Epigenetics and Expression of the Wnt Signaling Pathway in Ulcerative Colitis
Turkish Journal of Gastroenterology, vol. 36, no. 8, pp. 508–514
Zuhal Altıntaş, Mehmet Emin Erdal, Engin Altıntaş
Correlation of hsa-mirna-342-3p and SOX 6 Expression with Diabetic Nephropathy Classification, Prognostic Histomorphological Parameters and Laboratory Findings in Diabetic Nephropathy
ANNALS OF DIAGNOSTIC PATHOLOGY, vol. 76, no. , pp. 152461–
Arslan Gozde, Karabulut Yasemin Yuyucu, Yeleser Irem, Erdal Mehmet Emin, Demir Serap, Ozdemir Asena ...
Expression levels and polymorphisms of the microRNA maturing components; diagnostic values of Drosha, DGCR8 and Dicer in patients with vitiligo
African Health Sciences, vol. 25, no. 2, pp. 141–152
Soner Aşır, Özlem İzci Ay, Mustafa Ertan Ay, Kenan Çevik, Gurbet Doğru Özdemir, Merve Türkegün Şengü...
Effects of electromagnetic radiation on neurogenesis and gene expression in amniocytes
TOXICOLOGICAL AND ENVIRONMENTAL CHEMISTRY, vol. 105, no. 8-10, pp. 1–21
Coşar Uzun, Nurten Erdal, Özlem İzci Ay, Ümit Karakaş, Didem Derici Yıldırım, Hüseyin Durukan, Mehme...
Expression levels and clinical significances of hsa-miR-29 family and their target genes in the bone marrow of patients with multiple myeloma
INDIAN JOURNAL OF EXPERIMENTAL BIOLOGY, vol. 61, no. 12, pp. 933–940
Kenan Çevik, Mustafa Ertan Ay, Özlem İzci Ay, Anıl Tombak, Didem Derici Yıldırım, Tuba Kabasakal, Me...
A Novel Gene and Comparison of Gene Expressions in Low- and High-Grade Renal Cell Carcinomas
annals of urology and nephrology, vol. 3, no. 4, pp. 1–6
Yasemin Yuyucu Karabulut, Funda Bozkurt Saygı, Funda Bozkurt, Öznur Bucak, Emre Çağatay Köse, Bahar ...
The expression of TRPV6 and PMCA1 in the mid-secretory endometrium of infertile patients with unexplained infertility and endometriosis
CUKUROVA MEDICAL JOURNAL, vol. 48, no. 3, pp. 815–824
Tuba Özcan Metin, Nafiye Yılmaz, Banu Coşkun Yılmaz, Şakir Necat Yılmaz, Mehmet Emin Erdal, İlay Bur...
Biomarker potential of hsa-miR-145-5p in peripheral whole blood of manic bipolar I patients
BRAZILIAN JOURNAL OF PSYCHIATRY, vol. 44, no. 4, pp. 378–387
Sevinç Tekin, Sevinç Sürer Tekin, Mehmet Emin Erdal, Mehmet Asoğlu, Özlem İzci Ay, Mustafa Ertan Ay,...
Role of 2.4 GHz radiofrequency radiation emitted from Wi-Fi on some miRNA and faty acids composition in brain
Electromagnetic Biology and Medicine, vol. 41, no. 3, pp. 281–292
Süleyman Daşdağ, Mehmet Zülkif Akdağ, Mehmet Başhan, Veysi Kızmaz, Nurten Erdal, Mehmet Emin Erdal, ...
miR-181a-5p is a potential candidate epigenetic biomarker in multiple sclerosis
GENOME, vol. 65, no. 11, pp. 547–561
Tuba Edgünlü, Şenay Görücü Yılmaz, Ufuk Emre Toprak, Ufuk Emre, Bahar Taşdelen, Oktay Kuru, Gülnihal...
The role of Wnt pathway antagonists in early-stage lung adenocarcinoma
MOLECULAR BIOLOGY REPORTS, vol. 49, no. 1, pp. 9–17
Arife Zeybek, Necdet Öz, Serdar Kalemci, Kürşad Tosun, Tuba Edgünlü, Mehmet Tuğhan Kızıltuğ, Leyla T...
Association of NRG3 and ERBB4 gene polymorphism with nicotine dependence in Turkish population
MOLECULAR BIOLOGY REPORTS, vol. 48, no. 6, pp. 5319–5326
Hale Güler Kara, Mehmet Emin Erdal, Şenay Görücü Yılmaz, Cem Şengül, Melike Ceyhan Balcı Şengül, Kam...
The role of CD1a expression in the diagnosis of cutaneous leishmaniasis, its relationship with leishmania species and clinicopathological features
DERMATOLOGIC THERAPY, vol. 34, no. 4, pp. 1–9
Yasemin Yuyucu Karabulut, Funda Bozkurt, Funda Kuş Bozkurt, Gülhan Orekici Temel, Ümit Türsen, Umit ...
CCAAT Enhancer-binding Protein Alpha (CEBPA) Gene Expression in a Cohort of Turkish Patients with Multiple Myeloma
TURK ONKOLOJI DERGISI-TURKISH JOURNAL OF ONCOLOGY, vol. 37, no. 1, pp. 41–45
Tuba Kabasakal, Mustafa Ertan Ay, Kenan Çevik, Anıl Tombak, Özlem İzci Ay, Mehmet Emin Erdal
C626G Polymorphism in the Apoptotic Death Receptor-4 TRAIL Binding Domain Associated with Recurrent Pregnancy Loss: Case-Control Research
Turkiye Klinikleri Journal of Medical Sciences, vol. 41, no. 4, pp. 478–484
Sevinç Tekin, Sevinç Sürer Tekin, Mustafa Ertan Ay, Hüseyin Durukan, Kenan Çevik, Özlem İzci Ay, Gur...
A Study Investigating the Role of 2 Candidate SNPs in Bax and Bcl-2 Genes in Alzheimer’s Disease
Puerto Rico Health Sciences Journal, vol. 39, no. 3, pp. 264–269
Mehmet Emin Erdal, Şenay Görücü Yılmaz, Mustafa Ertan Ay, Hale Güler Kara, Hale Gür Kara, Aynur Özge...
MicroRNA dysregulation in manic and euthymic patients with bipolar disorder
Journal of Affective Disorders, vol. 261, no. , pp. 84–90
Mehmet Akif Camkurt, İbrahim Fatih Karababa, Mehmet Emin Erdal, Sultan Basmacı Kandemir, Gabrıel R F...
900 MHz Radiofrequency radiation has potential to increase the expression of rno-miR-145-5p in brain
Jounal of International Dental and Medical Research, vol. 12, no. 4, pp. 1652–1358
Süleyman Daşdağ, Mehmet Emin Erdal, Nurten Erdal, Bahar Taşdelen, Mehmet Tughan Kızıltuğ, Mehmet Zül...
Beyin kökenli nörotrofik faktör, nörotrofin-3 ve nörotrofin-4 gen ekspresyon değişimleri majör depresyonun patogenezinde etkili midir?
Anadolu Psikiyatri Dergisi, vol. 20, no. 0, pp. 1–588
Damla Yüksel, Damla Yüksel Balım, Özlem İzci Ay, Mustafa Ertan Ay, Ümit Karakaş, Ayşe Nur İnci Kenar...
