Prof. Dr. EDA TAHİR TURANLI

LOW-DIMENSIONAL AND NANOSTRUCTURED MATERIALS AND DEVICES: PROPERTIES, SYNTHESIS, CHARACTERIZATION, MODELLING AND APPLICATIONS , ss.579-587, 2016 (SCI-Expanded)

Methylation Analysis of HLA-B Locus in Familial Behcet Syndrome

Turanli E., Koprulu P., UĞURLU S., Yazici H., Seyahi E.

ARTHRITIS & RHEUMATOLOGY , cilt.67, 2015 (SCI-Expanded)

CSF Proteomics Identifies Specific and Shared Pathways for Multiple Sclerosis Clinical Subtypes

Avsar T., Durasi I. M., Uygunoglu U., Tutuncu M., Demirci N. O., Saip S., et al.

PLOS ONE , cilt.10, sa.5, 2015 (SCI-Expanded)

Protein biomarkers for multiple sclerosis: semi-quantitative analysis of cerebrospinal fluid candidate protein biomarkers in different forms of multiple sclerosis

Avsar T., Korkmaz D., TÜTÜNCÜ M., Demirci N. O., SAİP S., Kamaşak M. E., et al.

MULTIPLE SCLEROSIS JOURNAL , cilt.18, sa.8, ss.1081-1091, 2012 (SCI-Expanded)

Analysis of MEFV exon methylation and expression patterns in familial Mediterranean fever

Kirectepe A. K., Kasapcopur O., Arisoy N., Erdem G. C., Hatemi G., Ozdogan H., et al.

BMC MEDICAL GENETICS , cilt.12, 2011 (SCI-Expanded)

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

Kirectepe A. K., Erdem G. C., Senturk N., Arisoy N., Hatemi G., Ozdogan H., et al.

INTERNATIONAL JOURNAL OF IMMUNOGENETICS , cilt.38, sa.4, ss.327-329, 2011 (SCI-Expanded)

The prevalence of Behcet's syndrome, familial Mediterranean fever, HLA-B51 and MEFV gene mutations among ethnic Armenians living in Istanbul, Turkey

Seyahi E., Turanli E., Mangan M. S., Celikyapi G., Oktay V., Cevirgen D., et al.

CLINICAL AND EXPERIMENTAL RHEUMATOLOGY , cilt.28, sa.4, 2010 (SCI-Expanded)

A TWIN STUDY IN BEHCET'S SYNDROME

Masatlioglu S., Seyahi E., Turanli E., FRESKO İ., GÖĞÜŞ F. N., Senates E., et al.

CLINICAL AND EXPERIMENTAL RHEUMATOLOGY , cilt.28, sa.4, 2010 (SCI-Expanded)

Common MEFV mutations and polymorphisms in an elderly population: an association with E148Q polymorphism and rheumatoid factor levels.

Turanli E., Beger T., Erdincler D., Curgunlu A., Karaman S., Karaca E., et al.

Clinical and experimental rheumatology , cilt.27, ss.340-3, 2009 (SCI-Expanded)

MEFV mutations in an elderly population

Tahir T. E., Beger T., Erdincler D., Curgunlu A., Karaman S., Karaca E., et al.

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

Ozbay F., Wigg K. G., Turanli E., Asherson P., Yazgan Y., Sandor P., et al.

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

Bagis H., Arat S., Mercan H., Aktoprakligil D., Caner M., Turanli E., et al.

JOURNAL OF EXPERIMENTAL ZOOLOGY PART A-ECOLOGICAL AND INTEGRATIVE PHYSIOLOGY , cilt.305A, sa.5, ss.420-427, 2006 (SCI-Expanded)

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

D'Souza U., Russ C., Tahir E., Mill J., McGuffin P., Asherson P., et al.

