Yayınlar

Yayınlar

Uluslararası Hakemli Dergilerde Yayınlanan Makaleler

1. Ozer L, Unsal E, Ayvaz Ö, Şen A, Baltaci V. Prenatal Cytogenetic Findings in 13.466 Cases of High-Risk Pregnant Women in One Laboratory. MN GORM. 2013 19(3): 139-147
2. Ozer L, Lembet A, Uğurlu N, Baltaci V, Balci S. Prenatally diagnosed case of 22q11.2 deletion syndrome associated with pulmonary artery aneurysm. Turk J Pediatr. 2012 Jan-Feb;54(1):74-6.
3. Ayvaz O., Hatırnaz S., Hatırnaz E., Ünsal E., Sinanoglu E.B., Ozer L., Kadı A.K., Baltacı V. First successful preimplantation genetic diagnosis of epidermolysis bullosa with pyloric atresia: Case study of a novel c.4505-4508insACTC mutation. J Assist Reprod Genet, 2012
4. Baltaci Volkan, Ayvaz OU, Unsal E, Aktaş Y, Baltaci A, Turhan F, Ozcan S, Sönmezer M The effectiveness of intracytoplasmic sperm injection combined with piezoelectric stimulation in infertile couples with total fertilization failure.. Fertil Steril. 2010 Aug;94(3):900-4. Epub 2009 May 21.
5. Ramantani G, Kohlhase J, Hertzberg C, Innes AM, Engel K, Hunger S, Borozdin W, Mah JK, Ungerath K, Walkenhorst H, Richardt HH, Buckard J, Bevot A, Siegel C, von Stülpnagel C, Ikonomidou C, Thomas K, Proud V, Niemann F, Wieczorek D, Häusler M, Niggemann P, Baltaci Volkan, Conrad K, Lebon P, Lee-Kirsch MA. Expanding the phenotypic spectrum of lupus erythematosus in AicardiGoutières syndrome. Arthritis Rheum. 2010 May;62(5):1469-77.
6. Ayvaz OU, Ekmekçi A, Baltaci Volkan, Onen HI, Unsal Evaluation of in vitro fertilization parameters and estrogen receptor alpha gene polymorphisms for women with unexplained infertility. E. J Assist Reprod Genet. 2009 Sep-Oct;26(9-10):503-10. Epub 2009 Oct 29.
7. Sonmezer M, Ozmen B, Atabekoglu CS, Baltaci Volkan. Do patients with heterozygote mutations in GALT gene have increased risk for impaired reproductive functions? Fertil Steril. 2009 Oct;92(4):e43; author reply e44. Epub 2009 Sep 5.
8. Balci S, AltuganFS, AlehanD, AyparE, Baltaci Volkan.A prenatally sonographically diagnosed conotruncal anomaly with mosaic type trisomy 21 and 22q11.2 microdeletion/DiGeorge syndrome.Genet Couns. 2009;20(4):373-7.
9. Unsal E, Aktaş Y, Uner O, BaltacI A, Ozcan S, Turhan F, Baltaci Volkan Successful application of preimplantation genetic diagnosis for 22q11syndrome.. Fertil Steril. 2008 Nov;90(5):2017.e11-3.Epub 2008 Sep 7.
10. Sher G, Keskintepe L, Keskintepe M, Ginsburg M, Maassarani G, Yakut T, Baltaci Volkan, Kotze D, Unsal E. Oocyte karyotyping by comparative genomic hybridization [correction of hybrydization] provides a highly reliable method for selecting "competent" embryos, markedly improving in vitro fertilization outcome: a multiphase study. Fertil Steril. 2007 May;87(5):1033-40. Epub 2007 Jan 29.
11. Taskiran C, Baltaci Volkan, Gunalp S. Globozoospermia: Do Y-chromosome microdeletions play a role in this rare spermatogenic disorder? J Reprod Med. 2006 Aug;51(8):628-34.
12. Baltaci Volkan, Satiroglu H, Kabukçu C, Unsal E, Aydinuraz B, Uner O, Aktas Y, Cetinkaya E, Turhan F, Aktan A Relationship between embryo quality and aneuploidies.. Reprod Biomed Online. 2006 Jan;12(1):77-82.
13. Balci S, Engiz O, Yilmaz Z, Baltaci Volkan. Partial trisomy (11;22) syndrome with manifestations of Goldenhar sequence due to maternal balanced t(11;22). Genet Couns. 2006;17(3):281-9
14. Baltaci Volkan, Satiroğlu H, Unsal E, Uner O, Ergün MA, Batioğlu S, Sönmezer M, Kabukçu C, Aydinuraz B, Aktaş Y. Preimplantation genetic diagnosis in two couples with balanced reciprocal translocations. Eur J Obstet Gynecol Reprod Biol. 2007 Sep;134(1):126-7. Epub 2006 Jul 31.
15. Aydos K, Demirel LC, Baltaci Volkan, Unlü C.Enzymatic digestion plus mechanical searching improves testicular sperm retrieval in non-obstructive azoospermia cases. Eur J Obstet Gynecol Reprod Biol. 2005 May 1;120(1):80-6.
16. Baltaci Volkan, Zeyneloglu HB. Increased frequency of sister-chromatid exchange and altered alkaline comet assay scores in superovulation cycles for unexplained infertility. Eur J Obstet Gynecol Reprod Biol. 2004 Mar 15;113(1):73-7.
17. Baltaci Volkan, Sardas S, Aytac B, Cakar S, Karakaya AE. Assessment of cytogenetic aberrations and comet assay in colorectal adenocarcinomas. Tumori. 2003 May-Jun;89(3):305-10.
18. Dündaröz R, Ulucan H, Aydin HI, Güngör T, Baltaci Volkan, Denli M, Sanisoğlu Y.Analysis of DNA damage using the comet assay in infants fed cow's milk. Biol Neonate. 2003;84(2):135-41.
19. Derbent M, Yilmaz Z, Baltaci Volkan, Saygili A, Varan B, Tokel K. Chromosome 22q11.2 deletion and phenotypic features in 30 patients with conotruncal heart defects. Am J Med Genet A. 2003 Jan 15;116A(2):129-35.
20. DündarözR, TürkbayT, Sürer I, Gök F, Denli M, Baltaci Volkan. DNA damage in children treated with imipramine for primary nocturnal enuresis. Pediatr Int.2002 Dec;44(6):617-21.
21. Zeyneloglu HB, Baltaci Volkan, Duran HE, Erdemli E, Batioglu S. Achievement of pregnancy in globozoospermia with Y chromosome microdeletion after ICSI. Hum Reprod. 2002Jul;17(7):1833-6.
22. Dündaröz R, Aydin HI, Ulucan H, Baltaci Volkan, Denli M, Gökçay E. Preliminary study on DNA damage in non breast-fed infants. Pediatr Int. 2002 Apr;44(2):127-30.
23. Baltaci Volkan, Kayikçioğlu F, Alpas I, Zeyneloğlu H, Haberal A. Sister chromatid exchange rate and alkaline comet assay scores in patients with ovarian cancer. Gynecol Oncol. 2002 Jan;84(1):62-6.
24. Aras S, YilmazG, Alpas I, Baltaci Volkan, TayançE, Aydin P.Retinal vein occlusion and factor V Leiden and prothrombin 20210 G:A mutations. Eur J Ophthalmol. 2001 Oct-Dec;11(4):351-5.
25. Dündaröz R, Ulucan H, Denli M, Karapinar K, Aydin HI, Baltaci Volkan. Evaluation of DNA damage using the comet assay in children on long-term benzathine penicillin for secondary prophylaxis of rheumatic fever. Pediatr Int. 2001 Jun;43(3):276-80.
26. Derbent M, Saygili A, Tokel K, Baltaci Volkan. Derbent M, Gurakan B, Saygil A, Baltaci Volkan, Balci S. Clin Dysmorphol. Popliteal pterygium associated with neonatal Marfan syndrome: case report. 2001 Jul;10(3):209-13.
