Academician
EVREN GÜMÜŞ
Doçent
Muğla Sıtkı Koçman Üniversitesi Tıp Fakültesi Dahili Tıp Bilimleri Bölümü
- RNA modifications and cancer4
- Genetic and Kidney Cyst Diseases3
- Genomic variations and chromosomal abnormalities3
- Neurogenetic and Muscular Disorders Research3
- Cancer-related gene regulation3
- Genetics and Neurodevelopmental Disorders3
- Lysosomal Storage Disorders Research2
- Skin and Cellular Biology Research2
- Hip disorders and treatments2
- Genomics and Rare Diseases2
- Connective tissue disorders research2
- Wnt/β-catenin signaling in development and cancer2
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Tıbbi Genetik
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.
- i10-index
- 13
- Total citations
- 282 Top 21% in Türkiye
- Per article
- 7.8
- FWCI
- 0.64 1.00 = world average
- World top 1%
- 0
- World top 10%
- 1
Most cited articles
- Suppression of premature transcription termination leads to reduced mRNA isoform diversity and neurodegeneration
- A novel COQ7 mutation causing primarily neuromuscular pathology and its treatment options
- The Frequency of MEFV Gene Mutations and Genotypes in Sanliurfa Province, South-Eastern Region of Turkey, after the Syrian Civil War by Using Next Generation Sequencing and Report of a Novel Exon 4 Mutation (I423T)
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. 6 articles (18 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 53 publications citing 33 DOI-bearing articles · 14 Türkiye-affiliated
- 2019 3
- 2020 18
- 2021 17
- 2022 7
- 2025 8
- Comprehensive clinical and genetic characterization of Bardet-Biedl Syndrome: insights from the largest Turkish cohort TR Şenol Demir et al. · European Journal of Pediatrics · 2025
- DOI 10.64898/2025.12.08.691990 2025
- DOI 10.1038/s41593-025-02050-w 2025
- DOI 10.1016/j.ymthe.2025.12.008 2025
- DOI 10.3390/biology14121637 2025
- DOI 10.1371/journal.pbio.3003231 2025
- DOI 10.1038/s41586-025-09613-8 2025
- DOI 10.1002/mds.70119 2025
- Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium TR Munis Dundar et al. · Functional & Integrative Genomics · 2022
- MEFV gene allele frequency and genotype distribution in 3230 patients’ analyses by next generation sequencing methods TR Berkay Kırnaz et al. · Gene · 2022
- DOI 10.1038/s41431-022-01048-3 2022
- DOI 10.3389/fnmol.2022.805158 2022
- DOI 10.1093/hmg/ddac046 2022
- DOI 10.1002/mgg3.1894 2022
- DOI 10.1007/s10815-021-02381-0 2022
- High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population TR Tadahiro Mitani et al. · The American Journal of Human Genetics · 2021
- Presentation of a new mutation in FMF and evaluating the frequency of distribution of the MEFV gene mutation in our region with clinical findings TR Abdullah Arpacı et al. · Molecular Biology Reports · 2021
- THE ROLE OF CHROMOSOME ANALYSIS IN MALE AND FEMALE INFERTILITY TR Burhan BALTA et al. · Kırıkkale Üniversitesi Tıp Fakültesi Dergisi · 2021
- Frequency and Distribution of MEFV Gene Mutation in Familial Mediterranean Fever Patients: A Single Center Experience TR Şebnem ÖZEMRİ SAĞ et al. · SDÜ Tıp Fakültesi Dergisi · 2021
- Ailesel akdeniz ateşi ön tanılı hastalarda MEFV mutasyonlarının gerçek zamanlı polimeraz zincir reaksiyonu ve yeni nesil dizileme ile karşılaştırmalı analizi-tek merkez deneyimi TR Onur TOKGÜN et al. · Pamukkale Medical Journal · 2021
- DOI 10.1002/humu.24190 2021
- DOI 10.3390/genes12070986 2021
- DOI 10.1016/j.xhgg.2021.100049 2021
- DOI 10.1101/2021.07.26.453809 2021
- DOI 10.1007/s00296-021-04913-4 2021
- DOI 10.1016/j.ejmg.2021.104280 2021
- DOI 10.17650/2073-8803-2020-15-3-4-65-77 2021
- DOI 10.14581/jer.21004 2021
- DOI 10.1038/s41572-021-00309-7 2021
- DOI 10.1186/s12883-021-02204-w 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; 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.
