Yayınlar & Eserler

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler
Diğer Dergilerde Yayınlanan Makaleler
Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

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

14.Ulusal Tıbbi Genetik Kongresi “Uluslararası Katılımlı”, Ankara, Türkiye, 20 - 22 Kasım 2020, ss.69 Creative Commons License

Myeloid Malignitesi Olan Hastalarda NGS Temelli Panel Test Kullanımı ve Sonuçları

14. ULUSAL TIBBİ GENETİK KONGRESİ “Uluslararası Katılımlı”, Ankara, Türkiye, 20 - 22 Kasım 2020, ss.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, Türkiye, 20 - 22 Şubat 2020, ss.38

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

6. Uluslararası Bilimsel AraĢtırmalar Kongresi, Şanlıurfa, Türkiye, 1 - 03 Kasım 2019, ss.14-15

Stuve-Wiedemann syndrome: a case report without osteorosis

58th Annual Meeting of the ESPE , Vienna, Avusturya, 19 - 21 Eylül 2019, ss.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, Türkiye, 1 - 03 Temmuz 2019

An Inherited Novel FGFR2 Variant: A Case Report

13.BALKAN GENETİK KONGRESİ, Edirne, Türkiye, 17 - 20 Nisan 2019, ss.136

An Inherited Novel FGFR2 Variant: A Case Report

13.BALKAN GENETİK KONGRESİ, Edirne, Türkiye, 17 - 20 Nisan 2019, ss.136

Coronal Synostosis Syndrome (Muenke Syndrome)

13.BALKAN GENETİK KONGRESİ, Edirne, Türkiye, 17 - 20 Nisan 2019, ss.143

Coronal Synostosis Syndrome (Muenke Syndrome)

13.BALKAN GENETİK KONGRESİ, Edirne, Türkiye, 17 - 20 Nisan 2019, ss.143

Orofaciodigital syndrome XVII: A rare case report

Uluslararası Katılımlı Erciyes Tıp Genetik Günleri 2019, Kayseri, Türkiye, 21 - 23 Şubat 2019, ss.42

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

Uluslararası Katılımlı Erciyes Tıp Genetik Günleri 2019, Kayseri, Türkiye, 21 - 23 Şubat 2019, ss.42

Orofaciodigital syndrome XVII:A rare case report

Uluslararası Katılımlı Erciyes Tıp Genetik Günleri 2019, Kayseri, Türkiye, 21 - 23 Şubat 2019, ss.42

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

Uluslararası Katılımlı Erciyes Tıp Genetik Günleri 2019, Kayseri, Türkiye, 21 - 23 Şubat 2019, ss.52-53

A case of Cri du Chat syndrome

Uluslararası Katılımlı Erciyes Tıp Genetik Günleri 2019, Kayseri, Türkiye, 21 - 23 Şubat 2019, ss.43

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

Uluslararası Katılımlı Erciyes Tıp Genetik Günleri 2019, Kayseri, Türkiye, 21 - 23 Şubat 2019, ss.42

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

Uluslararası Katılımlı Erciyes Tıp Genetik Günleri 2019, Kayseri, Türkiye, 21 - 23 Şubat 2019, ss.52-53

A case of Cri du Chat syndrome

Uluslararası Katılımlı Erciyes Tıp Genetik Günleri 2019, Kayseri, Türkiye, 21 - 23 Şubat 2019, ss.43

Nadir Bir Genetik Hastalık Olan Kleidokranial Displazi Olgu Sunumu

Uluslararası Katılımlı 13. Ulusal Tıbbi Genetik Kongresi, Türkiye, 7 - 11 Kasım 2018

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

Uluslararası Katılımlı 13. Ulusal Tıbbi Genetik Kongresi, Türkiye, 7 - 11 Kasım 2018

A Case Report of Rarely Genetic Condition Cleidocranial Dysplasia

ULUSLARARASI KATILIMLI 13.ULUSAL TIBBİ GENETİK KONGRESİ, Türkiye, 7 - 11 Kasım 2018, cilt.30, ss.95

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

International Multidisciplinary Symposium on Drug Research and Development, Erzurum, Türkiye, 5 - 07 Ekim 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 Temmuz 2017

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

15th International Congress of Histochemistry and Cytochemistry (ICHC 2017), Antalya, Türkiye, 18 - 21 Mayıs 2017 Sürdürülebilir Kalkınma

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 Mayıs 2017, ss.79

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 Eylül 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 Aralık 2015

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

2nd international conference on advanced engineering technology (2nd ICAET), Incheon, Güney Kore, 11 - 13 Aralık 2015

Kronik otitis medialı hastalarda mtDNA delesyonlarının araştırılması

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

Auralı Migren ile GABA Reseptörleri Arasındaki İlişki.

