Mehmet Emin ERDAL
Mehmet Emin ERDAL
Professor, Department of Medical Biology and Genetics, Faculty of Medicine, Mersin University
Verified email at mersin.edu.tr - Homepage
Title
Cited by
Cited by
Year
A review of executive function deficits in autism spectrum disorder and attention-deficit/hyperactivity disorder
F Craig, F Margari, AR Legrottaglie, R Palumbi, C De Giambattista, ...
Neuropsychiatric disease and treatment 12, 1191, 2016
2602016
Serotonin transporter gene polymorphism in irritable bowel syndrome
C Pata, ME Erdal, E Derici, A Yazar, A Kanık, O Ulu
The American journal of gastroenterology 97 (7), 1780-1784, 2002
1812002
Extracellular matrix protein 1 gene (ECM1) mutations in lipoid proteinosis and genotype-phenotype correlation
T Hamada, V Wessagowit, AP South, GHS Ashton, I Chan, N Oyama, ...
Journal of investigative dermatology 120 (3), 345-350, 2003
1582003
Utilizing ethnic-specific differences in minor allele frequency to recategorize reported pathogenic deafness variants
AE Shearer, RW Eppsteiner, KT Booth, SS Ephraim, J Gurrola II, ...
The American Journal of Human Genetics 95 (4), 445-453, 2014
1302014
Significance of serotonin transporter gene 5-HTTLPR and variable number of tandem repeat polymorphism in attention deficit hyperactivity disorder
SS Zoroğlu, ME Erdal, B Alaşehirli, N Erdal, E Sivasli, H Tutkun, HA Savaş, ...
Neuropsychobiology 45 (4), 176-181, 2002
1272002
DRD4 and DAT1 polymorphisms modulate human gamma band responses
T Demiralp, CS Herrmann, ME Erdal, T Ergenoglu, YH Keskin, M Ergen, ...
Cerebral Cortex 17 (5), 1007-1019, 2007
1112007
Catechol-O-methyltransferase gene polymorphism in schizophrenia: evidence for association between symptomatology and prognosis
H Herken, ME Erdal
Psychiatric Genetics 11 (2), 105-109, 2001
952001
Significance of serotonin transporter gene polymorphism in migraine
M Yılmaz, ME Erdal, H Herken, O Cataloluk, Ö Barlas, YA Bayazıt
Journal of the neurological sciences 186 (1-2), 27-30, 2001
922001
Tardive dyskinesia is not associated with the polymorphisms of 5-HT2A receptor gene, serotonin transporter gene and catechol-o-methyltransferase gene
H Herken, ME Erdal, Ö Böke, HA Savaş
European Psychiatry 18 (2), 77-81, 2003
772003
Cytokine polymorphism in patients with migraine: some suggestive clues of migraine and inflammation
IA Yılmaz, A Özge, ME Erdal, TG Edgünlü, SE Çakmak, OÖ Yalın
Pain Medicine 11 (4), 492-497, 2010
722010
T102C and–1438 G/A polymorphisms of the 5-HT2A receptor gene in Turkish patients with obsessive–compulsive disorder
Ş Tot, ME Erdal, K Yazıcı, AE Yazıcı, Ö Metin
European psychiatry 18 (5), 249-254, 2003
702003
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
SS Zoroglu, ME Erdal, N Erdal, S Ozen, B Alasehirli, E Sivasli
Neuropsychobiology 47 (1), 17-20, 2003
692003
Significance of the catechol-O-methyltransferase gene polymorphism in migraine
ME Erdal, H Herken, M Yilmaz, YA Bayazit
Molecular brain research 94 (1-2), 193-196, 2001
662001
Effects of 2.4 GHz radiofrequency radiation emitted from Wi-Fi equipment on microRNA expression in brain tissue
S Dasdag, MZ Akdag, ME Erdal, N Erdal, OI Ay, ME Ay, SG Yilmaz, ...
International journal of radiation biology 91 (7), 555-561, 2015
652015
Lack of Association of catechol‐O‐Methyltransferase Gene Polymorphism in Obsessive–Compulsive Disorder
ME Erdal, Ş Tot, K Yazıcı, A Yazıcı, H Herken, P Erdem, E Derici, ...
Depression and anxiety 18 (1), 41-45, 2003
652003
Association of the T102C polymorphism of 5-HT2A receptor gene with aura in migraine
ME Erdal, H Herken, M Yılmaz, YA Bayazıt
Journal of the neurological sciences 188 (1-2), 99-101, 2001
592001
Association between tumor necrosis factor-alpha gene promoter polymorphism at position-308 and acne in Turkish patients
K Baz, ME Erdal, F Söylemez, U Güvenç, B Taşdelen, G Ikizoğlu
Archives of dermatological research 300 (7), 371, 2008
572008
Association of serotonin transporter gene polymorphism with obstructive sleep apnea syndrome
M Ylmaz, YA Bayazit, TU Ciftci, ME Erdal, M Urhan, O Kokturk, ...
The Laryngoscope 115 (5), 832-836, 2005
562005
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)
IÖ Barlas, M Sezgin, ME Erdal, G Sahin, HC Ankarali, ZM Altintas, ...
Rheumatology international 29 (4), 383, 2009
502009
T102C polymorphism of the 5‐HT2A receptor gene may be associated with temporomandibular dysfunction
N Mutlu, ME Erdal, H Herken, G Oz, YA Bayazıt
Oral diseases 10 (6), 349-352, 2004
502004
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