Altuğ Koç

667 total citations
53 papers, 356 citations indexed

About

Altuğ Koç is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Altuğ Koç has authored 53 papers receiving a total of 356 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 16 papers in Pediatrics, Perinatology and Child Health and 15 papers in Molecular Biology. Recurrent topics in Altuğ Koç's work include Prenatal Screening and Diagnostics (16 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetic factors in colorectal cancer (5 papers). Altuğ Koç is often cited by papers focused on Prenatal Screening and Diagnostics (16 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetic factors in colorectal cancer (5 papers). Altuğ Koç collaborates with scholars based in Türkiye, United States and Germany. Altuğ Koç's co-authors include Mehmet Ali Ergün, E. Ferda Perçin, Taha Reşid Özdemir, Meral Yirmibeş Karaoğuz, Özgür Kırbıyık, Peyamı Cınaz, Mehmet Özeren, Naciye Sinem Gezer, Kadri Karaer and Aysun Bıdecı and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Altuğ Koç

50 papers receiving 326 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Altuğ Koç Türkiye 11 157 107 80 44 33 53 356
Mohammad Yahya Vahidi Mehrjardi Iran 13 68 0.4× 184 1.7× 22 0.3× 32 0.7× 11 0.3× 38 323
Suzanne S. Fei United States 13 55 0.4× 172 1.6× 70 0.9× 21 0.5× 13 0.4× 31 412
Faouzi Mâazoul Tunisia 13 345 2.2× 424 4.0× 51 0.6× 28 0.6× 17 0.5× 46 567
Ping Ye United States 9 54 0.3× 220 2.1× 34 0.4× 19 0.4× 58 1.8× 18 384
Sophie Brisset France 16 378 2.4× 194 1.8× 183 2.3× 40 0.9× 133 4.0× 39 585
Elena Bianchi Italy 12 114 0.7× 135 1.3× 65 0.8× 32 0.7× 8 0.2× 27 419
Roberto Quadrelli United States 10 186 1.2× 345 3.2× 72 0.9× 82 1.9× 39 1.2× 26 602
Richa Sharma India 12 104 0.7× 230 2.1× 33 0.4× 35 0.8× 82 2.5× 23 427
Alicia Vaglio United States 7 159 1.0× 338 3.2× 53 0.7× 72 1.6× 31 0.9× 24 548
Jostein Westvik Norway 9 172 1.1× 246 2.3× 35 0.4× 31 0.7× 21 0.6× 14 364

Countries citing papers authored by Altuğ Koç

Since Specialization
Citations

This map shows the geographic impact of Altuğ Koç's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Altuğ Koç with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Altuğ Koç more than expected).

Fields of papers citing papers by Altuğ Koç

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Altuğ Koç. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Altuğ Koç. The network helps show where Altuğ Koç may publish in the future.

