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- Publications
- Influence
Significance of Serotonin Transporter Gene 5-HTTLPR and Variable Number of Tandem Repeat Polymorphism in Attention Deficit Hyperactivity Disorder
- Salih Zoroğlu, M. Erdal, +5 authors H. Herken
- Psychology, Medicine
- Neuropsychobiology
- 1 July 2002
The purpose of this study was to evaluate the relationship between attention deficit hyperactivity disorder (ADHD) and polymorphism of the two regions of the 5-HTT gene [variable number of tandem… Expand
Utilizing ethnic-specific differences in minor allele frequency to recategorize reported pathogenic deafness variants.
- A. Shearer, Robert W. Eppsteiner, +29 authors R. J. Smith
- Biology, Medicine
- American journal of human genetics
- 2 October 2014
Ethnic-specific differences in minor allele frequency impact variant categorization for genetic screening of nonsyndromic hearing loss (NSHL) and other genetic disorders. We sought to evaluate all… Expand
Extracellular matrix protein 1 gene (ECM1) mutations in lipoid proteinosis and genotype-phenotype correlation.
- T. Hamada, V. Wessagowit, +19 authors J. McGrath
- Biology, Medicine
- The Journal of investigative dermatology
- 1 March 2003
The autosomal recessive disorder lipoid proteinosis results from mutations in extracellular matrix protein 1 (ECM1), a glycoprotein expressed in several tissues (including skin) and composed of two… Expand
DRD4 and DAT1 polymorphisms modulate human gamma band responses.
- T. Demiralp, C. Herrmann, +4 authors H. Beydaği
- Biology, Medicine
- Cerebral cortex
- 1 May 2007
Gamma oscillations (30-80 Hz) have been demonstrated to be important for perceptual and cognitive processes. Animal and in vitro studies have revealed possible underlying generation mechanisms of the… Expand
Cytokine polymorphism in patients with migraine: some suggestive clues of migraine and inflammation.
- I. Yılmaz, A. Ozge, M. Erdal, T. Edgünlü, S. E. Cakmak, Osman Ozgür Yalin
- Medicine
- Pain medicine
- 1 April 2010
OBJECTIVE
There are contrasting results obtained in migraineurs concerning the levels and the role of both pro-inflammatory and anti-inflammatory cytokines. In this study, the association of the… Expand
Significance of serotonin transporter gene polymorphism in migraine
- Mustafa Yılmaz, M. Erdal, H. Herken, O. Çataloluk, Y. Bayazıt
- Medicine
- Journal of the Neurological Sciences
- 1 May 2001
OBJECTIVE
To elucidate significance of the serotonin transporter gene (STG) polymorphism in migraine, and to address the polymorphic patterns of STG, both in the migraineurs and healthy people in… Expand
Effects of 2.4 GHz radiofrequency radiation emitted from Wi-Fi equipment on microRNA expression in brain tissue
- S. Dasdag, M. Akdag, +6 authors K. Yeğin
- Biology, Medicine
- International journal of radiation biology
- 16 March 2015
Abstract Purpose: MicroRNAs (miRNA) play a paramount role in growth, differentiation, proliferation and cell death by suppressing one or more target genes. However, their interaction with… Expand
T102C and -1438 G/A polymorphisms of the 5-HT2A receptor gene in Turkish patients with obsessive-compulsive disorder.
- S. Tot, M. Erdal, K. Yazici, A. Yazıcı, O. Metin
- Psychology, Medicine
- European psychiatry : the journal of the…
- 1 August 2003
OBJECTIVE
This study aimed to investigate the possible association between T102C and -1438 G/A polymorphism in the 5-HT2A receptor gene and susceptibility to and clinical features of… Expand
Long term and excessive use of 900 MHz radiofrequency radiation alter microRNA expression in brain
- S. Dasdag, M. Akdag, +6 authors K. Yeğin
- Biology, Medicine
- International journal of radiation biology
- 27 January 2015
Abstract Purpose: We still do not have any information on the interaction between radiofrequency radiation (RF) and miRNA, which play paramount role in growth, differentiation, proliferation and cell… Expand
Lack of association with TNF-alpha-308 promoter polymorphism in patients with vitiligo.
- A. C. Yazıcı, M. Erdal, +4 authors U. Tursen
- Medicine
- Archives of dermatological research
- 2006
Vitiligo is an acquired depigmentary disorder of the skin, characterized by incomplete penetrance, multiple susceptibility loci and genetic heterogeneity. An immunologic hypothesis is currently… Expand