Oscar Diaz‐Horta

1.3k total citations
13 papers, 530 citations indexed

About

Oscar Diaz‐Horta is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, Oscar Diaz‐Horta has authored 13 papers receiving a total of 530 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Sensory Systems and 3 papers in Genetics. Recurrent topics in Oscar Diaz‐Horta's work include Hearing, Cochlea, Tinnitus, Genetics (6 papers), Congenital heart defects research (3 papers) and Genomics and Rare Diseases (2 papers). Oscar Diaz‐Horta is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (6 papers), Congenital heart defects research (3 papers) and Genomics and Rare Diseases (2 papers). Oscar Diaz‐Horta collaborates with scholars based in United States, Türkiye and Iran. Oscar Diaz‐Horta's co-authors include Mustafa Tekin, Joseph Foster, Susan H. Blanton, Güney Bademci, Duygu Duman, Filiz Başak Cengiz, Amjad Farooq, Fatoş Yalçınkaya, Yao‐Shan Fan and Zeynep Birsin Özçakar and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Human Genetics.

In The Last Decade

Oscar Diaz‐Horta

13 papers receiving 523 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Oscar Diaz‐Horta United States 10 235 231 103 89 85 13 530
Rachel E. Hardisty-Hughes United Kingdom 12 221 0.9× 227 1.0× 67 0.7× 46 0.5× 53 0.6× 15 568
Aslı Sırmacı Türkiye 14 437 1.9× 385 1.7× 262 2.5× 92 1.0× 191 2.2× 15 860
Ahmet Karagüzel Türkiye 11 236 1.0× 222 1.0× 95 0.9× 39 0.4× 104 1.2× 24 458
Laurence Jonard France 15 379 1.6× 301 1.3× 102 1.0× 33 0.4× 135 1.6× 36 742
Kwanghyuk Lee United States 13 297 1.3× 103 0.4× 145 1.4× 44 0.5× 42 0.5× 23 546
Margriet Verstreken Belgium 14 480 2.0× 504 2.2× 70 0.7× 91 1.0× 285 3.4× 24 913
Flavio Faletra Italy 15 251 1.1× 87 0.4× 267 2.6× 29 0.3× 29 0.3× 84 649
Susan Kupka Germany 15 346 1.5× 350 1.5× 36 0.3× 92 1.0× 143 1.7× 36 725
Koichiro Higashi Japan 12 347 1.5× 184 0.8× 141 1.4× 22 0.2× 78 0.9× 29 596

Countries citing papers authored by Oscar Diaz‐Horta

Since Specialization
Citations

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

Fields of papers citing papers by Oscar Diaz‐Horta

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Oscar Diaz‐Horta. 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 Oscar Diaz‐Horta. The network helps show where Oscar Diaz‐Horta may publish in the future.

Co-authorship network of co-authors of Oscar Diaz‐Horta

This figure shows the co-authorship network connecting the top 25 collaborators of Oscar Diaz‐Horta. A scholar is included among the top collaborators of Oscar Diaz‐Horta 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 Oscar Diaz‐Horta. Oscar Diaz‐Horta is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

13 of 13 papers shown
1.
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
2.
Diaz‐Horta, Oscar, Güney Bademci, Suna Tokgöz-Yılmaz, et al.. (2019). Novel variant p.E269K confirms causative role of PLS1 mutations in autosomal dominant hearing loss. Clinical Genetics. 96(6). 575–578. 5 indexed citations
3.
Diaz‐Horta, Oscar, Clemer Abad, Filiz Başak Cengiz, et al.. (2018). Ripor2 is involved in auditory hair cell stereociliary bundle structure and orientation. Journal of Molecular Medicine. 96(11). 1227–1238. 9 indexed citations
4.
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
5.
Chakchouk, Imen, M’hamed Grati, Güney Bademci, et al.. (2015). Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53. Molecular Genetics and Genomics. 290(4). 1327–1334. 17 indexed citations
6.
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
7.
Walz, Katherina, Paul M. Neilsen, Joseph Foster, et al.. (2014). Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome. Human Genetics. 134(2). 181–190. 40 indexed citations
8.
Diaz‐Horta, Oscar, M’hamed Grati, Alexandra A. DeSmidt, et al.. (2014). FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing. Proceedings of the National Academy of Sciences. 111(27). 9864–9868. 58 indexed citations
9.
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
10.
Thorson, Willa, Oscar Diaz‐Horta, Joseph Foster, et al.. (2013). De novo ACTG2 mutations cause congenital distended bladder, microcolon, and intestinal hypoperistalsis. Human Genetics. 133(6). 737–742. 72 indexed citations
11.
Özçakar, Zeynep Birsin, Joseph Foster, Oscar Diaz‐Horta, et al.. (2013). DNASE1L3Mutations in Hypocomplementemic Urticarial Vasculitis Syndrome. Arthritis & Rheumatism. 65(8). 2183–2189. 98 indexed citations
12.
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
13.
Diaz‐Horta, Oscar, Aslı Sırmacı, Dan Doherty, et al.. (2012). GPSM2 mutations in Chudley–McCullough syndrome. American Journal of Medical Genetics Part A. 158A(11). 2972–2973. 17 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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