Yayınlar & Eserler

Yayın Ağı
Makaleler 65
Tümü (65)
SCI-E, SSCI, AHCI (58)
SCI-E, SSCI, AHCI, ESCI (62)
ESCI (4)
Scopus (60)
TRDizin (5)
Diğer Yayınlar (1)

1. Impact of LAMA5 Variants on Immune Cell Infiltration Using 2D Blood Brain Barrier Culture Model of Multiple Sclerosis (P2-18.004)

Siva A., Voyvoda U., Cotuk K., Efe H., Karisik S. N., Reda M., et al.
NEUROLOGY , cilt.106, sa.11_Supplement_1, ss.1-2, 2026 (SCI-Expanded, Scopus)

2. Human TBK1 deficiency: An expanded spectrum from autoinflammation to viral encephalitis.

Akalu Y., Taft J., Berger T., Rostásy K., Dafsari H. S., Schönrade H., et al.
Journal of human immunity , cilt.2, sa.2, 2026 (Hakemli Dergi)

3. Genetic Influences on Disease-Modifying Therapy Response in Multiple Sclerosis: Current Insights and Future Directions

Reda M. D., Siva A., TAHİR TURANLI E.
Balkan Medical Journal , cilt.43, sa.4, ss.174-182, 2026 (SCI-Expanded, Scopus, TRDizin) Creative Commons License

4. Molecular Consequences of CCN6 Variants Encoding WISP3 in Progressive Pseudorheumatoid Dysplasia

Guven Tasbicen G., Tufan A., Savsar B., Bulbul A. A., Tonbul Z., Guzel E., et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES , cilt.26, ss.1-33, 2025 (SCI-Expanded, Scopus)

5. Exome sequencing reveals low-frequency and rare variant contributions to multiple sclerosis susceptibility in Turkish families.

Büyükgöl F., Gürdamar B., Aluçlu M. U., Beckmann Y., Bilguvar K., Boz C., et al.
Scientific reports , cilt.15, sa.1, ss.11682, 2025 (SCI-Expanded, Scopus)

6. Profiling of five urinary exosomal miRNAs for the differential diagnosis of patients with diabetic kidney disease and focal segmental glomerulosclerosis.

Trabulus S., Zor M. S., Alagoz S., Dincer M. T., Meşe M., Yilmaz E., et al.
PloS one , cilt.19, sa.10, 2024 (SCI-Expanded, Scopus)

7. A rare case of uncharacterized autoinflammatory disease: Patient carrying variations in NLRP3 and TNFRSF1A genes.

Kilinc O. C., Gayibova K., Onen M. O., Onat U. I., Bülbül A. A., Timucin A. C., et al.
American journal of medical genetics. Part A , cilt.194, sa.10, 2024 (SCI-Expanded, Scopus)

8. Investigation of Novel Variants in Familial Multiple Sclerosis Through Family-based Association Tests and Segregation Analyses (S17.007)

Siva A., Bülbül A. A., Everest E., Tutuncu M., Uygunoglu U., Saip S., et al.
NEUROLOGY , cilt.102, sa.7_supplement_1, ss.102, 2024 (SCI-Expanded, Scopus)

9. HLA-B gene methylation and expression in Behçet's syndrome: a potential role of epigenetics in the pathogenesis.

Özkılınç Önen M., Everest E., Demirci T., Köprülü Şen P., Kızıltepe Kısakesen E., Özgüler Y., et al.
Clinical and experimental rheumatology , 2024 (SCI-Expanded, Scopus)

10. Var3PPred: variant prediction based on 3-D structure and sequence analyses of protein-protein interactions on autoinflammatory diseases

Bülbül A. A., TİMUÇİN E., TİMUÇİN A. C., SEZERMAN O. U., TAHİR TURANLI E.
PeerJ , cilt.12, sa.5, 2024 (SCI-Expanded, Scopus)

11. A two-step purification platform for efficient removal of Fab-related impurities: A case study for Ranibizumab

Tatli O., Oz Y., Dingiloglu B., Yalcinkaya D., Basturk E., Korkmaz M., et al.
HELIYON , cilt.9, sa.11, 2023 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma

12. Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype

Özkılınç Önen M., Onat U. İ., Uğurlu S., Timuçin A. C., Öz Arslan D., Everest E., et al.
RHEUMATOLOGY , sa.9, ss.3188-3196, 2023 (SCI-Expanded, Scopus)

