Publications & Works

Published journal articles indexed by SCI, SSCI, and AHCI
Articles Published in Other Journals
Refereed Congress / Symposium Publications in Proceedings

A Novel NPR2 Mutation in Two Turkish Siblings with Acromesomelic Dysplasia Maroteaux Type

14.Ulusal Tıbbi Genetik Kongresi “Uluslararası Katılımlı”, Ankara, Turkey, 20 - 22 November 2020, pp.69 Creative Commons License

14. ULUSAL TIBBİ GENETİK KONGRESİ “Uluslararası Katılımlı”, Ankara, Turkey, 20 - 22 November 2020, pp.23 Creative Commons License

A case of myhre syndrome with a very rare finding: Severe constipation

V. International Participated Erciyes Medical Genetics Days Congress, Kayseri, Turkey, 20 - 22 February 2020, pp.38

Farklı Nano-Kalsiyum Fosfat Nanopartiküllerin Sentezi ve Ġ n V tro Toksisite Değerlendirmesi

6. Uluslararası Bilimsel AraĢtırmalar Kongresi, Şanlıurfa, Turkey, 1 - 03 November 2019, pp.14-15

Stuve-Wiedemann syndrome: a case report without osteorosis

58th Annual Meeting of the ESPE , Vienna, Austria, 19 - 21 September 2019, pp.378-379 Creative Commons License identifier

COMPARATIVE EVALUATION OF ANTI-ALZHEIMER ACTIVITY BY L- AND D-PENICILLAMINE

International Muldisciplinary Symposium on Drug Research Development (DRD 2019), Malatya, Turkey, 1 - 03 July 2019

An Inherited Novel FGFR2 Variant: A Case Report

13.BALKAN GENETİK KONGRESİ, Edirne, Turkey, 17 - 20 April 2019, pp.136

An Inherited Novel FGFR2 Variant: A Case Report

13.BALKAN GENETİK KONGRESİ, Edirne, Turkey, 17 - 20 April 2019, pp.136

Coronal Synostosis Syndrome (Muenke Syndrome)

13.BALKAN GENETİK KONGRESİ, Edirne, Turkey, 17 - 20 April 2019, pp.143

Coronal Synostosis Syndrome (Muenke Syndrome)

13.BALKAN GENETİK KONGRESİ, Edirne, Turkey, 17 - 20 April 2019, pp.143

Orofaciodigital syndrome XVII: A rare case report

Uluslararası Katılımlı Erciyes Tıp Genetik Günleri 2019, Kayseri, Turkey, 21 - 23 February 2019, pp.42

A case of Rubinstein Taybisyndrome with a very rare finding;Dandy Walker malformation

Uluslararası Katılımlı Erciyes Tıp Genetik Günleri 2019, Kayseri, Turkey, 21 - 23 February 2019, pp.42

Orofaciodigital syndrome XVII:A rare case report

Uluslararası Katılımlı Erciyes Tıp Genetik Günleri 2019, Kayseri, Turkey, 21 - 23 February 2019, pp.42

45,X and SRY positive male with infertility: A case report

Uluslararası Katılımlı Erciyes Tıp Genetik Günleri 2019, Kayseri, Turkey, 21 - 23 February 2019, pp.52-53

A case of Cri du Chat syndrome

Uluslararası Katılımlı Erciyes Tıp Genetik Günleri 2019, Kayseri, Turkey, 21 - 23 February 2019, pp.43

A case of Rubinstein Taybi syndrome with a very rare finding; Dandy Walker malformation

Uluslararası Katılımlı Erciyes Tıp Genetik Günleri 2019, Kayseri, Turkey, 21 - 23 February 2019, pp.42

45,X and SRY positive male withinfertility: A case report

Uluslararası Katılımlı Erciyes Tıp Genetik Günleri 2019, Kayseri, Turkey, 21 - 23 February 2019, pp.52-53

A case of Cri du Chat syndrome

Uluslararası Katılımlı Erciyes Tıp Genetik Günleri 2019, Kayseri, Turkey, 21 - 23 February 2019, pp.43

Nadir Bir Genetik Hastalık Olan Kleidokranial Displazi Olgu Sunumu

Uluslararası Katılımlı 13. Ulusal Tıbbi Genetik Kongresi, Turkey, 7 - 11 November 2018

A Case of Two Siblings with VLDLR-Associated Cerebellar Hypoplasia.

Uluslararası Katılımlı 13. Ulusal Tıbbi Genetik Kongresi, Turkey, 7 - 11 November 2018

A Case Report of Rarely Genetic Condition Cleidocranial Dysplasia

ULUSLARARASI KATILIMLI 13.ULUSAL TIBBİ GENETİK KONGRESİ, Turkey, 7 - 11 November 2018, vol.30, pp.95

Nickel boride nanoparticle toxicity and microarray analysis on human pulmonary alveolar cells

International Multidisciplinary Symposium on Drug Research and Development, Erzurum, Turkey, 5 - 07 October 2017

Toxico-genomic approaches of cobalt boride nanoparticles on human pulmonary alveolar cells

19th International Conference on Healthcare Life-Science Research (ICHLSR), 28-29 July 2017,Barcelona, Spain, 28 - 29 July 2017

Viability and apoptotic activation of melatonin-treated human breast cancer cells.

