Education
1988 - 1993
1988 - 1993Doctorate
Howard University, United States Of America
1979 - 1985
1979 - 1985Undergraduate
Ankara University, Tıp Fakültesi, Tıp Pr., Turkey
Dissertations
1993
1993Doctorate
Retinoik asid’in insan kolon adenokanserlerinde proliferasyon ve diferansiyasyona etkisi
Howard University
Foreign Languages
C1 Advanced
C1 AdvancedEnglish
Research Areas
Medical Genetics
Bioinformatics
Academic Positions
1999 - Continues
1999 - ContinuesAssistant Professor
Ankara University, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü
Courses
Undergraduate
Undergraduate
DÖNEM 3 DOLAŞIM, SOLUNUM, NEFROLOJİ
DÖNEM 3 FARMAKOLOJİ, PATOLOJİ, GENETİK VE RADYASYON FİZİĞİ
DÖNEM 4 NÖROLOJİ STJ MODÜLÜ
DÖNEM 3 ENFEKSİYON HASTALIKLARI VE KLİNİK MİKROBİYOLOJİ, ONKOLOJİ, RADYOLOJİ
DÖNEM 1 HÜCRE MODÜLÜ
DÖNEM 4 İÇ HASTALIKLARI 1 STAJ MODÜLÜ AİLESEL KANSER SENDROMLARI
CELL BIOLOGY INTRODUCTION TO HUMAN EMBRYOLOGY
DÖNEM 4 STJ MODÜLÜ NÖRODEJENERATİF HASTALIKLARIN GENETİĞİ
DÖNEM 4 İÇ HASTALIKLARI 1 STAJ MODÜLÜ AİLESEL ve KALITSAL KANSERLER
Supervised Theses
2020
2020Expertise In Medicine
Multiple myeloma hastalarında LncRNA LUNAR1 ekspresyon analizi
TUNCALI T. (Advisor)
E.GÖKPINAR(Student)
2013
2013Expertise In Medicine
Neoplazi şüphesi nedeniyle uygulanan endometrium biyopsilerinde ve neoplazi tanısı ile histerektomi uygulanan olgularda mikrosatellit instabilitesinin araştırılması
TUNCALI T. (Advisor)
C.EKİCİ(Student)
2010
2010Expertise In Medicine
Fanconi anemisinde FANCD2 monoubikitinasyonu saptanmasına dayalı tarama yönteminin klinikte uygulanabilirliği
TUNCALI T. (Advisor)
B.SAĞLAM(Student)
2004
2004Postgraduate
Ailesel akdeniz ateşi hastalarında ve normal bireylerde Mica geni üçlü tekrar polimorfizmin saptanması ve karşılaştırılması
TUNCALI T. (Advisor)
B.YALÇIN(Student)
2003
2003Expertise In Medicine
İnsan promiyelositik lösemi hücrelerinde proliferasyon ve diferansiyasyona etkili ajanların telomeraz aktivitesine etkisi
TUNCALI T. (Advisor)
A.İLKAY(Student)
Journal articles indexed in SCI, SSCI, and AHCI
2025
2025Familial Multiple Myeloma: Insights From Epidemiology and Underlying Germline Genetic Predisposition to the Clinic
Akkus E., TUNCALI T., Beksac M.
Clinical Lymphoma, Myeloma and Leukemia
, 2025 (SCI-Expanded)
2024
2024A Germline Variant of BNIP1 Gene (rs28199) is Associated with Familial Multiple Myeloma
AKKUŞ E., TUNCALI T., Akin H. Y., SALİHOĞLU A., Sevindik O. G., Kirkizlar H. O., et al.
CLINICAL LYMPHOMA MYELOMA & LEUKEMIA
, 2024 (SCI-Expanded)
2024
2024Germline genetic variants in Turkish familial multiple myeloma/monoclonal gammopathy of undetermined significance cases
AKKUŞ E., TUNCALI T., Akin H. Y., Aydin Y., Besisik S. K., GÜRKAN E., et al.
BRITISH JOURNAL OF HAEMATOLOGY
, vol.204, no.3, pp.931-938, 2024 (SCI-Expanded)
2024
2024X-linked Dyskeratosis Congenita Case with Mutation 1058C>T(p.Ala353Val) in Dyskerine Gene
ÖKTEM A., KUŞÇU D. D., TUNCALI T., Kahraman U., ÖZBOLAT S.