13. 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)

14. Prospective outcome analysis of multiple sclerosis cases reveals candidate prognostic cerebrospinal fluid markers.

Everest E., Uygunoglu U., Tutuncu M., Bulbul A. A., Onat U. İ., Unal M., et al.
PloS one , cilt.18, sa.6, 2023 (SCI-Expanded, Scopus)

15. A novel BH3 mimetic Bcl-2 inhibitor promotes autophagic cell death and reduces in vivo Glioblastoma tumor growth

Calis S., Dogan B., Durdagi S., Celebi A., Yapicier O., Kilic T., et al.
Cell Death Discovery , cilt.8, sa.1, 2022 (SCI-Expanded, Scopus) Creative Commons License

16. Investigating the role of common and rare variants in multiplex multiple sclerosis families reveals an increased burden of common risk variation

Everest E., Ahangari M., Uygunoglu U., Tutuncu M., Bulbul A. A., Saip S., et al.
SCIENTIFIC REPORTS , cilt.12, sa.1, 2022 (SCI-Expanded, Scopus)

17. Transcriptomics and Proteomics Analyses Reveal JAK Signaling and Inflammatory Phenotypes during Cellular Senescence in Blind Mole Rats: The Reflections of Superior Biology

Inci N., Akyildiz E. O., Bülbül A. A., Tahir Turanlı E., Akgun E., Baykal A. T., et al.
BIOLOGY-BASEL , cilt.11, sa.9, 2022 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma

18. Genome-wide analysis of schizophrenia and multiple sclerosis identifies shared genomic loci with mixed direction of effects

Ahangari M., Everest E., Nguyen T., Verrelli B. C., Webb B. T., Bacanu S., et al.
Brain, Behavior, and Immunity , cilt.104, ss.183-190, 2022 (SCI-Expanded, Scopus)

19. 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, 2022 (ESCI, Scopus) Creative Commons License Sürdürülebilir Kalkınma

20. COVID-19 vaccine candidates and vaccine development platforms available worldwide

DUMAN N., ALzaidi Z., Aynekin B., Taskin D., Demirors B., YILDIRIM A., et al.
JOURNAL OF PHARMACEUTICAL ANALYSIS , cilt.11, sa.6, ss.675-682, 2021 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

21. Investigation of multiple sclerosis-related pathways through the integration of genomic and proteomic data

Everest E., Ulgen E., UYGUNOĞLU U., TÜTÜNCÜ M., SAİP S., SEZERMAN O. U., et al.
PEERJ , cilt.9, 2021 (SCI-Expanded, Scopus)

22. LACC1 deficiency links juvenile arthritis with autophagy and metabolism in macrophages

Omarjee O., Mathieu A., Quiniou G., Moreews M., Ainouze M., Frachette C., et al.
JOURNAL OF EXPERIMENTAL MEDICINE , cilt.218, sa.3, 2021 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

23. Investigation of neuro-inflammatory parameters in a cuprizone induced mouse model of multiple sclerosis

Avsar T., Celikyapi Erdem G., Terzioglu G., Tahir Turanlı E.
TURKISH JOURNAL OF BIOLOGY , cilt.45, sa.5, ss.644-656, 2021 (SCI-Expanded, Scopus, TRDizin)

24. Preparation and in vitro characterization of monoclonal antibody ranibizumab conjugated magnetic nanoparticles for ocular drug delivery

Ayata N., SEZER A. D., Bucak S., Turanli E.
BRAZILIAN JOURNAL OF PHARMACEUTICAL SCIENCES , cilt.56, 2020 (SCI-Expanded, Scopus)

25. Peripheral blood mononuclear cell proteome profile in Behcet's syndrome

Aydin A. K., Ozguler Y., Ucar D., KASAP M., AKPINAR G., Seyahi E., et al.
RHEUMATOLOGY INTERNATIONAL , cilt.40, sa.1, ss.65-74, 2020 (SCI-Expanded, Scopus)

26. A 9.5-year-old boy with recurrent neurological manifestations and severe hypertension, treated initially for polyarteritis nodosa, was subsequently diagnosed with adenosine deaminase type 2 deficiency (DADA2) which responded to anti-TNF-alpha

