Ali Sazcı

1.3k total citations
42 papers, 993 citations indexed

About

Ali Sazcı is a scholar working on Molecular Biology, Rheumatology and Genetics. According to data from OpenAlex, Ali Sazcı has authored 42 papers receiving a total of 993 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 13 papers in Rheumatology and 9 papers in Genetics. Recurrent topics in Ali Sazcı's work include Folate and B Vitamins Research (13 papers), Liver Disease Diagnosis and Treatment (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Ali Sazcı is often cited by papers focused on Folate and B Vitamins Research (13 papers), Liver Disease Diagnosis and Treatment (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Ali Sazcı collaborates with scholars based in Türkiye, Germany and United Kingdom. Ali Sazcı's co-authors include Emel Ergül, İhsan Kara, Güner Kaya, Gamze Kılıç, Gürler Akpınar, Nuh Zafer Cantürk, Neşe Tuncer, Zafer Utkan, Cem İ̇smail Küçükali and Cem Aygün and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gene and Fertility and Sterility.

In The Last Decade

Ali Sazcı

42 papers receiving 955 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ali Sazcı Türkiye 19 412 255 185 168 156 42 993
Emel Ergül Türkiye 16 379 0.9× 213 0.8× 169 0.9× 147 0.9× 138 0.9× 35 884
Ranjana Poddar United States 18 423 1.0× 425 1.7× 52 0.3× 79 0.5× 82 0.5× 29 1.2k
Areeg El‐Gharbawy United States 17 446 1.1× 299 1.2× 37 0.2× 249 1.5× 80 0.5× 31 1.1k
Zoltán Szolnoki Hungary 20 131 0.3× 308 1.2× 49 0.3× 100 0.6× 77 0.5× 54 971
Carolina Gravina Italy 17 124 0.3× 348 1.4× 121 0.7× 129 0.8× 58 0.4× 40 921
Aurelio Jara‐Prado Mexico 13 147 0.4× 170 0.7× 168 0.9× 152 0.9× 34 0.2× 32 627
Eija Hämäläinen Finland 18 38 0.1× 433 1.7× 248 1.3× 172 1.0× 67 0.4× 27 1.2k
Qing Lin China 11 239 0.6× 174 0.7× 90 0.5× 45 0.3× 38 0.2× 25 595
Kelly Claire Simon United States 13 102 0.2× 227 0.9× 102 0.6× 71 0.4× 78 0.5× 32 1.2k
Wenli Sheng China 13 150 0.4× 200 0.8× 60 0.3× 42 0.3× 63 0.4× 39 641

Countries citing papers authored by Ali Sazcı

Since Specialization
Citations

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

Fields of papers citing papers by Ali Sazcı

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ali Sazcı

This figure shows the co-authorship network connecting the top 25 collaborators of Ali Sazcı. A scholar is included among the top collaborators of Ali Sazcı 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 Ali Sazcı. Ali Sazcı 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.. (2019). Female gender specific association of the Reelin (RELN) gene rs7341475 variant with schizophrenia. Molecular Biology Reports. 46(3). 3411–3416. 14 indexed citations
3.
Sazcı, Ali & Halil Atilla Idrısoğlu. (2019). Pregnancy in Parkinson's disease with PARK2 mutations. Clinical Parkinsonism & Related Disorders. 1. 52–53. 1 indexed citations
4.
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
5.
Sazcı, Ali, et al.. (2016). Transcription factor 4 gene rs9960767 polymorphism in bipolar disorder. Biomedical Reports. 5(4). 506–510. 1 indexed citations
6.
Sazcı, Ali, et al.. (2014). Association of rs62063857 Variant of the Saitohin Gene with Parkinson’s Disease. Cellular and Molecular Neurobiology. 35(1). 115–121. 3 indexed citations
7.
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
8.
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
9.
10.
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
11.
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
12.
Kasap, Murat & Ali Sazcı. (2008). The comparison of VEGFR-1-binding domain of VEGF-A with modelled VEGF-C sheds light on receptor specificity. Journal of Theoretical Biology. 253(3). 446–451. 1 indexed citations
13.
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
14.
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
15.
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
16.
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
17.
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
18.
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
19.
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
20.
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

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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