-
Main field Sağlık Bilimleri Temel AlanıPoints rank #7,864/ 39,749 top 19.8% At university #61/ 315Score 29.65 journal 29.4 · OA add 0.25
- Article rank10,443/39,749
- Scopus rank5,930/39,749
- WoS rank5,644/39,749
- YÖKSİS45
- Scopus39
- WoS39
-
Side field Tıbbi GenetikPoints rank #85/ 250 top 34.0% At university #1/ 1Score 29.65 journal 29.4 · OA add 0.25
- Article rank93/250
- Scopus rank77/250
- WoS rank74/250
- YÖKSİS45
- Scopus39
- WoS39
Works 45
YÖKSİS and OpenAlex records: index distribution, journals published in, a filterable article list and the other output types.
Indexes and citation percentiles
?Other counts
Scopus (SJR)
- YÖKSİS rows 39
WoS (JCR)
- YÖKSİS rows 39
Articles
Articles with YÖKSİS and OpenAlex source split; narrow by quartile or TR Index.
Journals with publications
38 journals
- American Journal of Medical Genetics, Part A 2
- Annals of Human Genetics 2
- Clinical Dysmorphology 2
- Fetal and Pediatric Pathology 2
- Gazi Medical Journal 2
- Human Mutation 2
- Journal of Pediatric Intensive Care 2
- ISSN 1300-2945 1
- ISSN 1303-328X 1
- ISSN 1304-9623 1
- ISSN 1309-4025 1
- ISSN 2146-6505 1
- ISSN 2148-0990 1
- American Journal of Neuroradiology 1
- Brain 1
- Cancer Investigation 1
- Cell Journal 1
- Dermatologica Sinica 1
- European Journal of Human Genetics 1
- European Journal of Medical Genetics 1
- Fresenius Environmental Bulletin (discontinued) 1
- Gene 1
- Ginekologia Polska 1
- Indian Journal of Orthopaedics 1
- Iranian Journal of Public Health 1
- Journal of Clinical Medicine 1
- Journal of Inherited Metabolic Disease 1
- Journal of Medical Genetics 1
- Journal of Neuroscience Research 1
- Journal of Pediatric Genetics 1
- Molecular Genetics and Metabolism Reports 1
- Neuron 1
- Ophthalmic Genetics 1
- Pain 1
- Revista Internacional de Andrologia 1
- Turkish Journal of Pediatrics 1
- Turk Pediatri Arsivi 1
- Van Medical Journal 1
Narrow down
Article list
- 2025 CHEK2 Germline Variants and Their Clinical Implications: Experience from a Turkish Hereditary Cancer Cohort YÖKSİS SJR Q3 JCR Q3 OpenAlex 32.6%
- 2023 BCKDK deficiency: a treatable neurodevelopmental disease amenable to newborn screening YÖKSİS SJR Q1 JCR Q1
- 2023 Sanat Temelli Özel Çalışma Modülü: Tıp Öğrencilerinin Görsel Düşünme ve İletişim Becerilerinin Geliştirilmesi YÖKSİS TR Index OpenAlex 63.8%
- 2022 Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711 YÖKSİS SJR Q1 JCR Q1 OpenAlex 89.1%
- 2022 Suppression of premature transcription termination leads to reduced mRNA isoform diversity and neurodegeneration YÖKSİS SJR Q1 JCR Q1 OpenAlex 85.2%
- 2022 Congenital insensitivity to pain: a novel mutation affecting a U12-type intron causes multiple aberrant splicing of SCN9A YÖKSİS SJR Q1 JCR Q1 OpenAlex 75.1%
