A Seller

3.8k total citations · 1 hit paper
24 papers, 1.7k citations indexed

About

A Seller is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, A Seller has authored 24 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Genetics and 4 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in A Seller's work include Mitochondrial Function and Pathology (6 papers), Metabolism and Genetic Disorders (4 papers) and Craniofacial Disorders and Treatments (4 papers). A Seller is often cited by papers focused on Mitochondrial Function and Pathology (6 papers), Metabolism and Genetic Disorders (4 papers) and Craniofacial Disorders and Treatments (4 papers). A Seller collaborates with scholars based in United Kingdom, United States and Australia. A Seller's co-authors include Jenny C. Taylor, Jiannis Ragoussis, Penny Clouston, Kate Thomson, Hugh Watkins, Stefano Colella, Helen Butler, Chris Holmes, Christopher Yau and Ghazala Mirza and has published in prestigious journals such as Nucleic Acids Research, Neurology and European Heart Journal.

In The Last Decade

A Seller

23 papers receiving 1.7k 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.

Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples

2016 451 citations Roddy Walsh, Kate Thomson et al. Genetics in Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A Seller United Kingdom	15	940	797	438	147	100	24	1.7k
Claudio Graziano Italy	20	695 0.7×	325 0.4×	183 0.4×	96 0.7×	91 0.9×	77	1.2k
Carol Saunders United States	22	744 0.8×	635 0.8×	119 0.3×	95 0.6×	72 0.7×	59	1.3k
Emma Clement United Kingdom	16	968 1.0×	294 0.4×	245 0.6×	141 1.0×	85 0.8×	37	1.3k
Shin‐ichiro Nishimatsu Japan	23	1.5k 1.6×	215 0.3×	304 0.7×	214 1.5×	134 1.3×	61	1.9k
Desirée du Sart Australia	26	888 0.9×	617 0.8×	130 0.3×	97 0.7×	168 1.7×	39	2.0k
Anas M. Alazami Saudi Arabia	22	857 0.9×	584 0.7×	60 0.1×	100 0.7×	95 0.9×	55	1.5k
P. Gallano Spain	20	1.0k 1.1×	287 0.4×	261 0.6×	116 0.8×	94 0.9×	65	1.4k
M Farrall United Kingdom	17	719 0.8×	439 0.6×	161 0.4×	162 1.1×	96 1.0×	31	1.3k
Isabelle Thiffault United States	23	822 0.9×	482 0.6×	76 0.2×	88 0.6×	67 0.7×	65	1.4k
Elizabeth A. Geiger United States	16	963 1.0×	473 0.6×	112 0.3×	37 0.3×	97 1.0×	20	1.2k

Countries citing papers authored by A Seller

Since Specialization

Citations

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

Fields of papers citing papers by A Seller

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A Seller

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Simpson, Siobhan, A Seller, & Michelle Bishop. (2019). Using the Findings of a National Survey to Inform the Work of England’s Genomics Education Programme. Frontiers in Genetics. 10. 1265–1265. 19 indexed citations

Bishop, Michelle, et al.. (2019). Genomic Education at Scale: The Benefits of Massive Open Online Courses for the Healthcare Workforce. Frontiers in Genetics. 10. 1094–1094. 4 indexed citations

Walsh, Roddy, Kate Thomson, James S. Ware, et al.. (2016). Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples. Genetics in Medicine. 19(2). 192–203. 451 indexed citations breakdown →

Bowman, Michael, Michael Oldridge, A O'Rourke, et al.. (2012). Gross deletions in TCOF1 are a cause of Treacher–Collins–Franceschetti syndrome. European Journal of Human Genetics. 20(7). 769–777. 39 indexed citations

Shanks, Morag, Susan M. Downes, Richard R. Copley, et al.. (2012). Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease. European Journal of Human Genetics. 21(3). 274–280. 104 indexed citations

Colella, Stefano, Christopher Yau, Jennifer M. Taylor, et al.. (2007). QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data. Nucleic Acids Research. 35(6). 2013–2025. 400 indexed citations

Wilkie, Andrew O.M., Elena G. Bochukova, Indira B. Taylor, et al.. (2007). Clinical dividends from the molecular genetic diagnosis of craniosynostosis†. American Journal of Medical Genetics Part A. 143A(16). 1941–1949. 66 indexed citations

Fratter, Carl, A O'Rourke, Jackie Marchington, et al.. (2006). Molecular genetic diagnosis of mitochondrial DNA depletion syndrome and Alpers syndrome. Journal of Medical Genetics. 43. 1 indexed citations

Bradley, Karin, Branca Cavaco, Michael R. Bowl, et al.. (2006). Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours. Clinical Endocrinology. 64(3). 299–306. 83 indexed citations

10.

Wilkie, Andrew O.M., Elena G. Bochukova, Indira B. Taylor, et al.. (2006). Clinical dividends from the molecular genetic diagnosis of craniosynostosis. American Journal of Medical Genetics Part A. 140A(23). 2631–2639. 80 indexed citations

11.

White, Helen, et al.. (2005). Accurate Detection and Quantitation of Heteroplasmic Mitochondrial Point Mutations by Pyrosequencing. Genetic Testing. 9(3). 190–199. 91 indexed citations

12.

Williams, Louise, Tracy Lester, H. Beaumont, et al.. (2005). A novel case of craniosynostosis caused by a 6p21 duplication that includes the entire RUNX2 gene. Journal of Medical Genetics. 42. 8 indexed citations

13.

Seller, A, et al.. (2004). Detection and estimation of heteroplasmy for mitochondrial mutations using NanoChip and Pyrosequencing technology. ePrints Soton (University of Southampton). 1 indexed citations

14.

Cockburn, D.J. & A Seller. (2003). Pulsed Field Gel Electrophoresis for Detection of Gene Rearrangements in Duchenne Muscular Dystrophy. Humana Press eBooks. 5. 283–298.

15.

Nixon, John, et al.. (2002). Service provision of complex mutation analysis: a technical and economic appraisal using dystrophin point mutation analysis as an example. Clinical Genetics. 62(1). 29–38. 1 indexed citations

16.

Poulton, Joanna, et al.. (2001). Progress in genetic counselling and prenatal diagnosis of maternally inherited mtDNA diseases. Journal of Medical Genetics. 38. 1 indexed citations

17.

Hardy, Carol, Farhat L. Khanim, Rosarelis Torres, et al.. (1999). Clinical and Molecular Genetic Analysis of 19 Wolfram Syndrome Kindreds Demonstrating a Wide Spectrum of Mutations in WFS1. The American Journal of Human Genetics. 65(5). 1279–1290. 159 indexed citations

18.

Zielenski, Julian, D. Markiewicz, Keith Schappert, et al.. (1995). Identification of six mutations (R31L, 441delA, 681delC, 1461ins4, W1089R, E1104X) in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Human Mutation. 5(1). 43–47. 16 indexed citations

19.

Roche, A., Maria Rita Passos‐Bueno, Reinaldo Issao Takata, et al.. (1995). Molecular characterization of further dystrophin gene microsatellites. Molecular and Cellular Probes. 9(5). 361–370. 7 indexed citations

20.

Shackleton, Sue, Jeremy Hull, Simon Dear, et al.. (1994). Identification of rare and novel mutations in the CFTR genes of CF patients in Southern England. Human Mutation. 3(2). 141–151. 13 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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