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Academician

ABDULBAKİ YILDIRIM

Araştırma Görevlisi

Erciyes Üniversitesi Tıp Fakültesi Dahili Tıp Bilimleri Bölümü

Research topics OpenAlex
  1. Ana Dal Sağlık Bilimleri Temel Alanı
  2. Yan Dal Tıbbi Genetik
Articles 13 YÖKSİS 13 · OpenAlex 0 Total citations 51 h-index 4 · OpenAlex OpenAlex coverage %100 matched 13 / 13 Q1 articles 1 Scopus · WoS Q1 1 Co-authors 31 1 Turkish institutions

Citation impact

Citation counts of the articles matched in OpenAlex, citing publications from Crossref and the Stanford/Elsevier list. Sources are shown separately and never added up.

OpenAlex YÖKSİS articles matched in OpenAlex: 13 + YÖKSİS · co-author record: 1
h-index 4 Percentile in Türkiye: 42 #869 of 1,439 at their university by h-index
i10-index
2
Total citations
51
Top 51% in Türkiye
Per article
3.6
FWCI
0.62
1.00 = world average
World top 1%
0
World top 10%
1

Most cited articles

  1. The impact and future of artificial intelligence in medical genetics and molecular medicine: an ongoing revolution 2024 world top 10% 18 citations
  2. COVID-19 vaccine candidates and vaccine development platforms available worldwide 2021 12 citations
  3. COVID-19 vaccine candidates and vaccine development platforms available worldwide 2021 9 citations
How is this computed?

h-index and citations are computed from the citation counts of this academic’s YÖKSİS articles matched in OpenAlex (not Google Scholar, WoS or Scopus). Unmatched articles are not included. 1 articles (9 citations) tagged with this academic’s YÖK author id in co-authors’ YÖKSİS records count only towards citations, h-index and i10; article counts, percentiles and rankings use their own YÖKSİS list.

Citing publications Crossref 2 publications citing 13 DOI-bearing articles
  • 2021 1
  • 2025 1
  1. DOI 10.1007/s12288-025-02244-z 2025
  2. DOI 10.3390/ph14121313 2021
Where does this list come from?

Extracted from the reference lists in Crossref’s public March 2026 data file; 20.3% of the file has been processed, so the list may be incomplete. Crossref citations are never added to or compared with the OpenAlex citation counts; the two sources have different coverage.

Field ranking

Position in the main-field, side-field and keyword cohorts by YÖKSİS article score; each card opens that ranking.

YÖKSİS ?

Works 13

YÖKSİS and OpenAlex records: index distribution, journals published in, a filterable article list and the other output types.

Indexes and citation percentiles

?
TR Index 0 articles
OpenAlex citation percentile
Top 1%0
Top 10%1
Avg · n 13 %48.8
Other counts

Scopus (SJR)

  • YÖKSİS rows 13

WoS (JCR)

  • YÖKSİS rows 13

Articles

Articles with YÖKSİS and OpenAlex source split; narrow by quartile or TR Index.

13articles

Journals with publications

9 journals

Narrow down

Scopus (SJR)
Q11 Q25 Q37 Q40
WoS (JCR)
Q11 Q23 Q39 Q40
TR Index
0articles

Article list

  1. 2026 First Report of a Novel Pathogenic Variant in the RREB1 Gene Associated With Obesity and Metabolic Syndrome Clinical Genetics DOI 10.1111/cge.70001 YÖKSİS SJR Q2 JCR Q3 OpenAlex 7.8%
  2. 2026 Germline Homozygous RAG1 Missense Variant Associated With Epstein-Barr Virus Negative Childhood Burkitt Lymphoma Journal of Pediatric Hematology/Oncology DOI 10.1097/MPH.0000000000003159 YÖKSİS SJR Q3 JCR Q3 OpenAlex 2.6%
  3. 2026 Epigenetic Clocks: Biological Aging, Disease, and Clinical Applications The EuroBiotech Journal DOI 10.2478/ebtj-2026-0014 YÖKSİS SJR Q3 JCR Q3 OpenAlex 58.4%
  4. 2026 Integrated Biotechnological Strategies for Planetary Health and Ecosystem Restoration The EuroBiotech Journal DOI 10.2478/ebtj-2026-0009 YÖKSİS SJR Q3 JCR Q3 OpenAlex 88.7%
  5. 2026 AI-Powered Synthetic Biology: Current Situation, Challenges, and Future Perspectives The EuroBiotech Journal DOI 10.2478/ebtj-2026-0015 YÖKSİS SJR Q3 JCR Q3 OpenAlex 58.1%
  6. 2025 Co-occurrence of homozygous ALMS1 variant, 17q11.2 mosaic and germline deletions, and VSX2 nonsense variant in a single family Molecular Biology Reports DOI 10.1007/s11033-025-11058-1 YÖKSİS SJR Q2 JCR Q3 OpenAlex 14.3%
  7. 2025 Messaging malignancy: Tumour-derived exosomes at the nexus of immune escape, vascular remodelling and metastatic competence The EuroBiotech Journal DOI 10.2478/ebtj-2025-0018 YÖKSİS SJR Q3 JCR Q3 OpenAlex 83.5%
  8. 2024 The impact and future of artificial intelligence in medical genetics and molecular medicine: an ongoing revolution Functional & Integrative Genomics DOI 10.1007/s10142-024-01417-9 YÖKSİS SJR Q2 JCR Q2 OpenAlex top 10% OpenAlex 90.9%
  9. 2024 Artificial cells: A potentially groundbreaking field of research and therapy The EuroBiotech Journal DOI 10.2478/ebtj-2024-0006 YÖKSİS SJR Q3 JCR Q3 OpenAlex 44.4%
  10. 2023 A New Case of Translocation T(2;7)(p23;q35) in Recurrent Pregnancy Loss Clinical Medicine & Research DOI 10.3121/cmr.2023.1766 YÖKSİS SJR Q2 JCR Q2 OpenAlex 6.4%
  11. 2022 Diagnosing Alström syndrome in a patient followed up with syndromic obesity for years Intractable & Rare Diseases Research DOI 10.5582/irdr.2022.01024 YÖKSİS SJR Q3 JCR Q2 OpenAlex 52.4%
  12. 2021 Detection of mutations in CML patients resistant to tyrosine kinase inhibitor: imatinib mesylate therapy Medical Oncology DOI 10.1007/s12032-021-01571-1 YÖKSİS SJR Q2 JCR Q3 OpenAlex 53.0%
  13. 2021 COVID-19 vaccine candidates and vaccine development platforms available worldwide Journal of Pharmaceutical Analysis DOI 10.1016/j.jpha.2021.09.004 YÖKSİS SJR Q1 JCR Q1 OpenAlex 74.1%

