Clive Hoggart

6.7k total citations · 2 hit papers
25 papers, 2.7k citations indexed

About

Clive Hoggart is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Clive Hoggart has authored 25 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 7 papers in Molecular Biology and 5 papers in Surgery. Recurrent topics in Clive Hoggart's work include Genetic Associations and Epidemiology (13 papers), Genetic Mapping and Diversity in Plants and Animals (11 papers) and Genetic and phenotypic traits in livestock (8 papers). Clive Hoggart is often cited by papers focused on Genetic Associations and Epidemiology (13 papers), Genetic Mapping and Diversity in Plants and Animals (11 papers) and Genetic and phenotypic traits in livestock (8 papers). Clive Hoggart collaborates with scholars based in United Kingdom, United States and Finland. Clive Hoggart's co-authors include David J. Balding, Paul McKeigue, Rick A. Kittles, Mark D. Shriver, John C. Whittaker, Maria De Iorio, David Clayton, Esteban J. Parra, Carolina Bonilla and Paul F. O’Reilly and has published in prestigious journals such as New England Journal of Medicine, Nature Genetics and Bioinformatics.

In The Last Decade

Clive Hoggart

24 papers receiving 2.6k 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.

Treatment of Multisystem Inflammatory Syndrome in Children

2021 196 citations Clive Hoggart, Jethro Herberg et al. profile →
Portability of 245 polygenic scores when derived from the UK Biobank and applied to 9 ancestry groups from the same cohort

2022 135 citations Florian Privé, Hugues Aschard et al. The American Journal of Human Genetics profile →

Peers

Countries citing papers authored by Clive Hoggart

Since Specialization

Citations

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

Fields of papers citing papers by Clive Hoggart

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Clive Hoggart

This figure shows the co-authorship network connecting the top 25 collaborators of Clive Hoggart. A scholar is included among the top collaborators of Clive Hoggart 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 Clive Hoggart. Clive Hoggart 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

#	Title	Journal	Authors	Indexed citations
1	Sibling similarity can reveal key insights into genetic architecture	eLife	Tade Souaiaia, Clive Hoggart et al.	0
2	Clinical and Genomic Prediction of Coronary Artery Disease Subtypes	Arteriosclerosis Thrombosis and Vascular Biology	Judit García‐González, Zhe Wang et al.	2
3	BridgePRS leverages shared genetic effects across ancestries to increase polygenic risk score portability	Nature Genetics	Clive Hoggart, Shing Wan Choi et al.	17
4	PRSet: Pathway-based polygenic risk score analyses and software	PLoS Genetics	Shing Wan Choi, Judit García‐González et al.	34
5	Portability of 245 polygenic scores when derived from the UK Biobank and applied to 9 ancestry groups from the same cohort breakdown →	The American Journal of Human Genetics	Florian Privé, Hugues Aschard et al.	135
6	A polygenic biomarker to identify patients with severe hypercholesterolemia of polygenic origin	Molecular Genetics & Genomic Medicine	Clive Hoggart, Karl‐Heinz Herzig et al.	9
7	Common Genetic Variations Associated with the Persistence of Immunity following Childhood Immunization	Cell Reports	Daniel O’Connor, Eileen Png et al.	21
8	Clinical Manifestations and Modes of Death among Patients with Ebola Virus Disease, Monrovia, Liberia, 2014	American Journal of Tropical Medicine and Hygiene	Linda Meta Mobula, Nathalie MacDermott et al.	10
9	Predicting IVIG resistance in UK Kawasaki disease	Archives of Disease in Childhood	Sarah L. Davies, Natalina Sutton et al.	93
10	Pathway-driven gene stability selection of two rheumatoid arthritis GWAS identifies and validates new susceptibility genes in receptor mediated signalling pathways	Human Molecular Genetics	Hariklia Eleftherohorinou, Clive Hoggart et al.	47
11	invertFREGENE: software for simulating inversions in population genetic data	Bioinformatics	Paul F. O’Reilly, Lachlan Coin et al.	11
12	Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels	Nature Genetics	John C. Chambers, Weihua Zhang et al.	186
13	Pathway Analysis of GWAS Provides New Insights into Genetic Susceptibility to 3 Inflammatory Diseases	PLoS ONE	Hariklia Eleftherohorinou, Victoria Wright et al.	119
14	Fregene: Simulation of realistic sequence-level data in populations and ascertained samples	BMC Bioinformatics	Marc Chadeau‐Hyam, Clive Hoggart et al.	54
15	Genome‐wide significance for dense SNP and resequencing data	Genetic Epidemiology	Clive Hoggart, Taane G. Clark et al.	137
16	Simultaneous Analysis of All SNPs in Genome-Wide and Re-Sequencing Association Studies	PLoS Genetics	Clive Hoggart, John C. Whittaker et al.	243
17	Assessing the Relative Ages of Admixture in the Bovine Hybrid Zones of Africa and the Near East Using X Chromosome Haplotype Mosaicism	Genetics	Abigail R Freeman, Clive Hoggart et al.	27
18	Design and Analysis of Admixture Mapping Studies	The American Journal of Human Genetics	Clive Hoggart, Mark D. Shriver et al.	231
19	Skin pigmentation, biogeographical ancestry and admixture mapping	Human Genetics	Mark D. Shriver, Esteban J. Parra et al.	394
20	Control of Confounding of Genetic Associations in Stratified Populations	The American Journal of Human Genetics	Clive Hoggart, Esteban J. Parra et al.	374

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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