Simon Heath

61.2k total citations · 2 hit papers
96 papers, 7.3k citations indexed

About

Simon Heath is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Simon Heath has authored 96 papers receiving a total of 7.3k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Genetics, 42 papers in Molecular Biology and 13 papers in Immunology. Recurrent topics in Simon Heath's work include Genetic Associations and Epidemiology (20 papers), Genetic Mapping and Diversity in Plants and Animals (14 papers) and Epigenetics and DNA Methylation (12 papers). Simon Heath is often cited by papers focused on Genetic Associations and Epidemiology (20 papers), Genetic Mapping and Diversity in Plants and Animals (14 papers) and Epigenetics and DNA Methylation (12 papers). Simon Heath collaborates with scholars based in United States, France and Spain. Simon Heath's co-authors include Marta Gut, Martin Farrall, William Cookson, Miriam F. Moffatt, Mark Lathrop, Erika von Mutius, Florence Démenais, Emmanuelle Bouzigon, David P. Strachan and Ellen M. Wijsman and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Simon Heath

94 papers receiving 7.2k citations

Hit Papers

A Large-Scale, Consortium-Based Genomewide Association St... 2007 2026 2013 2019 2010 2007 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Simon Heath United States 37 2.8k 2.4k 1.5k 1.4k 737 96 7.3k
Timothy J. Aitman United Kingdom 44 3.2k 1.1× 2.6k 1.1× 894 0.6× 839 0.6× 850 1.2× 140 7.1k
Jeanine J. Houwing‐Duistermaat Netherlands 48 2.1k 0.7× 1.2k 0.5× 988 0.7× 741 0.5× 481 0.7× 231 6.9k
Michael A. Simpson United Kingdom 44 2.7k 1.0× 1.2k 0.5× 859 0.6× 649 0.5× 626 0.8× 161 6.3k
Kristin Ardlie United States 37 4.4k 1.6× 4.1k 1.7× 1.5k 1.0× 610 0.4× 746 1.0× 71 9.7k
Yukinori Okada Japan 43 2.2k 0.8× 3.1k 1.3× 1.3k 0.9× 509 0.4× 396 0.5× 171 7.5k
Jayne S. Danska Canada 35 2.9k 1.0× 1.3k 0.5× 2.3k 1.5× 697 0.5× 710 1.0× 87 6.5k
Eleftheria Zeggini United Kingdom 47 2.9k 1.0× 3.8k 1.6× 748 0.5× 598 0.4× 962 1.3× 192 7.7k
Robert P. Erickson United States 49 4.7k 1.7× 3.2k 1.3× 964 0.6× 2.6k 1.9× 788 1.1× 350 10.7k
Melanie Bahlo Australia 47 3.3k 1.2× 2.1k 0.9× 1.5k 1.0× 598 0.4× 325 0.4× 203 9.3k
Terry F. Davies United States 61 3.3k 1.2× 3.7k 1.5× 2.7k 1.8× 1.0k 0.7× 1.1k 1.5× 349 13.4k

