» Publications

SCI-SSCI or SCI Expanded Articles

.S. Demir, H. Gurkan, D. Eker, S. Yalcintepe, E. Atli, E. Atli, RETROSPECTIVE ANALYSIS OF ALPHA GLOBIN COPY NUMBER VARIATIONS DETERMINED BY MLPA IN THE TRAKYA REGION, 10.26650/IUITFD.2021.880592, JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI, vol. 84, no. 3, pp. 348-353, 2021.

.I. GÖRKER, H. GÜRKAN, S. ULUSAL, E. ATLI, G. AYAZ, C. CEYLAN, H. TOZKIR, M. A. ALTAY, A. EROL, Otizm Spektrum Bozuklugu Tanisi Alan Türk Çocuk ve Ergenlerde Mikrodizin Karsilastirilmali Genomik Hibridizasyon Yöntemi Ile Kopya Sayisi Degisikliklerinin Arastirilmasi, Nöropsikiyatri Arsivi, vol. 55, no. 3, pp. 215-219, 4, 2018.

.G. I. Ç. UZUN, C. N. SAYIN, H. GÜRKAN, N. Ç. ALADAG, E. ATLI, C. INAN, S. E. GÜRSOY, H. SUTCU, Ü. Ö. VATANSEVER, F. G. VAROL, Deletion of macro domain containing 2(MACRO D2) associated withtransient hydrops fetalis, Taiwanese Journal of Obstetrics and Gynecology, 12, 2018.

.E. ATLI, H. GÜRKAN, S. ULUSAL, Y. KARAL, I. E. ATLI, H. TOZKIR, Identification of a novel homozygous TBC1D24 mutation in a Turkish family with DOORS syndrome, Clinical Dysmorphology, vol. 27, pp. 1-, 1, 2018.

.C. INAN, C. N. SAYIN, N. Z. A. DOLGUN, H. GÜRKAN, S. E. GÜRSOY, G. I. Ç. UZUN, H. SUTCU, S. ATES, E. ATLI, F. G. VAROL, Prenatal diagnosis of chromosomal polymorphisms: most commonly observed polymorphism on Chromosome 9 have associations with low PAPP-A values, The Journal of Maternal-Fetal Neonatal Medicine, vol. 31, pp. 1-8, 12, 2017.

.S. ULUSAL, H. GÜRKAN, E. ATLI, A. S. ÖZAL, M. ÇIFTDEMIR, H. TOZKIR, Y. KARAL, H. GÜÇLÜ, D. EKER, I. GÖRKER, Genetic analyses of the NF1 gene in Turkish neurofibromatosis type I patients and definition of three novel variants, Balkan Journal of Medical Genetics, vol. 20, no. 1, pp. 13-20, 1, 2017.

.H. M. MÜSLÜMANOGLU, E. TEPELI, S. ULUSAL, E. ATLI, M. ÖZDEMIR, The analysis of the relationship between A1298C and C677T polymorphisms of the MTHFR gene with prostate cancer in Eskisehir population, Genetic Testing and Molecular Biomarkers, 10, 2009.

International Articles

.I. E. ATLI, H. GÜRKAN, H. TOZKIR, Y. ÖZEN, S. ULUSAL, E. ATLI, F. G. VAROL, C. N. SAYIN, Cytogenetic Analysis and Thrombophilia Associated Gene Mutations of Couples with Recurrent Miscarriage, Journal of Fertilization: In Vitro - IVF-Worldwide, Reproductive Medicine, Genetics & Stem Cell Biology, vol. 4, no. 3, 1, 2016.

International Conference Proceedings

.S. DEMIR, H. TOZKIR, H. GÜRKAN, E. ATLI, D. EKER, A. H. TEZEL, A. Y. SEZER, I. ÇIÇIN, C. H. KARLIKAYA, A. Y. KARAMUSTAFAOGLU, Screening for germline variations of cancer related genes in patients with the diagnosis of different cancers and hereditary cancer predisposition syndromes, European Human Genetics Conference, Milan, Italy, MILANO-ITALYA.

.C. INAN, C. N. SAYIN, H. GÜRKAN, S. E. GÜRSOY, G. I. Ç. UZUN, H. SÜTCÜ, E. ATLI, F. G. VAROL, A case of amniotic band syndrome, 16th World Congress in Fetal Medicine, Ljubljana-SLOVENYA.

