David Bourn

2.4k citations

33 papers · 604 indexed · h-index 13

Impact in

Nephrology top 5%
- Renal Diseases and Glomerulopathies
Neurology top 10%
- Neurofibromatosis and Schwannoma Cases

Papers in ⓘ

Equine 1
Neurology 5
- Neurofibromatosis and Schwannoma Cases 5

Co-authors: D. Gareth Evans (4 shared papers)Tom Strachan (3 shared papers)Simon Carter (1 shared paper)T Strachan (3 shared papers)Lisa Strain (2 shared papers)Natalia A. Trayanova (3 shared papers)Judith Goodship (2 shared papers)Yves Pirson (1 shared paper)
Journals: Human Genetics (3 papers)Human Molecular Genetics (2 papers)The Journal of Laryngology & Otology (2 papers)Philosophical Transactions of the Royal Society A Mathematical Physical and Engineering Sciences (1 paper)PLoS Medicine (1 paper)
Partner nations: United Kingdom United States Czechia

In The Last Decade

David Bourn

32 papers receiving 595 citations

Peers

Countries citing papers authored by David Bourn

Since Specialization

Citations

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

Fields of papers citing papers by David Bourn

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside David Bourn, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with David Bourn Line = papers co-authored together David Bourn links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 33 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Atypical Haemolytic Uraemic Syndrome Associated with a Hybrid Complement Gene PLoS Medicine ·Julian P. Venables, Lisa Strain, Danny Routledge, David Bourn, Helen M Powell, Paul Warwicker, Martha Diaz-Torres, Anne Sampson, Paul Mead, Michelle Webb, Yves Pirson, Michael S. Jackson, Anne E. Hughes, Katrina Wood, Judith A. Goodship, Timothy H.J. Goodship	2006	165
2	Germline mutations in the neurofibromatosis type 2 tumour suppressor gene Human Molecular Genetics ·David Bourn, Simon Carter, Susan Mason, D. Gareth Evans, Tom Strachan	1994	78
3	A mutation in the neurofibromatosis type 2 tumor-suppressor gene, giving rise to widely different clinical phenotypes in two unrelated individuals. PubMed ·David Bourn, S. A. Carter, D. Gareth Evans, Judith Goodship, Hugh B. Coakham, T Strachan	1994	55
4	Virtual Electrode‐Induced Positive and Negative Graded Responses: Journal of Cardiovascular Electrophysiology ·Natalia A. Trayanova, Richard A. Gray, David Bourn, James Eason	2003	34
5	Pilot of BRAF mutation analysis in indeterminate, suspicious and malignant thyroid FNA cytology Cytopathology ·Samantha Johnson, Steven Hardy, Catherine C. Roberts, David Bourn, Ujjal K. Mallick, Petros Perros	2014	31
6	Diagnostic issues in a family with late onset type 2 neurofibromatosis. Journal of Medical Genetics ·D. Gareth Evans, David Bourn, Andrew J. Wallace, Richard Ramsden, John Mitchell, T Strachan	1995	24
7	Eleven novel mutations in the NF2 tumour suppressor gene Human Genetics ·David Bourn, D. Gareth Evans, Susan Mason, Selahattin Tekeş, L. Trueman, Tom Strachan	1995	22
8	Thirst perception and arginine vasopressin production in a kindred with an activating mutation of the type 2 vasopressin receptor: the pathophysiology of nephrogenic syndrome of inappropriate antidiuresis European Journal of Endocrinology ·Saket Gupta, Tim Cheetham, H Lambert, C.R. Roberts, David Bourn, Malcolm Coulthard, Stephen G. Ball	2009	21
9	Highly polymorphic dinucleotide repeat at the NF2 gene Human Genetics ·David Bourn, Tom Strachan	1995	19
10	Genotype–phenotype correlations in Cornelia de Lange syndrome: Behavioral characteristics and changes with age American Journal of Medical Genetics Part A ·Joanna Moss, Jessica Penhallow, Morad Ansari, Stephanie Barton, David Bourn, David Fitzpatrick, Judith Goodship, Peter Hammond, Catherine Roberts, Alice Welham, Chris Oliver	2017	18
11	Duplications of GPC3 and GPC4 genes in symptomatic female carriers of Simpson-Golabi-Behmel syndrome type 1 European Journal of Medical Genetics ·Schaida Schirwani, Antonio Novelli, M. Cristina Digilio, David Bourn, Valerie Wilson, Catherine Roberts, Bruno Dallapiccola, Emma Hobson	2018	16
