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SCI-SSCI or SCI Expanded Articles

  • An unknown chromosomal aberration in a patient with chronic lymphocytic leukemia: Extra isochromosome 4q (March 2019)
  • FOXF2 is required for cochlear development in humans and mice (December 2018)
  • Prenatal diagnosis of a new case: De novo balanced non-Robertsonian translocation involving t(15;22)(p11.2;q11.2) (December 2018)
  • A large posterior encephalocele associated with severe ventriculomegaly, cerebellar atrophy and transposition of the great arteries (June 2018)
  • Prenatal diagnosis of chromosomal polymorphisms: most commonly observed polymorphism on Chromosome 9 have associations with low PAPP-A values (December 2017)
  • Identification of a novel homozygous TBC1D24 mutation in a Turkish family with DOORS syndrome. (December 2017)
  • Görker I,Gürkan H, Demir Ulusal S, Atlı E, Ikbal Atlı E. DOI: 10.1515/bjmg-2016-0041 A 9-YEAR-OLD-GIRL WITH PHELAN McDERMID SYNDROME, WHO HAD BEEN DIAGNOSED WITH AN AUTISM SPECTRUM DISORDER (January 2017)
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  • Cihan Inan, N. Cenk Sayın, Emine Atlı, Selma Ulusal, Selen Erzincan, Isil Uzun, Hakan Gurkan & Füsun G. Varol show less Pages 339-343 Published online: 16 Jun 2016 Tetrasomy 18p in a Twin Pregnancy with Diverse Expression in Both Fetuses (May 2016)
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  • Eİ Atli, H Gürkan, Ü Vatansever, S Ulusal, H Tozkir Balkan Journal of Medical Genetics 18 (2), 77-82 A CASE WITH EMANUEL SYNDROME:EXTRA DERIVATIVE 22 CHROMOSOME INHERITED FROM THE MOTHER (April 2016)
  • R Kalkan, E Atli - Critical Reviews™ in Eukaryotic Gene Expression Volume 26, 2016 Issue 2 pages 137-142 The impacts of miRNAs in Glioblastoma Progression, Treatment and Prognosis (March 2016)
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  • Eİ Atli, R Kalkan, M Özdemir, HE Aydın, A Arslantaş, S Artan African Health Sciences 16 (1), 218-226 RARβ gene methylation is a candidate for primary glioblastoma treatment planning. (March 2016)
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  • R Kalkan, Eİ Atli, M Özdemir, E Çiftçi, HE Aydin, S Artan, A Arslantaş Gene 554 (1), 81-86 IDH1 mutations is prognostic marker for primary glioblastoma multiforme but MGMT hypermethylation is not prognostic for primary glioblastoma multiforme (January 2015)
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  • EI Atli, R Kalkan, E Ciftci, E ÖZKARA, O ÇİLİNGİR, M ÖZDEMİR, Z ÖZBEK, ... Journal of Neurological Sciences 31 (4) IDH2 Mutations in Primary Glioblastoma (September 2014)

International Articles

  • De Novo Subtelomeric 6p25.3 Deletion with Duplication of 6q23.3-q27: Genotype–Phenotype Correlation (June 2019)
  • EI Atli, H Gurkan, H Tozkir, Y Ozen, S Ulusal JFIV Reprod Med Genet 4, 189 Cytogenetic Analysis and Thrombophilia-Associated Gene Mutations of Couples with Recurrent Miscarriage (August 2016)
  • Atli EI, Yakicier C, Akin A (2016) Anaplastic Lymphoma Kinase (ALK) Rearrangement and EGFR Mutations in Lung Adenocarcinoma. Adv Oncol Res Treat 1:103. (March 2016)