- 2022 Phenotypic and mutational spectrum of ROR2-related Robinow syndrome YÖKSİS SJR Q1 JCR Q2 OpenAlex 79.2%
- 2022 A Newborn with Infantile-Onset Pompe Disease Improving after Administration of Enzyme Replacement Therapy: Case Report YÖKSİS SJR Q4 JCR Q4 OpenAlex 9.7%
- 2022 The link between miR-96 levels and the developmental dysplasia of the hip YÖKSİS TR Index SJR Q4 JCR Q4 OpenAlex 12.4%
- 2022 A novel COQ7 mutation causing primarily neuromuscular pathology and its treatment options YÖKSİS SJR Q3 JCR Q4 OpenAlex 86.1%
- 2022 A Novel In-Frame Type Deletion in CHST3 Gene in A Patient with Spondyloepiphyseal Dysplasia YÖKSİS OpenAlex 56.9%
- 2021 Bi-allelic TTC5 variants cause delayed developmental milestones and intellectual disability YÖKSİS SJR Q1 JCR Q1
- 2021 A novel homozygous RIPK4 variant in a family with severe Bartsocas-Papas syndrome YÖKSİS SJR Q2 JCR Q3 OpenAlex 47.5%
- 2021 A different look at genetic factors in individuals with non-obstructive azoospermia or oligospermia in our research study: To whom, which threshold, when, in what way? YÖKSİS SJR Q3 JCR Q4
- 2021 Clinical and exome sequencing findings in seven children with Bardet-Biedl syndrome from Turkey YÖKSİS SJR Q3 JCR Q4 OpenAlex 72.1%
- 2021 The Association Between BMP-2, UQCC1 and CX3CR1 Polymorphisms and the Risk of Developmental Dysplasia of the Hip YÖKSİS SJR Q3 JCR Q4 OpenAlex 67.9%
- 2021 An epilepsy‐associated ACTL6B variant captures neuronal hyperexcitability in a human induced pluripotent stem cell model YÖKSİS SJR Q2 JCR Q2
- 2021 Response to Letter to the Editor: "Atrioventricular canal defect is an infrequent congenital heart disease that can be observed in Bardet-Biedl syndrome" YÖKSİS SJR Q3 JCR Q4
- 2020 A Homozygous 1.16 Megabases Microdeletion at 8p22 Including The Whole TUSC3 in A Three Years Old Girl with Intellectual Disability and Speech Delay YÖKSİS SJR Q3 JCR Q4
- 2020 Responsiveness of sphingosine phosphate lyase insufficiency syndrome to vitamin B6 cofactor supplementation YÖKSİS SJR Q1 JCR Q1
Projects 3
-
2018 Gelişimsel kalça displazisi (GKD) olan hastalarda CX3CR1,UQCC ve BMP-2 genlerindeki polimorfizmlerin ve miR-96ekspresyonunun değerlendirilmesi
-
2014 SEREBRAL PALSİLİ ÇOCUKLARDA APOLİPOPROTEİN-E VE INTERLÖKİN-6 POLİMORFİZMLERİNİN İNCELENMESİ
-
2015 Normozoospermik ve nonnormozoospermik sperm örneklerinde DNA fragmentasyon oranlarının sperm anöploidilerine etkisi
Books 2
-
2025 HEMATOLOJİK HASTALIKLARIN FİZYOPATOLOJİK TEMELLERİ
-
2025 HEMATOLOJİK HASTALIKLARIN FİZYOPATOLOJİK TEMELLERİ
Proceedings 26 See all (26) →
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2018 Examination of Acute and Chronic Effects of Air Diving on Dynamic Tiyol-Disulfide Homoeostasis in Professional Divers
