.; Guney, A.; Tursen, U.; Kaya, T.; Tursen, B.; Erdal, M. Microchimerism in Behcet's disease. INTERNATIONAL JOURNAL OF DERMATOLOGY, 2014, 53, 832-837. 400 + 10
https://dx.doi.org/10.1111/j.1365-4632.2012.05804.x


Times Cited: 2
102. Herken, H.; Erdal, M.; Kenar, A.; Unal, G.; Cakaloz, B.; Ay, M.; Yucel, E.; Edgunlu, T.; Sengul, C. Association of SNAP-25 Gene Ddel and Mnll Polymorphisms with Adult Attention Deficit Hyperactivity Disorder. PSYCHIATRY INVESTIGATION, 2014, 11, 476-480. 600 + 10
https://dx.doi.org/10.4306/pi.2014.11.4.476


Times Cited: 2
101. Balkan, M.; Atar, M.; Erdal, M.; Rustemoglu, A.; Yildiz, I.; Gunesacar, R.; Hatipoglu, N.; Bodakci, M.; Ay, O.; Cevik, K. Possible Association of FAS and FASLG Polymorphisms with the Risk of Idiopathic Azoospermia in Southeast Turkey. GENETIC TESTING AND MOLECULAR BIOMARKERS, 2014, 18, 383-388. 450 + 0
https://dx.doi.org/10.1089/gtmb.2013.0454

100. Sengul, M.; Sengul, C.; Erdal, M.; Ay, O.; Efe, M.; Ay, M.; Herken, H. Association of the DRD2 TaqIA, 5-HT1B A-161T, and CNR1 1359 G/A Polymorphisms with Alcohol Dependence. KLINIK PSIKOFARMAKOLOJI BULTENI-BULLETIN OF CLINICAL PSYCHOPHARMACOLOGY, 2014, 24, 115-121. 600 + 0
https://dx.doi.org/10.5455/bcp.20131229022915

99. Kandemir, H.; Erdal, M.; Selek, S.; Ay, O.; Karababa, I.; Kandemir, S.; Ay, M.; Yilmaz, S.; Bayazit, H.; Tasdelen, B. Evaluation of several micro RNA (miRNA) levels in children and adolescents with attention deficit hyperactivity disorder. NEUROSCIENCE LETTERS, 2014, 580, 158-162. 550 + 0
https://dx.doi.org/10.1016/j.neulet.2014.07.060

98. Kandemir, H.; Erdal, M.; Selek, S.; Ay, .; Karababa, .; Kandemir, S.; Ay, M.; Yılmaz, .; Bayazıt, H.; Taşdelen, B. Evaluation of several micro RNA (miRNA) levels in children and adolescents with attention deficit hyperactivity disorder. NEUROSCIENCE LETTERS, 2014, 580, 158-162. 550 + 5
http://dx.doi.org/10.1016/j.neulet.2014.07.060


Times Cited: 1
97. Edgnulu, T.; Ozge, A.; Erdal, N.; Kuru, O.; Erdal, M. Association Analysis of the Functional MAOA Gene Promoter and MAOB Gene Intron 13 Polymorphisms in Tension Type Headache Patients. ADVANCES IN CLINICAL AND EXPERIMENTAL MEDICINE, 2014, 23, 901-906. 500 + 0
http://www.advances.umed.wroc.pl/pdf/2014/23/6/901.pdf

96. Kenar, A.; Ay, O.; Herken, H.; Erdal, M. Association of VAMP-2 and Syntaxin 1A Genes with Adult Attention Deficit Hyperactivity Disorder. PSYCHIATRY INVESTIGATION, 2014, 11, 76-83. 650 + 20
https://dx.doi.org/10.4306/pi.2014.11.1.76


Times Cited: 4
95. Altintas, E.; Altintas, Z.; Sezgin, O.; Ucbilek, E.; Nayir, E.; Erdal, M.; Polat, A.; Orekeci, G. Polymorphisms in methylenetetrahydrofolate reductase gene: Their impact on liver steatosis and fibrosis of chronic hepatitis c patients. SCIENTIFIC RESEARCH PUBLISHING, INC,, 2014, 04, 73-80. 250 + 0
http://dx.doi.org/10.4236/ojgas.2014.42013

94. Shearer, A.; Eppsteiner, R.; Booth, K.; Ephraim, S.; Gurrola, J.; Simpson, A.; Black-ziegelbein, E.; Joshi, S.; Ravi, H.; Erdal, M. Utilizing Ethnic-Specific Differences in Minor Allele Frequency to Recategorize Reported Pathogenic Deafness Variants. AMERICAN JOURNAL OF HUMAN GENETICS, 2014, 95, 445-453. 100 + 40
https://dx.doi.org/10.1016/j.ajhg.2014.09.001


Times Cited: 8
93. Edgnülü, T.; özge, A.; Erdal, N.; Kuru, O.; Erdal, M. Association Analysis of the Functional MAOA Gene Promoter and MAOB Gene Intron 13 Polymorphisms in Tension Type Headache Patients. WROCLAW MEDICAL UNIVERSITY, 2014, 23, 901-906. 500 + 0
http://dx.doi.org/10.17219/acem/37333

2013
92. Zamani, A.; Barlas, I.; Durakbasi-dursun, G.; Ural, O.; Erdal, M.; Yildirim, M. Evaluation of death pathway genes FAS and FASL polymorphisms in chronic HBV infection. INTERNATIONAL JOURNAL OF IMMUNOGENETICS, 2013, 40, 482-487. 450 + 5
https://dx.doi.org/10.1111/iji.12056

Publications_003.pdf


Times Cited: 1
91. Alasehirli, B.; Akcali, A.; Demiryurek, A.; Ozel, A.; Erdal, M.; Neyal, M. Lack of Association Between the C276T Polymorphism of the Neuronal Nitric Oxide Synthase Gene and Migraine. INTERNATIONAL JOURNAL OF NEUROSCIENCE, 2013, 123, 50-54. 450 + 5
https://dx.doi.org/10.3109/00207454.2012.724743


Times Cited: 1
90. Ulger, M.; Emekdas, G.; Aslan, G.; Tas, D.; ılvan, A.; Tezcan, S.; Calikoglu, M.; Erdal, M.; Kartaloglu, Z. Determination of the Cytokine Gene Polymorphism and Genetic Susceptibility in Tuberculosis Patients. MIKROBIYOLOJI BULTENI, 2013, 47, 250-264. 100 + 20
Publications_020.pdf


Times Cited: 4
89. Sezgin, M.; Barlas, I.; Yildir, S.; Turkoz, G.; Ankarah, H.; Sahin, G.; Erdal, M. Apoptosis-related Fas and FasL gene polymorphisms' associations with knee osteoarthritis. RHEUMATOLOGY INTERNATIONAL, 2013, 33, 2039-2043. 200 + 5
https://dx.doi.org/10.1007/s00296-013-2688-1


Times Cited: 1
88. Kenar, A.; Edgunlu, T.; Herken, H.; Erdal, M. Association of Synapsin III Gene with Adult Attention Deficit Hyperactivity Disorder. DNA AND CELL BIOLOGY, 2013, 32, 430-434. 650 + 0
https://dx.doi.org/10.1089/dna.2012.1937

87. Kurtulus, P.; Tursen, U.; Erdal, M. Microchimerism in vitiligo. JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 2013, 27, 795-796. 1000 + 5
https://dx.doi.org/10.1111/j.1468-3083.2012.04657.x


Times Cited: 1
86. Edgunlu, T.; Ozge, A.; Yalin, O.; Kul, S.; Erdal, M. A Study of the Impact of Death Receptor 4 (DR4) Gene Polymorphisms in Alzheimer's Disease. BALKAN MEDICAL JOURNAL, 2013, 30, 268-272. 500 + 15
https://dx.doi.org/10.5152/balkanmedj.2013.7455


Times Cited: 3
85. Yildir, S.; Sezgin, M.; Barlas, I.; Turkoz, G.; Ankarali, H.; Sahin, G.; Erdal, M. Relation of the Fas and FasL gene polymorphisms with susceptibility to and severity of rheumatoid arthritis. RHEUMATOLOGY INTERNATIONAL, 2013, 33, 2637-2645. 200 + 25
https://dx.doi.org/10.1007/s00296-013-2793-1


Times Cited: 5
2012
84. Barlas, I.; Semiz, U.; Erdal, M.; Algul, A.; Ay, O.; Ates, M.; Camdeviren, H.; Basoglu, C.; Herken, H. Association between dopamine beta hydroxylase gene polymorphism and age at onset in male schizophrenia. ACTA NEUROPSYCHIATRICA, 2012, 24, 176-182. 500 + 5
https://dx.doi.org/10.1111/j.1601-5215.2011.00617.x


Times Cited: 1
83. Edgunlu, T.; Ozge, A.; Yalin, O.; Kul, S.; Erdal, M. Genetic Variants of Synaptic Vesicle and Presynaptic Plasma Membrane Proteins In Alzheimer's Disease. NOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY, 2012, 49, 294-299. 500 + 0
https://dx.doi.org/10.4274/npa.y6244

82. Varma, G.; Karadag, F.; Erdal, M.; Ay, O.; Aydin, E.; Edgunlu, T.; Herken, H. The relationship DRD3 Ser9Gly polymorphisms and cognitive functions in schizophrenia: a preliminary study. ANADOLU PSIKIYATRI DERGISI-ANATOLIAN JOURNAL OF PSYCHIATRY, 2012, 13, 184-190. 600 + 0
Publications_022.pdf