NO ASSOCIATION OF THE LEPTIN (RS17151919) AND LEPTIN RECEPTOR (RS3790434) GENE POLYMORPHISMS WITH IRRITABLE BOWEL SYNDROME IN TURKISH POPULATION
WORLD JOURNAL OF ADVANCE HEALTHCARE RESEARCH, vol. 3, no. 1, pp. 126–131
Kenan Çevik, Mustafa Ertan Ay, Fehmi Ateş, Özlem İzci Ay, Ümit Karakaş, Mehmet Emin Erdal
Genetic Predisposition to Unexplained Recurrent Pregnancy Loss: Killer Cell Immunoglobulin-Like Receptor Gene Polymorphisms as Potential Biomarkers
Genetic Testing and Molecular Biomarkers, vol. 23, no. 1, pp. 57–65
Mustafa Ertan Ay, Özlem İzci Ay, Filiz Evşen Çayan, Sevinç Tekin, Ümit Karakaş, Didem Derici Yıldırı...
MicroRNA dysregulation in bipolar manic and euthymic patients
, vol. 85, no. 10, pp. S250–250
İbrahim Fatih Karababa, Akif Camkurt, Mehmet Emin Erdal, Sultan Basmacı Kandemir, Hüseyin Bayazit, M...
Tekrarlayan gebelik kayıplarında FAS ve FASLG polimorfizmlerinin TaqMan SNP genotiplendirme yöntemi ile belirlenmesi
Cukurova Medical Journal, vol. 44, no. 4, pp. 1303–1309
Mustafa Ertan Ay, Özlem İzci Ay, Kenan Çevik, Gurbet Doğru, Gurbet Doğru Özdemir, Fatma Söylemez, Fi...
No Association of Leptin (rs17151919 and Leptin Receptor (rs3790434) Gene Polymorphisms and Irritable Bowel Syndrome in Turkish Population
World Journal of Advance Healthcare Research, vol. 3, no. 1, pp. 125–131
Kenan Çevik, Mustafa Ertan Ay, Fehmi Ateş, Özlem İzci Ay, Ümit Karakaş, Mehmet Emin Erdal
Diagnostic Value of MiR-125b as a Potential Biomarker for Stage I Lung Adenocarcinoma
Current Molecular Medicine, vol. 19, no. 3, pp. 216–227
Arife Zeybek, Serdar Kalemci, Necdet Öz, Tuba Edgünlü, Mehmet Tuğhan Kızıltuğ, Mehmet Kızıltuğ, Kürş...
miRNA expression profile is altered differentially in the rat brain compared to blood after experimental exposure to 50 Hz and 1 mT electromagnetic field
Progress in Biophysics and Molecular Biology, vol. 132, no. , pp. 35–42
Mehmet Emin Erdal, Şenay Görücü Yılmaz, Serkan Gürgül, Coşar Uzun, Didem Derici Yıldırım, Nurten Erd...
Effect of EGF on Bax, Bcl-2 and Fas Expression in Ulcerous Disease and N87 Cell Line
Journal of Clinical Gastroenterology and Treatment, vol. 3, no. 2, pp. 1–8
Fatma Söylemez, Özlem İzci Ay, Mustafa Ertan Ay, Engin Altıntaş, Çağatay Han Türkseven, Mehmet Emin ...
Vitamin D gene polymorphism in multiple myeloma, chronic lymphocytic leukemia and chronic myeloid leukemia
, vol. 05, no. 05, pp. –
Anıl Tombak, Mustafa Ertan Ay, Mehmet Emin Erdal, Gurbet Doğru Özdemir, Fatma Söylemez, Emel Gürkan,...
Association of microRNA-related gene polymorphisms and idiopathic azoospermia in a south-east Turkey population
Biotechnology Biotechnological Equipment, vol. 31, no. 2, pp. 356–362
Özlem İzci Ay, Mehmet Emin Erdal, Mahmut Balkan, Aydın Rüstemoğlu, Aydın Rustemoğlu, Murat Atar, Nam...
MİYELOPROLİFERATİF NEOPLAZMLARAMOLEKÜLER GENETİK YAKLAŞIM
Nobel Medicus, vol. , no. , pp. –
Gurbet Doğru, Özlem İzci Ay, Mustafa Ertan Ay, Kenan Çevik, Mehmet Emin Erdal, Anıl Tombak, Ümit Kar...
Investigation of expressions of certain microRNAs in patients with Alzheimer’xxs disease.
, vol. 7, no. Suppl 1, pp. S1–S86
Mehmet Tuğhan Kızıltuğ, Mehmet Emin Erdal, Aynur Özge, Bahar Taşdelen
The role of certain gene polymorphisms involved in the apoptotic pathways in polycythemia vera and essential thrombocytosis
Advances in Clinical and Experimental Medicine, vol. 26, no. 5, pp. 761–765
Gurbet Doğru, Özlem İzci Ay, Mehmet Emin Erdal, Mustafa Ertan Ay, Anıl Tombak, Ümit Karakaş, Umit Ka...
Effect of EGF on Bax, Bcl-2 and Fas expression in ulcerous disease and N87 cell line
Bratislava Medical Journal, vol. 118, no. 11, pp. 695–701
Fatma Söylemez, Özlem İzci Ay, Mustafa Ertan Ay, Çağatay Han Türkseven, Engin Altıntaş, Mehmet Emin ...
Regulating the Regulators in Attention-Deficit/Hyperactivity Disorder: A Genetic Association Study of microRNA Biogenesis Pathways
OMICS: A Journal of Integrative Biology, vol. 21, no. 6, pp. 352–358
Ümit Karakaş, Özlem İzci Ay, Mustafa Ertan Ay, Wang Weı, Wei Wang, Wang Wei, Mehmet Ali Sungur, Kena...
Effects of Huperzin-A on the Beta-amyloid accumulation in the brain and skeletal muscle cells of a rat model for Alzheimer’xxs disease
Life Sciences, vol. 184, no. , pp. 47–57
Çağatay Han Türkseven, Belgin Büyükakıllı, Ebru Ballı, Derya Yetkin, Mehmet Emin Erdal, Şenay Görücü...
MicroRNA related gene polymorphism and idiopathic azoospermia
, vol. 283, no. 21, pp. 3889–3897
Mahmut Balkan, Özlem İzci Ay, Mehmet Emin Erdal, Aydın Rüstemoğlu, Murat Atar, Namık Kemal Hatipoğlu...
Investigation of Dysregulation of Several MicroRNAs in Peripheral Blood of Schizophrenia Patients
Clinical Psychopharmacology and Neuroscience, vol. 14, no. 3, pp. 256–260
Ma Çamkurt, Mehmet Akif Çamkurt, Mehmet Akif Camkurt, İbrahim Fatih Karababa, Mehmet Emin Erdal, Hüs...
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, vol. 12, no. , pp. 1141–1149
Ömer Başay, Bürge Kabukçu Başay, Hüseyin Alaçam, Önder Öztürk, Ahmet Büber, Şenay Görücü Yılmaz, Yıl...
Brain Derived Neurotrophic Factor Gene Val66Met Polymorphism Is a Risk Factor for Attention Deficit Hyperactivity Disorder in a Turkish Sample
Psychiatry Investigation, vol. 13, no. 5, pp. 518–525
Önder Öztürk, Bürge Kabukçu Başay, Ahmet Büber, Ömer Basey, Hüseyin Alaçam, Ali Bacanlı, Şenay Görüc...
Front Cover
FEBS Journal, vol. 283, no. S1, pp. 30–30
Mahmut Balkan, Özlem İzci Ay, Mehmet Emin Erdal, Aydın Rüstemoğlu, Murat Atar, Namık Kemal Hatipoğlu...
