Yayınlar & Eserler

Yayın Ağı
Makaleler 20
Tümü (20)
SCI-E, SSCI, AHCI (19)
SCI-E, SSCI, AHCI, ESCI (19)
Scopus (19)
TRDizin (1)
Diğer Yayınlar (1)

1. Borate and magnetic core containing layered gadolinium hydroxide hybrid materials: A potential agent for cancer diagnosis and treatment

İÇTEN O., AY A. N., Tuncdemir B. E., MERGEN H.
JOURNAL OF MOLECULAR STRUCTURE , cilt.1354, 2026 (SCI-Expanded, Scopus) identifier

2. Lipoid proteinosis and epilepsy: Molecular analysis

TECELLİOĞLU M., KAMIŞLI Ö., ACAR C., MERGEN H., SÖZEN M. M., KARADUMAN T., et al.
Annals of Medical research , cilt.26, sa.4, ss.744-747, 2019 (Hakemli Dergi)

3. Promoter hypermethylation of p16 and APC in gastrointestinal cancer patients

ERDEM B., KUCUKYILDIRIM S., Saglar E., POLAT Z., MERGEN H.
TURKISH JOURNAL OF GASTROENTEROLOGY , cilt.25, sa.5, ss.512-517, 2014 (SCI-Expanded, Scopus, TRDizin) Sürdürülebilir Kalkınma identifier identifier identifier

4. A large deletion of the AVPR2 gene causing severe nephrogenic diabetes insipidus in a Turkish family

Saglar E., DENIZ F., ERDEM B., KARADUMAN T., YONEM A., CAGILTAY E., et al.
ENDOCRINE , cilt.46, sa.1, ss.148-153, 2014 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

5. Early sign of atherosclerosis in slow coronary flow and relationship with angiotensin-converting enzyme I/D polymorphism

Tanriverdi H., Evrengul H., Mergen H., Acar C., Seleci D., Kuru O., et al.
HEART AND VESSELS , cilt.22, sa.1, ss.1-8, 2007 (SCI-Expanded, Scopus) identifier identifier identifier

6. Lack of association between the serotonin transporter and tryptophan hydroxylase gene polymorphisms and completed suicide

Mergen H., Demirel B., Akar T., Senol E.
PSYCHIATRIC GENETICS , cilt.16, sa.2, ss.53, 2006 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

7. Molecular scanning for mutations in the insulin receptor substrate-1 (Irs-1) gene in Turkish with type 2 diabetes mellitus

Orkunoglu Suer F. E., MERGEN H., Bolu E., Ozata M.
Endocrine Journal , cilt.52, sa.5, ss.593-598, 2005 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier

8. Mitochondrial DNA sequence variation in the Anatolian peninsula (Turkey)

Mergen H., Oner R., Oner C.
JOURNAL OF GENETICS , cilt.83, sa.1, ss.39-47, 2004 (SCI-Expanded, Scopus) identifier identifier

9. A novel melanocortin 4 receptor (MC4R) gene mutation associated with morbid obesity

Mergen M., Mergen H., Ozata M., Oner R., Oner C.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , cilt.86, sa.7, ss.3448-3451, 2001 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

10. Vitamin d-receptor gene polymorphisms and vertebral bone density in men with idiopathic hypogonadotrophic hypogonadism

Ozisik G., MERGEN H., Ozata M., Uyanik C., Caglayan S., Turan M., et al.
Medical Science Monitor , cilt.7, sa.2, ss.233-237, 2001 (SCI-Expanded, Scopus) identifier identifier identifier

11. Severe beta-thalassemia in frameshift codon 6 (-A) homozygotes: Effects of haplotype on phenotype

Birben E., Oner C., Oner R., Mergen H., Yesilipek A., Gumruk F., et al.
HEMOGLOBIN , cilt.25, sa.4, ss.441-445, 2001 (SCI-Expanded, Scopus) identifier identifier identifier

12. Beta-thalassemia intermedia associated with homozygosity for the -87 (C-->T) mutation in a Turkish family.

Gumruk F., Mergen H., Oner R., Ozcebe O., Sayinalp N., Oner C., et al.
Hemoglobin , cilt.24, sa.1, ss.23-9, 2000 (SCI-Expanded, Scopus) identifier identifier identifier

13. Woodhouse and Sakati syndrome (MIM 241080): Report of a new patient

Gul D., Ozata M., Mergen H., Odabasi Z., Mergen M.
Clinical Dysmorphology , cilt.9, sa.2, ss.123-125, 2000 (SCI-Expanded, Scopus) identifier identifier identifier

14. Effect of alpha-gene numbers on the expression of beta-thalassemia intermedia, beta-thalassemia and (delta beta)(0)-thalassemia traits

Altay C., Oner C., Oner R., Gumruk F., Mergen H., Gurgey A.
HUMAN HEREDITY , cilt.48, sa.3, ss.121-125, 1998 (SCI-Expanded, Scopus) identifier identifier identifier

15. Coexistence of Hb Lepore-Boston-Washington (delta 87Gln-beta-IVS-II-8) with alpha-thalassemia [alpha(-5NT)alpha/alpha alpha]

Oner C., Oner R., Balkan H., Gumruk F., Gurgey A.
HEMOGLOBIN , cilt.22, sa.3, ss.273-276, 1998 (SCI-Expanded, Scopus) identifier

16. Hb H disease with homozygosity for red cell G6PD deficiency in a Turkish female

Oner C., Oner R., Birben E., Balkan H., Gumruk F., Gurgey A., et al.
HEMOGLOBIN , cilt.22, sa.2, ss.157-160, 1998 (SCI-Expanded, Scopus) identifier identifier identifier

17. Genotype-phenotype analysis in HbS-beta-thalassemia

Altay C., Oner C., Oner R., Mesci L., Balkan H., Tuzmen S., et al.
HUMAN HEREDITY , cilt.47, sa.3, ss.161-164, 1997 (SCI-Expanded, Scopus) identifier identifier identifier

18. Molecular analysis of the Turkish form of deletion-inversion (delta beta)circle thalassaemia

Oner C., Oner R., Balkan H., Gurgey A., Yalcin A., Avcu F., et al.
BRITISH JOURNAL OF HAEMATOLOGY , cilt.96, sa.2, ss.229-234, 1997 (SCI-Expanded, Scopus) identifier identifier identifier

19. The molecular basis of Hb H disease in Turkey

Oner C., Gurgey A., Oner R., Balkan H., Gumruk F., Baysal E., et al.
HEMOGLOBIN , cilt.21, sa.1, ss.41-51, 1997 (SCI-Expanded, Scopus) identifier identifier identifier

20. A novel (delta beta)(0)-thalassemia due to a similar to 30-kb deletion observed in a Turkish family

Oner R., Oner C., Erdem G., Balkan H., ÖZDAĞ SEVGİLİ H., Erkan M., et al.
ACTA HAEMATOLOGICA , cilt.96, sa.4, ss.232-236, 1996 (SCI-Expanded, Scopus) identifier
Metrikler

Yayın

94

Yayın (WoS)

49

Yayın (Scopus)

49

Atıf (WoS)

540

H-İndeks (WoS)

13

Atıf (Scopus)

510

H-İndeks (Scopus)

13

Atıf (Scholar)

4

H-İndeks (Scholar)

1

Atıf (TrDizin)

1

H-İndeks (TrDizin)

1

Atıf (Diğer Toplam)

2

Proje

29

Tez Danışmanlığı

21

Açık Erişim

8
BM Sürdürülebilir Kalkınma Amaçları