.G. I. Ç. UZUN, C. N. SAYIN, H. GÜRKAN, N. Ç. ALADAG, E. ATLI, C. INAN, S. E. GÜRSOY, Ü. Ö. VATANSEVER, F. G. VAROL, Hydrops fetalis with deletion of macrodomain containing 2, 16 th World Congress in Fetal Medicine, -SLOVENYA.

.H. TOZKIR, S. ULUSAL, H. GÜRKAN, E. ATLI, Y. KARAL, T. S. KARASALIHOGLU, Four novel pathogenic variants in TSC2 gene of Turkish patients with tuberous sclerosis complex, EUROPEAN HUMAN GENETICS CONFERENCE.

.H. GÜRKAN, I. GÖRKER, E. ATLI, I. E. ATLI, S. ULUSAL, D. EKER, H. TOZKIR, ArrayCGH analysis in patients with intellectual disability/developmental delay in Turkish Children living in Trakya Region, EUROPEAN HUMAN GENETICS CONFERENCE.

.H. GÜRKAN, S. ULUSAL, H. TOZKIR, E. ATLI, I. E. ATLI, Genetic screening for chromosomal abnormalities Y chromosome microdeletions and copy number variationin infertile male patients living in the Trakya region of Turkey, ESHG Conference 2016.

.S. ULUSAL, H. GÜRKAN, E. ATLI, A. S. ÖZAL, H. TOZKIR, Comprehensive analysis of NF1 gene by using targeted resequencing and multiplex ligation dependent probeamplification in patients with neurofibromatosis type I, ESHG Conference 2016.

.H. TOZKIR, S. ULUSAL, E. ATLI, A. Y. SEZER, H. GÜRKAN, N. TUNÇBILEK, Results of BRCA1 and BRCA2 mutation screening with next generation sequencing in a cohort of breast andovarian cancer patients in Trakya region of Turkey, ESHG Conference 2016.

.C. INAN, C. N. SAYIN, H. GÜRKAN, E. ATLI, G. I. Ç. UZUN, S. E. GÜRSOY, I. E. ATLI, F. G. VAROL, Schizencephaly Case Accompanied By Deletion of Chromosome 22q13 32, 15th World Congress in Fetal Medicine.

National Articles

.I. E. ATLI, H. GÜRKAN, H. TOZKIR, G. E. ÜMIT, S. DEMIR, S. YALÇINTEPE, E. ATLI, M. A. DEMIR, Multiple Myelom (MM) Tanisi Alan Olgularda Kromozomal Degisimler, Gaziosmanpasa Üniversitesi Tip Fakültesi Dergisi, no. 1, pp. 8-19, 10, 2018.

National Conference Proceedings

.H. GÜRKAN, E. ATLI, Ü. Ö. VATANSEVER, I. E. ATLI, Y. ÖZEN, Ç. AKURUT, H. TOZKIR, A. B. ACUNAS, 3q22.2-q22.3 Deletion and 16p11.2 Microduplication Syndrome in a Patient with Blepharophimosis, Ptosis, Epicanthus Inversus Syndrome, Erciyes Medical Genetics Days, -TÜRKIYE.

.S. ULUSAL, H. TOZKIR, H. GÜRKAN, A. Y. SEZER, E. ATLI, E. TASTEKIN, N. TUNÇBILEK, F. G. VAROL, Pathogenic Variations of Brca1 and Brca2 Genes in the Breast and/or Ovarian Cancer Patients Living in Trakya Region of Turkey, Erciyes Medical Genetics Days, -TÜRKIYE.

Awards

.Sözlü Sunum Üçüncülük Ödülü, COAGULATION FACTOR X GENE MUTATIONS IN FIVE PATIENTS WITH FACTOR X DEFFICIENCY baslikli sözlü sunum gerçeklestirilmistir. , Yil: 2016, ERCIYES ÜNIVERSITESI, ERCIYES ÜNIVERSITESI.

Other

.E. Atli, S. Yalcintepe, E. Atli, S. Demir, H. Gurkan, A Child with 5q Deletion and Accompanying Chiari 1 Malformation, 10.1007/s12098-020-03451-4, INDIAN JOURNAL OF PEDIATRICS, vol. 87, no. 9, pp. 766-766, 2020.