SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler
Integrated Genomic and Proteomic Analyses of Multiple Sclerosis
NEUROLOGY
, cilt.88, 2017 (SCI-Expanded)

A NOVEL Missense Mvk mutation in a Family with Familial Mediterranean Fever-like Disease
ARTHRITIS & RHEUMATOLOGY
, cilt.68, 2016 (SCI-Expanded)

Methylation Analysis of HLA-B Locus in Familial Behcet Syndrome
ARTHRITIS & RHEUMATOLOGY
, cilt.67, 2015 (SCI-Expanded)

MEFV mutations in an elderly population
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
, cilt.26, sa.2, ss.200, 2008 (SCI-Expanded)

Analysis of the dopamine beta hydroxylase gene in Gilles de la Tourette syndrome
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
, cilt.141B, sa.6, ss.673-677, 2006 (SCI-Expanded)




Stable transmission and expression of the hepatitis B virus total genome in hybrid transgenic mice until F10 generation
JOURNAL OF EXPERIMENTAL ZOOLOGY PART A-ECOLOGICAL AND INTEGRATIVE PHYSIOLOGY
, cilt.305A, sa.5, ss.420-427, 2006 (SCI-Expanded)




Association analysis of MAOA and COMT with neuroticism assessed by peers
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
, sa.1, ss.90-96, 2003 (SCI-Expanded)



Evaluation of the genes for the adrenergic receptors alpha 2A and alpha 1C and Gilles de la Tourette syndrome
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
, cilt.119B, sa.1, ss.54-59, 2003 (SCI-Expanded)



Functional promoter VNTR for MAOA: Identification of two novel alleles and analyses of association with neuroticism, depression and anxiety.
AMERICAN JOURNAL OF MEDICAL GENETICS
, cilt.96, sa.4, ss.561-562, 2000 (SCI-Expanded)

Diğer Dergilerde Yayınlanan Makaleler
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler
Kondroisit Hücre Hatlarında Progresif Psödoromatoid Displazi Hastalık Geni Olan CCN6’daki Patojenik Varyantların Fonksiyonel Araştırmaları
9th International Congress of the Molecular Biology Association of Turkey, İzmir, Türkiye, 12 - 14 Eylül 2024, ss.1-138, (Özet Bildiri)
Analysis of Familial Exome Analysis Tools
8. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 21 - 23 Eylül 2023, ss.1, (Özet Bildiri)
Genetic and Functional Activity Analyses of ADA2 in Patients with Deficiency of Adenosine Deaminase 2
American Society of Human Genetics Annual Meeting, Washington, Amerika Birleşik Devletleri, 1 - 05 Kasım 2023, ss.258, (Özet Bildiri)
Comprehensive Analysis of Low-Frequency Genetic Variants through Exome Sequencing in Familial Multiple Sclerosis
75. American Society of Human Genetics Congress, Washington, Amerika Birleşik Devletleri, 1 - 05 Kasım 2023, ss.1, (Özet Bildiri)
Identification of a splice variant in PSMB10 gene in a multiply affected family with undiagnosed autoinflammatory syndrome.”
European Society of Human Genetics conference (ESHG 2023), Glasgow, İngiltere, 10 - 13 Haziran 2023, ss.1, (Özet Bildiri)
JAK/STAT signaling during cellular senescence process in primary fibroblast of blind mole rats
IUBMB-FEBS-PABMB Congress , Lisbon, Portekiz, 10 Temmuz 2022, ss.1-2, (Özet Bildiri)
Cellular senescence-related inflammation and JAK-STAT signaling in long-lived Blind Mole-Rats
8th International Congress of Molecular Biology Association of Turkey, İstanbul, Türkiye, 9 Haziran - 12 Temmuz 2022, (Yayınlanmadı)
NADİR BİR OLGU: ADENOZİN DEAMİNAZ-2 EKSİKLİĞİ
54. TÜRK PEDİATRİ KONGRESİ, Türkiye, 6 - 10 Mayıs 2018, (Özet Bildiri)
Behçet Sendromunda Proteom Analizleri
XVIII. Ulusal Romatoloji Kongresi, Türkiye, 18 - 22 Ekim 2017, (Tam Metin Bildiri)
Genetic Analysis of Inherited Autoinflammatory Disorders
9th International Congress of Familial Mediterranean Fever and Systemic Auto-Inflammatory Diseases, 4 - 07 Mayıs 2017, (Tam Metin Bildiri)
Genetic analysis of inherited autoinflammatory disorders
9th International Congress of Familial Mediterranean Fever and Systemic Auto-Inflammatory Diseases, Girne, Kıbrıs (Kktc), 4 - 07 Mayıs 2017, (Özet Bildiri)
Integrated Genomic and Proteomic Analyses of Multiple Sclerosis
American Academy of Neurology 69th Annual Meeting, 22 - 28 Nisan 2017, (Tam Metin Bildiri)
Çocukluk çağı nadir otoenflamatuvar hastalıkların genetik tanısı
III. Çocuk Romatoloji Kongresi, Türkiye, 21 - 24 Nisan 2016
Suggestive linkage to chromosomal regions 13q13 3 and 21q22 2 in families with Multiple Sclerosis
European Conference of Human Genetics, 6 - 09 Haziran 2015
Kitaplar
Nanomedicine
Low Dimensional and Nanostructured Materials and Devices, , Editör, Springer International Publishing, ss.579-587, 2016