Publications & Works

Publication Network
Articles 30
All (30)
SCI-E, SSCI, AHCI (12)
SCI-E, SSCI, AHCI, ESCI (14)
ESCI (2)
Scopus (14)
TRDizin (6)
Other Publications (12)

1. Cytogenetic findings in children with postnatal growth retardation.

Demirhan O., Tanrıverdi N., Demirhan Ö. F., Süleymanova D.
Global Journal of Medical Research: F Diseases , vol.19, no.6, pp.11-14, 2019 (Peer-Reviewed Journal) Creative Commons License

2. Frequency and types of chromosomal abnormalities in acute lymphoblastic leukemia patients in Turkey

Demirhan O., Tanrıverdi N., Süleymanova D.
Arca Community Med Public Health , vol.5, no.2, pp.55-61, 2019 (Scopus) Creative Commons License

3. ”Chromosomal alterations in patients with breast cancer”,

DEMİRHAN O., TANRIVERDİ N., PAZARBAŞI A., süleymanova D.
European Journal Of Human Genetics , vol.26, pp.536, 2018 (SCI-Expanded, Scopus) Sustainable Development

4. Frequencies and distributions of sex chromosome abnormalities in females with the Turner phenotype: a long-term retrospective study in the southern region of Turkey

TANRıVERDI N., Demirhan O., SÜLEYMANOVA D., PAZARBAŞı A.
Turkish journal of medical sciences , vol.47, pp.1447-1455, 2017 (SCI-Expanded, Scopus, TRDizin) identifier identifier identifier

5. Frequencies and distributions of sex chromosome abnormalities in females with Turner phenotype in south region of Turkey.

TANRIVERDİ N., DEMİRHAN O., süleymanova D., PAZARBAŞI A.
Turkish Journal Of Medical Sciences , vol.47, no.5, pp.1445-1457, 2017 (SCI-Expanded, Scopus, TRDizin)

6. Chromosomal aberrations in Turkish infertile couples with reproductive problems

DEMİRHAN O., TANRIVERDİ N., SÜLEYMANOVA D.
Global Journal of Fertility and Research , vol.1, pp.6-10, 2016 (Peer-Reviewed Journal)

7. Chromosomal Analysis of Couples with Bad Obstetric History

DEMİRHAN O., TANRIVERDİ N., SÜLEYMANOVA D.
Journal of Clinical Developmental Biology , vol.1, pp.16, 2016 (Peer-Reviewed Journal)

8. Chromosomal analyses of 1510 couples who have experienced recurrent spontaneous abortions

TUNÇ E., TANRIVERDİ N., DEMİRHAN O., SÜLEYMANOVA D., ÇETİNEL N.
REPRODUCTIVE BIOMEDICINE ONLINE , vol.32, no.4, pp.414-419, 2016 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

9. Chromosomal aberrations in Turkish infertile couples with reproductive problems”, , vol.1, pp.6-10, 2016

DEMİRHAN O., TANRIVERDİ N., süleymanova D.
Global Journal of Fertility and Research , vol.1, pp.6-10, 2016 (Peer-Reviewed Journal)

10. Demirhan O., Tanriverdi N., Süleymanova D., ”Chromosomal Analysis of Couples with Bad Obstetric History

DEMİRHAN O., TANRIVERDİ N., süleymanova D.
Journal of Clinical Developmental Biology, , vol.1, pp.16-19, 2016 (Peer-Reviewed Journal)

11. Report of a new case with pentasomy X and novel clinical findings.

DEMİRHAN O., TANRIVERDİ N., YILMAZ M. B., KOCATÜRK SEL S., LÜLEYAP H. Ü.
BALKAN JOURNAL OF MEDICAL GENETICS , vol.18, no.1, pp.85-92, 2015 (SCI-Expanded, Scopus)

12. Report of a new case with pentasomy X and novel clinical findings.

DEMİRHAN O., TANRIVERDİ N., YILMAZ M. B., KOCATÜRK SEL S., LÜLEYAP H. Ü.
BALKAN JOURNAL OF MEDICAL GENETICS , vol.18, no.1, pp.85-92, 2015 (SCI-Expanded, Scopus)

