Stephen Clayton

4.3k total citations · 1 hit paper
7 papers, 1.4k citations indexed

About

Stephen Clayton is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Stephen Clayton has authored 7 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Plant Science. Recurrent topics in Stephen Clayton's work include Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (3 papers) and Chromosomal and Genetic Variations (2 papers). Stephen Clayton is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (3 papers) and Chromosomal and Genetic Variations (2 papers). Stephen Clayton collaborates with scholars based in United Kingdom, Belgium and Estonia. Stephen Clayton's co-authors include Diana Rajan, Helen V. Firth, Manuel Corpas, A. Paul Bevan, Nigel P. Carter, Yves Moreau, Shola M. Richards, Steven Van Vooren, Tomas Fitzgerald and Rosemary E. Kelsell and has published in prestigious journals such as Bioinformatics, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Stephen Clayton

7 papers receiving 1.4k 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.

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

2009 1.2k citations Helen V. Firth, Shola M. Richards et al. The American Journal of Human Genetics profile →

Peers

Countries citing papers authored by Stephen Clayton

Since Specialization

Citations

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

Fields of papers citing papers by Stephen Clayton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephen Clayton

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

All Works

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7 of 7 papers shown

#	Work	Indexed citations
1	The Economics Scholars Program: Creating a professional economics research conference for undergraduate students 2020 ·The Journal of Economic Education ·Stephen Clayton, (unknown)	1
2	Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disorders 2018 ·Genetics in Medicine ·Caroline F. Wright, Jeremy F. McRae, Stephen Clayton, Giuseppe Gallone, Stuart Aitken, Tomas Fitzgerald, (unknown), Elena Prigmore, Diana Rajan, Jenny Lord, Alejandro Sifrim, Rosemary E. Kelsell, Michael Parker, Jeffrey C. Barrett, Matthew E. Hurles, David Fitzpatrick, Helen V. Firth	193
3	Auditory Function in the Tc1 Mouse Model of Down Syndrome Suggests a Limited Region of Human Chromosome 21 Involved in Otitis Media 2012 ·PLoS ONE ·Stephanie Kuhn, Neil J. Ingham, Selina Pearson, Susan Gribble, Stephen Clayton, Karen P. Steel, Walter Marcotti	7
4	Interpretation of Genomic Copy Number Variants Using DECIPHER 2012 ·Current Protocols in Human Genetics ·Manuel Corpas, Eugene Bragin, Stephen Clayton, A. Paul Bevan, Helen V. Firth	10
5	aCGH.Spline—an R package for aCGH dye bias normalization 2011 ·Bioinformatics ·Tomas Fitzgerald, Lee Larcombe, Solena Le Scouarnec, Stephen Clayton, Diana Rajan, Nigel P. Carter, Richard Redon	4
6	FoSTeS, MMBIR and NAHR at the human proximal Xp region and the mechanisms of human Xq isochromosome formation 2011 ·Human Molecular Genetics ·George Koumbaris, (unknown), (unknown), Marios Ioannides, Christodoulos Christodoulou, Tomas Fitzgerald, Diana Rajan, Stephen Clayton, Sophia Kitsiou‐Tzeli, Joris Vermeesch, Nicos Skordis, Pavlos Antoniou, Ants Kurg, Ioannis Georgiou, Nigel P. Carter, Philippos C. Patsalis	29
7	DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources breakdown → 2009 ·The American Journal of Human Genetics ·Helen V. Firth, Shola M. Richards, A. Paul Bevan, Stephen Clayton, Manuel Corpas, Diana Rajan, Steven Van Vooren, Yves Moreau, (unknown), Nigel P. Carter	1200

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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