Academician
TİMUR TUNCALI
DOÇENT
ANKARA ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Tıbbi Genetik
A quick look at recorded outputs — details below.
- Articles 34
- Projects 0
- Books 0
- Proceedings 27
- Patents 0
- Artistic 0
Scopus (SJR)
Q1
7
Q2
11
Q3
7
Q4
4
WoS (JCR)
Q1
4
Q2
5
Q3
9
Q4
12
TR Index
8
articles
Field+year+type normalized OpenAlex percentiles — not Clarivate ESI / SciVal.
Top 1% articles
0
Top 10% articles
1
Avg percentile
54.0%
Top 1% share
0.0%
Top 10% share
3.4%
Articles
Articles with YÖKSİS and OpenAlex source split; narrow by quartile or TR Index.
Article list
- 2026 Diagnostic Yield and Clinical Utility of Genetic Testing in Turkish Adults with Suspected Inherited Kidney Disease: Insights from a Population with High Parental Consanguinity YÖKSİS TR Index JCR Q4 OpenAlex 47.0%
- 2025 Somatic variants and frequencies of familial myeloma germline predisposition genes among patients within the CoMMpass dataset YÖKSİS SJR Q2 JCR Q2 OpenAlex 29.9%
- 2025 Familial Multiple Myeloma: Insights From Epidemiology and Underlying Germline Genetic Predisposition to the Clinic YÖKSİS SJR Q2 JCR Q1 OpenAlex 80.0%
- 2024 X-linked Dyskeratosis Congenita Case with Mutation 1058C>T(p.Ala353Val) in Dyskerine Gene YÖKSİS SJR Q3 JCR Q3 OpenAlex 60.6%
- 2023 Germline genetic variants in Turkish familial multiple myeloma/monoclonal gammopathy of undetermined significance cases YÖKSİS SJR Q1 JCR Q1 OpenAlex 81.4%
- 2023 Contribution of genotypes in Prothrombin and Factor V Leiden to COVID-19 and disease severity in patients at high risk for hereditary thrombophilia YÖKSİS SJR Q1 JCR Q1 OpenAlex 81.5%
- 2022 Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium YÖKSİS SJR Q2 JCR Q3 OpenAlex 75.1%
- 2022 Phenotypic and molecular characterization of five patients with PIK3CA‐related overgrowth spectrum (PROS) YÖKSİS SJR Q2 JCR Q3 OpenAlex 77.8%
- 2021 Right Anterior Theta Hypersynchrony as a Quantitative Measure Associated with Autistic Traits and K-Cl Cotransporter KCC2 Polymorphism YÖKSİS SJR Q1 JCR Q2 OpenAlex 64.6%
- 2021 ROHMM-A flexible hidden Markov model framework to detect runs of homozygosity from genotyping data YÖKSİS SJR Q1 JCR Q2 OpenAlex 69.5%
- 2021 Coexistence of Ovarian Granulose Cell Tumor, Congenital Adrenal Hyperplasia, and Triple Translocation: Is a Consequence or Coincidence? YÖKSİS SJR Q3 JCR Q4 OpenAlex 39.6%
- 2021 Kromozom 3 Dengesizliği Olan Bir Olgunun Genotip Fenotip Korelasyonu YÖKSİS OpenAlex 10.8%
- 2018 A Novel PTCH1 Frameshift Mutation Leading to Nevoid Basal Cell Carcinoma Syndrome YÖKSİS SJR Q3 JCR Q4 OpenAlex 58.7%
- 2015 Seckel syndrome with cutaneous pigmentary changes two siblings and a review of the literature YÖKSİS SJR Q3 JCR Q3 OpenAlex 18.0%
- 2014 Epstein Barr Virus Negative Post Transplant Lymphoproliferative Diseases Three Distinct Cases from a Single Center YÖKSİS TR Index SJR Q4 JCR Q4 OpenAlex 6.2%
- 2013 Oesophageal achalasia misdiagnosed as uncontrolled asthma YÖKSİS TR Index SJR Q2 JCR Q4 OpenAlex 60.4%
- 2013 An Evaluation of the Phenotypic Features of Fanconi Anemia Together with DEB/MMC Positivity in 199 Turkish Patients YÖKSİS SJR Q3 JCR Q4 OpenAlex 8.5%
- 2011 Association of methylenetetrahydrofolate reductase C677T-A1298C polymorphisms with risk for esophageal adenocarcinoma, Barretts esophagus, and reflux esophagitis YÖKSİS SJR Q2 JCR Q3 OpenAlex 86.3%
- 2007 The contribution of genotypes at the MICA gene triplet repeat polymorphisms and MEFV mutations to amyloidosis and course of the disease in the patients with familial Mediterranean fever YÖKSİS SJR Q2 JCR Q4 OpenAlex 62.0%
- 2007 Colobomatous macrophthalmia with microcornea syndrome maps to the 2p23 p16 region YÖKSİS SJR Q2 JCR Q3 OpenAlex 61.6%