Prof. Dr. Yusuf TUNCA | AVESİS

Akademik Veri Yönetim Sistemi

Yayınlar & Eserler

Makaleler 59

1. Phenotypes and genotypes in non-consanguineous and consanguineous primary microcephaly: High incidence of epilepsy

Duerinckx S., Désir J., Perazzolo C., Badoer C., Jacquemin V., Soblet J., et al.

Molecular Genetics and Genomic Medicine , cilt.9, sa.9, 2021 (SCI-Expanded, Scopus)

2. Gülhane Medical Journal

Dergisi G. T., Gülqelik M. A., TUNCA Y., Gürkök S., Sönmez Y. A., TaȘqi I., et al.

Gulhane Medical Journal , cilt.62, sa.4, ss.1-8, 2020 (Scopus, TRDizin)

3. Classifying dysmorphic syndromes by using artificial neural network based hierarchical decision tree

Özdemir M. E., Telatar Z., Eroğul O., TUNCA Y.

Australasian Physical and Engineering Sciences in Medicine , cilt.41, sa.2, ss.451-461, 2018 (SCI-Expanded, Scopus)

4. Autosomal recessive primary microcephaly due to ASPM mutations: An update

Létard P., Drunat S., Vial Y., Duerinckx S., Ernault A., Amram D., et al.

Human Mutation , cilt.39, sa.3, ss.319-332, 2018 (SCI-Expanded, Scopus)

5. Association of retinal vein occlusion, homocysteine, and the thrombophilic mutations in a Turkish population: A case-control study

KÖYLÜ M. T., Kucukevcilioglu M., Erdurman F. C., DURUKAN A. H., Sobacı G., TORUN D., et al.

Ophthalmic Genetics , cilt.38, sa.4, ss.352-356, 2017 (SCI-Expanded, Scopus)

6. MEFV gene mutation frequency and distribution of mutations in FMF patients: Analysis of a large group of patients from a single center FMF hastalarindaki MEFV gen mutasyon sikliği ve mutasyonlarin dağilimi: Tek bir merkezden geniş bir hasta grubunun analizi

TORUN D., TEKGÖZ E., Kavuş H., Öztuna A., Akar H., Çinar M., et al.

Gulhane Medical Journal , cilt.59, sa.1, ss.24-27, 2017 (Scopus, TRDizin)

7. Karyotype analysis results in girls followed with short stature Boy kisaliği nedeni ile takip edilen kiz çocuklarinda karyotip analizi sonuçlarimiz

TORUN D., Kavuş H., Öztuna A., Akar H., Akin O., TUNCA Y.

Gulhane Medical Journal , cilt.59, sa.1, ss.21-23, 2017 (Scopus, TRDizin)

8. Examining the ethical dilemmas in terminating the pregnancy through the basic ethical principles Temel etik ilkeler çerçevesinde gebeliğin sonlandırılmasındaki etik ikilemlere bir Bakış

Kurt E., TUNCA Y.

Haseki Tip Bulteni , cilt.54, sa.2, ss.57-61, 2016 (Scopus, TRDizin)

9. Central nervous system abnormalities and psychomotor retardation in a girl with a 15.4-mb deletion of 14q12 q21.2 and a 550-kb deletion of 18p11.23: Microarray delineation of an unbalanced chromosome rearrangement and a literature review

TORUN D., ARSLAN M., Akar H., Karaer K., ÜNAY B., TUNCA Y.

Genetic Counseling , cilt.27, sa.2, ss.165-176, 2016 (SCI-Expanded, Scopus)

10. A case with 18p deletion and dystonia and review of the literature

Tekeli H., Kendirli M. T., Şenol M. G., DEMİR S., Yaşar H., Toğrol R. E., et al.

Neurology Asia , cilt.20, sa.3, ss.287-290, 2015 (SCI-Expanded, Scopus)

11. Existe uma relacao entre a artrite gotosa e as mutacoes geneticas da febre familiar do Mediterraneo? Existe uma relação entre a artrite gotosa e as mutações genéticas da febre familiar do Mediterrâneo?

SARI İ., Simsek I., TUNCA Y., Kisacik B., ERDEM H., Pay S., et al.

Revista Brasileira de Reumatologia , cilt.55, sa.4, ss.325-329, 2015 (SCI-Expanded, Scopus)

12. Biomedical visual data analysis to build an intelligent diagnostic decision support system in medical genetics

Kuru K., Niranjan M., TUNCA Y., Osvank E., Azim T.