27. Derbent M, Tokel K., Saygı A, Baltacı Volkan. Pulmonary artery sling in a case of trisomy 18. Am J Med Genet. 2001 Jun 15;101(2):184-5.
28. ErgIn T, Baltaci Volkan, Zeyneloglu HB, Duran EH, ErgenelI MH, Batioglu S.Non-invasive early prenatal diagnosis using fluorescent in situ hybridization on transcervical cells: comparison of two different methods for retrieval. Eur J Obs Gynecol Reprod Biol. 2001 Mar;95(1):37-41.
29. Dündaröz R, OzisikT, Baltaci Volkan, KarapinarK, Aydin HI, Denli M.Sister-chromatid exchange analysis on long-term benzathine penicillin for secondary prophylaxis of rheumatic fever. Indian JPediatr. 2001 Feb;68(2):121-2.
30. Oto S, Ozbek N, Baltaci Volkan, Demirhan B, Aydin P Isolated granulocytic myelodysplasia in a child with unilateral retinoblastoma.. J Pediatr Ophthalmol Strabismus. 2000 Sep-Oct;37(5):302-4.
31. Akyol D, Mungan T, Baltaci Volkan.A comparative study of genotoxic effects in the treatment of trichomonas vaginalis infection: metronidazole or nalidixic acid. Arch Gynecol Obstet. 2000 Jul;264(1):20-3.
32. Kayikçioğlu F, Güneş M, Baltaci Volkan, Koçak M, Alpas I, Haberal A. Sister-chromatid exchange frequencies in postmenopausal hormone replacement patients. Mutat Res. 2000 Jul 20;452(1):37-9.
33. Zeyneloglu HB, Baltaci Volkan, Ege S, Haberal A, Batioglu S.Detection of chromosomal abnormalities by fluorescent in-situ hybridization in immotile viable spermatozoa determined by hypo-osmotic sperm swelling test. Hum Reprod. 2000 Apr;15(4):853-6.
34. Atalay F, Baltaci Volkan, Alpas I, Savas I, AtikcanS, Balci S. Sister chromatid exchange rate from pleural fluid cells in patients with malignant esothelioma. Mutat Res.2000 Feb 16;465(1-2):159-63.
35. Volkan Baltacı, Sevim Balcı A Reply to Zenker and Dörr.. Acta Pediatr (2000) 751,
36. Denli M, Aydin HI, Dündaröz R, Özışık T, Erdem E, Baltacı V GenotoxicityEvaluation in Female Patients on Valproik acid Monotheray Using Alkaline Single cell Gell Electrophoresis (Comet Assay). Eastern Journal of Medicine (2000) 5 (2), 61-63
37. Arican A, Ozbek N, Baltaci Volkan, Haberal M Philadelphia chromosome (+) T-cell acute lymphoblastic leukemia after renal transplantation.. Transplant Proc. 1999 Dec;31(8):3242-3.
38. Baltaci Volkan, Ors R, Kaya M, Balci S.A case associated with Walker Warburg syndrome phenotype and homozygous pericentric inversion 9: coincidental finding or aetiological factor? Acta Paediatr. 1999 May;88(5):579-83.
39. Akyol D, Mungan T, Baltaci Volkan, Kozinoglu H, Oguz S, Oztekin O, Gökmen O. Clinical assessment of EMA/CO induced DNA damage in peripheral blood lymphocytes of high-risk gestational trophoblastic tumor patients. Eur J Gynaecol Oncol. 1999;20(2):150-5.
40. Chromosomal Baltaci V, Aygün N, Akyol D, Karakaya AE, SardaĢ S. aberrations and alkaline comet assay in families with habitual abortion. Mutat Res. 1998 Sep 1;417(1):47-55.
41. Baltaci Volkan, Kiliç A. A new application for reconstruction of areola with transplantation of cultured autologous melanocytes. Plast Reconstr Surg. 1998 Apr;101(4):1056-9.
42. Özer L., Ünsal E., Aktuna S., Baltaci V., Çelikkol P., Akyiğit F., Şen A., Ayvaz Ö., Balci S. Mandibuloacral dysplasia and LMNA A529V mutation in Turkish patients with severe skeletal changes and absent breast development. Clinical Dysmorhology. 2016
43. Unsal E, Turan V, Aktuna S, Hurdag C, Bereketoglu G, Canillioglu Y, Baltaci A, Ozcan S, Karayalcin R, Batirbaygil H, Baltaci V. Effects of Pentoxifylline and Platelet Activating Factor on Sperm DNA Damage. Eur J Obstet Gynecol Reprod Biol, 2015
44. Oktay K, Baltaci V, Sonmezer M, Turan V, Unsal E, Baltaci A, Aktuna S, Moy F. Oogonial Precursor Cell-Derived Autologous Mitochondria Injection to Improve Outcomes in Women With Multiple IVF Failures Due to Low Oocyte Quality: A Clinical Translation. Reprod Sci, 22: 1612-1617, 2015
45. Kurtulgan H.K, Özer L., Yıldırım M., Unsal E, Aktuna S, Baltaci V,Nejmiye Akkuş and İlhan Sezgin. Recombinant chromosome with partial 14q trisomy due to maternal pericentric inversion. Molecular Cytogenetics. 8:92 DOI 10.1186/s13039-015-0195-2015
46. Karakaya C, Guzeloglu-Kayisli O, Uyar A, Kallen AN, Babayev E, Bozkurt N, Unsal E, Karabacak O, Seli E. Poor ovarian response in women undergoing in vitro fertilization is associated with altered microRNA expressionin cumulus cells. Fertil Steril, 103: 1469-1476, 2015
47. Titus S, Li Fang, Stobezki R, Akula K, Unsal E, Jeong K, Dickler M, Robson M, Moy F, Goswami S, Oktay K. Impairment of BRCA1-Related DNA Double-Strand Break Repair Leads to Ovarian Aging in Mice and Humans. Sci Transl Med 5, 172ra21 2013
48. Batıoğlu A.S., Şahin U, Gürlek B, Öztürk N & Ünsal E. The Efficacy of Melatonin Administration on Oocyte Quality Gynecological Endocrinology, cilt:28, sayı:2, 91-93, 2012
49. Inanç B, Elçin AE, Unsal E, Balos K, Parlar A, Elçin YM. Artif Differentiation of Human Embryonic Stem Cells on Periodontal Ligament Fibroblasts İn Vitro.Organs. 32(2):100-9. 2007
50. BALTACI V. ,AKTAS Y.,ÜNSAL E.,AYVAZ Ö.,TURHAN F.,SINANOGLU B.,SEN S.,BALTACI A. (2014). The Effect of Piezoelectric Stimulation in Patients with Low Fertilization Potential. Human Genetics& Embryology, 4(1), 1-5.(Özgün Makale), (Kontrol No: 2687427)
51. ÜNER AYVAZ ÖZGE,EKMEKÇİ ABDULLAH,BALTACI VOLKAN,ÖNEN HACER İLKE,ÜNSAL EVRİM (2009). Evaluation of in vitro fertilization parameters and estrogen receptor alpha gene polymorphisms for women with unexplained infertility. Journal of Assisted Reproduction and Genetics, 26(9-10), 503-510., Doi: 10.1007/s10815-009-9354-2, (Kontrol No: 866721)
52. SHER GEOFFREY,KESİNTEPE LEVENT,KESINTEPE MERAL,GINSBURG MIKE,MAASSARANI GHANIMA,YAKUT TAHSİN,BALTACI VOLKAN,KOTZE DIRK,ÜNSAL EVRİM (2007). Oocyte karyotyping by comparative genomic hybrydization provides a highly reliable method for selecting “competent” embryos, markedly improving in vitro fertilization outcome: a multiphase study. Fertility and Sterility, 87(5), 1033-1040., Doi: 10.1016/j.fertnstert.2006.08.108, (Kontrol No: 2614020)
53. Özer, L., Aktuna, S., Unsal, E., Ünal, M. A., Sahin, G., & Baltaci, V. (2022). A novel SLC35D1 variant causing milder phenotype of Schneckenbecken dysplasia in a large pedigree. American Journal of Medical Genetics Part A, 188(10), 3078-3083.
