John Barber

6.8k total citations
106 papers, 3.1k citations indexed

About

John Barber is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, John Barber has authored 106 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Genetics, 36 papers in Molecular Biology and 19 papers in Plant Science. Recurrent topics in John Barber's work include Genomic variations and chromosomal abnormalities (45 papers), Chromosomal and Genetic Variations (17 papers) and Congenital heart defects research (13 papers). John Barber is often cited by papers focused on Genomic variations and chromosomal abnormalities (45 papers), Chromosomal and Genetic Variations (17 papers) and Congenital heart defects research (13 papers). John Barber collaborates with scholars based in United Kingdom, United States and Germany. John Barber's co-authors include Edward J. Hollox, John A.L. Armour, I. Karen Temple, Ronald D. Miller, N R Dennis, David Robinson, R J Gardner, Viv Maloney, Deborah Mackay and James C. Nicholson and has published in prestigious journals such as Journal of the American College of Cardiology, Diabetes and Genome Research.

In The Last Decade

John Barber

102 papers receiving 2.9k citations

Peers

Countries citing papers authored by John Barber

Since Specialization

Citations

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

Fields of papers citing papers by John Barber

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of John Barber

This figure shows the co-authorship network connecting the top 25 collaborators of John Barber. A scholar is included among the top collaborators of John Barber 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 Barber. John Barber 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	Experiences of Parent Coaches in an Intervention for Parents of Young Children Newly Diagnosed with Type 1 Diabetes 2024 ·Children ·Carrie Tully, (unknown), Wendy Levy, (unknown), John Barber, (unknown), Marisa E. Hilliard, Maureen Monaghan, Randi Streisand	0
2	Directly Transmitted 12.3-Mb Deletion with a Consistent Phenotype in the Variable 11q21q22.3 Region 2020 ·Cytogenetic and Genome Research ·(unknown), Mira Kharbanda, Mark S. Bateman, David Hunt, (unknown), Amanda Collins, David J. Bunyan, Morag N. Collinson, (unknown), (unknown), John Barber	1
3	8p23.1 duplication syndrome; common, confirmed, and novel features in six further patients 2013 ·American Journal of Medical Genetics Part A ·John Barber, Jill A. Rosenfeld, Nicola Foulds, (unknown), Mark S. Bateman, N. Simon Thomas, Samantha Baker, Viv Maloney, (unknown), Wendy E. Smith, Valerie Banks, Sara Ellingwood, (unknown), Lakshmi Mehta, Keith Eddleman, Michael Marble, (unknown), John A. Crolla, Allen N. Lamb	33
4	Expansion of a 12-kb VNTR containing the REXO1L1 gene cluster underlies the microscopically visible euchromatic variant of 8q21.2 2013 ·European Journal of Human Genetics ·Christine Tyson, Andrew J. Sharp, Monica Hrynchak, Siu Li Yong, Edward J. Hollox, Peter E. Warburton, John Barber	17
5	A Novel Pseudo-Dicentric Variant of 16p11.2–q11.2 Contains Euchromatin from 16p11.2–p11.1 and Resembles Pathogenic Duplications of Proximal 16q 2012 ·Cytogenetic and Genome Research ·John Barber, Charlotte Brasch‐Andersen, V.K. Maloney, Shuwen Huang, Mark S. Bateman, Jesper Graakjær, (unknown), Christina Fagerberg	3
6	16p11.2–p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2 2012 ·European Journal of Human Genetics ·John Barber, Victoria L. Hall, Viv Maloney, Shuwen Huang, Angharad M. Roberts, Angela F. Brady, (unknown), (unknown), Marianne Volleth, Thomas Liehr, Karl Mehnert, Mark S. Bateman, Helen White	34