81. Sengul, C.; Erdal, M.; Sengul, C.; Ay, O.; Efe, M.; Ay, M.; Herken, H. ASSOCIATION OF THE DRD2 TAQIA, 5-HT1B A-161T AND CNR1 1359 G/A POLYMORPHISMS WITH ALCOHOL DEPENDENCE: A SINGLE CENTER EXPERIENCE IN DENIZLI PROVINCE OF TURKEY. EUROPEAN PSYCHIATRY, 2012, 27, 0-0. 350 + 0
Publications_021.pdf

2011
80. Basoglu, C.; Oner, O.; Ates, A.; Algul, A.; Bez, Y.; Cetin, M.; Herken, H.; Erdal, M.; Munir, K. Synaptosomal-Associated Protein 25 Gene Polymorphisms and Antisocial Personality Disorder: Association With Temperament and Psychopathy. CANADIAN JOURNAL OF PSYCHIATRY-REVUE CANADIENNE DE PSYCHIATRIE, 2011, 56, 341-347. 100 + 25
Publications_010.pdf


Times Cited: 5
79. Urhan-kucuk, M.; Erdal, M.; Ozen, M.; Kul, S.; Herken, H. Is the dopamine D3 receptor mRNA on blood lymphocytes help to for identification and subtyping of schizophrenia?. MOLECULAR BIOLOGY REPORTS, 2011, 38, 2569-2572. 800 + 10
https://dx.doi.org/10.1007/s11033-010-0396-4


Times Cited: 2
78. Virit, O.; Erdal, M.; Savas, H.; Barlas, I.; Yumru, M.; Gokdogan, T.; Ozen, M.; Herken, H. Catechol-O-methyltransferase gene Val108/158Met polymorphism in bipolar disorder. NEUROLOGY PSYCHIATRY AND BRAIN RESEARCH, 2011, 17, 46-50. 650 + 0
https://dx.doi.org/10.1016/j.npbr.2011.02.002

77. Varma, G.; Karadag, F.; Erdal, M.; Ay, O.; Levent, N.; Tekkanat, C.; Gokdogan, T.; Herken, H. Effects of catechol-O-methyltransferase enzyme Val158Met polymorphism on cognitive functions in schizophrenic patients. KLINIK PSIKOFARMAKOLOJI BULTENI-BULLETIN OF CLINICAL PSYCHOPHARMACOLOGY, 2011, 21, 24-32. 550 + 5
Publications_009.pdf


Times Cited: 1
76. Oner, O.; Akin, A.; Herken, H.; Erdal, M.; Ciftci, K.; Ay, M.; Bicer, D.; Oncu, B.; Bozkurt, O.; Muenir, K. Association Among SNAP-25 Gene DdeI and MnlI Polymorphisms and Hemodynamic Changes During Methylphenidate Use: A Functional Near-Infrared Spectroscopy Study. JOURNAL OF ATTENTION DISORDERS, 2011, 15, 628-637. 350 + 25
https://dx.doi.org/10.1177/1087054710374597


Times Cited: 5
2010
75. Deniz, M.; Bayazit, Y.; Celenk, F.; Karabulut, H.; Yilmaz, A.; Gunduz, B.; Saridogan, C.; Dagli, M.; Erdal, M.; Menevse, A. Significance of Serotonin Transporter Gene Polymorphism in Tinnitus. OTOLOGY & NEUROTOLOGY, 2010, 31, 19-24. 100 + 20
https://dx.doi.org/10.1097/MAO.0b013e3181c2dcbc


Times Cited: 4
74. Sengul, C.; Erdal, M.; Aydin, N.; Sengul, C.; Barlas, O.; Aynacioglu, S.; Herken, H. The relation between IRS-1 Gly972Arg (insulin receptor substrate) gene polymorphism and olanzapine induced weight gain. ANADOLU PSIKIYATRI DERGISI-ANATOLIAN JOURNAL OF PSYCHIATRY, 2010, 11, 18-22. 700 + 5
Publications_012.pdf


Times Cited: 1
73. ısi, H.; Oral, D.; Yildiz, T.; Ates, G.; Sinir, C.; Ay, O.; Turkoz, G.; Erdal, M. THE TUMOR NECROSIS FACTOR-A-308 G/A POLYMORPHISM AND THE TUMOR NECROSIS FACTOR-RELATED APOPTOSIS-INDUCING LIGAND POLYMORPHISMS, IN ASTHMATIC PATIENTS AND HEALTHY SUBJECTS. BIOTECHNOLOGY & BIOTECHNOLOGICAL EQUIPMENT, 2010, 24, 1638-1643. 100 + 5
https://dx.doi.org/10.2478/V10133-010-0018-2


Times Cited: 1
72. Balkan, M.; Gedik, A.; Akkoc, H.; Ay, O.; Erdal, M.; ısi, H.; Budak, T. FSHR Single Nucleotide Polymorphism Frequencies in Proven Fathers and Infertile Men in Southeast Turkey. JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY, 2010, Article ID: 640318. 400 + 70
https://dx.doi.org/10.1155/2010/640318


Times Cited: 14
71. Sevinc, E.; Erdal, M.; Sengul, C.; Cakaloz, B.; Ergundu, T.; Herken, H. Association of Adult Attention Deficit Hyperactivity Disorder With Dopamine Transporter Gene, Dopamine D3 Receptor, and Dopamine D4 Receptor Gene Polymorphisms. KLINIK PSIKOFARMAKOLOJI BULTENI-BULLETIN OF CLINICAL PSYCHOPHARMACOLOGY, 2010, 20, 196-203. 750 + 0
Publications_011.pdf

70. Sengul, C.; Erdal, M.; Aydin, N.; Sengul, C.; Barlas, O.; Aynacioglu, S.; Herken, H. The relation between IRS-1 Gly972Arg (insulin receptor substrate) gene polymorphism and olanzapine induced weight gain. ANADOLU PSIKIYATRI DERGISI-ANATOLIAN JOURNAL OF PSYCHIATRY, 2010, 11, 18-22. 700 + 5

Times Cited: 1
69. Cakmak, S.; Ozge, A.; Ucbilek, E.; Sezgin, O.; Soylemez, F.; Erdal, E.; Temel, G.; Kanik, E. The investigation of common clinical and genetic indicators of migraine, episodic tension type headache and irritable bowel syndrome. JOURNAL OF HEADACHE AND PAIN, 2010, 11, S44-S45. 0 + 0
68. ısi, H.; Erdal, M.; Akdeniz, S.; Oral, D.; Ay, O.; Tekes, S.; Sula, B.; Edgunlu, T.; Balkan, M.; Budak, T. THE TUMOR NECROSIS FACTOR-A (TNF-A) GENE-308 G/A POLYMORPHISM AND THE TUMOR NECROSIS FACTOR-RELATED APOPTOSIS-INDUCING LIGAND (TRAIL) GENE POLYMORPHISMS IN BEHCET'S DISEASE. BIOTECHNOLOGY & BIOTECHNOLOGICAL EQUIPMENT, 2010, 24, 2014-2019. 550 + 0
https://dx.doi.org/10.2478/V10133-010-0055-X

67. Yilmaz, I.; Ozge, A.; Erdal, M.; Edgunlu, T.; Cakmak, S.; Yalin, O. Cytokine Polymorphism in Patients with Migraine: Some Suggestive Clues of Migraine and Inflammation. PAIN MEDICINE, 2010, 11, 492-497. 650 + 110
Publications_013.pdf


Times Cited: 22
66. Ozen, M.; Yumru, M.; Erdal, M.; Herken, H.; Savas, H. A Sex-Related Genetic Difference in Bipolar Disorder: Tryptophan Hydroxylase 1 Gene 218 A > C Polymorphism. NOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY, 2010, 47, 96-100. 700 + 5
https://dx.doi.org/10.4274/npa.5326


Times Cited: 1
2009
65. Sengul, C.; Erdal, E.; Herken, H.; Aydin, N.; Karadag, F.; Barlas, O.; Ergundu, T. Synaptosomal-associated protein (SNAP-25) polymorphisms and response to olanzapine in schizophrenia patients. KLINIK PSIKOFARMAKOLOJI BULTENI-BULLETIN OF CLINICAL PSYCHOPHARMACOLOGY, 2009, 19, S145-S146. 0 + 0
64. Kaleagasi, H.; Edgunlu, T.; Erdal, M.; Dogu, O. The ARG399GLN Polymorphism in DNA Repair Gene XRCC1 Does Not Alter Risk of Parkinson's Disease. JOURNAL OF NEUROLOGICAL SCIENCES-TURKISH, 2009, 26, 185-189. 750 + 0
63. Barlas, I.; Cetin, M.; Erdal, M.; Semiz, U.; Basoglu, C.; Ay, M.; Herken, H.; Uzun, O. Lack of Association Between DRD3 Gene Polymorphism and Response to Clozapine in Turkish Schizoprenia Patients. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2009, 150B, 56-60. 550 + 45
https://dx.doi.org/10.1002/ajmg.b.30770


Times Cited: 9
62. Bayazit, Y.; Yilmaz, M.; Erdal, M.; Ciftci, T.; Ceylan, A.; Kokturk, O.; Celenk, F.; Kemaloglu, Y. Role of nitric oxide synthase gene intron 4 and exon 7 polymorphisms in obstructive sleep apnea syndrome. EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY, 2009, 266, 449-454. 550 + 30
https://dx.doi.org/10.1007/s00405-008-0763-0