Aneuploidy findings on two different pregnancy loss materials from the same mother
European Journal of Human Genetics, vol. 24, no. e1, pp. 407–408
İlay Buran, Mustafa Ertan Ay, Gurbet Doğru, Özlem İzci Ay, Ümit Karakaş, Kenan Çevik, Damla Yüksel, ...
White matter alterations related to attention-deficit hyperactivity disorder and COMT val158met polymorphism: children with valine homozygote attention-deficit hyperactivity disorder have altered white matter connectivity in the right cingulum (cingulate gyrus)
Neuropsychiatric Disease and Treatment, vol. 12, no. , pp. 969–981
Bürge Kabukçu Başay, Ahmet Büber, Ömer Başay, Hüseyin Alaçam, Önder Öztürk, Serkan Süren, S Süren, Ö...
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, vol. 45, no. 3, pp. 392–393
Kaan Savaşoğlu, Mehmet Emin Erdal
Can Peripheral MicroRNA Expression Data Serve as Epigenomic Upstream Biomarkers of Alzheimer s Disease
OMICS: A Journal of Integrative Biology, vol. 20, no. 8, pp. 456–461
Şenay Görücü Yılmaz, Mehmet Emin Erdal, Aynur Özge, Mehmet Ali Sungur
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, vol. 20, no. 7, pp. 1373–1378
Ayşe Nur İnci Kenar, Ga Ünal, Hale Gürel, B Albuz, Y Kıroğlu, Mehmet Emin Erdal, Hasan Herken
Association of the Neuropeptide Y LEU7PRO rs16139 and NEUREXIN 3 rs760288 polymorphisms with alcohol dependence
Klinik Psikofarmakoloji Bülteni, vol. 26, no. 1, pp. 15–20
Abdullah Cem Şengül, Mehmet Emin Erdal, Melike Ceyhan Balcı Şengül, Özlem İzci Ay, Ahmet Büber, Ahme...
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, vol. 14, no. 2, pp. 184–193
Önder Öztürk, Hüseyin Alaçam, Bürge Kabukçu Başay, Ömer Başay, Ahmet Büber, Özlem İzci Ay, Kadir Ağl...
SNP Variation in MicroRNA Biogenesis Pathway Genes as a New Innovation Strategy for Alzheimer Disease Diagnostics
Alzheimer Disease & Associated Disorders, vol. 30, no. 3, pp. 203–209
Şenay Görücü Yılmaz, Mehmet Emin Erdal, Aynur Özge, Mehmet Ali Sungur
Synapsin Polymorphisms Could Be Correlated with Stroop Simple Reaction Time Scores
American Journal of Molecular Biology, vol. 06, no. 01, pp. 25–32
Ahmet Büber, Bürge Kabukçu Başay, Burge Kabukçu Başay, Ömer Başay, Önder Öztürk, Hüseyin Alaçam, Kem...
Lack of association of DRD3 and CNR1 polymorphisms with premenstrual dysphoric disorders
Iranian Journal of Reproductive Medicine, vol. 13, no. 4, pp. 221–226
Mesut Yıldız, Mehmet Vural, Mehmet Emin Erdal, Özlem İzci Ay, Şenay Görücü Yılmaz, İbrahim Fatih Kar...
Long term and excessive use of 900 MHz radiofrequency radiation alter microRNA expression in brain
International Journal of Radiation Biology, vol. 91, no. 4, pp. 306–311
Süleyman Daşdağ, Mehmet Zülküf Akdağ, Mehmet Zülkif Akdağ, Nurten Erdal, Mehmet Emin Erdal, Özlem İz...
Microribonucleic acid dysregulations in children and adolescents with obsessive compulsive disorderMicroribonucleic acid dysregulations in children and adolescents with obsessive compulsive disorder
Neuropsychiatric Disease and Treatment, vol. 11, no. , pp. 1695–1701
Hasan Kandemir, Mehmet Emin Erdal, Salih Selek, Özlem İzci Ay, İbrahim Fatih Karababa, Sultan Basmac...
Microribonucleic acid dysregulations in children and adolescents with obsessive–compulsive disorder
Neuropsychiatric Disease and Treatment, vol. 11, no. , pp. 1695–1701
Hasan Kandemir, Mehmet Emin Erdal, Salih Selek, Özlem İzci Ay, İbrahim Fatih Karababa, Mustafa Ertan...
MicroRNA Expression Analysis in Patients with Primary Myelofibrosis, Polycythemia vera and Essential Thrombocythemia
Indian Journal of Hematology and Blood Transfusion, vol. 31, no. 4, pp. 416–425
Anıl Tombak, Özlem İzci Ay, Mehmet Emin Erdal, Mehmet Ali Sungur, Mehmet Ali Uçar, Aydan Akdeniz, Ey...
Folate Metabolism Gene Polymorphisms and Risk for Down Syndrome Offspring in Turkish Women
Genetic Testing and Molecular Biomarkers, vol. 19, no. 4, pp. 191–197
Özlem İzci Ay, Mustafa Ertan Ay, Mehmet Emin Erdal, Filiz Evşen Çayan, Sevinç Sürer, Sevinç Sürer Te...
Microchimerism in alopecia areata
International Journal of Dermatology, vol. 54, no. 11, pp. 448–452
Terzi Erdinç, Bilal Bulut, Ümit Türsen, Tamer İrfan Kaya, Tursen Belma, Türsen Belma, Mehmet Emin Er...
Association of microRNA Biogenesis Pathway Gene Variants and Alcohol Dependence Risk
DNA and Cell Biology, vol. 34, no. 3, pp. 220–226
Hüseyin Gedik, Mehmet Emin Erdal, Şenay Görücü Yılmaz, Abdullah Cem Şengül, Melike Ceyhan Balcı Şeng...
Lack of Associations Between CLU and PICALM Gene Polymorphisms and Alzheimer s Disease in a Turkish Population
IDEGGYOGYASZATI SZEMLE-CLINICAL NEUROSCIENCE, vol. 68, no. 3-4, pp. 113–120
Aysun Şen, Aysu Şen, Mehtap Arslan, Mehmet Emin Erdal, Özlem İzci Ay, Şenay Görücü Yılmaz, Erhan Kur...
Evaluation of TLR2 and TLR4 Polymorphisms in Chronic HBV Infection
British Journal of Medicine and Medical Research, vol. 7, no. 3, pp. 195–202
Ayşe Gül Zamani, Ayşegül Zamani, Mehmet Emin Erdal, Hatice Gül Dursun, Özlem İzci Ay, Onur Ural, Tub...
Effects of 2 4 GHz radiofrequency radiation emitted from Wi Fi equipment on microRNA expression in brain tissue
International Journal of Radiation Biology, vol. 91, no. 7, pp. 555–561
Süleyman Daşdağ, Mehmet Zülküf Akdağ, Mehmet Zülkif Akdağ, Mehmet Emin Erdal, Nurten Erdal, Özlem İz...
Interleukin 1 receptor antagonist gene polymorphism adverse pregnancy outcome and periodontitis in Turkish women
Archives of Oral Biology, vol. 60, no. 12, pp. 1777–1783
Nezahat Arzu Kayar, Nilgün Özlem Alptekin, Mehmet Emin Erdal
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, vol. 23, no. 6, pp. 901–906
Tuba Edgünlü, Aynur Özge, Nurten Erdal, Oktay Kuru, Osman Kuru, Mehmet Emin Erdal
Association of the DRD2 TaqIA, 5-HT1B A-161T, and CNR1 1359 G/A polymorphisms with alcohol dependence
Klinik Psikofarmakoloji Bülteni, vol. 24, no. 2, pp. 115–121
Balcı Sengul Melike Ceyhan, Melike Ceyhan Balcı Şengül, Abdullah Cem Şengül, Cem Sengul, Mehmet Emin...
