Robert J. Osborne

4.8k total citations · 1 hit paper
27 papers, 2.2k citations indexed

About

Robert J. Osborne is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Robert J. Osborne has authored 27 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 6 papers in Genetics. Recurrent topics in Robert J. Osborne's work include Genetic Neurodegenerative Diseases (8 papers), Cancer Genomics and Diagnostics (6 papers) and Muscle Physiology and Disorders (5 papers). Robert J. Osborne is often cited by papers focused on Genetic Neurodegenerative Diseases (8 papers), Cancer Genomics and Diagnostics (6 papers) and Muscle Physiology and Disorders (5 papers). Robert J. Osborne collaborates with scholars based in United Kingdom, United States and Canada. Robert J. Osborne's co-authors include Charles A. Thornton, Krzysztof Sobczak, Xiaoyan Lin, Maurice S. Swanson, Thurman M. Wheeler, John D. Lueck, Robert T. Dirksen, Stephen Welle, Melissa Cline and Marion Hamshere and has published in prestigious journals such as Nature, Science and Nucleic Acids Research.

In The Last Decade

Robert J. Osborne

26 papers receiving 2.2k citations

Hit Papers

Population dynamics of no... 2018 2026 2020 2023 2018 100 200 300

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Robert J. Osborne 1.7k 821 379 318 288 27 2.2k
Brenda Lilly 2.1k 1.2× 220 0.3× 407 1.1× 355 1.1× 149 0.5× 54 3.1k
António Duarte 3.1k 1.8× 400 0.5× 241 0.6× 561 1.8× 205 0.7× 54 4.1k
Mary Shago 1.4k 0.8× 132 0.2× 613 1.6× 183 0.6× 224 0.8× 57 2.3k
Van N. Pham 1.6k 0.9× 371 0.5× 116 0.3× 208 0.7× 115 0.4× 24 2.2k
Luc Pardanaud 2.6k 1.5× 604 0.7× 249 0.7× 270 0.8× 150 0.5× 46 3.4k
Arndt F. Siekmann 2.1k 1.2× 285 0.3× 155 0.4× 318 1.0× 128 0.4× 43 3.0k
Anthony B. Firulli 3.3k 1.9× 172 0.2× 713 1.9× 362 1.1× 97 0.3× 85 4.0k
Jacquelyn Joseph‐Silverstein 1.2k 0.7× 256 0.3× 172 0.5× 357 1.1× 59 0.2× 20 1.8k
Alison Miyamoto 1.7k 1.0× 162 0.2× 193 0.5× 194 0.6× 98 0.3× 17 2.1k
Jürgen Neesen 582 0.3× 312 0.4× 475 1.3× 84 0.3× 150 0.5× 54 1.5k

Countries citing papers authored by Robert J. Osborne

Since Specialization
Citations

This map shows the geographic impact of Robert J. Osborne'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. Osborne 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. Osborne more than expected).