54. KARTAL, B., HATİPOĞLU, M. T., KAYIŞLI, Ü. A., KILIÇ, S. H., ÜNSAL, E., & ÖZOĞUL, C. (2019). INVESTIGATION OF ENDOPLASMIC RETICULUM SIGNAL PROTEINS IN CUMULUS CELLS WITH NORMAL, HYPERRESPONSIVE, HYPORESPONSIVE AND POLYCYSTIC OVARY SYNDROMES. International Journal of Health Services Research and Policy, 4(2), 74-83.
55. Gencer Öncül EB, Duman D, Eminoğlu FT, Aktuna S, Duman MT .<https://pubmed.ncbi.nlm.nih.gov/34928236/> Whole Mitochondrial Genome Analysis in Turkish Patients with Mitochondrial Diseases..Balkan Med J. 2022Mar 14;39(2):96-106. doi: 10.5152/balkanmedj.2021.21141. Epub 2021 Dec20.PMID: 34928236
56. Ibis MA, Aydos K, Baltaci V, Aktuna S, Yaman O .<https://pubmed.ncbi.nlm.nih.gov/35570072/> Can PCNA and LIM15 gene expression levels predict sperm retrieval success in men with non-obstructive azoospermia?.Rev Int Androl. 2022 Oct;20 Suppl 1:S31-S38. doi: 10.1016/j.androl.2021.04.002. Epub 2022 May 12.PMID: 35570072
57. Stadhouders, R., Aktuna, S., Thongjuea, S., Aghajanirefah, A., Pourfarzad, F., van IJcken, W., ... & Soler, E. (2014). HBS1L-MYB intergenic variants modulate fetal hemoglobin via long-range MYB enhancers. The Journal of clinical investigation, 124(4), 1699-1710.
58. Stadhouders, R., Aktuna, S., Thongjuea, S., Aghajanirefah, A., Pourfarzad, F., van IJcken, W., ... & Soler, E. (2014). HBS1L-MYB intergenic variants modulate fetal hemoglobin via long-range MYB enhancers. The Journal of clinical investigation, 124(4), 1699-1710.
59. Ozer L, Aktuna S, Unsal E, Baltaci A, Baltaci V. An Incidental Detection of a Cryptic Complex Chromosome Rearrangement Found During NGS Based PGT-SR: A Case Report .Journal of Reproduction & Infertility, 2022; 23(4):303-309.
60. Sayın Kocakap DB, Gündüz Ö, Özer L , Durak M .Case Report For Two Sıblıngs Carryıng Neurofıbromatosıs Type 1 Wıth A Rare Nf1: C.5392c>T Mutatıon. Balkan Journal of Medical Genetics. 2021, 24(2):1-5.
61. Özer L, Ruhi HI, Bökesoy I, Analysis of Xq27.3 Fragility Using the Micronucleus‑Fluorescence In situ Hybridization Assay, Genome Integrity, 2020; 11: 1-7.
62. Özgün N , Özer L, Yaramış A, A rare cause of epileptic encephalopathy: a beta-propellerprotein associated neurodegeneration case with a newmutation and literature review. The Turkish Journal of Pediatrics 2020; 62: 109-113.
63. Neuray C, Maroofian R, Scala M, Sultan T, Pai SP, Mojarrad M, Khashab HE, deHoll L, Yue W, Alsaif HS, Zanetti M, Bello O, Person R, Eslahi A, Khazaei Z, Feizabadi HM, Efthymiou S, SYNaPS Study Group, El-Bassyouni HT, Soliman DR, Tekes S, Ozer L, Baltaci V, Khan S, Beetz C, Amr KS, Salpietro V, Jamshidi Y, Alkuraya FS, Houlden H. Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants. Brain 2020; 143:2388–2397.
64. Akıncı A, Türkkahraman D, Tekedereli İ, Özer L, Evren B, Şahin İ, Kalkan T, Çürek Y, Çamtosun E, Döğer E, Bideci A, Güven A, Eren E, Sangün Ö, Çayır A, Bilir P, Törel Ergür A, Ercan O. Novel Mutations in Obesity-related Genes in Turkish Children with Non-syndromic Early Onset Severe Obesity: A Multicentre Study. J Clin Res Pediatr Endocrinol. 2019;11(4):341-349.
65. Ozer L, Elgun S, Ozdemir B, Ozmeric N. Arginine-Nitric Oxide-Polyamine metabolism in periodontal disease. J Periodontology. 2011, 82(2): 320-8.

Uluslararası Bilimsel Toplantılarda Sunulan ve Bildiri Kitabında (Proceedings) Basılan Bildiriler

1. Volkan BALTACI, Davut GÜL, Aysun SOĞUKPINAR, B. Sıtkı SAYLI (1992). A t(2q;15q) translocation in a family with habitual abortion and prenatal diagnosis in a recent pregnancy. European Society of Human Genetics 24th annual meeting, 27-31 May 1992 pp: 41-42.
2. Davut GÜL, Volkan BALTACI, M. SARILMAZ (1992). An Ahlers-Danlos-Like phenotype with 18pchromosome constitution. European Society of Human Genetics 24th annual meeting, 27-31 May 1992 pp:83.
3. B. Sıtkı SAYLI, Volkan BALTACI, E. GEZDER, Davut GÜL (1992). Two or more conditions in one individual or in two sibs stressing genetic services. European Society of Human Genetics 24th annual meeting, 27-31 May 1992 pp:134.
4. Sinan SÖNMEZ, Yasemin SÖNMEZ, Volkan BALTACI (1993). Chromosomal effect of phototherapy applied to the newborns with hyperbiluribinemia. European Society of Human Genetics 25th annual meeting, 6-9 May 1993 Barcelona pp:102.
5. Volkan BALTACI, Aysun BALTACI, Sinan SÖNMEZ (1993). Cytogenetic analysis in blighted ovum and missed abortion cases with CVS before the termination. European Society of Human Genetics 25th annual meeting, 6-9 May 1993 Barcelona pp:111.
6. Sıtkı ÖZTAŞ, Sedat KADANALI, Sinan SÖNMEZ, Mevlüt İKBAL, Volkan BALTACI, Ġrfan BATAT (1996). The case report of the stillbirth with Roberts-sc phocomelia syndromes. Abstract of th 28th meeting of the ESHG, London, April 1996, pp: 123.
7. Mevlüt İKBAL, Volkan BALTACI, Sıtkı ÖZTAŞ, Sinan SÖNMEZ, Mevlit KORKMAZ, Ġrfan BATAT (1996). Cerebro-Oculo-Facio-Skelatal (COFS) syndrome .n a 3 years old boy. Abstract of th 28th meeting of the ESHG, London, April 1996, pp: 122.
8. Muhterem BAHÇE, Gönül OĞUR, Necat İMİRAZLİOĞLU, Seçkin ÖZEN, Volkan BALTACI, E.VAMOS (1996). Repeated fetal loss in two related first cousin marriages with couples all carrying the same translocation t(13q;14q). Abstract of th 28th meeting of the ESHG, London, April 1996, pp: 35.
9. Volkan BALTACI, Nedret HIZEL, Hakan DURAN, Hulusi ZEYNELOĞLU, Sertaç BATIOĞLU (1998). Fetal sex determination from maternal peripheral blood by polymerase chain reaction. XIV. International Congress “ The fetus as a patient”. February, 1998 pp:84.
10. Volkan BALTACI, Neslihan AYGÜN, Didem AKYOL, Hakan DURAN, Semra SARDAġ (1998). Chromosamal aberrations and alkaline comer assay in families with habitual abortion. XIV. International Congress “ The fetus as a patient”. February, 1998 pp:84.
