Tracy Campbell

3.8k citations

47 papers · 1.7k indexed · h-index 19

Co-authors: John Collinge Simon Mead Mark Poulter Jonathan Beck Jerome Whitfield Michael P. Alpers Mark S. Palmer Elizabeth Fisher
Topics: Prion Diseases and Protein Misfolding (26 papers)Neurological diseases and metabolism (19 papers)Trace Elements in Health (14 papers)
Cited by: Neurology Nutrition and Dietetics Molecular Biology
Journals: Science New England Journal of Medicine The Lancet
Partner nations: United Kingdom United States Australia

In The Last Decade

Tracy Campbell

43 papers receiving 1.7k citations

Peers

Countries citing papers authored by Tracy Campbell

Since Specialization

Citations

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

Fields of papers citing papers by Tracy Campbell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tracy Campbell

This figure shows the co-authorship network connecting the top 25 collaborators of Tracy Campbell. A scholar is included among the top collaborators of Tracy Campbell 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 Tracy Campbell. Tracy Campbell 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	Enhanced efficiency fertilizers, potato production, and nitrate leaching in the Wisconsin Central Sands 2025 ·Journal of Environmental Quality ·Tracy Campbell,Matthew D. Ruark,(unknown),Birl Lowery	0
2	Quantifying the spatiotemporal variability of nitrate in irrigation water across the Wisconsin Central Sands 2023 ·Journal of Environmental Quality ·Tracy Campbell,(unknown),(unknown),Christopher J. Kucharik	2
3	Estimation of the number of inherited prion disease mutation carriers in the UK 2022 ·European Journal of Human Genetics ·(unknown),Tracy Campbell,Lee Darwent,Peter Rudge,John Collinge,Simon Mead	3
4	Prion protein gene mutation detection using long-read Nanopore sequencing 2022 ·Scientific Reports ·François Kroll,Athanasios Dimitriadis,Tracy Campbell,Lee Darwent,John Collinge,Simon Mead,Emmanuelle Viré	6
5	Case report of homozygous E200D mutation of PRNP in apparently sporadic Creutzfeldt-Jakob disease 2021 ·BMC Neurology ·Ahamad Hassan,Tracy Campbell,Lee Darwent,(unknown),Alison Green,John Collinge,Simon Mead	6
6	Altered DNA methylation profiles in blood from patients with sporadic Creutzfeldt–Jakob disease 2020 ·Acta Neuropathologica ·(unknown),(unknown),Tracy Campbell,Tony Bélicard,Adam R. Smith,Rebecca G. Smith,Rachel Raybould,Jonathan M. Schott,Katie Lunnon,Peter Sarkies,John Collinge,Simon Mead,Emmanuelle Viré	16
7	Evaluating the causality of novel sequence variants in the prion protein gene by example 2018 ·Neurobiology of Aging ·Tze How Mok,(unknown),Zane Jaunmuktane,Tracy Campbell,Susan Joiner,Jonathan D. F. Wadsworth,Laszlo L. P. Hosszu,Sebastian Brandner,(unknown),Thomas Truelsen,Eva Løbner Lund,(unknown),John Collinge,Simon Mead	10
8	Rare structural genetic variation in human prion diseases 2015 ·Neurobiology of Aging ·Ana Lukić,James Uphill,Craig Brown,John S. Beck,Mark Poulter,Tracy Campbell,Gary Adamson,Holger Hummerich,Jerome Whitfield,Claudia Ponto,Inga Zerr,Sarah E. Lloyd,John Collinge,Simon Mead	6
9	C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies 2013 ·Neurology ·Davina J. Hensman Moss,Mark Poulter,Jon Beck,Jason Hehir,James M. Polke,Tracy Campbell,(unknown),Ese Mudanohwo,Peter McColgan,Andrea Haworth,Edward J. Wild,Mary G. Sweeney,Henry Houlden,Simon Mead,Sarah J. Tabrizi	137