Times Cited: 6
61. Varma, S.; Karadag, F.; Erdal, M.; Tekkanat, C.; ınciay, O.; Tumkaya, S.; Gokdogan, T.; Levent, N.; Herken, H. Role of serotonine transporter gene polymorphism in cognitive functions in patients with schizophrenia. KLINIK PSIKOFARMAKOLOJI BULTENI-BULLETIN OF CLINICAL PSYCHOPHARMACOLOGY, 2009, 19, S19-S23. 500 + 0
60. Herken, H.; Erdal, E.; Sengul, C.; Yucel, E.; Cakaloz, B.; Kenar, A.; Ay, E.; Ergundu, T. Attention deficit hyperactivity disorder associaton with synaptosomal-associated protein (snap-25) polymorphisms. KLINIK PSIKOFARMAKOLOJI BULTENI-BULLETIN OF CLINICAL PSYCHOPHARMACOLOGY, 2009, 19, S142-S143. 0 + 0
59. Herken, H.; Erdal, M.; Aydin, N.; Sengul, C.; Karadag, F.; Barlas, O.; Akin, F. The Association of Olanzapine-Induced Weight Gain with Peroxisome Proliferator-Activated Receptor-gamma 2 Pro12Ala Polymorphism in Patients with Schizophrenia. DNA AND CELL BIOLOGY, 2009, 28, 515-519. 700 + 95
https://dx.doi.org/10.1089/dna.2009.0893


Times Cited: 19
58. Barlas, I.; Sezgin, M.; Erdal, M.; Sahin, G.; Ankarali, H.; Altintas, Z.; Tuerkmen, E. Association of (1,607) 1G/2G polymorphism of matrix metalloproteinase-1 gene with knee osteoarthritis in the Turkish population (knee osteoarthritis and MMPs gene polymorphisms). RHEUMATOLOGY INTERNATIONAL, 2009, 29, 383-388. 600 + 65
https://dx.doi.org/10.1007/s00296-008-0705-6


Times Cited: 13
2008
57. Gursoy, S.; Erdal, M.; Alasehirli, B.; Aydeniz, A.; Erdal, N. TaqI polymorphism of the vitamin-D receptor gene and quality of life in postmenopausal Turkish women. TURKISH JOURNAL OF MEDICAL SCIENCES, 2008, 38, 21-26. 800 + 0
56. Sezgin, M.; Barlas, I.; Ankarali, H.; Altintas, Z.; Turkmen, E.; Gokdogan, T.; Sahin, G.; Erdal, M. Tumour necrosis factor alpha-308G/A gene polymorphism: lack of association with knee osteoarthritis in a Turkish population. CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 2008, 26, 763-768. 100 + 25

Times Cited: 5
55. Baz, K.; Erdal, M.; Yazici, A.; Soylemez, F.; Guvenc, U.; Tasdelen, B.; ıkizoglu, G. Association between tumor necrosis factor-alpha gene promoter polymorphism at position-308 and acne in Turkish patients. ARCHIVES OF DERMATOLOGICAL RESEARCH, 2008, 300, 371-376. 700 + 90
https://dx.doi.org/10.1007/s00403-008-0871-0


Times Cited: 18
54. Kirtak, N.; ınaloz, H.; Akcali, C.; Erdal, M.; Herken, H.; Yildirim, M.; Erguven, H. Association of serotonin transporter gene-linked polymorphic region and variable number of tandem repeat polymorphism of the serotonin transporter gene in lichen simplex chronicus patients with psychiatric status. INTERNATIONAL JOURNAL OF DERMATOLOGY, 2008, 47, 1069-1072. 500 + 5
https://dx.doi.org/10.1111/j.1365-4632.2008.03821.x


Times Cited: 1
53. Sengul, C.; Erdal, M.; Aydin, N.; Karadag, F.; Ay, O.; Sengul, M.; Aynacioglu, S.; Herken, H. Effects of drd3 and dat gene polymorphisms on schizophrenia and response to olanzapine. EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2008, 18, S406-S407. 650 + 0
https://dx.doi.org/10.1016/S0924-977X(08)70589-3

52. Gursoy, S.; Erdal, M.; Sezgin, M.; Barlas, I.; Aydeniz, A.; Alasehirli, B.; Sahin, G. Which genotype of MAO gene that the patients have are likely to be most susceptible to the symptoms of fibromyalgia?. RHEUMATOLOGY INTERNATIONAL, 2008, 28, 307-311. 700 + 50
https://dx.doi.org/10.1007/s00296-007-0454-y


Times Cited: 10
51. Etoz, O.; Ataoglu, H.; Erdal, M. Association between tryptophan hydroxylase gene polymorphism and painful non-osseous temporomandibular disorders. SAUDI MEDICAL JOURNAL, 2008, 29, 1352-1354. 1000 + 20

Times Cited: 4
2007
50. Sezgin, M.; Erdal, M.; Altintas, Z.; Ankarali, H.; Barlas, I.; Turkmen, E. Lack of association polymorphisms of the IL1RN, IL1A, and IL1B genes with knee osteoarthritis in Turkish patients. CLINICAL AND INVESTIGATIVE MEDICINE, 2007, 30, 86-92. 750 + 55
Publications_023.pdf


Times Cited: 11
49. Sengull, C.; Herken, H.; Erdal, M.; Aydin, N.; Barlas, O.; Aynacioglu, S.; Basdemir, M. The relation between insulin receptor substrate-1 gene and olanzapine-induced weight gain and smoking in schizophrenia patients. EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2007, 17, S433-S433. 600 + 0
https://dx.doi.org/10.1016/S0924-977X(07)70653-3

48. Demiralp, T.; Herrmann, C.; Erdal, M.; Ergenoglu, T.; Keskin, Y.; Ergen, M.; Beydagi, H. DRD4 and DAT1 polymorphisms modulate human gamma band responses. CEREBRAL CORTEX, 2007, 17, 1007-1019. 600 + 275
https://dx.doi.org/10.1093/cereor/bhl011


Times Cited: 55
47. Erdal, N.; Herken, H.; Yilmaz, M.; Erdal, M.; Bayazit, Y. The A218C polymorphism of tryptophan hydroxylase gene and migraine. JOURNAL OF CLINICAL NEUROSCIENCE, 2007, 14, 249-251. 600 + 30
https://dx.doi.org/10.1016/j.jocn.2006.04.018


Times Cited: 6
46. Ay, M.; Ay, I.; Soylemez, F.; Erdal, M. Deletion of 8p: a case of a child with multiple congenital anomalies. CHROMOSOME RESEARCH, 2007, 15, 62-62. 650 + 0
45. Bayazit, Y.; Yilmaz, M.; Kokturk, O.; Erdal, M.; Ciftci, T.; Gokdogan, T.; Kemaloglu, Y.; ıleri, F. Association of GABA(B)R1 receptor gene polymorphism with obstructive sleep apnea syndrome. ORL-JOURNAL FOR OTO-RHINO-LARYNGOLOGY AND ITS RELATED SPECIALTIES, 2007, 69, 190-197. 450 + 25
https://dx.doi.org/10.1159/000099230


Times Cited: 5
2006
44. Tok, E.; Ertunc, D.; Bilgin, O.; Erdal, M.; Kaplanoglu, M.; Dilek, S. PPAR-gamma 2 Pro12Ala polymorphism is associated with weight gain in women with gestational diabetes mellitus. EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 2006, 129, 25-30. 550 + 85
https://dx.doi.org/10.1016/j.ejogrb.2006.03.016


Times Cited: 17
43. Ozturk, O.; Erdal, M.; Zoroglu, S.; Alasehirli, B.; Yuce, M. Association analysis of the functional monoamine oxidase a gene promoter (MAO-LPR) polymorphism in attention-dericit/hyperactivity disorder in a Turkish sample. NEUROLOGY PSYCHIATRY AND BRAIN RESEARCH, 2006, 13, 65-70. 800 + 0
42. Ergenoglu, T.; Herrmann, C.; Erdal, M.; Keskin, Y.; Ergen, M.; Beydagi, H.; Demiralp, T. Polymorphisms of DRD4 and DAT1 modulate human gamma band responses. INTERNATIONAL JOURNAL OF PSYCHOPHYSIOLOGY, 2006, 61, 377-377. 600 + 0
41. Herken, H.; Erdal, M.; Cetin, M.; Barlas, O.; Basoglu, C.; Uzun, O.; Selek, S.; Gokdogan, T. Association between 5-HT2A receptor gene T102C and 1438G/apolymorphism and clozapine treatment response. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2006, 141B, 786-787. 650 + 0
40. Tok, E.; Ertunc, D.; Bilgin, O.; Erdal, M.; Kaplanogtu, M.; Dilek, S. Association of insulin receptor substrate-1 G972R variant with baseline characteristics of the patients with gestational diabetes mellitus. AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2006, 194, 868-872. 550 + 55
https://dx.doi.org/10.1016/j.ajog.2005.08.067


Times Cited: 11
39. Bayazit, Y.; Erdal, M.; Yilmaz, M.; Ciftci, T.; Soylemez, F.; Gokdogan, T.; Kokturk, O.; Kemaloglu, Y.; Koybasioglu, A. Insulin receptor substrate gene polymorphism is associated with obstructive sleep apnea syndrome in men. LARYNGOSCOPE, 2006, 116, 1962-1965. 600 + 30
https://dx.doi.org/10.1097/01.mlg.0000235933.74319.80


Times Cited: 6
38. Yazici, A.; Erdal, M.; Kaya, T.; ıkizoglu, G.; Savasoglu, K.; Camdeviren, H.; Tursen, U. Lack of association with TNF-alpha-308 promoter polymorphism in patients with vitiligo. ARCHIVES OF DERMATOLOGICAL RESEARCH, 2006, 298, 46-49. 700 + 50
https://dx.doi.org/10.1007/s00403-006-0664-2


Times Cited: 10
2005
37. Erdal, N.; Erdal, M.; Gurgul, S. Lack of effect of extremely low frequency electromagnetic fields on cyclin-dependent kinase 4 inhibitor gene p18(INK4C) in electric energy workers. ARCHIVES OF MEDICAL RESEARCH, 2005, 36, 120-123. 1000 + 0
https://dx.doi.org/10.1016/j.arcmed.2004.12.015