Countries citing papers authored by Simon Heath

Since Specialization
Citations

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

Fields of papers citing papers by Simon Heath

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Simon Heath

This figure shows the co-authorship network connecting the top 25 collaborators of Simon Heath. A scholar is included among the top collaborators of Simon Heath 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 Simon Heath. Simon Heath is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Duran‐Ferrer, Martí, Diego Mallo, Ferran Nadeu, et al.. (2025). Fluctuating DNA methylation tracks cancer evolution at clinical scale. Nature. 645(8081). 764–773. 2 indexed citations
2.
Castel, Victoria, et al.. (2023). Evaluation of circulating tumor DNA by electropherogram analysis and methylome profiling in high-risk neuroblastomas. Frontiers in Oncology. 13. 1037342–1037342. 9 indexed citations
3.
Becker, Philipp, Cristina Frías-López, Marc Dabad, et al.. (2022). A method for multiplexed full-length single-molecule sequencing of the human mitochondrial genome. Nature Communications. 13(1). 5902–5902. 17 indexed citations
4.
Bonet, Jose, Marc Dabad, Simon Heath, et al.. (2021). DeepMP: a deep learning tool to detect DNA base modifications on Nanopore sequencing data. Bioinformatics. 38(5). 1235–1243. 18 indexed citations
5.
Sáez, María Eugenia, Javier Varona Santos, Cristina Nuevo‐Tapioles, et al.. (2019). PD-1 signaling affects cristae morphology and leads to mitochondrial dysfunction in human CD8+ T lymphocytes. Journal for ImmunoTherapy of Cancer. 7(1). 151–151. 96 indexed citations
6.
Merkel, Angelika, Marcos Fernández-Callejo, Santiago Marco‐Sola, et al.. (2018). gemBS: high throughput processing for DNA methylation data from bisulfite sequencing. Bioinformatics. 35(5). 737–742. 33 indexed citations
7.
Libertini, Emanuele, Simon Heath, Rifat Hamoudi, et al.. (2016). Saturation analysis for whole-genome bisulfite sequencing data. Nature Biotechnology. 34(7). 691–693. 23 indexed citations
8.
Narni-Mancinelli, Émilie, Baptiste N. Jaeger, Claire Bernat, et al.. (2012). Tuning of Natural Killer Cell Reactivity by NKp46 and Helios Calibrates T Cell Responses. Science. 335(6066). 344–348. 150 indexed citations
9.
Raineri, Emanuele, Luca Ferretti, Anna Esteve‐Codina, et al.. (2012). SNP calling by sequencing pooled samples. BMC Bioinformatics. 13(1). 239–239. 53 indexed citations
10.
Heath, Simon, Van C. Willis, Karin J. Purdie, et al.. (2011). Clinically Significant Human Papilloma Virus in Squamous Cell Carcinoma of the Head and Neck in UK Practice. Clinical Oncology. 24(1). e18–e23. 36 indexed citations
11.
Darmanis, Spyros, Rachel Yuan Nong, Agneta Siegbahn, et al.. (2011). ProteinSeq: High-Performance Proteomic Analyses by Proximity Ligation and Next Generation Sequencing. PLoS ONE. 6(9). e25583–e25583. 75 indexed citations
12.
Zinovieva, Elena, Catherine Bourgain, Amir Kadi, et al.. (2009). Comprehensive Linkage and Association Analyses Identify Haplotype, Near to the TNFSF15 Gene, Significantly Associated with Spondyloarthritis. PLoS Genetics. 5(6). e1000528–e1000528. 46 indexed citations
13.
Flori, Laurence, Sébastien Fritz, Florence Jaffrézic, et al.. (2009). The Genome Response to Artificial Selection: A Case Study in Dairy Cattle. PLoS ONE. 4(8). e6595–e6595. 173 indexed citations
14.
Sakuntabhai, Anavaj, Isabelle Casadémont, Chayanon Peerapittayamongkol, et al.. (2008). Correction: Genetic Determination and Linkage Mapping of Plasmodium falciparum Malaria Related Traits in Senegal. PLoS ONE. 3(4). 4 indexed citations
15.
Shmulewitz, Dvora, Simon Heath, Maude L. Blundell, et al.. (2006). Linkage analysis of quantitative traits for obesity, diabetes, hypertension, and dyslipidemia on the island of Kosrae, Federated States of Micronesia. Proceedings of the National Academy of Sciences. 103(10). 3502–3509. 53 indexed citations
16.
Serre, Jean‐Louis, et al.. (2006). Diagnostic techniques in genetics. John Wiley & Sons eBooks. 1 indexed citations
17.
Rothenbühler, Anya, Delphine Fradin, Simon Heath, et al.. (2006). Weight-Adjusted Genome Scan Analysis for Mapping Quantitative Trait Loci for Menarchal Age. The Journal of Clinical Endocrinology & Metabolism. 91(9). 3534–3537. 26 indexed citations
18.
Liu, Hui, Simon Heath, Christina Sobin, et al.. (2002). Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia. Proceedings of the National Academy of Sciences. 99(6). 3717–3722. 245 indexed citations
19.
Gordon, Derek, Simon Heath, Xin Liu, & Jürg Ott. (2001). A Transmission/Disequilibrium Test That Allows for Genotyping Errors in the Analysis of Single-Nucleotide Polymorphism Data. The American Journal of Human Genetics. 69(2). 371–380. 121 indexed citations
20.
Daw, E. Warwick, Simon Heath, & Ellen M. Wijsman. (1999). Multipoint Oligogenic Analysis of Age-at-Onset Data with Applications to Alzheimer Disease Pedigrees. The American Journal of Human Genetics. 64(3). 839–851. 76 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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