James O’Sullivan

4.7k total citations
40 papers, 2.0k citations indexed

About

James O’Sullivan is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, James O’Sullivan has authored 40 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 14 papers in Genetics and 4 papers in Genetics. Recurrent topics in James O’Sullivan's work include Retinal Development and Disorders (8 papers), RNA regulation and disease (6 papers) and Connexins and lens biology (3 papers). James O’Sullivan is often cited by papers focused on Retinal Development and Disorders (8 papers), RNA regulation and disease (6 papers) and Connexins and lens biology (3 papers). James O’Sullivan collaborates with scholars based in United Kingdom, United States and South Africa. James O’Sullivan's co-authors include Sanjeev S. Bhaskar, Graeme C. Black, Jill Urquhart, Simon G. Williams, William G. Newman, Simon Ramsden, Sarah B. Daly, Georgina Hall, Miriam J. Smith and D. Gareth Evans and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Journal of Clinical Investigation.

In The Last Decade

James O’Sullivan

37 papers receiving 2.0k citations

Peers

Countries citing papers authored by James O’Sullivan

Since Specialization

Citations

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

Fields of papers citing papers by James O’Sullivan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by James O’Sullivan. 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 James O’Sullivan. The network helps show where James O’Sullivan may publish in the future.

Co-authorship network of co-authors of James O’Sullivan

This figure shows the co-authorship network connecting the top 25 collaborators of James O’Sullivan. A scholar is included among the top collaborators of James O’Sullivan 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 James O’Sullivan. James O’Sullivan 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	Beta‐cell death and dysfunction drives hyperglycaemia in organ donors 2023 ·Diabetes Obesity and Metabolism ·(unknown), Angela Summers, James O’Sullivan, Catherine Fullwood, Neil A. Hanley, John Casey, Shareen Forbes, Miranda Rosenthal, Paul Johnson, Pratik Choudhary, (unknown), James Shaw, Daniel Neiman, Ruth Shemer, Benjamin Gläser, Yuval Dor, Titus Augustine, Martin K. Rutter, David van Dellen	4
2	Biallelic loss of function variants in STAG3 result in primary ovarian insufficiency 2021 ·Reproductive BioMedicine Online ·Leigh Demain, (unknown), (unknown), Emma Miles, Cheryl T. Fitzgerald, (unknown), Glenda M. Beaman, James O’Sullivan, Raymond T. O’Keefe, William G. Newman	7
3	A challenging case of sporadic melanocytoma of the jugular foramen 2021 ·Neurochirurgie ·Carmine Antonio Donofrio, Federico Roncaroli, (unknown), Marta Pereira, James O’Sullivan, (unknown), Gillian Potter, (unknown), Scott Rutherford	2
4	Kidney Single-Cell Atlas Reveals Myeloid Heterogeneity in Progression and Regression of Kidney Disease 2020 ·Journal of the American Society of Nephrology ·Bryan R. Conway, Eoin O’Sullivan, Carolynn Cairns, James O’Sullivan, Daniel J. Simpson, Angela Salzano, Katie Connor, Peng Ding, Duncan C. Humphries, Kevin Stewart, (unknown), Riinu Pius, Neil C. Henderson, C Bénézech, Prakash Ramachandran, David A. Ferenbach, Jeremy Hughes, Tamir Chandra, Laura Denby	130
5	Infantile fibrosarcoma with TPM3-NTRK1 fusion in a boy with Bloom syndrome 2020 ·Familial Cancer ·S M Huson, (unknown), (unknown), (unknown), Roberto Paredes, D. Gareth Evans, Daniel Baumhoer, James O’Sullivan, (unknown), Detlev Schindler, Stefan Meyer	7
6	A homozygous missense variant in CHRM3 associated with familial urinary bladder disease 2019 ·Clinical Genetics ·Glenda M. Beaman, (unknown), Keng Wee Teik, Jill Urquhart, (unknown), James O’Sullivan, Sanjeev S. Bhaskar, K Wood, Huw B. Thomas, Raymond T. O’Keefe, Adrian S. Woolf, Helen M. Stuart, William G. Newman	9
7	Intracranial Angiomatoid Fibrous Histiocytoma with EWSR1-CREB Family Fusions: A Report of 2 Pediatric Cases 2019 ·World Neurosurgery ·Athanasios Konstantinidis, Edmund Cheesman, James O’Sullivan, (unknown), Shivaram Avula, Barry Pizer, John‐Paul Kilday	34
8	Refining the Mouse Subtotal Nephrectomy in Male 129S2/SV Mice for Consistent Modeling of Progressive Kidney Disease With Renal Inflammation and Cardiac Dysfunction 2019 ·Frontiers in Physiology ·James O’Sullivan, (unknown), (unknown), Carolynn Cairns, Andy Boyd, Matthew A. Bailey, Adrian Thomson, Jeremy Hughes, C Bénézech, Bryan R. Conway, Laura Denby	10