13. Report of a new case with pentasomy X and novel clinical findings.

DEMİRHAN O., tanrıverdi n., Yilmaz M., Kocaturk-Sel S., Inandiklioglu N.
Balkan J Med Genet. , vol.18, no.1, pp.85-92, 2015 (Peer-Reviewed Journal)

14. The frequency and types of chromosomal aberrations in the patients with hypogonodism

DEMİRHAN O., TANRIVERDİ N., SÜLEYMANOVA D., ÇETİNEL N., Yaşar Y.
Human Genetics and Embryology , vol.5, pp.124-129, 2015 (Peer-Reviewed Journal)

15. REPORT OF A NEW CASE WITH PENTASOMY X AND NOVEL CLINICAL FINDINGS

DEMİRHAN O., TANRIVERDİ N., YILMAZ M., Kocaturk-Sel S., INANDIKLIOGLU N., Luleyap U., et al.
BALKAN JOURNAL OF MEDICAL GENETICS , vol.18, no.1, pp.85-92, 2015 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

16. Demirhan O., Tanriverdi N., Süleymanova D., Çetinel N., Yaşar Y., ”The frequency and types of chromosomal aberrations in the patients with hypogonodism”,

DEMİRHAN O., TANRIVERDİ N., süleymanova D., ÇETİNEL N.
Human Genetics and Embryology , vol.5, pp.124-129, 2015 (Peer-Reviewed Journal)

17. Frequency and Types of Chromosomal Abnormalities in Turkish Women with Amenorrhea

DEMİRHAN O., TANRIVERDİ N., TUNC E., INANDIKIOGLU N., SULEYMANOVA D.
JOURNAL OF PEDIATRIC AND ADOLESCENT GYNECOLOGY , vol.27, no.5, pp.274-277, 2014 (SCI-Expanded, Scopus) Sustainable Development identifier identifier identifier

18. INHERITANCE OF A CHROMOSOME 3 AND 21 TRANSLOCATION IN THE FETUSES, WITH ONE ALSO HAVING TRISOMY 21, IN THREE PREGNANCIES IN ONE FAMILY

PAZARBAŞI A., DEMİRHAN O., ALPTEKİN D., ÖZGÜNEN F. T., ÖZPAK L., YILMAZ M., et al.
BALKAN JOURNAL OF MEDICAL GENETICS , vol.16, no.2, pp.91-96, 2013 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

19. A newborn with klinefelter and trisomy 18 syndrome: Case report

OZLU F., Yapicioǧlu H., SATAR M., NARLI N., ÖZCAN K., TANRIVERDİ N., et al.
Turkiye Klinikleri Pediatri , vol.21, no.3, pp.173-174, 2012 (Scopus) identifier

20. THE CLINICAL EFFECTS OF ISOCHROMOSOME Xq IN KLINEFELTER SYNDROME: REPORT OF A CASE AND REVIEW OF LITERATURE

DEMİRHAN O., PAZARBAŞI A., TANRIVERDİ N., ARIDOGAN A., KARAHAN D.
GENETIC COUNSELING , vol.20, no.3, pp.235-242, 2009 (SCI-Expanded, Scopus) identifier identifier identifier

21. THE EFFECT OF A DE NOVO PERICENTRIC INVERSION (10)(p11.1;q22.1) ON AGGRESSIVE BEHAVIOR AND HYPERACTIVITY

Demirhan O., PAZARBAŞI A., TUNC E., KARAHAN D., TANRIVERDI N., AVCI A., et al.
GENETIC COUNSELING , vol.20, no.1, pp.69-71, 2009 (SCI-Expanded, Scopus) identifier identifier identifier

22. Yarık dudak ve yarık damak görülen çocuklarda Klienfelter Sendromu ve genetik danışmanlık: İki vaka sunumu.

SÜLEYMANOVA D., NARLI N., DEMİRHAN O., YAPICIOĞLU YILDIZDAŞ H., TANRIVERDİ N., SATAR M.
Türkiye Klinikleri Tıp Bilimleri Dergisi , vol.22, no.3, pp.297-300, 2002 (TRDizin)

23. Cinsiyet Gelişim Bozukluğu Olan Çocuklarda Kromozom Düzensizlikleri. 1999, 24:153-157.

DEMİRHAN O., Süleymanova D., tanrıverdi n.
Ç.Ü. Tıp Fak. Derg. , vol.24, pp.153-157, 1999 (Peer-Reviewed Journal)

