Robert J. Morell

9.1k total citations
81 papers, 5.2k citations indexed

About

Robert J. Morell is a scholar working on Molecular Biology, Sensory Systems and Cognitive Neuroscience. According to data from OpenAlex, Robert J. Morell has authored 81 papers receiving a total of 5.2k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 46 papers in Sensory Systems and 15 papers in Cognitive Neuroscience. Recurrent topics in Robert J. Morell's work include Hearing, Cochlea, Tinnitus, Genetics (46 papers), Hearing Loss and Rehabilitation (15 papers) and RNA regulation and disease (11 papers). Robert J. Morell is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (46 papers), Hearing Loss and Rehabilitation (15 papers) and RNA regulation and disease (11 papers). Robert J. Morell collaborates with scholars based in United States, Pakistan and Poland. Robert J. Morell's co-authors include Thomas B. Friedman, Edward R. Wilcox, Sheikh Riazuddin, Andrew J. Griffith, Zubair M. Ahmed, Saima Riazuddin, James H. Asher, Inna A. Belyantseva, Konrad Noben‐Trauth and Sally A. Camper and has published in prestigious journals such as Science, New England Journal of Medicine and Cell.

In The Last Decade

Robert J. Morell

81 papers receiving 5.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert J. Morell United States 36 3.1k 2.9k 1.2k 666 492 81 5.2k
Inna A. Belyantseva United States 37 2.5k 0.8× 3.2k 1.1× 1.4k 1.2× 783 1.2× 563 1.1× 58 4.9k
Andrew J. Griffith United States 41 3.6k 1.2× 4.3k 1.5× 1.8k 1.5× 921 1.4× 401 0.8× 117 6.8k
Sandrine Marlin France 39 3.4k 1.1× 1.7k 0.6× 653 0.5× 559 0.8× 577 1.2× 117 8.3k
Kenneth R. Johnson United States 42 2.3k 0.8× 2.8k 1.0× 1.0k 0.9× 1.0k 1.5× 470 1.0× 102 5.5k
A. Amraoui France 40 3.2k 1.0× 2.6k 0.9× 886 0.7× 609 0.9× 821 1.7× 130 5.4k
Saima Riazuddin United States 34 2.4k 0.8× 2.2k 0.8× 982 0.8× 346 0.5× 535 1.1× 101 4.0k
Qing Yin Zheng United States 35 1.9k 0.6× 2.4k 0.8× 887 0.7× 811 1.2× 244 0.5× 119 5.0k
Richard J. Goodyear United Kingdom 41 1.9k 0.6× 3.3k 1.1× 1.0k 0.9× 1.0k 1.5× 387 0.8× 72 4.5k
Hannie Kremer Netherlands 44 5.1k 1.7× 2.3k 0.8× 1.1k 0.9× 494 0.7× 728 1.5× 188 8.0k
Kirk W. Beisel United States 42 2.7k 0.9× 2.8k 0.9× 565 0.5× 653 1.0× 302 0.6× 123 6.6k

Countries citing papers authored by Robert J. Morell

Since Specialization
Citations

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

Fields of papers citing papers by Robert J. Morell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert J. Morell. 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 Robert J. Morell. The network helps show where Robert J. Morell may publish in the future.

