Banu Nur

983 total citations
36 papers, 358 citations indexed

About

Banu Nur is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Banu Nur has authored 36 papers receiving a total of 358 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 15 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Banu Nur's work include Genomic variations and chromosomal abnormalities (7 papers), Craniofacial Disorders and Treatments (6 papers) and Connective tissue disorders research (5 papers). Banu Nur is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Craniofacial Disorders and Treatments (6 papers) and Connective tissue disorders research (5 papers). Banu Nur collaborates with scholars based in Türkiye, Netherlands and Canada. Banu Nur's co-authors include Ercan Mıhçı, Özgül M. Alper, Mehmet Bayram, Adem Kuşgöz, Mevlüt Çelikoğlu, Saadettin Kayıpmaz, Elanur Yılmaz, Pınar Gençpınar, Şenay Haspolat and Özgür Duman and has published in prestigious journals such as Gene, Cytogenetic and Genome Research and Neuromuscular Disorders.

In The Last Decade

Banu Nur

32 papers receiving 339 citations

Peers

Banu Nur

GENET

ARCHE

SURGE

Ondřej Souček Czechia

Young Pyo Chang South Korea

Dawn Earl United States

Valerie L. Prenger United States

Silvia Vannelli Italy

Mahmoud F. Elsaid Qatar

Ziva Ben Neriah Israel

J. M. Cant� Mexico

Kleber Simônio Parreira Brazil

Jean‐Michel Pedespan France

Ondřej Souček Czechia

Banu Nur

157 ×1.0

183 ×1.5

GENET

5 ×0.1

ARCHE

43 ×0.8

SURGE

3 ×0.1

Citations per year, relative to Banu Nur Banu Nur (= 1×) peers Ondřej Souček

Countries citing papers authored by Banu Nur

Since Specialization

Citations

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

Fields of papers citing papers by Banu Nur

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Banu Nur

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

Nur, Banu, et al.. (2024). A Case with Angelman Syndrome Carried de novo der(15q;15q) By de novo Paternal Uniparental Disomy. DergiPark (Istanbul University). 11(1). 40–46.

Albayrak, Hatice Mutlu, et al.. (2023). Expanding the clinical and molecular features of trichorhino- phalangeal syndrome with a novel variant. The Turkish Journal of Pediatrics. 65(1). 81–95. 2 indexed citations

Uysal, Hilmi, et al.. (2022). Evaluation of exonic copy numbers of SMN1 and SMN2 genes in SMA. Gene. 823. 146322–146322. 2 indexed citations

Yılmaz, Elanur, Banu Nur, Ercan Mıhçı, et al.. (2022). Novel Gene Variants Associated with Primary Ciliary Dyskinesia. The Indian Journal of Pediatrics. 89(7). 682–691. 5 indexed citations

Altunoğlu, Umut, Kıvanç Çefle, Ercan Mıhçı, et al.. (2021). Skeletal and molecular findings in 51 Cleidocranial dysplasia patients from Turkey. American Journal of Medical Genetics Part A. 185(8). 2488–2495. 9 indexed citations

Şimşek‐Kiper, Pelin Özlem, Ekim Z. Taşkıran, Ümüt Arslan, et al.. (2020). Further defining the clinical and molecular spectrum of acromesomelic dysplasia type maroteaux: a Turkish tertiary center experience. Journal of Human Genetics. 66(6). 585–596. 3 indexed citations

Yılmaz, Elanur, et al.. (2019). Recent Advances in Craniosynostosis. Pediatric Neurology. 99. 7–15. 27 indexed citations

Yılmaz, Elanur, Ercan Mıhçı, Banu Nur, & Özgül M. Alper. (2019). Coronal craniosynostosis due to TCF12 mutations in patients from Turkey. American Journal of Medical Genetics Part A. 179(11). 2241–2245. 1 indexed citations

Nur, Banu, et al.. (2018). The clinical spectrum of a rare chromosomal abnormality: Isochromosome 18p.. PubMed. 27(2). 223–31. 1 indexed citations

10.

Akıncı, Gülçin, Haluk Topaloğlu, Tevfik Demir, et al.. (2017). Clinical spectra of neuromuscular manifestations in patients with lipodystrophy: A multicenter study. Neuromuscular Disorders. 27(10). 923–930. 22 indexed citations

11.

Mıhçı, Ercan, et al.. (2017). Celiac disease in patients with Williams-Beuren syndrome.. PubMed. 57(6). 599–604. 12 indexed citations

12.

Nur, Banu, et al.. (2016). Bone mineral density in patients with mucopolysaccharidosis type III. Journal of Bone and Mineral Metabolism. 35(3). 338–343. 10 indexed citations

13.

Karayılmaz, Hüseyin, et al.. (2015). Comprehensive dental management in a Hallermann-Streiff syndrome patient with unusual radiographic appearance of teeth. Nigerian Journal of Clinical Practice. 18(4). 559–559. 6 indexed citations

14.

Nur, Banu, et al.. (2015). Chanarin-Dorfman syndrome: Genotype-Phenotype Correlation. European Journal of Medical Genetics. 58(4). 238–242. 27 indexed citations

15.

Toru, Havva Serap, Banu Nur, Cem Yaşar Sanhal, et al.. (2015). Perinatal Diagnostic Approach to Fetal Skeletal Dysplasias: Six Years Experience of a Tertiary Center. Fetal and Pediatric Pathology. 34(5). 287–306. 7 indexed citations

16.

Gençpınar, Pınar, et al.. (2014). Epidural capillary hemangioma: A review of the literature. Clinical Neurology and Neurosurgery. 126. 99–102. 15 indexed citations

17.

Nur, Banu, et al.. (2014). Clinicogenetic Study of Turkish Patients With Syndromic Craniosynostosis and Literature Review. Pediatric Neurology. 50(5). 482–490. 19 indexed citations

18.

Nur, Banu, et al.. (2013). Possible autosomal recessive inheritance in an infant with acrofacial dysostosis similar to nager syndrome. American Journal of Medical Genetics Part A. 161(9). 2311–2315. 10 indexed citations

19.

Nur, Banu, et al.. (2012). Validity of demirjian and nolla methods for dental age estimation for Northeastern Turkish children aged 5-16 years old. Medicina oral, patología oral y cirugía bucal. 17(5). e871–e877. 70 indexed citations

20.

Nur, Banu, Özgür Duman, Nihal Olgaç Dündar, et al.. (2011). Interleukin-6 Gene Polymorphism in Febrile Seizures. Pediatric Neurology. 46(1). 36–38. 22 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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