Nazlı Kara

1.0k total citations
23 papers, 689 citations indexed

About

Nazlı Kara is a scholar working on Molecular Biology, Nephrology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Nazlı Kara has authored 23 papers receiving a total of 689 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Nephrology and 5 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Nazlı Kara's work include Inflammasome and immune disorders (4 papers), Renal Diseases and Glomerulopathies (3 papers) and Vasculitis and related conditions (3 papers). Nazlı Kara is often cited by papers focused on Inflammasome and immune disorders (4 papers), Renal Diseases and Glomerulopathies (3 papers) and Vasculitis and related conditions (3 papers). Nazlı Kara collaborates with scholars based in Türkiye, United States and Czechia. Nazlı Kara's co-authors include Nermin Uncu, Nilgün Çakar, Fatoş Yalçınkaya, Zeynep Birsin Özçakar, Mesı̇ha Ekı̇m, Özgür Kasapçopur, Ayşı̇n Bakkaloğlu, Atilla Halil Elhan, Beyza Doğanay Erdoğan and Ali Düzova and has published in prestigious journals such as American Journal of Kidney Diseases, Lara D. Veeken and International Journal of Cardiology.

In The Last Decade

Nazlı Kara

22 papers receiving 660 citations

Peers

Nazlı Kara

IMMUN

NEPHR

PRM

SURGE

Necmiye Tümer Türkiye

Mehmet Bülbül Türkiye

Emma Allain‐Launay France

Yoshimitsu Gotoh Japan

Atif Awan Ireland

Joshua Kausman Australia

T. Messiaen Belgium

Thierry Schurmans Belgium

Gülay Demircin Türkiye

Christine Chamberlain United States

Necmiye Tümer Türkiye

Nazlı Kara

418 ×1.0

148 ×0.7

IMMUN

243 ×1.5

NEPHR

125 ×0.9

PRM

139 ×1.1

SURGE

Citations per year, relative to Nazlı Kara Nazlı Kara (= 1×) peers Necmiye Tümer

Countries citing papers authored by Nazlı Kara

Since Specialization

Citations

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

Fields of papers citing papers by Nazlı Kara

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nazlı Kara

This figure shows the co-authorship network connecting the top 25 collaborators of Nazlı Kara. A scholar is included among the top collaborators of Nazlı Kara 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 Kara. Nazlı Kara 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

Kara, Nazlı, et al.. (2025). Epidemiology and healthcare utilization in motor neuron disease in Czechia. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 26(5-6). 541–549.

Canpolat, Nur, Seha Saygılı, Nazlı Kara, et al.. (2021). A splice site mutation in the TSEN2 causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome. Clinical Genetics. 101(3). 346–358. 7 indexed citations

Karakuş, Nevin, et al.. (2017). Influence of the MIF polymorphism −173G > C on Turkish postmenopausal women with osteoporosis. Zeitschrift für Rheumatologie. 77(7). 629–632. 4 indexed citations

Özçakar, Zeynep Birsin, Fatoş Yalçınkaya, Nilgün Çakar, et al.. (2011). Application of the new pediatric criteria and Tel Hashomer criteria in heterozygous patients with clinical features of FMF. European Journal of Pediatrics. 170(8). 1055–1057. 21 indexed citations

Bilginer, Yelda, Rezan Topaloğlu, Ayfer Alikaşifoğlu, et al.. (2009). Low cortisol levels in active juvenile idiopathic arthritis. Clinical Rheumatology. 29(3). 309–314. 9 indexed citations

Yalçınkaya, Fatoş, Zeynep Birsin Özçakar, Nilgün Çakar, et al.. (2009). A new set of criteria for the diagnosis of familial Mediterranean fever in childhood. Lara D. Veeken. 48(4). 395–398. 335 indexed citations

Acar, Banu Çelikel, Fatoş Yalçınkaya, Nilgün Çakar, et al.. (2008). The outcome for pediatric patients on peritoneal dialysis. Journal of Nephrology. 21(3). 394–399. 3 indexed citations

Ünal, Sevim, Ebru Arhan, Nazlı Kara, Nermin Uncu, & Didem Aliefendioğlu. (2008). Breast‐feeding‐associated hypernatremia: Retrospective analysis of 169 term newborns. Pediatrics International. 50(1). 29–34. 68 indexed citations

Çakar, Nilgün, Zeynep Birsin Özçakar, Suat Fítöz, et al.. (2008). Renal Involvement in Childhood Vasculitis. Nephron Clinical Practice. 108(3). c202–c206. 8 indexed citations

10.

Özçakar, Zeynep Birsin, Fatoş Yalçınkaya, Nilgün Çakar, et al.. (2008). MEFV Mutations Modify the Clinical Presentation of Henoch-Schönlein Purpura. The Journal of Rheumatology. 35(12). 2427–2429. 49 indexed citations

11.

Uçar, Tayfun, Ercan Tutar, Fatoş Yalçınkaya, et al.. (2008). Global left-ventricular function by tissue Doppler imaging in pediatric dialysis patients. Pediatric Nephrology. 23(5). 779–785. 20 indexed citations

12.

Özçakar, Zeynep Birsin, Filiz Başak Cengiz, Nilgün Çakar, et al.. (2006). Analysis of NPHS2 mutations in Turkish steroid-resistant nephrotic syndrome patients. Pediatric Nephrology. 21(8). 1093–1096. 13 indexed citations

13.

Özçakar, Zeynep Birsin, Fatoş Yalçınkaya, Ercan Tutar, et al.. (2006). Hypertension and Left Ventricular Hypertrophy in Pediatric Peritoneal Dialysis Patients: Ambulatory Blood Pressure Monitoring and Echocardiographic Evaluation. Nephron Clinical Practice. 104(2). c101–c106. 15 indexed citations

14.

Aydın, Fatma, et al.. (2006). Lack of association between leptin G2548A gene polymorphism and Behçet's disease. Journal of the European Academy of Dermatology and Venereology. 21(1). 68–71. 4 indexed citations

15.

Özkaya, Nuray, et al.. (2004). Primary nephrotic syndrome during childhood in Turkey. Pediatrics International. 46(4). 436–438. 24 indexed citations

16.

Kara, Nazlı, et al.. (2003). Cardiac abnormalities in children with systemic lupus erythematosus. The Turkish Journal of Pediatrics. 45(4). 301–305. 15 indexed citations

17.

Özen, Seza, U Saatçi, A Bakkaloğlu, et al.. (1999). Implications of certain genetic polymorphisms in scarring in vesicoureteric reflux: Importance of ace polymorphism. American Journal of Kidney Diseases. 34(1). 140–145. 51 indexed citations

18.

Kara, Nazlı, et al.. (1997). Cardiac involvement in childhood polyarteritis nodosa. International Journal of Cardiology. 60(3). 257–262. 13 indexed citations

19.

Küçüködük, Ş., et al.. (1996). Partial trisomy 18q. The Indian Journal of Pediatrics. 63(3). 393–396. 1 indexed citations

20.

Bağcı, Hasan, et al.. (1994). A case of hypogonadism with a translocation: t (4; 12) (q25; q24.2). The Indian Journal of Pediatrics. 61(4). 421–426. 5 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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