Utilizing Ethnic Specific Differences in Minor Allele Frequency to Recategorize Reported Pathogenic Deafness Variants
The American Journal of Human Genetics, vol. 95, no. 4, pp. 445–453
Shearer A Eliot, Eppsteiner Robert W, Kevin T Booth, Sean S Ephraim, José Gurrola, Allen Simpson, E ...
Is catechol o methyltransferase gene polymorphism a risk factor in the development of premenstrual syndrome
Clinical and Experimental Reproductive Medicine, vol. 41, no. 2, pp. 62–67
Esma Öztürk Deveci, Adnan İncebıyık, Salih Selek, Aysun Camuzcuoğlu, Neşe Gül Hilali, Hakan Camuzcuo...
Evaluation of several micro RNA (miRNA) levels in children and adolescents with attention deficit hyperactivity disorder
Neuroscience Letters, vol. 580, no. , pp. 158–162
Hasan Kandemir, Mehmet Emin Erdal, Salih Selek, Özlem İzci Ay, Ay Özlem İzci, İbrahim Fatih Karababa...
Association of FAS Gene Promoter Functional Polymorphisms and the Risk of Vitiligo in Turkish Populations
Journal of the Turkish Academy of Dermatology, vol. , no. , pp. –
Ümit Türsen, Tamer İrfan Kaya, Bilal Bulut, Mehmet Emin Erdal, Özlem İzci Ay, Özlem Ay, Türsen Belma...
Association of SNAP-25 GeneDdel andMnll Polymorphisms with Adult Attention Deficit Hyperactivity Disorder
Psychiatry Investigation, vol. 11, no. 4, pp. 476–480
Hasan Herken, Mehmet Emin Erdal, Ayşe Nur İnci Kenar, Gonca Ayşe Ünal, Ayşe Ünal, Burcu Çakaloz, Mu...
Association of VAMP-2 and Syntaxin 1A Genes with Adult Attention Deficit Hyperactivity Disorder
Psychiatry Investigation, vol. 11, no. 1, pp. 76–83
Ayşe Nur İnci Kenar, Özlem İzci Ay, Mehmet Emin Erdal, Hasan Herken
In-vitro research of epidermal growth factor on the gene expressions associated with the apoptosis in the gastric epithelial cells of ulcerous patients
FEBS JOURNAL, vol. , no. , pp. –
Fatma Söylemez, Mehmet Emin Erdal, Özlem İzci Ay
Polymorphisms in methylenetetrahydrofolate reductase gene Their impact on liver steatosis and fibrosis of chronic hepatitis c patients
Open Journal of Gastroenterology, vol. 04, no. 02, pp. 73–80
Engin Altıntaş, Zuhal Altıntaş, Zuhal Altıntaş, Orhan Sezgin, Tuba Edgünlü, Enver Üçbilek, Üçbilek E...
Possible Association of FAS and FASLG Polymorphisms with the Risk of Idiopathic Azoospermia in Southeast Turkey
Genetic Testing and Molecular Biomarkers, vol. 18, no. 6, pp. 383–388
Mahmut Balkan, Murat Atar, Mehmet Emin Erdal, Aydın Rustemoğlu, İsmail Yıldız, Aydın Rüstemoğlu, Ram...
The effect of genetic variations of methylene tetrahydropholate reductase gene polymorphisms on ribavirin induced anemia in hepatitis C patients
Journal of Liver:Disease Transplantation, vol. 02, no. 01, pp. –
Zuhal Altıntaş, Engin Altıntaş, Orhan Sezgin, Tuba Edgünlü, Enver Üçbilek, Erdinç Nayır, İbrahim Öme...
Tüberküloz Hastalarında Sitokin Gen Polimorfizmi ve Genetik Yatkınlığın Belirlenmesi
Mikrobiyoloji Bülteni, vol. 47, no. 2, pp. 250–264
Mahmut Ülger, Gürol Emekdaş, Gönül Aslan, Dilaver Taş, Ahmet İlvan, Seda Tezcan Ülger, Mukadder Çalı...
Determination of the cytokine gene polymorphism and genetic susceptibility in tuberculosis patients
Mikrobiyol Bul, vol. 47, no. 2, pp. 250–264
Mahmut Ülger, Gürol Emekdaş, Gönül Aslan, Dilaver Taş, Ahmet İlvan, Seda Tezcan Ülger, Mukadder Çalı...
Relation of the Fas and FasL gene polymorphisms with susceptibility to and severity of rheumatoid arthritis
Rheumatology International, vol. 33, no. 10, pp. 2637–2645
Seyfi Yıldır, Günşah Şahin, Melek Sezgin, İbrahim Ömer Barlas, Gözde Türköz, Türköz Gözde, Handan An...
A Study of the Impact of Death Receptor 4 (DR4) Gene Polymorphisms in Alzheimer's Disease
Balkan Medical Journal, vol. 30, no. 3, pp. 268–272
Tuba Edgünlü, Aynur Özge, Oö Yalın, Osman Özgür Yalın, Seval Kul, Erdal Me, Mehmet Emin Erdal
Apoptosis related Fas and FasL gene polymorphisms associations with knee osteoarthritis
Rheumatology International, vol. 33, no. 8, pp. 2039–2043
Melek Sezgin, İbrahim Ömer Barlas, Seyfi Yıldır, Türköz Gözde, Gözde Türköz, Handan Ankaralı, Ankara...
Association of Synapsin III Gene with Adult Attention Deficit Hyperactivity Disorder
DNA and Cell Biology, vol. 32, no. 8, pp. 430–434
Ayşe Nur İnci Kenar, Tuba Edgünlü, Hasan Herken, Mehmet Emin Erdal
Evaluation of death pathway genes FAS and FASL polymorphisms in chronic HBV infection
International Journal of Immunogenetics, vol. 40, no. 6, pp. 482–487
A G Zamani, Ayşegül Zamani, İbrahim Ömer Barlas, G Durakbasi Dursun, Hatice Gül Dursun, O Ural, Onur...
Microchimerism in Behçet s disease
International Journal of Dermatology, vol. 53, no. 7, pp. 832–837
Alp Ruken, Ruken Alp, Güney Ayşegül, Aysequl U Guney, Ayşegül Güney, Ümit Türsen, Tamer İrfan Kaya, ...
Alzheimer Hastalığında Sinaptik Vezikül ve Presinaptik Plazma Membran Proteinlerinin Genetik Varyantları
Nöro Psikiyatri Arşivi, vol. 49, no. 4, pp. 294–299
Tuba Edgünlü, Aynur Özge, Osman Özgür Yalın, Seval Kul, Mehmet Emin Erdal
The relationship DRD3 Ser9Gly polimorphisms and cognitive functions in schizophrenia preliminary study
Anadolu Psikiyatri Dergisi-Anatolian Journal of Psychiatry, vol. 13, no. 3, pp. 184–190
Gülfizar Varma, Rukiye Filiz Karadağ, Mehmet Emin Erdal, Özlem İzci Ay, Emel Aydın, Tuba Edgünlü, Ha...