International Conference Proceedings

  • Genomic Changes in Patients with Short Stature (October 2019)
  • Rare Observed X Chromosome Changes in Different Cases (October 2019)
  • Copy Number Variation (CNV) in Patients Diagnosed with Growth Retardation (July 2019)
  • Prenatal management and pregnancy outcomes in fetuses with cystic hygroma (April 2019)
  • A six - year retrospective study of amniocentesis: one centre experience (April 2019)
  • A case of encephalocele (June 2017)
  • ArrayCGH analysis in patients with intellectual disability/developmental delay in Turkish Children living in Trakya Region (June 2017)
  • 3q22.2-q22.3 Deletion and 16p11.2 Microduplication Syndrome in a Patient with Blepharophimosis, Ptosis, Epicanthus Inversus Syndrome (May 2017)
  • E. I. Atlı, H. Gürkan, G. E. Pamuk, C. Akurut, H. Tozkır, A. M. Demir. A novel cytogenetic abberation is extra isochromosome 4q in chronic lymphocytic leukemia patient. European Human Genetics Conference-2016, (ESHG-2016). 21-24 May 2016, Conference venue: CCIB, Barcelona, Spain. E-P12.036 (Mayıs 2016) (May 2016)
  • Kalkan R.Atli EI,European Human Genetics Conference-2016, (ESHG-2016). 21-24 May 2016 The prognostic importance of the MGMT and RARβ gene hypermethylation in Primary Glioblastoma (May 2016)
  • E. Atli, H. Gurkan, S. Demir Ulusal, Y. Karal, E. I. Atli, H. Tozkir. A novel mutation of TBC1D24 identified in a Turkish family with DOORS syndrome. European Human Genetics Conference-2016, (ESHG-2016). 21-24 May 2016, Conference venue: CCIB, Barcelona, Spain. P11.051 (Mayıs 2016) (May 2016)
  • H. Gurkan, S. Demir Ulusal, H. Tozkır, E. Atlı, E. I. Atlı, D. Eker. Genetic screening for chromosomal abnormalities, Y chromosome microdeletions and copy number variation in infertile male patients living in the Trakya region of Turkey. European Human Genetics Conference-2016, (ESHG-2016). 21-24 May 2016, Conference venue: CCIB, Barcelona, Spain. P01.051 (Mayıs 2016) (May 2016)
  • Yasemim Özen, Hakan Gürkan, Ülfet Vatansever Özbek, Emine İkbal Atlı, Damla Eker, Betül Acunaş. A case report: 13q21-qter deletion with digital anomalies, duodenal atresia and anal atresia. 10th European Cytogenetics Conference 4 - 7 July 2015 Strasbourg Convention & Exhibition Centre Strasbourg, France (Temmuz 2015) (July 2015)
  • H. Gurkan, U. Vatansever, E. I. Atlı, D. Eker, S. Ulusal, N. A. Çiftdemir, H. Tozkır. Genotype-phenotype correlation in three patients with Wolf-Hirschhorn syndrome. European Human Genetics Conference. June 6 - 9, 2015 Glasgow, Scotland, United Kingdom, (Haziran 2015) (June 2015)
  • Inan C, Sayın NC, Gurkan H, Erzincan SG, Ulusal S, Atlı EI, Varol FG. Both siblings affected by tetrasomy 18p in a dichorionic twin pregnancy. 14th World Congress in Fetal Medicine, 21-25 June 2015, Crete, Greece (Haziran 2015) (June 2015)
  • R.Kalkan, E.I.Atli, IDH1 mutations in a Turkey series of primary glioblastoma, FEBS EMBO 2014 Conference, Paris, France, 30 August-4 September, 2014, FEBS Journal Volume 281 (Suppl. 1)(2014)65-783, P475 (August 2014)
  • E.İ. Atli, , R. Özkut, S. Artan, A. Arslantaş, M. Özdemir. European Journal of Cancer Volume 50, Supplement 4, May 2014,Pages e37,http://dx.doi.org/10.1016/j.ejca.2014.03.142 IDH2 mutations in Turkish patients with primary glioblastoma (May 2014)
  • E.İ. Atli, , R. Özkut, S. Artan, A. Arslantaş, M. Özdemir. European Journal of Cancer. Vol. 50, 05/2014; 50:e37. DOI: 10.1016/j.ejca.2014.03.144 RARβ methylation in Turkish patients with primary glioblastoma. (May 2014)
  • E.İ. Atli,M.C. Yakicier, A. Akin,European Journal of Cancer,Volume 50, Supplement 4, May 2014, Pages e37,6th Asian Oncology Summit and 10th Annual Conference of the Organisation for Oncology and Translational Research,P0097 ALK rearrangements in turkish patients with lung adenocarcinoma (May 2014)
  • E. I. Atli , R. Kalkan , S. Artan. FEBS Journal 281 (Suppl. 1) (2014) 65–783 IDH2 MUTATIONS IN TURKISH PATIENTS WITH PRIMAR GLIOBLASTOMA (May 2014)
  • E. I. Atli , R. Kalkan , S. Artan. FEBS Journal 281 (Suppl. 1) (2014) 65–783 4.RARB gene methylation in primary glioblastomas, (May 2014)

International Conferences and Symposiums

  • Novel MID1 mutation in a patient with X-linked Opitz G/BBB syndrome (April 2019)
  • Inan C, Sayin NC, Gurkan H, Atli E, Uzun I, Erzincan SG, Sutcu H, Dogan S, Atli EI, Varol FG. A Schizencephaly Case Accompanied By Deletion of Chromosome 22q13. 32. 15th World Congress in Fetal Medicine, Palma de Mallorca 2016 (Haziran 2016) (June 2016)

National Articles

  • R KALKAN, Eİ ATLI Türk Nöroşirürji Dergisi 24 (3), 239-249 Genetics of Glioblastoma; Past and Present (June 2014)

