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YAYINLARIMIZ
  1. Oocyte maturation abnormalities – A systematic review of the evidence and mechanisms in a rare but difficult to manage fertility pheneomina. Hatırnaz Ş, Hatırnaz ES, Ellibeş Kaya A, Hatırnaz K, Soyer Çalışkan C, Sezer Ö, Dokuzeylül Güngor N, Demirel C, Baltacı V, Tan S, Dahan M.Turk J Obstet Gynecol. 2022 Mar 28;19(1):60-80. doi: 10.4274/tjod.galenos.2022.76329.
  1. Can PCNA and LIM15 gene expression levels predict sperm retrieval success in men with non-obstructive azoospermia? Ibis MA, Aydos K, Baltaci V, Aktuna S, Yaman O. Rev Int Androl. 2022 May 12:S1698-031X(22)00039-5. doi: 10.1016/j.androl.2021.04.002.
  1. Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants. Neuray C, Maroofian R, Scala M, Sultan T, Pai GS, Mojarrad M, Khashab HE, deHoll L, Yue W, Alsaif HS, Zanetti MN, Bello O, Person R, Eslahi A, Khazaei Z, Feizabadi MH, 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. 2020 Aug 1;143(8):2388-2397. doi: 10.1093/brain/awaa178.
  1. Mandibuloacral Dysplasia and LMNA A529V mutation in Turkish patients with Severe Skeletal Changes and Absent Breast Development. Ozer  L, Unsal E, Aktuna S, Baltaci V, Akyiğit F, Ayvaz O, Balci S.. Clin Dysmophol. 2016 Jul;25(3):91-7
 
