H Herken

Summary

Publications

  1. ncbi Association of the T102C polymorphism of 5-HT2A receptor gene with aura in migraine
    M E Erdal
    Department of Medical Biology and Genetics, Faculty of Medicine, Mersin University, Mersin, Turkey
    J Neurol Sci 188:99-101. 2001
  2. ncbi Significance of the catechol-O-methyltransferase gene polymorphism in migraine
    M Emin Erdal
    Department of Medical Biology and Genetics, Faculty of Medicine, Mersin University, Mersin, Turkey
    Brain Res Mol Brain Res 94:193-6. 2001
  3. ncbi Catechol-O-methyltransferase gene polymorphism in schizophrenia: evidence for association between symptomatology and prognosis
    H Herken
    Department of Psychiatry, Medical Faculty of Gaziantep University, Kolejtepe, Turkey
    Psychiatr Genet 11:105-9. 2001
  4. ncbi Possible association of temporomandibular joint pain and dysfunction with a polymorphism in the serotonin transporter gene
    H Herken
    Department of Psychiatry, Medical Faculty of Gaziantep University, Gaziantep, Turkey
    Am J Orthod Dentofacial Orthop 120:308-13. 2001
  5. ncbi Tardive dyskinesia is not associated with the polymorphisms of 5-HT2A receptor gene, serotonin transporter gene and catechol-o-methyltransferase gene
    Hasan Herken
    Department of Psychiatry, Medical Faculty of Gaziantep University, City, Gaziantep, Turkey
    Eur Psychiatry 18:77-81. 2003
  6. ncbi T102C polymorphisms at the 5-HT2A receptor gene in Turkish schizophrenia patients: a possible association with prognosis
    Hasan Herken
    Department of Psychiatry, Medical Faculty of Gaziantep University, Kolejtepe Hastanesi, 27200, TR Gaziantep, Turkey
    Neuropsychobiology 47:27-30. 2003
  7. ncbi Significance of serotonin transporter gene polymorphism in migraine
    M Yilmaz
    Department of Neurology, Faculty of Medicine, Gaziantep University, Kolejtepe, Gaziantep, Turkey
    J Neurol Sci 186:27-30. 2001
  8. doi Is the dopamine D3 receptor mRNA on blood lymphocytes help to for identification and subtyping of schizophrenia?
    M Urhan-Kucuk
    Department of Molecular Biology and Genetics, Adiyaman University, Faculty of Science and Letter, Adiyaman, Turkey
    Mol Biol Rep 38:2569-72. 2011
  9. ncbi Association of T102C polymorphism of the 5-HT2A receptor gene with psychiatric status in fibromyalgia syndrome
    S Gursoy
    Department of PMR, Medical Hospital, Kolejtep Gaziantep, Turkey
    Rheumatol Int 21:58-61. 2001
  10. ncbi Evidence that the activities of erythrocyte free radical scavenging enzymes and the products of lipid peroxidation are increased in different forms of schizophrenia
    H Herken
    Gaziantep University, Faculty of Medicine, Department of Psychiatry, Gaziantep, Turkey
    Mol Psychiatry 6:66-73. 2001

