Güney Bademci

3.3k total citations
63 papers, 1.1k citations indexed

About

Güney Bademci is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, Güney Bademci has authored 63 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 23 papers in Sensory Systems and 19 papers in Genetics. Recurrent topics in Güney Bademci's work include Hearing, Cochlea, Tinnitus, Genetics (23 papers), Genomics and Rare Diseases (11 papers) and Ear Surgery and Otitis Media (9 papers). Güney Bademci is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (23 papers), Genomics and Rare Diseases (11 papers) and Ear Surgery and Otitis Media (9 papers). Güney Bademci collaborates with scholars based in United States, Türkiye and United Kingdom. Güney Bademci's co-authors include Mustafa Tekin, Susan H. Blanton, Duygu Duman, Jeffery M. Vance, Joseph Foster, Shengru Guo, Eden R. Martin, Liyong Wang, Stephan Züchner and Tahir Atık and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and SHILAP Revista de lepidopterología.

In The Last Decade

Güney Bademci

62 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Güney Bademci United States 19 582 356 331 166 155 63 1.1k
Michael R. Bowl United Kingdom 27 836 1.4× 551 1.5× 355 1.1× 201 1.2× 105 0.7× 49 1.9k
Francine M. Jodelka United States 18 883 1.5× 416 1.2× 142 0.4× 131 0.8× 63 0.4× 23 1.2k
Teresa Jaijo Spain 22 984 1.7× 597 1.7× 151 0.5× 264 1.6× 56 0.4× 58 1.4k
Isabelle Schrauwen United States 25 690 1.2× 525 1.5× 336 1.0× 323 1.9× 75 0.5× 105 1.8k
Emanuela Leonardi Italy 20 461 0.8× 243 0.7× 125 0.4× 106 0.6× 63 0.4× 38 850
Hashem Shahin Palestinian Territory 15 697 1.2× 756 2.1× 171 0.5× 318 1.9× 73 0.5× 17 1.2k
Pavel Seeman Czechia 22 778 1.3× 299 0.8× 289 0.9× 387 2.3× 148 1.0× 99 1.6k
Guntram Borck Germany 27 876 1.5× 113 0.3× 681 2.1× 136 0.8× 114 0.7× 65 1.7k
Jun Shen United States 20 807 1.4× 555 1.6× 307 0.9× 116 0.7× 18 0.1× 44 1.6k
P J Willems Belgium 17 611 1.0× 559 1.6× 280 0.8× 264 1.6× 24 0.2× 36 1.3k

Countries citing papers authored by Güney Bademci

Since Specialization
Citations

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

Fields of papers citing papers by Güney Bademci

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Güney Bademci

This figure shows the co-authorship network connecting the top 25 collaborators of Güney Bademci. A scholar is included among the top collaborators of Güney Bademci 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 Güney Bademci. Güney Bademci 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.
Grajewski, Alana, et al.. (2025). Genome sequencing reveals novel variants in a diverse population with congenital anterior segment anomalies. Scientific Reports. 15(1). 518–518. 2 indexed citations
2.
Eberl, Daniel F., Güney Bademci, Stephanie Bivona, et al.. (2025). De novo variants in CDKL1 and CDKL2 are associated with neurodevelopmental symptoms. The American Journal of Human Genetics. 112(4). 846–862. 1 indexed citations
3.
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
4.
Forghani, Irman, Stephanie Bivona, Alejo A. Morales, et al.. (2024). EFEMP1 haploinsufficiency causes a Marfan‐like hereditary connective tissue disorder. American Journal of Medical Genetics Part A. 194(6). e63556–e63556. 1 indexed citations
5.
Dohrn, Maike F., Güney Bademci, Adriana Rebelo, et al.. (2024). Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autism. Annals of Clinical and Translational Neurology. 11(4). 1075–1079. 1 indexed citations
6.
Bivona, Stephanie, et al.. (2023). H4C5 missense variant leads to a neurodevelopmental phenotype overlapping with Angelman syndrome. American Journal of Medical Genetics Part A. 191(7). 1911–1916.
7.
Thorson, Willa, et al.. (2023). Deletion of first noncoding exon in ANKRD11 leads to KBG syndrome. American Journal of Medical Genetics Part A. 191(4). 1044–1049. 2 indexed citations
8.
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
9.
Vona, Barbara, María Costales, Rocío González‐Aguado, et al.. (2020). Radixin modulates the function of outer hair cell stereocilia. Communications Biology. 3(1). 792–792. 10 indexed citations
10.
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
11.
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
12.
Clavijo, Raul I., Himanshu Arora, Samuel M. Cohen, et al.. (2018). Whole Exome Sequencing of a Consanguineous Turkish Family Identifies a Mutation in GTF2H3 in Brothers With Spermatogenic Failure. Urology. 120. 86–89. 9 indexed citations
13.
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
14.
Tekin, Demet, Denise Yan, Güney Bademci, et al.. (2016). A next-generation sequencing gene panel (MiamiOtoGenes) for comprehensive analysis of deafness genes. Hearing Research. 333. 179–184. 34 indexed citations
15.
Atık, Tahir, Hüseyin Önay, Ayça Aykut, et al.. (2015). Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss. PLoS ONE. 10(11). e0142154–e0142154. 49 indexed citations
16.
Atık, Tahir, Güney Bademci, Oscar Diaz‐Horta, Susan H. Blanton, & Mustafa Tekin. (2015). Whole-exome sequencing and its impact in hereditary hearing loss. Genetics Research. 97. e4–e4. 42 indexed citations
17.
Atık, Tahir, Asuman Koparır, Güney Bademci, et al.. (2015). Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome. Orphanet Journal of Rare Diseases. 10(1). 128–128. 34 indexed citations
18.
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
19.
Edwards, Yvonne J. K., Gary W. Beecham, William K. Scott, et al.. (2011). Identifying Consensus Disease Pathways in Parkinson's Disease Using an Integrative Systems Biology Approach. PLoS ONE. 6(2). e16917–e16917. 60 indexed citations
20.
Çilingir, Oğuz, et al.. (2006). A novel mutation in the ARS (component B) gene encoding SLURP-1 in a Turkish family with mal de Meleda. British Journal of Dermatology. 155(2). 467–469. 8 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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