Indian Journal of Dermatology
, vol.69, no.1, pp.106, 2024 (SCI-Expanded)
2023
2023Contribution of genotypes in Prothrombin and Factor V Leiden to COVID-19 and disease severity in patients at high risk for hereditary thrombophilia.
Kiraz A., Sezer O., ALEMDAR A., Canbek S., Duman N., BİŞGİN A., et al.
Journal of medical virology
, vol.95, no.2, 2023 (SCI-Expanded)
2022
2022Phenotypic and molecular characterization of five patients with <i>PIK3CA</i>-related overgrowth spectrum (PROS)
Ili E., Tasdelen E., Durmaz C. D., ALTINER Ş., TUNCALI T., Martinez-Glez V., et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
, vol.188, no.6, pp.1792-1800, 2022 (SCI-Expanded)
2022
2022Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium
DÜNDAR M., FAHRİOGLU U., Yildiz S. H., Bakir-Gungor B., TEMEL Ş. G., AKIN H., et al.
FUNCTIONAL & INTEGRATIVE GENOMICS
, vol.22, no.3, pp.291-315, 2022 (SCI-Expanded)
2022
2022A case report of an atypical FIP1L1-PDGFRA fusion in a patient with hypereosinophilia
EKİNCİ S., CENGİZ SEVAL G., KARABULUT H. G., Vicdan A., YÜKSEL S., KUZU I., et al.
EUROPEAN JOURNAL OF HUMAN GENETICS
, vol.30, no.SUPPL 1, pp.222, 2022 (SCI-Expanded)
2022
2022Clinical findings in 22q11.2 microdeletion syndrome: case series
ALTINER Ş., TUNCALI T., KUTLAY N., KARABULUT H. G., ILGIN RUHİ H.
EUROPEAN JOURNAL OF HUMAN GENETICS
, vol.30, no.SUPPL 1, pp.325, 2022 (SCI-Expanded)
2022
2022Evaluation of Plasma Cell Molecular Cytogenetic Findings of Myeloma Patients: One-Year Single-Center Experience
KAPLAN İ., CESUR BALTACI H. N., ALTINER Ş., EKİNCİ S., VİCDAN N. A., KARABULUT H. G., et al.
EUROPEAN JOURNAL OF HUMAN GENETICS
, vol.30, no.SUPPL 1, pp.413, 2022 (SCI-Expanded)
2022
2022ROHMM-A flexible hidden Markov model framework to detect runs of homozygosity from genotyping data
Celik G., TUNCALI T.
HUMAN MUTATION
, vol.43, no.2, pp.158-168, 2022 (SCI-Expanded)
2022
2022Right Anterior Theta Hypersynchrony as a Quantitative Measure Associated with Autistic Traits and K-Cl Cotransporter KCC2 Polymorphism
Aykan S., Puglia M. H., Kalaycioglu C., Pelphrey K. A., Tuncalı T., Nalçacı E.
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
, vol.52, no.1, pp.61-72, 2022 (SSCI)
2018
2018A Novel PTCH1 Frameshift Mutation Leading to Nevoid Basal Cell Carcinoma Syndrome
Durmaz C. D., Evans G., Smith M. J., Ertop P., Akay B. N., TUNCALI T.
CYTOGENETIC AND GENOME RESEARCH
, vol.154, no.2, pp.57-61, 2018 (SCI-Expanded)
2016
2016Lack of the Association of the PTPN22 C1858T Gene Polymorphism With Susceptibility to Familial Mediterranean Fever
KÜÇÜKŞAHİN O., Seker Z., ŞAHİN A., KINIKLI G., TUNCALI T., Turgay M., et al.
ARCHIVES OF RHEUMATOLOGY
, no.2, pp.107-111, 2016 (SCI-Expanded)
2015
2015Resting-State EEG Alpha Power in Healthy Individuals with Autistic Traits
Zergeroglu S., GÜRSES E., TUNCALI T., Yilmaz S., ÖZGÜVEN H., Kalaycioglu C.
ACTA PHYSIOLOGICA
, vol.215, pp.22, 2015 (SCI-Expanded)
2015
2015Follow-up of del(5)q MDS patients with or without other chromosomal abnormalities
Turedi O., Ataca P., TUNCALI T., Atilla E., Vicdan A., Durmaz C. D., et al.
CHROMOSOME RESEARCH
, vol.23, 2015 (SCI-Expanded)
2015
2015Seckel syndrome with cutaneous pigmentary changes: two siblings and a review of the literature
KILIÇ A., Cakmak S. K., TUNCALI T., Koz O., Ozhamamci E., Yasun O., et al.