9	Non lethal Raine syndrome and differential diagnosis 2016 ·European Journal of Medical Genetics ·Siham Chafai Elalaoui, (unknown), Ilham Ratbi, Jill Urquhart, James O’Sullivan, Sanjeev S. Bhaskar, Simon G. Williams, (unknown), Jaber Lyahyai, (unknown), Imane Cherkaoui Jaouad, (unknown), William G. Newman, Abdelaziz Sefiani	32
10	Whole Genome Sequencing Increases Molecular Diagnostic Yield Compared with Current Diagnostic Testing for Inherited Retinal Disease 2016 ·Ophthalmology ·Jamie M. Ellingford, Stephanie Barton, Sanjeev S. Bhaskar, Simon G. Williams, Panagiotis I. Sergouniotis, James O’Sullivan, Janine A. Lamb, Rahat Perveen, Georgina Hall, William G. Newman, Richard D. Unwin, Stephen A. Roberts, (unknown), Rick Tearle, S. C. Bayliss, Simon Ramsden, Andrea H. Németh, Graeme C. Black	93
11	MiR-204 is responsible for inherited retinal dystrophy associated with ocular coloboma 2015 ·Proceedings of the National Academy of Sciences ·Iván Conte, Kristen D. Hadfield, Sara Barbato, Sabrina Carrella, Mariateresa Pizzo, (unknown), Annamaria Carissimo, Marianthi Karali, Louise F. Porter, Jill Urquhart, (unknown), James O’Sullivan, Forbes Manson, Stephan C. F. Neuhauss, Sandro Banfi, Graeme C. Black	84
12	Expanding the genetic and phenotypic spectrum of popliteal pterygium disorders 2015 ·American Journal of Medical Genetics Part A ·Elizabeth J. Leslie, James O’Sullivan, Michael L. Cunningham, Ankur Singh, Steven L. Goudy, (unknown), Lamia Alsubaie, (unknown), (unknown), A. Jeannette M. Hoogeboom, Martine Dunnwald, Seema Kapoor, Pawina Jiramongkolchai, Jennifer Standley, J. Robert Manak, Jeffrey C. Murray, Michael J. Dixon	32
13	Pinpointing clinical diagnosis through whole exome sequencing to direct patient care: a case of Senior-Loken syndrome 2015 ·The Lancet ·Jamie M. Ellingford, Panagiotis I. Sergouniotis, Rachel Lennon, Sanjeev S. Bhaskar, Simon G. Williams, (unknown), James O’Sullivan, Georgina Hall, Simon Ramsden, I. Christopher Lloyd, Adrian S. Woolf, Graeme C. Black	21
14	A clinical molecular genetic service for United Kingdom families with choroideraemia 2013 ·European Journal of Medical Genetics ·Simon Ramsden, Anna O’Grady, Tracy Fletcher, James O’Sullivan, (unknown), Stephanie Barton, Georgina Hall, Anthony T. Moore, Andrew R. Webster, Graeme C. Black	16
15	Loss-of-function mutations in SMARCE1 cause an inherited disorder of multiple spinal meningiomas 2013 ·Nature Genetics ·Miriam J. Smith, James O’Sullivan, Sanjeev S. Bhaskar, Kristen D. Hadfield, Gemma Poke, John Caird, Saba Sharif, Diana Eccles, David Fitzpatrick, Daniel Rawluk, Daniel du Plessis, William G. Newman, D. Gareth Evans	168
16	A paradigm shift in the delivery of services for diagnosis of inherited retinal disease 2012 ·Journal of Medical Genetics ·James O’Sullivan, (unknown), Sanjeev S. Bhaskar, Jonathan E. Dickerson, Georgina Hall, Anna O’Grady, Andrew R. Webster, Simon Ramsden, Graeme C. Black	124
17	Exome Sequence Identifies RIPK4 as the Bartsocas- Papas Syndrome Locus 2011 ·The American Journal of Human Genetics ·Karen S. Mitchell, James O’Sullivan, Caterina Missero, Ed Blair, Rose Richardson, Beverley Anderson, Dario Antonini, Jeffrey C. Murray, Alan Shanske, Brian C. Schutte, Rose-Anne Romano, Satrajit Sinha, Sanjeev S. Bhaskar, Graeme C. Black, Jill Dixon, Michael J. Dixon	73
18	Exome Sequencing Identifies CCDC8 Mutations in 3-M Syndrome, Suggesting that CCDC8 Contributes in a Pathway with CUL7 and OBSL1 to Control Human Growth 2011 ·The American Journal of Human Genetics ·Dan Hanson, Philip Murray, James O’Sullivan, Jill Urquhart, Sarah B. Daly, Sanjeev S. Bhaskar, Leslie G. Biesecker, Mars Skae, Claire E. L. Smith, Trevor Cole, Jeremy Kirk, Kate Chandler, Helen Kingston, Dian Donnai, Peter Clayton, Graeme C. Black	88
19	Missense Mutations in a Retinal Pigment Epithelium Protein, Bestrophin-1, Cause Retinitis Pigmentosa 2009 ·The American Journal of Human Genetics ·Alice E. Davidson, I. D. Millar, Jill Urquhart, (unknown), Yusrah Shweikh, Neil R. A. Parry, James O’Sullivan, Geoffrey J. Maher, Martin McKibbin, Susan M. Downes, Andrew Lotery, Samuel G. Jacobson, Peter de Nully Brown, Graeme C. Black, Forbes Manson	135
20	The Transcription Factor Onecut-2 Controls the Microphthalmia-Associated Transcription Factor Gene 2001 ·Biochemical and Biophysical Research Communications ·Patrick Jacquemin, Vincent Lannoy, James O’Sullivan, Andrew Read, Frédéric P. Lemaigre, Guy Rousseau	33

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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