Increased Risk of Non Melanoma Skin Cancer in DNA Repair Gene XRCC1 Polymorphism
Journal of the Turkish Academy of Dermatology, vol. 6, no. 3, pp. 184–190
Şakir Ünal, Mehmet Emin Erdal, Ferit Demirkan, Özkaya Mahmut, Mahmut Özakaya, Emrah Arslan, Ümit Tür...
Lack of Association Between the C276T Polymorphism of the Neuronal Nitric Oxide Synthase Gene and Migraine
International Journal of Neuroscience, vol. 123, no. 1, pp. 50–54
Belgin Alaşehirli, Aylin Akçalı, Abdullah Tuncay Demiryürek, Ayşe Özel, Mehmet Emin Erdal, Ayşe Müni...
Microchimerism in vitiligo
Journal of the European Academy of Dermatology and Venereology, vol. 27, no. 6, pp. 795–796
İnandıoğlu Pınar, Pınar Kurtuluş, Ümit Türsen, Mehmet Emin Erdal
Association between dopamine beta hydroxylase gene polymorphism and age at onset in male schizophrenia
Acta Neuropsychiatrica, vol. 24, no. 3, pp. 176–182
İbrahim Ömer Barlas, Mehmet Emin Erdal, Ümit Başar Semiz, Umit Semiz, Ayhan Algül, Özlem İzci Ay, Ma...
Synaptosomal Associated Protein 25 Gene Polymorphisms and AntisocialPersonality Disorder Association With Temperament and Psychopathy
CANADIAN JOURNAL OF PSYCHIATRY-REVUE CANADIENNE DE PSYCHIATRIE, vol. 56, no. 6, pp. 341–347
Cengiz Başoğlu, Öner Özgür, Alpay Ateş, Ayhan Algül, Yasin Bez, Mesut Çetin, Hasan Herken, Mehmet Em...
Effects of catechol O methyltransferase enzyme Val158Met polymorphism on cognitive functions in schizophrenic patients
KLINIK PSIKOFARMAKOLOJI BULTENI-BULLETIN OF CLINICAL PSYCHOPHARMACOLOGY, vol. 21, no. 1, pp. 24–32
Gülfizar Varma, Rukiye Filiz Karadağ, Mehmet Emin Erdal, Özlem İzci Ay, Neslihan Levent, Çiğdem Tekk...
Lack of association between COMT gene polymorphism and treatment outcome in major depression
Journal of Mood Disorders, vol. 1, no. 1, pp. 19–24
S Selek, Salih Selek, Mehmet Cemal Kaya, Mc Kaya, Mehmet Emin Erdal, M Bulut, Mahmut Bulut, Murat Er...
Catechol O methyltransferase gene Val108 158Met polymorphism in bipolar disorder
Neurology, Psychiatry and Brain Research, vol. 17, no. 2, pp. 46–50
Osman Virit, Mehmet Emin Erdal, Haluk Asuman Savaş, Haluk Savaş, İbrahim Ömer Barlas, Mehmet Yumru, ...
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, vol. 24, no. 3, pp. 2014–2019
Hilmi İsi, Mehmet Emin Erdal, Sedat Akdeniz, Diclehan Oral, Özlem İzci Ay, Selahattin Tekeş, Bilal S...
Association Among SNAP-25 Gene DdeI and MnlI Polymorphisms and Hemodynamic Changes During Methylphenidate Use
Journal of Attention Disorders, vol. 15, no. 8, pp. 628–637
Özgür Öner, Ata Akın, Hasan Herken, Mehmet Emin Erdal, K Çifçi, Koray Çiftçi, Rifat Koray Çiftçi, Mu...
FSHRSingle Nucleotide Polymorphism Frequencies in Proven Fathers and Infertile Men in Southeast Turkey
Journal of Biomedicine and Biotechnology, vol. 2010, no. 2010, pp. 1–5
Mahmut Balkan, Abdullah Gedik, Hasan Akkoç, Özlem İzci Ay, Mehmet Emin Erdal, Hilmi İsi, Turgay Buda...
Synaptosomal-associated protein (SNAP-25) polymorphisms and response to olanzapine in schizophrenia patients
Anatolian Journal of Psychiatry, vol. 11, no. , pp. 18–22
Cem Şengül, Mehmet Emin Erdal, Nazan Aydın, Ceyhan Balcı Şengül, İbrahim Ömer Barlas, Ahmet Şükrü Ay...
Significance of Serotonin Transporter Gene Polymorphism in Tinnitus
Otology & Neurotology, vol. 31, no. 1, pp. 19–24
Murat Deniz, Yıldırım Ahmet Bayazıt, Fatih Çelenk, Hayriye Karabulut, Akın Yılmaz, Bülent Gündüz, Ça...
The relation between IRS 1 Gly972Arg insulin receptor substrate genepolymorphism and olanzapine induced weight gain
Anadolu Psikiyatri Dergisi-Anatolian Journal of Psychiatry, vol. 11, no. 1, pp. 18–22
C Şengül, Abdullah Cem Şengül, Mehmet Emin Erdal, Nazan Aydın, N Aydın, Melike Ceyhan Balcı Şengül, ...
Association of Adult Attention Deficit HyperactivityDisorder With Dopamine Transporter Gene Dopamine D3Receptor and Dopamine D4 Receptor Gene Polymorphisms
Bulletin of Clinical Psychopharmacology, vol. 20, no. , pp. 196–203
Erinç Sevinç, Mehmet Emin Erdal, Abdullah Cem Şengül, Burcu Çakaloz, Tuba Edgünlü, Hasan Herken
Is the dopamine D3 receptor mRNA on blood lymphocytes help to for identification and subtyping of schizophrenia
Molecular Biology Reports, vol. 38, no. 4, pp. 2569–2572
Meral Urhan Küçük, Mehmet Emin Erdal, Murat Eren Özen, Seval Kul, Hasan Herken
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, vol. 24, no. 1, pp. 1638–1643
Hilmi İsi, Diclehan Oral, T Yıldız, Tekin Yıldız, G Ateş, C Sinir, Özlem İzci Ay, Gözde Türköz, Mehm...
Cytokine Polymorphism in Patients with Migraine Some Suggestive Cluesof Migraine and Inflammation
Pain Medicine, vol. 11, no. 4, pp. 492–497
İbrahim Arda Yılmaz, Aynur Özge, Mehmet Emin Erdal, Edgünlü Tuğba Gökdoğan, Tuba Edgünlü, Çakmak Sem...
Role of serotonine transporter gene polymorphism in cognitive functions in patients with schizophrenia
KLINIK PSIKOFARMAKOLOJI BULTENI-BULLETIN OF CLINICAL PSYCHOPHARMACOLOGY, vol. 19, no. 1, pp. 19–23
Gülfizar Varma, Rukiye Filiz Karadağ, Mehmet Emin Erdal, Ç Tekkanat, Özlem İzci Ay, Tuba Edgünlü, N ...
The Association of Olanzapine Induced Weight Gain with Peroxisome Proliferator Activated Receptor 2 Pro12Ala Polymorphism in Patients with Schizophrenia
DNA and Cell Biology, vol. 28, no. 10, pp. 515–519
Hasan Herken, Mehmet Emin Erdal, Nazan Aydın, Nazan Aydin, Abdullah Cem Şengül, Cem Sengul, Filiz Ka...
