Yayınlar & Eserler

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Diğer Dergilerde Yayınlanan Makaleler

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

Analysis of Familial Exome Analysis Tools

8. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 21 - 23 Eylül 2023, ss.1

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

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

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

Increased Burden of Susceptibility Variants in Familial Multiple Sclerosis

Annual Meeting of the American-Academy-of-Neurology, Toronto, Kanada, 25 Nisan - 01 Mayıs 2020, cilt.94 identifier

Genetic screening in the clinical suspicion of autoinflammatory diseases

European Biotechnology Congress, Valencia, İspanya, 11 - 13 Nisan 2019, cilt.305 identifier

Candidate Gene Search For Autosomal Dominant Behcet's Disease Through Whole Exome Sequencing

51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, İtalya, 16 - 19 Haziran 2018, cilt.27, ss.936 identifier

Investigation of Peripheral Blood Mononuclear Cells (PBMC) Proteome Profile in Behcet's Disease

51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, İtalya, 16 - 19 Haziran 2018, cilt.27, ss.201-202 identifier

URINARY EXOSOMAL MIRNA LEVELS REVEAL NEW POTENTIAL BIOMARKERS IN TYPE 2 DIABETIC NEPHROPATHY AND FSGS

56th Congress of the European-Renal-Association (ERA)-European-Dialysis-and-Transplant-Association (EDTA) - Burden, Access and Disparities in Kidney Disease, Budapest, Macaristan, 13 - 16 Haziran 2019, cilt.34, ss.214 identifier

Lack of Low-Frequency Complete-Penetrance Coding Variants Responsible from Familial Multiple Sclerosis

71st Annual Meeting of the American-Academy-of-Neurology (AAN), Pennsylvania, Amerika Birleşik Devletleri, 4 - 10 Mayıs 2019, cilt.92 identifier

LACC1 mutations in familial form of juvenile idiopathic arthritis

50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Danimarka, 27 - 30 Mayıs 2017, cilt.26, ss.915 identifier

WHOLE GENOME LINKAGE AND EXOME SEQUENCING ANALYSES IN TAKAYASU ARTERITIS FAMILIES

Congress of the European-League-Against-Rheumatism (EULAR), Amsterdam, Hollanda, 13 - 16 Haziran 2018, cilt.77, ss.231-232 Creative Commons License identifier

Identification of Multiple Sclerosis Related Pathways through Genome-Proteome Correlations

ACTRIMS Forum, California, Amerika Birleşik Devletleri, 1 - 03 Şubat 2018, cilt.24, ss.99 identifier

ANTI TNF-ALPHA THERAPY WOULD BE LIFESAVING IN DEFICIENCY OF ADENOSINE DEAMINASE-2

Annual European Congress of Rheumatology, Madrid, İspanya, 14 - 17 Haziran 2017, cilt.76, ss.1402-1403 Creative Commons License identifier

Genetic Analysis of Inherited Autoinflammatory Disorders

9th International Congress of Familial Mediterranean Fever and Systemic Auto-Inflammatory Diseases, 4 - 07 Mayıs 2017

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

Potential biomarkers for different clinical subtypes of multiple sclerosis

32nd Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS), London, Kanada, 14 - 17 Eylül 2016, cilt.22, ss.585-586 identifier

Çocukluk çağı nadir otoenflamatuvar hastalıkların genetik tanısı

III. Çocuk Romatoloji Kongresi, Türkiye, 21 - 24 Nisan 2016

The Frequency of MEFV gene variation in adult onset still disease and gout

International Congress of Familial Mediterreanen Fever and Systemic Autoinflammatory Diseases, 30 Eylül - 03 Ekim 2015

Functional effects of a tandem duplication polymorphism in the 5 ' flanking region of the DRD4 gene

10th World Congress of Psychiatric Genetics, Brussels, Belçika, 9 - 13 Ekim 2002, cilt.114, ss.880 identifier

Kitap & Kitap Bölümleri

Behçet Hastalığı: Genetik ve Epigenetik Araştırmalar

Behçet Hastalığı, Emire Seyahi, Editör, Türkiye Klinikleri Yayınevi, Ankara, ss.21-28, 2020 Sürdürülebilir Kalkınma

Nanomedicine

Low Dimensional and Nanostructured Materials and Devices, , Editör, Springer International Publishing, ss.579-587, 2016

Metrikler

Yayın

91

Atıf (WoS)

1128

H-İndeks (WoS)

16

Atıf (Scopus)

1213

H-İndeks (Scopus)

16

Proje

5

Tez Danışmanlığı

22

Açık Erişim

10
BM Sürdürülebilir Kalkınma Amaçları