11. Hulusi B ZEYNELOĞLU, Volkan BALTACI, Sevinç EGE, Ali HABERAL, Sertaç BATIOĞLU (1998) Detection of chromosomal abnormalities in immotile viable spermatozoa determined by hyposmolar sperm swelling test. 16th World Congress on Fertility and Sterility and 54th Annual Meeting of the American Society for Reproductive Medicine. October 4-9, 1998 pp445.
12. Sümer ARAS, İdil ALPAS, Volkan BALTACI, Gürsel YILMAZ, Pınar AYDIN (1999). Association of retinal vein thrombosis with factor V 1691 G:A (Leiden) and prothrombin 20210 G : A mutation. 31st Annual Meeting of the European Society of Human Genetics 29 May-1June 1999 pp116.
13. Figen ATALAY, Volkan BALTACI, İdil ALPAS, Sümer ARAS, S.ATĠKCAN, Sevim BALCI (1999) Sister chromatid exchange (SCE) rate from pleural fluid cells in patients with malign mesotelioma 31st Annual Meeting of the European Society of Human Genetics 29 May-1June 1999 pp 83.
14. Volkan BALTACI, KürĢat TOKEL, Berkan GÜRAKAN, Namık ÖZBEK, İdil ALPAS, Sümer ARAS (1999) Unbalanced t(3;11)(p23;q24) in two sisters with Jacobsen syndrome. 31st Annual Meeting of the European Society of Human Genetics 29 May-1June 1999 pp72.
15. İdil ALPAS, Sümer ARAS, Volkan BALTACI, Sertaç BATIOĞLU, Esra KUŞÇU, Ali HABERAL (1999) Which is the most advantaged for prenatal non-invasive fetal diagnosis? Maternal plasma, serum or extracted DNA? 31st Annual Meeting of the European Society of Human Genetics 29 May-1June 1999 pp78.
16. Merve Aydin, Suleyman Aktuna, Evrim Unsal, Leyla Ozer, Volkan Baltaci. “NGS Based PGT-A / PGT-SR: Data from >7000 Embryos”, PGDIS, 18th International Conference on Preimplantation Genetics, Geneva, Switzerland (April 15-18, 2019)
17. Leyla Ozer, Merve Aydin, Evrim Unsal, Suleyman Aktuna, Volkan Baltaci. “Additional Data for Controversial Inter-chromosomal Effect Susceptibility in PGT-SR Patients”, PGDIS, 18th International Conference on Preimplantation Genetics, Geneva, Switzerland (April 15-18, 2019)
18. Evrim Unsal, Suleyman Aktuna, Merve Aydin, Leyla Ozer, Volkan Baltaci. “Improved IVF Success of Combined PGT-M and PGT-A Applications”, PGDIS, 18th International Conference on Preimplantation Genetics, Geneva, Switzerland (April 15-18, 2019)
19. Süleyman Aktuna, Evrim Unsal, Leyla Ozer, Merve Aydin, Volkan Baltaci. “Simultaneous PGT-M Applications for Multiple Genetic Conditions”, PGDIS, 18th International Conference on Preimplantation Genetics, Geneva, Switzerland (April 15-18, 2019)
20. Leyla Ozer, Merve Aydin, Suleyman Aktuna, Evrim Unsal, Volkan Baltaci. “Chromosomal Microarray Analysis in Diagnosis of Patients with Congenital Abnormalities, Developmental Delay, Intellectual Disability, Autism: A One Year Retrospective Analysis”, 13th Balkan Congress of Human Genetics, Edirne, Turkey (April 17-20, 2019)
21. Özer L Ünsal E, Aydın M, Aktuna S, Duman D, Çelikkol P, Şen S, Baltacı A, Özcan S , Karayalçın R, Biri A, Baltacı V. Development of NGS based genetic testing for female infertility TSRM Üreme Sağlığı ve İnfertilite Kongresi, Antalya, Türkiye (2018)
22. Özer L, Ünsal E, Aktuna S, Aydın M, Duman D, Çelikkol P, Şen S, Baltacı A, Özcan S , Karayalçın R, Biri A, Baltacı V. Comprehensive Next Generation Sequencing(NGS) based panel for male infertility TSRM Üreme Sağlığı ve İnfertilite Kongresi, Antalya, Türkiye (2018)
23. Aydın, M., Ünsal, E., Aktuna, S., Özer, L., Çelikkol, P., Duman, T., Batırbaygil, H., Şen, S., Baltacı, A., Baltacı, V. “Our Experience Following NGS Based PGT-A on >6000 Embryos”, TSRM Üreme Sağlığı ve İnfertilite Kongresi, Antalya, Türkiye (2018)
24. Aktuna, S., Ünsal, E., Aydın, M., Özer, L., Atik, A., Duman, T., Baltacı, A., Baltacı, V. “Haploid Cell Assessment Approach: Predictive Value of Spermatogenesis Biomarkers”, TSRM Üreme Sağlığı ve İnfertilite Kongresi, Antalya, Türkiye (2018)
25. Ünsal, E., Aktuna, S., Aydın, M., Çelikkol, P., Duman, T., Atik, A., Karayalçın, R., Baltacı, A., Baltacı, V. “The Importance of Combining 24 Chromosome Screening with Preimplantation Genetic Diagnosis of Monogenic Diseases”, TSRM Üreme Sağlığı ve İnfertilite Kongresi, Antalya, Türkiye (2018)
26. Aktuna, S., Ünsal, E., Özer, L., Abbasi, M., Aydın, M., Duman, T., Baltacı, V. “Testing Sperm DNA Fragmentation with Flow Cytometry : A New ERA for Robust and Standardised DNA Integrity Evaluation”, TSRM Üreme Sağlığı ve İnfertilite Kongresi, Antalya, Türkiye (2018
27. Aktuna, S., Ünsal, E., Özer, L., Abbasi, M., Aydın, M., Duman, T., Baltacı, V. “Testing Sperm DNA Fragmentation with Flow Cytometry : A New ERA for Robust and Standardised DNA Integrity Evaluation”, TSRM Üreme Sağlığı ve İnfertilite Kongresi, Antalya, Türkiye (2018)
28. Baltacı, V., Ünsal, E., Özer, L., Aktuna, S., Aydın, M., Atik, A., Abbasi, M., Biri, A. “Flow Cytometric Analysis of Post Meiotic Spermatids”, TSRM Üreme Sağlığı ve İnfertilite Kongresi, Antalya, Türkiye (2018)
29. Aktuna, S.;Unsal, E.;Ozer, L.;Kolsal, G.;Polat, S.;Baltaci, A.;Duman, T.;Hurdag, C.;Aydos, K.;Baltaci, V. DMC1 is an encouraging biomarker for non-obstructive azoospermia patients. ESHRE 2017
30. Ozer L , Aktuna S, Unsal E, Çelikkol. P, Aydın M., Duman T., Baltacı A , Baltacı V. Aneuploidy rates of next-generation sequencing in preimplantation genetic diagnosis for balanced translocation carriers PGD IS 2017
31. Baltaci V, Unsal E Ozer E , Aktuna S , Atik A , Baltacı A Are Metabolıc Disorder Carriers Subject To Poor Ovarian Response İn Pgd Cycles ? PGD IS 2017
32. Unsal E , Aktuna S , Ozer E , Aydın M.,, Duman T.,, Çelikkol. P, Baltacı A, Baltaci V What Next Generation Sequencing Brings to Preimplantation Genetic Testing PGD IS 2017
33. Özer L., Trujıllano D., ÜNSAL E., Aktuna S., Akyiğit F., Çelikkol P., Rolfs A., Baltacı V. (2016). Novel  PGAP1 Gene Mutation in Patients with Mental Retardation  in a Turkish family.  European Society of Human Genetics Congress
34. ÜNSAL E (2016). Open and Closed Blastocyst Vitrification of Biopsied Embryos. UARM CONGRESS UKRAINE 2016 (Davetli konusmacı) (Kontrol No: 2728401)
