Peter K. Joshi

27.7k total citations · 1 hit paper
29 papers, 1.3k citations indexed

About

Peter K. Joshi is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Peter K. Joshi has authored 29 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 15 papers in Molecular Biology and 4 papers in Rheumatology. Recurrent topics in Peter K. Joshi's work include Genetic Associations and Epidemiology (14 papers), Genetic Mapping and Diversity in Plants and Animals (5 papers) and Genetic and phenotypic traits in livestock (4 papers). Peter K. Joshi is often cited by papers focused on Genetic Associations and Epidemiology (14 papers), Genetic Mapping and Diversity in Plants and Animals (5 papers) and Genetic and phenotypic traits in livestock (4 papers). Peter K. Joshi collaborates with scholars based in United Kingdom, United States and Canada. Peter K. Joshi's co-authors include James F. Wilson, David W. Clark, Michèle Ramsay, Francisco C. Ceballos, Harry Campbell, Paul R. H. J. Timmers, Joris Deelen, Tōnu Esko, Paul McKeigue and Athina Spiliopoulou and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Communications.

In The Last Decade

Peter K. Joshi

29 papers receiving 1.3k 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.

Runs of homozygosity: windows into population history and trait architecture

2018 485 citations Peter K. Joshi, David W. Clark et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Peter K. Joshi United Kingdom	17	683	434	112	95	94	29	1.3k
Kristy Lee United States	21	899 1.3×	586 1.4×	329 2.9×	190 2.0×	23 0.2×	55	1.9k
Jeanne C. Beck United States	18	436 0.6×	968 2.2×	195 1.7×	85 0.9×	53 0.6×	43	2.0k
Seiji Tanaka Japan	26	301 0.4×	1.7k 3.9×	107 1.0×	64 0.7×	87 0.9×	88	2.3k
Andrew Bakshi Australia	15	1.5k 2.2×	1.1k 2.4×	270 2.4×	111 1.2×	34 0.4×	32	2.6k
James G. Wilson United States	23	418 0.6×	383 0.9×	82 0.7×	35 0.4×	143 1.5×	49	1.8k
Andrea Angius Italy	31	569 0.8×	942 2.2×	209 1.9×	86 0.9×	32 0.3×	100	2.5k
Mark M. Iles United Kingdom	23	471 0.7×	514 1.2×	141 1.3×	72 0.8×	13 0.1×	79	1.5k
Sebastian Schönherr Austria	17	884 1.3×	768 1.8×	93 0.8×	24 0.3×	40 0.4×	54	1.7k
Peter Gerke Germany	21	388 0.6×	615 1.4×	26 0.2×	185 1.9×	513 5.5×	38	1.5k
James Boocock United States	18	364 0.5×	375 0.9×	29 0.3×	41 0.4×	115 1.2×	34	766

Countries citing papers authored by Peter K. Joshi

Since Specialization

Citations

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

Fields of papers citing papers by Peter K. Joshi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter K. Joshi. 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 Peter K. Joshi. The network helps show where Peter K. Joshi may publish in the future.

Co-authorship network of co-authors of Peter K. Joshi

This figure shows the co-authorship network connecting the top 25 collaborators of Peter K. Joshi. A scholar is included among the top collaborators of Peter K. Joshi 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 Peter K. Joshi. Peter K. Joshi 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

Kentistou, Katherine A., Jian’an Luan, Laura B. L. Wittemans, et al.. (2023). Large scale phenotype imputation and in vivo functional validation implicate ADAMTS14 as an adiposity gene. Nature Communications. 14(1). 307–307. 2 indexed citations

Timmers, Paul R. H. J., Evgeny Tiys, Saori Sakaue, et al.. (2022). Mendelian randomization of genetically independent aging phenotypes identifies LPA and VCAM1 as biological targets for human aging. Nature Aging. 2(1). 19–30. 27 indexed citations

Kuo, Feng-Chih, Matt J. Neville, Rugivan Sabaratnam, et al.. (2022). HOTAIR interacts with PRC2 complex regulating the regional preadipocyte transcriptome and human fat distribution. Cell Reports. 40(4). 111136–111136. 32 indexed citations

Farré, Xavier, Paul R. H. J. Timmers, Peter K. Joshi, et al.. (2021). Comparative Analysis of Mammal Genomes Unveils Key Genomic Variability for Human Life Span. Molecular Biology and Evolution. 38(11). 4948–4961. 24 indexed citations