BIOLOGICAL PSYCHIATRY , cilt.56, sa.9, ss.691-697, 2004 (SCI-Expanded)

Joint analysis of the DRD5 marker concludes association with attention-deficit/hyperactivity disorder confined to the predominantly inattentive and combined subtypes

Lowe N., Kirley A., Hawi Z., Sham P., Wickham H., Kratochvil C., et al.

AMERICAN JOURNAL OF HUMAN GENETICS , cilt.74, sa.2, ss.348-356, 2004 (SCI-Expanded)

Association analysis of MAOA and COMT with neuroticism assessed by peers

Eley T., Tahir E., Angleitner A., Harriss K., McClay J., Plomin R., et al.

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

Xu C., Ozbay F., Wigg K., Shulman R., Tahir E., Yazgan Y., et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS , cilt.119B, sa.1, ss.54-59, 2003 (SCI-Expanded)

Association study of a dopamine transporter polymorphism and attention deficit hyperactivity disorder in UK and Turkish samples

Curran S., Mill J., Tahir E., Kent L., Richards S., Gould A., et al.

MOLECULAR PSYCHIATRY , cilt.6, sa.4, ss.425-428, 2001 (SCI-Expanded)

Functional promoter VNTR for MAOA: Identification of two novel alleles and analyses of association with neuroticism, depression and anxiety.

Eley T., Tahir E., Angleitner A., Fombonne E., Galsworthy M., Plomin R., et al.

AMERICAN JOURNAL OF MEDICAL GENETICS , cilt.96, sa.4, ss.561-562, 2000 (SCI-Expanded)

Association and linkage of DRD4 and DRD5 with attention deficit hyperactivity disorder (ADHD) in a sample of Turkish children

Tahir E., Yazgan Y., Cirakoglu B., Ozbay F., Waldman I., Asherson P.

MOLECULAR PSYCHIATRY , cilt.5, sa.4, ss.396-404, 2000 (SCI-Expanded)

No association between low- and high-activity catecholamine-methyl-transferase (COMT) and attention deficit hyperactivity disorder (ADHD) in a sample of Turkish children

Tahir E., Curran S., Yazgan Y., Ozbay F., Cirakoglu B., Asherson P.

AMERICAN JOURNAL OF MEDICAL GENETICS , cilt.96, sa.3, ss.285-288, 2000 (SCI-Expanded)

A family-based association study of a Turkish ADHD population: Findings of DRD4, DAT1, DRD5, and DBH.

Tahir E., Yazgan Y., Cirakoglu B., Asherson P.

MOLECULAR PSYCHIATRY , cilt.4, 1999 (SCI-Expanded)

A linkage study of the N-methyl-D-aspartate receptor subunit gene loci and schizophrenia in southern African Bantu-speaking families

Riley B., Tahir E., Rajagopalan S., MogudiCarter M., Faure S., Weissenbach J., et al.

PSYCHIATRIC GENETICS , cilt.7, sa.2, ss.57-74, 1997 (SCI-Expanded)

Preliminary results from a linkage study of the N-methyl-D-aspartate (NMDA) receptor subunit genes in a sample of southern African Bantu-speaking families multiply affected with schizophrenia

Riley B., Tahir E., MogudiCarter M., Rajagopalan S., Faure S., Weissenbach J., et al.

SCHIZOPHRENIA RESEARCH , cilt.18, sa.2-3, 1996 (SCI-Expanded)

Diğer Dergilerde Yayınlanan Makaleler

A case with febrile attacks and vasculopathy associated with ADA2 and MEFV pathogenic variants.

Parlar K., Tahir Turanli E., Nuhoglu Kantarci E., Hacioglu A., Kirectepe Aydin A., Ayla A. Y., et al.

Modern rheumatology case reports , 2023 (ESCI)

Translation of Cellular Senescence to Novel Therapeutics: Insights From Alternative Tools and Models.

Inci N., Kamali D., Akyildiz E. O., Tahir Turanli E., Bozaykut P.