POSTEPY DERMATOLOGII I ALERGOLOGII
, vol.32, no.6, pp.470-474, 2015 (SCI-Expanded)
2014
2014Epstein-Barr Virus-Negative Post-Transplant Lymphoproliferative Diseases: Three Distinct Cases from a Single Center
Bakanay S. M., KAYGUSUZ G., TOPÇUOĞLU P., ŞENGÜL Ş., TUNCALI T., KEVEN K., et al.
TURKISH JOURNAL OF HEMATOLOGY
, vol.31, no.1, pp.79-83, 2014 (SCI-Expanded)
2013
2013An evaluation of the phenotypic features of fanconi anemia together with DEB/MMC positivity in 199 turkish patients Fanconi anemisinin fenotipik Özelliklerinin DEB/MMC pozitifligi ile birlikte 199 türk hastada degerlendirilmesi
Yürür-Kutlay N., TUNCALI T., ILGIN RUHİ H., KARABULUT H. G., Tukun A.
Turkiye Klinikleri Journal of Medical Sciences
, vol.33, no.1, pp.1-8, 2013 (SCI-Expanded)
2013
2013Oesophageal achalasia misdiagnosed as uncontrolled asthma Kontrolsüz astım tanısıyla izlenen özefageal akalazya olgusu
AYDIN Ö., YÜKSEL C., TUNCALI T., ÖZKAN M., KAYA A., Ökten I., et al.
Tuberkuloz ve Toraks
, vol.61, no.2, pp.147-151, 2013 (SCI-Expanded)
2011
2011Clinical Applicability of FANCD2 Mono-Ubiquitination Test for Fanconi Anemia Diagnosis and a Suggestion for an Algorithm
Ada B. S., TUNCALI T., Ertem M., ILGIN RUHİ H.
TURKISH JOURNAL OF BIOCHEMISTRY-TURK BIYOKIMYA DERGISI
, vol.36, no.2, pp.175-182, 2011 (SCI-Expanded)
2007
2007Colobomatous macrophthalmia with microcornea syndrome maps to the 2p23-p16 region
Elcioglu N. H., Akin B., Toker E., Elcioglu M., Kaya A., Tuncali T., et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
, vol.143A, no.12, pp.1308-1312, 2007 (SCI-Expanded)
2007
2007The contribution of genotypes at the MICA gene triplet repeat polymorphisms and MEFV mutations to amyloidosis and course of the disease in the patients with familial Mediterranean fever
Turkcapar N., Tuncali T., Kutlay S., Burhan B. Y., Kinikli G., ERTÜRK Ş., et al.
RHEUMATOLOGY INTERNATIONAL
, vol.27, no.6, pp.545-551, 2007 (SCI-Expanded)
2007
2007TBX1 gene mutation screening in patients with non-syndromic Fallot tetralogy
Cabuk F., KARABULUT H. G., Tuncali T., Karademir S., Bozdayi M., Tukun A.
TURKISH JOURNAL OF PEDIATRICS
, vol.49, no.1, pp.61-68, 2007 (SCI-Expanded)
2006
2006A fourth locus for hereditary hemorrhagic telangiectasia maps to chromosome 7
Bayrak-Toydemir P., McDonald J., Alkarsu N., Toydemir R. M., Calderon F., Tuncali T., et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
, vol.140A, no.20, pp.2155-2162, 2006 (SCI-Expanded)
2004
2004Is vitamin D hypothesis for schizophrenia valid? Independent segregation of psychosis in a family with vitamin-D-dependent rickets type IIA
Ozer S., Ulusahin A., Ulusoy S., Okur H., Coskun T., Tuncali T., et al.
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY
, vol.28, no.2, pp.255-266, 2004 (SCI-Expanded)
2002
2002Retinoik asit ile in vitro insan kolon adenokanser hücrelerinde baskılanan proliferasyonda protein kinaz C enzim aktivitesinde değişim
TUNCALI T.
Turkish Journal Of Biochemistry-Turk Biyokimya Dergisi , vol.27, no.4, pp.145-152, 2002 (SCI-Expanded)
2000
2000Mental retardation with rare fragile site expressed at 2q11
Tukun A., Renda Y., Topcu M., Tuncali T., Bokesoy I.