Artificial Intelligence in Medicine , cilt.62, sa.2, ss.105-118, 2014 (SCI-Expanded, Scopus)

13. Investigation of the association between paraoxonase-1 gene polymorphisms and response to therapy in chronic hepatitis C patients Kronik Hepatit C Enfeksiyonu Olan Hastalarda Paraoksonaz-1 Gen Polimorfizmi ile Tedaviye Yanit Arasindaki ̄lişkinin Araştirilmasi

KIRATLI K., GÜL H. C., ARTUK C., Kozan S., Öztuna A., TUNCA Y., et al.

Mikrobiyoloji Bulteni , cilt.48, sa.4, ss.596-605, 2014 (SCI-Expanded, Scopus, TRDizin)

14. A polymorphism in ERAP1 is associated with susceptibility to ankylosing spondylitis in a Turkish population

Cinar M., Akar H., YILMAZ S., Simsek I., Karkucak M., Sagkan R. I., et al.

Rheumatology International , cilt.33, sa.11, ss.2851-2858, 2013 (SCI-Expanded, Scopus)

15. The presence of MEFV gene mutations in patients with primary osteoarthritis who require surgery

YILMAZ S., ERDEM H., Tunay S., TORUN D., Genc H., TUNCA Y., et al.

Korean Journal of Internal Medicine , cilt.28, sa.5, ss.594-598, 2013 (Scopus)

16. Prenatal diagnosis of an autosomal translocation with regular trisomy 21

TUNCA Y., Deveci M. S., Koc A., Kaya H., Alanbay I., Coksuer H., et al.

Fetal and Pediatric Pathology , cilt.32, sa.3, ss.210-212, 2013 (SCI-Expanded, Scopus)

17. Travelling after amniocentesis: Answer to a frequent question

KARAŞAHİN K. E., Ozturk M., Çoksuer H., TORUN D., TUNCA Y.

Journal of Obstetrics and Gynaecology , cilt.33, sa.4, ss.343-345, 2013 (SCI-Expanded, Scopus)

18. The investigation of angiotensin converting enzyme I/D and plasminogen activator inhibitor-1 4G/5G polymorphisms in venous thromboembolism patients Venöz tromboembolili hastalarda anjiyotensin dönüştürücü enzim I/D ve plazminojen aktivatör inhibitör-1 4G/5G gen polimorfizmlerinin araştırılması

Kaya H., Karkucak M., SalIfoǧlu H., TORUN D., Kozan S., TUNCA Y.

Tuberkuloz ve Toraks , cilt.61, sa.2, ss.88-95, 2013 (Scopus, TRDizin)

19. The status of telomerase enzyme activity in benign and malignant gynaecologic pathologies

Gül L., Dündar Ö., Bodur S., TUNCA Y., Tütüncü L.

Balkan Medical Journal , cilt.30, sa.3, ss.287-292, 2013 (SCI-Expanded, Scopus, TRDizin)

20. Ring chromosome 21 in the differential diagnosis of waddling gait

ARSLAN M., YİŞ U., VURUCU S., TUNCA Y., ÜNAY B., Akin R.

Brain and Development , cilt.34, sa.9, ss.792-795, 2012 (SCI-Expanded, Scopus)

21. Rheumatic and autoimmune diseases may have a role in disease progression of myelodysplastic syndrome Ramatolojik ve otoimmün hastalıkların myelodisplastik sendromun progresyonunda rolü olabilir

Kozan S., TORUN D., TUNCA Y., Beyan C., Ifran A., Kaptan M. K., et al.

Turkiye Klinikleri Journal of Medical Sciences , cilt.32, sa.4, ss.910-916, 2012 (Scopus)

22. The effect of cytogenetic analysis results on prognosis in cases with myelodysplastic syndrome Miyelodisplastik sendrom olgularinda sitogenetik analiz sonuçlarinin hasta prognozuna etkisi

GÜRAN Ş., Beyan C., TUNCA Y., Kozan S., TORUN D., Ifran A., et al.

Gulhane Medical Journal , cilt.53, sa.2, ss.104-106, 2011 (Scopus, TRDizin)

23. Blood oxidative stress biomarkers in patients with Familial Mediterranean Fever (FMF)

Celik S., Oktenli C., Terekeci H., Ipcioglu O., Sanisoglu Y., Sayan O., et al.

Aktuelle Rheumatologie , cilt.35, sa.6, ss.382-385, 2010 (SCI-Expanded, Scopus)

24. The rate of MEFV gene mutations in hematolymphoid neoplasms

Celik S., Erikci A., TUNCA Y., Sayan O., Terekeci H., Umur E., et al.

International Journal of Immunogenetics , cilt.37, sa.5, ss.387-391, 2010 (SCI-Expanded, Scopus)

25. High frequency of MEFV gene mutations in patients with myeloid neoplasm

Oktenli C., Sayan O., Celik S., Erikci A. A., TUNCA Y., Terekeci H. M., et al.

