ABDULLAH ALPER BÜLBÜL

Yayın Ağı

Makaleler 8

1. Molecular Consequences of CCN6 Variants Encoding WISP3 in Progressive Pseudorheumatoid Dysplasia

Guven Tasbicen G., Tufan A., Savsar B., Bulbul A. A., Tonbul Z., Guzel E., et al.

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES , cilt.26, ss.1-33, 2025 (SCI-Expanded, Scopus)

2. Exome sequencing reveals low-frequency and rare variant contributions to multiple sclerosis susceptibility in Turkish families.

Büyükgöl F., Gürdamar B., Aluçlu M. U., Beckmann Y., Bilguvar K., Boz C., et al.

Scientific reports , cilt.15, sa.1, ss.11682, 2025 (SCI-Expanded, Scopus)

3. Adaptation to space conditions of novel bacterial species isolated from the International Space Station revealed by functional gene annotations and comparative genome analysis

Szydlowski L. M., Bulbul A. A., Simpson A. C., Kaya D. E., Singh N. K., Sezerman U. O., et al.

MICROBIOME , cilt.12, sa.1, 2024 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

4. A rare case of uncharacterized autoinflammatory disease: Patient carrying variations in NLRP3 and TNFRSF1A genes.

Kilinc O. C., Gayibova K., Onen M. O., Onat U. I., Bülbül A. A., Timucin A. C., et al.

American journal of medical genetics. Part A , cilt.194, sa.10, 2024 (SCI-Expanded, Scopus)

5. Var3PPred: variant prediction based on 3-D structure and sequence analyses of protein-protein interactions on autoinflammatory diseases

Bülbül A. A., TİMUÇİN E., TİMUÇİN A. C., SEZERMAN O. U., TAHİR TURANLI E.

PeerJ , cilt.12, sa.5, 2024 (SCI-Expanded, Scopus)

6. Prospective outcome analysis of multiple sclerosis cases reveals candidate prognostic cerebrospinal fluid markers.

Everest E., Uygunoglu U., Tutuncu M., Bulbul A. A., Onat U. İ., Unal M., et al.

PloS one , cilt.18, sa.6, 2023 (SCI-Expanded, Scopus)

7. Investigating the role of common and rare variants in multiplex multiple sclerosis families reveals an increased burden of common risk variation

Everest E., Ahangari M., Uygunoglu U., Tutuncu M., Bulbul A. A., Saip S., et al.

SCIENTIFIC REPORTS , cilt.12, sa.1, 2022 (SCI-Expanded, Scopus)

8. Transcriptomics and Proteomics Analyses Reveal JAK Signaling and Inflammatory Phenotypes during Cellular Senescence in Blind Mole Rats: The Reflections of Superior Biology

Inci N., Akyildiz E. O., Bülbül A. A., Tahir Turanlı E., Akgun E., Baykal A. T., et al.

BIOLOGY-BASEL , cilt.11, sa.9, 2022 (SCI-Expanded, Scopus)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 5

1. Identification of a splice variant in PSMB10 gene in a multiply affected family with undiagnosed autoinflammatory syndrome

Gecgel M., Bulbul A. A., Sigli D., ONAT U. İ., Ugurlu S., Tahir Turanlı E.

56th Annual Conference of the European-Society-of-Human-Genetics (ESHG), Glasgow, İngiltere, 10 - 13 Haziran 2023, cilt.32, ss.175, (Özet Bildiri)

2. Analysis of Familial Exome Analysis Tools

Tahir Turanlı E., Bülbül A. A., Siva A.

8. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 21 - 23 Eylül 2023, ss.1, (Özet Bildiri)

3. Comprehensive Analysis of Low-Frequency Genetic Variants through Exome Sequencing in Familial Multiple Sclerosis

Tahir Turanlı E., Bülbül A. A., Siva A., Sezerman O. U.

75. American Society of Human Genetics Congress, Washington, Amerika Birleşik Devletleri, 1 - 05 Kasım 2023, ss.1, (Özet Bildiri)

4. JAK/STAT signaling during cellular senescence process in primary fibroblast of blind mole rats

İnci N., Akyıldız E. O., Bülbül A. A., Tahir Turanlı E., Bozaykut Eker P.

IUBMB-FEBS-PABMB Congress , Lisbon, Portekiz, 10 Temmuz 2022, ss.1-2, (Özet Bildiri)

5. Prospective Analysis of Cerebrospinal Fluid Protein Levels Reveals Candidate Biomarkers for Disability Outcome in Multiple Sclerosis

Siva A., Everest E., UYGUNOĞLU U., Yavuz D., Bulbul A. A., TÜTÜNCÜ M., et al.

Annual Meeting of the American-Academy-of-Neurology, Toronto, Kanada, 25 Nisan - 01 Mayıs 2020, cilt.94, (Özet Bildiri)

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H-İndeks (WoS)

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