BRAIN & DEVELOPMENT
, vol.22, no.8, pp.498-500, 2000 (SCI-Expanded)
1993
1993RETINOIC ACID INHIBITS GROWTH OF HT29 CELLS AND DECREASES ORNITHINE DECARBOXYLASE LEVELS INVITRO
TUNCALI T., DILLON M., SMOOT D., DICKSON L., BREMNER T., ASSEFFA A.
GASTROENTEROLOGY
, vol.104, no.4, 1993 (SCI-Expanded)
1988
1988A SEMI-ITERATIVE METHOD FOR DERIVATION OF CONCENTRATION-RESPONSE PARAMETERS
ONARAN H. O., TUNCALI T., BOKESOY T.
JOURNAL OF PHARMACOLOGICAL METHODS
, vol.19, no.1, pp.39-45, 1988 (SCI-Expanded)
Articles Published in Other Journals
2021
2021Genotype Phenotype Correlation of A Case Having Chromosome 3 Imbalance
Taşdelen E., Gökpınar İli E., Altıner Ş., Ceylan A. C., Tuncalı T.
Ankara Üniversitesi Tıp Fakültesi Mecmuası
, vol.74, no.3, pp.365-369, 2021 (Peer-Reviewed Journal)
2021
2021Molecular Testing for Thalassemia: Mutation Detection According to Referral Reasons and Demographic Data
ALTINER Ş., KARABULUT H. G., EKİNCİ S., Vicdan A., KUTLAY N., TUNCALI T., et al.
ERCIYES MEDICAL JOURNAL
, vol.43, no.5, pp.449-451, 2021 (ESCI)
2021
2021Coexistence of Ovarian Granulose Cell Tumor, Congenital Adrenal Hyperplasia, and Triple Translocation: Is a Consequence or Coincidence?
AKBULUT A. S., Ceylan S. D., TUNCALI T., Sogutcu N.
JOURNAL OF GASTROINTESTINAL CANCER
, vol.52, no.2, pp.508-514, 2021 (ESCI)
2021
2021Comparative Analysis and Validation of CIBMTR Early Relapse Risk Score with ISS and R-ISS: Single Center Experience from Ankara University
Seval G. C., Bozdag S. C., Toprak S. K., Yuksel M. K., Topcuoglu P., Arslan O., et al.
Transplantation and Cellular Therapy
, vol.27, no.3, pp.401, 2021 (Scopus)
2017
2017Akut Miyeloid Lösemide Kromozomal Anomaliler: Tek Merkezden 417 Olgunun Sitogenetik Sonuçları
KUTLAY N., TUNCALI T., KARABULUT H. G., AKALIN İ., ILGIN RUHİ H., VİCDAN N. A., et al.
Ankara Üniversitesi Tıp Fakültesi Mecmuası , vol.70, no.1, pp.37-51, 2017 (Peer-Reviewed Journal)
2013
2013An evaluation of the phenotypic features of fanconi anemia together with DEB/MMC positivity in 199 turkish patients
KUTLAY N., TUNCALI T., ILGIN RUHİ H., KARABULUT H. G., TÜKÜN F. A.
Türkiye Klinikleri Tip Bilimleri Dergisi , vol.33, no.1, pp.1-8, 2013 (Scopus)
1992
1992Augmentation of the release of leukotriene B4 by indomethacin from human peripheral blood mononuclear cells
TUNCALI T., MELLİ M., Ayhan I., Turker R., Vigano T., Folco G.
Doga - Turkish Journal of Medical Sciences
, vol.16, no.3, pp.163-166, 1992 (Scopus)
Papers Presented at Peer-Reviewed Scientific Conferences
2024
2024Aynı Hastalık Farklı Klinik: A20 Haplo Yetersizliği
SÜLEYMAN M., HASKOLOĞLU Z. Ş., DEVECİ N., İSLAMOĞLU C., ERKMEN H., BAYLAN T., et al.
10. KLİNİK İMMÜNOLOJİ KONGRESİ, Antalya, Turkey, 15 April 2024
2022
2022Yetişkin Akut Miyeloid Lösemi/Miyelodisplastik Sendrom Hastalarında Konvansiyonel Sitogenetik İncelemenin Kompleks Karyotip Saptamadaki Gücü
Altıner Ş., Vicdan N. A., Kutlay N., Tuncalı T., Karabulut H. G., Ilgın Ruhi H.
15.Uulsal Tıbbi Genetik Kongresi, Muğla, Turkey, 9 - 13 November 2022, pp.102-103
2022
2022Cytogenetic evaluation in myelodysplastic syndrome
LEBLEBİCİ C. B., ALTINER Ş., VİCDAN N. A., KUTLAY N., TUNCALI T., KARABULUT H. G., et al.
