Duygu Duman

2.7k total citations
42 papers, 1.4k citations indexed

About

Duygu Duman is a scholar working on Sensory Systems, Molecular Biology and Neurology. According to data from OpenAlex, Duygu Duman has authored 42 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Sensory Systems, 19 papers in Molecular Biology and 11 papers in Neurology. Recurrent topics in Duygu Duman's work include Hearing, Cochlea, Tinnitus, Genetics (22 papers), Ear Surgery and Otitis Media (10 papers) and Vestibular and auditory disorders (10 papers). Duygu Duman is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (22 papers), Ear Surgery and Otitis Media (10 papers) and Vestibular and auditory disorders (10 papers). Duygu Duman collaborates with scholars based in Türkiye, United States and Iran. Duygu Duman's co-authors include Mustafa Tekin, Aslı Sırmacı, Filiz Başak Cengiz, Güney Bademci, Michail Spiliopoulos, Susan H. Blanton, Hatice Akay, Hi̇lal Özdağ, Mary‐Claire King and Tom Walsh and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and The Journal of Immunology.

In The Last Decade

Duygu Duman

40 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Duygu Duman Türkiye 19 697 601 303 268 205 42 1.4k
Aslı Sırmacı Türkiye 14 437 0.6× 385 0.6× 262 0.9× 191 0.7× 92 0.4× 15 860
Nabiha Salem Lebanon 19 1.1k 1.5× 664 1.1× 252 0.8× 208 0.8× 203 1.0× 36 1.6k
Héla Azaiez United States 20 860 1.2× 1.2k 1.9× 260 0.9× 393 1.5× 113 0.6× 45 1.7k
Carla Nishimura United States 24 828 1.2× 1.0k 1.7× 300 1.0× 402 1.5× 740 3.6× 33 2.3k
Shin‐ichiro Kitajiri Japan 20 787 1.1× 644 1.1× 83 0.3× 604 2.3× 91 0.4× 57 1.6k
Philippe Vago France 20 422 0.6× 262 0.4× 297 1.0× 81 0.3× 143 0.7× 89 1.2k
Ingrid Zwaenepoel France 11 789 1.1× 537 0.9× 116 0.4× 198 0.7× 54 0.3× 12 1.3k
Yelena Bykhovskaya United States 29 1.3k 1.8× 485 0.8× 131 0.4× 189 0.7× 65 0.3× 45 2.1k
Anand N. Mhatre United States 24 866 1.2× 916 1.5× 189 0.6× 327 1.2× 38 0.2× 46 1.8k
Nahid G. Robertson United States 22 616 0.9× 1.1k 1.9× 82 0.3× 726 2.7× 118 0.6× 31 1.7k

Countries citing papers authored by Duygu Duman

Since Specialization
Citations

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

Fields of papers citing papers by Duygu Duman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Duygu Duman

This figure shows the co-authorship network connecting the top 25 collaborators of Duygu Duman. A scholar is included among the top collaborators of Duygu Duman 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 Duygu Duman. Duygu Duman 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.
Ramzan, Memoona, Duygu Duman, M. Tayyar Kalcıoğlu, et al.. (2025). Human organoids for rapid validation of gene variants linked to cochlear malformations. Human Genetics. 144(4). 375–389.
2.
Ramzan, Memoona, Clemer Abad, Shengru Guo, et al.. (2024). Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2. European Journal of Human Genetics. 32(6). 639–646. 2 indexed citations
3.
Duman, Duygu, Turçin Saridogan, Memoona Ramzan, et al.. (2023). Dispersed DNA variants underlie hearing loss in South Florida’s minority population. Human Genomics. 17(1). 103–103. 4 indexed citations
4.
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
5.
Ocak, Emre, Duygu Duman, & Mustafa Tekin. (2019). Genetic Causes of Inner Ear Anomalies: a Review from the Turkish Study Group for Inner Ear Anomalies. Balkan Medical Journal. 36(4). 206–211. 9 indexed citations
6.
Guo, Shengru, Vladimir Camarena, Gaofeng Wang, et al.. (2019). A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss. Human Genetics. 138(10). 1071–1075. 18 indexed citations
7.
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
8.
Duman, Duygu, Aslı Sırmacı, Güney Bademci, et al.. (2017). Research of genetic bases of hereditary non-syndromic hearing loss. Türk Pediatri Arşivi. 52(3). 122–132. 7 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.
Bademci, Güney, et al.. (2014). Evidence for genotype–phenotype correlation for OTOF mutations. International Journal of Pediatric Otorhinolaryngology. 78(6). 950–953. 13 indexed citations
12.
Diaz‐Horta, Oscar, Duygu Duman, Joseph Foster, et al.. (2013). Correction: Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss. PLoS ONE. 8(5). 7 indexed citations
13.
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
14.
Duman, Duygu. (2012). Autosomal recessive nonsyndromic deafness genes: a review. Frontiers in bioscience. 17(7). 2213–2213. 113 indexed citations
15.
Yariz, Kemal O., Tom Walsh, Michail Spiliopoulos, et al.. (2011). Inherited mutation of the luteinizing hormone/choriogonadotropin receptor (LHCGR) in empty follicle syndrome. Fertility and Sterility. 96(2). e125–e130. 64 indexed citations
16.
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
17.
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
18.
Sırmacı, Aslı, Tom Walsh, Hatice Akay, et al.. (2010). MASP1 Mutations in Patients with Facial, Umbilical, Coccygeal, and Auditory Findings of Carnevale, Malpuech, OSA, and Michels Syndromes. The American Journal of Human Genetics. 87(5). 679–686. 106 indexed citations
19.
Tekin, Mustafa, Hatice Akay, Suat Fítöz, et al.. (2008). Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia. Clinical Genetics. 73(6). 554–565. 41 indexed citations
20.
Sırmacı, Aslı, Duygu Duman, & Mustafa Tekin. (2006). The c.IVS1+1G>A mutation intheGJB2 gene is prevalent and large deletions involving theGJB6 gene are not present in the Turkish population. Journal of Genetics. 85(3). 213–216. 49 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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