Duygu Duman

2.7k citations

42 papers · 1.4k indexed · h-index 19

Co-authors: Mustafa Tekin Aslı Sırmacı Filiz Başak Cengiz Güney Bademci Michail Spiliopoulos Susan H. Blanton Hatice Akay Hi̇lal Özdağ
Topics: Hearing, Cochlea, Tinnitus, Genetics (22 papers)Ear Surgery and Otitis Media (10 papers)Vestibular and auditory disorders (10 papers)
Cited by: Sensory Systems Otorhinolaryngology Neurology
Journals: Proceedings of the National Academy of Sciences Journal of Clinical Investigation The Journal of Immunology
Partner nations: Türkiye United States Iran

In The Last Decade

Duygu Duman

40 papers receiving 1.3k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Human organoids for rapid validation of gene variants linked to cochlear malformations 2025 ·Human Genetics ·(unknown),Memoona Ramzan,Duygu Duman,(unknown),(unknown),M. Tayyar Kalcıoğlu,Suat Fítöz,(unknown),Shengru Guo,Derek M. Dykxhoorn,Mustafa Tekin	0
2	Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2 2024 ·European Journal of Human Genetics ·Memoona Ramzan,(unknown),Clemer Abad,Shengru Guo,(unknown),Özgül M. Alper,(unknown),Tahir Atık,Duygu Duman,Güney Bademci,Barbara Vona,M. Tayyar Kalcıoğlu,Katherina Walz,Mustafa Tekin	2
3	Dispersed DNA variants underlie hearing loss in South Florida’s minority population 2023 ·Human Genomics ·(unknown),(unknown),(unknown),Duygu Duman,Turçin Saridogan,Memoona Ramzan,(unknown),Xue Zhong Liu,Adrien A. Eshraghi,Michael E. Hoffer,Simón I. Angeli,Güney Bademci,Susan H. Blanton,Carson Smith,Fred F. Telischi,Mustafa Tekin	4
4	Whole Mitochondrial Genome Analysis in Turkish Patients With Mitochondrial Diseases 2021 ·Balkan Medical Journal ·(unknown),Duygu Duman,Fatma Tuba Eminoğlu,Süleyman Aktuna,Mustafa Duman	2
5	Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development 2020 ·Journal of Clinical Investigation ·Güney Bademci,Clemer Abad,Filiz Başak Cengiz,(unknown),Armağan İncesulu,Shengru Guo,Suat Fítöz,Emine İkbal Atlı,(unknown),Selma Demır,(unknown),(unknown),(unknown),Duygu Duman,Hakan Gürkan,Cynthia C. Morton,Derek M. Dykxhoorn,Katherina Walz,Mustafa Tekin	15
6	Dysfunction of GRAP , encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss 2019 ·Proceedings of the National Academy of Sciences ·Chong Li,Güney Bademci,(unknown),Oscar Diaz‐Horta,Yi Zhu,Jiaqi Liu,(unknown),Clemer Abad,(unknown),Duygu Duman,Filiz Başak Cengiz,Suna Tokgöz-Yılmaz,Susan H. Blanton,Amjad Farooq,Katherina Walz,R. Grace Zhai,Mustafa Tekin	12
7	Genetic Causes of Inner Ear Anomalies: a Review from the Turkish Study Group for Inner Ear Anomalies 2019 ·Balkan Medical Journal ·Emre Ocak,Duygu Duman,Mustafa Tekin	9
8	A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss 2019 ·Human Genetics ·(unknown),(unknown),Shengru Guo,Vladimir Camarena,Gaofeng Wang,Suna Tokgöz-Yılmaz,Duygu Duman,Güney Bademci,Mustafa Tekin	18
9	Identification of candidate gene FAM183A and novel pathogenic variants in known genes: High genetic heterogeneity for autosomal recessive intellectual disability 2018 ·PLoS ONE ·(unknown),Katherine E. Masih,Nursel Elçioğlu,(unknown),(unknown),Filiz Başak Cengiz,(unknown),(unknown),(unknown),(unknown),Shengru Guo,Duygu Duman,Güney Bademci,Mustafa Tekin	18
10	Novel EYA1 variants causing Branchio-oto-renal syndrome 2017 ·International Journal of Pediatric Otorhinolaryngology ·(unknown),(unknown),Selçuk Arslan,(unknown),Hakan Gürkan,Selma Demır,Reza Maroofian,(unknown),(unknown),(unknown),Nursel Elçioğlu,Ibis Menéndez,Mahdiyeh Behnam,Joseph Foster,Shengru Guo,(unknown),Filiz Başak Cengiz,Duygu Duman,Güney Bademci,Mustafa Tekin	15