European Human Genetics Conference, Viyana, Austria, 11 - 14 June 2022
2022
2022Evaluation of Plasma Cell Molecular Cytogenetic Findings of Myeloma Patients: One-Year Single-Center Experience
KAPLAN İ., CESUR BALTACI H. N., ALTINER Ş., EKİNCİ S., VİCDAN N. A., KARABULUT H. G., et al.
ESHG 2021, 28 August 2022, pp.413
2021
2021Familyal Adenomatöz Polipozis’de Genetik Test Ve Danışmanın Önemi: Bir Aile Örneği
ALTINER Ş., TUNCALI T.
1. Ulusal Hemotoonkogenetik kongresi, Antalya, Turkey, 25 - 28 November 2021
2021
2021Kütanöz T Hücreli Lenfomada Görülen Konvansiyonel Sitogenetik ve Akım Sitometri Bulguları
LEBLEBİCİ C. B., ALTINER Ş., VİCDAN N. A., KUTLAY N., TUNCALI T., KARABULUT H. G., et al.
1. Ulusal HematoOnkoGenetik Kongresi, Antalya, Turkey, 25 - 28 November 2021
2021
2021Son İki Yılda Kliniğimize Başvuran Yeni Tanı AML Hastalarında Genetik Parametrelerin Değerlendirilmesi
SEVİM B., KURTÇU O., ALTINER Ş., EKİNCİ S., VİCDAN N. A., TUNCALI T., et al.
1. Ulusal HematoOnkoGenetik Kongresi, Antalya, Turkey, 25 - 28 November 2021
2021
2021Multiple Miyelom Hastalarının Plazma Hücrelerindeki Moleküler Sitogenetik İnceleme Sonuçları: Ankara Üniversitesi Deneyimi
KAPLAN İ., CESUR BALTACI H. N., ALTINER Ş., EKİNCİ S., VİCDAN N. A., KARABULUT H. G., et al.
1. Ulusal HematoOnkoGenetik Kongresi, Antalya, Turkey, 25 November 2021, pp.29
2021
2021Clinical findings in 22q11.2 microdeletion syndrome: case series
ALTINER Ş., TUNCALI T., KUTLAY N., KARABULUT H. G., ILGIN RUHİ H.
European Human Genetics Virtual Conference, 28 - 31 August 2021
2021
2021MULTİPL MİYELOMDA OTOLOG PRİFERİK KÖK HÜCRE NAKLİ SONRASI ERKEN NÜKSÜ BELİRLEMEDE CIBMTR, ISS VE R-ISS SKORLAMA SİSTEMLERİNİN KARŞILAŞTIRILMASI
CENGİZ SEVAL G., CİVRİZ BOZDAĞ S., TOPRAK S. K., YÜKSEL M., TOPÇUOĞLU P., ARSLAN Ö., et al.
13. Ulusal kemik İliği Transplantasyonu ve Hücresel Tedaviler Kongresi, 02 April 2021
2020
202014q32.31q32.33 Delesyon Olgu Sunumu
ACAR M. O., ALTINER Ş., KENDİRLİ T., KUTLAY N., TUNCALI T.
14.Ulusal Tıbbi Genetik Kongresi “Uluslararası Katılımlı”, Ankara, Turkey, 14 October 2020, vol.31, (Summary Text)
2020
2020ROHMM, a flexible HMM approach for detecting homozygosity using next generation sequencing data
ÇELİK G., TUNCALI T.
ESHG Conference - EUROPEAN JOURNAL OF HUMAN GENETICS, 6 - 09 June 2020, vol.28, pp.668
2012
2012AB0028 Effect of genetic polymorphism of PTPN22 protein tyrosine phosphatase non receptor type 22 on progress and course of disease in familial mediterrenean fever
Seker Z., KÜÇÜKŞAHİN O., ŞAHİN A., TUNCALI T., KINIKLI G., TURGAY T. M.
EULAR 2012, 6 - 09 June 2012, vol.71, pp.639
2019
2019ATN1 gene mutation in patients with Huntington disease-like phenotype
KARABULUT H. G., GÖKOĞLU M., Altıner Ş., DURMAZ C. D., GÖKPINAR İLİ E., VİCDAN N. A., et al.
