Güney Bademci

3.4k citations

67 papers · 1.2k · h-index 19

Impact in

Sensory Systems top 1%
- Hearing, Cochlea, Tinnitus, Genetics
Neurology top 5%
- Parkinson's Disease Mechanisms and Treatments
- Vestibular and auditory disorders

Papers in

Molecular Biology 30
- RNA regulation and disease 6
Sensory Systems 24
- Hearing, Cochlea, Tinnitus, Genetics 24

Co-authors: Mustafa Tekin (48 shared papers)Susan H. Blanton (11 shared papers)Duygu Duman (20 shared papers)Joseph Foster (12 shared papers)Jeffery M. Vance (7 shared papers)Shengru Guo (15 shared papers)Eden R. Martin (6 shared papers)Liyong Wang (5 shared papers)
Journals: PLoS ONE (4 papers)International Journal of Pediatric Otorhinolaryngology (3 papers)Clinical Genetics (3 papers)Proceedings of the National Academy of Sciences (2 papers)Human Mutation (2 papers)
Partner nations: United States Türkiye United Kingdom

In The Last Decade

Güney Bademci

63 papers receiving 1.2k citations

Peers

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-authors

The 25 scholars most cited alongside Güney Bademci, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Güney Bademci Line = papers co-authored together Güney Bademci links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 67 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia The American Journal of Human Genetics ·Aslı Sırmacı, Michail Spiliopoulos, Francesco Brancati, Eric Powell, Duygu Duman, Alex Abrams, Güney Bademci, Emanuele Agolini, Shengru Guo, Berrin Konuk, Aslı Kavaz, Susan H. Blanton, M. Cristina Digilio, Bruno Dallapiccola, Juan I. Young, Stephan Züchner, Mustafa Tekin	2011	173
2	Comparison of Three Targeted Enrichment Strategies on the SOLiD Sequencing Platform PLoS ONE ·Dale J. Hedges, Toumy Guettouche, Shan Yang, Güney Bademci, Ashley Diaz, Ashley Andersen, William Hulme, Sara B. Linker, Arpit Mehta, Yvonne J. K. Edwards, Gary W. Beecham, Eden R. Martin, Margaret A. Pericak‐Vance, Stephan Züchner, Jeffery M. Vance, John R. Gilbert	2011	61
3	Identifying Consensus Disease Pathways in Parkinson's Disease Using an Integrative Systems Biology Approach PLoS ONE ·Yvonne J. K. Edwards, Gary W. Beecham, William K. Scott, Sawsan Khuri, Güney Bademci, Demet Tekin, Eden R. Martin, Zhijie Jiang, Deborah C. Mash, Jarlath M.H. ffrench‐Mullen, Margaret A. Pericak‐Vance, Nicholas F. Tsinoremas, Jeffery M. Vance	2011	60
4	C9ORF72 Intermediate Repeat Copies Are a Significant Risk Factor for Parkinson Disease Annals of Human Genetics ·Karen Nuytemans, Güney Bademci, Martin M. Kohli, Gary W. Beecham, Liyong Wang, Juan I. Young, Fatta B. Nahab, Eden R. Martin, John R. Gilbert, Michael Benatar, Jonathan L. Haines, William K. Scott, Stephan Züchner, Margaret A. Pericak‐Vance, Jeffery M. Vance	2013	60
5	FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing Proceedings of the National Academy of Sciences ·Oscar Diaz‐Horta, Asli Subasioglu-Uzak, M’hamed Grati, Alexandra A. DeSmidt, Joseph Foster, Lei Cao, Güney Bademci, Suna Tokgöz-Yılmaz, Duygu Duman, Filiz Başak Cengiz, Clemer Abad, Rahul Mittal, Susan H. Blanton, Xue Z. Liu, Amjad Farooq, Katherina Walz, Zhongmin Lu, Mustafa Tekin	2014	58
6	Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss PLoS ONE ·Tahir Atık, Hüseyin Önay, Ayça Aykut, Güney Bademci, Tayfun Kirazlı, Mustafa Tekin, Ferda Özkınay	2015	49
7	Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease Neurology ·Karen Nuytemans, Güney Bademci, Vanessa Inchausti, Amy Dressen, Daniel D. Kinnamon, Arpit Mehta, Liyong Wang, Stephan Züchner, Gary W. Beecham, Eden R. Martin, William K. Scott, Jeffery M. Vance	2013	49
8	Variants in CIB2 cause DFNB48 and not USH1J Clinical Genetics ·Kevin T. Booth, Kimia Kahrizi, Mojgan Babanejad, Hossein Daghagh, Güney Bademci, Sanaz Arzhangi, Davood Zare‐Abdollahi, Duygu Duman, A. Amraoui, Mustafa Tekin, Hossein Najmabadi, Héla Azaiez, Richard J. Smith	2017	44
9	Whole-exome sequencing and its impact in hereditary hearing loss Genetics Research ·Tahir Atık, Güney Bademci, Oscar Diaz‐Horta, Susan H. Blanton, Mustafa Tekin	2015	42