Books 2

  1. 2023 Oncology: Genomics, Precision Medicine and Therapeutic Targets Springer ISBN 978-981-99-1528-6 Kitap Bölümü · Bilimsel Kitap
  2. 2021 Türkiye Klinikleri Tıbbi Genetik Türkiye Klinikleri Tıp Bilimleri Dergisi ISBN 978-625-401-430-7 Kitap Bölümü · Bilimsel Kitap

Proceedings 4

  1. — Molecular analysis of SMN1 and SMN2 genes with the patients pre-diagnosed with spinal muscular atrophy INTERNATIONAL ERCIYES MEDICAL, MEDICAL GENETICS CONGRESS
  2. 2025 Expanding the Phenotypic Spectrum of OTX2 Mutations: A Case Report EUROPEAN BIOTECHNOLOGY CONGRESS 2025
  3. 2024 Artificial intelligence applications in personalised treatment approaches of genetic diseasesapproaches of genetic diseases EUROPEAN BIOTECHNOLOGY CONGRESS 2024
  4. 2025 The role of a deep intronic variant in the SHH gene in the molecular pathogenesis of Dundar Acropectoral syndromecular pathogenesis of Dundar Acropectoral syndrome EUROPEAN BIOTECHNOLOGY CONGRESS 2024

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Collaboration network

From the author lists of YÖKSİS publication records. Duplicate records of a work count once; institutions are co-authors’ current YÖKSİS affiliations.

Co-authors
31
With an akaturk profile
10
Turkish institutions
1
Co-authored works
%92

Academic co-authors 10

  1. MUNİS DÜNDAR Profesör · Erciyes Üniversitesi same university 11
  2. HİLAL AKALIN Öğretim Görevlisi (uygulamalı Birim) · Erciyes Üniversitesi same university 2
  3. NURİYE GÖKÇE Araştırma Görevlisi · Erciyes Üniversitesi same university 2
  4. NİHAL HATİPOĞLU Profesör · Erciyes Üniversitesi same university 2
  5. ALPER ÖZCAN Doçent · Erciyes Üniversitesi same university 1
  6. DUYGU GÜLMEZ SEVİM Doçent · Erciyes Üniversitesi same university 1
  7. MUSA KARAKÜKCÜ Profesör · Erciyes Üniversitesi same university 1
  8. OSMAN UĞUR SEZERMAN Profesör · Acıbadem Mehmet Ali Aydınlar Üniversitesi 1
  9. TUĞÇE BOZKURT YOZGATLI Doktor Öğretim Üyesi · Acıbadem Mehmet Ali Aydınlar Üniversitesi 1
  10. YUSUF ÖZKUL Profesör · Erciyes Üniversitesi same university 1

National collaboration 1 institutions

Within own university12 joint works · Erciyes Üniversitesi

  1. Acıbadem Mehmet Ali Aydınlar Üniversitesi 1 works · 2 academics

Other co-authors (incl. international) 21

DUYGU TAŞKIN YILDIRIM 4NURANA MAMMADOVA 3SATYA PRAKASH 2AL. ETARIOLA BACUDİLEK ÇİÇEKLEMBIT NEILUISA PASCUCCIMAHMUT ÇERKEZ ERGÖRENMARIA RACHELE CECCARINIMARTIN KOLLERMATTEO BERTELLIMUSTAFA YAKUBİMİCHEL SALZETMİKAİL DEMİRNIKOLA ZHELEVRADKE KANEVARATNESH LALRÜMEYSA ATASAYTOMMASO BECCARIİZEM OLCAY ŞAHİN

Authors without an akaturk profile (international researchers, retired or former academics, students, clinicians) are grouped by name spelling; short forms such as “Gulluce M.” join the single full name they match.