  1. Prenatal Cytogenetic Findings in 13.466 Cases of High-Risk Pregnant Vomen in One Laboratory. Ozer L,  Unsal E, Ayvaz Ö, Şen A, Baltaci V. MN GORM. 2013 19(3): 139-147
  2. Genetic Aspects of Recurrent Miscarriages Volkan Baltaci, and Ege Baltaci JSM Invitro Fertilisation. 2016.  1 (1):  2002
  1. Oogonial Precursor Cell-Derived Autologous Mitochondria Injection to Improve Outcomes in Women With Multiple IVF Failures Due to Low Oocyte Quality: A Clinical Translation Oktay K,Baltaci V, Sonmezer M, Turan V, Unsal E, Baltaci A, Aktuna S, Moy F. Reprod Sci. 2015 Dec;22(12):1612-7
  1. Effects of pentoxifylline and platelet activating factor on sperm DNA damage. Unsal E, Turan V, Aktuna S, Hurdag C, Bereketoglu G, Canillioglu Y, Baltacı A, Ozcan S, Karayalcin R, Batırbaygil H, Baltacı V. Eur J Obstet Gynecol Reprod Biol. 2016 Feb;197:125-9.
  1. Recombinant chromosome with partial 14 q trisomy due to maternal pericentric inversion. Kurtulgan HK, Özer L, Yıldırım ME, Ünsal E, Aktuna S, Baltacı V, Akkuş N, Sezgin İ Mol Cytogenet. 2015 Nov 21;8:92
  1. Prenatally diagnosed case of 22q11.2 deletion syndrome associated with pulmonary artery aneurysm. Ozer L, Lembet A, Uğurlu N,Baltaci V, Balci S. Turk J Pediatr. 2012 Jan-Feb;54(1):74-6.
  2. A prenatally sonographically diagnosed conotruncal anomaly with mosaic type trisomy 21 and 22q11.2 microdeletion/DiGeorge syndrome. Balci S, AltuganFS, AlehanD, AyparE, Baltaci V. Genet Couns. 2009;20(4):373-7.
  3. Expanding the phenotypic spectrum of lupus erythematosus in Aicardi-Goutières syndrome. 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 V, Conrad K, Lebon P, Lee-Kirsch MA. Arthritis Rheum. 2010 May;62(5):1469-77.
  4. Evaluation of in vitro fertilization parameters and estrogen receptor alpha gene polymorphisms for women with unexplained infertility. Ayvaz OU, Ekmekçi A, Baltaci V, Onen HI, Unsal E. J Assist Reprod Genet. 2009 Sep-Oct;26(9-10):503-10. Epub 2009 Oct 29.
  5. Do patients with heterozygote mutations in GALT gene have increased risk for impaired reproductive functions? Sonmezer M, Ozmen B, Atabekoglu CS, Baltaci V. Fertil Steril. 2009 Oct;92(4):e43; author reply e44. Epub 2009 Sep 5.
  6. The effectiveness of intracytoplasmic sperm injection combined with piezoelectric stimulation in infertile couples with total fertilization failure. Baltaci V, Ayvaz OU, Unsal E, Aktaş Y, Baltaci A, Turhan F, Ozcan S, Sönmezer M. Fertil Steril. 2010 Aug;94(3):900-4. Epub 2009 May 21.
  7. Successful application of preimplantation genetic diagnosis for Leigh syndrome. Unsal E, Aktaş Y, Uner O, BaltacI A, Ozcan S, Turhan F, Baltaci V. Fertil Steril. 2008 Nov;90(5):2017.e11-3. Epub 2008 Sep 7.
  8. 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. Sher G, Keskintepe L, Keskintepe M, Ginsburg M, Maassarani G, Yakut T, Baltaci V, Kotze D, Unsal E. Fertil Steril. 2007 May;87(5):1033-40. Epub 2007 Jan 29.
  9. Partial trisomy (11;22) syndrome with manifestations of Goldenhar sequence due to maternal balanced t(11;22). Balci S, Engiz O, Yilmaz Z, Baltaci V. Genet Couns. 2006;17(3):281-9.
  10. Globozoospermia: Do Y-chromosome microdeletions play a role in this rare spermatogenic disorder? Taskiran C, Baltaci V, Gunalp S. J Reprod Med. 2006 Aug;51(8):628-34.
  11. .Preimplantation genetic diagnosis in two couples with balanced reciprocal translocations.
Baltaci V, Satiroğlu H, Unsal E, Uner O, Ergün MA, Batioğlu S, Sönmezer M, Kabukçu C, Aydinuraz B, Aktaş Y. Eur J Obstet Gynecol Reprod Biol. 2007 Sep;134(1):126-7. Epub 2006 Jul 31.
  1. Relationship between embryo quality and aneuploidies. Baltaci V, Satiroglu H, Kabukçu C, Unsal E, Aydinuraz B, Uner O, Aktas Y, Cetinkaya E, Turhan F, Aktan A. Reprod Biomed Online. 2006 Jan;12(1):77-82.
  2. Enzymatic digestion plus mechanical searching improves testicular sperm retrieval in non-obstructive azoospermia cases. Aydos K, Demirel LC, Baltaci V, Unlü C. Eur J Obstet Gynecol Reprod Biol. 2005 May 1;120(1):80-6.
  3. Increased frequency of sister-chromatid exchange and altered alkaline comet assay scores in superovulation cycles for unexplained infertility. Baltaci V, Zeyneloglu HB. Eur J Obstet Gynecol Reprod Biol. 2004 Mar 15;113(1):73-7.
  4. Assessment of cytogenetic aberrations and comet assay in colorectal adenocarcinomas. Baltaci V, Sardas S, Aytac B, Cakar S, Karakaya AE. Tumori. 2003 May-Jun;89(3):305-10.
  5. Analysis of DNA damage using the comet assay in infants fed cow’s milk. Dündaröz R, Ulucan H, Aydin HI, Güngör T, Baltaci V, Denli M, Sanisoğlu Y. Biol Neonate. 2003;84(2):135-41.
  6. Chromosome 22q11.2 deletion and phenotypic features in 30 patients with conotruncal heart defects. Derbent M, Yilmaz Z, Baltaci V, Saygili A, Varan B, Tokel K. Am J Med Genet A. 2003 Jan 15;116A(2):129-35.
  7. DNA damage in children treated with imipramine for primary nocturnal enuresis.
DündarözR, TürkbayT, Sürer I, Gök F, Denli M, Baltaci V. Pediatr Int.2002 Dec;44(6):617-21.
  1. Achievement of pregnancy in globozoospermia with Y chromosome microdeletion after ICSI.
Zeyneloglu HB, Baltaci V, Duran HE, Erdemli E, Batioglu S. Hum Reprod. 2002Jul;17(7):1833-6.
  1. Preliminary study on DNA damage in non breast-fed infants. Dündaröz R, Aydin HI, Ulucan H, Baltaci V, Denli M, Gökçay E. Pediatr Int. 2002 Apr;44(2):127-30.
  2. .Retinal vein occlusion and factor V Leiden and prothrombin 20210 G:A mutations. Aras S, YilmazG, Alpas I, Baltaci V, TayançE, Aydin P.Eur J Ophthalmol. 2001 Oct-Dec;11(4):351-5.