36. Yilmaz, M.; Bayazit, Y.; Ciftci, T.; Erdal, M.; Urhan, M.; Kokturk, O.; Kemaloglu, Y.; ınal, E. Association of serotonin transporter gene polymorphism with obstructive sleep apnea syndrome. LARYNGOSCOPE, 2005, 115, 832-836. 450 + 30
https://dx.doi.org/10.1097/01.MLG.0000157334.88700.E6


Times Cited: 6
35. Ertunc, D.; Tok, E.; Aktas, A.; Erdal, M.; Dilek, S. The importance of IRS-1 Gly972Arg polymorphism in evaluating the response to metformin treatment in polycystic ovary syndrome. HUMAN REPRODUCTION, 2005, 20, 1207-1212. 600 + 90
https://dx.doi.org/10.1093/humrep/deh747


Times Cited: 18
34. Tok, E.; Aktas, A.; Ertunc, D.; Erdal, M.; Dilek, S. Evaluation of glucose metabolism and reproductive hormones in polycystic ovary syndrome on the basis of peroxisome proliferator-activated receptor (PPAR)-gamma 2 Pro12Ala genotype. HUMAN REPRODUCTION, 2005, 20, 1590-1595. 600 + 140
https://dx.doi.org/10.1093/humrep/deh769


Times Cited: 28
33. Dilek, S.; Ertunc, D.; Tok, E.; Erdal, M.; Aktas, A. Association of Gly972Arg variant of insulin receptor substrate-1 with metabolic features in women with polycystic ovary syndrome. FERTILITY AND STERILITY, 2005, 84, 407-412. 600 + 110
https://dx.doi.org/10.1016/j.fertnstert.2005.01.133


Times Cited: 22
2004
32. Mutlu, N.; Erdal, M.; Herken, H.; Oz, G.; Bayazit, Y. T102C polymorphism of the 5-HT2A receptor gene may be associated with temporomandibular dysfunction. ORAL DISEASES, 2004, 10, 349-352. 800 + 95
https://dx.doi.org/10.1111/j.1601-0825.2004.01037.x


Times Cited: 19
31. Pata, C.; Erdal, M.; Yazici, K.; Camdeviren, H.; Ozkaya, M.; Ulu, O. Association of the -1438 G/A and 102 T/C polymorphism of the 5-Ht2A receptor gene with irritable bowel syndrome 5-Ht2A gene polymorphism in irritable bowel syndrome. JOURNAL OF CLINICAL GASTROENTEROLOGY, 2004, 38, 561-566. 750 + 165
https://dx.doi.org/10.1097/00004836-200408000-00005


Times Cited: 33
30. Erdal, M.; Tursen, U.; Kaya, T.; Kanik, A.; Derici, E.; ıkizoglu, G. Association between Cathechol-O-Metyltransferase polymorphism and psoriasis. INTERNATIONAL JOURNAL OF DERMATOLOGY, 2004, 43, 312-314. 850 + 5
https://dx.doi.org/10.1111/j.1365-4632.2004.01992.x


Times Cited: 1
2003
29. Tot, S.; Erdal, M.; Yazici, K.; Yazici, A.; Metin, O. T102C and-1438 G/A polymorphisms of the 5-HT2A receptor gene in Turkish patients with obsessive-compulsive disorder. EUROPEAN PSYCHIATRY, 2003, 18, 249-254. 800 + 130
https://dx.doi.org/10.1016/S0924-9338(03)00066-X


Times Cited: 26
28. Hasan, H.; Erdal, M.; Boke, O.; Savas, H. Tardive dyskinesia is not associated with the polymorphisms of 5-HT2A receptor gene, serotonin transporter gene and catechol-o-methyltransferase gene. EUROPEAN PSYCHIATRY, 2003, 18, 77-81. 850 + 0
https://dx.doi.org/10.1016/S0924-9338(03)00005-1

27. Hamada, T.; Wessagowit, V.; South, A.; Ashton, G.; Chan, I.; Oyama, N.; Siriwattana, A.; Jewhasuchin, P.; Charuwichitratana, S.; Thappa, D. Extracellular matrix protein 1 gene (ECM1) mutations in lipoid proteinosis and genotype-phenotype correlation. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 120, 345-350. 0 + 285
https://dx.doi.org/10.1046/j.1523-1747.2003.12073.x


Times Cited: 57
26. Erdal, M.; Yilmaz, M.; Herken, H.; Kocoglu, H.; Bayazit, Y. The 1438G/A polymorphism of the 5-HT2A receptor gene is associated with aura in migraine. PAIN CLINIC, 2003, 15, 315-319. 900 + 15
https://dx.doi.org/10.1163/156856903767650853


Times Cited: 3
25. Erdal, M.; Herken, H.; Mutlu, M.; Bayazit, Y. Significance of catechol-O-methyltransferase gene polymorphism in myofacial pain syndrome. PAIN CLINIC, 2003, 15, 309-313. 950 + 25
https://dx.doi.org/10.1163/156856903767650844


Times Cited: 5
24. Duran, I.; Erdal, M.; Ozgur, Z.; Gokdogan, T.; Erdal, N. Relationship between estrogen receptor gene polymorphism and periodontal diseases.. JOURNAL OF DENTAL RESEARCH, 2003, 82, B317-B317. 800 + 0
23. Erdal, M.; Tot, S.; Yazici, K.; Yazici, A.; Herken, H.; Erdem, P.; Derici, E.; Camdeviren, H. Lack of association of catechol-O-methyltransferase gene polymorphism in obsessive-compulsive disorder. DEPRESSION AND ANXIETY, 2003, 18, 41-45. 750 + 165
https://dx.doi.org/10.1002/da.10114


Times Cited: 33
22. Erdal, M.; Duran, L.; Erdal, N.; Ozgur, Z.; Bodur, S. Relationship between vitamin D receptor gene polyrnorphism and periodontal diseases.. JOURNAL OF DENTAL RESEARCH, 2003, 82, B363-B363. 900 + 0
21. Erdal, M.; Herken, H.; Yilmaz, M.; Bayazit, Y. Monoamine oxidase-A gene promoter polymorphism in female migraineurs. PAIN CLINIC, 2003, 15, 455-458. 950 + 5
https://dx.doi.org/10.1163/156856903770196854


Times Cited: 1
20. Gursoy, S.; Erdal, M.; Herken, H.; Madenci, E.; Alasehirli, B.; Erdal, N. Significance of catechol-O-methyltransferase gene polymorphism in fibromyalgia syndrome. RHEUMATOLOGY INTERNATIONAL, 2003, 23, 104-107. 750 + 670
https://dx.doi.org/10.1007/s00296-002-0260-5


Times Cited: 134
19. Zoroglu, S.; Erdal, M.; Erdal, N.; Ozen, S.; Alasehirli, B.; Sivasli, E. No evidence for an association between the T102C and 1438 G/A polymorphisms of the serotonin 2A receptor gene in attention deficit/hyperactivity disorder in a Turkish population. NEUROPSYCHOBIOLOGY, 2003, 47, 17-20. 750 + 110
https://dx.doi.org/10.1159/000068870


Times Cited: 22
18. Herken, H.; Erdal, M.; Erdal, N.; Aynacioglu, S. T102C polymorphisms at the 5-HT2A receptor gene in Turkish schizophrenia patients: A possible association with prognosis. NEUROPSYCHOBIOLOGY, 2003, 47, 27-30. 850 + 65
https://dx.doi.org/10.1159/000068872


Times Cited: 13
17. Sengun, A.; Duran, I.; Erdal, M.; Ozkaya, M.; Ozturk, B.; Ozer, F. Vitamin D receptor gene polymorphism is associated with dental caries.. JOURNAL OF DENTAL RESEARCH, 2003, 82, B100-B100. 650 + 0
2002
16. Pata, C.; Erdal, M.; Derici, E.; Yazar, A.; Kanik, A.; Ulu, O. Serotonin transporter gene polymorphism in irritable bowel syndrome. AMERICAN JOURNAL OF GASTROENTEROLOGY, 2002, 97, 1780-1784. 750 + 445
Publications_008.pdf


Times Cited: 89
15. Tot, S.; Erdal, M.; Yazici, K.; Herken, H.; Yazici, A.; Buturak, V. 5-HT2A T102C gene polymorphism in Turkish patients with obsessive-compulsive disorder. EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2002, 12, S336-S336. 750 + 0
14. Nacak, M.; Aynacioglu, A.; Filiz, A.; Cascorbi, I.; Erdal, M.; Yilmaz, N.; Ekinci, E.; Roots, I. Association between the N-acetylation genetic polymorphism and bronchial asthma. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2002, 54, 671-674. 350 + 80
https://dx.doi.org/10.1046/j.1365-2125.2002.01670.x


Times Cited: 16
13. Kaya, T.; Erdal, M.; Tursen, U.; Camdeviren, H.; Gunduz, O.; Soylemez, F.; ıkizoglu, G. Association between vitamin D receptor gene polymorphism and psoriasis among the Turkish population. ARCHIVES OF DERMATOLOGICAL RESEARCH, 2002, 294, 286-289. 700 + 85
https://dx.doi.org/10.1007/s00403-002-0326-y


Times Cited: 17
12. Gursoy, S.; Erdal, M.; Herken, H.; Madenci, E.; Alasehirli, B. Absence of association of the serotonin transporter gene polymorphism with the mentally healthy subset of fibromyalgia patients (vol 21, pg 194, 2002). CLINICAL RHEUMATOLOGY, 2002, 21, 351-351. 800 + 0
11. Gursoy, S.; Erdal, E.; Herken, H.; Madenci, E.; Alasehirli, B. Absence of association of the serotonin transporter gene polymorphism with the mentally healthy subset of fibromyalgia patients. CLINICAL RHEUMATOLOGY, 2002, 21, 194-197. 0 + 285
https://dx.doi.org/10.1007/s10067-002-8284-5