Collaborators

Detail Information

Publications12

  1. ncbi Association of the T102C polymorphism of 5-HT2A receptor gene with aura in migraine
    M E Erdal
    Department of Medical Biology and Genetics, Faculty of Medicine, Mersin University, Mersin, Turkey
    J Neurol Sci 188:99-101. 2001
    ..To find out the significance of the 5-HT2A receptor gene polymorphism in migraine. Study design: A PCR study in which 61 migraineurs and 44 healthy controls were included...
  2. ncbi Significance of the catechol-O-methyltransferase gene polymorphism in migraine
    M Emin Erdal
    Department of Medical Biology and Genetics, Faculty of Medicine, Mersin University, Mersin, Turkey
    Brain Res Mol Brain Res 94:193-6. 2001
    ..Although altered catecholamine activity due to polymorphism of COMT gene may be one of the mechanisms involved in the pathogenesis of migraine, these mechanisms are not related to presence or absence of aura...
  3. ncbi Catechol-O-methyltransferase gene polymorphism in schizophrenia: evidence for association between symptomatology and prognosis
    H Herken
    Department of Psychiatry, Medical Faculty of Gaziantep University, Kolejtepe, Turkey
    Psychiatr Genet 11:105-9. 2001
    ..Further studies are required to better understand the association of symptomatology of schizophrenia and other psychiatric disorders with COMT gene polymorphism...
  4. ncbi Possible association of temporomandibular joint pain and dysfunction with a polymorphism in the serotonin transporter gene
    H Herken
    Department of Psychiatry, Medical Faculty of Gaziantep University, Gaziantep, Turkey
    Am J Orthod Dentofacial Orthop 120:308-13. 2001
    ..12/12 genotype may have a protective role against temporomandibular joint pain and dysfunction...
  5. ncbi Tardive dyskinesia is not associated with the polymorphisms of 5-HT2A receptor gene, serotonin transporter gene and catechol-o-methyltransferase gene
    Hasan Herken
    Department of Psychiatry, Medical Faculty of Gaziantep University, City, Gaziantep, Turkey
    Eur Psychiatry 18:77-81. 2003
    ..The pathophysiology of tardive dyskinesia (TD) is not completely understood.Aim. - To assess the relationship of TD with 5-HT2A receptor gene, serotonin transporter gene (5 HTT), and catechol-o-methyltransferase (COMT) gene polymorphisms...
  6. ncbi T102C polymorphisms at the 5-HT2A receptor gene in Turkish schizophrenia patients: a possible association with prognosis
    Hasan Herken
    Department of Psychiatry, Medical Faculty of Gaziantep University, Kolejtepe Hastanesi, 27200, TR Gaziantep, Turkey
    Neuropsychobiology 47:27-30. 2003
    ..Serotonergic system abnormalities have been implicated in the pathogenesis of schizophrenia. The 5-HT2A receptor gene polymorphism has long been implicated to play a role in the pathogenesis of schizophrenia...
  7. ncbi Significance of serotonin transporter gene polymorphism in migraine
    M Yilmaz
    Department of Neurology, Faculty of Medicine, Gaziantep University, Kolejtepe, Gaziantep, Turkey
    J Neurol Sci 186:27-30. 2001
    ..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 this country...
  8. doi Is the dopamine D3 receptor mRNA on blood lymphocytes help to for identification and subtyping of schizophrenia?
    M Urhan-Kucuk
    Department of Molecular Biology and Genetics, Adiyaman University, Faculty of Science and Letter, Adiyaman, Turkey
    Mol Biol Rep 38:2569-72. 2011
    ..030) while no difference was detected between control subjects and schizophrenics. We concluded that the levels of DRD3 mRNA can help understanding and severity of clinical manifestations in schizophrenia...
  9. ncbi Association of T102C polymorphism of the 5-HT2A receptor gene with psychiatric status in fibromyalgia syndrome
    S Gursoy
    Department of PMR, Medical Hospital, Kolejtep Gaziantep, Turkey
    Rheumatol Int 21:58-61. 2001
    ..CONCLUSION. T102C polymorphism of the 5-HT2A receptor gene is not associated with the etiology of FS. Our results also indicate that the T/T genotype may be responsible for psychiatric symptoms of FS...
  10. ncbi Evidence that the activities of erythrocyte free radical scavenging enzymes and the products of lipid peroxidation are increased in different forms of schizophrenia
    H Herken
    Gaziantep University, Faculty of Medicine, Department of Psychiatry, Gaziantep, Turkey
    Mol Psychiatry 6:66-73. 2001
    ..It is proposed that antioxidant status may be changed in schizophrenia and thus may induce lipid peroxidation. Therefore, oxidative stress may have a pathophysiological role in all the subtypes of schizophrenia...
  11. ncbi T102C polymorphism of the 5-HT2A receptor gene may be associated with temporomandibular dysfunction
    N Mutlu
    Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Selcuk University, Konya, Turkey
    Oral Dis 10:349-52. 2004
    ..To assess whether a relationship existed between the T102C polymorphism of 5-HT2A receptor gene and temporomandibular dysfunction...
  12. ncbi An apparently dominant bipolar affective disorder (BPAD) locus on chromosome 20p11.2-q11.2 in a large Turkish pedigree
    U Radhakrishna
    Division of Medical Genetics, University of Geneva Medical School, Geneva, Switzerland
    Eur J Hum Genet 9:39-44. 2001
    ..Haplotype analysis enabled the mapping of the BPAD locus in this family between markers D20S186 and D20S109, to a region of approximately 42 cM...