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2019 The Evaluation of Glutaric Aciduria Type 1 Patients Which Were Diagnosed and Followed at Harran University Medical Faculty Hospital Between January 2017 and December 2018
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2013 A NOVEL MUTATION IN RIPK4 CAUSE THE BARTSOCAS-PAPAS SYNDROME
-
2014 A rare case with de novo Isochromosome 18p Syndrome
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2018 Yeni Tanımlanan Bir Mutasyon Eşliğinde Ailesel Hiperkolesterolemi Vakalarının Değerlendirilmesi
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
- 261
- With an akaturk profile
- 48
- Turkish institutions
- 23
- Co-authored works
- %64
Academic co-authors 48
- MERYEM KARACA Doktor Öğretim Üyesi · İstanbul Üniversitesi 4
- BEYHAN DURAK ARAS Profesör · Eskişehir Osmangazi Üniversitesi 3
- ÖZLEM ÖZ Doçent · Harran Üniversitesi 3
- BARAN SARIKAYA Profesör · Sağlık Bilimleri Üniversitesi 2
- COŞKUN YARAR Profesör · Eskişehir Osmangazi Üniversitesi 2
- EBRU TEMİZ Doçent · Harran Üniversitesi 2
- KÜRŞAT BORA ÇARMAN Profesör · Eskişehir Osmangazi Üniversitesi 2
- MELTEM BOR Doktor Öğretim Üyesi · İstanbul Üniversitesi 2
- OĞUZ ÇİLİNGİR Profesör · Eskişehir Osmangazi Üniversitesi 2
- SERKAN SİPAHİOĞLU Profesör · Ordu Üniversitesi 2
Show all (48)
- SEVİLHAN ARTAN Profesör · Eskişehir Osmangazi Üniversitesi 2
- ÖZKAN İLHAN Doçent · Muğla Sıtkı Koçman Üniversitesi same university 2
- ANIL YÜCEL Araştırma Görevlisi · Muğla Sıtkı Koçman Üniversitesi same university 1
- ATAMAN GÖNEL Profesör · Sanko Üniversitesi 1
- BAKİ VOLKAN ÇETİN Doçent · Harran Üniversitesi 1
- BAYRAM TORAMAN Doktor Öğretim Üyesi · Karadeniz Teknik Üniversitesi 1
- BURCU ÖZTÜRK HİŞMİ Doçent · Marmara Üniversitesi 1
- BÜLENT KATI Profesör · Harran Üniversitesi 1
- CELAL BOZKURT Doçent · Sağlık Bilimleri Üniversitesi 1
- CELAL ERBAŞ Öğretim Görevlisi (ders Vermekle Görevli) · Çukurova Üniversitesi 1
- ELİF YILMAZ GÜLEÇ Doçent · İstanbul Medeniyet Üniversitesi 1
- EROL ERKAN Doktor Öğretim Üyesi · Aydın Adnan Menderes Üniversitesi 1
- ERSAN KALAY Profesör · Karadeniz Teknik Üniversitesi 1
- ESER ÖRDEK Doktor Öğretim Üyesi · Hatay Mustafa Kemal Üniversitesi 1
- EYYUP SABRİ PELİT Profesör · Harran Üniversitesi 1
- FATMA TUBA EMİNOĞLU Profesör · Ankara Üniversitesi 1
- GÖKHAN YILDIZ Doktor Öğretim Üyesi · Karadeniz Teknik Üniversitesi 1
- GÖZDE YEŞİL SAYIN Profesör · İstanbul Atlas Üniversitesi 1
- GÖZDE ŞAHİN VURAL Doçent · Balıkesir Üniversitesi 1
- GÜLAY CAN YILMAZ Doçent · Muğla Sıtkı Koçman Üniversitesi same university 1
- HAKİM ÇELİK Profesör · Harran Üniversitesi 1