15th International Congress of Histochemistry and Cytochemistry (ICHC 2017), Antalya, Turkey, 18 - 21 May 2017 Sustainable Development

Supplementation of Propolis Protects Human Lymphocytes in vitro from the Genotoxic Damage by Imazalil

I. International Congress on Medicinal and Aromatic Plants ”Natural and Healthy Life, 10 - 12 May 2017, pp.79

Boron Compounds Ameliorates the Human Alveolar Epithelial Cell Death Induced by 2 3 7 8 Tetrachlorodibenzo P Dioxin

1st International Mediterranean Science and Engineering Congress (IMSEC 2016), 26 - 28 October 2016

Genotoxic and Cytotoxic Responses to Tellurium Dioxide Nanoparticles In Vitro Protection by Boric Acid

3rd International Conference on Advanced Technology and Sciences (ICAT'16), 1 - 03 September 2016

Boron Compounds Counteracts Oxidative Stress Mediated Genotoxicity Induced By Fe3O4 Nanoparticles In Vitro

2nd International Conference on Advanced Engineering Technology (2nd ICAET) by Incheon National University, 11 - 13 December 2015

Boron compounds counteracts oxidative stress mediated genotoxicity induced by Fe3O4 nanoparticles in vitro

2nd international conference on advanced engineering technology (2nd ICAET), Incheon, South Korea, 11 - 13 December 2015

Kronik otitis medialı hastalarda mtDNA delesyonlarının araştırılması

36. Türk Ulusal Kulak Burun Boğaz ve Baş Boyun Cerrahisi kongresi, Antalya, Turkey, 5 - 08 November 2014

Auralı Migren ile GABA Reseptörleri Arasındaki İlişki.

11.Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.164

Kronik otitis mediadaki işitme kaybının sebebi mitokondriyal DNA delesyonları olabilir mi

11. Uluslararası Kulak Burun Boğaz ve Baş Boyun Cerrahisi kongresi, 17 - 19 April 2014

Asrosite/Neuron Ratio And Its Importance On Glutamate Toxicity

8th FENS Forum of Neuroscience, Barselona, Spain, 14 - 18 July 2012, vol.6, pp.140

THE EFFECTS OF ASCORBIC ACID ON LISTERINE TOXICITY IN VITRO

INTERNATIONAL SYMPOSIUM ON DRUG RESEARCH AND DEVELOPMENT, Turkey, 27 - 29 May 2011

The genotoxic potentials of some atypic anthipsychotic drugs on human lymphocytes

International Symposium on Drug Research and Development “From Chemistry to Medicine, 27 - 29 May 2011

Translocated X inactivation in a patient with t(X;19)

9th National Medical Genetics Congress of Turkish Medical Genetics Society with International Participation, İstanbul, Turkey, 1 - 05 December 2010, pp.118-119

A case with Crouzon syndrome without craniosynostosis

9th National Medical Genetics Congress of Turkish Medical Genetics Society with International Participation, İstanbul, Turkey, 1 - 05 December 2010, pp.34

Translocated X inactivation in a patient with t(X;19)

9th National Medical Genetics Congress of Turkish Medical Genetics Society with International Participation, İstanbul, Turkey, 1 - 05 December 2010, pp.118-119

A case with Crouzon syndrome without craniosynostosis

9th National Medical Genetics Congress of Turkish Medical Genetics Society with International Participation, İstanbul, Turkey, 1 - 05 December 2010, pp.34

A case with Cri du chat syndrome and 45,XX, der(5) t(521)(p13q10), -21 karyotype.

9th National Medical Genetics Congress of Turkish Medical Genetics Society with International Participation, İstanbul, Turkey, 1 - 05 December 2010, pp.119

A case with Cri du chat syndrome and 45,XX, der(5) t(521)(p13q10), -21 karyotype.

9th National Medical Genetics Congress of Turkish Medical Genetics Society with International Participation, İstanbul, Turkey, 1 - 05 December 2010, pp.119

Genotoxic and biochemical effects of wastewater samples from a local fat plant in Erzurum Turkey

BIES08: Blacksea International Environmental Symposium, 25-29 August 2008, 187, Giresun, TURKEY., Giresun, Turkey, 25 - 29 August 2008

Mozaik olmayan 49 XYYYY karyotipli bir vaka

8. Ulusal Tıbbi Genetik Kongresi, Çanakkale, Turkey, 6 - 09 May 2008

Familial t 2 5 in a Patient with micropenis

6. European Cytogenetics Conference, 7 - 10 July 2007, vol.15, pp.82-83

Homozygous inv(5) in a family with recurrent fetal loses

6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, vol.15, pp.39 identifier

Translocation (X;2) in a patient with premature ovarian failure

6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, vol.15, pp.59-60 identifier

Familial T(12;21) followed through four generations

6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, vol.15, pp.59 identifier
Books & Book Chapters

Alzheimer Hastalığı ve Herediter Demanslar

in: Nörogenetikte Güncel Gelişmeler, Çam Fethi Sırrı, Editor, Türkiye Klinikleri, Ankara, pp.6-11, 2023

MİTOKONDRİ, MİTOKONDRİYAL DNA VE HASTALIKLARI

in: TIBBİ GENETİK VE KLİNİK UYGULAMALARI, MUNİS DÜNDAR, Editor, MGRUP MATBAACILIK, Kayseri, pp.163-176, 2016
Metrics

Publication

190

Citation (WoS)

857

H-Index (WoS)

15

Citation (Scopus)

1036

H-Index (Scopus)

17

Citation (Scholar)

22

H-Index (Scholar)

2

Citiation (Sum Other)

2

Project

9

Thesis Advisory

2

Open Access

14
UN Sustainable Development Goals