Arş. Gör. BURAK BAŞER

Yayın Ağı

Makaleler 8

1. The Association of MCP-1 Level and MCP-1 -2518 A/G and CCR2 190 G/A Gene Polymorphisms with COPD and Pulmonary Hypertension

YILDIRIM M. E., BERK S., KÜÇÜK KURTULGAN H., TEKİN G., TEKİN Y. K., BAŞER B., et al.

GAZI MEDICAL JOURNAL , cilt.32, sa.1, ss.28-32, 2021 (ESCI, Scopus)

2. Analysis of PKD1 and PKD2 Gene Mutations for Autosomal Dominant Polycystic Kidney Disease Cases in Turkish Population

SEZGİN İ., KAYATAŞ M., KÜÇÜK KURTULGAN H., YILDIRIM M. E., BAŞER B., TİMÜÇİN M., et al.

TURKISH JOURNAL OF NEPHROLOGY , cilt.29, sa.4, ss.304-309, 2020 (ESCI)

3. Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in Central Anatolia

YILDIRIM M. E., Kurtulgan H. K., ÖZDEMİR Ö., KILIÇGÜN H., Aydemir D. S., Baser B., et al.

ANNALS OF SAUDI MEDICINE , cilt.39, sa.6, ss.382-387, 2019 (SCI-Expanded, Scopus)

4. The type and prevalence of chromosomal abnormalities in couples with recurrent first trimester abortions: A Turkish retrospective study

YILDIRIM M. E., KARAKUŞ S., Kurtulgan H. K., Baser B., Sezgin I.

JOURNAL OF GYNECOLOGY OBSTETRICS AND HUMAN REPRODUCTION , cilt.48, sa.7, ss.521-525, 2019 (SCI-Expanded, Scopus)

5. Ocular and Genetic Characteristics Observed in Two Cases of Fish-Eye Disease

Ustaoglu M., Solmaz N., BAŞER B., KÜÇÜK KURTULGAN H., Onder F.

CORNEA , cilt.38, sa.3, ss.379-383, 2019 (SCI-Expanded)

6. A case of weill-marchesani syndrome with a novel mutation and vitamin d deficiency

YILDIRIM M. E., VURAL ÖZEÇ A., KÜÇÜK KURTULGAN H., KILIÇGÜN H., BAŞER B.

JOURNAL OF CLINICAL AND ANALYTICAL MEDICINE , cilt.9, sa.6, ss.578-580, 2018 (ESCI)

7. Megacystis Microcolon Intestinal Hypoperistalsis Syndrome in Which a Different De Novo Actg2 Mutation was Detected: A Case Report

Korgali E., YAVUZ A., ÇAĞLAR ŞİMŞEK C. E., GÜNEY C., KÜÇÜK KURTULGAN H., BAŞER B., et al.

FETAL AND PEDIATRIC PATHOLOGY , cilt.37, sa.2, ss.109-116, 2018 (SCI-Expanded, Scopus)

8. 8q22.3 q24.23 duplication in a patient with oral frenulum and normal intellectual development

KÜÇÜK KURTULGAN H., YILDIRIM M. E., BAŞER B., SEZGİN İ.

MOLECULAR CYTOGENETICS , cilt.10, 2017 (SCI-Expanded)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 1

1. 8q22.3 q24.23 duplication in a patient with oral frenulum andnormal intellectual development

KÜÇÜK KURTULGAN H., YILDIRIM M. E., BAŞER B., SEZGİN İ.

11th European Cytogenetics Conference, İtalya, 1 - 04 Temmuz 2017, cilt.10, ss.19, (Özet Bildiri)

Metrikler

Arş. Gör. BURAK BAŞER

Yayınlar & Eserler

1. The Association of MCP-1 Level and MCP-1 -2518 A/G and CCR2 190 G/A Gene Polymorphisms with COPD and Pulmonary Hypertension

2. Analysis of PKD1 and PKD2 Gene Mutations for Autosomal Dominant Polycystic Kidney Disease Cases in Turkish Population

3. Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in Central Anatolia

4. The type and prevalence of chromosomal abnormalities in couples with recurrent first trimester abortions: A Turkish retrospective study

5. Ocular and Genetic Characteristics Observed in Two Cases of Fish-Eye Disease

6. A case of weill-marchesani syndrome with a novel mutation and vitamin d deficiency

7. Megacystis Microcolon Intestinal Hypoperistalsis Syndrome in Which a Different De Novo Actg2 Mutation was Detected: A Case Report

8. 8q22.3 q24.23 duplication in a patient with oral frenulum and normal intellectual development

1. 8q22.3 q24.23 duplication in a patient with oral frenulum andnormal intellectual development

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Yayın (WoS)

Yayın (Scopus)

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H-İndeks (WoS)

Atıf (Scopus)

H-İndeks (Scopus)

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