11.Ulusal Tıbbi Genetik Kongresi, İstanbul, Türkiye, 24 - 27 Eylül 2014, ss.164

Kronik otitis mediadaki işitme kaybının sebebi mitokondriyal DNA delesyonları olabilir mi

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

Asrosite/Neuron Ratio And Its Importance On Glutamate Toxicity

8th FENS Forum of Neuroscience, Barselona, İspanya, 14 - 18 Temmuz 2012, cilt.6, ss.140

Determination of Cisplatin Induced Neurotoxicity in New Born rat Neuron Culture

4. cell membranes and free radical research, Isparta, Türkiye, 11 - 13 Haziran 2012, cilt.4

THE EFFECTS OF ASCORBIC ACID ON LISTERINE TOXICITY IN VITRO

INTERNATIONAL SYMPOSIUM ON DRUG RESEARCH AND DEVELOPMENT, Türkiye, 27 - 29 Mayıs 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 Mayıs 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, Türkiye, 1 - 05 Aralık 2010, ss.118-119

A case with Crouzon syndrome without craniosynostosis

9th National Medical Genetics Congress of Turkish Medical Genetics Society with International Participation, İstanbul, Türkiye, 1 - 05 Aralık 2010, ss.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, Türkiye, 1 - 05 Aralık 2010, ss.118-119

A case with Crouzon syndrome without craniosynostosis

9th National Medical Genetics Congress of Turkish Medical Genetics Society with International Participation, İstanbul, Türkiye, 1 - 05 Aralık 2010, ss.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, Türkiye, 1 - 05 Aralık 2010, ss.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, Türkiye, 1 - 05 Aralık 2010, ss.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, Türkiye, 25 - 29 Ağustos 2008

Mozaik olmayan 49 XYYYY karyotipli bir vaka

8. Ulusal Tıbbi Genetik Kongresi, Çanakkale, Türkiye, 6 - 09 Mayıs 2008

Familial t 2 5 in a Patient with micropenis

6. European Cytogenetics Conference, 7 - 10 Temmuz 2007, cilt.15, ss.82-83

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

6th European Cytogenetics Conference, İstanbul, Türkiye, 7 - 10 Temmuz 2007, cilt.15, ss.39 identifier

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

6th European Cytogenetics Conference, İstanbul, Türkiye, 7 - 10 Temmuz 2007, cilt.15, ss.59-60 identifier

Familial T(12;21) followed through four generations

6th European Cytogenetics Conference, İstanbul, Türkiye, 7 - 10 Temmuz 2007, cilt.15, ss.59 identifier

Spontaneous fetal losses in a family with t(1;8): an evidence of Malsegregation

6th European Cytogenetics Conference, İstanbul, Türkiye, 7 - 10 Temmuz 2007, cilt.15, ss.83 identifier
Kitap & Kitap Bölümleri

Alzheimer Hastalığı ve Herediter Demanslar

Nörogenetikte Güncel Gelişmeler, Çam Fethi Sırrı, Editör, Türkiye Klinikleri, Ankara, ss.6-11, 2023

MİTOKONDRİ, MİTOKONDRİYAL DNA VE HASTALIKLARI

TIBBİ GENETİK VE KLİNİK UYGULAMALARI, MUNİS DÜNDAR, Editör, MGRUP MATBAACILIK, Kayseri, ss.163-176, 2016
Metrikler

Yayın

189

Atıf (WoS)

857

H-İndeks (WoS)

15

Atıf (Scopus)

1029

H-İndeks (Scopus)

17

Atıf (Scholar)

2

H-İndeks (Scholar)

1

Atıf (Diğer Toplam)

2

Proje

9

Tez Danışmanlığı

2

Açık Erişim

14
BM Sürdürülebilir Kalkınma Amaçları