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, Robert T. Dirksen, John D. Lueck, 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

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Population dynamics of normal human blood inferred from somatic mutations

2018 374 citations Henry Lee-Six, Nina Friesgaard Øbro et al. Nature profile →

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	5mC and 5hmC methylation sequencing: the power of 6-base sequencing in a multiomic era 2025 ·Epigenomics ·R. M. M. Crawford, (unknown), Stephen Riffle, (unknown), Robert J. Osborne	1
2	Abstract 5573: Validation of Aspyre Clinical Test for Lung at low input levels: Simplified genomic profiling for NSCLC with minimal tissue requirements 2025 ·Cancer Research ·(unknown), Katherine Knudsen, (unknown), Rebecca Palmer, (unknown), Ryan Evans, Eleanor R. Gray, (unknown), Robert J. Osborne, (unknown), Wendy J. Levin, (unknown)	0
3	Ultra-sensitive molecular detection of gene fusions from RNA using ASPYRE 2022 ·BMC Medical Genomics ·Eleanor R. Gray, (unknown), (unknown), Kristine von Bargen, (unknown), (unknown), Ana-Luisa Silva, (unknown), (unknown), (unknown), Simonetta Andreazza, Alessandro Tomassini, (unknown), (unknown), Robert J. Osborne, (unknown)	2
4	Reliable detection of somatic mutations in solid tissues by laser-capture microdissection and low-input DNA sequencing 2020 ·Nature Protocols ·Peter Ellis, Luiza Moore, Mathijs A. Sanders, Timothy Butler, Simon Brunner, Henry Lee-Six, Robert J. Osborne, Ben W. Farr, Tim Coorens, Andrew Lawson, Alex Cagan, Mike Stratton, Iñigo Martincorena, Peter J. Campbell	67
5	Abstract 3097: Analytical development of the RaDaRTM assay, a highly sensitive and specific assay for the monitoring of minimal residual disease 2020 ·Cancer Research ·Giovanni Marsico, Garima Sharma, (unknown), Sophie Hackinger, Tim Forshew, Karen Howarth, Jamie L. Platt, Nitzan Rosenfeld, Robert J. Osborne	9
6	Population dynamics of normal human blood inferred from somatic mutations breakdown → 2018 ·Nature ·Henry Lee-Six, Nina Friesgaard Øbro, Mairi Shepherd, Sebastian Großmann, Kevin J. Dawson, Miriam Belmonte, Robert J. Osborne, Brian J.P. Huntly, Iñigo Martincorena, Elizabeth Anderson, Laura P. O’Neill, Michael R. Stratton, Elisa Laurenti, Anthony R. Green, David G. Kent, Peter J. Campbell	374
7	High concentrations of lead and barium in hair of the rural population caused by water pollution in the Thar Jath oilfields in South Sudan 2016 ·Forensic Science International ·Fritz Pragst, (unknown), (unknown), (unknown), David Quig, Robert J. Osborne, Christian Runge, (unknown)	41
8	A method for counting PCR template molecules with application to next-generation sequencing 2011 ·Nucleic Acids Research ·(unknown), Robert J. Osborne, Sydney Brenner, Conrad Lichtenstein	125
9	Bone morphogenetic protein 7 (BMP7) mutations are associated with variable ocular, brain, ear, palate, and skeletal anomalies 2010 ·Human Mutation ·Alexander W. Wyatt, Robert J. Osborne, Helen Stewart, Nicola Ragge	66
10	Aberrant alternative splicing and extracellular matrix gene expression in mouse models of myotonic dystrophy 2010 ·Nature Structural & Molecular Biology ·(unknown), Melissa Cline, Robert J. Osborne, Daniel L. Tuttle, Tyson A. Clark, John P. Donohue, Megan P. Hall, Lily Shiue, Maurice S. Swanson, Charles A. Thornton, Manuel Ares	269
11	Androgenetic complete mole with trisomy 13: Report of a case with microsatellite genotyping and review of the literature 2010 ·Pathology - Research and Practice ·Valérie Dubé, Kathy Chun, Robert J. Osborne, Christopher Sherman, Sharon Nofech‐Mozes, Nadia Ismiil, (unknown), Mahmoud A. Khalifa	7
12	Reversal of RNA Dominance by Displacement of Protein Sequestered on Triplet Repeat RNA 2009 ·Science ·Thurman M. Wheeler, Krzysztof Sobczak, John D. Lueck, Robert J. Osborne, Xiaoyan Lin, Robert T. Dirksen, Charles A. Thornton	303
13	Seeing clearly: the dominant and recessive nature ofFOXE3in eye developmental anomalies 2009 ·Human Mutation ·Sı̇bel Aylı̇n Uğur İşerı̇, Robert J. Osborne, Martin Farrall, Alexander W. Wyatt, Ghazala Mirza, Gudrun Nürnberg, (unknown), H. Herbert, Angela Martin, Muhammad Sajid Hussain, J. R. O. Collin, Mark Lathrop, Peter Nürnberg, Jiannis Ragoussis, Nicola Ragge	67
14	Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulators 2009 ·Human Genetics ·Gaia Gestri, Robert J. Osborne, Alexander W. Wyatt, Dianne Gerrelli, Susan Gribble, Helen Stewart, Alan Fryer, David J. Bunyan, Katrina Prescott, J. R. O. Collin, Tomas Fitzgerald, David Robinson, Nigel P. Carter, Stephen W. Wilson, Nicola Ragge	60
15	Novel heterozygousOTX2mutations and whole gene deletions in anophthalmia, microphthalmia and coloboma 2008 ·Human Mutation ·Alexander W. Wyatt, Preeti Bakrania, David J. Bunyan, Robert J. Osborne, John A. Crolla, Alison Salt, Carmen Ayuso, Ruth Newbury‐Ecob, Yassir Abou-Rayyah, J. R. O. Collin, David Robinson, Nicola Ragge	82
16	Cell-free cloning of highly expanded CTG repeats by amplification of dimerized expanded repeats 2007 ·Nucleic Acids Research ·Robert J. Osborne, Charles A. Thornton	23
17	Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy 2006 ·Neurology ·Robert J. Osborne, Stephen Welle, Shannon L. Venance, Charles A. Thornton, Rabi Tawil	112
18	RNA-dominant diseases 2006 ·Human Molecular Genetics ·Robert J. Osborne, Charles A. Thornton	169
19	Chloride channelopathy in myotonic dystrophy resulting from loss of posttranscriptional regulation for CLCN1 2006 ·American Journal of Physiology-Cell Physiology ·John D. Lueck, Codrin Lungu, Ami Mankodi, Robert J. Osborne, Stephen Welle, Robert T. Dirksen, Charles A. Thornton	54
20	An entomopoxvirus homologue of the vaccinia virus D13L-encoded 'rifampicin resistance' protein 1996 ·Journal of General Virology ·Robert J. Osborne, (unknown), Alagacone Sriskantha, J. Lai‐Fook, (unknown), David J. Dall	14

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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