Emel Ergül

1.2k total citations
35 papers, 884 citations indexed

About

Emel Ergül is a scholar working on Molecular Biology, Rheumatology and Genetics. According to data from OpenAlex, Emel Ergül has authored 35 papers receiving a total of 884 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 12 papers in Rheumatology and 7 papers in Genetics. Recurrent topics in Emel Ergül's work include Folate and B Vitamins Research (12 papers), Genomic variations and chromosomal abnormalities (4 papers) and Amyotrophic Lateral Sclerosis Research (3 papers). Emel Ergül is often cited by papers focused on Folate and B Vitamins Research (12 papers), Genomic variations and chromosomal abnormalities (4 papers) and Amyotrophic Lateral Sclerosis Research (3 papers). Emel Ergül collaborates with scholars based in Türkiye, Germany and United States. Emel Ergül's co-authors include Ali Sazcı, İhsan Kara, Güner Kaya, Gürler Akpınar, Gamze Kılıç, Nuh Zafer Cantürk, Zafer Utkan, Cem İ̇smail Küçükali, Neşe Tuncer and Sadettin Hülagü and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gene and Fertility and Sterility.

In The Last Decade

Emel Ergül

35 papers receiving 851 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Emel Ergül Türkiye 16 379 213 169 147 138 35 884
Ali Sazcı Türkiye 19 412 1.1× 255 1.2× 185 1.1× 168 1.1× 156 1.1× 42 993
Qing Lin China 11 239 0.6× 174 0.8× 90 0.5× 45 0.3× 38 0.3× 25 595
Carolina Gravina Italy 17 124 0.3× 348 1.6× 121 0.7× 129 0.9× 58 0.4× 40 921
Ann Bowron United Kingdom 13 255 0.7× 424 2.0× 36 0.2× 79 0.5× 58 0.4× 29 997
Zoltán Szolnoki Hungary 20 131 0.3× 308 1.4× 49 0.3× 100 0.7× 77 0.6× 54 971
Antonio Masala Italy 16 119 0.3× 157 0.7× 49 0.3× 50 0.3× 46 0.3× 69 902
Eija Hämäläinen Finland 18 38 0.1× 433 2.0× 248 1.5× 172 1.2× 67 0.5× 27 1.2k
Lance H. Rodan United States 17 64 0.2× 285 1.3× 52 0.3× 118 0.8× 152 1.1× 48 763
John H. Walter United Kingdom 20 589 1.6× 874 4.1× 51 0.3× 210 1.4× 46 0.3× 39 1.9k
Kimmo Kontula Finland 21 45 0.1× 560 2.6× 76 0.4× 182 1.2× 116 0.8× 40 1.5k

Countries citing papers authored by Emel Ergül

Since Specialization
Citations

This map shows the geographic impact of Emel Ergül'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 Emel Ergül with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Emel Ergül more than expected).

Fields of papers citing papers by Emel Ergül

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Emel Ergül. 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 Emel Ergül. The network helps show where Emel Ergül may publish in the future.