Co-authorship network of co-authors of Altuğ Koç

This figure shows the co-authorship network connecting the top 25 collaborators of Altuğ Koç. A scholar is included among the top collaborators of Altuğ Koç based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Altuğ Koç. Altuğ Koç is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Çağlayan, Ahmet Okay, et al.. (2024). Clinical and Molecular Analysis in Patients with Peutz-Jeghers Syndrome. The Turkish Journal of Gastroenterology. 35(5). 374–384. 1 indexed citations
2.
Göksel, Tuncay, Su Özgür, Aslı Teti̇k Vardarli, et al.. (2024). Prognostic and predictive role of liquid biopsy in lung cancer patients. Frontiers in Oncology. 13. 1275525–1275525. 2 indexed citations
3.
Ellıdokuz, Hülya, et al.. (2024). New treatment alternatives for primary and metastatic colorectal cancer by an integrated transcriptome and network analyses. Scientific Reports. 14(1). 8762–8762. 3 indexed citations
4.
Gülhan, İbrahim, et al.. (2022). High Risk of Gestational Trophoblastic Neoplasia Development in Recurrent Hydatidiform Moles with NLRP7 Pathogenic Variations. SHILAP Revista de lepidopterología. 25(2). 45–50. 1 indexed citations
5.
Bayram, Meral Torun, et al.. (2022). Late onset Bartter syndrome: Bartter syndrome type 2 presenting with isolated nephrocalcinosis and high parathyroid hormone levels mimicking primary hyperparathyroidism. Journal of Pediatric Endocrinology and Metabolism. 35(10). 1298–1301. 1 indexed citations
6.
Çağlayan, Ahmet Okay, Altuğ Koç, Tufan Çankaya, et al.. (2022). Evaluation of hereditary/familial breast cancer patients with multigene targeted next generation sequencing panel and MLPA analysis in Turkey. Cancer Genetics. 262-263. 118–133. 6 indexed citations
7.
8.
Işık, Zerrin, et al.. (2022). In silico identification of novel biomarkers for key players in transition from normal colon tissue to adenomatous polyps. PLoS ONE. 17(4). e0267973–e0267973. 2 indexed citations
9.
Koç, Altuğ, et al.. (2021). PCR-Free Methodology for Detection of Single-Nucleotide Polymorphism with a Cationic Polythiophene Reporter. ACS Sensors. 6(3). 950–957. 8 indexed citations
10.
Koç, Altuğ, et al.. (2020). Warburg Micro Syndrome 1 due to Segmental Paternal Uniparental Isodisomy of Chromosome 2 Detected by Whole-Exome Sequencing and Homozygosity Mapping. Cytogenetic and Genome Research. 160(6). 309–315. 2 indexed citations
11.
Özdemir, Taha Reşid, et al.. (2019). Evaluation of chromosomal abnormalities and Y-chromosome microdeletions in 1696 Turkish cases with primary male infertility: A single-center study. SHILAP Revista de lepidopterología. 46(2). 95–100. 7 indexed citations
12.
Kırbıyık, Özgür, et al.. (2019). First-Line Molecular Genetic Evaluation of Autosomal Recessive Non-Syndromic Hearing Loss. SHILAP Revista de lepidopterología. 57(3). 140–148. 2 indexed citations
13.
Koç, Altuğ. (2018). MİCHEL FOUCAULT’NUN “BİYOPOLİTİKA” KAVRAMININ TEORİK ÇERÇEVESİ. DergiPark (Istanbul University). 2(2). 193–218.
14.
Koç, Altuğ, et al.. (2018). Fetal HLA-G alleles and their effect on miscarriage. Advances in Clinical and Experimental Medicine. 27(9). 1233–1237. 7 indexed citations
15.
Koç, Altuğ, Taha Reşid Özdemir, Özgür Kırbıyık, et al.. (2017). QF-PCR in invasive prenatal diagnosis: a single-center experience in Turkey. TURKISH JOURNAL OF MEDICAL SCIENCES. 47(1). 142–147. 3 indexed citations
16.
Bayol, Ümit, et al.. (2016). Investigating KRAS/BRAF mutation in oropharyngeal squamous cell carcinomas: a preliminary study. The Turkish Journal of Ear Nose and Throat. 26(5). 265–267. 2 indexed citations
17.
Koç, Altuğ, Abdullah Ekmekçi, & Onur Özer. (2013). A case of dup(3q) syndrome.. PubMed. 24(4). 381–5. 1 indexed citations
18.
Ergün, Mehmet Ali, Meral Yirmibeş Karaoğuz, Altuğ Koç, et al.. (2010). The Apolipoprotein E Gene and Taq1A Polymorphisms in Childhood Obesity. Genetic Testing and Molecular Biomarkers. 14(3). 343–345. 10 indexed citations
19.
Koç, Altuğ, et al.. (2009). Prenatal diagnosis of mosaic ring 22 duplication/deletion with terminal 22q13 deletion due to abnormal first trimester screening and choroid plexus cyst detected on ultrasound. Journal of obstetrics and gynaecology research. 35(5). 978–982. 14 indexed citations
20.
Yeşilkaya, Ediz, Altuğ Koç, Aysun Bıdecı, et al.. (2008). CTLA4 Gene Polymorphisms in Children and Adolescents with Autoimmune Thyroid Diseases. Genetic Testing. 12(3). 461–464. 17 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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