Ali Dursun

2.0k total citations
97 papers, 995 citations indexed

About

Ali Dursun is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, Ali Dursun has authored 97 papers receiving a total of 995 indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Clinical Biochemistry, 48 papers in Molecular Biology and 21 papers in Physiology. Recurrent topics in Ali Dursun's work include Metabolism and Genetic Disorders (51 papers), Mitochondrial Function and Pathology (19 papers) and Neonatal Health and Biochemistry (12 papers). Ali Dursun is often cited by papers focused on Metabolism and Genetic Disorders (51 papers), Mitochondrial Function and Pathology (19 papers) and Neonatal Health and Biochemistry (12 papers). Ali Dursun collaborates with scholars based in Türkiye, United States and Denmark. Ali Dursun's co-authors include Turgay Coşkun, Ayşegül Tokatlı, Rıza Köksal Özgül, Serap Sivri, H. Serap Kalkanoğlu, Hatice Serap Sivri, Yılmaz Yıldız, Didem Aliefendioğlu, Mustafa Özsütçü and Abdülkadir Koçer and has published in prestigious journals such as SHILAP Revista de lepidopterología, Free Radical Biology and Medicine and International Journal of Molecular Sciences.

In The Last Decade

Ali Dursun

88 papers receiving 966 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ali Dursun Türkiye	17	438	434	215	165	145	97	995
Diana Ballhausen Switzerland	19	356 0.8×	546 1.3×	347 1.6×	158 1.0×	167 1.2×	46	1.1k
Judit García‐Villoria Spain	24	511 1.2×	673 1.6×	189 0.9×	218 1.3×	135 0.9×	73	1.3k
Dimitar Gavrilov United States	15	437 1.0×	403 0.9×	345 1.6×	152 0.9×	121 0.8×	35	901
Ayşegül Tokatlı Türkiye	17	575 1.3×	610 1.4×	249 1.2×	184 1.1×	116 0.8×	101	1.3k
Lock Hock Ngu Malaysia	18	299 0.7×	503 1.2×	181 0.8×	113 0.7×	242 1.7×	59	899
David Coman Australia	20	302 0.7×	583 1.3×	302 1.4×	149 0.9×	227 1.6×	79	1.2k
Carolina Fischinger Moura de Souza Brazil	19	362 0.8×	507 1.2×	427 2.0×	279 1.7×	183 1.3×	110	1.2k
Zuhair N. Al‐Hassnan Saudi Arabia	18	291 0.7×	549 1.3×	166 0.8×	114 0.7×	248 1.7×	78	1.0k
Jim McGill Australia	15	376 0.9×	306 0.7×	243 1.1×	198 1.2×	182 1.3×	34	829
Klaas J. Wierenga United States	21	305 0.7×	579 1.3×	137 0.6×	118 0.7×	221 1.5×	43	1.4k

Countries citing papers authored by Ali Dursun

Since Specialization

Citations

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

Fields of papers citing papers by Ali Dursun

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ali Dursun

This figure shows the co-authorship network connecting the top 25 collaborators of Ali Dursun. A scholar is included among the top collaborators of Ali Dursun 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 Dursun. Ali Dursun is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Dursun, Ali, et al.. (2025). Metabolomics and Lipidomics Explore Phenotype-Specific Molecular Signatures for Phenylketonuria. International Journal of Molecular Sciences. 26(15). 7171–7171.

Ayhan, Selda & Ali Dursun. (2024). ELFN1 is a new extracellular matrix (ECM)-associated protein. Life Sciences. 352. 122900–122900. 1 indexed citations

Gülbakan, Basri, Rıza Köksal Özgül, Rahşan Göçmen, et al.. (2024). Exploring metabolic alterations in PYCR2 deficiency: Unveiling pathways and clinical presentations of hypomyelinating leukodystrophy 10. American Journal of Medical Genetics Part A. 194(9). e63645–e63645.

