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Academician

NİHAN BİLGE KAMER

Doktor Öğretim Üyesi

Trakya Üniversitesi Mühendislik Fakültesi Genetik Ve Biyomühendislik Bölümü

Research topics OpenAlex
  1. Ana Dal Sağlık Bilimleri Temel Alanı
  2. Yan Dal Tıbbi Genetik
Articles 10 YÖKSİS 10 · OpenAlex 0 Total citations 354 h-index 5 · OpenAlex OpenAlex coverage %100 matched 10 / 10 Q1 articles 2 Scopus · WoS Q1 3 Co-authors 13 2 Turkish institutions

Citation impact

OpenAlex YÖKSİS articles matched in OpenAlex: 10
h-index 5 Percentile in Türkiye: 60 #296 of 1,121 at their university by h-index
i10-index
4
Total citations
354
Top 16% in Türkiye
Per article
35.4
FWCI
1.88
1.00 = world average
World top 1%
0
World top 10%
2

Most cited articles

  1. CLP1 founder mutation links tRNA splicing and maturation to cerebellar development and neurodegeneration. 2014 world top 10% 284 citations
  2. Fraser syndrome due to mutations in GRIP1--clinical phenotype in two families and expansion of the mutation spectrum. 2014 20 citations
  3. Mild nasal clefting may be predictive for ALX4 heterozygotes 2014 17 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. h-index on the OpenAlex author profile: 1.

Citing publications

Crossref 86 publications citing 10 DOI-bearing articles · 7 Türkiye-affiliated

2016 12019 112020 372021 222022 112025 32026 1

  1. 10.1016/j.celrep.2025.116729 2026
  2. Deciphering the role of tRNA-derived fragments in neurological and psychiatric disease pathogenesis TR Huseyin Kocakusak et al. · Frontiers in Cellular Neuroscience · 2025
  3. Revisiting Wiedemann-Steiner Syndrome: Novel KMT2A Variants and Broadened Clinical Spectrum TR Zehra Manav Yiğit et al. · Balkan Medical Journal · 2025
  4. 10.1007/s12032-025-03142-0 2025
  5. Suppression of premature transcription termination leads to reduced mRNA isoform diversity and neurodegeneration TR Geneva R. LaForce et al. · Neuron · 2022
  6. A splice site mutation in the <scp> <i>TSEN2</i> </scp> causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome TR Nur Canpolat et al. · Clinical Genetics · 2022
  7. 10.1242/bio.058928 2022
  8. 10.1111/jcmm.17245 2022
  9. 10.4103/1673-5374.314315 2022
  10. 10.1002/wrna.1717 2022
  11. 10.1093/bioinformatics/btab883 2022
  12. 10.1007/s00109-022-02189-0 2022
  13. 10.1186/s12935-022-02481-6 2022
  14. 10.1016/j.bbadis.2021.166314 2022
  15. 10.4103/jpcdoh.jpcdoh_17_21 2022
  16. The first adolescent case of Fraser syndrome 3, with a novel nonsense variant in <i>GRIP1</i> TR Mine Koprulu et al. · American Journal of Medical Genetics Part A · 2021
  17. <i>ALX</i>-Related Frontonasal Dysplasias: Clinical Characteristics and Surgical Management TR Ibrahim Vargel et al. · The Cleft Palate Craniofacial Journal · 2021
  18. 10.1016/j.ejpn.2020.08.011 2021
  19. 10.1016/b978-0-12-817990-1.00004-4 2021
  20. 10.1038/s41419-021-04108-6 2021
  21. 10.3233/jad-200917 2021
  22. 10.1016/j.ygeno.2021.06.039 2021
  23. 10.14336/ad.2021.0115 2021
  24. 10.1073/pnas.2020429118 2021
  25. 10.1007/s12311-020-01224-5 2021
  26. 10.1016/j.bbrc.2021.07.036 2021
  27. 10.1126/sciadv.abh0494 2021
  28. 10.1093/hmg/ddab107 2021
  29. 10.1073/pnas.2110730118 2021
  30. 10.1093/molehr/gaab026 2021

Showing the 30 most recent.

Where does this list come from?

Extracted from the reference lists in Crossref’s public March 2026 data file; 18.4% 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

YÖKSİS ?

