John F. Peden

55.3k citations

27 papers · 1.9k indexed · h-index 16

Co-authors: Andrew T. Lloyd Paul M. Sharp Martin Farrall Nigel J. Saunders Derek W. Hood Michele Stenico E. Richard Moxon Anders Hamsten
Topics: Genomics and Phylogenetic Studies (7 papers)RNA and protein synthesis mechanisms (7 papers)Genetic Associations and Epidemiology (5 papers)
Cited by: Microbiology Nephrology Cancer Research
Journals: Blood Bioinformatics PLoS ONE
Partner nations: United Kingdom Sweden Italy

In The Last Decade

John F. Peden

25 papers receiving 1.9k citations

Peers

Countries citing papers authored by John F. Peden

Since Specialization

Citations

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

Fields of papers citing papers by John F. Peden

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John F. Peden. 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 John F. Peden. The network helps show where John F. Peden may publish in the future.

Co-authorship network of co-authors of John F. Peden

This figure shows the co-authorship network connecting the top 25 collaborators of John F. Peden. A scholar is included among the top collaborators of John F. Peden 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 John F. Peden. John F. Peden 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	A dedicated caller for DUX4 rearrangements from whole-genome sequencing data 2025 ·BMC Medical Genomics ·(unknown),Stefano Berri,John F. Peden,(unknown),Claire Fielding,(unknown),Helen Northen,David J. McBride,Peter J. Campbell,Jennifer Becq,Sarra Ryan,David Bentley,Christine J. Harrison,Anthony V. Moorman,Mark T. Ross,Martina Mijušković	1
2	Whole genome sequencing provides comprehensive genetic testing in childhood B-cell acute lymphoblastic leukaemia 2023 ·Leukemia ·Sarra Ryan,John F. Peden,Zoya Kingsbury,Claire Schwab,Terena James,Petri Pölönen,Martina Mijušković,(unknown),(unknown),(unknown),Dale J. Hedges,Kathryn G. Roberts,Charles G. Mullighan,Ajay Vora,Lisa J. Russell,(unknown),Anthony V. Moorman,David Bentley,Christine J. Harrison,Mark T. Ross	41
3	Familial congenital cataract, coloboma, and nystagmus phenotype with variable expression caused by mutation in PAX6 in a South African family. 2018 ·PubMed ·(unknown),(unknown),Mark T. Ross,David Bentley,Margarida Mendes Lopes,John F. Peden,Zoya Kingsbury,(unknown),(unknown),Trevor Carmichael,Michèle Ramsay,Susan Williams	19
4	Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour 2011 ·Human Molecular Genetics ·John F. Peden,Martin Farrall	102
5	HLA Has Strongest Association with IgA Nephropathy in Genome-Wide Analysis 2010 ·Journal of the American Society of Nephrology ·John Feehally,Martin Farrall,Anne Boland,Daniel P. Gale,Marta Gut,Simon Heath,Ashish Kumar,John F. Peden,Patrick H. Maxwell,David L. Morris,Sandosh Padmanabhan,Timothy J. Vyse,Anna Zawadzka,Andrew J. Rees,Mark Lathrop,Peter J. Ratcliffe	191
6	Relationship between CAD Risk Genotype in the Chromosome 9p21 Locus and Gene Expression. Identification of Eight New ANRIL Splice Variants 2009 ·PLoS ONE ·Lasse Folkersen,Theodosios Kyriakou,Anuj Goel,John F. Peden,Anders Mälarstig,Gabrielle Paulsson‐Berne,Anders Hamsten,(unknown),Anders Franco‐Cereceda,Anders Gabrielsen,Per Eriksson	132
7	Quantitative Trait Genetic Linkage Analysis of Body Mass Index in Familial Coronary Artery Disease 2008 ·Human Heredity ·Claudia Specchia,Simona Barlera,Benedetta Chiodini,Enrico Nicolis,Martin Farrall,John F. Peden,Rory Collins,Hugh Watkins,Gianni Tognoni,Maria Grazia Franzosi	2
