Eğitim Bilgileri
1996 - 2000
1996 - 2000Doktora
Marmara Üniversitesi, Sağlık Bilimleri Enstitüsü, Tıbbi Biyoloji Ve Genetik Anabilim Dalı, Türkiye
1994 - 1995
1994 - 1995Yüksek Lisans
University of London-Imperial College of Science, Technology and Medicine, Life Sciences, Human Molecular Genetics, İngiltere
1991 - 1994
1991 - 1994Lisans
University of Nottingham, Life Sciences, Genetics, İngiltere
Yaptığı Tezler
2005
2005Yüksek Lisans
A Linkage Study of NMDAR1 Receptors and Schizophrenia
2000
2000Doktora
Dikkat eksikliği aşırı hareketlilik bozukluğunun dopamin genleri ile ilişkisi
Marmara Üniversitesi, Sağlık Bilimleri Enstitüsü
Araştırma Alanları
Genomiks
Akademik Unvanlar / Görevler
2021 - Devam Ediyor
2021 - Devam EdiyorProf. Dr.
Acıbadem Mehmet Ali Aydınlar Üniversitesi, Mühendislik ve Doğa Bilimleri Fakültesi, Moleküler Biyoloji ve Genetik
2016 - 2021
2016 - 2021Prof. Dr.
İstanbul Teknik Üniversitesi, Fen-Edebiyat, Moleküler Biyoloji Ve Genetik
2009 - 2016
2009 - 2016Doç. Dr.
İstanbul Teknik Üniversitesi, Fen-Edebiyat, Moleküler Biyoloji Ve Genetik
2005 - 2010
2005 - 2010Yrd. Doç. Dr.
İstanbul Teknik Üniversitesi, Fen-Edebiyat, Moleküler Biyoloji Ve Genetik
2004 - 2005
2004 - 2005Öğretim Görevlisi Dr.
İstanbul Teknik Üniversitesi, Fen-Edebiyat, Moleküler Biyoloji Ve Genetik
2001 - 2003
2001 - 2003Öğretim Görevlisi Dr.
Boğaziçi Üniversitesi, Fen-Edebiyat Fakültesi, Moleküler Biyoloji Ve Genetik Bölümü
Yönetimsel Görevler
2023 - Devam Ediyor
2023 - Devam EdiyorAnabilim/Bilim Dalı Başkanı
Acıbadem Mehmet Ali Aydınlar Üniversitesi, Fen Bilimleri Enstitüsü
2021 - Devam Ediyor
2021 - Devam EdiyorAnabilim/Bilim Dalı Başkanı
Acıbadem Mehmet Ali Aydınlar Üniversitesi, Fen Bilimleri Enstitüsü, Moleküler ve Translasyonel Biyotıp Tezli Yüksek Lisans Programı
2021 - Devam Ediyor
2021 - Devam EdiyorAnabilim/Bilim Dalı Başkanı
Acıbadem Mehmet Ali Aydınlar Üniversitesi, Mühendislik ve Doğa Bilimleri Fakültesi, Molecular Biology and Genetics
Verdiği Dersler
Yönetilen Tezler
2022
2022Yüksek Lisans
Analysis of total ada activity in peripheral blood mononuclear cells (PBMCs) of DADA2 patients
Tahir Turanlı E. (Danışman)
T.DEMİRCİ(Öğrenci)
2022
2022Doktora
Investigation of Familial Multiple Sclerosis Genetics
Tahir Turanlı E. (Danışman)
E.EVEREST(Öğrenci)
2021
2021Yüksek Lisans
The relationship between urinary exosomal miRNA levels and renal outcome in type 2 diabetic nephropathy patients
Tahir Turanlı E. (Danışman)
M.SEYİT(Öğrenci)
2021
2021Yüksek Lisans
VARIANT PATHOGENICITY PREDICTION TOOL BASED ON PROTEIN-PROTEIN INTERACTIONS AND THE EFFECTS OF VARIANTS ON 3-DIMENSIONAL PROTEIN STRUCTURE:A MODEL FOR MONOGENIC AUTOINFLAMMATORY DISORDERS
Tahir Turanlı E. (Danışman)
A.ALPER(Öğrenci)
2020
2020Yüksek Lisans
Disease gene identification using linkage and exome analysis
Tahir Turanlı E. (Danışman)
D.YAVUZ(Öğrenci)
2019
2019Doktora
Disease gene identification using linkage and exome analyses
Tahir Turanlı E. (Danışman)
İ.KARACAN(Öğrenci)
2019
2019Yüksek Lisans
Investigation of MEFV gene expression and pyrin levels in familial mediterranean fever and behçet syndrome
Tahir Turanlı E. (Danışman)
M.ÇİFTÇİ(Öğrenci)
2019
2019Yüksek Lisans
Investigation of novel genes in autosomal dominant Behçet syndrome
Tahir Turanlı E. (Danışman)
G.TURAN(Öğrenci)
2019
2019Doktora
Differential expression of proteins in active and inactive phases of Behçet's syndrome