Co-authorship network of co-authors of Robert J. Morell

This figure shows the co-authorship network connecting the top 25 collaborators of Robert J. Morell. A scholar is included among the top collaborators of Robert J. Morell 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 Robert J. Morell. Robert J. Morell 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.
Jin, Wenwen, Na Liu, Liliana Catherine Patiño, et al.. (2025). Activin A activation of Smad3 mitigates innate inflammation in mouse models of psoriasis and sepsis. Journal of Clinical Investigation. 135(9). 1 indexed citations
2.
Faridi, Rabia, Pamela Stratton, Noemi Salmeri, et al.. (2024). Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome. Clinical Genetics. 105(5). 584–586. 4 indexed citations
3.
Roux, Isabelle, Cristina Fenollar‐Ferrer, Parna Chattaraj, et al.. (2023). CHD7 variants associated with hearing loss and enlargement of the vestibular aqueduct. Human Genetics. 142(10). 1499–1517. 8 indexed citations
4.
Yao, Chen, Tyrone Dowdy, Wenwen Jin, et al.. (2023). TGF-β uncouples glycolysis and inflammation in macrophages and controls survival during sepsis. Science Signaling. 16(797). eade0385–eade0385. 42 indexed citations
5.
Chibly, Alejandro, Vaishali Patel, Marit H. Aure, et al.. (2023). Neurotrophin signaling is a central mechanism of salivary dysfunction after irradiation that disrupts myoepithelial cells. npj Regenerative Medicine. 8(1). 17–17. 16 indexed citations
6.
Faridi, Rabia, Kelly King, Christopher Zalewski, et al.. (2020). Vestibular phenotype‐genotype correlation in a cohort of 90 patients with Usher syndrome. Clinical Genetics. 99(2). 226–235. 24 indexed citations
7.
Morell, Robert J., Rafal T. Olszewski, Risa Tona, et al.. (2020). Noncoding Microdeletion in Mouse Hgf Disrupts Neural Crest Migration into the Stria Vascularis, Reduces the Endocochlear Potential, and Suggests the Neuropathology for Human Nonsyndromic Deafness DFNB39. Journal of Neuroscience. 40(15). 2976–2992. 23 indexed citations
8.
Hoa, Michael, Rafal T. Olszewski, Xiaoyi Li, et al.. (2020). Characterizing Adult Cochlear Supporting Cell Transcriptional Diversity Using Single-Cell RNA-Seq: Validation in the Adult Mouse and Translational Implications for the Adult Human Cochlea. Frontiers in Molecular Neuroscience. 13. 13–13. 37 indexed citations
9.
Bondioli, K. R., et al.. (2016). Molecular markers located on the DGAT1, CAST, and LEPR genes and their associations with milk production and fertility traits in Holstein cattle. Genetics and Molecular Research. 15(1). 11 indexed citations
10.
Brewer, Carmen C., Christopher Zalewski, Kelly King, et al.. (2016). Heritability of non-speech auditory processing skills. European Journal of Human Genetics. 24(8). 1137–1144. 25 indexed citations
11.
Raza, Muhammad Hashim, Rafael Mattera, Robert J. Morell, et al.. (2015). Association between Rare Variants in AP4E1, a Component of Intracellular Trafficking, and Persistent Stuttering. The American Journal of Human Genetics. 97(5). 715–725. 55 indexed citations
12.
Riazuddin, Saima, Shaheen N. Khan, Zubair M. Ahmed, et al.. (2005). Mutations in TRIOBP, Which Encodes a Putative Cytoskeletal-Organizing Protein, Are Associated with Nonsyndromic Recessive Deafness. The American Journal of Human Genetics. 78(1). 137–143. 76 indexed citations
13.
Ahmed, Zubair M., Robert J. Morell, Saima Riazuddin, et al.. (2003). Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37. The American Journal of Human Genetics. 72(5). 1315–1322. 151 indexed citations
14.
Zhu, Mei, Tao Yang, Shu‐Chen Wei, et al.. (2003). Mutations in the γ-Actin Gene (ACTG1) Are Associated with Dominant Progressive Deafness (DFNA20/26). The American Journal of Human Genetics. 73(5). 1082–1091. 149 indexed citations
15.
Wilcox, Edward R., Sadaf Naz, Saima Riazuddin, et al.. (2001). Mutations in the Gene Encoding Tight Junction Claudin-14 Cause Autosomal Recessive Deafness DFNB29. Cell. 104(1). 165–172. 344 indexed citations
16.
Noben‐Trauth, Konrad, et al.. (1998). Tectorin-β (Tectb)Maps to Mouse Chromosome 19. Genomics. 53(3). 419–420. 2 indexed citations
17.
Morell, Robert J., et al.. (1997). Apparent Digenic Inheritance of Waardenburg Syndrome Type 2 (WS2) and Autosomal Recessive Ocular Albinism (AROA). Human Molecular Genetics. 6(5). 659–664. 68 indexed citations
18.
Morell, Robert J., Yong Liang, James H. Asher, et al.. (1995). Analysis of short tandem repeat (STR) allele frequency distributions in a Balinese population. Human Molecular Genetics. 4(1). 85–91. 10 indexed citations
19.
Morell, Robert J., Thomas B. Friedman, & James H. Asher. (1993). A plus-one frameshift mutation in PAX3 alters the entire deduced amino acid sequence of the paired box in a Waardenburg syndrome type 1 (WS1) family. Human Molecular Genetics. 2(9). 1487–1488. 20 indexed citations
20.
Asher, James H., Robert J. Morell, & Thomas B. Friedman. (1991). Confirmation of the Location of a Waardenburg Syndrome Type I Mutation on Human Chromosome 2qa. Annals of the New York Academy of Sciences. 630(1). 295–297. 2 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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