Filiz Başak Cengiz

1.7k total citations
25 papers, 750 citations indexed

About

Filiz Başak Cengiz is a scholar working on Sensory Systems, Molecular Biology and Genetics. According to data from OpenAlex, Filiz Başak Cengiz has authored 25 papers receiving a total of 750 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Sensory Systems, 11 papers in Molecular Biology and 7 papers in Genetics. Recurrent topics in Filiz Başak Cengiz's work include Hearing, Cochlea, Tinnitus, Genetics (13 papers), Vestibular and auditory disorders (6 papers) and Ear Surgery and Otitis Media (5 papers). Filiz Başak Cengiz is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (13 papers), Vestibular and auditory disorders (6 papers) and Ear Surgery and Otitis Media (5 papers). Filiz Başak Cengiz collaborates with scholars based in Türkiye, United States and United Kingdom. Filiz Başak Cengiz's co-authors include Mustafa Tekin, Duygu Duman, Aslı Sırmacı, Hi̇lal Özdağ, Joseph Foster, Suat Fítöz, Oscar Diaz‐Horta, Güney Bademci, Susan H. Blanton and Ibis Menéndez and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and PLoS ONE.

In The Last Decade

Filiz Başak Cengiz

25 papers receiving 740 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Filiz Başak Cengiz Türkiye 16 419 408 186 152 123 25 750
Aslı Sırmacı Türkiye 14 385 0.9× 437 1.1× 191 1.0× 262 1.7× 124 1.0× 15 860
Güney Bademci United States 19 356 0.8× 582 1.4× 166 0.9× 331 2.2× 102 0.8× 63 1.1k
Duygu Duman Türkiye 19 601 1.4× 697 1.7× 268 1.4× 303 2.0× 166 1.3× 42 1.4k
Laurence Jonard France 15 301 0.7× 379 0.9× 135 0.7× 102 0.7× 66 0.5× 36 742
Margriet Verstreken Belgium 14 504 1.2× 480 1.2× 285 1.5× 70 0.5× 170 1.4× 24 913
Nanna Dahl Rendtorff Denmark 19 223 0.5× 487 1.2× 109 0.6× 136 0.9× 61 0.5× 40 816
Barbara Vona Germany 15 450 1.1× 349 0.9× 193 1.0× 137 0.9× 129 1.0× 64 751
Mohamed Drira Tunisia 12 517 1.2× 431 1.1× 192 1.0× 62 0.4× 119 1.0× 16 779
Nele Hilgert Belgium 11 585 1.4× 410 1.0× 237 1.3× 125 0.8× 179 1.5× 12 847
Susan Kupka Germany 15 350 0.8× 346 0.8× 143 0.8× 36 0.2× 72 0.6× 36 725

Countries citing papers authored by Filiz Başak Cengiz

Since Specialization
Citations

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

Fields of papers citing papers by Filiz Başak Cengiz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Filiz Başak Cengiz