International Journal of Hematology , cilt.91, sa.5, ss.758-761, 2010 (SCI-Expanded, Scopus)

26. Specific polymorphisms of IL-1β genes (-511, +3953) and their probable effects on IL-1β production in idiopatic hypogonadotropic hypogonadism Idiopatik hipogonadotropik hipogonadizm hastalarinda IL-1β genlerindeki spesifik (-511, +3953) polimorfizmler ve bunlarin IL-1β üretimindeki olasi etkileri

Muşabak U., Bolu E., ILIKÇI SAĞKAN R., TUNCA Y., GÜRAN Ş., Gül D., et al.

Turkiye Klinikleri Journal of Medical Sciences , cilt.30, sa.6, ss.1814-1819, 2010 (SCI-Expanded, Scopus)

27. Genetic appoproch in cases with disorders of sexual development Cinsel farklılaşma bozukluǧu olan olgularda genetik yaklaşım

Bahçe M., TUNCA Y., Gül D., Imirzalioǧlu N., Emre Taşçilar M., Bolu E., et al.

Gulhane Medical Journal , cilt.51, sa.4, ss.223-228, 2009 (Scopus, TRDizin)

28. Analysis of the dermatoglyphics in Turkish patients with Klinefelter's syndrome

Sirri Cam F., Gul D., TUNCA Y., Fistik T., Ozdemir Erdogan M., Yildiz H., et al.

Hereditas , cilt.145, sa.4, ss.163-166, 2008 (SCI-Expanded, Scopus)

29. Placental mesenchymal dysplasia associated with trisomy 13: Sonographic findings

Müngen E., Dundar Ö., MUHCU M., Haholu A., TUNCA Y.

Journal of Clinical Ultrasound , cilt.36, sa.7, ss.454-456, 2008 (SCI-Expanded, Scopus)

30. A very frequent mutation and remarkable association of R761H with M694V mutations in Turkish familial Mediterranean fever patients

Demirkaya E., TUNCA Y., Gok F., Ozen S., Gul D.

Clinical Rheumatology , cilt.27, sa.6, ss.729-732, 2008 (SCI-Expanded, Scopus)

31. The role of ace gene polymorphism in the development of angioedema secondary to angiotensin converting enzyme inhibitors and angiotensin II receptor blockers

Gulec M., Caliskaner Z., TUNCA Y., Ozturk S., Bozoglu E., Gul D., et al.

Allergologia et Immunopathologia , cilt.36, sa.3, ss.134-140, 2008 (Scopus)

32. The rate and significance of Mediterranean fever gene mutations in patients with ankylosing spondylitis: A three-month, longitudinal clinical study

Cinar M., Dinc A., Simsek I., ERDEM H., Koc B., Pay S., et al.

Rheumatology International , cilt.29, sa.1, ss.37-42, 2008 (SCI-Expanded, Scopus)

33. Association of Prune belly syndrome and horse shoe kidney (case report) Prune belly sendromu ve at nalı böbrek birlikteliǧi (olgu sunumu)

Özcan A., GÜNAL A., Alömeroǧlu M., Temel Ceyhan S., TUNCA Y., Başer I.

Gulhane Medical Journal , cilt.50, sa.4, ss.276-278, 2008 (Scopus, TRDizin)

34. Clinical and intraoral findings of a patient with tricho-rhino-phalangeal syndrome type I

KARAÇAY Ş., SAYGUN N. I., TUNCA Y., Imirzalioglu N., Guvenc G.

Journal of Indian Society of Pedodontics and Preventive Dentistry , cilt.25, sa.1, ss.43-45, 2007 (Scopus)

35. Translocation (2;11)(p21;q23) in a patient with polycythemia vera: A novel clonal chromosome abnormality [2]

Acar K., Sucak G. T., YAĞCI A. M., TUNCA Y., Haznedar R.

American Journal of Hematology , cilt.81, sa.11, ss.891, 2006 (SCI-Expanded, Scopus)

36. Novel mutations in prenatal diagnosis of primary microcephaly [1]

Desir J., Abramowicz M., TUNCA Y.

Prenatal Diagnosis , cilt.26, sa.10, ss.989, 2006 (SCI-Expanded, Scopus)

37. Prenatal diagnosis of primary microcephaly in two consanguineous families by confrontation of morphometry with DNA data

TUNCA Y., VURUCU S., Parma J., Akin R., Désir J., Baser I., et al.