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
13
With an akaturk profile
8
Turkish institutions
2
Co-authored works
%100

Academic co-authors 8

  1. HÜLYA KAYSERİLİ KARABEY Profesör · Koç Üniversitesi 8
  2. UMUT ALTUNOĞLU Doçent · Koç Üniversitesi 4
  3. BİRSEN KARAMAN Profesör · İstanbul Üniversitesi 3
  4. ZEHRA OYA UYGUNER Profesör · İstanbul Üniversitesi 2
  5. AYÇA DİLRUBA ASLANGER Doçent · İstanbul Üniversitesi 1
  6. GÜZİN TUNCA ALPARSLAN Doktor Öğretim Üyesi · Trakya Üniversitesi same university 1
  7. HAKAN GÜRKAN Profesör · Trakya Üniversitesi same university 1
  8. RECEP HAS Profesör · İstanbul Üniversitesi 1

National collaboration 2 institutions

Within own university2 joint works · Trakya Üniversitesi

  1. Koç Üniversitesi 8 works · 2 academics
  2. İstanbul Üniversitesi 5 works · 4 academics

Other co-authors (incl. international) 5

ATIL YÜKSEL 3SEHER BAŞARAN 3Ece ÇepniİBRAHİM KAMERİSMİHAN MERVE TEKİN

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.

Indexes and citation percentiles

?
TR Index 2 articles
OpenAlex citation percentile
Top 1%0
Top 10%2
Avg · n 10 %59.4
Other counts

Scopus (SJR)

  • YÖKSİS rows 10

WoS (JCR)

  • YÖKSİS rows 10

Articles

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

10articles

Journals with publications

7 journals

Narrow down

Scopus (SJR)
Q12 Q26 Q30 Q42
WoS (JCR)
Q13 Q20 Q35 Q42
TR Index
2articles

Article list

  1. 2026 Understanding the dynamic behavior of wild-type and mutant LARS1 proteins: insight from comparative molecular dynamics simulations Journal of Biomolecular Structure and Dynamics DOI 10.1080/07391102.2026.2713057 YÖKSİS SJR Q2 JCR Q3 OpenAlex 80.0%
  2. 2025 The Importance of Genetic Diagnosis in Rare Diseases Balkan Medical Journal DOI 10.4274/balkanmedj.galenos.2025.2025-270125 YÖKSİS TR Index SJR Q2 JCR Q1 OpenAlex top 10% OpenAlex 96.1%
  3. 2022 Biallelic TERT variant leads to Hoyeraal-Hreidarsson syndrome with additional dyskeratosis congenita findings. American journal of medical genetics. Part A DOI 10.1002/ajmg.a.62602 YÖKSİS SJR Q2 JCR Q3 OpenAlex 57.5%
  4. 2021 HOLOPROSENCEPHALY: CHROMOSOMAL ABNORMALITIES IN THE ETIOPATHOGENESIS OF 127 ANTENATAL CASES İstanbul Tıp Fakültesi Dergisi DOI 10.26650/IUITFD.2020.0071 YÖKSİS TR Index SJR Q4 JCR Q4 OpenAlex 4.3%
  5. 2020 Array-comparative Genomic Hybridization Results in Clinically Affected Cases with Apparently Balanced Chromosomal Rearrangements. Balkan journal of medical genetics : BJMG DOI 10.2478/bjmg-2020-0026 YÖKSİS SJR Q4 JCR Q4 OpenAlex 16.3%
  6. 2020 Follow-Up Studies of cf-DNA Testing from 101 Consecutive Fetuses and Related Ultrasound Findings. Ultraschall in der Medizin (Stuttgart, Germany : 1980) DOI 10.1055/a-0651-0459 YÖKSİS SJR Q1 JCR Q1 OpenAlex 11.1%
  7. 2014 Newly described clinical features in two siblings with MACS syndrome and a novel mutation in RIN2. American journal of medical genetics. Part A DOI 10.1002/ajmg.a.36277 YÖKSİS SJR Q2 JCR Q3 OpenAlex 72.4%
  8. 2014 Fraser syndrome due to mutations in GRIP1--clinical phenotype in two families and expansion of the mutation spectrum. American journal of medical genetics. Part A DOI 10.1002/ajmg.a.36343 YÖKSİS SJR Q2 JCR Q3 OpenAlex 85.6%
  9. 2014 CLP1 founder mutation links tRNA splicing and maturation to cerebellar development and neurodegeneration. Cell DOI 10.1016/j.cell.2014.03.049 YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 98.8%
  10. 2014 Mild nasal clefting may be predictive for ALX4 heterozygotes AMERICAN JOURNAL OF MEDICAL GENETICS PART A DOI 10.1002/ajmg.a.36578 YÖKSİS SJR Q2 JCR Q3 OpenAlex 72.2%

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