7	A de novo 4q34 interstitial deletion of at least 9.3 Mb with no discernible phenotypic effect 2010 ·American Journal of Medical Genetics Part A ·Mark S. Bateman, Sarju Mehta, Lionel Willatt, (unknown), (unknown), Simon Zwolinski, (unknown), Ingrid Simonic, Kristin M. Abbott, John Barber	25
8	Transmitted duplication of 8p23.1–8p23.2 associated with speech delay, autism and learning difficulties 2008 ·European Journal of Human Genetics ·(unknown), Angela Barnicoat, (unknown), (unknown), (unknown), Shuwen Huang, Viv Maloney, N. Simon Thomas, David J. Bunyan, (unknown), John Barber	61
9	Defensins and the dynamic genome: What we can learn from structural variation at human chromosome band 8p23.1 2008 ·Genome Research ·Edward J. Hollox, John Barber, Anthony J. Brookes, John A.L. Armour	76
10	Novel deletion variants of 9q13–q21.12 and classical euchromatic variants of 9q12/qh involve deletion, duplication and triplication of large tracts of segmentally duplicated pericentromeric euchromatin 2006 ·European Journal of Human Genetics ·Lionel Willatt, John Barber, (unknown), Ingrid Simonic, F. Lucy Raymond, Zoe Docherty, Caroline Mackie Ogilvie	12
11	A study of reciprocal translocations and inversions detected by light microscopy with special reference to origin, segregation, and recurrent abnormalities 2003 ·American Journal of Medical Genetics Part A ·Sheila Youings, (unknown), Sarah Ennis, John Barber, Patricia A. Jacobs	38
12	Amplification of a pseudogene cassette underlies euchromatic variation of 16p at the cytogenetic level 1999 ·Human Genetics ·John Barber, (unknown), Christine A Joyce, (unknown)	32
13	Inherited Interstitial Duplications of Proximal 15q: Genotype-Phenotype Correlations 1997 ·The American Journal of Human Genetics ·C.E. Browne, N R Dennis, E.R. Maher, (unknown), James C. Nicholson, James Sillibourne, John Barber	143
14	RAPIDIN SITU HARVESTING AND CYTOGENETIC ANALYSIS OF PERINATAL TISSUE SAMPLES 1996 ·Prenatal Diagnosis ·Andrew Fisher, Annette E. Cockwell, (unknown), N. Gregson, Paul L. Campbell, (unknown), (unknown), John Barber, John A. Crolla	11
15	A wooden bowl from Loch a 'Ghlinne Bhig, Bracadale, Skye 1994 ·Proceedings of the Society of Antiquaries of Scotland ·(unknown), John Barber, (unknown), (unknown), (unknown)	2
16	Identification of the FRAXE fragile site in two families ascertained for X linked mental retardation. 1993 ·Journal of Medical Genetics ·Geraldine Flynn, Mark C. Hirst, Samantha J.L. Knight, John MacPherson, John Barber, A Flannery, Kay E. Davies, Veronica J. Buckle	52
17	Mosaic tetrasomy 8p: Molecular cytogenetic confirmation and measurement of glutathione reductase and tissue plasminogen activator levels 1993 ·American Journal of Medical Genetics ·Andrew Fisher, John Barber, John A. Crolla, Rowena S. James, A. N. Lestas, Ian Jennings, Nicholas R. Dennis	13
18	Abstracts of the annual scientific meeting of the Association of Clinical Cytogeneticists held on 3 to 5 July 1991 at Earnshaw Hall, Sheffield 1992 ·Journal of Medical Genetics ·David Mutton, (unknown), Eva Alberman, Martin Bobrow, John Barber, (unknown), (unknown), JDA Delhanty, Roland Ede, Chris Clarke, Simon Zwolinski, Charles E. Leonard, (unknown), Ralph Ellis, (unknown), John W. Crawford	1
19	Ocular choristomas 1989 ·Survey of Ophthalmology ·Ahmad M. Mansour, John Barber, Robert Reinecke, Frederick M. Wang	107
20	Analytical techniques for the investigation of non-artefactual wood from prehistoric and medieval sites 1982 ·Proceedings of the Society of Antiquaries of Scotland ·Anne Crone, John Barber	10

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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