Mounier, Ninon, Chiara Auwerx, Eirini Marouli, et al.. (2021). Composite trait Mendelian randomization reveals distinct metabolic and lifestyle consequences of differences in body shape. Communications Biology. 4(1). 1064–1064. 11 indexed citations

Zheng, Ning, Yakov A. Tsepilov, Sodbo Sharapov, et al.. (2021). Nontrivial Replication of Loci Detected by Multi-Trait Methods. Frontiers in Genetics. 12. 627989–627989. 3 indexed citations

Barnes, Catriona L. K., Caroline Hayward, David J. Porteous, et al.. (2021). Contribution of common risk variants to multiple sclerosis in Orkney and Shetland. European Journal of Human Genetics. 29(11). 1701–1709. 6 indexed citations

Bretherick, Andrew D., Oriol Canela‐Xandri, Peter K. Joshi, et al.. (2020). Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits. PLoS Genetics. 16(7). e1008785–e1008785. 21 indexed citations

Timmers, Paul R. H. J., J.J. Kerssens, Jon Minton, et al.. (2020). Trends in disease incidence and survival and their effect on mortality in Scotland: nationwide cohort study of linked hospital admission and death records 2001–2016. BMJ Open. 10(3). e034299–e034299. 5 indexed citations

10.

Shadrina, Alexandra S., Tatiana Shashkova, Anna A. Torgasheva, et al.. (2020). Prioritization of causal genes for coronary artery disease based on cumulative evidence from experimental and in silico studies. Scientific Reports. 10(1). 10486–10486. 21 indexed citations

11.

Timmers, Paul R. H. J., James F. Wilson, Peter K. Joshi, & Joris Deelen. (2020). Multivariate genomic scan implicates novel loci and haem metabolism in human ageing. Nature Communications. 11(1). 3570–3570. 92 indexed citations

12.

Lenárt, Peter, et al.. (2019). Male mortality rates mirror mortality rates of older females. Scientific Reports. 9(1). 10589–10589. 13 indexed citations

13.

Li, Xue, Xiangrui Meng, Yazhou He, et al.. (2019). Genetically determined serum urate levels and cardiovascular and other diseases in UK Biobank cohort: A phenome-wide mendelian randomization study. PLoS Medicine. 16(10). e1002937–e1002937. 94 indexed citations

14.

Gilbert, Edmund, Seamus O’Reilly, Michaël Merrigan, et al.. (2019). The genetic landscape of Scotland and the Isles. Proceedings of the National Academy of Sciences. 116(38). 19064–19070. 22 indexed citations

15.

Li, Xue, Xiangrui Meng, Athina Spiliopoulou, et al.. (2018). MR-PheWAS: exploring the causal effect of SUA level on multiple disease outcomes by using genetic instruments in UK Biobank. Annals of the Rheumatic Diseases. 77(7). 1039–1047. 59 indexed citations

16.

McDaid, Aaron F., Peter K. Joshi, Eleonora Porcu, et al.. (2017). Bayesian association scan reveals loci associated with human lifespan and linked biomarkers. Nature Communications. 8(1). 15842–15842. 47 indexed citations

17.

Zheng, Ning, Youngjo Lee, Peter K. Joshi, et al.. (2017). A Selection Operator for Summary Association Statistics Reveals Allelic Heterogeneity of Complex Traits. The American Journal of Human Genetics. 101(6). 903–912. 8 indexed citations

18.

Pirastu, Nicola, Peter K. Joshi, Paul S. de Vries, et al.. (2017). GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk. Nature Communications. 8(1). 1584–1584. 62 indexed citations

19.

Cáceres, Alejandro, Tōnu Esko, Irene Pappa, et al.. (2016). Ancient Haplotypes at the 15q24.2 Microdeletion Region Are Linked to Brain Expression of MAN2C1 and Children's Intelligence. PLoS ONE. 11(6). e0157739–e0157739. 1 indexed citations

20.

Joshi, Peter K., James Prendergast, Ross M. Fraser, et al.. (2013). Local Exome Sequences Facilitate Imputation of Less Common Variants and Increase Power of Genome Wide Association Studies. PLoS ONE. 8(7). e68604–e68604. 8 indexed citations

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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