- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Tıbbi Genetik
Citation impact
OpenAlex YÖKSİS articles matched in OpenAlex: 2 + YÖKSİS · co-author record: 8
h-index
8
Percentile in Türkiye: 28
Without large collaborations: h 7 · 1 papers
#93 of 178 at their university by h-index
- i10-index
- 8
- Total citations
- 576 Top 46% in Türkiye
- Per article
- 57.6
- FWCI
- 1.94 1.00 = world average
- World top 1%
- 0
- World top 10%
- 2
Most cited articles
- Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia
- Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis Microtia and Microdontia
- Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss A report of five novel mutations
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. 8 articles (521 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. h-index on the OpenAlex author profile: 2.
Field ranking
YÖKSİS ?-
Main field Sağlık Bilimleri Temel AlanıPoints rank #24,958/ 39,749 top 62.8% At university #77/ 122Score 5.6 journal 5.6 · OA add 0
- Article rank20,186/39,749
- Scopus rank26,871/39,749
- WoS rank26,681/39,749
- YÖKSİS20
- Scopus3
- WoS3
-
Side field Tıbbi GenetikPoints rank #196/ 250 top 78.4% At university #1/ 1Score 5.6 journal 5.6 · OA add 0
- Article rank163/250
- Scopus rank213/250
- WoS rank212/250
- YÖKSİS20
- Scopus3
- WoS3
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
- 60
- With an akaturk profile
- 6
- Turkish institutions
- 5
- Co-authored works
- %100
Academic co-authors 6
- ALİ KEMAL OĞUZ Profesör · Başkent Üniversitesi 1
- AYŞE GÜLDEM KİLCİLER Profesör · Bandırma Onyedi Eylül Üniversitesi 1
- BEYZA DOĞANAY Doçent · Ankara Üniversitesi 1
- SERAP TEBER Profesör · Ankara Üniversitesi 1
- UFUK KUTLUANA Profesör · Pamukkale Üniversitesi 1
- ŞAZİYE ARMAĞAN İNCESULU Profesör · Eskişehir Osmangazi Üniversitesi 1
National collaboration 5 institutions
- Ankara Üniversitesi 2 works · 2 academics
- Bandırma Onyedi Eylül Üniversitesi 1 works · 1 academics
- Başkent Üniversitesi 1 works · 1 academics
- Eskişehir Osmangazi Üniversitesi 1 works · 1 academics
- Pamukkale Üniversitesi 1 works · 1 academics
Other co-authors (incl. international) 54
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Show all (54)
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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
?Top 1%0
Top 10%0
Avg · n 2
%69.0
Other counts
Scopus (SJR)
- YÖKSİS rows 3
WoS (JCR)
- YÖKSİS rows 3
Articles
Articles with YÖKSİS and OpenAlex source split; narrow by quartile or TR Index.
Journals with publications
3 journals
Narrow down
Article list
- 2020 The Association Between The PNPLA3 I148M Polymorphism And Nonalcoholic Fatty Liver Disease YÖKSİS TR Index SJR Q4 JCR Q4
- 2018 Potential effects of metformin in DNA BER system based on oxidativestatus in type 2 diabetes YÖKSİS SJR Q1 JCR Q2 OpenAlex 80.3%
- 2017 Role of metformin on base excision repair pathway in p53 wild-type H2009 and HepG2 cancer cells YÖKSİS SJR Q2 JCR Q3 OpenAlex 57.7%
- 2015 Is There An Association Between Two STAT4 Gene Polymorphisms and Rheumatoid Arthrirtis in Turkish Population YÖKSİS
- 2011 Mutations in ANKRD11 cause KBG syndrome characterized by intellectual disability skeletal malformations and macrodontia YÖKSİS
- 2011 Primer ve Nüks Pterjiyumda Siklooksijenaz 2 ve Ki 67 Ekspresyonu YÖKSİS
- 2010 Partial Deletion of the Long Arm of Chromosome 13 q32q33 2 Associated with Mental Retardation Choanal Atresia and Fish Mouth YÖKSİS
- 2009 Loss of function mutations in ATP6V0A2 impair vesicular trafficking tropoelastin secretion and cell survival YÖKSİS
- 2009 Homozygous mutations in the 15 hydroxyprostaglandin dehydrogenase gene in patients with primary hypertrophic osteoarthropathy YÖKSİS
- 2009 Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss a report of five novel mutations YÖKSİS
- 2009 Current Advances in the Genetic Basis of Rheumatoid Arthritis YÖKSİS
- 2009 A complex TFAP2A allele is associated with branchio oculo facial syndrome and inner ear malformation in a deaf child YÖKSİS
- 2009 Dikkat Eksikliği Hiperaktivite Bozukluğu ve Genetik YÖKSİS
- 2009 A New Sox9 Gene Mutation in a Case of Campomelic Dysplasia YÖKSİS
- 2008 Rubinstein Taybi syndrome with normal FISH result and CREBBP gene analysis a case report YÖKSİS
- 2008 Severe muscle eye brain disease is associated with a homozygous mutation in the POMGnT1 gene YÖKSİS
- 2008 Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis microtia and microdontia YÖKSİS
- 2007 A novel mutation in TRIM37 is associated with mulibrey nanism in a Turkish boy YÖKSİS
- 2007 Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis microtia and microdontia YÖKSİS
- 2006 Expression of cyclooxygenase 2 in orbital fibroadipose connective tissues of Graves ophthalmopathy patients YÖKSİS