Sahin S., Adrovic A., Barut K., Baran S., Turanli E., Canpolat N., et al.
PAEDIATRICS AND INTERNATIONAL CHILD HEALTH , cilt.40, sa.1, ss.65-68, 2020 (SCI-Expanded, Scopus)

27. Diagnostic utility of a targeted next-generation sequencing gene panel in the clinical suspicion of systemic autoinflammatory diseases: a multi-center study

Karacan I., Balamir A., Ugurlu S., Aydin A. K., Everest E., Zor S., et al.
RHEUMATOLOGY INTERNATIONAL , cilt.39, sa.5, ss.911-919, 2019 (SCI-Expanded, Scopus)

28. Atypical phenotype of an old disease or typical phenotype of a new disease: deficiency of adenosine deaminase 2

Cakan M., Aktay-Ayaz N., Karadag S. G., Tahir-Turanli E., Stafstrom K., Bainter W., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.61, sa.3, ss.413-417, 2019 (SCI-Expanded, Scopus, TRDizin)

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

Kilic H., ŞAHİN S., Duman C., Adrovic A., BARUT K., Turanli E., et al.
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , cilt.23, sa.3, ss.466-472, 2019 (SCI-Expanded, Scopus)

30. 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

31. A Novel ATP6V0A2 Mutation Causing Recessive Cutis Laxa with Unusual Manifestations of Bleeding Diathesis and Defective Wound Healing

Karacan I., Kucukkaya R. D., KARAKUŞ F. N., SOLAKOĞLU S., Tolun A., Hancer V. S., et al.
TURKISH JOURNAL OF HEMATOLOGY , cilt.36, sa.1, ss.29-36, 2019 (SCI-Expanded, Scopus, TRDizin)

32. 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)

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

BAŞARAN H. Ö., Uncu N., ÇAKAR N., Turanli E., KİREMİTCİ S., Aydin F., et al.
RHEUMATOLOGY INTERNATIONAL , cilt.38, sa.8, ss.1571-1576, 2018 (SCI-Expanded, Scopus)

34. LACC1 Gene Defects in Familial Form of Juvenile Arthritis

Karacan I., Ugurlu S., ŞAHİN S., Everest E., KASAPÇOPUR Ö., Tolun A., et al.
JOURNAL OF RHEUMATOLOGY , cilt.45, sa.5, ss.726-728, 2018 (SCI-Expanded, Scopus)

35. Familial Mediterranean fever in childhood: a single-center experience

BARUT K., ŞAHİN S., Adrovic A., Sinoplu A. B., Yucel G., Pamuk G., et al.
RHEUMATOLOGY INTERNATIONAL , cilt.38, sa.1, ss.67-74, 2018 (SCI-Expanded, Scopus)

36. Clinical, imaging and genotypical features of three deceased and five surviving cases with ADA2 deficiency

ŞAHİN S., Adrovic A., BARUT K., Ugurlu S., Turanli E., Ozdogan H., et al.
RHEUMATOLOGY INTERNATIONAL , cilt.38, sa.1, ss.129-136, 2018 (SCI-Expanded, Scopus)

37. 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, Scopus, TRDizin) Creative Commons License

38. Alternatively spliced MEFV transcript lacking exon 2 and its protein isoform pyrin-2d implies an epigenetic regulation of the gene in inflammatory cell culture models

Erdem G. C., Erdemir S., Abaci I., Aydin A. K. K., Everest E., Turanli E.
GENETICS AND MOLECULAR BIOLOGY , cilt.40, sa.3, ss.688-697, 2017 (SCI-Expanded, Scopus)

39. Integrated Genomic and Proteomic Analyses of Multiple Sclerosis

Everest E., Uygunoglu U., Tutuncu M., SAİP S., SEZERMAN O. U., Siva A., et al.
NEUROLOGY , cilt.88, 2017 (SCI-Expanded, Scopus)

40. Other autoinflammatory disease genes in an FMF-prevalent population: a homozygous MVK mutation and a heterozygous TNFRSF1A mutation in two different Turkish families with clinical FMF

Karacan I., UĞURLU S. Y., Tolun A., Turanli E., Ozdogan H.
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY , cilt.35, sa.6, 2017 (SCI-Expanded, Scopus)

41. A NOVEL Missense Mvk mutation in a Family with Familial Mediterranean Fever-like Disease

Karacan I., UĞURLU S., Tolun A., Turanli E., Ozdogan H.
ARTHRITIS & RHEUMATOLOGY , cilt.68, 2016 (SCI-Expanded, Scopus)

