David T. Bonthron

14.7k citations

130 papers · 7.9k indexed · 2 hit papers · h-index 45

Molecular Biology top 2%
Genetics top 0.5%
Endocrinology, Diabetes and Metabolism top 1%
Hematology top 1%
Pediatrics, Perinatology and Child Health top 1%

Co-authors: Bruce E. Hayward Stuart H. Orkin Lisa Strain Ian Carr Eamonn Sheridan Tucker Collins Alexander F. Markham David Ginsburg
Topics: Genetic Syndromes and Imprinting (22 papers)Genomic variations and chromosomal abnormalities (19 papers)Genomics and Rare Diseases (17 papers)
Cited by: Genetics Hematology Immunology and Allergy
Journals: Nature Science New England Journal of Medicine
Partner nations: United Kingdom United States Japan

In The Last Decade

David T. Bonthron

129 papers receiving 7.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Correction: Corrigendum: Endogenous fructose production and metabolism in the liver contributes to the development of metabolic syndrome

2013 725 citations Christine P. Diggle, Aruna Asipu et al. profile →
Platelet-derived growth factor B chain promoter contains a cis-acting fluid shear-stress-responsive element.

1993 507 citations David T. Bonthron et al. profile →

Peers

Countries citing papers authored by David T. Bonthron

Since Specialization

Citations

This map shows the geographic impact of David T. Bonthron'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 T. Bonthron with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David T. Bonthron more than expected).