24. Cinsiyet Gelişim Bozukluğu Olan Çocuklarda Kromozom Düzensizlikleri

DEMİRHAN O., süleymanova D., TANRIVERDİ N.
CUKUROVA MEDICAL JOURNAL , vol.24, pp.153-157, 1999 (TRDizin)

25. Results of cytogenetic investigation in adolescent patients with primary or secondary amenorrhea.

TEMOÇIN K., VARDAR M. A., SÜLEYMANOVA D., OZER E., TANRıVERDI N., Demirhan O., et al.
Journal of pediatric and adolescent gynecology , vol.10, pp.86-8, 1997 (SCI-Expanded, Scopus) identifier identifier identifier

26. Down Sendromlu Çocuklar Ve Ailelerinde Genetik Araştırmalar

Süleymanova D., Temoçin K., tanrıverdi n., DEMİRHAN O.
Ç.Ü. Tıp Fak. Derg. , vol.20, pp.75-79, 1995 (Peer-Reviewed Journal)

27. Cri-Du-Chat" Sendromunda Fenotipik Bulgulara Göre Tanı Konma Zorluğu

DEMİRHAN O., Süleymanova D., tanrıverdi n., ark. v.
Ç.Ü.Tıp Fakültesi Derg. , vol.20, no.4, pp.235-239, 1995 (Peer-Reviewed Journal)

28. Dismorfogenezle Yeni Doğan Bebeğin Tanısında Sitogenetik Araştırmanın Önemi

Süleymanova D., tanrıverdi n., DEMİRHAN O., ark. v.
Ç.Ü. Tıp Fak. Derg. , vol.20, no.4, pp.230-234, 1995 (Peer-Reviewed Journal)

29. Demirhan O, Süleymanova D, Tanrıverdı N, Önenlı N, Duman N.”Cri-Du-Chat” Sendromunda Fenotipik Bulgulara Göre Tanı Konma Zorluğu

DEMİRHAN O., süleymanova D., TANRIVERDİ N.
CUKUROVA MEDICAL JOURNAL , vol.20, no.4, pp.235-239, 1995 (ESCI, TRDizin)

30. Ellis-Van Creveld Sendromu (Chondroectodermal Dypl

Temoçin K., DEMİRHAN O., TANRIVERDİ N.
CUKUROVA MEDICAL JOURNAL , vol.19, pp.234-238, 1994 (ESCI, TRDizin)
Papers Presented at Peer-Reviewed Scientific Conferences 15

1. Chromosomal Abnormalities identified at prenatal diagnosis

PAZARBAŞI A., DEMİRHAN O., LÜLEYAP H. Ü., ÖZPAK L., ILGAZ N. S., USLU İ. N., et al.
Innovation in Medicine Meeting 4, Gaziantep, Turkey, 11 - 13 October 2018, pp.60-69, (Full Text)

2. Amniyosentez iile prenatal tanı konulan 7821 olguda kromozom analizi sonuçları

PAZARBAŞI A., DEMİRHAN O., LÜLEYAP H. Ü., ÖZPAK L., ILGAZ N. S., USLU İ. N., et al.
15.Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Muğla, Turkey, 26 - 29 October 2017, (Summary Text)

3. Chromosomal alteraĕons in paĕents with breast cancer

DEMİRHAN O., TANRIVERDİ N., PAZARBAŞI A.
Eurpean Human Genetics Conference, Kopenhag, DANIMARKA, 27 - 30 May 2017, (Full Text) Sustainable Development

4. Chromosomal alteration in patients with breast cancer

DEMİRHAN O., tanrıverdi n., Süleymanova D.
Eurpean Human Genetics Conference, Kpenhag, Denmark, 27 May 2017 - 30 June 2015, vol.P12, pp.454, (Full Text) Sustainable Development

5. Results of Karyotype Analysis of 7766 Pregnancies Prenataly Identified with Amniocentesis in Turkey

PAZARBAŞI A., DEMİRHAN O., LÜLEYAP H. Ü., ÖZPAK L., Ilgaz N. S., USLU İ. N., et al.
Innovation in Medicine Meetings 3, Gaziantep, Turkey, 11 - 13 May 2017, (Summary Text)

6. . Frequencies and distributions of sex chromosome abnormalities in females with Turner phenotype in south region of Turkey.