Yıldız, Yılmaz, et al.. (2021). DNACJ12 deficiency in patients with unexplained hyperphenylalaninemia: two new patients and a novel variant. Metabolic Brain Disease. 36(6). 1405–1410. 8 indexed citations

Yıldız, Yılmaz, et al.. (2021). Correction to: DNAJC12 deficiency in patients with unexplained hyperphenylalaninemia: two new patients and a novel variant. Metabolic Brain Disease. 36(6). 1411–1411. 1 indexed citations

Dursun, Ali, Dilek Yalnızoğlu, Kader Karlı Oğuz, et al.. (2021). Biallelic mutations in ELFN1 gene associated with developmental and epileptic encephalopathy and joint laxity. European Journal of Medical Genetics. 64(11). 104340–104340. 7 indexed citations

Özdemir, Dilşad Foto, Yılmaz Yıldız, Ali Dursun, et al.. (2018). Cognitive and behavioral impairment in mild hyperphenylalaninemia. The Turkish Journal of Pediatrics. 60(6). 617–624. 10 indexed citations

Özgül, Rıza Köksal, Dilek Yalnızoğlu, Ayşegül Tokatlı, et al.. (2017). Two Turkish siblings with MEGDEL syndrome due to novel SERAC1 gene mutation.. PubMed. 57(4). 388–393. 6 indexed citations

Alikaşifoğlu, Ayfer, Nurgün Kandemir, Munis Dündar, et al.. (2016). A Nonvirilized form of Classic 3[beta]-Hydroxysteroid Dehydrogenase Deficiency Due to a Homozygous S218P Mutation in the HSD3B2 Gene in a Girl with Classic Phenylketonuria. 86. 1 indexed citations

10.

Ünal, Özlem, Hülya Gökmen-Özel, Turgay Coşkun, et al.. (2016). Sapropterin dihydrochloride treatment in Turkish hyperphenylalaninemic patients under age four.. PubMed. 57(3). 213–8. 7 indexed citations

11.

Yıldız, Yılmaz, Ali Dursun, Ayşegül Tokatlı, Turgay Coşkun, & Hatice Serap Sivri. (2016). Late-diagnosed phenylketonuria in an eight-year-old boy with dyslexia and attention-deficit hyperactivity disorder. The Turkish Journal of Pediatrics. 58(1). 94–96. 9 indexed citations

12.

Karaca, Mehmet, Burcu Öztürk Hişmi, Rıza Köksal Özgül, et al.. (2013). High prevalence of cerebral venous sinus thrombosis (CVST) as presentation of cystathionine beta-synthase deficiency in childhood: Molecular and clinical findings of Turkish probands. Gene. 534(2). 197–203. 6 indexed citations

13.

Özgül, Rıza Köksal, Halil Dündar, Turgay Coşkun, et al.. (2013). Galactosemia in the Turkish population with a high frequency of Q188R mutation and distribution of Duarte-1 and Duarte-2 variations. Journal of Human Genetics. 58(10). 675–678. 9 indexed citations

14.

Ünal, Özlem, Burcu Öztürk Hişmi, Turgay Coşkun, et al.. (2012). Detection of other inborn errors of metabolism in hyperphenylalaninemic babies picked up on narrow-spectrum screening programs. The Turkish Journal of Pediatrics. 54(4). 409–412. 2 indexed citations

15.

Taşkesen, Mustafa, Turgay Coşkun, Figen Gürakan, et al.. (2011). A Zinc Sulphate-Resistant Acrodermatitis Enteropathica Patient with a Novel Mutation in SLC39A4 Gene. JIMD Reports. 2. 25–28. 9 indexed citations

16.

Özgül, Rıza Köksal, Turgay Coşkun, Mehmet Ali Karaca, et al.. (2011). Identification of Mutations and Evaluation of Cardiomyopathy in Turkish Patients with Primary Carnitine Deficiency. JIMD Reports. 3. 17–23. 20 indexed citations

17.

Dursun, Ali, Rıza Köksal Özgül, Aytemiz Gürgey, et al.. (2008). Familial pulmonary arterial hypertension, leucopenia, and atrial septal defect: a probable new familial syndrome with multisystem involvement. Clinical Dysmorphology. 18(1). 19–23. 16 indexed citations

18.

Ichida, Kimiyoshi, Halil İbrahim Aydın, Makoto Hosoyamada, et al.. (2006). A Turkish Case with Molybdenum Cofactor Deficiency. Nucleosides Nucleotides & Nucleic Acids. 25(9-11). 1087–1091. 9 indexed citations

19.

Sozen, Mert, Ros Whittall, Cihan Öner, et al.. (2005). The molecular basis of familial hypercholesterolaemia in Turkish patients. Atherosclerosis. 180(1). 63–71. 34 indexed citations

20.

Tüysüz, Beyhan, Ali Dursun, Tufan Kutlu, et al.. (2001). HLA‐DQ alleles in patients with celiac disease in Turkey. Tissue Antigens. 57(6). 540–542. 18 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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