Tahir Turanlı E. (Danışman)
K.ASLI(Öğrenci)
2018
2018Yüksek Lisans
Expression analysis of hla-b gene in sporadic behcet syndrome patients
Tahir Turanlı E. (Danışman)
E.KIZILTEPE(Öğrenci)
2017
2017Yüksek Lisans
TRANSCRIPTION ANALYSIS OF HLA-B GENE IN SPORADIC BEHCET SYNDROME PATIENTS
Tahir Turanlı E. (Danışman)
E.Kızıltepe(Öğrenci)
2017
2017Doktora
Investigation of the possible effect of intragenic MEFV gene CpG island methylation on mRNA transcription and pyrin localization
Tahir Turanlı E. (Danışman)
G.ERDEM(Öğrenci)
2016
2016Yüksek Lisans
Investigation of notch signalling pathway proteins as potential biomarkers for differentiating multiple sclerosis subtypes
Tahir Turanlı E. (Danışman)
Z.ÖZTÜRK(Öğrenci)
2016
2016Yüksek Lisans
Analysis of mefv variations, expression and pyrin levels in familial mediterranean fever disease
Tahir Turanlı E. (Danışman)
N.SEVİNÇ(Öğrenci)
2016
2016Yüksek Lisans
A genetic analysis of autoinflammatory diseases
Tahir Turanlı E. (Danışman)
A.BALAMİR(Öğrenci)
2015
2015Yüksek Lisans
MEFV mutation analysis in familial Mediterranean fever, gout and adult-onset still's diseases
Tahir Turanlı E. (Danışman)
S.GILA(Öğrenci)
2015
2015Yüksek Lisans
A linkage analysis and a genome-wide association study on familial multiple sclerosis
Tahir Turanlı E. (Danışman)
E.EVEREST(Öğrenci)
2015
2015Doktora
Investigation of molecular pathways and biomarkers in Multiple sclerosis clinical subtypes
Tahir Turanlı E. (Danışman)
T.AVŞAR(Öğrenci)
2015
2015Yüksek Lisans
Analysis of histone modifications in familial Mediterranean fever patients using chromatin immunoprecipitation sequencing assay
Tahir Turanlı E. (Danışman)
B.FİDAN(Öğrenci)
2015
2015Yüksek Lisans
Genetic and epigenetic analyses of hla-b5 gene in familial behçet syndrome pedigrees
Tahir Turanlı E. (Danışman)
P.KÖPRÜLÜ(Öğrenci)
2013
2013Yüksek Lisans
A study on the localization of alternative MEFV transcripts in neutrophil-like cells
Tahir Turanlı E. (Danışman)
Ş.ERDEMİR(Öğrenci)
2013
2013Yüksek Lisans
Analysis of MEFV gene alternatively spliced transcripts expression patterns in cell culture models
Tahir Turanlı E. (Danışman)
İ.ABACI(Öğrenci)
SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler
2025
2025Exome 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)
2024
2024Profiling 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)
2024
2024A rare case of uncharacterized autoinflammatory disease: Patient carrying variations in NLRP3 and TNFRSF1A genes
Kılınç Ö. C., Gayibova K., Ozkilinc Onen M., Onat U. İ., Bülbül A., Timuçin A. C., et al.
AMERICAN JOURNAL OF MEDICAL GENETICS, PART A , ss.1-9, 2024 (SCI-Expanded)
2024
2024HLA-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)
2023
2023A two-step purification platform for efficient removal of Fab-related impurities: A case study for Ranibizumab
Tatlı Ö., Tahir Turanlı E., Dinler Doğanay G.
HELIYON
, cilt.9, sa.11, ss.1-16, 2023 (SCI-Expanded)
2023
2023Detection 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)
2023
2023Prospective outcome analysis of multiple sclerosis cases reveals candidate prognostic cerebrospinal fluid markers.
Everest E., Uygunoglu U., Tutuncu M., Bulbul A., Onat U. İ., Unal M., et al.
PloS one
, cilt.18, sa.6, 2023 (SCI-Expanded)
2022
2022A 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)
2022
2022Investigating 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., Saip S., et al.