Fields of papers citing papers by Robert J. Osborne

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of Robert J. Osborne. A scholar is included among the top collaborators of Robert J. Osborne 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. Osborne. Robert J. Osborne 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.
Crawford, R. M. M., et al.. (2025). 5mC and 5hmC methylation sequencing: the power of 6-base sequencing in a multiomic era. Epigenomics. 18(1). 101–115. 1 indexed citations
2.
Knudsen, Katherine, Rebecca Palmer, Ryan Evans, et al.. (2025). Abstract 5573: Validation of Aspyre Clinical Test for Lung at low input levels: Simplified genomic profiling for NSCLC with minimal tissue requirements. Cancer Research. 85(8_Supplement_1). 5573–5573.
3.
Gray, Eleanor R., Kristine von Bargen, Ana-Luisa Silva, et al.. (2022). Ultra-sensitive molecular detection of gene fusions from RNA using ASPYRE. BMC Medical Genomics. 15(1). 215–215. 2 indexed citations
4.
Ellis, Peter, Luiza Moore, Mathijs A. Sanders, et al.. (2020). Reliable detection of somatic mutations in solid tissues by laser-capture microdissection and low-input DNA sequencing. Nature Protocols. 16(2). 841–871. 67 indexed citations
5.
Marsico, Giovanni, Garima Sharma, Sophie Hackinger, et al.. (2020). Abstract 3097: Analytical development of the RaDaRTM assay, a highly sensitive and specific assay for the monitoring of minimal residual disease. Cancer Research. 80(16_Supplement). 3097–3097. 9 indexed citations
6.
Lee-Six, Henry, Nina Friesgaard Øbro, Mairi Shepherd, et al.. (2018). Population dynamics of normal human blood inferred from somatic mutations. Nature. 561(7724). 473–478. 374 indexed citations breakdown →
7.
Pragst, Fritz, et al.. (2016). High concentrations of lead and barium in hair of the rural population caused by water pollution in the Thar Jath oilfields in South Sudan. Forensic Science International. 274. 99–106. 41 indexed citations
8.
Osborne, Robert J., et al.. (2011). A method for counting PCR template molecules with application to next-generation sequencing. Nucleic Acids Research. 39(12). e81–e81. 125 indexed citations
9.
Dubé, Valérie, Kathy Chun, Robert J. Osborne, et al.. (2010). Androgenetic complete mole with trisomy 13: Report of a case with microsatellite genotyping and review of the literature. Pathology - Research and Practice. 206(11). 776–781. 7 indexed citations
10.
Wyatt, Alexander W., Robert J. Osborne, Helen Stewart, & Nicola Ragge. (2010). Bone morphogenetic protein 7 (BMP7) mutations are associated with variable ocular, brain, ear, palate, and skeletal anomalies. Human Mutation. 31(7). 781–787. 66 indexed citations
11.
Cline, Melissa, Robert J. Osborne, Daniel L. Tuttle, et al.. (2010). Aberrant alternative splicing and extracellular matrix gene expression in mouse models of myotonic dystrophy. Nature Structural & Molecular Biology. 17(2). 187–193. 269 indexed citations
12.
Wheeler, Thurman M., Krzysztof Sobczak, John D. Lueck, et al.. (2009). Reversal of RNA Dominance by Displacement of Protein Sequestered on Triplet Repeat RNA. Science. 325(5938). 336–339. 303 indexed citations
13.
Gestri, Gaia, Robert J. Osborne, Alexander W. Wyatt, et al.. (2009). Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulators. Human Genetics. 126(6). 791–803. 60 indexed citations
14.
İşerı̇, Sı̇bel Aylı̇n Uğur, Robert J. Osborne, Martin Farrall, et al.. (2009). Seeing clearly: the dominant and recessive nature ofFOXE3in eye developmental anomalies. Human Mutation. 30(10). 1378–1386. 67 indexed citations
15.
Wyatt, Alexander W., Preeti Bakrania, David J. Bunyan, et al.. (2008). Novel heterozygousOTX2mutations and whole gene deletions in anophthalmia, microphthalmia and coloboma. Human Mutation. 29(11). E278–E283. 82 indexed citations
16.
Osborne, Robert J. & Charles A. Thornton. (2007). Cell-free cloning of highly expanded CTG repeats by amplification of dimerized expanded repeats. Nucleic Acids Research. 36(4). e24–e24. 23 indexed citations
17.
Osborne, Robert J., Stephen Welle, Shannon L. Venance, Charles A. Thornton, & Rabi Tawil. (2006). Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy. Neurology. 68(8). 569–577. 112 indexed citations
18.
Osborne, Robert J. & Charles A. Thornton. (2006). RNA-dominant diseases. Human Molecular Genetics. 15(suppl_2). R162–R169. 169 indexed citations
19.
Lueck, John D., Codrin Lungu, Ami Mankodi, et al.. (2006). Chloride channelopathy in myotonic dystrophy resulting from loss of posttranscriptional regulation for CLCN1. American Journal of Physiology-Cell Physiology. 292(4). C1291–C1297. 54 indexed citations
20.
Osborne, Robert J., et al.. (1996). An entomopoxvirus homologue of the vaccinia virus D13L-encoded 'rifampicin resistance' protein. Journal of General Virology. 77(5). 839–846. 14 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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