- HALUK AKIN Profesör · Ege Üniversitesi 1
- HALİL ÇİFTÇİ Profesör · Harran Üniversitesi 1
- HATİCE AKAY Profesör · Başkent Üniversitesi 1
- HÜLYA ELBE Profesör · Muğla Sıtkı Koçman Üniversitesi same university 1
- HÜLYA KAYSERİLİ KARABEY Profesör · Koç Üniversitesi 1
- MEHMET ALTAY ÜNAL Doçent · Ankara Üniversitesi 1
- MEHMET ALİ ERGÜN Profesör · Gazi Üniversitesi 1
- MERVE YAZOL Doktor Öğretim Üyesi · Gazi Üniversitesi 1
- MUNİS DÜNDAR Profesör · Erciyes Üniversitesi 1
- TAHA BAHSİ Profesör · Üsküdar Üniversitesi 1
- TUBA DİNÇER Doçent · Karadeniz Teknik Üniversitesi 1
- TURAN DEMİRCAN Profesör · İzmir Bakırçay Üniversitesi 1
- ZEHRA MANAV YİĞİT Doktor Öğretim Üyesi · Aydın Adnan Menderes Üniversitesi 1
- ÖZGÜR YILMAZ Öğretim Görevlisi (ders Vermekle Görevli) · Çukurova Üniversitesi 1
- İDRİS ER Araştırma Görevlisi · Karadeniz Teknik Üniversitesi 1
- İSMAİL KOYUNCU Profesör · Harran Üniversitesi 1
- ŞEYDA NUR DAĞLI Doktor Öğretim Üyesi · İstinye Üniversitesi 1
National collaboration 23 institutions
Within own university4 joint works · Muğla Sıtkı Koçman Üniversitesi
- Harran Üniversitesi 7 works · 8 academics
- İstanbul Üniversitesi 4 works · 2 academics
- Eskişehir Osmangazi Üniversitesi 3 works · 5 academics
- Ankara Üniversitesi 2 works · 2 academics
- Gazi Üniversitesi 2 works · 2 academics
- Ordu Üniversitesi 2 works · 1 academics
- Sağlık Bilimleri Üniversitesi 2 works · 2 academics
- Aydın Adnan Menderes Üniversitesi 1 works · 2 academics
- Balıkesir Üniversitesi 1 works · 1 academics
- Başkent Üniversitesi 1 works · 1 academics
Show all (23)
- Ege Üniversitesi 1 works · 1 academics
- Erciyes Üniversitesi 1 works · 1 academics
- Hatay Mustafa Kemal Üniversitesi 1 works · 1 academics
- Karadeniz Teknik Üniversitesi 1 works · 5 academics
- Koç Üniversitesi 1 works · 1 academics
- Marmara Üniversitesi 1 works · 1 academics
- Sanko Üniversitesi 1 works · 1 academics
- Çukurova Üniversitesi 1 works · 2 academics
- Üsküdar Üniversitesi 1 works · 1 academics
- İstanbul Atlas Üniversitesi 1 works · 1 academics
- İstanbul Medeniyet Üniversitesi 1 works · 1 academics
- İstinye Üniversitesi 1 works · 1 academics
- İzmir Bakırçay Üniversitesi 1 works · 1 academics
Other co-authors (incl. international) 213
ASHLEIGH SCHAFFER 3MARTIN ZENKER 3EBRU TUNÇEZ 2GENEVA LAFORCE 2Helen C. Miranda 2Jingyi Liu 2Katherine Johnson 2OZAN KOÇAK 2SİBEL LAÇİNEL GÜRLEVİK 2ZAFER YÜKSEL 2Özgür Yüksekdağ 2ABDULLAH A ALANGARIABDÜLLATİF BAKIRALPER GEZDİRİCİALWIN LOHALİ ERDAL GÜNEŞANNEKARIN KAHLERTANNICK TOUTAINARIANA KARIMINEJADARISHA RASHEEDARMAĞAN ÖZGÜRAUSTIN LARSONAi LinAida OrmazabalAidin ForoutanAlexander A L JorgeAlfonso OyarzábalAngad JollyAngela M Vianna‐MorganteAngeles García-CazorlaAntonio Richieri‐CostaAriadne R LimaBENJAMIN W DARBROBENOMRAN TAWFEGBONNIE SULLIVANBR SULLIVANBarbara M FerreiraBassam R AliBekim SadikovicBoris Keren