12	<i>CYLD Genetic</i> Testing for Brooke-Spiegler Syndrome, Familial Cylindromatosis and Multiple Familial Trichoepitheliomas PLoS Currents ·Anna Dubois, Valerie Wilson, David Bourn, Neil Rajan	2015	15
13	Novel Low-Voltage MultiPulse Therapy to Terminate Atrial Fibrillation JACC. Clinical electrophysiology ·Fu Siong Ng, Ondřej Toman, Jan Petrů, Petr Peichl, Roger A. Winkle, Vivek Y. Reddy, Petr Neužil, R. Hardwin Mead, Norman Qureshi, Zachary I. Whinnett, David Bourn, M. Brent Shelton, Josef Kautzner, Arjun D. Sharma, Mélèze Hocini, Michel Haı̈ssaguerre, Nicholas S. Peters, Igor R. Efimov	2021	12
14	Is CFTR-delF508 Really Absent from the Apical Membrane of the Airway Epithelium? PLoS ONE ·Lee A. Borthwick, Phil Botha, Bernard Verdon, Malcolm Brodlie, Aaron Gardner, David Bourn, Gail Johnson, Michael A. Gray, Andrew J. Fisher	2011	12
15	Phenotypic Variations of Cartilage Hair Hypoplasia: Granulomatous Skin Inflammation and Severe T Cell Immunodeficiency as Initial Clinical Presentation in Otherwise Well Child with Short Stature Journal of Clinical Immunology ·Liza McCann, Jo McPartland, D Barge, Lisa Strain, David Bourn, Eduardo Calonje, Julian Verbov, Andrew Riordan, George Kokai, Chris M. Bacon, Michael Wright, Mario Abinun	2013	11
16	Incidence and outcomes for adults diagnosed with acute myeloid leukemia in the north of England: a real world study Leukemia & lymphoma ·Andrew McGregor, Deborah Moulton, Nick Bown, Gavin Cuthbert, David Bourn, Susanna Mathew, Raymond Dang, Philip Mounter, Gail Jones	2015	10
17	Protease and Amylase in the digestive tract ofBarbus paludinosus Hydrobiologia ·A Cockson, David Bourn	1973	8
18	Chromosomal assignment of a large tRNA gene cluster (tRNALeu, tRNAGln, tRNALys, tRNAArg, tRNAGly) to 17p13.1 Human Genetics ·Norma Morrison, J.P. Goddard, David H. Ledbetter, E. Boyd, David Bourn, J. M. Connor	1991	8
19	Diverse presentations of cutaneous mosaicism occur in CYLD cutaneous syndrome and may result in parent-to-child transmission Journal of the American Academy of Dermatology ·Majid Arefi, Valerie Wilson, Siobhan Muthiah, Simon Zwolinski, Dalvir Bajwa, Paul Brennan, Katie Blasdale, David Bourn, John Burn, Mauro Santibanez‐Koref, Neil Rajan	2019	7
20	Characterization of the relationship between preshock state and virtual electrode polarization-induced propagated graded responses resulting in arrhythmia induction Heart Rhythm ·David Bourn, Richard A. Gray, Natalia A. Trayanova	2006	6

About David Bourn

David Bourn is a scholar working on Equine, Neurology, Hematology, Dermatology and Pulmonary and Respiratory Medicine, having authored 33 papers that have together received 604 indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (5 papers), Cardiac electrophysiology and arrhythmias (4 papers), RNA modifications and cancer (4 papers), RNA and protein synthesis mechanisms (4 papers), Electrolyte and hormonal disorders (3 papers), Sarcoma Diagnosis and Treatment (3 papers), Ion Transport and Channel Regulation (3 papers) and RNA Research and Splicing (2 papers). The work is most often cited by research in Nephrology (107 citations), Neurology (179 citations), Immunology (178 citations), Hematology (90 citations) and Physiology (30 citations). David Bourn has collaborated with scholars based in United Kingdom, United States and Czechia. Frequent co-authors include D. Gareth Evans, Tom Strachan, Simon Carter, T Strachan, Lisa Strain, Natalia A. Trayanova, Judith Goodship, Yves Pirson, Paul Mead and Michelle Webb. Their work appears in journals such as Human Genetics, Human Molecular Genetics, The Journal of Laryngology & Otology, Philosophical Transactions of the Royal Society A Mathematical Physical and Engineering Sciences and PLoS Medicine.

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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