42. Nanomedicine

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

43. 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, Scopus)

44. 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, Scopus) Creative Commons License

45. 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)

46. 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, Scopus)

47. 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, Scopus)

48. 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, Scopus)

49. 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, Scopus)

50. 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, Scopus)

51. 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, Scopus)

52. 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, Scopus)

53. 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, Scopus)

54. 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)

55. 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, Scopus)

56. 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, Scopus)

57. 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, Scopus)

58. 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, Scopus)

59. 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, Scopus)

60. 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)

61. 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, Scopus)

62. 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, Scopus)

63. 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, Scopus)

64. 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, Scopus)

65. 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, Scopus)
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 41

1. Functional Investigation of Pathogenic Variants in CCN6 Causing Progressive Pseudorheumatoid Dysplasia

GÜVEN TAŞBİÇEN G., Tonbul Z., Tufan A., Savsar B., Guzel E., BAYRAM AKÇAPINAR G., et al.
58th Conference of the European-Society-of-Human-Genetics (ESHG), Milan, İtalya, 24 - 27 Mayıs 2025, cilt.33, ss.409, (Özet Bildiri)

2. Impact of LAMA5 Variants on Immune Cell Infiltration using 2D Blood Brain Barrier Culture Model of Multiple Sclerosis

Voyvoda U., Karisik S. N., Reda M. D., Efe H., Cotuk ., Cakici B., et al.
6th International Molecular Immunology and Immunogenetics Congress (MIMIC-VI), İstanbul, Türkiye, 28 - 30 Nisan 2025, ss.1-2, (Özet Bildiri)

3. Analysis of the Interaction Between PTP-PEST and PSTPIP1 in an In Vitro Cell Culture Model

Tonbul Z., Tahir Turanlı E., Onat U. İ.
MIMIC-VI, İstanbul, Türkiye, 28 - 30 Nisan 2025, ss.99, (Özet Bildiri)

4. Telomere Attrition and Oxidative Stress as Candidate Modulators of Multiple Sclerosis Progression

Turanli E., Gurz E., Voyvoda U., Reda D., Tonbul Z., Savsar B., et al.
Annual Meeting of the American-Academy-of-Neurology (AAN), California, Amerika Birleşik Devletleri, 5 - 09 Nisan 2025, cilt.104, (Özet Bildiri)

5. Exome-sequencing of Turkish Families with Multiple Sclerosis: Low Frequency and Rare Variant Contributions into Susceptibility

Buyukgol F., GÜRDAMAR B., Bulbul A., Sezerman O. U., Everest E., Voyvoda U., et al.
Annual Meeting of the American-Academy-of-Neurology (AAN), California, Amerika Birleşik Devletleri, 5 - 09 Nisan 2025, cilt.104, (Özet Bildiri)

6. Evaluating Multiple Sclerosis Risk Prediction in Families Through Comprehensive Polygenic Risk Score Analysis

Bülbül A. A., Timuçin E., Tahir Turanli E.
9th International Congress of the Molecular Biology Association of Turkey, İzmir, Türkiye, 12 - 14 Eylül 2024, ss.1-138, (Özet Bildiri)

7. Kondroisit Hücre Hatlarında Progresif Psödoromatoid Displazi Hastalık Geni Olan CCN6’daki Patojenik Varyantların Fonksiyonel Araştırmaları

Güven Taşbiçen G., Tahir Turanlı E., Alanay Y.
9th International Congress of the Molecular Biology Association of Turkey, İzmir, Türkiye, 12 - 14 Eylül 2024, ss.1-138, (Özet Bildiri)

8. Unveiling the Role of PSMB10 Gene Splice Variant in Dominantly Inherited Auto- inflammatory Disease: Insights into Autophagy Interaction and Clinical Im

Savsar B., Tonbul Z., Onat U. İ., Sever E., Uğurlu S., Öz Arslan D., et al.
Molbiyokon24, İzmir, Türkiye, 12 - 14 Eylül 2024, ss.241, (Özet Bildiri) Creative Commons License

9. 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, (Yayınlanmadı)

10. Analysis of Familial Exome Analysis Tools

Tahir Turanlı E., Bülbül A. A., Siva A.
8. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 21 - 23 Eylül 2023, ss.1, (Özet Bildiri)

