Nazlı Başak

2.0k total citations
15 papers, 295 citations indexed

About

Nazlı Başak is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Nazlı Başak has authored 15 papers receiving a total of 295 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 5 papers in Neurology. Recurrent topics in Nazlı Başak's work include Mitochondrial Function and Pathology (5 papers), Genetic Neurodegenerative Diseases (4 papers) and Neurological diseases and metabolism (2 papers). Nazlı Başak is often cited by papers focused on Mitochondrial Function and Pathology (5 papers), Genetic Neurodegenerative Diseases (4 papers) and Neurological diseases and metabolism (2 papers). Nazlı Başak collaborates with scholars based in Türkiye and Germany. Nazlı Başak's co-authors include Heinrich G. Köchel, Hans Küntzel, Roland Netzker, Colin M. Lazarus, Aslı Çetin, Osman Çiftçi, Murat Emre, Haşmet Hanağası, Peter Heutink and Anamika Giri and has published in prestigious journals such as Cell, Nucleic Acids Research and Parkinsonism & Related Disorders.

In The Last Decade

Nazlı Başak

13 papers receiving 284 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nazlı Başak Türkiye	6	190	35	35	31	28	15	295
Xiuying Duan China	10	233 1.2×	9 0.3×	30 0.9×	19 0.6×	13 0.5×	15	342
Valentina Siino Sweden	9	93 0.5×	8 0.2×	15 0.4×	11 0.4×	14 0.5×	20	218
Jay M. Sage United States	8	240 1.3×	13 0.4×	7 0.2×	6 0.2×	33 1.2×	11	359
Susana R. Valdéz Argentina	11	50 0.3×	9 0.3×	12 0.3×	36 1.2×	13 0.5×	32	309
Changmei Chen China	9	98 0.5×	11 0.3×	6 0.2×	7 0.2×	29 1.0×	18	323
Belén Tizón Spain	7	178 0.9×	18 0.5×	40 1.1×	3 0.1×	23 0.8×	11	336
Moon-Yong Cha United States	2	176 0.9×	11 0.3×	35 1.0×	11 0.4×	7 0.3×	2	338
D. T. Brown United Kingdom	9	677 3.6×	8 0.2×	18 0.5×	5 0.2×	55 2.0×	10	747
Xiaoling Guo China	8	91 0.5×	6 0.2×	14 0.4×	14 0.5×	33 1.2×	17	227
Charles G. Rosa United States	11	126 0.7×	6 0.2×	25 0.7×	18 0.6×	16 0.6×	16	318

Countries citing papers authored by Nazlı Başak

Since Specialization

Citations

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

Fields of papers citing papers by Nazlı Başak

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nazlı Başak

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

All Works

Sort: Min cites: Since: Top N: Style:

15 of 15 papers shown

Şenel, Gülçin Benbir, et al.. (2022). Adult-Onset Treatable Leukodystrophy: Cerebrotendinous Xanthomatosis. Digital Collections portal (Koç University). 60(4). 106–109.

Başak, Nazlı, et al.. (2018). Shunt tapping versus lumbar puncture for evaluating cerebrospinal fluid infections in pediatric population.. Turkish Neurosurgery. 29(2). 275–278. 3 indexed citations

Seçıl, Yaprak, et al.. (2018). Two Families with SOD1 (L144F) and C9orf72 Gene Mutations and an Overview of Amyotrophic Lateral Sclerosis. Turkish Journal Of Neurology. 24(2). 159–164. 1 indexed citations

Başak, Nazlı, et al.. (2017). Coenzyme Q10 deficiency; A treatable autosomal recessive cerebellar ataxias. European Journal of Paediatric Neurology. 21. e136–e136. 2 indexed citations

Hanağası, Haşmet, Anamika Giri, Ece Kartal, et al.. (2016). A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish family. Parkinsonism & Related Disorders. 29. 117–120. 24 indexed citations

Çiftçi, Osman, et al.. (2014). Hesperidin protects testicular and spermatological damages induced by cisplatin in rats. Andrologia. 47(7). 793–800. 60 indexed citations

Kurul, Semra Hız, Uluç Yiş, Ali İrfan Güzel, et al.. (2013). Evaluation of the Cases with Friedreich Ataxia. 55(2). 123–123.

Kaplan, Yüksel, et al.. (2010). Phenotypic differences in a large family with Kennedy's disease from the Middle Black Sea region of Turkey. Amyotrophic Lateral Sclerosis. 11(1-2). 148–153. 4 indexed citations

Hanağası, Haşmet, et al.. (2009). Mitochondrial Pathology in Muscle of a Patient with a Novel Parkin Mutation. International Journal of Neuroscience. 119(10). 1572–1583. 7 indexed citations

10.

Kaplan, Yüksel, et al.. (2008). Phenotypic differences in a large family with Kennedy's disease from the Middle Black Sea region of Turkey. Amyotrophic Lateral Sclerosis. 1–6. 2 indexed citations

11.

Dırık, Eray, et al.. (2007). Spinocerebellar Ataxia Type 2 in a Turkish Family. Journal of Child Neurology. 22(7). 891–894. 5 indexed citations

12.

Akar, Nejat, et al.. (2001). Homozygous ß-Thalassemia (FCS8-AA) and Hereditary Spherocytosis in the Same Patient.. PubMed. 18(2). 137–41. 2 indexed citations

13.

Uysal, Zümrüt, Yıldız Yildirmak, Nejat Akar, Nazlı Başak, & Şükrü Cin. (1998). α-Thalassemia and Hereditary Spherocytosis in the Same Patient: The Interaction of two Diseases. Pediatric Hematology and Oncology. 15(3). 271–276. 7 indexed citations

14.

Netzker, Roland, Heinrich G. Köchel, Nazlı Başak, & Hans Küntzel. (1982). Nucleotide sequence ofAspergillus nidulansmitochondrial genes coding for ATPase subunit 6, cytochrome oxidase subunit 3, seven unidentified proteins, four tRNAs and L-rRNA. Nucleic Acids Research. 10(15). 4783–4794. 111 indexed citations

15.

Köchel, Heinrich G., Colin M. Lazarus, Nazlı Başak, & Hans Küntzel. (1981). Mitochondrial tRNA gene clusters in Aspergillus nidulans: Organization and nucleotide sequence. Cell. 23(2). 625–633. 67 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.

Explore authors with similar magnitude of impact