Times Cited: 57
10. Zoroglu, S.; Erdal, M.; Alasehirli, B.; Erdal, N.; Sivasli, E.; Tutkun, H.; Savas, H.; Herken, H. Significance of serotonin transporter gene 5-HTTLPR and variable number of tandem repeat polymorphism in attention deficit hyperactivity disorder. NEUROPSYCHOBIOLOGY, 2002, 45, 176-181. 650 + 325
https://dx.doi.org/10.1159/000063667


Times Cited: 65
9. Tursen, U.; Kaya, T.; Erdal, M.; Derici, E.; Gunduz, O.; ıkizoglu, G. Association between catechol-O-methyltransferase polymorphism and vitiligo. ARCHIVES OF DERMATOLOGICAL RESEARCH, 2002, 294, 143-146. 650 + 155
https://dx.doi.org/10.1007/s00403-002-0295-1


Times Cited: 31
8. Herken, H.; Erdal, M.; Aynacioglu, A.; Barlas, O.; Cataloluk, O.; Esgi, K.; Brockmoller, J.; Kaiser, R. Frequency of the 17-bp variable number of tandem repeat polymorphism in Turkish schizophrenic patients. SCHIZOPHRENIA RESEARCH, 2002, 58, 99-100. 650 + 30
https://dx.doi.org/10.1016/S0920-9964(01)00391-7


Times Cited: 6
7. Tot, S.; Erdal, M.; Yazici, K.; Herken, H.; Yazici, A.; Bal, N. Catechol-O-methyltransferase gene polymorphism in Turkish patients with obsessive-compulsive disorder. EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2002, 12, S406-S406. 750 + 0
2001
6. Yilmaz, M.; Erdal, M.; Herken, H.; Cataloluk, O.; Barlas, O.; Bayazit, Y. Significance of serotonin transporter gene polymorphism in migraine. JOURNAL OF THE NEUROLOGICAL SCIENCES, 2001, 186, 27-30. 750 + 225
https://dx.doi.org/10.1016/S0022-510X(01)00491-9


Times Cited: 45
5. Herken, H.; Erdal, M. Catechol-O-methyltransferase gene polymorphism in schizophrenia: evidence for association between symptomatology and prognosis. PSYCHIATRIC GENETICS, 2001, 11, 105-109. 1000 + 270
https://dx.doi.org/10.1097/00041444-200106000-00009


Times Cited: 54
4. Erdal, M.; Herken, H.; Yilmaz, M.; Bayazit, Y. Significance of the catechol-O-methyltransferase gene polymorphism in migraine. MOLECULAR BRAIN RESEARCH, 2001, 94, 193-196. 950 + 80
Publications_014.pdf


Times Cited: 16
3. Gursoy, S.; Erdal, M.; Herken, H.; Madenci, E.; Alasehirli, B. Association of T102C polymorphism of the 5-HT2A receptor gene with pyschiatric status in fibromyalgia syndrome. RHEUMATOLOGY INTERNATIONAL, 2001, 21, 58-61. 800 + 195
https://dx.doi.org/10.1007/s002960100130


Times Cited: 39
2. Herken, H.; Erdal, M.; Mutlu, N.; Barlas, O.; Cataloluk, O.; Oz, F.; Guray, E. Possible association of temporomandibular joint pain and dysfunction with a polymorphism the serotonin transporter gene. AMERICAN JOURNAL OF ORTHODONTICS AND DENTOFACIAL ORTHOPEDICS, 2001, 120, 308-313. 700 + 160
https://dx.doi.org/10.1067/mod.2001.115307


Times Cited: 32
1. Erdal, M.; Herken, H.; Yilmaz, M.; Bayazit, Y. Association of the T102C polymorphism of 5-HT2A receptor gene with aura in migraine. JOURNAL OF THE NEUROLOGICAL SCIENCES, 2001, 188, 99-101. 950 + 115
https://dx.doi.org/10.1016/S0022-510X(01)00556-1


Times Cited: 23
International - Covered by Other International Indexes 260
2015
2. Yıldız, M.; vural, M.; Erdal, M.; Ay, .; Yılmaz, .; Karababa, .; Selek, S. Lack of association of DRD3 and CNR1 polymorphisms with premenstrual dysphoric disorders. IRANIAN JOURNAL OF REPRODUCTIVE MEDICINE , 2015, 13, 221-226. 120 + 0
Publications_004.pdf

2005
1. Mutlu, N.; Erdal, M.; Herken, H.; Ozkaya, M.; Erdal, N.; Oz, G.; Bayazit, Y. Monoamine oxidase-A gene promoter polymorphism in temporomandibular joint pain and dysfunction. THE PAIN CLINIC, 2005, 17, 39-44. 140 + 0
http://dx.doi.org/10.1163/1568569053421663

National - Covered by ULAKBIM 420
2016
3. Erdal, M.; Yılmaz, . microRNA Studies and Reflection to Psychiatry.. TURKIYE KLINIKLERI J PSYCHIATRY-SPECIAL TOPICS, 2016, 9, 16-24. 200 + 0
Publications_005.pdf

2015
2. Tezol, .; Delibaş, A.; Ay, .; Karakaş, .; Taşdelen, B.; Erdal, M. MicroRNA Gene Polymorphisms in Congenital Anomalies of the Kidney and Urinary Tract. CUKUROVA MEDICAL JOURNAL, 2015, 40, 439-451. 80 + 0
Publications_001.pdf

2012
1. Unal , .; Erdal, M.; Demirkan, F.; özkaya, M.; Arslan, E.; Türsen, .; Camdeviren, H. Increased Risk of Non-Melanoma Skin Cancer in DNA Repair Gene XRCC1 Polymorphism. J TURK ACAD DERMATOL, 2012, 6, 1-5. 140 + 0
10.6003/jtad.1263a1

Publications_002.pdf

National - SCI/SCI-Expanded category 0
2017
2. Karakaş, .; Izci ay, .; Ay, M.; Wang, W.; Sungur, M.; çevik, K.; Doğru, G.; Erdal, M. . OMICS: A JOURNAL OF INTEGRATIVE BIOLOGY, 2017, 21, 352-358. 0 + 0
10.1089/omi.2017.0048

1. Türkseven, .; Büyükakıllı, B.; Ballı, E.; Yetkin, D.; Erdal, M.; Görücü yılmaz, .; şahin, L. . LIFE SCIENCES, 2017, 184, 47-57. 0 + 0
10.1016/j.lfs.2017.07.012

International - Chapter(s) in Book 50
1. Ay, .; çokaklı, E.; Erdal, M.; Ay, M.; çokaklı, M. RESEARCHES ON SCIENCE AND ART iN 21 ST CENTURY TURKEY, ISBN: 978-605-180-771-3, Gece Publishing, Number of print: 1, Total Printing Number: 500, 1548 Page, English, Ankara, Turkey, 2017. 50
International - Full text - Poster 35

1. Metin, T.; Yılmaz, N.; Yılmaz, B.; Yılmaz, N.; Erdal, M.; Buran, İ.; Temel, G., EXPRESSION OF TRPV6 AND PMCA1 IN THE MID-SECRETORY ENDOMETRIUM OF INFERTILE PATIENTS WITH ENDOMETRIOSIS AND UNEXPLAINED INFERTILITY . 19th World Congress on IVF in conjunction with 6th Society of Reproductive Medicine and Surgery Congress, 2017-10-04, 2017-10-08, ANTALYA, Turkey, 2017. 35

International - Abstract - Oral 250

6. Tombak, A.; Ay, M.; Erdal, M.; Doğru, G.; Söylemez, F.; Gürkan, E.; Paydaş, S., Vitamin D gene polymorphism in multiple myeloma, chronic lymphocytic leukemia and chronic myeloid leukemia. 9th International Conference on Leukemia and Hematologic Oncology, 2017-10-05, 2017-10-06, London, England / United Kingdom, 2017. 60
Scientific_Meetings_005.pdf

5. Balım, D.; Ay, Ö.; Karakas, Ü.; Ay, M.; Kenar, A.; Yıldırım , D.; Erdal , M., Investigation of Expression Levels of Brain Derived Neurotrophic Factor Neurotrophin-3 and Neurotrophin-4 in Patient with Major Depression. . 3Rd International Conference On Science, Ecology And Technology (Iconsete’2017), 2017-08-14, 2017-08-16, Roma, Italy, 2017. 20

4. Kızıltuğ, M.; Erdal, M.; Özge, A.; Taşdelen, B., Investigation of expressions of certain microRNAs in patients with Alzheimer's disease. . 15th Turkish Neuroscience Congress , 2017-05-07, 2017-05-10, Sakarya, Turkey, 2017. 85
http://www.anatomy.org.tr/issue/2017s1/pdf/03.pdf

3. Doğru, G.; Ay , Ö.; Tursen, Ü.; Ay, M.; Çevik, K.; Karakaş, Ü.; Yıldırım , D., EFFECT OF MIR-3680, MIR-4495, MIR-6824-5P EXPRESSION LEVELS IN VITILIGO, OP-019. 2nd International Dermatology and Cosmetology Congress,, 2017-03-15, 2017-03-18, İstanbul, Turkey, 2017. 10

2. Balkan, M.; İzci Ay, Ö.; Erdal, M.; Rustemoğlu, A.; Atar, M.; Hatipoğlu, N.; Yıldız, İ., MicroRNA-related Gene Polymorphisms and Idiopathic Azoospermia. 41st Federation of European Biochemical Societies (FEBS) congress, 2016-09-03, 2016-09-08, Aydın/Kuşadası, Turkey, 2016. 45
http://onlinelibrary.wiley.com/doi/10.1111/febs.13805/pdf

