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Academician

TARIK DÜZENLİ

ARAŞTIRMA GÖREVLİSİ

GAZİ ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ

Research topics OpenAlex
  1. Ana Dal Sağlık Bilimleri Temel Alanı
  2. Yan Dal Tıbbi Genetik
Academic summary YÖKSİS and OpenAlex counted separately.
Articles 6
YÖKSİS6 OpenAlex0
Projects 0
Books 2
Proceedings 0

Citation impact

OpenAlex YÖKSİS articles matched in OpenAlex: 6
h-index 2 Percentile in Türkiye: 29 #1,701 of 2,179 at their university by h-index
i10-index
0
Total citations
11
Top 68% in Türkiye
Per article
1.8
FWCI
0.80
1.00 = world average
World top 1%
0
World top 10%
0

Most cited articles

  1. Expanding the phenotype and genotype in Thauvin-Robinet-Faivre syndrome: A new patient with a novel variant and additional clinical findings. 2023 3 citations
  2. Identifying the Fourth Patient With Spastic Paraplegia 90, Extending the Phenotype Spectrum 2026 2 citations
  3. Exome Sequencing in Adults with Unexplained Liver Disease: Diagnostic Yield and Clinical Impact 2025 2 citations

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.

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
16
With an akaturk profile
6
Turkish institutions
0
Co-authored works
%100

Academic co-authors 6

  1. AYŞE TANA ASLAN Profesör · Gazi Üniversitesi same university 1
  2. BAHAR BÜYÜKKARAGÖZ Profesör · Gazi Üniversitesi same university 1
  3. BETÜL SEHER UYSAL Doçent · Gazi Üniversitesi same university 1
  4. ESRA SERDAROĞLU Doçent · Gazi Üniversitesi same university 1
  5. MEHMET CİNDORUK Profesör · Gazi Üniversitesi same university 1
  6. SİNAN SARI Profesör · Gazi Üniversitesi same university 1

National collaboration 0 institutions

Within own university4 joint works · Gazi Üniversitesi

No joint work with another Turkish university.

Other co-authors (incl. international) 10

GÜLSÜM KAYHAN 5ABDULLAH SEZER 2FERDA EMRİYE PERÇİN 2Ali BabazadeBerkay UlaşHURİYE ÇETİNKENAN MORALNERGİZ ERKMENSERDAR MERMERVUSALA YUSUFOVA

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.

Index quartiles

?
Scopus (SJR) 6
  • Q1 0 %0.0
  • Q2 6 %100.0
  • Q3 0 %0.0
  • Q4 0 %0.0
WoS (JCR) 6
  • Q1 1 %16.7
  • Q2 0 %0.0
  • Q3 3 %50.0
  • Q4 2 %33.3
TR Index 0 articles
OpenAlex citation percentile
Top 1%0
Top 10%0
Avg · n 6 %71.7
Other counts

Scopus (SJR)

  • YÖKSİS rows 7

WoS (JCR)

  • YÖKSİS rows 7

Articles

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

6articles

Journals with publications

4 journals

Narrow down

Scopus (SJR)
Q10 Q26 Q30 Q40
WoS (JCR)
Q11 Q20 Q33 Q42
TR Index
0articles

Article list

  1. 2026 Identifying the Fourth Patient With Spastic Paraplegia 90, Extending the Phenotype Spectrum Clinical Genetics DOI 10.1111/cge.70009 YÖKSİS SJR Q2 JCR Q3 OpenAlex 71.1%
  2. 2025 Exome Sequencing in Adults with Unexplained Liver Disease: Diagnostic Yield and Clinical Impact Diagnostics DOI 10.3390/diagnostics15162010 YÖKSİS SJR Q2 JCR Q1 OpenAlex 80.1%
  3. 2025 Dual Diagnosis of Sifrim–Hitz–Weiss Syndrome and Neurofibromatosis Type 1: Expanding the Phenotype of Cardiac Features in Sifrim–Hitz–Weiss Syndrome and Quick Literature Review American Journal of Medical Genetics Part A DOI 10.1002/ajmg.a.64099 YÖKSİS SJR Q2 JCR Q4 OpenAlex 65.1%
  4. 2024 Geleophysic dysplasia and Weill-Marchesani syndrome: ADAMTSL2 a possible common gene Ophthalmic Genetics DOI 10.1080/13816810.2024.2358973. 2 YÖKSİS records YÖKSİS SJR Q2 JCR Q4 OpenAlex 72.1%
  5. 2024 Letter to the Editor regarding “New cases of recently described Thauvin-Robinet-Faivre syndrome with a novel homozygous FIBP gene variant” by Kılıç and Koşukçu, “An investigation of the etiology and follow-up findings in 35 children with overgrowth syndromes, including biallelic SUZ12 variant” by Yüksel Ülker et al. and “Expanding the phenotype and genotype in Thauvin-Robinet-Faivre syndrome: A new patient with a novel variant and additional clinical findings” by Duzenli et al. American Journal of Medical Genetics Part A DOI 10.1002/ajmg.a.63507 YÖKSİS SJR Q2 JCR Q3
  6. 2023 Expanding the phenotype and genotype in Thauvin-Robinet-Faivre syndrome: A new patient with a novel variant and additional clinical findings. American Journal of Medical Genetics Part A DOI 10.1002/ajmg.a.63300 YÖKSİS SJR Q2 JCR Q3 OpenAlex 69.7%

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