Yayınlar & Eserler

Yayın Ağı
SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler 6

1. NELF knockout is associated with impaired pubertal development and subfertility

Quaynor S. D., Ko E. K., Chorich L. P., Sullivan M. E., Demir D., Waller J. L., et al.
MOLECULAR AND CELLULAR ENDOCRINOLOGY , cilt.407, sa.C, ss.26-36, 2015 (SCI-Expanded) Creative Commons License identifier identifier identifier

2. Assessment of women who applied for the uterine transplant project as potential candidates for uterus transplantation

Akar M., Ozekinci M., Alper O., Demir D., Cevikol C., Bilekdemir A. M., et al.
JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH , cilt.41, sa.1, ss.12-16, 2015 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

3. Mitochondrial ATPase Subunit 6 and Cytochrome B Gene Variations in Obese Turkish Children

DEMIR D., TURKKAHRAMAN D., SAMUR A. A., LULECI G., Akcurin S., Alper O. M.
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.6, sa.4, ss.209-215, 2014 (SCI-Expanded) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

4. Clinicogenetic Study of Turkish Patients With Syndromic Craniosynostosis and Literature Review

Nur B., Pehlivanoglu S., Mıhçı E., Calıskan M., Demır D., Alper O. M., et al.
PEDIATRIC NEUROLOGY , cilt.50, sa.5, ss.482-490, 2014 (SCI-Expanded) Creative Commons License identifier identifier identifier

5. Differential expression of nasal embryonic LHRH factor (NELF) variants in immortalized GnRH neuronal cell lines

QUAYNOR S. D., Goldberg L. Y., KO E. K., Stanley R. K., Demir D., KIM H., et al.
MOLECULAR AND CELLULAR ENDOCRINOLOGY , cilt.383, sa.1-2, ss.32-37, 2014 (SCI-Expanded) Creative Commons License identifier identifier identifier

6. Novel and rare CFTR gene mutations in Turkish patients with congenital aplasia of vas deferens

Akin Y., DEMIR D., GORGISEN G., LULECI G., Alper O. M., WATANABE C. S., et al.
ANDROLOGIA , cilt.46, sa.2, ss.198-199, 2014 (SCI-Expanded) identifier identifier identifier
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 5

1. Association of Several Genetic Variants with Myocardial Infarction: A Pilot Study in Mediterranean Region

MANGUOĞLU A. E., Alper O., Küçük M., Pehlivanoğlu S., DEMİR D., ERENGİN K. H., et al.
9. Ulusal Tıbbi Genetik Kongresi, İstanbul, Türkiye, 1 - 05 Aralık 2010, ss.87, (Tam Metin Bildiri)

2. ASSOCIATION OS SEVERAL GENETIC VARIANTS WITH MYOCARDIAL INFARCTION A PILOT STUDY IN A MEDITERRANEAN REGION

MANGUOĞLU AYDEMİR A. E., ALPER Ö., KÜÇÜK M., PEHLİVANOĞLU S., DEMİR D., ERENGİN K. H., et al.
9 th NATIONAL MEDICAL GENETICS CONGRESS OF TURKISH MEDICAL GENETICS SOCIETY WITH INTERNATIONAL PARTICIPATION, 1 - 05 Aralık 2010, cilt.78, (Özet Bildiri)

3. Association of Several Genetic Variants with Myocardial Infarction: A Pilot Study in Mediterranean Region

MANGUOĞLU A. E., Alper O., Küçük M., Pehlivanoğlu S., DEMİR D., ERENGİN K. H., et al.
9. Ulusal Tıbbi Genetik Kongresi, İstanbul, Türkiye, 1 - 05 Aralık 2010, ss.87, (Tam Metin Bildiri)

4. Association of Several Genetic Variants with Myocardial Infarction: A Pilot Study in Mediterranean Region

MANGUOĞLU A. E., Alper O., Küçük M., Pehlivanoğlu S., DEMİR D., ERENGİN K. H., et al.
9. Ulusal Tıbbi Genetik Kongresi, İstanbul, Türkiye, 1 - 05 Aralık 2010, ss.87, (Tam Metin Bildiri)

5. Prenatal diagnosis of partial trisomy 18 (18p11.2-qter) in a fetus associated with increased nuchal translucency

DEMIR D., MENDILCIOGLU I., PESTERELI E., Mihci E., CALISKAN M. O., LULECI G.
6th European Cytogenetics Conference, İstanbul, Türkiye, 7 - 10 Temmuz 2007, cilt.15, ss.129, (Özet Bildiri) identifier
Metrikler

Yayın

11

Yayın (WoS)

7

Yayın (Scopus)

6

Atıf (WoS)

40

H-İndeks (WoS)

4

Atıf (Scopus)

51

H-İndeks (Scopus)

4

Açık Erişim

3
BM Sürdürülebilir Kalkınma Amaçları