Publications & Works

Articles Published in Journals That Entered SCI, SSCI and AHCI Indexes

Peripheral blood mononuclear cell proteome profile in Behcet's syndrome

RHEUMATOLOGY INTERNATIONAL, vol.40, no.1, pp.65-74, 2020 (Journal Indexed in SCI) identifier identifier identifier

Spectrum of the neurologic manifestations in childhood-onset cryopyrin-associated periodic syndrome

EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, vol.23, no.3, pp.466-472, 2019 (Journal Indexed in SCI) identifier identifier identifier

C3 glomerulopathy in NLRP12-related autoinflammatory disorder: case-based review

RHEUMATOLOGY INTERNATIONAL, vol.38, no.8, pp.1571-1576, 2018 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

LACC1 Gene Defects in Familial Form of Juvenile Arthritis

JOURNAL OF RHEUMATOLOGY, vol.45, no.5, pp.726-728, 2018 (Journal Indexed in SCI) identifier identifier identifier

Familial Mediterranean fever in childhood: a single-center experience

RHEUMATOLOGY INTERNATIONAL, vol.38, no.1, pp.67-74, 2018 (Journal Indexed in SCI) identifier identifier identifier

Nanomedicine

LOW-DIMENSIONAL AND NANOSTRUCTURED MATERIALS AND DEVICES: PROPERTIES, SYNTHESIS, CHARACTERIZATION, MODELLING AND APPLICATIONS, pp.579-587, 2016 (Journal Indexed in SCI) identifier

Increased expression of exon 2 deleted MEFV transcript in familial Mediterranean fever patients

INTERNATIONAL JOURNAL OF IMMUNOGENETICS, vol.38, no.4, pp.327-329, 2011 (Journal Indexed in SCI) identifier identifier identifier

A twin study in Behçet's syndrome.

Clinical and experimental rheumatology, vol.28, 2010 (Journal Indexed in SCI Expanded) identifier identifier

A TWIN STUDY IN BEHCET'S SYNDROME

CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, vol.28, no.4, 2010 (Journal Indexed in SCI) identifier

Analysis of the dopamine beta hydroxylase gene in Gilles de la Tourette syndrome

AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, no.6, pp.673-677, 2006 (Journal Indexed in SCI) identifier identifier identifier

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, no.5, pp.420-427, 2006 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

Association analysis of MAOA and COMT with neuroticism assessed by peers

AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, no.1, pp.90-96, 2003 (Journal Indexed in SCI) identifier identifier identifier

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, no.1, pp.54-59, 2003 (Journal Indexed in SCI) identifier identifier identifier

Articles Published in Other Journals

Refereed Congress / Symposium Publications in Proceedings

Increased Burden of Susceptibility Variants in Familial Multiple Sclerosis

Annual Meeting of the American-Academy-of-Neurology, Toronto, Canada, 25 April - 01 May 2020, vol.94 identifier

Genetic screening in the clinical suspicion of autoinflammatory diseases

European Biotechnology Congress, Valencia, Spain, 11 - 13 April 2019, vol.305 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, Italy, 16 - 19 June 2018, vol.27, pp.201-202 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, Italy, 16 - 19 June 2018, vol.27, pp.936 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, Hungary, 13 - 16 June 2019, vol.34, pp.214 Sustainable Development 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, United States Of America, 4 - 10 May 2019, vol.92 identifier

LACC1 mutations in familial form of juvenile idiopathic arthritis

50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.915 identifier

Whole genome linkage and exome sequencing analyses in an autosomal recessive Takayasu arteritis family

50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.323 identifier

WHOLE GENOME LINKAGE AND EXOME SEQUENCING ANALYSES IN TAKAYASU ARTERITIS FAMILIES

Congress of the European-League-Against-Rheumatism (EULAR), Amsterdam, Netherlands, 13 - 16 June 2018, vol.77, pp.231-232 Creative Commons License identifier

Identification of Multiple Sclerosis Related Pathways through Genome-Proteome Correlations

ACTRIMS Forum, California, United States Of America, 1 - 03 February 2018, vol.24, pp.99 identifier

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

Annual European Congress of Rheumatology, Madrid, Spain, 14 - 17 June 2017, vol.76, pp.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 May 2017

Genetic Analysis of Inherited Autoinflammatory Disorders

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

Genetic analysis of inherited autoinflammatory disorders

9th International Congress of Familial Mediterranean Fever and Systemic Auto-Inflammatory Diseases, Girne, Cyprus (Kktc), 4 - 07 May 2017

Integrated Genomic and Proteomic Analyses of Multiple Sclerosis

American Academy of Neurology 69th Annual Meeting, 22 - 28 April 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, Canada, 14 - 17 September 2016, vol.22, pp.585-586 identifier

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

International Congress of Familial Mediterreanen Fever and Systemic Autoinflammatory Diseases, 30 September - 03 October 2015

A Case with Febrile Attacks and Vasculopathy Associated with ADA2 and MEFV Gene Mutations

International Congress of FMF and Systemic Autoinflammatory Diseases, 30 September - 03 October 2015

Proteomic analysis: identification of candidate protein biomarkers in the CSF and serum samples of patients with clinically different multiple sclerosis subtypes

28th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis, Lyon, France, 10 - 13 October 2012, vol.18, pp.263-264 identifier

Books & Book Chapters

Behçet Hastalığı: Genetik ve Epigenetik Araştırmalar

in: Behçet Hastalığı, Emire Seyahi, Editor, Türkiye Klinikleri Yayınevi, Ankara, pp.21-28, 2020 Sustainable Development

Nanomedicine

in: Low Dimensional and Nanostructured Materials and Devices, , Editor, Springer International Publishing, pp.579-587, 2016