Clemer Abad

702 total citations
20 papers, 360 citations indexed

About

Clemer Abad is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Clemer Abad has authored 20 papers receiving a total of 360 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Sensory Systems. Recurrent topics in Clemer Abad's work include Hearing, Cochlea, Tinnitus, Genetics (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Clemer Abad is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Clemer Abad collaborates with scholars based in United States, Türkiye and Argentina. Clemer Abad's co-authors include Katherina Walz, Mustafa Tekin, Juan I. Young, David F. Callen, Paul M. Neilsen, Denis Gallagher, Matthew P. Krause, David R. Kaplan, Stephen W. Scherer and Gonzalo I. Cancino and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Brain.

In The Last Decade

Clemer Abad

19 papers receiving 356 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Clemer Abad United States 10 238 178 57 57 32 20 360
Emma Bedoukian United States 13 238 1.0× 119 0.7× 26 0.5× 61 1.1× 16 0.5× 31 375
Muriel Holder France 9 283 1.2× 185 1.0× 22 0.4× 92 1.6× 8 0.3× 14 408
Vera Beyer Germany 9 181 0.8× 168 0.9× 61 1.1× 36 0.6× 14 0.4× 15 318
Bellinda van den Helm Netherlands 11 320 1.3× 201 1.1× 30 0.5× 36 0.6× 16 0.5× 17 465
Lauren Chessum United Kingdom 7 163 0.7× 51 0.3× 24 0.4× 61 1.1× 12 0.4× 8 265
MaryPat Jones United States 9 153 0.6× 144 0.8× 17 0.3× 31 0.5× 9 0.3× 9 326
Olinda Alegria-Prévot France 5 205 0.9× 62 0.3× 33 0.6× 167 2.9× 56 1.8× 6 435
Cynthia C. Morton United States 8 178 0.7× 81 0.5× 29 0.5× 150 2.6× 23 0.7× 8 407
Greta Gillies Australia 9 302 1.3× 216 1.2× 11 0.2× 62 1.1× 16 0.5× 13 481
Fernando Arena United States 7 352 1.5× 171 1.0× 38 0.7× 60 1.1× 34 1.1× 8 477

Countries citing papers authored by Clemer Abad

Since Specialization
Citations

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

Fields of papers citing papers by Clemer Abad

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Clemer Abad

This figure shows the co-authorship network connecting the top 25 collaborators of Clemer Abad. A scholar is included among the top collaborators of Clemer Abad 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 Clemer Abad. Clemer Abad 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.
Abad, Clemer, et al.. (2025). Cutaneous squamous cell carcinoma rechallenge with pembrolizumab. 3. 100707–100707.
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.
Abad, Clemer, María Gabriela Otero, Anthony J. Griswold, et al.. (2024). Gatad2b, associated with the neurodevelopmental syndrome GAND, plays a critical role in neurodevelopment and cortical patterning. Translational Psychiatry. 14(1). 33–33. 3 indexed citations
4.
Rebelo, Adriana, Clemer Abad, Maike F. Dohrn, et al.. (2024). SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insights. Brain. 147(9). 3131–3143. 5 indexed citations
5.
Camarena, Vladimir, Monique Williams, Alejo A. Morales, et al.. (2024). ADAMTSL2 mutations determine the phenotypic severity in Geleophysic Dysplasia. JCI Insight. 9(5). 5 indexed citations
6.
Abad, Clemer, et al.. (2024). Fatal septicemia in 2 South American camelids with caudal C3-pyloric-duodenal adenocarcinoma. Journal of Veterinary Diagnostic Investigation. 36(3). 473–476. 1 indexed citations
7.
Chen, Xiao‐Ya, Clemer Abad, Zheng‐Yi Chen, et al.. (2021). Generation and characterization of a P2rx2 V60L mouse model for DFNA41. Human Molecular Genetics. 30(11). 985–995. 3 indexed citations
8.
Abad, Clemer, et al.. (2020). Bromodomain Protein BRD4 Is Essential for Hair Cell Function and Survival. Frontiers in Cell and Developmental Biology. 8. 576654–576654. 4 indexed citations
9.
Bademci, Güney, Clemer Abad, Filiz Başak Cengiz, et al.. (2020). Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development. Journal of Clinical Investigation. 130(8). 4213–4217. 15 indexed citations
10.
Seabra, Catarina M., Tatsiana Aneichyk, Serkan Erdin, et al.. (2020). Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neurons. Molecular Autism. 11(1). 45–45. 11 indexed citations
11.
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
12.
13.
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
14.
Abad, Clemer, et al.. (2017). Rai1 Haploinsufficiency Is Associated with Social Abnormalities in Mice. Biology. 6(2). 25–25. 13 indexed citations
15.
Voronova, Anastassia, Denis Gallagher, Mark Zander, et al.. (2015). Ankrd11 is a chromatin regulator involved in autism that is essential for neural development. SpringerPlus. 4(S1). 4 indexed citations
16.
Gallagher, Denis, Anastassia Voronova, Mark Zander, et al.. (2014). Ankrd11 Is a Chromatin Regulator Involved in Autism that Is Essential for Neural Development. Developmental Cell. 32(1). 31–42. 119 indexed citations
17.
Camarena, Vladimir, Lei Cao, Clemer Abad, et al.. (2014). Disruption of Mbd5 in mice causes neuronal functional deficits and neurobehavioral abnormalities consistent with 2q23.1 microdeletion syndrome. EMBO Molecular Medicine. 6(8). 1003–1015. 26 indexed citations
18.
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
19.
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
20.
Cao, Lei, Jéssica Molina, Clemer Abad, et al.. (2013). Correct developmental expression level of Rai1 in forebrain neurons is required for control of body weight, activity levels and learning and memory. Human Molecular Genetics. 23(7). 1771–1782. 15 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Emma Bedoukian Breakdown of academic impact, for papers by Muriel Holder Breakdown of academic impact, for papers by Vera Beyer Breakdown of academic impact, for papers by Bellinda van den Helm Breakdown of academic impact, for papers by Lauren Chessum Breakdown of academic impact, for papers by MaryPat Jones Breakdown of academic impact, for papers by Olinda Alegria-Prévot Breakdown of academic impact, for papers by Cynthia C. Morton Breakdown of academic impact, for papers by Greta Gillies Breakdown of academic impact, for papers by Fernando Arena
Rankless by CCL
2026