Yayınlar & Eserler

Yayın Ağı
Makaleler 13
Tümü (13)
SCI-E, SSCI, AHCI (13)
SCI-E, SSCI, AHCI, ESCI (13)
Scopus (13)

1. A case series of joubert syndrome evaluated with whole exome sequencing and the utility of optical genome mapping in the diagnosis

KİRAZ A., Erdogan M., Balta B., GÜMÜŞ H., Mutlu M. B., MAMMADOVA N., et al.
Neurogenetics , cilt.26, sa.1, 2025 (SCI-Expanded, Scopus) identifier identifier identifier identifier

2. Contribution of genotypes in Prothrombin and Factor V Leiden to COVID-19 and disease severity in patients at high risk for hereditary thrombophilia.

Kiraz A., Sezer O., ALEMDAR A., Canbek S., Duman N., BİŞGİN A., et al.
Journal of medical virology , cilt.95, sa.2, 2023 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

3. Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium

DÜNDAR M., FAHRİOGLU U., Yildiz S. H., Bakir-Gungor B., TEMEL Ş. G., AKIN H., et al.
FUNCTIONAL & INTEGRATIVE GENOMICS , cilt.22, sa.3, ss.291-315, 2022 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

4. Increased vitamin D receptor gene expression and rs11568820 and rs4516035 promoter polymorphisms in autistic disorder

Balta B., GÜMÜŞ H., BAYRAMOV R., Bayramov K. K., Erdogan M., Oztop D. B., et al.
MOLECULAR BIOLOGY REPORTS , cilt.45, sa.4, ss.541-546, 2018 (SCI-Expanded, Scopus) identifier identifier identifier

5. Interstitial deletion 5p14.1-p15.2 and 5q14.3-q23.2 in a patient with clubfoot, blepharophimosis, arthrogryposis, and multiple congenital abnormalities

Balta B., Erdogan M., Ergul A. B., SAHİN Y., ÖZCAN A.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A , cilt.173, sa.10, ss.2798-2802, 2017 (SCI-Expanded, Scopus) identifier identifier identifier

6. The Association of Brain-Derived Neurotrophic Factor Gene Polymorphism with Obstructive Sleep Apnea Syndrome and Obesity

Yuksekkaya M., TUTAR N., Buyukoglan H., DÜNDAR M., YILMAZ I., GÜLMEZ I., et al.
LUNG , cilt.194, sa.5, ss.839-846, 2016 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

7. Prenatal diagnosis of intestinal volvulus in a foetus with homozygous M470V cystic fibrosis gene polymorphism

KUTUK M., BALTA B., DOĞANAY S., Guzel M., ÖZGÜN M. T.
Journal of Obstetrics and Gynaecology , cilt.35, sa.5, ss.522-525, 2015 (SCI-Expanded, Scopus) identifier identifier identifier

8. A c.1244G>A (p.Arg415Gln) mutation in SH3BP2 gene causes cherubism in a Turkish family: Report of a family with review of the literature

SEKERCI A., Balta B., DÜNDAR M., Hu Y., Reichenberger E., ETOZ O., et al.
MEDICINA ORAL PATOLOGIA ORAL Y CIRUGIA BUCAL , cilt.19, sa.4, 2014 (SCI-Expanded, Scopus) Creative Commons License identifier identifier

9. Is there relation between COL4A1/A2 mutations and antenatally detected fetal intraventricular hemorrhage?

Kutuk M. S., Balta B., Kodera H., Matsumoto N., Saitsu H., Doganay S., et al.
CHILDS NERVOUS SYSTEM , cilt.30, sa.3, ss.419-424, 2014 (SCI-Expanded, Scopus) identifier identifier identifier

10. AN UNCOMMON CAUSE OF INFERTILITY: Y;1 TRANSLOCATION AND PGD TRIAL

DÜNDAR M., Balta B., Bahadir O., Acar H., BAYDİLLİ N., Baltaci V., et al.
GENETIC COUNSELING , cilt.25, sa.3, ss.353-355, 2014 (SCI-Expanded, Scopus) identifier identifier

11. The role of TNF-alpha and PAI-1 gene polymorphisms in familial Mediterranean fever

DÜNDAR M., Kiraz A., Balta B., Emirogullari E. F., ZARARSIZ G., Yurci A., et al.
MODERN RHEUMATOLOGY , cilt.23, sa.1, ss.140-145, 2013 (SCI-Expanded, Scopus) identifier identifier identifier

12. The Role of TNF-? and PAI-1 In Familial Mediterranean Fever (FMF)

DÜNDAR M., Kiraz A., BALTA B., ŞENER E. F., ZARARSIZ G., ARSLAN D., et al.
MODERN RHEUMATOLOGY , cilt.23, sa.1, ss.140-145, 2013 (SCI-Expanded, Scopus)

13. A Case of Dichorionic Twin Pregnancy Concordant for Bilateral Cleft Lip and Palate and Discordant for Spina Bifida; Schisis Association

KUTUK M. S., ÖZGÜN M. T., Uludag S., AKGÜN H., Balta B.
FETAL AND PEDIATRIC PATHOLOGY , cilt.32, sa.5, ss.371-374, 2013 (SCI-Expanded, Scopus) identifier
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 1

1. Association of PAI-1 and TNF-? Gene Polymorphisms In Familial Mediterranean Fever (FMF) Patients.

DÜNDAR M., Kiraz A., Balta B., EMİROĞULLARI E. F., YURCİ M. A., BAŞKOL M.
9th Balkan Congress of Medical Genetics, Romanya, 1 - 04 Eylül 2011, (Tam Metin Bildiri)
Diğer Yayınlar 1

1. A case of 46, XX, t(2;17)(q37.1;q25) with recurrent miscarriage. Current Opinion in Biotechnology, Volume 22, Supplement 1, European Biotechnology Congress

Colak F., Dogan M., Uzak A., Erdogan M., Karabulut S., Balta B., et al.
Diğer, ss.107, 2011
Metrikler

Yayın

15

Yayın (WoS)

13

Yayın (Scopus)

13

Atıf (WoS)

62

H-İndeks (WoS)

5

Atıf (Scopus)

74

H-İndeks (Scopus)

6

Atıf (Scholar)

25

H-İndeks (Scholar)

2

Proje

2

Açık Erişim

1
BM Sürdürülebilir Kalkınma Amaçları