Simon Holden

7.3k total citations
35 papers, 585 citations indexed

About

Simon Holden is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Simon Holden has authored 35 papers receiving a total of 585 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 15 papers in Genetics and 5 papers in Surgery. Recurrent topics in Simon Holden's work include Congenital heart defects research (5 papers), Genetic and rare skin diseases. (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Simon Holden is often cited by papers focused on Congenital heart defects research (5 papers), Genetic and rare skin diseases. (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Simon Holden collaborates with scholars based in United Kingdom, France and United States. Simon Holden's co-authors include Thomas B. Stoker, Roger A. Barker, Julia C. Greenland, Sarah Mason, David Collier, Christine Patch, Evangelos Vassos, Cathryn M. Lewis, F. Lucy Raymond and David St Clair and has published in prestigious journals such as Human Molecular Genetics, Gene and Thorax.

In The Last Decade

Simon Holden

32 papers receiving 559 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Simon Holden 296 219 88 87 61 35 585
Soo‐Mi Park 464 1.6× 258 1.2× 74 0.8× 52 0.6× 31 0.5× 39 794
Zhenhong Nan 284 1.0× 86 0.4× 70 0.8× 92 1.1× 85 1.4× 15 703
Marcello Niceta 489 1.7× 304 1.4× 60 0.7× 52 0.6× 37 0.6× 53 810
Katharina Steindl 411 1.4× 323 1.5× 46 0.5× 49 0.6× 34 0.6× 50 698
Reza Maroofian 307 1.0× 131 0.6× 65 0.7× 55 0.6× 44 0.7× 57 667
Josef Ekstein 407 1.4× 193 0.9× 44 0.5× 170 2.0× 48 0.8× 27 851
Zhijian Yang 319 1.1× 129 0.6× 52 0.6× 61 0.7× 102 1.7× 52 585
Nam Suk Sim 211 0.7× 175 0.8× 68 0.8× 52 0.6× 31 0.5× 31 531
Rachel Schot 355 1.2× 260 1.2× 78 0.9× 62 0.7× 57 0.9× 35 686
Isabelle Maystadt 514 1.7× 516 2.4× 51 0.6× 94 1.1× 30 0.5× 32 946

Countries citing papers authored by Simon Holden

Since Specialization
Citations

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

Fields of papers citing papers by Simon Holden

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Simon Holden

This figure shows the co-authorship network connecting the top 25 collaborators of Simon Holden. A scholar is included among the top collaborators of Simon Holden 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 Holden. Simon Holden 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.
Parry, David, Mihail Halachev, Kathleen A. Williamson, et al.. (2023). Short-read whole genome sequencing identifies causative variants in most individuals with previously unexplained aniridia. Journal of Medical Genetics. 61(3). 250–261. 4 indexed citations
2.
Brasch‐Andersen, Charlotte, Niels Ove Illum, Tiffany Busa, et al.. (2021). Mono‐allelic loss of YTHDF3 and neurodevelopmental disorder: clinical features of four individuals with 8q12.3 deletions. Clinical Genetics. 101(2). 208–213. 2 indexed citations
3.
Holden, Simon, Judith Babar, Jürgen Herre, et al.. (2021). Combining clinical, radiological and genetic approaches to pneumothorax management. Thorax. 77(2). 196–198. 3 indexed citations
4.
Stoker, Thomas B., Simon Holden, & Roger A. Barker. (2021). Correction to: Late‑onset Huntington’s disease associated with CAG repeat lengths of 30 and 31. Journal of Neurology. 268(10). 3920–3920. 1 indexed citations
5.
Rytina, Ed, et al.. (2020). Pseudoxanthoma elasticum presenting without typical skin changes. Clinical and Experimental Dermatology. 45(4). 518–520. 2 indexed citations
6.
Holden, Simon, Rhona MacLeod, Zosia Miedzybrodzka, et al.. (2019). A case-note review of continued pregnancies found to be at a high risk of Huntington’s disease: considerations for clinical practice. European Journal of Human Genetics. 27(8). 1215–1224. 4 indexed citations
7.
Andrews, Katrina, et al.. (2019). Taking consent for neonatal microarray analysis as a screen for genomic rearrangements: are paediatricians equipped for the genomic era?. Archives of Disease in Childhood. 105(10). 1021–1022. 1 indexed citations
8.
Reid, Emma, Hywel Williams, Glenn Anderson, et al.. (2017). Mutations in SLC25A22: hyperprolinaemia, vacuolated fibroblasts and presentation with developmental delay. Journal of Inherited Metabolic Disease. 40(3). 385–394. 15 indexed citations
9.
Λεωνίδου, Ανδρέας, Melita Irving, Simon Holden, & Marcos Katchburian. (2016). Recurrent missense mutation of GDF5 (p.R438L) causes proximal symphalangism in a British family. World Journal of Orthopedics. 7(12). 839–839. 6 indexed citations
10.
Brouillard, Pascal, Laurence M. Boon, Nicole Revençu, et al.. (2013). Genotypes and Phenotypes of 162 Families with a <b><i>Glomulin</i></b> Mutation. Molecular Syndromology. 4(4). 157–164. 33 indexed citations
11.
McGowan, Ruth, Sarah J. Ross, Susan Holloway, et al.. (2012). Results of Duchenne muscular dystrophy family screening in practice: leaks rather than cascades?. Clinical Genetics. 83(2). 187–190. 6 indexed citations
12.
McGowan, Ruth, Sulekha Rajagopalan, Alasdair G. W. Hunter, et al.. (2011). X‐linked VACTERL with hydrocephalus syndrome: Further delineation of the phenotype caused by FANCB mutations. American Journal of Medical Genetics Part A. 155(10). 2370–2380. 30 indexed citations
13.
Vassos, Evangelos, David Collier, Simon Holden, et al.. (2010). Penetrance for copy number variants associated with schizophrenia. Human Molecular Genetics. 19(17). 3477–3481. 119 indexed citations
14.
Holden, Simon, et al.. (2010). A de novo duplication of Xp11.22–p11.4 in a girl with intellectual disability, structural brain anomalies, and preferential inactivation of the normal X chromosome. American Journal of Medical Genetics Part A. 152A(7). 1735–1740. 13 indexed citations
15.
Mellerio, Jemima E., et al.. (2009). PORCNgene mutations and the protean nature of focal dermal hypoplasia. British Journal of Dermatology. 160(5). 1103–1109. 23 indexed citations
16.
Reardon, William, et al.. (2007). Bipolar affective disorder associated with 11q24.2 disruption—A second report. American Journal of Medical Genetics Part A. 143A(12). 1263–1267. 2 indexed citations
17.
Holden, Simon, et al.. (2007). Prenatal diagnosis of Harlequin ichthyosis presenting as distal arthrogryposis using three‐dimensional ultrasound. Prenatal Diagnosis. 27(6). 566–567. 19 indexed citations
18.
Holden, Simon, et al.. (2006). Fanconi anaemia complementation group B presenting as X linked VACTERL with hydrocephalus syndrome. Journal of Medical Genetics. 43(9). 750–754. 48 indexed citations
19.
Holden, Simon, et al.. (2004). Cloning, genomic organization, alternative splicing and expression analysis of the human gene WNK3 (PRKWNK3). Gene. 335. 109–119. 54 indexed citations
20.

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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