Prenatal Diagnosis , cilt.26, sa.5, ss.449-453, 2006 (SCI-Expanded, Scopus)

38. Is there a different phenotype for Familial Mediterranean Fever arthritis in Çorum and its vicinity? Çorum i̇li ve çevresinde ailesel akdeniz ateşi artriti olarak farkli bir fenotip mi var?

Solmazgül E., TUNCA Y., Şahan B., KAPLAN M., Demírci M., NALBANT S.

Turkiye Klinikleri Journal of Medical Sciences , cilt.26, sa.1, ss.20-23, 2006 (Scopus)

39. Synchronous double malignancies of renal cell carcinoma and acute myeloid leukemia: An unreported co-existence [1]

Beyan C., Kaptan K., TUNCA Y., Ifran A., GÜRAN Ş.

American Journal of Hematology , cilt.80, sa.2, ss.164, 2005 (SCI-Expanded, Scopus)

40. A chronic myeloid leukemia-like syndrome case with del (12) (p12) in a Li-Fraumeni syndrome family

GÜRAN Ş., Beyan C., Nevruz O., Yakicier C., TUNCA Y.

Clinical and Laboratory Haematology , cilt.27, sa.2, ss.135-138, 2005 (Scopus)

41. Trisomy 8 finding treatment of imatinib mesylate in chronic myeloid leukemia cases

TUNCA Y., GÜRAN Ş.

Experimental Hematology , cilt.33, sa.2, ss.151, 2005 (SCI-Expanded, Scopus)

42. The role of secondary chromosomal abnormalities in the progression of chronic myeloid leukemia cases Kronik miyelositer lösemi olgularinda philadelphia kromozomu haricindeki sitogenetik anomalilerin prognoza etkisi

Nevruz O., GÜRAN Ş., Beyan C., Ifran A., TUNCA Y., Kaptan K., et al.

Turkiye Klinikleri Journal of Medical Sciences , cilt.25, sa.2, ss.174-177, 2005 (Scopus, TRDizin)

43. Prenatal diagnosis history of a Li-Fraumeni syndrome family [3]

GÜRAN Ş., TUNCA Y.

Cancer Genetics and Cytogenetics , cilt.157, sa.2, ss.191, 2005 (SCI-Expanded, Scopus)

44. The cytogenetic results of the cases who had chronic myeloproliferative disorders except chronic myeloid leukemia Kroni̇k mi̇yelosi̇ter lösemi̇ dişi kroni̇k mi̇yeloproli̇ferati̇f hastaliǧi olan olgularimizda si̇togeneti̇k i̇nceleme sonuçlari

Nevruz O., GÜRAN Ş., Beyan C., Ifran A., TUNCA Y., Kaptan K., et al.

Gulhane Medical Journal , cilt.47, sa.1, ss.11-13, 2005 (Scopus, TRDizin)

45. Our treatment results in patients with ANNL over 60 years old 60 Yaş üzeri̇ akut nonlenfosi̇ter lösemi̇ olgularimizda tedavi̇ sonuçlari

Nevruz O., Beyan C., GÜRAN Ş., Ifran A., TUNCA Y., Kaptan K., et al.

Gulhane Medical Journal , cilt.46, sa.4, ss.276-279, 2004 (Scopus, TRDizin)

46. A case of Zellweger syndrome with clonal 46, XX, t(1;2) (q43;q21) cytogenetic abnormality Klonal 46XX, t(1;2) (q43;q21) si̇togeneti̇k anomali̇si̇ i̇le karakteri̇ze Zellweger sendromu olgusu

GÜRAN Ş., Bal F., TUNCA Y.

Erciyes Tip Dergisi , cilt.26, sa.3, ss.145-148, 2004 (Scopus, TRDizin)

47. New heritable fragile site at 15q13 in both members of a nonconsanguineous couple

Karadeniz N. N., TUNCA Y., Imirzalioǧlu N.

American Journal of Medical Genetics , cilt.118 A, sa.3, ss.290-292, 2003 (SCI-Expanded, Scopus)

48. Deletion of RBM and DAZ in azoospermia: Evaluation by PRINS

Kadandale J. S., Wachtel S. S., TUNCA Y., Martens P. R., Wilroy R. S., Tharapel A. T.

American Journal of Medical Genetics , cilt.107, sa.2, ss.105-108, 2002 (SCI-Expanded, Scopus)

49. Third case of WAGR syndrome with severe obesity and constitutional deletion of chromosome (11)(p12p14) [2]

Gül D., Oǧur G., TUNCA Y., Özcan O.

American Journal of Medical Genetics , cilt.107, sa.1, ss.70-71, 2002 (Scopus)

50. Long-term survival in Patau syndrome

TUNCA Y., Kadandale J. S., Pivnick E. K.