Co-authorship network of co-authors of Emel Ergül

This figure shows the co-authorship network connecting the top 25 collaborators of Emel Ergül. A scholar is included among the top collaborators of Emel Ergül 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 Emel Ergül. Emel Ergül 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.
Sazcı, Ali, et al.. (2021). Investigation of some variations of superoxide dismutase gene family in Turkish sporadic amyotrophic lateral sclerosis patients. SHILAP Revista de lepidopterología. 3. 100013–100013. 1 indexed citations
2.
Sazcı, Ali, et al.. (2016). Nicotinamide-N-Methyltransferase gene rs694539 variant and migraine risk. The Journal of Headache and Pain. 17(1). 93–93. 13 indexed citations
3.
Sazcı, Ali, et al.. (2013). Association of Nicotinamide- N -Methyltransferase Gene rs694539 Variant with Patients with Nonalcoholic Steatohepatitis. Genetic Testing and Molecular Biomarkers. 17(11). 849–853. 23 indexed citations
4.
Ergül, Emel, et al.. (2012). ZNF804A rs1344706 Variant and Schizophrenia in a Romanian Population from Cluj Napoca. Genetic Testing and Molecular Biomarkers. 16(9). 1135–1137. 6 indexed citations
5.
Sazcı, Ali, et al.. (2012). Gender-Specific Association of Methylenetetrahydrofolate Reductase Gene Polymorphisms with Sporadic Amyotrophic Lateral Sclerosis. Genetic Testing and Molecular Biomarkers. 16(7). 716–721. 10 indexed citations
6.
7.
Ergül, Emel, Ali Sazcı, & İhsan Kara. (2011). Methylenetetrahydrofolate Reductase Gene Polymorphisms in Turkish Children with Attention-Deficit/Hyperactivity Disorder. Genetic Testing and Molecular Biomarkers. 16(1). 67–69. 15 indexed citations
8.
Ergül, Emel, et al.. (2011). TP53 Arg72Pro polymorphism in Turkish patients with sporadic amyotrophic lateral sclerosis. Neurobiology of Aging. 32(11). 2107.e1–2107.e2. 4 indexed citations
9.
Sazcı, Ali, Gürler Akpınar, Cem Aygün, et al.. (2008). Association of Apolipoprotein E Polymorphisms in Patients with Non-Alcoholic Steatohepatitis. Digestive Diseases and Sciences. 53(12). 3218–3224. 66 indexed citations
10.
Kasap, Murat, Ali Sazcı, Gürler Akpınar, & Emel Ergül. (2007). Apolipoprotein E phylogeny and evolution. Cell Biochemistry and Function. 26(1). 43–50. 9 indexed citations
11.
Sazcı, Ali, Emel Ergül, Cem Aygün, et al.. (2007). Methylenetetrahydrofolate reductase gene polymorphisms in patients with nonalcoholic steatohepatitis (NASH). Cell Biochemistry and Function. 26(3). 291–296. 32 indexed citations
12.
Sazcı, Ali, Emel Ergül, Neşe Tuncer, Gürler Akpınar, & İhsan Kara. (2006). Methylenetetrahydrofolate reductase gene polymorphisms are associated with ischemic and hemorrhagic stroke: Dual effect of MTHFR polymorphisms C677T and A1298C. Brain Research Bulletin. 71(1-3). 45–50. 85 indexed citations
13.
Kasap, Murat, Ali Sazcı, Emel Ergül, & Gürler Akpınar. (2006). Molecular phylogenetic analysis of methylenetetrahydrofolate reductase family of proteins. Molecular Phylogenetics and Evolution. 42(3). 838–846. 4 indexed citations
14.
Sazcı, Ali, et al.. (2005). Male factor infertility associated with a familial translocation t(1;13)(q24;q10). Fertility and Sterility. 83(5). 1548.e19–1548.e21. 3 indexed citations
15.
Sazcı, Ali, Emel Ergül, Güner Kaya, & İhsan Kara. (2004). Genotype and allele frequencies of the polymorphic methylenetetrahydrofolate reductase gene in Turkey. Cell Biochemistry and Function. 23(1). 51–54. 60 indexed citations
16.
Sazcı, Ali, et al.. (2004). Association of the C677T and A1298C polymorphisms of methylenetetrahydrofolate reductase gene in patients with essential tremor in Turkey. Movement Disorders. 19(12). 1472–1476. 28 indexed citations
17.
Sazcı, Ali, Emel Ergül, Cem İ̇smail Küçükali, et al.. (2004). Catechol-O-methyltransferase gene Val108/158Met polymorphism, and susceptibility to schizophrenia: association is more significant in women. Molecular Brain Research. 132(1). 51–56. 48 indexed citations
18.
Ergül, Emel, Ali Sazcı, Zafer Utkan, & Nuh Zafer Cantürk. (2003). Polymorphisms in the MTHFR Gene Are Associated with Breast Cancer. Tumor Biology. 24(6). 286–290. 84 indexed citations
19.
Kara, İhsan, Ali Sazcı, Emel Ergül, Güner Kaya, & Gamze Kılıç. (2003). Association of the C677T and A1298C polymorphisms in the 5,10 methylenetetrahydrofolate reductase gene in patients with migraine risk. Molecular Brain Research. 111(1-2). 84–90. 135 indexed citations
20.
Ergül, Emel. (2001). Molecular Genetics of Breast Cancer. DergiPark (Istanbul University). 4 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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