Frontiers in aging , cilt.3, ss.828058, 2022 (Hakemli Dergi)

Chemerin rs17173608 Gene Polymorphism is not Associated with Type 2 Diabetes Mellitus: a Cross-sectional Study.

Olt S., Öznas O., Bağış H., Turanlı E.

Folia medica , cilt.61, ss.69-75, 2019 (Hakemli Dergi) Sürdürülebilir Kalkınma

Quality assurance of genetic laboratories and the EBTNA practice certification, a simple standardization assurance system for a laboratory network

Precone V., DÜNDAR M., Beccari T., Turanli E., Cecchin S., Marceddu G., et al.

EUROBIOTECH JOURNAL , cilt.2, sa.4, ss.215-258, 2018 (ESCI)

Role of genetics in pediatric rheumatology

Turanli E., Everest E., Balamir A., Aydin A. K., KASAPÇOPUR Ö.

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , cilt.52, sa.3, ss.113-121, 2017 (ESCI)

Based on neuro-degeneration and inflammation in animal models of multiple sclerosis Multipl sklerozda nöro-dejenerasyon ve enflamasyon temelli hayvan modelleri

Avşar T., SİVA A., Altuǧ T., TAHİR TURANLI E.

Turkish Journal of Immunology , cilt.18, sa.2, ss.10, 2012 (Scopus)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler

A rare case of uncharacterised autoinflammatory disease: patient carrying variations in NLRP3 and TNFRSF1A genes

Kılınç Ö. C., Gayibova K., Durucan İ., Özkılınç Önen M., Onat U. İ., Bülbül A., et al.

European Congress of Rheumatology, Vienna, Avusturya, 12 - 15 Haziran 2024

Analysis of Familial Exome Analysis Tools

Tahir Turanlı E., Bülbül A., Siva A.

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

Everest E., Ozkilinc Onen M., Demirci T., Timuçin A. C., Sahin S., Kasapcopur O., et al.

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

Tahir Turanlı E., Bülbül A., Siva A., Sezerman O. U.

75. American Society of Human Genetics Congress, Washington, Amerika Birleşik Devletleri, 1 - 05 Kasım 2023, ss.1

Identification of a splice variant in PSMB10 gene in a multiply affected family with undiagnosed autoinflammatory syndrome.”

Tahir Turanlı E., Geçgel M., Onat U. İ., Uğurlu S., Bülbül A., Siğli D.

European Society of Human Genetics conference (ESHG 2023), Glasgow, İngiltere, 10 - 13 Haziran 2023, ss.1

JAK/STAT signaling during cellular senescence process in primary fibroblast of blind mole rats

İnci N., Akyıldız E. O., Bülbül A. A., Tahir Turanlı E., Bozaykut Eker P.

IUBMB-FEBS-PABMB Congress , Lisbon, Portekiz, 10 Temmuz 2022, ss.1-2

Cellular senescence-related inflammation and JAK-STAT signaling in long-lived Blind Mole-Rats

Inci N., Akyıldız E. O., Tahir Turanlı E., Bulbul A., Savsar B., Çolak F., et al.

8th International Congress of Molecular Biology Association of Turkey, İstanbul, Türkiye, 9 Haziran - 12 Temmuz 2022

Prospective Analysis of Cerebrospinal Fluid Protein Levels Reveals Candidate Biomarkers for Disability Outcome in Multiple Sclerosis

Siva A., Everest E., UYGUNOĞLU U., Yavuz D., Bulbul A., TÜTÜNCÜ M., et al.

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

Increased Burden of Susceptibility Variants in Familial Multiple Sclerosis

Everest E., UYGUNOĞLU U., TÜTÜNCÜ M., SAİP S., Duman T., Riley B., et al.

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

Genetic screening in the clinical suspicion of autoinflammatory diseases

Turanli E.

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

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

UĞURLU S., Turan G., Karacan I., DAŞDEMİR S., Seven M., Duz M. B., et al.