SCIENTIFIC REPORTS
, cilt.12, sa.1, 2022 (SCI-Expanded)
2022
2022Genome-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)
2022
2022Transcriptomics 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
, cilt.11, ss.1253-1267, 2022 (SCI-Expanded)
2021
2021COVID-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)
2021
2021Investigation 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)
2021
2021LACC1 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)
2021
2021Investigation 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)
2020
2020Peripheral 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)
2020
2020Preparation 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)
2020
2020A 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)
2019
2019Diagnostic 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)
2019
2019Atypical 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)
2019
2019Spectrum 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)
2019
2019A 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)
2018
2018C3 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)
2018
2018LACC1 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)
2018
2018Clinical, 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)
2018
2018Familial 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)
2017
2017Alternatively 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)
2017
2017Integrated 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)
2017
2017Other 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)
2016
2016A 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)
2016
2016Nanomedicine
Turanli E., Everest E.
LOW-DIMENSIONAL AND NANOSTRUCTURED MATERIALS AND DEVICES: PROPERTIES, SYNTHESIS, CHARACTERIZATION, MODELLING AND APPLICATIONS
, ss.579-587, 2016 (SCI-Expanded)
2015
2015Methylation 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)
2015
2015CSF 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)
2012
2012Protein 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)
2011
2011Analysis 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)
2011
2011Increased 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)
2010
2010The 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)
2010
2010A 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)
2009
2009Common 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)
2008
2008MEFV 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)
2006
2006Analysis 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)
2006
2006Stable 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)
2004
2004Functional 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)
2004
2004Joint 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)
2003
2003Association 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)
2003
2003Evaluation 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)
2001
2001Association 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)
2000
2000Functional 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)
2000
2000Association 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)
2000
2000No 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)
1999
1999A 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)
1997
1997A 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)
1996
1996Preliminary 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
2023
2023A 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)
2022
2022Translation 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)
2019
2019Chemerin 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)
2018
2018Quality 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)
2017
2017Role 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)
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler
2024
2024A 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)
2023
2023Analysis 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, (Özet Bildiri)
2023
2023Genetic 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)
2023
2023Comprehensive 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, (Özet Bildiri)
2023
2023Identification 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)
2022
2022JAK/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)
2022
2022Cellular 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)
2020
2020Prospective 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, (Özet Bildiri)
2020
2020Increased 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)
2019
2019Genetic screening in the clinical suspicion of autoinflammatory diseases
Turanli E.
European Biotechnology Congress, Valencia, İspanya, 11 - 13 Nisan 2019, cilt.305, (Özet Bildiri)
2018
2018Investigation 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)
2018
2018Candidate 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)
2019
2019URINARY 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)
2019
2019Lack 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)
2017
2017LACC1 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)
2018
2018WHOLE 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)
2018
2018NADİR 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)
2018
2018Identification 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)
2017
2017Behçet 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)
2017
2017TREX 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)
2017
2017WHOLE 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)
2017
2017ANTI 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)
2017
2017Genetic 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)
2017
2017Genetic 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, (Özet Bildiri)
2017
2017Integrated 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)
2016
2016A 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)
2016
2016Potential 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)
2016
2016Çocukluk çağı nadir otoenflamatuvar hastalıkların genetik tanısı
TAHİR TURANLI E.
III. Çocuk Romatoloji Kongresi, Türkiye, 21 - 24 Nisan 2016
2015
2015The 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
2015
2015A 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
2015
2015Suggestive 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
2012
2012Proteomic 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)
2002
2002Functional 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
2020
2020Behçet 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
2016
2016Nanomedicine
TAHİR TURANLI E., EVEREST E.
Low Dimensional and Nanostructured Materials and Devices, , Editör, Springer International Publishing, ss.579-587, 2016
Desteklenen Projeler
2024 - 2026
2024 - 2026AİLESEL MULTİPL SKLEROZ HASTALARINDA POLİGENİK RİSK SKORLARININ VE METABOLİT PROFİLLERİNİN KAPSAMLI ARAŞTIRILMASI
TÜSEB B Grubu AR-GE Projesi
Tahir Turanlı E. (Yürütücü)
2023 - 2026
2023 - 2026Investigation of functional roles of LAMA5 gene variants identified in a cohort of Turkish multiple sclerosis families on the disease pathophysiology
TÜBİTAK Projesi
Timuçin A. C., Tahir Turanlı E. (Yürütücü), Onat U. İ.
2024 - 2025
2024 - 2025Progresif Psödoromatoid Displazi Hastalığı Geni Olan CCN6’de in vitro Oluşturulan Patojenik Varyantların Fonksiyonel Analizleri
Diğer Resmi Kurumlarca Desteklenen Proje
Güven G., Tahir Turanlı E. (Yürütücü), Alanay Y.
