Frederic Depreux

1.4k total citations
21 papers, 1.1k citations indexed

About

Frederic Depreux is a scholar working on Molecular Biology, Sensory Systems and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Frederic Depreux has authored 21 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 8 papers in Sensory Systems and 4 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Frederic Depreux's work include Hearing, Cochlea, Tinnitus, Genetics (6 papers), Muscle Physiology and Disorders (6 papers) and RNA Research and Splicing (4 papers). Frederic Depreux is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (6 papers), Muscle Physiology and Disorders (6 papers) and RNA Research and Splicing (4 papers). Frederic Depreux collaborates with scholars based in United States, Canada and United Kingdom. Frederic Depreux's co-authors include David E. Gerrard, A.L. Grant, Christine E. Seidman, Megan J. Puckelwartz, Elizabeth M. McNally, S. G. Cornelius, Shaoquan Ji, Michael E. Spurlock, Glenn Frank and Gawain M. Willis and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Clinical Investigation.

In The Last Decade

Frederic Depreux

21 papers receiving 1.1k citations

Peers

Frederic Depreux
Nobuko Hagiwara United States
Hong‐Xiang Liu United States
Erwin van Wijk Netherlands
Kevin J. Sonnemann United States
G. Bulfield United Kingdom
Frederic Depreux
Citations per year, relative to Frederic Depreux Frederic Depreux (= 1×) peers Roberta Sacchetto

Countries citing papers authored by Frederic Depreux

Since Specialization
Citations

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

Fields of papers citing papers by Frederic Depreux

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Frederic Depreux

This figure shows the co-authorship network connecting the top 25 collaborators of Frederic Depreux. A scholar is included among the top collaborators of Frederic Depreux 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 Frederic Depreux. Frederic Depreux 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.
Depreux, Frederic, Francine M. Jodelka, Frank Rigo, et al.. (2017). Rescue of Outer Hair Cells with Antisense Oligonucleotides in Usher Mice Is Dependent on Age of Treatment. Journal of the Association for Research in Otolaryngology. 19(1). 1–16. 38 indexed citations
2.
Cherep, Lucia A., et al.. (2017). Antisense oligonucleotide therapy rescues disruptions in organization of exploratory movements associated with Usher syndrome type 1C in mice. Behavioural Brain Research. 338. 76–87. 19 indexed citations
3.
Semerci, Fatih, Aleksandar Bajić, Juan Manuel Encinas, et al.. (2017). Lunatic fringe-mediated Notch signaling regulates adult hippocampal neural stem cell maintenance. eLife. 6. 42 indexed citations
4.
Depreux, Frederic, Lingyan Wang, Han Jiang, et al.. (2016). Antisense oligonucleotides delivered to the amniotic cavityin uteromodulate gene expression in the postnatal mouse. Nucleic Acids Research. 44(20). gkw867–gkw867. 30 indexed citations
5.
Basch, Martín L., Fatih Semerci, Frederic Depreux, et al.. (2016). Fine-tuning of Notch signaling sets the boundary of the organ of Corti and establishes sensory cell fates. eLife. 5. 66 indexed citations
6.
Depreux, Frederic, Megan J. Puckelwartz, Don Wolfgeher, et al.. (2015). Disruption of the lamin A and matrin-3 interaction by myopathic LMNA mutations. Human Molecular Genetics. 24(15). 4284–4295. 26 indexed citations
7.
Puckelwartz, Megan J., Frederic Depreux, & Elizabeth M. McNally. (2011). Gene expression, chromosome position and lamin A/C mutations. Nucleus. 2(3). 162–167. 40 indexed citations
8.
Puckelwartz, Megan J., Gene Kim, Yuan Zhang, et al.. (2009). Nesprin-1 mutations in human and murine cardiomyopathy. Journal of Molecular and Cellular Cardiology. 48(4). 600–608. 107 indexed citations
9.
Zvaritch, Elena, Éric Bombardier, Frederic Depreux, et al.. (2009). Ca 2+ dysregulation in Ryr1 I4895T/wt mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods. Proceedings of the National Academy of Sciences. 106(51). 21813–21818. 52 indexed citations
10.
Depreux, Frederic, J. M. Scheffler, A.L. Grant, C. A. Bidwell, & David E. Gerrard. (2009). Molecular cloning and characterization of porcine calcineurin-α subunit expression in skeletal muscle. Journal of Animal Science. 88(2). 562–571. 7 indexed citations
11.
Depreux, Frederic, Keith N. Darrow, David A. Conner, et al.. (2008). Eya4-deficient mice are a model for heritable otitis media. Journal of Clinical Investigation. 118(2). 651–8. 75 indexed citations
12.
Alcalai, Ronny, Michael Arad, Frederic Depreux, et al.. (2007). Hypertrophy, electrical abnormalities, autophagic vacuoles accumulation and cardiac fibrosis in LAMP2 cardiomyopathy mouse model. Progress in Pediatric Cardiology. 24(1). 73–74. 2 indexed citations
13.
Zvaritch, Elena, Frederic Depreux, Ryan E. Loy, et al.. (2007). An Ryr1 I4895T mutation abolishes Ca 2+ release channel function and delays development in homozygous offspring of a mutant mouse line. Proceedings of the National Academy of Sciences. 104(47). 18537–18542. 62 indexed citations
14.
Schönberger, Jost, Libin Wang, Jordan T. Shin, et al.. (2005). Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss. Nature Genetics. 37(4). 418–422. 154 indexed citations
15.
Eggert, J. M., Frederic Depreux, A. P. Schinckel, A.L. Grant, & David E. Gerrard. (2002). Myosin heavy chain isoforms account for variation in pork quality. Meat Science. 61(2). 117–126. 70 indexed citations
16.
Depreux, Frederic, A.L. Grant, D. B. Anderson, & David E. Gerrard. (2002). Paylean alters myosin heavy chain isoform content in pig muscle1. Journal of Animal Science. 80(7). 1888–1894. 38 indexed citations
17.
Depreux, Frederic, A.L. Grant, & David E. Gerrard. (2002). Influence of halothane genotype and body-weight on myosin heavy chain composition in pig muscle as related to meat quality. Livestock Production Science. 73(2-3). 265–273. 38 indexed citations
18.
Depreux, Frederic, et al.. (2000). Quantification of myosin heavy chain isoform in porcine muscle using an enzyme-linked immunosorbent assay. Meat Science. 56(3). 261–269. 30 indexed citations
19.
Depreux, Frederic. (2000). Role of MRFs and calcineurin in modulating muscle fiber type. Purdue e-Pubs (Purdue University System). 1 indexed citations
20.
Ji, Shaoquan, S. G. Cornelius, Glenn Frank, et al.. (1998). Myostatin expression in porcine tissues: tissue specificity and developmental and postnatal regulation. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology. 275(4). R1265–R1273. 197 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

Rankless by CCL
2026