11. PPP1R32 PROTEİN VARYANTININ İNFLAMAZOM AKTİVİTESİNİN İN VİTRO HÜCRE KÜLTÜRÜ MODELİNDE ARAŞTIRILMASI

Tahir Turanlı E., Tonbul Z., Onat U. İ., Kasapçopur Ö.
XXVI ULUSAL İMMÜNOLOJİ KONGRESİ, Ankara, Türkiye, 11 - 13 Kasım 2023, ss.94, (Özet Bildiri) Creative Commons License

12. 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, (Özet Bildiri)

13. Comprehensive Analysis of Low-Frequency Genetic Variants through Exome Sequencing in Familial Multiple Sclerosis

Tahir Turanlı E., Bülbül A. A., Siva A., Sezerman O. U.
75. American Society of Human Genetics Congress, Washington, Amerika Birleşik Devletleri, 1 - 05 Kasım 2023, ss.1, (Özet Bildiri)

14. 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, (Özet Bildiri)

15. 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, (Özet Bildiri)

16. 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, (Yayınlanmadı)

17. 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, (Özet Bildiri)

18. 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. A., TÜTÜNCÜ M., et al.
Annual Meeting of the American-Academy-of-Neurology, Toronto, Kanada, 25 Nisan - 01 Mayıs 2020, cilt.94, (Özet Bildiri)

19. Genetic screening in the clinical suspicion of autoinflammatory diseases

Turanli E.
European Biotechnology Congress, Valencia, İspanya, 11 - 13 Nisan 2019, cilt.305, (Özet Bildiri)

20. 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.
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, (Özet Bildiri)

21. 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, (Özet Bildiri)

22. 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, (Özet Bildiri)

23. 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, (Özet Bildiri)

24. 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, (Özet Bildiri)

25. 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, (Özet Bildiri) Creative Commons License

26. 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, (Özet Bildiri)

27. 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, (Özet Bildiri)

28. 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, (Tam Metin Bildiri)

29. 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, (Özet Bildiri) Creative Commons License

30. 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, (Özet Bildiri) Creative Commons License

31. 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, (Özet Bildiri) Creative Commons License

32. 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, (Tam Metin Bildiri)

33. 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, (Tam Metin Bildiri)

34. 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, (Tam Metin Bildiri)

35. 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, (Özet Bildiri)

36. Çocukluk çağı nadir otoenflamatuvar hastalıkların genetik tanısı

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

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

ÖZDOĞAN A. H., UĞURLU S., TAHİR TURANLI E., Hacıoğlu A., Aslı K. A.
International Congress of FMF and Systemic Autoinflammatory Diseases, 30 Eylül - 03 Ekim 2015

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

UĞURLU S., Emekli A. S., TAHİR TURANLI E., Benyakar S. G., Çelikyapi Erdem G., ÖZDOĞAN A. H., et al.
International Congress of Familial Mediterreanen Fever and Systemic Autoinflammatory Diseases, 30 Eylül - 03 Ekim 2015

39. Suggestive linkage to chromosomal regions 13q13 3 and 21q22 2 in families with Multiple Sclerosis

EVEREST E., Avşar T., SİVA A., Uygunoğlu U., Tütüncü M., SAİP S., et al.
European Conference of Human Genetics, 6 - 09 Haziran 2015

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

Avsar T., UYGUNOĞLU U., TÜTÜNCÜ M., Demirci N. O., SAİP S., SİVA A., et al.
28th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis, Lyon, Fransa, 10 - 13 Ekim 2012, cilt.18, ss.263-264, (Özet Bildiri)

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

D'Souza U., Russ C., Tahir E., Browes C., Mill J., McGuffin P., et al.
10th World Congress of Psychiatric Genetics, Brussels, Belçika, 9 - 13 Ekim 2002, cilt.114, ss.880, (Özet Bildiri)
Kitaplar 2

1. Behçet Hastalığı: Genetik ve Epigenetik Araştırmalar

Tahir Turanlı E., Kireçtepe Aydın A., Özkılınç Önen M.
Behçet Hastalığı, Emire Seyahi, Editör, Türkiye Klinikleri Yayınevi, Ankara, ss.21-28, 2020 Sürdürülebilir Kalkınma

2. Nanomedicine

TAHİR TURANLI E., EVEREST E.
Low Dimensional and Nanostructured Materials and Devices, Springer International Publishing, ss.579-587, 2016