11	Identification of Copy Number Variants Through Whole-Exome Sequencing in Autosomal Recessive Nonsyndromic Hearing Loss 2014 ·Genetic Testing and Molecular Biomarkers ·Güney Bademci,Oscar Diaz‐Horta,Shengru Guo,Duygu Duman,Derek Van Booven,Joseph Foster,Filiz Başak Cengiz,Susan H. Blanton,Mustafa Tekin	26
12	Evidence for genotype–phenotype correlation for OTOF mutations 2014 ·International Journal of Pediatric Otorhinolaryngology ·(unknown),Güney Bademci,Duygu Duman,Hatice Akay,Suna Tokgöz-Yılmaz,Mustafa Tekin	13
13	Autosomal recessive nonsyndromic deafness genes: a review 2012 ·Frontiers in bioscience ·Duygu Duman	113
14	Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss 2012 ·PLoS ONE ·Oscar Diaz‐Horta,Duygu Duman,Joseph Foster,Aslı Sırmacı,Michael Gonzalez,Nejat Mahdieh,(unknown),Mortaza Bonyadi,Filiz Başak Cengiz,Ibis Menéndez,(unknown),Yvonne J. K. Edwards,Stephan Züchner,Susan H. Blanton,Mustafa Tekin	127
15	Inherited mutation of the luteinizing hormone/choriogonadotropin receptor (LHCGR) in empty follicle syndrome 2011 ·Fertility and Sterility ·Kemal O. Yariz,Tom Walsh,(unknown),Michail Spiliopoulos,Duygu Duman,Göğşen Önalan,Mary‐Claire King,Mustafa Tekin	64
16	Screening of 38 Genes Identifies Mutations in 62% of Families with Nonsyndromic Deafness in Turkey 2010 ·Genetic Testing and Molecular Biomarkers ·Duygu Duman,Aslı Sırmacı,Filiz Başak Cengiz,Hi̇lal Özdağ,Mustafa Tekin	71
17	Recurrent and Private MYO15A Mutations Are Associated with Deafness in the Turkish Population 2010 ·Genetic Testing and Molecular Biomarkers ·Filiz Başak Cengiz,Duygu Duman,Aslı Sırmacı,Suna Tokgöz-Yılmaz,Seyra Erbek,Hatice Akay,Armağan İncesulu,Yvonne J. K. Edwards,Hi̇lal Özdağ,Xue Z. Liu,Mustafa Tekin	38
18	MASP1 Mutations in Patients with Facial, Umbilical, Coccygeal, and Auditory Findings of Carnevale, Malpuech, OSA, and Michels Syndromes 2010 ·The American Journal of Human Genetics ·Aslı Sırmacı,Tom Walsh,Hatice Akay,Michail Spiliopoulos,Yıldırım Bayezıt Şakalar,(unknown),Duygu Duman,Amjad Farooq,Mary‐Claire King,Mustafa Tekin	106
19	Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia 2008 ·Clinical Genetics ·Mustafa Tekin,Hatice Akay,Suat Fítöz,Stefanie Birnbaum,(unknown),Levent Sennaroğlu,Armağan İncesulu,(unknown),(unknown),Şenol Şentürk,(unknown),(unknown),E Tunçbilek,Nance We,Duygu Duman	41
20	The c.IVS1+1G>A mutation intheGJB2 gene is prevalent and large deletions involving theGJB6 gene are not present in the Turkish population 2006 ·Journal of Genetics ·Aslı Sırmacı,Duygu Duman,Mustafa Tekin	49

About Duygu Duman

Duygu Duman is a scholar working on Sensory Systems, Otorhinolaryngology and Neurology, having authored 42 papers that have together received 1.4k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (22 papers), Ear Surgery and Otitis Media (10 papers) and Vestibular and auditory disorders (10 papers). The work is most often cited by research in Sensory Systems (601 citations), Otorhinolaryngology (166 citations) and Neurology (268 citations). Duygu Duman has collaborated with scholars based in Türkiye, United States and Iran. Frequent co-authors include Mustafa Tekin, Aslı Sırmacı, Filiz Başak Cengiz, Güney Bademci, Michail Spiliopoulos, Susan H. Blanton, Hatice Akay, Hi̇lal Özdağ, Tom Walsh and Mary‐Claire King. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and The Journal of Immunology.

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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