10	Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome Orphanet Journal of Rare Diseases ·Tahir Atık, Asuman Koparır, Güney Bademci, Joseph Foster, Umut Altunoğlu, Gül Yeşiltepe Mutlu, Sarah Bowdin, Nursel Elçioğlu, Gulsen Akay Tayfun, Sevinç Şahin Atik, Mustafa Özen, Ferda Özkınay, Yasemin Alanay, Hülya Kayserili, Steffen Thiel, Mustafa Tekin	2015	35
11	A next-generation sequencing gene panel (MiamiOtoGenes) for comprehensive analysis of deafness genes Hearing Research ·Demet Tekin, Denise Yan, Güney Bademci, Yong Feng, Shengru Guo, Joseph Foster, Susan H. Blanton, Mustafa Tekin, Xuezhong Liu	2016	34
12	Identification of Copy Number Variants Through Whole-Exome Sequencing in Autosomal Recessive Nonsyndromic Hearing Loss 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	2014	26
13	Tyrosine Hydroxylase Gene: Another Piece of the Genetic Puzzle of Parkinson’s Disease CNS & Neurological Disorders - Drug Targets ·Güney Bademci, Jeffery M. Vance, Liyong Wang	2012	23
14	Dominant deafness–onychodystrophy syndrome caused by an ATP6V1B2 mutation Clinical Case Reports ·Ibis Menéndez, Claudia Carranza, Mariana Herrera‐Cruz, Nely Marroquín, Joseph Foster, Filiz Başak Cengiz, Güney Bademci, Mustafa Tekin	2017	22
15	A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease Human Mutation ·Güney Bademci, Todd L. Edwards, André Luiz Quintanilha Torres, William K. Scott, Stephan Züchner, Eden R. Martin, Jeffery M. Vance, Liyong Wang	2010	22
16	Common genes for non-syndromic deafness are uncommon in sub-Saharan Africa: A report from Nigeria International Journal of Pediatric Otorhinolaryngology ·Akeem O. Lasisi, Güney Bademci, Joseph Foster, Susan H. Blanton, Mustafa Tekin	2014	22
17	Novel Causative Variants in DYRK1A, KARS, and KAT6A Associated with Intellectual Disability and Additional Phenotypic Features Journal of Pediatric Genetics ·Clark R. Murray, Samantha Abel, Matthew McClure, Joseph Foster, Maria Walke, Parul Jayakar, Güney Bademci, Mustafa Tekin	2017	20
18	A Mayan founder mutation is a common cause of deafness in Guatemala Clinical Genetics ·Claudia Carranza, Ibis Menéndez, (unknown), P. Castellanos, C. Amado, Fausto Maldonado, Laura Rosales, Nancy Escobar, Mónica Guerra, D. Alvarez, Joseph Foster, Shengru Guo, Susan H. Blanton, Güney Bademci, Mustafa Tekin	2015	19
19	Novel domain-specific POU3F4 mutations are associated with X-linked deafness: examples from different populations BMC Medical Genetics ·Güney Bademci, Akeem O. Lasisi, Kemal O. Yariz, Paola Montenegro, Ibis Menéndez, Rodrigo Vinueza, Rosario Paredes, Germania Moreta, Aslı Subaşıoğlu, Susan H. Blanton, Suat Fítöz, Armağan İncesulu, Levent Sennaroğlu, Mustafa Tekin	2015	19
20	Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53 Molecular Genetics and Genomics ·Imen Chakchouk, M’hamed Grati, Güney Bademci, Mariem Ben Saïd, Qi Ma, Amine Chakroun, Joseph Foster, Denise Yan, Duygu Duman, Oscar Diaz‐Horta, Abdelmonem Ghorbel, Rahul Mittal, Amjad Farooq, Mustafa Tekin, Saber Masmoudi, Xue Zhong Liu	2015	18

About Güney Bademci

Güney Bademci is a scholar working on Molecular Biology, Sensory Systems, Genetics, Neurology and Otorhinolaryngology, having authored 67 papers that have together received 1.2k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (24 papers), Genomics and Rare Diseases (10 papers), Ear Surgery and Otitis Media (7 papers), RNA regulation and disease (6 papers), Genetics and Neurodevelopmental Disorders (6 papers), Vestibular and auditory disorders (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Parkinson's Disease Mechanisms and Treatments (5 papers). The work is most often cited by research in Sensory Systems (356 citations), Neurology (134 citations), Otorhinolaryngology (67 citations), Genetics (306 citations) and Neurology (143 citations). Güney Bademci has collaborated with scholars based in United States, Türkiye and United Kingdom. Frequent co-authors include Mustafa Tekin, Susan H. Blanton, Duygu Duman, Joseph Foster, Jeffery M. Vance, Shengru Guo, Eden R. Martin, Liyong Wang, Stephan Züchner and Tahir Atık. Their work appears in journals such as PLoS ONE, International Journal of Pediatric Otorhinolaryngology, Clinical Genetics, Proceedings of the National Academy of Sciences and Human Mutation.

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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