35. Özer L., Ünsal E., Aktuna S., Duman M.T., Çelikkol P., Kutlu N. K., Koçak İ., Baltacı V. (2016). Whole Exom Sequencıng Enables Preımplantatıon Genetıc Dıagnosıs For Couples Wıth Undıagnosed Dısorders.  PGD IS 2016
36. Ünsal E., Aktuna S., Özer L., Koçak İ., ,Akyiğit F., Güney E., Baltacı A., Duman M.T.,Almacıoğlu H., Baltacı V. (2016). First NGS Based Comprehensive Chromosome Screening Data From Turkey. PGD IS 2016
37. Aktuna S., Ünsal E., Özer L., Duman M. T., Çelikkol P., Kutlu N. K., Baltacı A., Baltacı V. (2016). PGD for variants of unknown significance (VUS) ; How to decide to perform or not to perform ?. PGD IS 2016
38. Ünsal E (2016). Open Versus Closed System for Vitrification: Pros and Cons. XIV. Annual Meeting of the Mediterranean Society for Reproductive Medicine (Davetli konusmacı) (Kontrol No: 2727496)
39. Oktay K., Sönmezer M., Baltacı V., Ünsal E., Aktuna S., Baltacı A, Turan V. (2015). Oogonıal Precursor Cell Derıved Autologous Mıtochondrıa Injectıon Improves Outcomes In Women Wıth Multıple Ivf Faılures Due To Low Oocyte Qualıty.  Society for Reproductive Investigation
40. Özer L, Ünsal E, Baltaci V, Aktuna S, Ayvaz Ö, Akyiğit F, Çelikkol P, Şen A, Balcı S. “Homozygous Ala529Val LMNA Mutation in Patients with Mandibuloacral Dysplasia in a Turkish family” ESHG, 2014
41. Aktuna, S.; Unsal, E.; Duman, T.; Ozer, L.; Akyigit, F.; Celikkol, P.; Baltaci, A.; Ozcan, S.; Baltaci, V “Preimplantation Genetic Diagnosis with Carrier Mapping Test: An Encouraging New Approach For Couples Without Molecular Diagnosis” Chromosome Research Dec 2014, Volume: 22   Issue: 4   Pages: 637-638 
42. Unsal E, Ayvaz Ö, Duman T, Özer L, Akyiğit F, Baltaci A, Baltaci V. “Preimplantation Genetic Diagnosis (PGD) for Single Gene Disorders with HLA typing: A Brief Report” Fertility and Sterility 2013, Volume: 100 Issue: 3   Supplement: S   Pages: S204-S204   Meeting Abstract: P-194
43. İlkan A, Aktuna A, Hürdağ C, Çanıllıoğlu Y, Duman T, Üner Ö, Özer L, Baltacı V, Ünsal E. “Mutation Analysis of Phospholipase C Zeta (PLCζ) in Patients With Low Fertilisation Rate” ESHRE, 2014
44. HÜRDAG C., CANILLIOGLU Y.E., KANDIL A.,YÜKSEL M.L, Ünsal E. KARPUZ V. (2013). The Morphological Evaluation in Azoospermia Cases of Testicular Tubular Tight Junctions. Microscopy Conference 2013 (Poster) (Kontrol No: 2633066)
45. HÜRDAG C., CANILLIOGLU Y.E., KANDIL A.,YÜKSEL M.L, Ünsal E. KARPUZ V. (2013). The Role of Nitric Oxide in Testicular Sperm Extraction (TESE). FEBS (Poster) (Kontrol No: 2633044)
46. Duman T., Unsal E., Ayvaz Ö., Demirel C.,Özer L.,Baltaci A., Akyigit F.,Baltaci V. (2013). Birth of Healthy Baby After Preimplantation Genetic Diagnosis of Junctional Epidermolysis Bullosa.. PGDIS 2013 (Poster) (Kontrol No: 872494)
47. Ayvaz Ö, Unsal E, Baltaci A, Duman T, Özer L, Akyiğit F, Baltaci V. “ Preimplantation Genetic Diagnosis for Mucopolysaccharidose Type I: Analysis of a Novel Indel Mutation”, FERTILITY AND STERILITY Sep 2013 Volume: 100 Issue: 3   Supplement: S   Pages: S206-S206   Meeting Abstract: P-203
48. Karakaya H, Ünsal E, Kandil A, Canıllıoğlu Y.E., Hürdağ C. The Effects of NOS Isoforms In Human Normospermia, Asthenospermia And Oligospermia Cases” Proceedings of the 4th International Congress on cell membranes and oxidative stress: Focus on calcium signalling ant TRP channels. Int. Proceedings Division Medimond, p 5-10,2012
49. Baltaci V, Satıroglu H, Aydınuraz B, Ünsal E, , Üner Ö, Çetinkaya E, Kabukçu C Aktas Y, Turhan F. (2006). A SIMPLIFIED BLASTOMERE FIXATION PROTOCOL FOR PGD APPLICATIONS. EUROPIAN SOCIETY OF HUMAN GENETICS (Poster) (Kontrol No: 868477)
50. Baltaci V, Satıroglu H, Ünsal E, Üner Ö, Ergün MA, Batıoglu S, Sönmezer M, Kabukçu C, Aydınuraz B, Turhan F, Aktas Y, (2005). Preimplantation genetic diagnosis in two couples with balanced reciprocal translocations. PGD-IS (Poster) (Kontrol No: 868698)
51. Baltaci E., Gumuslu S., Alpas I., Erdem M., Karabacak O., Tiras M.B. and Guner H. (2002). Is there any effect of severe oligozoospermia on fertilization, embryo quality and pregnancy in ICSI patients?. ESHRE 2002 (Özet bildiri) (Kontrol No: 868992)
52. Comprehensive Carrier Screening Strategy for Challenging Genomic Conditions Evrim Ünsal, Süleyman Aktuna, Leyla Özer, Merve Polat, Volkan Baltacı ;Yüksek Ihtisas Univ., Ankara, Turkey. European Human Genetics Virtual Conference 2021 August 28-31, 2021
53. Embryo transfer decision dilemma in PGT-M: Dominant or recessive inheritance, Süleyman Aktuna, Merve Polat, Evrim Ünsal, Leyla Özer, Volkan Baltacı; Yüksek Ihtisas Univ., Ankara, Turkey. European Human Genetics Virtual Conference 2021 August 28-31, 2021
54. What we learned from PGT-M data: Overview of 162 single gene disorder cases, Merve Polat, Leyla Özer, Süleyman Aktuna, Evrim Ünsal, Volkan Baltacı, Yüksek Ihtisas Univ., Ankara, Turkey. European Human Genetics Virtual Conference 2021 August 28-31, 2021
55. The Shift Towards Rare: Increased Frequency of Rare PGT-M Cases Leyla Özer, Süleyman Aktuna, Evrim Ünsal, Merve Polat, Volkan Baltacı, Yüksek Ihtisas Univ., Ankara, Turkey. European Human Genetics Virtual Conference 2021 August 28-31, 2021
56. Evrim Unsal, Leyla Ozer, Merve Aydin, Suleyman Aktuna, Volkan Baltaci.How Effectıve is Target Sequence Enrıchment Durıng Whole Genome Amplıfıcatıon On The Improvement Of PGT-M Results? American Society for Reproductive Medicine , (17-21 Ekim 2020) , Online
57. Merve Aydin, Volkan Baltaci, Leyla Ozer, Evrim Unsal, Suleyman Aktuna. Is it Possible to Detect All Segmental Chromosomal Imbalances with NGS Using Custom Analysis Algorithms? American Society for Reproductive Medicine , (17-21 Ekim 2020) , Online
58. Suleyman Aktuna, Volkan Baltaci, Evrim Unsal, Leyla Ozer, Merve Aydin, How Effective is Universal Carrier Screening To Encompass Turkish Population Mutation Profile? American Society for Reproductive Medicine , (17-21 Ekim 2020) , Online
59. Warren, K., Unsal, E., Aktuna, S., Aydin, M., Baltaci, V., & Jasper, M. J. (2017). WGA and NGS read length significantly impact mitochondrial characterisation. Fertility and Sterility, 108(3), e289.