The ARG399GLN polymorphism in DNA repair gene XRCC1 does not alter risk of Parkinson's Disease
Journal of Neurological Sciences (Turkish), vol. 26, no. 2, pp. 185–189
Şükrü Hakan Kaleağası, Tuba Edgünlü, Mehmet Emin Erdal, Okan Doğu
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, vol. 29, no. 4, pp. 383–388
Barlas I Ömer, İbrahim Ömer Barlas, Melek Sezgin, Günşah Şahin, Mehmet Emin Erdal, Erdal M Emin, Sah...
Association between tumor necrosis factor alpha gene promoter polymorphism at position 308 and acne in Turkish patients
Archives of Dermatological Research, vol. 300, no. 7, pp. 371–376
K Baz, Güliz İkizoğlu, Kıymet Baz, Mehmet Emin Erdal, Ayça Yazıcı, Ac Yazıcı, F Söylemez, Fatma Söyl...
Association between tryptophan hydroxylase gene polymorphism and painfulnon osseous temporomandibular disorders
SAUDI MEDICAL JOURNAL, vol. 29, no. 9, pp. 1352–1354
Etoz Osman, Hanife Ataoğlu, Mehmet Emin Erdal
Taq I polymorphism of the vitamin-D receptor gene and quality of life in postmenopausal Turkish women
Turkish Journal of Medical Sciences, vol. 38, no. 1, pp. 21–26
Savaş Gürsoy, Mehmet Emin Erdal, Belgin Alaşehirli, Ali Akdeniz, Nurten Erdal
Tumour necrosis factor alpha 308G A gene polymorphism lack of association with knee osteoarthritis in a Turkish population
Clinical and Experimental Rheumatology, vol. 26, no. 5, pp. 763–768
Melek Sezgin, İbrahim Ömer Barlas, Handan Çamdeviren Ankaralı, Handan Ankaralı, Zuhal Mert Altıntaş,...
Lack of association between DRD3 gene polymorphism and response to clozapine in Turkish schizoprenia patients
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 150B, no. 1, pp. 56–60
İbrahim Ömer Barlas, Mesut Çetin, M Çetin, Mehmet Emin Erdal, Ümit Başar Semiz, Ub Semiz, Mustafa Er...
Role of nitric oxide synthase gene intron 4 and exon 7 polymorphisms in obstructive sleep apnea syndrome
European Archives of Oto-Rhino-Laryngology, vol. 266, no. 3, pp. 449–454
Yıldırım Ahmet Bayazıt, Metin Yılmaz, Mehmet Emin Erdal, Tansu Ulukavak Çiftçi, Alper Ceylan, Oğuz K...
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, vol. 47, no. 10, pp. 1069–1072
Necmettin Kırtak, Hüseyin Serhat İnalöz, Cenk Akçalı, Mehmet Emin Erdal, Hasan Herken, Mehmet Yıldır...
Serotonin transporter gene polymorphisms in patients with chronic tension type headache A preliminary study
Neurology India, vol. 56, no. 2, pp. 156–160
Aylin Akarcalı, Mehmet Cengiz Tataroğlu, Mehmet Emin Erdal, Neriman Aydın, Sacide Pehlivan
Lack of association polymorphisms of the IL1RN IL1A and IL1B genes with knee osteoarthritis in Turkish patients
Clin Invest Med, vol. 30, no. 2, pp. 86–92
Melek Sezgin, M Sezgin, Mehmet Emin Erdal, Zm Altıntaş, Zuhal Altıntaş, Altıntaş Zuhal Mert, Handan ...
The A218C polymorphism of tryptophan hydroxylase gene and migraine
Journal of Clinical Neuroscience, vol. 14, no. 3, pp. 249–251
Nurten Erdal, Hasan Herken, Mustafa Yılmaz, Mehmet Emin Erdal, Yıldırım Ahmet Bayazıt
Which genotype of MAO gene that the patients have are likely to be most susceptible to the symptoms of fibromyalgia
Rheumatology International, vol. 28, no. 4, pp. 307–311
Savaş Gürsoy, Mehmet Emin Erdal, Melek Sezgin, İbrahim Ömer Barlas, Ali Aydeniz, Belgin Alaşehirli, ...
Association of GABA B R1 Receptor Gene Polymorphism with Obstructive Sleep Apnea Syndrome
ORL, vol. 69, no. 3, pp. 190–197
Yıldırım Ahmet Bayazıt, Metin Yılmaz, Oğuz Köktürk, Mehmet Emin Erdal, Tansu Ulukavak Çiftçi, Tuba E...
Deletion of 8p: a case of a child with multiple congenital anomalies
Chromosome Research, vol. , no. , pp. –
Mustafa Ertan Ay, Özlem İzci Ay, Fatma Söylemez, Mehmet Emin Erdal
DRD4 and DAT1 Polymorphisms Modulate Human Gamma Band Responses
Cerebral Cortex, vol. 17, no. 5, pp. 1007–1019
Tamer Demiralp, C S Herrmann, Cristoph S Herrmann, Mehmet Emin Erdal, Tolgay Ergenoğlu, Hatice Yasem...
lack of association with tnf alpha 308 promoter polymorphism in patients with vitiligo
ARCHIVES OF DERMATOLOGICAL RESEARCH, vol. 298, no. 1, pp. 46–49
Güliz İkizoğlu, Tamer İrfan Kaya, Ayça Yazıcı, Mehmet Emin Erdal, Savaşoğlu Ka, Handan Çamdeviren, Ü...
Association of the 1438G A Polymorphism of the 5 HT 2A Receptor Gene with Obstructive Sleep Apnea Syndrome
ORL, vol. 68, no. 3, pp. 123–128
Yıldırım Ahmet Bayazıt, Metin Yılmaz, Tansu Ulukavak Çiftçi, Mehmet Emin Erdal, Oğuz Köktürk, Tuba E...
Association Analysis of the Functional Monoamine Oxidase A Gene Promoter MAO LPR Polymorphism in Attention Deficit Hyperactivity Disorder in a Turkish Sample
Neurology Psychiatry and Brain Research, vol. 13, no. , pp. 65–70
Ömer Mucahit Öztürk, Mehmet Emin Erdal, Süleyman Salih Zoroğlu, Belgin Alaşehirli, Murat Yüce
Lack of association between the 308GA polymorphism of the tumor necrosis factor alpha gene and temporomandibular dysfunction
The Pain Clinic, vol. 18, no. 2, pp. 175–180
A Osman Etoz, Mehmet Emin Erdal, Hasan Herken, Yıldırım Ahmet Bayazıt, Murat Necip Mutlu
PPAR g2 Pro12Ala polymorphism is associated with weight gain in women with gestational diabetes mellitus
European Journal of Obstetrics Gynecology and Reproductive Biology, vol. 129, no. 1, pp. 25–30
Celalettin Ekrem Tok, Devrim Ertunç, Özlem Bilgin, Mehmet Emin Erdal, Mustafa Kaplanoğlu, Saffet Dil...
Insulin Receptor Substrate Gene Polymorphism Is Associated With Obstructive Sleep Apnea Syndrome in Men
The Laryngoscope, vol. 116, no. 11, pp. 1962–1965
Yıldırım Ahmet Bayazıt, Ya Bayazit, Mehmet Emin Erdal, M Yilmaz, Metin Yılmaz, Tu Ciftci, Tansu Uluk...