10	Detection of prion infection in variant Creutzfeldt-Jakob disease: a blood-based assay 2011 ·The Lancet ·Julie Ann Edgeworth,Michael Farmer,(unknown),(unknown),Jonathan Beck,Tracy Campbell,Jessica Lowe,Simon Mead,Peter Rudge,John Collinge,Graham S. Jackson	134
11	PRNP allelic series from 19 years of prion protein gene sequencing at the MRC Prion Unit 2010 ·Human Mutation ·(unknown),Mark Poulter,Tracy Campbell,Gary Adamson,(unknown),Rita Guerreiro,Graham S. Jackson,James C. Stevens,Hadi Manji,John Collinge,Simon Mead	65
12	A Novel Protective Prion Protein Variant that Colocalizes with Kuru Exposure 2009 ·New England Journal of Medicine ·Simon Mead,Jerome Whitfield,Mark Poulter,(unknown),James Uphill,Tracy Campbell,(unknown),Holger Hummerich,Jon Beck,Charles A. Mein,Claudio Verzilli,John C. Whittaker,Michael P. Alpers,John Collinge	119
13	Distinct glycoform ratios of protease resistant prion protein associated with PRNP point mutations 2006 ·Brain ·Andrew F. Hill,Susan Joiner,Jonathan Beck,Tracy Campbell,Andrew Dickinson,Mark Poulter,Jonathan D. F. Wadsworth,John Collinge	78
14	Balancing Selection at the Prion Protein Gene Consistent with Prehistoric Kurulike Epidemics 2003 ·Science ·Simon Mead,Michael P. H. Stumpf,Jerome Whitfield,Jonathan Beck,Mark Poulter,Tracy Campbell,(unknown),David B. Goldstein,Michael P. Alpers,Elizabeth Fisher,John Collinge	276
15	Sporadic—but Not Variant—Creutzfeldt-Jakob Disease Is Associated with Polymorphisms Upstream of PRNP Exon 1 2001 ·The American Journal of Human Genetics ·Simon Mead,Sukhvir P. Mahal,John S. Beck,Tracy Campbell,Martin Farrall,Elizabeth Fisher,John Collinge	74
16	Pathogenic presenilin 1 mutations (P436S & I143F) in early-onset Alzheimer's disease in the UK 1999 ·Human Mutation ·Mark S. Palmer,Jonathan Beck,Tracy Campbell,(unknown),(unknown),Nick C. Fox,(unknown),Martin N. Rossor,John Collinge	16
17	Advantages of Higher Level Thinking for At Risk Children. 1996 ·The rural educator ·Tracy Campbell,(unknown)	4
18	Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene 1996 ·Human Genetics ·Otto Windl,Maureen Dempster,J. Peter Estibeiro,Richard Lathe,Rajith de Silva,Thomas Esmonde,Robert Will,Anthea Springbett,Tracy Campbell,Katie Sidle,Mark S. Palmer,John Collinge	164
19	A prion disease with a novel 96-base pair insertional mutation in the prion protein gene 1996 ·Neurology ·Tracy Campbell,Mark S. Palmer,R. G. Will,(unknown),Philip J. Luthert,John Collinge	50
20	Deletions in the prion protein gene are not associated with CJD 1993 ·Human Molecular Genetics ·Mark S. Palmer,Sukhvir P. Mahal,Tracy Campbell,Andrew F. Hill,Katie Sidle,Jean Laplanche,John Collinge	71

About Tracy Campbell

Tracy Campbell is a scholar working on Neurology, Nutrition and Dietetics and Molecular Biology, having authored 47 papers that have together received 1.7k indexed citations. Recurring topics across this work include Prion Diseases and Protein Misfolding (26 papers), Neurological diseases and metabolism (19 papers) and Trace Elements in Health (14 papers). The work is most often cited by research in Neurology (837 citations), Nutrition and Dietetics (515 citations) and Molecular Biology (1.4k citations). Tracy Campbell has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include John Collinge, Simon Mead, Mark Poulter, Jonathan Beck, Jerome Whitfield, Michael P. Alpers, Mark S. Palmer, Elizabeth Fisher, Jon Beck and Katie Sidle. Their work appears in journals such as Science, New England Journal of Medicine and The Lancet.

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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