1. Kenar, A.; Unal, G.; Guler, H.; Albuz, B.; Kiroglu, Y.; Erdal, M.; Herken , H., The relationship between DAT1 Gene and Effects of Methylphenidate Use in Adult ADHD: A magnetic resonance spectroscopy study . 8. Uluslararası Psikofarmakoloji Kongresi & 4. Uluslararası Çocuk ve Ergen Psikofarmakolojisi Sempozyumu, , 2016-04-20, 2016-04-24, Antalya, Turkey, 2016. 30

International - Abstract - Poster 232

11. Dasdag, S.; Akdag, Z.; Erdal, M.; Kiziltug, M.; Tasdelen, B.; Erdal , N., Microrna Expression In Brain After Long Term And Excessive Exposure Of 2.4 Ghz Radiofrequency Radiation (Wi Fi). 13th Nanoscience and Nanotechnology Conference, 2017-10-22, 2017-10-25, Antalya, Turkey, 2017. 32

10. Daşdağ, S.; Akdağ, M.; Erdal , M.; Kızıltuğ, M.; Taşdelen, B.; Erdal, N., Do Long Term And Excessive Exposure of 900 Mhz Radiofrequency Radiation Emitted from Mobile Phones Alter Microrna Expression in Brain?. 22nd International Biomedıcal Science & Technology Symposium, 2017-05-12, 2017-05-14, Ankara, Turkey, 2017. 32

9. Avşar, I.; Nacak, M.; Erdal , M.; Aydın, N.; Gök, Ş.; Herken, H.; Yarış, E., The Frequency Distributions of CYP3A4*22 in Turkish Population.. 7th European Congress of Pharmacology (EPHAR2016), 2016-06-26, 2016-06-30, İSTANBUL, Turkey, 2016. 25

8. Dasdag, S.; Akdag, Z.; Erdal, M.; Erdal, N.; Ay, O.; Ay, M.; Yılmaz, S., Long term and excessive use of 900 MHz radiofrequency radiation alter microRNA expression in brain. . BioEM2016 (The Joint Annual Meeting of The Bioelectromagnetics Society and the European BioElectromagnetics Association co-organized with the European COST EMF-MED Action BM1309), 2016-06-05, 2016-06-10, Ghent, Belgium, 2016. 25

7. Buran, İ.; Ay, M.; Doğru, G.; Ay, Ö.; Karakaş, Ü.; Çevik, K.; Yüksel, D., Aneuploidy findings on two different pregnancy loss materials from the same mother. . The European Human Genetics Conference, , 2016-05-21, 2016-05-24, Barcelona, Spain, 2016. 5

6. Yuksel, D.; Ay , Ö.; Ay, M.; Tezol, Ö.; Doğru, G.; Çevik, K.; Karakaş, Ü., The case o der(5)t(5;14)mat caused by adjacent I meiotic segregation in prenatal diagnosis. . The European Human Genetics Conference, 2016-05-21, 2016-05-24, Barcelona, Spain, 2016. 5

5. Tursen, B.; Ulut, B.; Guvenc, U.; Kaya, T.; Yilmaz, Ş.; Kızıltug, M.; Terzi , E., Microchimerism in chronic idiopathic urticari . 5th International Conference on Clinical & Experimental Dermatology, 2015-07-13, 2015-07-15, New Orleans, United States of America, 2015. 5
Scientific_Meetings_004.pdf

4. Altintas, Z.; Ucbilek, E.; Erdal, M.; Sezgin, O.; Altintas, E., Methylation and Expression of the Genes That Have a Role in the WNT Signaling Pathway in Ulcerative Colitis.. 46th Annual Digestive Disease Week (DDW) Washington, DC. GASTROENTEROLOGY Volume: 148, Issue: 4 Pages: S694-S694 Supplement: 1, 2015-05-16, 2015-05-19, Washington, United States of America, 2015. 35
Scientific_Meetings_003.pdf

3. Yildiz, M.; Vural, M.; Erdal, M.; Ay, O.; Yilmaz, S.; Karababa, I.; Selek, S., No association of DRD3 and CNR1 polymorphisms in premenstrual dysphoric disorder . 7. Uluslararası Psikofarmakoloji Kongresi ve 3. Uluslararası Çocuk ve Ergen Psikofarmakolojisi Sempozyumu , 2015-04-15, 2015-06-19, Antalya, Turkey, 2015. 30
Scientific_Meetings_001.pdf

2. Camkurt, M.; Karababa, I.; Erdal, M.; Kandemir, S.; Bayazit, H.; Ay, M.; Kandemir, H., Blood microRNA dysregulation in schizophrenia. 7. Uluslararası Psikofarmakoloji Kongresi ve 3. Uluslararası Çock ve Ergen Psikofarmakolojisi Sempozyumu, 2015-04-15, 2015-06-19, Antalya, Turkey, 2015. 22
Scientific_Meetings_002.pdf

1. Bacanli,, A.; Süren, S.; Yazıcı, K.; Aygüneş, D.; Kosova, B.; Erdal, M.; Herken, H., Imaging Genetics of DSM-V Proposed Attention Deficit Hyperactivity Disorder Subtypes. . XXIst World Congress on Psychiatric Genetics,, 2013-10-17, 2013-10-21, Boston, MASSACHUSETTS, United States of America, 2013. 15

National - Abstract - Poster 16

2. AY, Ö.; AY, M.; DOĞRU, G.; KARAKAŞ, Ü.; ÇEVİK, K.; YÜKSEL, D.; ÇAYAN, F., Evaluation of Prenatal Cytogenetic Data with in-situ Culture Method. . Uluslarası Katılımlı Gevher Nesibe Tıp Günleri, Tıbbi Genetik ve Klinik Uygulamaları Kongresi. , 2016-03-11, 2016-03-13, Kayseri, Turkey, 2016. 2

1. Tombak, A.; Ay , M.; Erdal, M.; Doğru, G.; Tiftik, E.; Söylemez, F.; Gürkan, E., Multiple Myeloma, Kronik Lenfositik Lösemi ve Kronik Miyeloid Lösemide Vitamin D Reseptör Gen Polimorfizmleri. Abstract:217 (P-50). 41. Ulusal Hematoloji Kongresi , 2015-10-21, 2015-10-24, Antalya, Turkey, 2015. 13

National - Manager 1700

17. INVESTIGATION OF CACNA1A, HCRTR2, F2RL1 GENE EXPRESSION LEVELS IN CLUSTER HEADACHE PATIENTS, BAP, Project Number: 2019-2-TP2-3522, 13000 TL, Manager, Continue... 100

16. Investigation of Expression Levels of mRNA, miRNA and lncRNAs Associated with Serotonergic System in Childhood Inflammatory Bowel Disease, BAP, Project Number: 2019-1-TP3-3493, 19500 TL, Manager, Continue... 100

15. Bipolar Mood Disorder Cases serotonin and dopamine Investigation of Some Related miRNA Expression Levels, BAP, Project Number: BAP-SBE TBB (ST) 2013-3 DR , 20000 TL, Manager, Continue... 100

14. Investigation of Expression Levels and Polymorphisms DICER1, DROSHA and XPO5 Genes in Psychotic Disorders., BAP, Project Number: 2018-1-TP2-2807, 10000 TL, Manager, Continue... 100

13. The Examination of Chemical Reprogramming Capacity of Amniocytes by Modification of Histone and Cellular Signaling Pathways. , BAP, Project Number: 2018-2-TP3-2922, 20000 TL, Manager, Continue... 100

12. Investigation of Expressions of Certain miRNAs in Patients with Alzheimer's Disease, BAP, Project Number: 2015-TP2-1195, 7000 TL, Manager, 2016,Completed. 100

11. Investigation of NRG3 and ErbB4 Gene Polymorphisms in Cigarette Dependent Individuals ., BAP, Project Number: BAP-SBE TBB (HG) 2014-4 YL , 10000 TL, Manager, 2015,Completed. 100

10. Sigara Bağımlısı Bireylerde Dopamin Beta Hidroksilaz geni ve 444 G/A Polimorfizmlerinin Araştırılması, BAP, Project Number: BAP-TF TBGAD (MEE) 2014-3 GP, 28000 TL, Manager, 2014,Completed. 100

9. Associated with Alzheimer's Disease In some miRNA (microRNA) into the expression and Polymorphisms, BAP, Project Number: BAP-SBE TB (ŞGY) 2010-4 DR , 20000 TL, Manager, 2013,Completed. 100

8. Ulcerative Colitis Some genes involved in the Wnt signaling pathway Methylation and Expression., BAP, Project Number: BAP-SBE TBG (ZMA) 2009-3 DR, 20000 TL, Manager, 2012,Completed. 100

7. Association of microRNA Biogenesis Pathway Gene Variants and Alcohol Dependence Risk. , BAP, Project Number: BAP-SBEM TM (HG) 2010-5 YL , 10000 TL, Manager, 2012,Completed. 100

6. Investigation on the Effect of the In-Vitro Expression of Genes Associated with Epidermal Growth Factor in Gastric Epithelial Cell Apoptosis of ulcer patients., TÜBİTAK, Project Number: SBAG- (108S108), 25000 TL, Manager, 2009,Completed. 100

5. Presinaptik proteinleri kodlayan genlerin polimorfizmleri ile Alzheimer hastalığı arasındaki ilişkinin araştırılması , BAP, Project Number: BAP-SBE TTB (TG) 2005-DR)., 10000 TL, Manager, 2009,Completed. 100

4. Matriks metalloproteaz-2 (-1306G/T) ve Matriks metalloproteaz-9 (-1162 C/T) polimorfizmleri ile lenfoid malignensi oluşum riski arasındaki ilişkinin araştırılması , BAP, Project Number: BAP-TFTTB(MEE)2005-2, 10000 TL, Manager, 2007,Completed. 100