Association of insulin receptor substrate 1 G972Rvariant with baseline characteristics of the patientswith gestational diabetes mellitus
American Journal of Obstetrics and Gynecology, vol. 194, no. 3, pp. 868–872
Celalettin Ekrem Tok, Devrim Tok, Özlem Bilgin, Mehmet Emin Erdal, Mustafa Kaplanoğlu, Saffet Dilek
Lack of association with TNF 308 promoter polymorphism in patients with vitiligo
Archives of Dermatological Research, vol. 298, no. 1, pp. 46–49
Ayça Yazıcı, Güliz İkizoğlu, Mehmet Emin Erdal, Tamer İrfan Kaya, Savaşoğlu Kaan, Kaan Savaşoğlu, Ça...
Association of Serotonin Transporter Gene Polymorphism with Obstructive Sleep Apnea Syndrome
The Laryngoscope, vol. 115, no. 5, pp. 832–836
Metin Yılmaz, Yıldırım Ahmet Bayazıt, Tansu Ulukavak Çiftçi, Mehmet Emin Erdal, Meral Urhan Küçük, K...
Monoamine oxidase A gene promoter polymorphism in temporomandibular joint pain and dysfunction
The Pain Clinic, vol. 17, no. 1, pp. 39–44
Necip Mutlu, Mehmet Emin Erdal, Hasan Herken, M Özkaya, Mahmut Özkaya, Nurten Erdal, Gülsüm Öz, Yıld...
The importance of IRS 1 Gly972Arg polymorphismin evaluating the response to metformin treatmentin polycystic ovary syndrome
Human Reproduction, vol. 20, no. 5, pp. 1207–1212
Dilek Ertunç, Celalettin Ekrem Tok, Atıl Aktaş, Mehmet Emin Erdal, Saffet Dilek
The 308 G A polymorphism of tumor necrosis factor alpha gene is not associated with migraine
The Pain Clinic, vol. 17, no. 4, pp. 389–393
Hasan Herken, Mehmet Emin Erdal, Mustafa Yılmaz, Kaan Savaşoğlu, Yıldırım Ahmet Bayazıt
Evaluation of glucose metabolism and reproductivehormones in polycystic ovary syndrome on the basisof peroxisome proliferator activated receptor PPAR g2 Pro12Ala genotype
Human Reproduction, vol. 20, no. 6, pp. 1590–1595
Celalettin Ekrem Tok, Atıl Aktaş, Devrim Tok, Mehmet Emin Erdal, Saffet Dilek
Lack of Effect of Extremely Low Frequency Electromagnetic Fields on Cyclin Dependent Kinase 4 Inhibitor Gene p18INK4C in Electric Energy Workers
Archives of Medical Research, vol. 36, no. 2, pp. 120–123
Nurten Erdal, Mehmet Emin Erdal, Serkan Gürgül
Association of Gly972Arg variant of insulin receptorsubstrate 1 with metabolic features in women withpolycystic ovary syndrome
FERTILITY AND STERILITY, vol. 84, no. 2, pp. 407–412
Saffet Dilek, Devrim Tok, Celalettin Ekrem Tok, Mehmet Emin Erdal, Atıl Aktaş
Association between Cathechol O Metyltransferase polymorphism and psoriasis
International Journal of Dermatology, vol. 43, no. 4, pp. 312–314
Mehmet Emin Erdal, Ümit Türsen, Tamer İrfan Kaya, Emine Arzu Kanık, Ebru Derici Eker, Güliz İkizoğlu...
T102C polymorphism of the 5 HT2A receptor gene may be associated with temporomandibular dysfunction
Oral Diseases, vol. 10, no. 6, pp. 349–352
Necip Mutlu, Mehmet Emin Erdal, Hasan Herken, Gülsüm Öz, Yıldırım Ahmet Bayazıt
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, vol. 38, no. 7, pp. 561–566
Cengiz Pata, Mehmet Emin Erdal, Mustafa Kemal Yazıcı, Handan Ankaralı, Mahmut Özkaya, Oğuz Ulu
Extracellular Matrix Protein 1 Gene ECM1 Mutations in Lipoid Proteinosis and Genotype Phenotype Correlation
Journal of Investigative Dermatology, vol. 120, no. 3, pp. 345–350
Takahiro Hamada, Hamada Takahiro, Vesarat Wessagowit, Wessagowit Vesarat, South Andrew P, Andrew P S...
Lack of Association of catechol O Methyltransferase Gene Polymorphism in Obsessive Compulsive Disorder
Depression and Anxiety, vol. 18, no. 1, pp. 41–45
Mehmet Emin Erdal, Şenel Tot, Şenel Acar, Mustafa Kemal Yazıcı, Aylin Ertekin Yazıcı, Hasan Herken, ...
Significance of catechol O methyltransferase gene polymorphismin fibromyalgia syndrome
Rheumatology International, vol. 23, no. 3, pp. 104–107
Savaş Gürsoy, Mehmet Emin Erdal, Hasan Herken, Ercan Madenci, Belgin Alaşehirli, Nurten Erdal
Tardive dyskinesia is not associated with the polymorphisms of 5 HT2A receptor gene serotonin transporter gene and catechol o methyltransferase gene
European Psychiatry, vol. 18, no. 2, pp. 77–81
Hasan Herken, Mehmet Emin Erdal, Ömer Böke, Haluk Asuman Savaş
Significance of catechol O methyltransferase gene polymorphism in myofacial pain syndrome
The Pain Clinic, vol. 15, no. 3, pp. 309–313
Mehmet Emin Erdal, Hasan Herken, Necip Mutlu, Yıldırım Ahmet Bayazıt
T102C and 1438 G A polymorphisms of the 5 HT2A receptor gene in Turkish patients with obsessive compulsive disorder
European Psychiatry, vol. 18, no. 5, pp. 249–254
Şenel Tot, Şenel Acar, Mehmet Emin Erdal, Mustafa Kemal Yazıcı, Aylin Ertekin Yazıcı, O Metin, Özmen...
Relationship between estrogen receptor gene polymorphism and periodontaldiseases
JOURNAL OF DENTAL RESEARCH, vol. 82, no. null, pp. 317–317
I Duran, Mehmet Emin Erdal, Z Özgür, Tuba Edgünlü, Nurten Erdal
The 1438G A polymorphism of the 5HT 2A receptor gene is associated with aura in migraine
The Pain Clinic, vol. 15, no. 3, pp. 315–319
Mehmet Emin Erdal, Mustafa Yılmaz, Hasan Herken, Hasan Kocaoğlu, Yıldırım Ahmet Bayazıt
Relationship between vitamin D receptor gene polyrnorphism andperiodontal diseases
JOURNAL OF DENTAL RESEARCH, vol. 82, no. null, pp. 363–363
Mehmet Emin Erdal, L Duran, Nurten Erdal, Z Özgür, S Bodur
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, vol. 47, no. 1, pp. 17–20
Süleyman Salih Zoroğlu, Mehmet Emin Erdal, Nurten Erdal, Ozen S, Sak&İnodot;R Özen, Belgin Alaşehirl...
Monoamine oxidase A gene promoter polymorphism in female migraineurs
The Pain Clinic, vol. 15, no. 4, pp. 455–458
Mehmet Emin Erdal, Hasan Herken, Mustafa Yılmaz, Yıldırım Ahmet Bayazıt
T102C Polymorphisms at the 5 HT2A Receptor Gene in Turkish Schizophrenia Patients A Possible Association with Prognosis
Neuropsychobiology, vol. 47, no. 1, pp. 27–30
Hasan Herken, Mehmet Emin Erdal, Nurten Erdal, Ahmet Şükrü Aynacıoğlu
Significance of Serotonin Transporter Gene 5 HTTLPR and Variable Number of Tandem Repeat Polymorphism in Attention Deficit Hyperactivity Disorder
Neuropsychobiology, vol. 45, no. 4, pp. 176–181
Süleyman Salih Zoroğlu, Mehmet Emin Erdal, Belgin Alaşehirli, Nurten Erdal, Ercan Sivaslı, Hamdi Tut...
