Yusuf Tunca

Summary

Affiliation: Gulhane Military Medical Academy
Country: Turkey

Publications

  1. ncbi request reprint Prenatal diagnosis of primary microcephaly in two consanguineous families by confrontation of morphometry with DNA data
    Yusuf Tunca
    Department of Medical Genetics, GATA, 06018 Etlik, Ankara, Turkey
    Prenat Diagn 26:449-53. 2006
  2. doi request reprint A polymorphism in ERAP1 is associated with susceptibility to ankylosing spondylitis in a Turkish population
    Muhammet Cinar
    Division of Rheumatology, Gulhane Military Medical Academy School of Medicine, Gn Tevfik Saglam Cad, 06018, Etlik, Ankara, Turkey
    Rheumatol Int 33:2851-8. 2013
  3. doi request reprint Association of retinal vein occlusion, homocysteine, and the thrombophilic mutations in a Turkish population: A case-control study
    Mehmet Talay Koylu
    A Department of Ophthalmology, Gulhane Military Medicine Academy, Ankara, Turkey
    Ophthalmic Genet . 2017
  4. ncbi request reprint [Investigation of the association between paraoxonase-1 gene polymorphisms and response to therapy in chronic hepatitis C patients]
    Kazım Kıratlı
    Gulhane Military Medical Academy, Department of Infectious Diseases and Clinical Microbiology, Ankara, Turkey
    Mikrobiyol Bul 48:596-605. 2014
  5. doi request reprint Prenatal diagnosis of an autosomal translocation with regular trisomy 21
    Yusuf Tunca
    Department of Medical Genetics, Gulhane Military Medical Academy, Ankara, Turkey
    Fetal Pediatr Pathol 32:210-2. 2013
  6. ncbi request reprint [The investigation of angiotensin converting enzyme I/D and plasminogen activator inhibitor-1 4G/5G polymorphisms in venous thromboembolism patients]
    Halide Kaya
    Department of Medical Biology, Gulhane Military Medical Academy, Ankara, Turkey
    Tuberk Toraks 61:88-95. 2013
  7. pmc The presence of MEFV gene mutations in patients with primary osteoarthritis who require surgery
    Sedat Yilmaz
    Division of Rheumatology, Gulhane School of Medicine, Ankara, Turkey
    Korean J Intern Med 28:594-8. 2013
  8. doi request reprint Ring chromosome 21 in the differential diagnosis of waddling gait
    Mutluay Arslan
    Gulhane Military Medical School, Department of Pediatrics, Division of Child Neurology, Etlik, Ankara, Turkey
    Brain Dev 34:792-5. 2012
  9. ncbi request reprint Novel mutations in prenatal diagnosis of primary microcephaly
    Julie Desir
    Prenat Diagn 26:989. 2006
  10. ncbi request reprint New heritable fragile site at 15q13 in both members of a nonconsanguineous couple
    Nadide Nilüfer Karadeniz
    Dr Zekai Tahir Burak Woman Hospital, Department of Medical Genetics, Hamamönü Ankara, Turkiye
    Am J Med Genet A 118:290-2. 2003

Collaborators

Detail Information

Publications10

  1. ncbi request reprint Prenatal diagnosis of primary microcephaly in two consanguineous families by confrontation of morphometry with DNA data
    Yusuf Tunca
    Department of Medical Genetics, GATA, 06018 Etlik, Ankara, Turkey
    Prenat Diagn 26:449-53. 2006
    ....
  2. doi request reprint A polymorphism in ERAP1 is associated with susceptibility to ankylosing spondylitis in a Turkish population
    Muhammet Cinar
    Division of Rheumatology, Gulhane Military Medical Academy School of Medicine, Gn Tevfik Saglam Cad, 06018, Etlik, Ankara, Turkey
    Rheumatol Int 33:2851-8. 2013
    ..In summary, an ERAP1 polymorphism was associated with AS in a Turkish population. The contributions of HLA-B27 and the rs26653 SNP to AS pathogenesis appear to be independent...
  3. doi request reprint Association of retinal vein occlusion, homocysteine, and the thrombophilic mutations in a Turkish population: A case-control study
    Mehmet Talay Koylu
    A Department of Ophthalmology, Gulhane Military Medicine Academy, Ankara, Turkey
    Ophthalmic Genet . 2017
    ..To compare homocysteine and thrombophilic mutations for the methylenetetrahydrofolate reductase (MTHFR) C677T, factor V Leiden, and prothrombin G20210A between retinal vein occlusion (RVO) and healthy controls in a Turkish population...
  4. ncbi request reprint [Investigation of the association between paraoxonase-1 gene polymorphisms and response to therapy in chronic hepatitis C patients]
    Kazım Kıratlı
    Gulhane Military Medical Academy, Department of Infectious Diseases and Clinical Microbiology, Ankara, Turkey
    Mikrobiyol Bul 48:596-605. 2014
    ....
  5. doi request reprint Prenatal diagnosis of an autosomal translocation with regular trisomy 21
    Yusuf Tunca
    Department of Medical Genetics, Gulhane Military Medical Academy, Ankara, Turkey
    Fetal Pediatr Pathol 32:210-2. 2013
    ..The postmortem pathologic examination of the fetus revealed that the findings of hypertelorism and right lung with two lobes are interesting novel findings of our cases associated with the breakpoints 3p21 and 8q24...
  6. ncbi request reprint [The investigation of angiotensin converting enzyme I/D and plasminogen activator inhibitor-1 4G/5G polymorphisms in venous thromboembolism patients]
    Halide Kaya
    Department of Medical Biology, Gulhane Military Medical Academy, Ankara, Turkey
    Tuberk Toraks 61:88-95. 2013
    ..In this study we aimed to investigate the role of angiotensin converting enzyme insersion/deletion (ACE I/D) and plasminogen activator inhibitor-1 4G/5G (PAI-1 4G/5G) polymorphism in the development of disease...
  7. pmc The presence of MEFV gene mutations in patients with primary osteoarthritis who require surgery
    Sedat Yilmaz
    Division of Rheumatology, Gulhane School of Medicine, Ankara, Turkey
    Korean J Intern Med 28:594-8. 2013
    ..Our aim was to investigate a possible causal relationship between FMF and osteoarthritis in a population in which FMF is quite common...
  8. doi request reprint Ring chromosome 21 in the differential diagnosis of waddling gait
    Mutluay Arslan
    Gulhane Military Medical School, Department of Pediatrics, Division of Child Neurology, Etlik, Ankara, Turkey
    Brain Dev 34:792-5. 2012
    ..Structural neurologic anomalies have also been described, but waddling gait due to lower motor neuron involvement has not been previously reported in association with ring 21...
  9. ncbi request reprint Novel mutations in prenatal diagnosis of primary microcephaly
    Julie Desir
    Prenat Diagn 26:989. 2006
  10. ncbi request reprint New heritable fragile site at 15q13 in both members of a nonconsanguineous couple
    Nadide Nilüfer Karadeniz
    Dr Zekai Tahir Burak Woman Hospital, Department of Medical Genetics, Hamamönü Ankara, Turkiye
    Am J Med Genet A 118:290-2. 2003
    ..While it looks like the fragile site is harmless in all carriers, having heterozygosity in the couple may lead to homozygous offspring that could result in fetal loss...