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

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

Aydın A. F., Ozguler Y., UÇAR D., Seyahi E., YAZICI H., Turanli E.

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

Trabulus S., Zor M. S., Turanli E., Dincer T., Alagoz S., Mese M., et al.

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

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

SİVA A., Everest E., UYGUNOĞLU U., TÜTÜNCÜ M., SAİP S., Duman T., et al.

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

LACC1 mutations in familial form of juvenile idiopathic arthritis

Karacan I., Ugurlu S., Sahin S., KASAPÇOPUR Ö., Tolun A., Ozdogan H., et al.

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

WHOLE GENOME LINKAGE AND EXOME SEQUENCING ANALYSES IN TAKAYASU ARTERITIS FAMILIES

Turanli E., Karacan I., Esatlioglu S. N., ŞAHİN S., KASAPÇOPUR Ö., Tolun A., et al.

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

NADİR BİR OLGU: ADENOZİN DEAMİNAZ-2 EKSİKLİĞİ

AYDIN M., BABAZADA K., TAŞDEMİR E., ŞAHİN S., ADROVIC A., TURAN O., et al.

54. TÜRK PEDİATRİ KONGRESİ, Türkiye, 6 - 10 Mayıs 2018

Identification of Multiple Sclerosis Related Pathways through Genome-Proteome Correlations

SİVA A., Everest E., Ulgen E., Uygunoglu U., Tutuncu M., Saip S., et al.

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

Behçet Sendromunda Proteom Analizleri

Kireçtepe Aydın A., ÖZGÜLER Y., SEYAHİ E., Yazıcı H., TAHİR TURANLI E.

XVIII. Ulusal Romatoloji Kongresi, Türkiye, 18 - 22 Ekim 2017

TREX 1 MUTATION IN THE MEMBERS OF A FAMILY WITH SYSTEMIC LUPUS ERYTHEMATOSUS AND ANTIPHOSPHOLIPID SYNDROME

UĞURLU S., Karacan I., Ozdogan H., Tolun A., Turanli E.

Annual European Congress of Rheumatology, Madrid, İspanya, 14 - 17 Haziran 2017, cilt.76, ss.1101

WHOLE GENOME LINKAGE AND EXOME SEQUENCING ANALYSES IN AN AUTOSOMAL RECESSIVE TAKAYASU ARTERITIS FAMILY

Karacan I., Esatoglu S. N., Turanli E., Tolun A., Seyahi E.

Annual European Congress of Rheumatology, Madrid, İspanya, 14 - 17 Haziran 2017, cilt.76, ss.208

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

ŞAHİN S., Adrovic A., BARUT K., UĞURLU S., Turanli E., Ozdogan H., et al.

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

Genetic Analysis of Inherited Autoinflammatory Disorders

TAHİR TURANLI E., Balamir A., KARACAN İ., Kireçtepe Aydın A., Sevinç N., Özkılınç M., et al.

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

Genetic analysis of inherited autoinflammatory disorders

TAHİR TURANLI E., BALAMİR A., KARACAN İ., KİREÇTEPE AYDIN A., SEVİNÇ N., ÖZKILINÇ M., et al.

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

Integrated Genomic and Proteomic Analyses of Multiple Sclerosis

EVEREST E., Uygunoğlu U., TÜTÜNCÜ M., SAİP S., SEZERMAN O. U., SİVA A., et al.

American Academy of Neurology 69th Annual Meeting, 22 - 28 Nisan 2017

A Novel Missense Mvk Mutation in a Family with Familial Mediterranean Fever like Disease

Karacan İ., UĞURLU S., Tolun A., TAHİR TURANLI E., ÖZDOĞAN A. H.

2016 ACR/ARHP Annual Meeting, 11 - 16 Kasım 2016

Potential biomarkers for different clinical subtypes of multiple sclerosis

Turanli E., Avsar T., Everest E., Öztürk Z., Şahin E., Oran D. C., et al.

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