13. Balkan Congress of Human Genetics, 17 - 20 April 2019, (Summary Text)
2019
2019ATN1 gene mutation in patients with Huntington disease-like phenotype
KARABULUT H. G., GÖKOĞLU M., ALTINER Ş., DURMAZ C. D., GÖKPINAR İLİ E., VİCDAN N. A., et al.
13th Balkan Congress of Human Genetics, Edirne, Turkey, 17 - 20 April 2019, (Summary Text)
2018
201822q11.2 delesyon sendromu örneği: Cayler Kardiyofasyel sendromu
KAPLAN İ., TAŞDELEN E., TUNCALI T.
13. Uluslararası Katılımlı Ulusal Tıbbi Genetik Kongresi, Turkey, 7 - 11 November 2018, (Summary Text)
2017
2017A case with chromosome 3 imbalance: duplication 3q and deletion 3p
Tasdelen E., Gokpinar E., TUNCALI T.
50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.956-957, (Summary Text)
2017
2017Nonclassical adrenal hyperplasia and polycystic ovary syndrome: evaluation of four cases
Ilgin-Ruhi H., Tasdelen E., Gokpinar E., Gokoglu M., TUNCALI T.
50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.149
2016
2016Multiple Konjenital anomali/mental retardasyonlu üç olguda subtelomerik FISH bulguları
ALTINER Ş., GÖKOĞLU M., TUNCALI T., KUTLAY N.
12. ULUSAL TIBBİ GENETİK KONGRESİ, İzmir, Turkey, 5 - 09 October 2016, (Summary Text)
2016
2016Perinatal outcomes in fetuses with cystic hygroma
SEVAL M. M., KATLAN D. C., YAKIŞTIRAN B., TUNCALI T., ILGIN RUHİ H., KOÇ F. A., et al.
XXV European Congress Perinatal Medicine, Maastricht, Netherlands, 15 - 18 June 2016
2016
2016Polymorphism of a potassium chloride transporter gene SLC12A5 is associated with autistic like traits in healthy individuals
AYKAN S., TUNCALI T., ÖZGÜVEN H., KALAYCIOĞLU C.
European Human Genetics Conference, Barselona, Spain, 21 - 24 May 2016, vol.24, pp.443
2016
2016Polymorphism of a potassium/chlorıde transporter gene SLC12A5 is associated with autistic-like traits in healthy individuals
AYKAN S., TUNCALI T., KALAYCIOĞLU C., ÖZGÜVEN H.
European Society of Human Genetics Conference 2016, 21 - 24 May 2016
2016
2016Partial trisomy 22q12 1 and monosomy 13q12 1 in a child due to maternal t 13 22 q12 1 q12 1
Altıner Ş., KUTLAY N., tos t., TUNCALI T.
The European Human Genetics Conference 2016, Barselona, Spain, 21 - 24 May 2016
2016
2016Evaluation of accompanying cytogenetic abnormalities and light chain profiles in 13q deleted MM patients
DURMAZ C. D., TUNCALI T., KUTLAY N., TÜREDİ Ö., ILGIN RUHİ H., VİCDAN N. A., et al.
The European Human Genetics Conference2016, Barselona, Spain, 21 - 24 May 2016
2016
2016Investigation of TBP gene mutations in patients with Huntington Disease phenotype
GÖKOĞLU M., KARABULUT H. G., TÜREDİ Ö., ALTINER Ş., DURMAZ C. D., GÖKPINAR E., et al.
The European Human Genetics Conference2016, Barselona, Spain, 21 - 24 May 2016
2016
2016Multiple Myelom ön tanılı hastalarda FISH yöntemi ile kromozomal anomalilerin belirlenmesi
DURMAZ C. D., TUNCALI T., KUTLAY N., VİCDAN N. A., KARABULUT H. G., TÜKÜN F. A., et al.
II. Hematolojik Genetik Sempozyumu, Turkey, 24 - 26 February 2016, (Summary Text)
2015
2015Resting-State EEG Alpha Power in Healthy Individuals with Autistic Traits
AYKAN S., GÜRSES E., TUNCALI T., YILMAZ S., ÖZGÜVEN H., KALAYCIOĞLU C.
41. Ulusal Fizyoloji Kongresi, Turkey, 9 - 13 September 2015
2015
2015EEG Alpha Power Changes During Sensory Processing in Individuals with Autistic Traits
Simge A. Z., Gürses E., Tuncalı T., Yılmaz S., Halise D. Ö., Kalaycıoğlu C.