Serotonin transporter gene polymorphism in irritable bowel syndrome
The American Journal of Gastroenterology, vol. 97, no. 7, pp. 1780–1784
Pata Cengiz, Cengiz Pata, Mehmet Emin Erdal, Ebru Derici Eker, Aziz Yazar, Emine Arzu Kanık, Oğuz Ul...
Association between the N acetylation genetic polymorphism and bronchial asthma
British Journal of Clinical Pharmacology, vol. 54, no. 6, pp. 671–674
Muradiye Nacak, Ahmet Şükrü Aynacıoğlu, Ingolf Cascorbı, Mehmet Emin Erdal, Necat Yılmaz, Erhan Ekin...
Association between vitamin D receptor gene polymorphism and psoriasis among the Turkish population
Archives of Dermatological Research, vol. 294, no. 6, pp. 286–289
Tı Kaya, Güliz İkizoğlu, Tamer İrfan Kaya, Mehmet Emin Erdal, Tursen Umut, Ümit Türsen, Çamdeviren H...
Absence of Association of the Serotonin Transporter Gene Polymorphism with the Mentally Healthy Subset of Fibromyalgia Patients
Clinical Rheumatology, vol. 21, no. 3, pp. 194–197
Savaş Gürsoy, Mehmet Emin Erdal, Hasan Herken, Ercan Madenci, Belgin Alaşehirli
Association between catechol O methyltransferase polymorphism and vitiligo
Archives of Dermatological Research, vol. 294, no. 3, pp. 143–146
Ümit Türsen, Tamer İrfan Kaya, Mehmet Emin Erdal, Ebru Derici Eker, Güliz İkizoğlu, Özgür Gündüz
Frequency of the 17 bp variable number of tandem repeat polymorphism in Turkish schizophrenic patients
Schizophrenia Research, vol. 58, no. 1, pp. 99–100
Hasan Herken, Mehmet Emin Erdal, Ahmet Şükrü Aynacıoğlu, İbrahim Ömer Barlas, Osman Çataloluk, Osman...
Association of the T102C polymorphism of 5 HT2A receptor gene with aura in migraine
Journal of the Neurological Sciences, vol. 188, no. 1-2, pp. 99–101
Mehmet Emin Erdal, Hasan Herken, Mustafa Yılmaz, Yıldırım Ahmet Bayazıt
Association of T102C polymorphism of the 5 HT2A receptor gene with pyschiatric status in fibromyalgia syndrome
Rheumatology International, vol. 21, no. 2, pp. 58–61
Savaş Gürsoy, Mehmet Emin Erdal, Hasan Herken, Ercan Madenci, Belgin Alaşehirli
Catechol O methyltransferase gene polymorphism in schizophrenia evidence for association between symptomatology and prognosis
Psychiatric Genetics, vol. 11, no. 2, pp. 105–109
Hasan Herken, Mehmet Emin Erdal
Significance of serotonin transporter gene polymorphism in migraine
Journal of the Neurological Sciences, vol. 186, no. 1-2, pp. 27–30
Mustafa Yılmaz, Mehmet Emin Erdal, Hasan Herken, Osman Çataloluk, İbrahim Ömer Barlas, Yıldırım Ahme...
Possible association of temporomandibular joint pain and dysfunction with a polymorphism in the serotonin transporter gene
American Journal of Orthodontics and Dentofacial Orthopedics, vol. 120, no. 3, pp. 308–313
Hasan Herken, Mehmet Emin Erdal, Necip Mutlu, N Mutlu, Osman Çataloluk, İbrahim Ömer Barlas, O Catal...
Significance of the catechol O methyltransferase gene polymorphism in migraine
Molecular Brain Research, vol. 94, no. 1-2, pp. 193–196
Mehmet Emin Erdal, Hasan Herken, Mustafa Yılmaz, Yıldırım Ahmet Bayazıt
Majör depresyon hastalarında BDNF gen polimorfizmi (rs6265) ile BDNF gen ekspresyon düzeylerinin araştırılması
Mersin Üniversitesi Sağlık Bilimleri Dergisi, vol. 16, no. 3, pp. 473–482
Ümit Karakaş, Kenan Çevik, Mustafa Ertan Ay, Gurbet Doğru Özdemir, Alper Zıblak, Ayşe Nur İnci Kenar...
Amniyotik sıvı hücrelerinde kök hücre pluripotensi belirteçlerinin ifadesi
Mersin Üniversitesi Sağlık Bilimleri Dergisi, vol. 12, no. 3, pp. 388–396
Mustafa Ertan Ay, Ezgi Çokaklı, Murat Çokaklı, Ümit Karakaş, Özlem İzci Ay, Hüseyin Durukan, Mehmet ...
The case of der 5 t 5 14 mat caused by adjacent I meiotic segregation in prenatal diagnosis
European Journal of Human Genetics, vol. 24, no. 1, pp. 417–417
Damla Yüksel, Özlem İzci Ay, Mustafa Ertan Ay, Özlem Tezol, Gurbet Doğru, Kenan Çevik, Ümit Karakaş,...
mikroRNA Çalışmaları ve Psikiyatriye Yansıması
Turkiye Klinikleri J Psychiatry-Special Topics, vol. 9, no. 1, pp. 16–24
Mehmet Emin Erdal, Şenay Görücü Yılmaz
MicroRNA Gene Polymorphisms in Congenital Anomalies of the Kidney and Urinary Tract
Çukurova Üniversitesi Tıp Fakültesi Dergisi, vol. 40, no. 3, pp. 439–451
Özlem Tezol, Ali Delibaş, Özlem İzci Ay, Ümit Karakaş, Bahar Taşdelen, Mehmet Emin Erdal, Mehmet Emi...
A Sex Related Genetic Difference in Bipolar Disorder Tryptophan Hydroxylase 1 Gene 218 A C Polymorphism
Archives of Neuropsychiatry, vol. 48, no. 3, pp. 1–1
Özen Murat Eren, Mehmet Yumru, Mehmet Emin Erdal, Hasan Herken, Haluk Asuman Savaş
Primer Myelofibrozis Polisitemia Vera ve Esansiyel Trombositoz Hastalarında Kantitatif Real Time PCR deltadeltaCT Comparative CT Metoduyla miRNA Ekspresyon Analizi
Türkiye Klinikleri Tıp Bilimleri Dergisi Supplement, vol. 31, no. 6, pp. 90–90
Özlem İzci Ay, Anıl Tombak, Fatma Söylemez, Ümit Karakaş, Didem Derici Yıldırım, Şenay Görücü Yılmaz...
lack of evidence for association between serotonin transporter gene poly morphism and obsesive compulsive disorder
yeni symposium, vol. 48, no. 1, pp. 31–39
Şenel Acar, Mehmet Emin Erdal, Mustafa Kemal Yazıcı, Aylin Ertekin Yazıcı, Ayşe Devrim Başterzi
Monoamine oxidase A gene polymorphism in Parkinson s Disease
JOURNAL OF NEUROLOGICAL SCIENCES (TURKISH), vol. , no. , pp. 98–104
Mustafa Serhan Sevim, Okan Doğu, Mehmet Emin Erdal, Mahmut Özkaya, Şükrü Hakan Kaleağası, Mihriban A...