60. Özer L., Trujıllano D., Ünsal E., Aktuna S., Akyiğit F., Çelikkol P., Rolfs A., Baltacı V. . Novel  PGAP1 Gene Mutation in Patients with Mental Retardation  in a Turkish family.  European Society of Human Genetics Congress 2016
61. Stadhouders, R; Aktuna, S; Thongjuea, S; Aghajanirefah, A; Pourfarzad, F; van Ijcken, W; Lenhard, B; Rooks, H; Best, S; Menzel, S; Grosveld, F; Thein, S L; Soler, E “HBS1L-MYB intergenic Variants Modulate Fetal Hemoglobin Via Long-Range MYB Enhancers “ <javascript:;> BLOOD Nov 2013 Volume: 122   Issue: 21   Meeting Abstract: 43
62. Amandine Breton, Laura Sonzogni, Andria Theodorou, Suleyman Aktuna, Stephan Menzel, Frank Grosveld, Sjaak Philipsen and Swee Lay Thein ‘ASH1L: A Novel Beta-Globin Gene Regulator in Humans?’ Blood 2015 126:641;
63. Ozer, L., M. Aydin, S. Aktuna, E. Unsal .The value of prenatal array to detect submicroscopic chromosomal imbalances in cases with abnormal fetal ultrasonographic findings: a retrospective study, ESHG Conference,2020.
64. Derya Beyza Sayın Kocakap, Hatice Karaca, Leyla Özer, Eser Bolat, Umut Tekin. A case of Basal Cell Nevus Syndrome with a new PTCH1 gene mutation: c.592A>T. 13th Balkan Congress of Human Genetics, 2019
65. Basak Celtikci, Semih Tangal, Leyla Ozer. The effects of human chorionic gonadotropin-based hormonal therapy on the expression levels of proliferating cell nuclear antigen.13th Balkan Congress of Human Genetics, 2019
66. L. Özer, E. Unsal, S. Aktuna, V. Baltacı, Two Different Genetic Diseases in the Same Patient, European Human Genetic Conference, 2018

Ulusal Hakemli Dergilerde Yayınlanan Makaleler

1. B. Sıtkı SAYLI, Volkan BALTACI (1992). Neurofibromotosis 1 and congenital deafness. Two mendelian conditions segregating in a family. Gazi Medical Journal 3: 171-174.
2. Volkan BALTACI, B. Sıtkı SAYLI (1992). Kamptodaktili eşliğiyle mikrosefali. Atatürk Üniversitesi Tıp Bülteni. 24: 87-90.
3. Volkan BALTACI, Aysun SOĞUKPINAR, Sinan SÖNMEZ (1993) Prenatal tanıda koryon vilus biyopsisi uygulama ve avantajları. Atatürk Üniversitesi Tıp Bülteni. Cilt 25, sayı 1 Ocak 1993.
4. Volkan BALTACI, Davut GÜL, Aysun SOĞUKPINAR, B. Sıtkı SAYLI (1994). A t(2q;15q) translocation in a family with habitual abortion and prenatal diagnosis in a recent pregnancy. Gazi Medical Journal 5: 91-93.
5. Volkan BALTACI, B. Sıtkı SAYLI, Aysun BALTACI, Ali HABERAL, Necat İMİRAZLİOĞLU (1996). Missed abortus blighted ovum öntanılı gebeliklerde terminasyon öncesi koryon villus örneklemesi ile sitogenetik incelemeler. Perinatoloji Dergisi. 4: 200-204.
6. Volkan BALTACI, Ali HABERAL, Aysun BALTACI, Muhterem BAHÇE, Necat İMİRAZLİOĞLU (1997). Prenatal tanıda koryon villus biyopsi yöntemlerinin değerlendirilmesi. Fatih Üniversitesi Tıp Fakültesi Yeni Tıp Dergisi. 14: 81-83.
7. Mevlit İKBAL, Volkan BALTACI, Sıtkı ÖZTAŞ, Sinan SÖNMEZ, Mevlüt KORKMAZ, Bahri ġEN (1997). A case of cerebro-ocub-facio-skeletal (COFS) syndrome. Fatih University University Medical Faculity The New Journal of Medicine. 14: 52-53.
8. Volkan BALTACI, Didem AKYOL, Sedat KADANLI. Risk assesment and prenatal diagnosis in a recent pregnancy of a family which has a child with Down Syndrome due to t(21q;21q) . TUBĠTAK Turkish Journal of Medical Sciences. 19. Kasım. 1997 tarihli ve sağ 97/34 sayılı kabul yazısı.
9. Muhterem BAHÇE, Necat İMİRAZLİOĞLU, Engin YILMAZ, R. Seçkin ÖZEN, Volkan BALTACI, Gönül OĞUR (1997). Tekrarlayan düĢüklerde fetal, maternal ve paternal sitogenetik incelemeler: 281 materyalin evaluasyonu. Gülhane Askeri Tıp Akademisi Bülteni. 30: 163-171.
10. Volkan BALTACI, Alparslan NUHOĞLU (1997). Prenatal t(7q;14q) balanced translocation carriage. Fatih University Medical Faculity The New Journal of Medicine. 14: 54-55.
11. Volkan BALTACI, Didem AKYOL, Davut GÜL, B. Sıtkı SAYLI (1998). Digital amputations caused by amniotic bands. TUBĠTAK Turkish Journal of Medical Sciences. 28: 701-703
12. Nedret HIZEL, Volkan BALTACI, Hakan DURAN, Hulusi ZEYNELOĞLU, Esra KUŞÇU, Mehmet ERGENELİ (1998). Anne kanında PCR ile prenatal cinsiyet tayini. Jinekoloji ve Obstetrik Bülteni. 7: 57-60.
13. Hulusi B. ZEYNELOĞLU, Sevinç EGE, Hakan E. DURAN, Volkan BALTACI, Tolga ERGİN, Sertaç BATIOĞLU IxaPrep: Yardımcı üreme teknolojisinde percoll'e alternatif bir yöntem (1998)12: 233-236
14. Volkan BALTACI (1998). Prenatal genetik tanı. Sürekli Tıp Eğitimi Dergisi. Cilt 7, sayı 3, 83-84.
15. Didem Akyol, Volkan BALTACI, Hakan KOZİNOĞLU, Kutlugil YÜKSEL, Saime KIġ, Nedim ÇĠÇEK, Tayfun GÜNGÖR (1999) Accessory Limb Attached to the Back. TUBĠTAK Turkish Journal of Medical Sciences 29: 199-201.
16. Volkan BALTACI, Hulusi B. ZEYNELOĞLU, Mehmet ERGENELİ, Sevinç EGE, İdil ALPAS, Sertaç BATIOĞLU (1999) IxaPrep ve Percoll gradienti sonrası X ve Y kromozomu taĢıyan sperm oranlarının çok renkli FISH yöntemi ile değerlendirilmesi. Jinekoloji ve Obstetrik Bülteni 8(1): 18-22.
17. Volkan BALTACI, Aysun BALTACI (1999) Amnıyosentez, Sakat bebek doğumlarına önlem. Popüler bilim dergisi, 64: (Mart) 25-29
18. Murat Derbent, Banu Bilezikçi, İdil Alpas, Volkan Baltacı. Fetal 45,X/46,XY mosaicism, cytogenetic and morphologic findings in pregnancy. Turkish Journal of Medical Sciences. (16/8/2000 tarihli kabul yazısı)
19. Dilbaz N., Dündar Öz R. Devrim Z., Aydın H.Ġ., Denli M., Baltacı Volkan. Analysis of DNA Damage using Comet Assay in Female Patients Treated with Flouxetin Against Depression. Kocatepe Tıp Dergisi. 2001, 2,79-86.