Cortical Interneurons in Health and Disease, Balears, Spain, 22 - 25 June 2015
2015
2015Resting State EEG Alpha Power in Healthy Individuals with Autistic Traits
Simge A. Z., Gürses E., Tuncalı T., Yılmaz S., Halise D. Ö., Kalaycıoğlu C.
41. Ulusal Fizyoloji Kongresi, Çanakkale, Turkey, 9 - 13 September 2015
2015
2015Follow up of del 5 q MDS patients with or without other chromosomal abnormalities
TÜREDİ Ö., ATACA P., TUNCALI T., ATİLLA E., VİCDAN N. A., DURMAZ C. D., et al.
10th European Cytogenetics Conference, 4 - 07 July 2015, pp.102
2015
2015Coexistence of ovary tumour congenital adrenal hyperplasia and triple translocation involving chromosome 9 11 and 12 Initial steps of defining new syndrome
AKBULUT S., DURMAZ S. A., TUNCALI T., SOGUTCU N.
17th European Congress of Endocrinology, Dublin, Ireland, 16 - 20 May 2015
2013
2013Talasemi ön tanısı ile incelenen 206 hastada saptanan mutasyonların başvuru nedenlerine göre dağılımı
BİÇER Ş., KARABULUT H. G., Ekinci S., Mutlu M. B., VİCDAN N. A., KUTLAY N., et al.
I. Hematolojik Genetik Sempozyumu, Turkey, 2 - 04 December 2013
2013
2013Akut lenfoblastik lösemide konvansiyonel sitogenetik, FISH ve real-time PCR yöntemlerinin birlikte kullanımının klinik yararı: tek merkezden 1050 olgunun sonuçları
Ekinci S., VİCDAN N. A., BİÇER Ş., Mutlu M. B., KUTLAY N., KARABULUT H. G., et al.
I. Hematolojik Genetik Sempozyumu, İzmir, Turkey, 2 - 04 December 2013, pp.52
2013
2013Multiple Myelomda konvansiyonel sitogenetik ve FISH yöntemlerinin birlikte kullanımının klinik yararı: Tek merkezden 1150 olgunun sonuçları
Mutlu M. B., VİCDAN N. A., BİÇER Ş., Ekinci S., KUTLAY N., KARABULUT H. G., et al.
I. Hematolojik Genetik Sempozyumu, İzmir, Turkey, 2 - 04 December 2013, pp.53
2010
2010New Mutations of CYP21 in Turkish Population
KUTLAY N., Faika S., BERBEROĞLU M., Çetinkaya E., Aycan Z., Kara C., et al.
European Human Genetics Conference, Gothenburg, Sweden, 12 - 15 June 2010
2009
2009Cytogenetic findings in 1493 patients with hematologic disorders from turkey
VİCDAN N. A., Dinççelik M., YARARBAŞ K., Faika S., AKALIN İ., Ada Sağlam B., et al.
Mediterranean Medical Genetics Meeting, Ankara, Turkey, 28 June - 01 July 2009
2008
2008Huntigton Hastalığı Genetik Test Sonuclarını Değerlendirilmesi
KARABULUT H. G., Sağlam B., Topcu V., VİCDAN N. A., KUTLAY N., TUNCALI T., et al.
VIII. Ulusal Tıbbi Genetik Kongresi, Çanakkale, Turkey, 6 - 09 May 2008
2007
2007Cytogenetics findings in a group of patients with acute lymphoblastic leukemia
KARABULUT H. G., Sağlam B., TUNCALI T., KUTLAY N., ILGIN RUHİ H., YARARBAŞ K., et al.
European Human Genetics Conference, Nice, France, 16 - 19 June 2007
2007
2007Cytogenetics in AML: results of 589 patients
KUTLAY N., TUNCALI T., KARABULUT H. G., Faika S., Ada Sağlam B., AKALIN İ., et al.
European Human Genetics Conference, Nice, France, 16 - 19 June 2007
2007
2007Cytogenetic evaluation of 506 myelodysplastic syndrome patiens
ILGIN RUHİ H., TUNCALI T., KUTLAY N., KARABULUT H. G., YARARBAŞ K., AKALIN İ., et al.
European Human Genetics Conference, Nice, France, 16 - 19 June 2007, (Summary Text)
2007
2007Secondary chromosomal abnormalities within Philadelphia positive Chronic Myeloid Leukemia
Sağlam B., YARARBAŞ K., AKALIN İ., ILGIN RUHİ H., TUNCALI T., KARABULUT H. G., et al.