2023 - 2025
2023 - 2025Multiple Skleroz'da Progesyon ile Telomer Uzunluğu ve Oksidatif Stres İlişkilerinin Araştırılması
Dernek (STK)
Tahir Turanlı E. (Yürütücü), Siva A., Gürz E.
2022 - 2025
2022 - 2025Genetically Engineering Experimental Models: Enhancement of Scientific and Technological excellence and innOvation potential to study NEurodevelopmental diseases (GEMSTONE)
UFUK AVRUPA Projesi
(Proje Özeti)
Onat F. (Yürütücü), Güven A. Z., Şahiner A. M., Süyen G., Şahin A., Öz Arslan D., et al.
2022 - 2024
2022 - 2024Progresif Psödoromatoid Displazi Geni Olan Ccn6'Daki Patojenik Varyantların İşlevsel Analizleri İçin Kondrosit Hücre Hatlarında Modellenmesi
TÜBİTAK Projesi
Tahir Turanlı E., Güven G.(Yürütücü)
2022 - 2024
2022 - 2024Progresif Psödoromatoid Displazi Geni olan CCN6’daki Patojenik Varyantların İşlevsel Analizleri İçin Kondrosit Hücre Hatlarında Modellenmesi
TÜBİTAK Projesi
Güven G. (Yürütücü), Alanay Y., Tahir Turanlı E.
2022 - 2024
2022 - 2024Pyrin İnflamazomunda PSTPIP1 Proteini Varyantlarının In Vitro Hücre Kültürü Modelinde Araştırılması
Yükseköğretim Kurumları Destekli Proje
(Proje Özeti)
Onat U. İ., Tahir Turanlı E. (Yürütücü)
2023 - 2023
2023 - 2023Otoenflamatuvar Ön Tanılı Ailede Ekzom Dizileme Yöntemleri ile Yepyeni Gen Araştırılması
Yükseköğretim Kurumları Destekli Proje
Tahir Turanlı E. (Yürütücü), Geçgel M.
Bilimsel Yayınlarda Hakemlikler
Temmuz 2023
Temmuz 2023GENES AND IMMUNITY
SCI-E Kapsamındaki Dergi
Bilimsel Projelerde Hakemlikler
Haziran 2024
Haziran 2024TÜBİTAK Projesi
1501 - Sanayi Ar-Ge Projeleri Destekleme Programı, ACC TEKNOLOJİ SANAYİ TİCARET ANONİM ŞİRKETİ, Türkiye
Kongre ve Sempozyum Katılımı Faaliyetleri
11 Kasım 2023 - 13 Kasım 2023
11 Kasım 2023 - 13 Kasım 202326. Ulusal İmmünoloji Kongresi
Katılımcı
Ankara-Türkiye
01 Kasım 2023 - 05 Kasım 2023
01 Kasım 2023 - 05 Kasım 202375. American Society of HUman Genetics Conference
Katılımcı
Washington-Amerika Birleşik Devletleri
16 Ekim 2023 - 18 Ekim 2023
16 Ekim 2023 - 18 Ekim 20238. Istanbul MS Days
Moderatör
İzmir-Türkiye
11 Ekim 2023 - 13 Ekim 2023
11 Ekim 2023 - 13 Ekim 20233rd INTERNATIONAL MATERIALS TECHNOLOGIES AND METALLURGY CONFERENCE-
Davetli Konuşmacı
İstanbul-Türkiye
03 Ekim 2023 - 04 Ekim 2023
03 Ekim 2023 - 04 Ekim 2023GEMSTONE Project's 1st Dissemination Event
Katılımcı
İstanbul-Türkiye
21 Eylül 2023 - 23 Kasım 2023
21 Eylül 2023 - 23 Kasım 20238.Uluslarası Erciyes Tıp Tıbbi Genetik Kongresi
Davetli Konuşmacı
Kayseri-Türkiye
Atıflar
Toplam Atıf Sayısı (SCOPUS): 1262
h-indeksi (SCOPUS): 16
Jüri Üyelikleri
Nisan-2024
Nisan 2024Tez Savunma (Doktora)
Gizem Alkurt İTÜ Doktora Sınavı - İstanbul Teknik Üniversitesi
Nisan-2024
Nisan 2024Tez Savunma (Doktora)
Seda Süsgün DETAE - İstanbul Üniversitesi
Mayıs-2023
Mayıs 2023Akademik Personel Sınavı
Ar-Gör Sınavı - Acıbadem Mehmet Ali Aydınlar Üniversitesi
Şubat-2023
Şubat 2023