20. Dündar Öz R. Devrim Z., Aydın H.İ., Denli M., Baltacı Volkan. Analysis of DNA Damage using Comet Assay in Female Patients Treated with Phenytoin For Epilepsy. Kocatepe Tıp Dergisi. 2001, 2,153-158.
21. Dündar Öz R. Çalışkaner A.Z. Türkbay T. Gök F., Dilbaz N., Baltacı Volkan. Sister Chromatid Exchange Analysis in Women Treated with Flouxetin for Depression. SDI Tıp Fakültesi Dergisi. 1999, 6(4),15-19.
22. Dündar Öz R. Aydın H.İ. Güngör T., Gök F. Denli M., Baltacı Volkan. Assesment of DNA Damage Induced by Carbamazepin in Epileptic Women. Kocatepe Tıp Dergisi. 2001, 2,87-93.
23. Evrim Ünsal, Tek Gen Hastalıklarının Preimplantasyon Genetik Tanısında 24 Kromozom Taramanın Önemi, BLAST PGT Özel Sayısı: Bölüm 1; Nisan 2019
24. Evrim Ünsal, Preimplantasyon Genetik Test Uygulamalarında Ivf Ve Genetik Tanı Laboratuvarı Koordinasyonu BLAST PGT Özel Sayısı: Bölüm 2; Temmuz 2019
25. Oktay N, Ersoy Ç.Y., Ünsal E, Hürdağ C. Normospermi ve astenospermi olgularda phospholipase C zeta’nın fertilizasyondaki etkisi. FNG & Bilim Tıp Dergisi 2016;2(2):121-129
26. Özdemir Y, Ünsal E, Hürdağ C. Pentoksifilin ve platelet aktive edici faktör sonrası spermatozoada meydana gelen ultrastrüktürel değişikliklerin kıyaslanması. FNG & Bilim Tıp Dergisi 2015;1(1):11-17
27. Hürdağ C., Çanıllıoğlu Y.E., Kandil A. , Yüksel M., Altun E., Ünsal E., The role of nitric oxide on spermatogenesis in infertile men with azoospermia D J Med Sci 2021;7(1):7-19, DOI: 10.5606/fng.btd.2021.25040
28. Kandil A., Çanıllıoğlu Y.E., Ünsal E., Karabulut S., Hürdağ C. .Ultrastructural Examination of Testicular Tissues and Evaluation of ZO-1 Protein Levels Obtained from Azoospermic Cases, J Exp Clin Med 2021; 38(3): 272-276 doi: 10.52142/omujecm.38.3.12
29. Flow Sitometrik Spermatoloji – Evrim Ünsal Blast, Ağustos 2021
30. Azospermik olguların tanısında moleküler yaklaşımlar Süleyman Aktuna; Blast, Ağustos 2021
31. Süleyman Aktuna ; Yeni Nesil Dizileme Uygulamaları ile PGT-M Uygulamalarında Güncel Durum, BLAST PGT Özel Sayısı: Bölüm 1; Nisan 2019

Ulusal Bilimsel Toplantılarda Sunulan ve Bildiri Kitabında Basılan Bildiriler

1. Volkan BALTACI, Ö. Ferit SARAÇOĞLU, Aysun SOĞUKPINAR, B. Sıtkı SAYLI (1992). Prenatal tanı amacıyla uyguladığımız kordosentez ve sonuçları. 3. Ulusal perinatoloji kongresi, 1-5 Mart, Bursa, pp: 080.
2. Hamit ÇELİK, Gül KAHVECİ, Volkan BALTACI, Günhan GÜRMAN (1995). Dyskeratosis Congenita’da oral bulgular ve sitokinlerin önemi. Türk Peiodontoloji Derneği XXV. Bilimsel Kongresi. 22-26 Mayıs 1995, pp:60.
3. Necat İMİRAZLİOĞLU, Seçkin ÖZEN, Muhterem BAHÇE, M.K. CENK, Yusuf TUNCA, Volkan BALTACI, ÖGönül OĞUR (1996). Down-XYY Syndrome: A case report. 2nd Balkan Meeting on Human Genetics. 3-6 September, Istanbul, pp:b-6.
4. Volkan BALTACI, Rahmi ÖRS, Murat KAYA, Mevlüt KORKMAZ, Mevlit İKBAL (1996). Any possible connection between the pericentric region of the chromosome 9 and the Warburg Syndrome. 2nd Balkan Meeting on Human Genetics. 3-6 September, Istanbul, pp:6-13.
5. Volkan BALTACI, Hakan DURAN, Zuhal EREN, Hulusi ZEYNELOĞLU, Sertaç BATIOĞLU, Ali HABERAL(1997) Prenatal Sex Determination from Maternal Peripheral Blood Using the Polymerase Chain Reaction. Turkish –Hellenic Scientific Meeting
6. Volkan BALTACI, Hulusi ZEYNELOĞLU, Sevinç EGE, Sertaç BATIOĞLU, Ali HABERAL (1998). Evalution of in vitro seperation of “X” and “Y” bearing spermatozoa by percoll and ixaprep gradients by double-labelled flourescence in-situ hybridisation. 3. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, 26-30 Nisan, Marmaris. Türkiye Kongre Kitapçığı, p:7 ve 34.
7. Cüneyt TUZUN, Serdar CEYLANER, Gülay CEYLANER, Nilüfer KARADENİZ, Volkan BALTACI, Oya GÖKMEN (1998). Dr. Zekai Tahir Burak Kadın Hastanesi Prenatal Tanı ve Genetik Merkezi. 3. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, 26-30 Nisan, Marmaris. Türkiye Kongre Kitapçığı, p: 93.
8. Ali HABERAL, Volkan BALTACI, Esra KUŞÇU, Fulya KAYIKÇIOĞLU, Idil ALPAS (1998) Sister chromatid exchange rate in patients with different stages of ovarian malignancies 6. Ulusal Jinekolojik Onkoloji Kongresi ve Mezuniyet Sonrası Eğitim Seminerleri Poster Özetleri 11-15 Ekim 1998 pp: 41.