This figure shows the co-authorship network connecting the top 25 collaborators of Filiz Başak Cengiz. A scholar is included among the top collaborators of Filiz Başak Cengiz 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 Filiz Başak Cengiz. Filiz Başak Cengiz 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.
Bademci, Güney, Clemer Abad, Filiz Başak Cengiz, et al.. (2020). Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development. Journal of Clinical Investigation. 130(8). 4213–4217. 15 indexed citations
2.
Li, Chong, Güney Bademci, Oscar Diaz‐Horta, et al.. (2019). Dysfunction of GRAP , encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss. Proceedings of the National Academy of Sciences. 116(4). 1347–1352. 12 indexed citations
3.
Su, Meng, Paul J. Benke, Güney Bademci, et al.. (2018). Monosomy chromosome 21 compensated by 21q22.11q22.3 duplication in a case with small size and minor anomalies. Molecular Cytogenetics. 11(1). 43–43. 2 indexed citations
4.
Masih, Katherine E., Nursel Elçioğlu, Filiz Başak Cengiz, et al.. (2018). Identification of candidate gene FAM183A and novel pathogenic variants in known genes: High genetic heterogeneity for autosomal recessive intellectual disability. PLoS ONE. 13(11). e0208324–e0208324. 18 indexed citations
5.
Arslan, Selçuk, Hakan Gürkan, Selma Demır, et al.. (2017). Novel EYA1 variants causing Branchio-oto-renal syndrome. International Journal of Pediatric Otorhinolaryngology. 98. 59–63. 15 indexed citations
6.
Menéndez, Ibis, et al.. (2017). Dominant deafness–onychodystrophy syndrome caused by an ATP6V1B2 mutation. Clinical Case Reports. 5(4). 376–379. 22 indexed citations
7.
Tokgöz-Yılmaz, Suna, et al.. (2016). Audiological findings in Noonan syndrome. International Journal of Pediatric Otorhinolaryngology. 89. 50–54. 2 indexed citations
8.
Özçakar, Zeynep Birsin, Duygu Duman, Filiz Başak Cengiz, et al.. (2015). <b><i>HPSE2</i></b> Mutations in Urofacial Syndrome, Non-Neurogenic Neurogenic Bladder and Lower Urinary Tract Dysfunction. ˜The œNephron journals/Nephron journals. 130(1). 54–58. 6 indexed citations
9.
Bademci, Güney, Oscar Diaz‐Horta, Shengru Guo, et al.. (2014). Identification of Copy Number Variants Through Whole-Exome Sequencing in Autosomal Recessive Nonsyndromic Hearing Loss. Genetic Testing and Molecular Biomarkers. 18(9). 658–661. 26 indexed citations
10.
Güneş, Nilay, Filiz Başak Cengiz, Duygu Duman, et al.. (2014). Branchio-oculo-facial syndrome in a newborn caused by a novel TFAP2A mutation.. PubMed. 25(1). 41–7. 4 indexed citations
11.
Diaz‐Horta, Oscar, Duygu Duman, Joseph Foster, et al.. (2012). Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss. PLoS ONE. 7(11). e50628–e50628. 127 indexed citations
12.
Duman, Duygu, Aslı Sırmacı, Filiz Başak Cengiz, Hi̇lal Özdağ, & Mustafa Tekin. (2010). Screening of 38 Genes Identifies Mutations in 62% of Families with Nonsyndromic Deafness in Turkey. Genetic Testing and Molecular Biomarkers. 15(1-2). 29–33. 71 indexed citations
13.
Cengiz, Filiz Başak, Duygu Duman, Aslı Sırmacı, et al.. (2010). Recurrent and Private MYO15A Mutations Are Associated with Deafness in the Turkish Population. Genetic Testing and Molecular Biomarkers. 14(4). 543–550. 38 indexed citations
14.
Tekin, Mustafa, Xia‐Juan Xia, Filiz Başak Cengiz, et al.. (2010). GJB2 Mutations in Mongolia: Complex Alleles, Low Frequency, and Reduced Fitness of the Deaf. Annals of Human Genetics. 74(2). 155–164. 52 indexed citations
15.
Parzefall, Thomas, Trevor Lucas, Wolf‐Dieter Baumgartner, et al.. (2009). A FGF3 mutation associated with differential inner ear malformation, microtia, and microdontia. The Laryngoscope. 120(2). 359–364. 19 indexed citations
16.
Tekin, Mustafa, Filiz Başak Cengiz, Tanıl Kendirli, et al.. (2007). Familial neonatal Marfan syndrome due to parental mosaicism of a missense mutation in the FBN1 gene. American Journal of Medical Genetics Part A. 143A(8). 875–880. 38 indexed citations
17.
Akçaboy, Meltem, Filiz Başak Cengiz, Bora İnceoğlu, et al.. (2007). The Effect of p.Arg25Cys Alteration in NKX2-5 on Conotruncal Heart Anomalies: Mutation or Polymorphism?. Pediatric Cardiology. 29(1). 126–129. 25 indexed citations
18.
Tekin, Mustafa, Burcu Öztürk Hişmi, Suat Fítöz, et al.. (2007). Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia. The American Journal of Human Genetics. 80(2). 338–344. 86 indexed citations
19.
Fítöz, Suat, et al.. (2007). SLC26A4 mutations are associated with a specific inner ear malformation. International Journal of Pediatric Otorhinolaryngology. 71(3). 479–486. 18 indexed citations
20.
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

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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