National Conference Proceedings

  • Hakan Gürkan, Emine İkbal Atlı, Yasemin Özen, Beril Karabacak, Çisem Akurut, Cenk Sayın, Füsun Varol, Hilmi Tozkır. Evaluation Of Chromosomal And Thrombophilia Panel Of Recurrent Miscarriages. Uluslararası Katkılı ‘Gevher Nesibe Tıp Günleri 2016 ve Tıbbi Genetik ve Klinik Uygulamaları Kongresi. 11-13 Şubat 2016, KAYSERİ. Sözlü Sunum (Şubat 2016) (February 2016)
  • Hilmi TOZKIR, Engin Atlı, Hakan GURKAN, Ulfet VATANSEVER OZBEK, Emine İkbal Atlı, Damla Eker, Ozge YAPICI UĞURLAR, Hakan GENCHELLAC, Betul ACUNAŞ. 1q23.3-q44 duplikasyonu ve Xq22.1-q28 delesyonu saptanan minör konjenital anomalileri olan bir yaşındaki kız olgu. 2.Ulusal Cocuk Genetik Sempozyumu/ 22-24 Ekim 2015, Samsun, (Ekim 2015) (October 2015)
  • Hakan Gurkan, Engin Atlı, Ulfet VATANSEVER OZBEK, Emine İkbal Atlı, Damla Eker, Yasemin KARAL, Sumeyra DOĞAN, Hakan GENCHELLAC. De novo kromozom 11q14.1-11q22.2 delesyonu, hipotonisite, bilateral pitozis ve ekzoftalmus saptanan kız olgu. 2.Ulusal Cocuk Genetik Sempozyumu/ 22-24 Ekim 2015, Samsun (Ekim 2015) (October 2015)
  • Emine İkbal Atlı, Hakan Gurkan, Selma Ulusal, Rıdvan Duran, Hilmi Tozkır. Ekstra derivatif kromozom 22 taşıyan bir olgu: Emanuel sendromu. 2.Ulusal Cocuk Genetik Sempozyumu/ 22-24 Ekim 2015, Samsun, (Ekim 2015) (October 2015)
  • Selma Ulusal, Hakan Gürkan, Beril Varnatopu, Damla Eker, Hilmi Tozkır, Emine İkbal Atlı, Havva Nur Kendirci. De novo r(21) Saptanan Bir Olgu. (Eylül 2014) (September 2014)
  • Atlı E.İ.,Akın A., Yakıcıer C.,XIII. Ulusal Tıbbi Biyoloji ve Genetik Kongresi Kuşadası, Akciğer Adenokarsinomlarında ALK Geni Yeniden Düzenlenmeleri (October 2013)
  • Cantürk M., Çilingir O., Özdemir M., Emre R., Aldemir Ö., Durak B., Çiçek İ., Önür, H., Artan S., VIII. Ulusal Tıbbi Genetik Kongresi 2008, Subtelomerik FISH yöntemiyle saptanan kriptik 14q delesyonu ve 19p duplikasyonlu olgu (May 2008)
  • Artan S., Uludağ A.,Şener T.,Durak B.,Çilingir O.,Çiçek E.İ.,Yurdakul H.,Kurtçu K.,VII. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi ,Prenatal Tanıda Saptanan t(10;12)(q22;q22) Vakası:Olgu Sunumu (May 2006)

Memberships

  • Turkish medical genetics association
  • The European Society of Human Genetics
  • TUBİTAK/ARBİS
  • European Cytogenetics Association

Editorial Positions

  • Advances in Oncology Research and Treatments (March 2016)

Referee Positions

  • MicroRNA-195 inhibits the proliferation and invasion of pancreatic cancer cells by targeting the fatty acid synthase/Wnt signaling pathway (May 2017)
  • Cause-Specific Mortality in Childhood Acute Lymphoblastic Leukemia at a Single Center in Iran (April 2017)
  • A CASE REPORT OF POEMS SYNDROME: A DIAGNOSTIC CHALLENGE (April 2017)
  • Neutrophil-to-lymphocyte and platelet-to-lymphocyte ratio help identify patients with non-small cell lung cancer and predict TNM stages (March 2017)
  • LDR GYNECOLOGICAL BRACHYTHERAPY BY Cs-137: DOSIMETRIC COMPARISON OF MACHESTER SYSTEM AND ICRU-38 (February 2017)
  • Role of Human PAPILLOMA Virus infection in Cancer Cervix: Review article (January 2017)
  • Metastatic Ewings Sarcoma: Revisiting the "Evidence on the Fence' (January 2017)
  • Relaxation and Guided Imagery for Parents of Offspring with Developmental Disabilities (January 2017)
  • Occurrence of Metachronous Multiple Malignancies. Review of the literature. Case of three Patients (April 2016)
  • Molecular characterization of mecA and SCCmec genes in pathogenic Staphylococcus spp. collected from hospitals in Taif region, KSA (March 2016)

Awards

  • INTERPRETATION OF CYTOGENETIC/FISH RESULTS İN MULTIPLE MYELOMA (February 2018)
  • Evaluation Of Chromosomal And Thrombophilia Panel Of Recurrent Miscarriages (February 2016)