Show all (213)
CAROLINE ROORYCKCaroline MartinezCecilia MelladoChaofan ZhangCharles E SchwartzChong A KimCindy SkinnerClarissa BuenoClaudia M B CarvalhoCydni CydniCynthia J CurryDANICA ROSSDAVID CHITAYATDAVID J AMORDENISE LIMENG GOHDENNY SCHANZEDaniele CartelliDonna M MuznyDébora R BertolaDécio BrunoniDİLAN ÇETİNAVCIELİF NUR KOÇAKEMILY TANGEVA BERMEJO SANCHEZEllen RichardsonEllen van BeusekomEmma FootittEric J WagnerErica C C Caldas RosaErica WuErika SalviFATIMA ABDELFATTAHFEDERICO TORTAFF HILDEBRANDTFRIEDHELM HILDEBRANDTFrancois BoemerFrançois G DebrayGAMZE MOCANGEMMA POKEGiuliana C CoattiGuiseppe LauriaGÜLTEN TUNCELHAVVA ÇOBANOĞULLARIHEINRICH STICHTHUI KIM YAPHUMERA MANZOORHan G BrunnerHans van BokhovenHaowei DuHirofumi OhashiIAN HAYESISAAC D LIUISOLINA RIANO GALANIlaria D'AmatoIrene MachadoIsabelle MaystadtJAMES A ENDRIZZIJD SABAJEFFREY B HODGINJENNIFER MCEVOYVENNERIJEREMY SELVAJOSEPH G GLEESONJULIE D SABAJack ReillyJames DavisonJames R LupskiJanson J WhiteJeff CollerJennifer KerkhofJiyong WangJoanne W DixonJordan S. FarrJordi Muchart LópezJulia NeugebauerJuliana F MazzeuJuliana R ConstanteKARIN CHENKATHERINA D MATHEWSKHALID ALHASANKK ALHASANKW MARTINLEE SANGMOONLUISA WEIBLars MørkridLucie Y AhnLyse RuaudMAHA ZAKIMAHMUT ÇERKEZ ERGÖRENMAIE WALSHMARIE LAURE VUILLAUMEMARKUS R WENKMEGAN A COOPERMERVE SAKAMERVE SAKA GÜVENÇMERYEM BETMEZOĞLUMILAN JIRSAMOHAMAD H KARIMINEJADMUHAMMED ŞEYHANLIMara S CordobaMarcela A ChiabaiMargherita MarchiMariela De Los SantosMarielle AldersMarjorie DixonMatthew L TedderMichael J FriezMirna AndelicMoez DawoodMustafa TekinNICOLE WEAVERNN WEAVERNURDAMLA SANDAL FİLİKCİNatalie WeinholdNeysa A P RegattieriNobuhiko OkamotoNouriya Al-SannaaOLIVIA WESTOtis PinkardPATRICK J MORRISONPATRICK SHANNONPERRINE PENNAMENPETER I BENKEPIMING ZHAOPINAR TULAYPatrick S TarpeyPaul Hoff BackePaulo A OttoPhillis LakemanPilar Rodríguez-PomboPing JiPolyxeni PhilippidouRASİME KALKANRachel HonjoRachel RachelRafael ArtuchRaffaella LombardiRaissa M Dandalo‐GirardiRichard A GibbsRinaldo W PereiraRobert PogueRoger E StevensonSABINE WEIDENSEESADAF NAZSIAVASH GHADERI SOHISIEGFRIED HEKIMISOLMAZ ÖZKANSTACEY KIAT HONG TAYSUHA SALIMSUONAVY KHUNG SAVATOVSKYShalini N JhangianiSonia PajaresStephanie D StowayStephen P RobertsonSteven A SkinnerSÖNKE WEINERTTadahiro MitaniTalyta M CanóThomas J SweetTrine TangeraasTulio C LinsUMUT FAHRİOĞLUUĞUR DEVECİV Reid SuttonVALENTINA STANLEYVIRANI ABBIRVineet AggarwalVirginia KimonisWEIXING OUYAVUZ BAYRAMYING WANGYVES SZNAJERZeynep Çoban AkdemirÜMMÜHAN ÖNCÜL DEMİRCAN
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.