3. Şizofreni Hastalarında Dopamin Reseptörü D3 (DRD3) mRNA Düzeyleri İle DRD3 Geni Ser9Gly Polimorfizmi Arasındaki İlişkinin Araştırılması , BAP, Project Number: BAP-TF TTB(MEE) 2004-3, 10000 TL, Manager, 2006,Completed. 100

2. Parkinson Hastalarında Serotonin Transporter Gen Polimorfizminin Araştırılması, BAP, Project Number: BAP SBE TBG (MÖ) 2002 YL, 5000 TL, Manager, 2003,Completed. 100

1. Monoamin Oksidaz Geni Polimorfizimlerinin Epizodik ve Kronik Gerilim Tipi Başağrısı ile İlişkisi, BAP, Project Number: BAP SBE TBG (TG) 2002 YL, 5000 TL, Manager, 2003,Completed. 100

National - Researcher 1000

20. Researching Expression Levels of miRNAs That is Considered to Increase Hemoglobin F Rates in Sickle Cell Anemia Patients, BAP, Project Number: 2015-TP3-1370, 21000 TL, Researcher, 2019,Completed. 50

19. Investigation ofSome miRNA expression levels associated with melanogenesis in vitiligo patients, BAP, Project Number: 2015-TP3-1204, 18000 TL, Researcher, 2018,Completed. 50

18. The investigation of the expression levels of miRNA processing genes DICER, DROSHA, XPO5, DGCR8, TARP2, AGO1 ve AGO2 in hematologic malignancies, BAP, Project Number: 2015-TP3-1205, 18000 TL, Researcher, 2018,Completed. 50

17. -, BAP, Project Number: 16/119, 20 TL, Researcher, 2017,Completed. 50

16. The examination of the expressions of proteins, functioning in calcium metabolism in the mid-secretuar endometrium of the unexplained infertile and endometriosis patients with implantation failure, which undergoing In Vitro Fertilization (IVF) programs , BAP, Project Number: 2015-TP3-1209, 15000 TL, Researcher, 2016,Completed. 50

15. Alzheimer hastalarının beyin ve iskelet kas hücrelerinde huperzine-a'nın amiloid-beta toksisitesi üzerine etkileri., BAP, Project Number: BAP-SBE BFB (ÇHT) 2013-1 YL, 10000 TL, Researcher, 2015,Completed. 50

14. Vitiligo Hastalığının Patogenezinde Fetal Mikrokimerizmin Rolü, BAP, Project Number: BAP-TF DTB (Pİ) 2010-4 TU, 20000 TL, Researcher, 2012,Completed. 50

13. Behçet Hastalığında IL-18 Promotor Gen -607 (C/A) Ve -137 (G/C) Polimorfizmi, , BAP, Project Number: BAP-TF DTB (RA) 2010-1 TU, 20000 TL, Researcher, 2012,Completed. 50

12. Tüberküloz Hastalarında Sitokin Gen Polimorfizmi Ve Genetik Yatkınlık , BAP, Project Number: BAP-SBE TM (MÜ) 2010-4 DR, 0 TL, Researcher, 2012,Completed. 50

11. Polisitemia Vera Ve Esansiyel Trombositoz Hastalarında Apoptotik Yolakta Görevli Gen Polimorfizmlerinin Araştırılması , BAP, Project Number: BAP-SBE TBG (GD) 2010-6 YL, 10000 TL, Researcher, 2012,Completed. 50

10. İrritabl Barsak Sendromlu Hastalarda Leptin Ve Leptin Reseptör Gen Polimorfizmlerinin Araştırılması, , BAP, Project Number: BAP-SBE TTB (KÇ) 2010-6 YL, 10000 TL, Researcher, 2012,Completed. 50

9. Kronik Lösemilerde Folat Metabolizmasında Rol Oynayan Bazı Gen Polimorfizmlerinin Etiyopatogenetik Önemi, , BAP, Project Number: BAP-TF DTB (ENT) 2010-3 A, 10000 TL, Researcher, 2011,Completed. 50

8. Romatoid Artritli Hastalarda Apopitozis İle İlişkili FAS (-670 G/A, -1377 G/A) Ve FAS-Ligand (-844 T/C, -IVS2nt -124 A/T) Gen Polimorfizmlerinin Hastalığa Duyarlılık Ve Hastalık Şiddeti İle İlişkisi, , BAP, Project Number: BAP-TF DTB (SY) 2009-5 TU, 20000 TL, Researcher, 2011,Completed. 50

7. Down Sendromu Öyküsü Olan Annelerde Folat/Homosistein Metabolizmasında Görevli Gen Polimorfizmlerinin Araştırılması, BAP, Project Number: BAP-TF TTB (ÖİA) 2009-2 , 0 TL, Researcher, 2011,Completed. 50

6. Hepatit C enfeksiyonu seyrinde düşük dansiteli lipoprotein, CD81 ve scavenger reseptör class B Tip 1’in polimorfizmlerinin etkisi. , BAP, Project Number: BAP-TF DTB (EK) 2008-1, 20000 TL, Researcher, 2009,Completed. 50

5. Tekrarlayan Gebelik Kayıplarında Death Receptor-4 (Dr-4.TRAIL-R1) Gen Polimorfizmlerinin Araştırılması., BAP, Project Number: BAP-SBE TBG (SS) 2008-10YL , 10000 TL, Researcher, 2009,Completed. 50

4. Postmenopozal osteoporetik kadınlarda beta 2 adrenarjik reseptör polimorfizminin etkisi,, BAP, Project Number: BAP-SBE TTB (FD)2006-YL, 5000 TL, Researcher, 2007,Completed. 50

3. Matriks Metalloproteinaz-1 (-1607 G -ins/del), Matriks Metalloproteinaz-2 (-1306 C/T) ve Matriks Metalloproteinaz-9 (-1562 C/T) Polimorfizmleri ile Osteoartrit Oluşum Riski Arasındaki İlişkinin Araştırılması. , BAP, Project Number: BAP-TF-TTB (İÖB) 2006-1, 62000 TL, Researcher, 2007,Completed. 50

2. The Effects on Event-Related Brain Potentials (ERP) of Gene Polymorphisms of neurotransmitter systems Event-Related Brain Potentials (ERP) , TÜBİTAK, Project Number: SBAG-2953 (104S488) , 0 TL, Researcher, 2006,Completed. 50

1. Sedanter erkeklerde beta 2 reseptör polimorfizm ile aerobik ve anaerobik kapasiteleri arasında ilişkilerin araştırılması, BAP, Project Number: TF TTB (HB) 2001-2, 0 TL, Researcher, 2002,Completed. 50

National - Advisor 0

1. The Possible Role of DNA Methylation and Demethylation Dynamics on Adult Olfactory Neurogenesis, TÜBİTAK, Project Number: 114S566, 373000 TL, Advisor, Continue... 0

Supervised Master Theses 1750

9. METİN BİRIŞIK, Detection of X and Y chromosomes by floresan in situ hybridization (FISH) method, Graduate School of Health Sciences, Gaziantep University, Completed. 200

8. MAHMUT ÖZKAYA, Investigation of serotonin transporter gene polymorphisms in parkinson's disease, Graduate School of Health Sciences, Mersin University, Completed. 200

7. SİBEL OĞUZKAN, Serum lipoprotein levels and ischemic heart disease is investigated by the method of serum proteins in polyacrylamide gel disc electrophoresis genetic polymorphism, Graduate School of Health Sciences, Gaziantep University, Completed. 200

6. HÜSEYİN GEDİK, A research on possible effects of gene polymorphisms in microRNA biogenesis pathway on alcohol dependence, Graduate School of Health Sciences, Mersin University, Completed. 200

5. TUBA GÖKDOĞAN, Investigation on genetic polymorphism of monoamine oxidase (MAO) in tension type headache, Graduate School of Health Sciences, Mersin University, Completed. 200

4. ZÜHAL MERT ALTINTAŞ, The effect of methylenetetrahydrofolate reductase gene polymorphisms and S-adenosylhomocysteine hydrolase genetic variations on ribavirin induced anemia in the patients with chronic hepatitis C, Graduate School of Health Sciences, Mersin University, Completed. 200

3. Mehmet Tuğhan KIZILTUĞ, Investigation of Expression of Certain miRNAs in Patients with Alzheimer's Disease, Graduate School of Health Sciences, Mersin University, 2016, Completed. 200

2. Hale GÜLER, The Investigation of ErbB4 and NRG3 gene polymorphism in individuals with smoking addiction, Graduate School of Health Sciences, Mersin University, 2015, Completed. 200

1. İlay BURAN, -, Graduate School of Health Sciences, Mersin University, 2015, Completed. 150

Supervised Expertise in Medicine Theses 400

1. KAAN SAVAŞOĞLU , Investigate the relationship between matrix metalloproteinase-2 -1306 c/t and matrix metalloproteinase-9 -1562 c/t polymorphisms and formation risk of lymphoid malignity, Others, Mersin University, Completed. 400

Supervised Doctorate Theses 2400

6. ŞENAY GÖRÜCÜ YILMAZ, Expressions of some miRNAs in Alzheimer patients and investigation of polymorphisms in genes involved in the miRNA formation pathway , Graduate School of Health Sciences, Mersin University, Completed. 400

5. ZUHAL MERT ALTINTAŞ, The expression and metylation of some Wnt signaling pathway genes which plays a role in ulcerative colitis, Graduate School of Health Sciences, Mersin University, Completed. 400

4. MERAL URHAN KÜÇÜK, Investigation of relationship between mrna levels of drd3 in human peripheral blood lymphocytes (pbl) and ser9gly polymorphism of drd3 gene in schizophrenia patients, Graduate School of Health Sciences, Mersin University, Completed. 400