TANRIVERDİ N., DEMİRHAN O., süleymanova D., PAZARBAŞI A.
SANKO ün. Innovation in medicine, 11 - 13 May 2017, (Summary Text)

7. Turner fenotipine sahip kadınlardaki cinsiyet kromozomu anomalilerinin sıklık ve dağılımları uzun süreli retrospektif çalışma

TANRIVERDİ N., DEMİRHAN O., süleymanova D., PAZARBAŞI A.
Innovation in Medicine Meetings 3, Turkey, 11 - 13 May 2017, pp.70, (Summary Text) Sustainable Development

8. Turner fenotipine sahip kadınlardaki cinsiyet kromozomu anomalilerinin sıklık ve dağılımları; uzun süreli retrospektif çalışma. Innovation in Medicine Meetings 3, May 11-13, 2017. Innovation summit book 2017; pp: 70. The University of Sanko, GAZİANTEP/TURKEY.

tanrıverdi n., DEMİRHAN O., ark. v.
Innovation in Medicine Meetings 3, Gaziantep, Turkey, 11 - 13 May 2017, pp.70, (Full Text) Sustainable Development

9. Chromosomal Abnormalities Identified at Prenatal Diagnosis of 7050 Pregnancies in Turkey Pregnancy Summit 2014 October 6 8 th London UK

PAZARBAŞI A., LÜLEYAP H. Ü., ALPTEKİN D., ÖZPAK L., ILGAZ N. S., USLU İ. N., et al.
Pregnancy Summit, 6 - 08 October 2014, (Summary Text)

10. Amniyosentez ile tanı prenatal tanı konulan 5671 olguda sitogenetik bulgular

PAZARBAŞI A., ALPTEKİN D., TUNÇ E., TANRIVERDİ N., DEMİRHAN O., Özgünen F. T., et al.
10. Ulusal Tıbbi Genetik Kongresi, Turkey, 19 - 23 December 2012

11. ?Lenfosit Kültürü ile Tanı Konulan 5800 Olgunun Karyotip Sonuçlarının Değerlendirilmesi

Tanrıverdi N., DEMİRHAN O., ark. v.
10. Ulusal Tıbbi Genetik Kongresi,, Bursa, Turkey, 19 - 23 December 2012, pp.26, (Full Text)

12. Amniyosentez Ile Prenatal Tanı Konulan 5671 Olguda Sitogennetik Bulgular

PAZARBAŞI A., ALPTEKİN D., TUNÇ E., TANRIVERDİ N., DEMİRHAN O., ÖZGÜNEN F. T., et al.
10. Ulusal Tıbbi Genetik Kongresi, Bursa, Turkey, 19 - 23 September 2012, vol.PB0177, pp.63, (Full Text)

13. "Genetic Polymorphisms In The Estrogen Receptor Alpha Gene In Turkish Patients With Familial Prostate Carcinoma"

PAZARBAŞI A., ALPTEKİN D., LÜLEYAP H. Ü., TANSUG Z., IZMIRLI M., YILMAZ M. B., et al.
IV. International Congress of Molecular Medicine, İstanbul, Turkey, 27 - 30 June 2011, vol.231, pp.97-98, (Full Text)

14. Perisentrik İnversiyon (10)(p11.1;q22.1)?un Agresif Davranış ve Hiperaktivite Üzerine Etkisi

PAZARBAŞI A., DEMİRHAN O., TANRIVERDİ N., AVCI A., YOLGA TAHİROĞLU A.
19. Ulusal Ulusal Çocuk ve Ergen Ruh Sağlığı ve Hastalıkları Kongresi, Hatay, Turkey, 14 - 16 April 2009, pp.134, (Full Text)

15. Atipik Yüz Görünümü Ve Zeka Geriliği Olan Bir Olguda Homolog Olmayan İki Kromozomun Her İki Eşleri Arasındaki Translokasyonun [T(16;19)(q24;q12)X2] Varlığı.

Tanrıverdi N., Süleymenova D., DEMİRHAN O., ark. v.
VIII. Ulusal Tıbbi Genetik Kongresi,, Çanakkale, Turkey, 6 - 09 May 2008, pp.160, (Full Text)
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45

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14

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14

Citation (WoS)

33

H-Index (WoS)

3

Citation (Scopus)

53

H-Index (Scopus)

4

Open Access

5
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