  3. Sister chromatid exchange rate and alkaline comet assay scores in patients with ovarian cancer. Baltaci V, Kayikçioğlu F, Alpas I, Zeyneloğlu H, Haberal A. Gynecol Oncol. 2002 Jan;84(1):62-6.
  4. Evaluation of DNA damage using the comet assay in children on long-term benzathine penicillin for secondary prophylaxis of rheumatic fever. Dündaröz R, Ulucan H, Denli M, Karapinar K, Aydin HI, Baltaci V. Pediatr Int. 2001 Jun;43(3):276-80.
  5. Popliteal pterygium associated with neonatal Marfan syndrome: case report.
Derbent M, Gurakan B, Saygil A, Baltaci V, Balci S. Clin Dysmorphol. 2001 Jul;10(3):209-13.
  1. Pulmonary artery sling in a case of trisomy 18. Derbent M, Saygili A, Tokel K, Baltaci V. Am J Med Genet. 2001 Jun 15;101(2):184-5.
  2. Sister-chromatid exchange analysis on long-term benzathine penicillin for secondary prophylaxis of rheumatic fever. Dündaröz R, OzisikT, Baltaci V, KarapinarK, Aydin HI, Denli M. Indian J Pediatr. 2001 Feb;68(2):121-2.
  3. Non-invasive early prenatal diagnosis using fluorescent in situ hybridization on transcervical cells: comparison of two different methods for retrieval. ErgIn T, Baltaci V, Zeyneloglu HB, Duran EH, ErgenelI MH, Batioglu S. Eur J Obs Gynecol Reprod Biol. 2001 Mar;95(1):37-41.
  4. Isolated granulocytic myelodysplasia in a child with unilateral retinoblastoma. Oto S, Ozbek N, Baltaci V, Demirhan B, Aydin P. J Pediatr Ophthalmol Strabismus. 2000 Sep-Oct;37(5):302-4.
  5. A comparative study of genotoxic effects in the treatment of trichomonas vaginalis infection: metronidazole or nalidixic acid. Akyol D, Mungan T, Baltaci V. Arch Gynecol Obstet. 2000 Jul;264(1):20-3.
  6. Sister-chromatid exchange frequencies in postmenopausal hormone replacement patients. Kayikçioğlu F, Güneş M, Baltaci V, Koçak M, Alpas I, Haberal A. Mutat Res. 2000 Jul 20;452(1):37-9.
  7. Detection of chromosomal abnormalities by fluorescent in-situ hybridization in immotile viable spermatozoa determined by hypo-osmotic sperm swelling test. Zeyneloglu HB, Baltaci V, Ege S, Haberal A, Batioglu S. Hum Reprod. 2000 Apr;15(4):853-6.
  8. Sister chromatid exchange rate from pleural fluid cells in patients with malignant esothelioma. Atalay F, Baltaci V, Alpas I, Savas I, AtikcanS, Balci S. Mutat Res.2000 Feb 16;465(1-2):159-63.
  9. Philadelphia chromosome (+) T-cell acute lymphoblastic leukemia after renal transplantation. Arican A, Ozbek N, Baltaci V, Haberal M. Transplant Proc. 1999 Dec;31(8):3242-3.
  10. Philadelphia chromosome (+) T-cell acute lymphoblastic leukaemia after renal ransplantation. Arican A, Ozbek N, Baltaci V, Haberal M. Nephrol Dial Transplant. 1999 Aug;14(8):2054-5.
  11. A case associated with Walker Warburg syndrome phenotype and homozygous pericentric inversion 9: coincidental finding or aetiological factor? Baltaci V, Ors R, Kaya M, Balci S. Acta Paediatr. 1999 May;88(5):579-83.
  12. Clinical assessment of EMA/CO induced DNA damage in peripheral blood lymphocytes of high-risk gestational trophoblastic tumor patients. Akyol D, Mungan T, Baltaci V, Kozinoglu H, Oguz S, Oztekin O, Gökmen O. Eur J Gynaecol Oncol. 1999;20(2):150-5.
  13. Chromosomal aberrations and alkaline comet assay in families with habitual abortion.
Baltaci V, Aygün N, Akyol D, Karakaya AE, Sardaş S. Mutat Res. 1998 Sep 1;417(1):47-55.
  1. A new application for reconstruction of areola with transplantation of cultured autologous melanocytes. Baltaci V, Kiliç A. Plast Reconstr Surg. 1998 Apr;101(4):1056-9.
  2. Next Generation Sequencing (NGS) based variation analysis: A new practical biomarker for beef tenderness assessment. Calik E, Baltaci V, Candogan K. Int J Agric Environ Food Sci 3(4): 233-239 (2019) DOI: 10.31015/jaefs.2019.4.6
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      7.2.  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 18p- chromosome constitution. European Society of Human Genetics 24th annual meeting, 27-31 May 1992 pp:83.
  3. 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, İrfan 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, İrfan 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 İMİRZALİOĞLU, 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 SARDAŞ (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.ATİKCAN, 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, Kürşat 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.
 
      7.3.  Yazılan uluslararası kitaplar veya kitaplarda bölümler
      7.4.  Ulusal hakemli dergilerde yayınlanan makaleler
  1. 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 İMİRZALİOĞLU (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 İMİRZALİOĞLU (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 ŞEN (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) . TUBİTAK Turkish Journal of Medical Sciences. Kasım. 1997 tarihli ve sağ 97/34 sayılı kabul yazısı.
  9. Muhterem BAHÇE, Necat İMİRZALİOĞLU, Engin YILMAZ, R. Seçkin ÖZEN, Volkan BALTACI, Gönül OĞUR (1997). Tekrarlayan düşüklerde 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. TUBİTAK 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 KIŞ, Nedim ÇİÇEK, Tayfun GÜNGÖR (1999) Accessory Limb Attached to the Back. TUBİTAK 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 taşıyan 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)

 

 

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