Clinical Dysmorphology , cilt.10, sa.2, ss.149-150, 2001 (SCI-Expanded, Scopus)

51. Hyperpigmentation along the lines of Blaschko with associated chromosome 14 mosaicism [1]

Kuwahara R., Henson T., TUNCA Y., Wilroy S.

Pediatric Dermatology , cilt.18, sa.4, ss.360-361, 2001 (SCI-Expanded, Scopus)

52. A case of Klinefelter's syndrome associated with unilateral renal aplasia

Ozata M., Yesilova Z., Saglam M., TUNCA Y.

Medical Science Monitor , cilt.6, sa.5, ss.1000-1002, 2000 (Scopus)

53. Localization of SRY by primed in situ labeling in XX and XY sex reversal

Kadandale J. S., Wachtel S. S., TUNCA Y., Sid Wilroy Jr. R., Martens P. R., Tharapel A. T.

American Journal of Medical Genetics , cilt.95, sa.1, ss.71-74, 2000 (SCI-Expanded, Scopus)

54. The role of bilateral choroid plexus cysts in prenatal diagnosis of double trisomy (Klinefelter-Edwards Syndrome) Double trizomi (Klinefelter-Edwards Sendromu) prenatal tanisinda bilateral koroid pleksus kistlerinin rolu

TUNCA Y., Ergun A., SOYSAL Y., Sefali M., Imirzalioglu N.

Jinekoloji ve Obstetri Bulteni , cilt.9, sa.2, ss.72-73, 2000 (Scopus)

55. Chromosomal localization of single copy genes SRY and SOX3 by primed in situ labeling (PRINS)

Kadandale J., TUNCA Y., Tharapel A.

Microbial and Comparative Genomics , cilt.5, sa.2, ss.71-74, 2000 (Scopus)

56. Hypomelanosis of Ito and a 'mirror image' whole chromosome duplication resulting in trisomy 14 mosaicism

TUNCA Y., Wilroy R. S., Kadandale J. S., Martens P. R., Gunther W. M., Tharapel A. T.

Annales de Genetique , cilt.43, sa.1, ss.39-43, 2000 (SCI-Expanded, Scopus)

57. Hereditary TP53 codon 292 and somatic P16(INK4A) codon 94 mutations in a Li-Fraumeni syndrome family

GÜRAN Ş., TUNCA Y., Imirzalioglu N.

Cancer Genetics and Cytogenetics , cilt.113, sa.2, ss.145-151, 1999 (SCI-Expanded, Scopus)

58. Application of the 'apt test' in prenatal diagnosis to evaluate the fetal origin of blood obtained by cordocentesis: Results of 30 pregnancies

Ogur G., Gül D., Özen S., Imirzalioglu N., Cankus G., TUNCA Y., et al.

Prenatal Diagnosis , cilt.17, sa.9, ss.879-882, 1997 (SCI-Expanded, Scopus)

59. Placental chorioangioma associated with fetal cardiac complication

DEMİRİZ M., TUNCA Y., Özcan A., Celasun B., Finci R.

Acta Obstetricia et Gynecologica Scandinavica , cilt.76, sa.7, ss.708-709, 1997 (SCI-Expanded, Scopus)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 3

1. Establishment of a diagnostic decision support system in genetic dysmorphology

Kuru K., Niranjan M., TUNCA Y.

11th IEEE International Conference on Machine Learning and Applications, ICMLA 2012, Boca Raton, FL, Amerika Birleşik Devletleri, 12 - 15 Aralık 2012, cilt.2, ss.164-169, (Tam Metin Bildiri)

2. Dysmorphic syndromes classification and recognition with computer assisted system

Erkinay M., Telatar Z., Eroǧul O., TUNCA Y.

9th IASTED International Conference on Biomedical Engineering, BioMed 2012, Innsbruck, Avusturya, 15 - 17 Şubat 2012, ss.47-51, (Tam Metin Bildiri)

3. Recognition of Down syndromes using image analysis Down sendromlu hastalarin görüntü analizi i̇le ayirt edilmesi

Eroǧul O., Sipahi M. E., TUNCA Y., VURUCU S.

2009 14th National Biomedical Engineering Meeting, BIYOMUT 2009, Balcova, Izmir, Türkiye, 20 - 22 Mayıs 2009, (Tam Metin Bildiri)

Metrikler

Yayın

62

Yayın (WoS)

45

Yayın (Scopus)

62

H-İndeks (WoS)

14

Atıf (Scopus)

594

H-İndeks (Scopus)

14

Proje

1

Tez Danışmanlığı

6

Açık Erişim

3