9. Volkan BALTACI, Hulusi ZEYNELOĞLU, İdil ALPAS, Esra KUŞÇU, Sümer ARAS, Ali HABERAL, Sertaç BATIOĞLU (1999) Anne kanında fetal DNA’nın belirlenmesinde en etkili materyal: Maternal serum, maternal plazma, maternal DNA? 7. Ulusal Perinatoloji Kongresi (Perinatoloji Dergisi) 7: (2) 39
10. Volkan BALTACI, Tolga ERGİN, Hulusi ZEYNELOĞLU, Mehmet H ERGENELİ, Esra KUŞÇU, Sertaç BATIOĞLU (1999) Transservikal hücrelerde in situ hibridizasyon (FISH) ile non invaziv erken prenatal tanı. 7. Ulusal Perinatoloji Kongresi (Perinatoloji Dergisi) 7: (2) 75
11. Evrim Ünsal. Embriyo Biyopsi Tekniğinin Preimplantasyon Genetik Test Sonuçlarına Etkisi, (Davetli Konuşmacı) Başkent İnfertilite Günleri, 14-15 Haziran 2019, Ankara
12. Evrim Ünsal, PGT - Mevcut Durum ve Gelecek Zorluklar (Davetli Konuşmacı), İnfertilite ve ART'de tartışmalı konular Sempozyumu, 23-24 Şubat 2019
13. Evrim Ünsal, Her Yönüyle Preimplantasyon Genetik Tanı uygulamaları (Davetli Konuşmacı) ,23-24 Mart. 2019, Zeynep Kamil Hastanesi, İstanbul
14. Evrim Ünsal. 3. Uluslarası Korı Gebelik Doğum ve Lohusalık Kongresi. (Davetli Konuşmacı) Yeni Nesil Dizileme Uygulamalarında Islak Laboratuvar Çalışmalarının Biyoinformatik Verilere Etkisi. 14 Şubat. 2019, Bolu
15. Evrim Ünsal. Klivaj Dönemi Arrestinde Erkeğe, Kadına veya Tekniğe Bağlı Faktörler Nelerdir? (Davetli Konuşmacı) 1. Çukurova IVF Günleri, 11-13 Ocak 2019, Adana
16. Evrim Ünsal, Prrekonsepsiyonel Genetik Taramada Tartışmalı Konular, (Davetli Konuşmacı) 8. Ulusal Üreme Sağlığı ve İnfertilite Kongresi (TSRM 2018),
17. Evrim Ünsal, Joyce Harper, Carmen Rubio, Kemal Özgür. (Panelist) Klinik Embriyoloji ve Genetik. Ovulasyon İndüksiyonu ve İnfertilitede Güncel Yaklaşımlar Sempozyumu, 4-7 Ekim 2018, Muğla
18. Evrim Ünsal. Improved IVF Success of Combined. PGT-M and PGT-A Applications18th International Conference on Preimplantation Genetics-PGDIS, Geneve (Switzerland) 15-18 April 2019
19. Unsal E., (2018). Prekonsepsiyonel Genetik Tramada Tartışmalı konular, (Davetli Konuşmacı) . Ulusal Üreme Sağlığı ve İnfertilite Kongresi. Antalya 8-11 Kasım 2018
20. Unsal E. HLA Uyumlu Kardeş Amaçlı PGD Uygulamaları Ve Güncel Durum. (Davetli Konuşmacı) I V. Türk Tıp Dünyası Kurultayı, 28-29 Ekim 2017. İstanbul
21. Unsal E. Tek Gen Hastalıklarının Preimplantasyon Genetik Tanısına Yönelik Algoritmalar. Tıbbi Genetikte Algoritmalar Sempozyumu, (Davetli Konuşmacı) 3. Haziran 2017. Ankara
22. AKTUNA S,ÜNSAL E.,KAYA C.,ÖZER L.,GÜNEY E.,BALTACI A.,DUMAN M. T.,ALMACIOGLU H.,BALTACI V. (2016). How 24 Chromosome Screening Improve the PGS efficacy. 11. Türk Alman Jinekoloji Kongresi, (Kontrol No: 2728309)
23. ÜNSAL E (2016). The Analysis of Blastomere and Trophectoderm – Whole Genomic Technologies: Microarrays and Next Generation Sequencing. 11. Türk Alman Jinekoloji Kongresi, (Kontrol No: 2728349)
24. Unsal E., Ayvaz Ö., Duman T., Özer L.,Akyigit F., Baltaci A.,Baltaci V (2013). Beta Talasemi Olgularında Preimplantasyon Genetik Tanı ve HLA Tiplemesi. 4. Ulusal Transplantasyon Immünolojisi ve Genetigi Kongresi., (Kontrol No: 872610)
25. Unsal E., (2012). Invaziv Embriyo Seçim Yöntemleri. Dördüncü Üreme Tıbbı Dernegi Kongresi, Antalya 26-29 Eylül 2013 (Kontrol No: 866666)
26. Unsal E (2011) Hemoglobinopatilerde Güncel Tedavi Yöntemleri ve Preimplantasyon Genetik Tanı ve Kök Hücre Nakli Paneli., Kök hücre ve kemik iliği için uygun donörün PGD ile sağlanması. Adana, 8.Mayıs.2011
27. Unsal E (2011) “Trans Atlantic Reproductive Technologies Network (TARTEN)” Congress, - Assessment of Sperm DNA Fragmentation Before ART. İstanbul. 14-17 Nisan 2011
28. Evrim Ünsal , Güncel Embriyo Biyopsi Teknikleri - 8. Üreme Tıbbı ve Cerrahisi Derneği Kongresi 28-31 Ekim 2021 -Antalya
29. Evrim Ünsal , PGT-M ve PGT-A beraber yapılabilir mi? 9. Üreme Sağlığı ve İnfertilite Kongresi 11-14 Kasım 2021 – Antalya
30. Ozer L.Duchenne Muskuler Distrofi’de Genetik Yaklaşımlar ve Korunma Yolları.1.Ulusal Dmd Sempozyumu Türkiye’de Dmd Farkındalığı: Tanı, Tedavi Ve Terapi Surecleri İle Biyopsikososyal Yaklaşımlar, Nisan 2019, Ankara
31. Leyla Ozer, Merve Aydin, Suleyman Aktuna, Evrim Unsal, Volkan Baltaci. "Testing for genetic causes of infertility: NGS based infertility panels" Sözlü Bildiri Erciyes Tıp Genetik Günleri 2019, Kayseri 2019
32. Derya Beyza Sayin Kocakap, Ozgur Gunduz, Leyla Ozer, Murat Durak A case of neurofibromatosis with a new neurofibromin mutation: c.5392C>T. Erciyes Tıp Genetik Günleri 2019
33. Leyla Özer, Hande Küçük Kurtulgan, Burak Başer, Evrim Ünsal, Süleyman Aktuna, İlhan Sezgin, Volkan Baltacı, De novo 10p15.3 microdeletion in monozygotic twins, Kayseri Genetik Günleri, 2018
34. L. Ozer , E. Unsal , S. Aktuna , P. Celikkol , I. Kocak, V. Baltacı. Whole-exome sequencing in undiagnosed genetic diseases: phenotype-genotype correlations. Ulusal Tıbbi Genetik Kongresi , Çeşme, Ekim 2016
35. L.Özer, İnsan Kalıtımının Ana Formları: Mendelian ve Mitokondriyal , Türk-Alman Jinekoloji Kongresi, Mayıs 2016
36. L.Özer, Kromozomal anomaliler için PGD , Türk-Alman Jinekoloji Kongresi, Mayıs 2016
37. Özer L, Karabulut HG, Tükün A, RuhiIlgın H, Xq27.3 Frajilitesinin MN-FISH ileDeğerlendirilmesi VIII. UlusalTıbbiGenetikKongresi; YazılıBildiriMayıs 2008, Çanakkale/Türkiye
38. Özer L., KurtuluşÖzmeriç N., Tokman B., Çakılcı B., Uyanık B., Boynueğri D., ÜlkarElgün S. Periodontal hastalıklardaArjinin-NitrikOksitMetabolizmasındakiDeğişiklikler; Poster Presentation , XX. UlusalBiyokimyaKongresi, Ekim 2008 Nevşehir/ Türkiye
39. Özer L, Ulkar B, Ozmeric N, ÜlkarElgünS.Nitric Oxide Pathway Alteration Due to Psychological Stress in Handball Players. XV. Meeting of Balkan Clinical Laboratory Federation; Poster Presentation, Eylül 2007, Antalya/ Türkiye
40. Yalçın B, Özer L, Akçay R, Özkal P, IlgınRuhi H, Bökesoy I. Sitogenetik Laboratuarında Kullanılan Yöntem ve Malzemelerin Kromozom Kırıklarına Etkisi; Poster Presentation, V. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Ekim 2002, Konya/ Türkiye
41. Çabuk F, Sayın B, Akçay R, Özer L, Aydos S, Kutlay N, Karabulut HG, IlgınRuhi H, Tükün A,Tuncalı T, Farklı Gebelik Dönemlerinde Tekrarlayan Kayıpları Olan Çiftlerde Sitogenetik Bulgular; Poster Presentation, Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Ekim 2002, Konya/ Türkiye
42. Özer L, Kutlay N, Tuncalı T, Aydos S, Karabulut HG, Sayın B, Gümüş G, Pekkurnaz G, IlgınRuhi H, Kaya Aİ, Akçay R, Çabuk F, Tükün A. AngelmanSendromu: Mikrodelesyon ve Klinik Bulgular; Oral Presentation, Ulusal Prenatal TanıveTıbbiGenetikKongresi, Ekim 2002, Konya/ Türkiye