3. FATMA SÖYLEMEZ, In-vitro research of epidermal growth factor on the gene expressions associated with the apoptosis in the gastric epithelial cells of ulcerous patients, Graduate School of Health Sciences, Mersin University, Completed. 400

2. TUBA GÖKDOĞAN EDGÜNLÜ, Investigation on genetic polymorphisms of presynaptic proteins genes in alzheimer disease, Graduate School of Health Sciences, Mersin University, Completed. 400

1. Sevinç SÜRER TEKİN, INVESTIGATION OF SOME DOPAMINE and SEROTONIN RELATED MICRORNA (miRNA) EXPRESSION LEVELS IN BIPOLAR DISORDER, Graduate School of Health Sciences, Mersin University, Completed. 400

International 50
1. Klinik Psikofarmakoloji Bülteni 24.Cilt Araştırma Ödülleri: Psikofarmakoloji Derneği, 2015-04-19, Antalya, Turkey. 0
2. Sözel Bildiri üçüncülük ödülü. Psikofarmakoloji Derneği, 2016-04-24, Antalya, Turkey. 50
3. , 2017-03-18, İSTANBUL, Turkey. 0
4. , 2017-10-08, İSTANBUL, Turkey. 0
National 350
1. , 2001-06-21, Cappadocia, Turkey. 25
2. , 2001-10-06, Antalya, Turkey. 25
3. , 2001-10-30, Antalya, Turkey. 25
4. , 2002-03-20, Eskişehir, Turkey. 25
5. , 2002-09-27, Marmaris Muğla, Turkey. 50
6. , 2005-11-20, Palandöken-Erzurum, Turkey. 25
7. , 2005-12-17, İstanbul, Turkey. 25
8. , 2007-04-08, K.K.T.C. Girne , Turkey. 50
9. , 2007-11-07, İstanbul, Turkey. 50
10. , 2011-09-15, İstanbul, Turkey. 50
1. Tıbbi Genetik Derneği , Member No: 113, Turkey, 1999-01-01-Continue.
2. Tıbbi Biyoloji ve Genetik Derneği , Member No: 112, Turkey, 1989-01-01-Continue.
3. Türk Biyofizik Derneği , Member No: 111, Turkey, 1986-01-01-Continue.
Term C.Code Course Faculty/College/Institute Department/Program T-A-C
Fall TBİY 101 Medical Biology Faculty of Dentistry Dentistry 3-1-4
Fall BİO 801 Specialty Area Institute of Health Sciences Department of Medical Biology 4-0-4
Fall BİO 802 Specialty Area Institute of Health Sciences Department of Medical Biology 4-0-4
Fall BİO 515 Methods For Genome Analysis Institute of Health Sciences Medical Biology 3-0-3
Fall BİO 514 Mutagens & Mutations Institute of Health Sciences Medical Biology 2-0-2
Fall BİO 613 Pharmacogenetics Institute of Health Sciences Medical Biology 2-0-2
Term C.Code Course Faculty/College/Institute Department/Program T-A-C
Spring TBİY 101 Medical Biology Faculty of Dentistry Dentistry 3-1-4
Spring BİO 610 Genetic Polymorphism Institute of Health Sciences Medical Biology 1-2-2
Spring SEM YL Seminar Institute of Health Sciences Institute of Health Sciences 0-0-0
Spring BİO 802 Specialty Area Institute of Health Sciences Department of Medical Biology 4-0-4
Spring BİO 801 Specialty Area Institute of Health Sciences Department of Medical Biology 4-0-4
Spring BİO 514 Mutagens & Mutations Institute of Health Sciences Medical Biology 2-0-2
Spring BİO 613 Pharmacogenetics Institute of Health Sciences Medical Biology 2-0-2
Fall TBİY 101 Medical Biology Faculty of Dentistry Dentistry 3-1-4
Fall BİO 515 Methods For Genome Analysis Institute of Health Sciences Medical Biology 3-0-3
Fall BİO 526 General Medical Biology Institute of Health Sciences Medical Biology 2-2-3
Fall SEM DR Seminar II Institute of Health Sciences Institute of Health Sciences 0-0-0
Fall SEM DR Seminar I Institute of Health Sciences Institute of Health Sciences 0-0-0
Fall BİO 802 Specialty Area Institute of Health Sciences Department of Medical Biology 4-0-4
Fall BİO 801 Specialty Area Institute of Health Sciences Department of Medical Biology 4-0-4
Fall BİO 514 Mutagens & Mutations Institute of Health Sciences Medical Biology 2-0-2
Term C.Code Course Faculty/College/Institute Department/Program T-A-C
Spring TBİY 102 Medical Biology Faculty of Dentistry Dentistry 3-1-4
Spring BİO 610 Genetic Polymorphism Institute of Health Sciences Medical Biology 1-2-2
Spring SEM YL Seminar Institute of Health Sciences Institute of Health Sciences 0-0-0
Spring SEM DR Seminar I Institute of Health Sciences Institute of Health Sciences 0-0-0
Spring BİO 515 Methods For Genome Analysis Institute of Health Sciences Medical Biology 3-0-3
Spring BİO 802 Specialty Area Institute of Health Sciences Department of Medical Biology 4-0-4
Spring BİO 801 Specialty Area Institute of Health Sciences Department of Medical Biology 4-0-4
Spring BİO 613 Pharmacogenetics Institute of Health Sciences Medical Biology 2-0-2
Fall TBİY 101 Medical Biology Faculty of Dentistry Dentistry 3-1-4
Fall SEM YL Seminar Institute of Health Sciences Institute of Health Sciences 0-0-0
Fall BİO 515 Methods For Genome Analysis Institute of Health Sciences Medical Biology 3-0-3
Fall BİO 618 Advanced Molecular Molecular Genetics Institute of Health Sciences Medical Biology 3-0-3
Fall BİO 802 Specialty Area Institute of Health Sciences Department of Medical Biology 4-0-4
Fall BİO 801 Specialty Area Institute of Health Sciences Department of Medical Biology 4-0-4
Fall BİO 514 Mutagens & Mutations Institute of Health Sciences Medical Biology 2-0-2
Term C.Code Course Faculty/College/Institute Department/Program T-A-C
Spring SEM DR Seminar I Institute of Health Sciences Institute of Health Sciences 0-0-0
Spring BİO 801 Specialty Area Institute of Health Sciences Department of Medical Biology 4-0-4
Spring BİO 613 Pharmacogenetics Institute of Health Sciences Medical Biology 2-0-2
Spring BİO 514 Mutagens & Mutations Institute of Health Sciences Medical Biology 2-0-2
Spring SEM YL Seminar Institute of Health Sciences Institute of Health Sciences 0-0-0
Fall BİO 604 Chemical Structure and Examination of Bo... Institute of Health Sciences Medical Biology 2-2-3
Fall SEM DR Seminar II Institute of Health Sciences Institute of Health Sciences 0-0-0
Fall BİO 801 Specialty Area Institute of Health Sciences Department of Medical Biology 4-0-4
Fall BİO 515 Methods For Genome Analysis Institute of Health Sciences Medical Biology 3-0-3
Fall BİO 610 Genetic Polymorphism Institute of Health Sciences Medical Biology 1-2-2
Term C.Code Course Faculty/College/Institute Department/Program T-A-C
Spring BİO 613 Pharmacogenetics Institute of Health Sciences Medical Biology 2-0-2
Spring BİO 801 Specialty Area Institute of Health Sciences Department of Medical Biology 4-0-4
Spring TEZ Thesis Institute of Health Sciences Institute of Health Sciences 0-0-0
Spring BİO 802 Specialty Area Institute of Health Sciences Department of Medical Biology 4-0-4
Spring SEM DR Seminar I Institute of Health Sciences Institute of Health Sciences 0-0-0
Spring BİO 526 General Medical Biology Institute of Health Sciences Medical Biology 2-2-3
Fall BİO 515 Methods For Genome Analysis Graduate School of Health Scie... MEDİCAL BİOLOGY 3-0-3
Fall BİO 514 Mutagens & Mutatıons Graduate School of Health Scie... MEDİCAL BİOLOGY 2-0-2
Fall BİO 604 Chemical Structure and Examination of Bo... Graduate School of Health Scie... MEDİCAL BİOLOGY 2-2-3
Term C.Code Course Faculty/College/Institute Department/Program T-A-C
Spring BİO 604 Chemical Structure and Examination of Bo... Graduate School of Health Scie... MEDİCAL BİOLOGY 2-2-3
Spring BİO 514 Mutagens & Mutatıons Graduate School of Health Scie... MEDİCAL BİOLOGY 2-0-2
Spring BİO 505 Technıques ın Medıcal Bıology Graduate School of Health Scie... MEDİCAL BİOLOGY 2-2-3
Fall BİO 610 Genetic Polymorphism Graduate School of Health Scie... MEDİCAL BİOLOGY 1-2-2
Fall BİO 515 Methods For Genome Analysis Graduate School of Health Scie... MEDİCAL BİOLOGY 3-0-3
Term C.Code Course Faculty/College/Institute Department/Program T-A-C
Fall BİO 515 Methods For Genome Analysis Graduate School of Health Scie... MEDİCAL BİOLOGY 3-0-3
Term C.Code Course Faculty/College/Institute Department/Program T-A-C
Spring BİO 610 Genetic Polymorphism Graduate School of Health Scie... MEDİCAL BİOLOGY 1-2-2
Spring BİO 514 Mutagens & Mutatıons Graduate School of Health Scie... MEDİCAL BİOLOGY 2-0-2
Fall BİO 613 Pharmacogenetics Graduate School of Health Scie... MEDİCAL BİOLOGY 2-0-2