Fields of papers citing papers by David T. Bonthron

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David T. Bonthron

This figure shows the co-authorship network connecting the top 25 collaborators of David T. Bonthron. A scholar is included among the top collaborators of David T. Bonthron 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 David T. Bonthron. David T. Bonthron 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	Inhibition of ketohexokinase prevents fructose-induced insulin resistance and endothelial dysfunction in high fat and sucrose-fed mice via enhancing energy expenditure 2024 ·European Heart Journal ·Hema Viswambharan,Asjad Visnagri,David T. Bonthron,Mark T. Kearney	0
2	Assessing the utility of long-read nanopore sequencing for rapid and efficient characterization of mobile element insertions 2020 ·Laboratory Investigation ·Christopher M. Watson,Laura A. Crinnion,Helen Lindsay,(unknown),(unknown),Rachel Robinson,Caroline Joyce,George A. Tanteles,(unknown),Sérgio D.J. Pena,Ian Carr,David T. Bonthron	12
3	A tubulin alpha 8 mouse knockout model indicates a likely role in spermatogenesis but not in brain development 2017 ·PLoS ONE ·Christine P. Diggle,Isabel Martínez‐Garay,Zoltán Molnár,Martin H. Brinkworth,Ed White,Ewan D. Fowler,Ruth Hughes,Bruce E. Hayward,Ian Carr,Christopher M. Watson,Laura A. Crinnion,Aruna Asipu,Ben Woodman,P. Louise Coletta,Alexander F. Markham,T. Neil Dear,David T. Bonthron,Michelle Peckham,Ewan E. Morrison,Eamonn Sheridan	23
4	Enhanced diagnostic yield in Meckel-Gruber and Joubert syndrome through exome sequencing supplemented with split-read mapping 2016 ·BMC Medical Genetics ·Christopher M. Watson,Laura A. Crinnion,Ian Berry,Sally M. Harrison,(unknown),Agne Antanaviciute,Ruth Charlton,Angus Dobbie,Ian Carr,David T. Bonthron	59
5	OVA: integrating molecular and physical phenotype data from multiple biomedical domain ontologies with variant filtering for enhanced variant prioritization 2015 ·Bioinformatics ·Agne Antanaviciute,Christopher M. Watson,Sally M. Harrison,(unknown),Laura A. Crinnion,Alexander F. Markham,David T. Bonthron,Ian Carr	19
6	Mutations Causing Familial Biparental Hydatidiform Mole Implicate C6orf221 as a Possible Regulator of Genomic Imprinting in the Human Oocyte 2011 ·The American Journal of Human Genetics ·David Parry,Clare V. Logan,Bruce E. Hayward,Michael Shires,Hanène Landolsi,Christine P. Diggle,Ian Carr,Cécile Rittore,Isabelle Touitou,Laurent Philibert,Rosemary A. Fisher,Masoumeh Fallahian,John Huntriss,Helen M. Picton,(unknown),Graham R. Taylor,Colin A. Johnson,David T. Bonthron,Eamonn Sheridan	174
7	Illuminator, a desktop program for mutation detection using short-read clonal sequencing 2011 ·Genomics ·Ian Carr,Joanne Morgan,Christine P. Diggle,Eamonn Sheridan,Alexander F. Markham,Clare V. Logan,Chris F. Inglehearn,Graham R. Taylor,David T. Bonthron	3
8	DominantMapper: Rule-based analysis of SNP data for rapid mapping of dominant diseases in related nuclear families 2011 ·Human Mutation ·Ian Carr,Colin A. Johnson,Alex Markham,Carmel Toomes,David T. Bonthron,Eamonn Sheridan	4
9	Common and recurrent HPGD mutations in Caucasian individuals with primary hypertrophic osteoarthropathy 2010 ·Lara D. Veeken ·Christine P. Diggle,Ian Carr,Emanuel Zitt,Katie Wusik,Robert J. Hopkin,Carlos E. Prada,Olga Calabrese,Olaf Rittinger,Marilynn Punaro,Alexander F. Markham,David T. Bonthron	40
10	Loss of expression of ZAC/PLAGL1 in diffuse large B‐cell lymphoma is independent of promoter hypermethylation 2010 ·Genes Chromosomes and Cancer ·Elizabeth M. A. Valleley,Sarah F. Cordery,Ian Carr,Kenneth MacLennan,David T. Bonthron	9
11	Shadow autozygosity mapping by linkage exclusion (SAMPLE): a simple strategy to identify the genetic basis of lethal autosomal recessive disorders 2009 ·Human Mutation ·Ian Carr,Katarzyna Szymańska,Eamonn Sheridan,Alexander F. Markham,David T. Bonthron,Colin A. Johnson	5
12	Mutation of the Variant α-Tubulin TUBA8 Results in Polymicrogyria with Optic Nerve Hypoplasia 2009 ·The American Journal of Human Genetics ·Mohammad Reza Abdollahi,Ewan E. Morrison,Tamara Sirey,Zoltán Molnár,Bruce E. Hayward,Ian Carr,Kelly Springell,(unknown),Mushtaq Ahmed,(unknown),Peter Corry,Daniela T. Pilz,Neil Stoodley,Yanick J. Crow,Graham R. Taylor,David T. Bonthron,Eamonn Sheridan	122
13	Structures of alternatively spliced isoforms of human ketohexokinase 2009 ·Acta Crystallographica Section D Biological Crystallography ·Chi H. Trinh,Aruna Asipu,David T. Bonthron,S.E.V. Phillips	33
14	Lack of involvement of known DNA methyltransferases in familial hydatidiform mole implies the involvement of other factors in establishment of imprinting in the human female germline 2003 ·BMC Genetics ·Bruce E. Hayward,Michel De Vos,(unknown),(unknown),John Huntriss,Helen M. Picton,Eamonn Sheridan,David T. Bonthron	40
15	A global disorder of imprinting in the human female germ line 2002 ·Nature ·(unknown),Bruce E. Hayward,Eamonn Sheridan,David T. Bonthron	170
16	cDNA Cloning, Genomic Organization, and Chromosomal Localization of a Novel Human Gene That Encodes a Kinesin-Related Protein Highly Similar to Mouse Kif3C 1998 ·Biochemical and Biophysical Research Communications ·Elizabeth A.R. Telford,(unknown),(unknown),Alexander F. Markham,Nicholas Lench,David T. Bonthron	6
17	Co-localization of the ketohexokinase and glucokinase regulator genes to a 500-kb region of Chromosome 2p23 1996 ·Mammalian Genome ·Bruce E. Hayward,Judy Fantes,Jon Warner,(unknown),J.P. Leek,Alex Markham,David T. Bonthron	21
18	Nager acrofacial dysostosis: minor familial manifestations supporting dominant inheritance 1993 ·Clinical Genetics ·David T. Bonthron,(unknown),D G Barr	11
19	Smal andHhal polymorphisms in the 5′ region of the human von Willebrand factor gene (F8VWF) 1991 ·Nucleic Acids Research ·Lisa Strain,David T. Bonthron,D. J. H. Brock	3
20	The human von Willebrand factor gene 1988 ·European Journal of Biochemistry ·David T. Bonthron,Stuart H. Orkin	36

About David T. Bonthron

David T. Bonthron is a scholar working on Genetics, Developmental Biology and Molecular Biology, having authored 130 papers that have together received 7.9k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (22 papers), Genomic variations and chromosomal abnormalities (19 papers) and Genomics and Rare Diseases (17 papers). The work is most often cited by research in Genetics (2.3k citations), Hematology (785 citations) and Immunology and Allergy (346 citations). David T. Bonthron has collaborated with scholars based in United Kingdom, United States and Japan. Frequent co-authors include Bruce E. Hayward, Stuart H. Orkin, Lisa Strain, Ian Carr, Eamonn Sheridan, Tucker Collins, Alexander F. Markham, David Ginsburg, Christine P. Diggle and Aruna Asipu. Their work appears in journals such as Nature, Science and New England Journal of 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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