European Human Genetics Conference, Nice, France, 16 - 19 June 2007, (Summary Text)
2007
2007Classification of chromosomal aberrations in a group of patients with chronic myeloproliferative disorders
TUNCALI T., KARABULUT H. G., ILGIN RUHİ H., KUTLAY N., Faika S., AKALIN İ., et al.
European Human Genetics Conference, Nice, France, 16 - 19 June 2007
2007
2007Cytogenetic findings in 357 patients with multiple myeloma
Ilgin-Ruhi I. A., KARABULUT H. G., KUTLAY N., TUNCALI T., Saglam B., Yararbas K., et al.
6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, vol.15, pp.215
2005
2005The contribution of genotypes at the mica gene triplet repeat polymorphisms and MEFV mutations to amyloidosis and course of the disease in the patients with Familial Mediterranean Fever
Turkcapar N., TUNCALI T., Kutlay S., Burhan B., Kinikli G., ERTÜRK Ş., et al.
Annual European Congress of Rheumatology, Vienna, Austria, 8 - 11 June 2005, vol.64, pp.543-544
2005
2005The contribution of genotypes at the mica gene triplet repeat polymorphisms and MEFV mutations to amyloidosis and course of the disease in the patients with familial Mediterranean fever
Turkcapar N., TUNCALI T., Kutlay S., Burhan B., ERTÜRK Ş., Kinikli G., et al.
42nd Annual Meeting of the European-Renal-Association/European-Dialysis-and-Transplant-Association (ERA-EDTA), İstanbul, Turkey, 4 - 07 June 2005, vol.20
2005
2005Evalution of clinical and cytogenetical criteria presets for the diagnostic approach in a large group of Fanconi anemia cases
TUNCALI T., Babaoğlu E., KUTLAY N., Akçay R., YARARBAŞ K., Faika S., et al.
European Human Genetics Conference, Prag, Czech Republic, 7 - 10 May 2005
2004
200446 X i Y q10 inv 9 p11q13 8 45 X inv 9 p11q13 22 Karyotipli Turner sendromu olgusu
AYDOS O. S., TUNCALI T.
6. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Antalya, Turkey, 21 - 24 April 2004
2002
2002Farklı gebelik dönemlerinde tekrarlayan kayıpları olan çiftlerde sitogenetik bulgular
Çabuk F., SAYIN KOCAKAP D. B., Akçay R., Özer L., AYDOS O. S., KUTLAY N., et al.
V.ULUSAL PRENATAL TANI ve TIBBİ GENETİK KONGRESİ, Turkey, 9 - 12 October 2002
2002
2002Angelman Sendromu: Mikrodelesyon ve Klinik Bulgular
Özer L., KUTLAY N., TUNCALI T., AYDOS O. S., KARABULUT H. G., SAYIN KOCAKAP D. B., et al.
V. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Turkey, 9 - 12 October 2002
1993
1993RETINOIC ACID INHIBITS GROWTH OF HT29 CELLS AND DECREASES ORNITHINE DECARBOXYLASE LEVELS INVITRO
TUNCALI T., DILLON M., SMOOT D., DICKSON L., BREMNER T., ASSEFFA A.
GASTROENTEROLOGY, United States Of America, 1 - 03 April 1993, vol.104, pp.458
Books
2006
2006Konak Genetikleri ve Farmakogenomik
TUNCALI T.
in: Moleküler Mikrobiyoloji, Alper Tekeli, Şemsettin Ustaçelebi, Editor, ANTIP, pp.643-679, 2006
Memberships and Roles in Scientific Organizations
1994 - Continues
1994 - ContinuesTıbbi Genetik Derneği
Member
Peer Reviews in Scientific Publications
November 2022
November 2022TURKISH JOURNAL OF GASTROENTEROLOGY
Journal Indexed in SCI-E
October 2017
October 2017TURKISH JOURNAL OF BIOCHEMISTRY
Journal Indexed in SCI-E
October 2014
October 2014TURKISH JOURNAL OF MEDICAL SCIENCES
Journal Indexed in SCI-E
Congress and Symposium Activities
04 December 2024 - 08 December 2024
04 December 2024 - 08 December 202416. Ulusal Tıbbi Genetik Kongresi
Invited Speaker
Antalya-Turkey
17 April 2019 - 20 April 2019
17 April 2019 - 20 April 2019
13. Balkan Congress of Human Genetics
Invited Speaker
Edirne-Turkey
Scholarships
1988 - 1993
1988 - 1993