8	Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p 2007 ·Human Molecular Genetics ·(unknown),John F. Peden,Stefan Lorkowski,Anuj Goel,Halit Ongen,Fiona Green,Robert Clarke,Rory Collins,Maria Grazia Franzosi,Gianni Tognoni,Udo Seedorf,Stephan Rust,Per Eriksson,Anders Hamsten,Martin Farrall,Hugh Watkins	389
9	Genome-Wide Mapping of Susceptibility to Coronary Artery Disease Identifies a Novel Replicated Locus on Chromosome 17 2006 ·PLoS Genetics ·Martin Farrall,Fiona R. Green,John F. Peden,Per Olsson,Robert Clarke,Mai‐Lis Hellénius,Stephan Rust,Jacob Lagercrantz,Maria Grazia Franzosi,H. Schulte,Alisoun H. Carey,Gunnar Olsson,Gerd Assmann,Gianni Tognoni,Rory Collins,Anders Hamsten,Hugh Watkins	55
10	Multiple QTL influence the serum Lp(a) concentration: a genome-wide linkage screen in the PROCARDIS study 2006 ·European Journal of Human Genetics ·Simona Barlera,Claudia Specchia,Martin Farrall,Benedetta Chiodini,Maria Grazia Franzosi,Stephan Rust,Fiona Green,Enrico Nicolis,John F. Peden,Gerd Assmann,Rory Collins,Anders Hamsten,Gianni Tognoni,Hugh Watkins	14
11	Bisphosphonates and their impact on patient treatment. 2006 ·PubMed ·Gregori M Kurtzman,Lee H Silverstein,John F. Peden	0
12	Inter-species horizontal transfer resulting in core-genome and niche-adaptive variation within Helicobacter pylori 2005 ·BMC Genomics ·Nigel J. Saunders,(unknown),John F. Peden,Stephen A. Jarvis	27
13	SNP cherry picker: maximizing the chance of finding an association with a disease SNP 2003 ·Bioinformatics ·Mark Harris,(unknown),John F. Peden,Chris Rawlings	4
14	Finding Secret Messages in DNA Microdots 2001 ·Warwick Research Archive Portal (University of Warwick) ·Stephen A. Jarvis,(unknown),John F. Peden,Nigel J. Saunders	1
15	Repeat‐associated phase variable genes in the complete genome sequence of Neisseria meningitidis strain MC58 2000 ·Molecular Microbiology ·Nigel J. Saunders,Alex C. Jeffries,John F. Peden,Derek W. Hood,Hervé Tettelin,Rino Rappuoli,E. Richard Moxon	192
16	Molecular cloning and phylogenetic analysis of the small cytoplasmic RNA fromListeria monocytogenes 1999 ·FEMS Microbiology Letters ·Tom Barry,Mary Margaret Kelly,Barry Glynn,John F. Peden	6
17	Simple sequence repeats in the Helicobacter pylori genome 1998 ·Molecular Microbiology ·Nigel J. Saunders,John F. Peden,Derek W. Hood,E. Richard Moxon	167
18	DNA sequence evolution: the sounds of silence 1995 ·Philosophical Transactions of the Royal Society B Biological Sciences ·Paul M. Sharp,Michalis Averof,Andrew T. Lloyd,Giorgio Matassi,John F. Peden	197
19	Upstream stimulators for recoding 1995 ·Biochemistry and Cell Biology ·(unknown),(unknown),John F. Atkins,John F. Peden,Senya Matsufuji,Tamiko Matsufuji,Rafaël Maldonado,Norma M. Wills,R.F. Gesteland,(unknown)	26
20	Codon usage: mutational bias, translational selection, or both? 1993 ·Biochemical Society Transactions ·Paul M. Sharp,Michele Stenico,John F. Peden,Andrew T. Lloyd	258

About John F. Peden

John F. Peden is a scholar working on Genetics, Molecular Biology and Gastroenterology, having authored 27 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (7 papers), RNA and protein synthesis mechanisms (7 papers) and Genetic Associations and Epidemiology (5 papers). The work is most often cited by research in Microbiology (159 citations), Nephrology (177 citations) and Cancer Research (300 citations). John F. Peden has collaborated with scholars based in United Kingdom, Sweden and Italy. Frequent co-authors include Andrew T. Lloyd, Paul M. Sharp, Martin Farrall, Nigel J. Saunders, Derek W. Hood, Michele Stenico, E. Richard Moxon, Anders Hamsten, Michalis Averof and Giorgio Matassi. Their work appears in journals such as Blood, Bioinformatics and PLoS ONE.

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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