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 Roger A. Barker, Julia C. Greenland, Thomas B. Stoker, Sarah Mason, David Collier, Christine Patch, F. Lucy Raymond, Evangelos Vassos, Cathryn M. Lewis 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

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Short-read whole genome sequencing identifies causative variants in most individuals with previously unexplained aniridia 2023 ·Journal of Medical Genetics ·(unknown), David Parry, Mihail Halachev, Kathleen A. Williamson, Kevin Donnelly, (unknown), Shipra Bhatia, Jeffrey T. Joseph, Simon Holden, Trine Prescott, Pierre Bitoun, Edwin P. Kirk, Ruth Newbury‐Ecob, Katherine Lachlan, Juan Bernar, Veronica van Heyningen, David Fitzpatrick, Alison Meynert	4
2	Mono‐allelic loss of YTHDF3 and neurodevelopmental disorder: clinical features of four individuals with 8q12.3 deletions 2021 ·Clinical Genetics ·(unknown), Charlotte Brasch‐Andersen, Niels Ove Illum, Tiffany Busa, Chantal Missirian, Kate Chandler, Simon Holden, Uffe Birk Jensen, Christina Fagerberg	2
3	Correction to: Late‑onset Huntington’s disease associated with CAG repeat lengths of 30 and 31 2021 ·Journal of Neurology ·Thomas B. Stoker, Simon Holden, Roger A. Barker	1
4	Combining clinical, radiological and genetic approaches to pneumothorax management 2021 ·Thorax ·(unknown), Simon Holden, Judith Babar, (unknown), (unknown), (unknown), Jürgen Herre, Martin Knolle, Eamonn R. Maher, Stefan J. Marciniak	3
5	Huntington’s disease: diagnosis and management 2021 ·Practical Neurology ·Thomas B. Stoker, Sarah Mason, Julia C. Greenland, Simon Holden, (unknown), Roger A. Barker	112
6	Pseudoxanthoma elasticum presenting without typical skin changes 2020 ·Clinical and Experimental Dermatology ·(unknown), Ed Rytina, Simon Holden, Natalie Burrows	2
7	A case-note review of continued pregnancies found to be at a high risk of Huntington’s disease: considerations for clinical practice 2019 ·European Journal of Human Genetics ·(unknown), Simon Holden, Rhona MacLeod, Zosia Miedzybrodzka, Andrea H. Németh, (unknown), (unknown), Oliver Quarrell, Angus Clarke	4
8	Taking consent for neonatal microarray analysis as a screen for genomic rearrangements: are paediatricians equipped for the genomic era? 2019 ·Archives of Disease in Childhood ·Katrina Andrews, (unknown), Elizabeth J. Radford, Ingrid Simonic, Simon Holden, Gusztáv Bélteki	1
9	031. COMPELLING CASE OF COPPER CONUNDRUM: OCCIPITAL HORN SYNDROME 2017 ·Lara D. Veeken ·(unknown), Amaka C Offiah, Simon Holden, Nicholas Shenker	1
10	Recurrent missense mutation of GDF5 (p.R438L) causes proximal symphalangism in a British family 2016 ·World Journal of Orthopedics ·Ανδρέας Λεωνίδου, Melita Irving, Simon Holden, Marcos Katchburian	6
11	Genotypes and Phenotypes of 162 Families with a <b><i>Glomulin</i></b> Mutation 2013 ·Molecular Syndromology ·Pascal Brouillard, Laurence M. Boon, Nicole Revençu, J. Berg, A. Dompmartin, Josée Dubois, Maria C. Garzón, Simon Holden, Loshan Kangesu, Christine Labrèze, Sally Ann Lynch, C McKeown, Raimundas Meškauskas, I. Quéré, Samira Syed, P. Vabres, Michel Wassef, John B. Mulliken, Miikka Vikkula, (unknown)	33
12	Results of Duchenne muscular dystrophy family screening in practice: leaks rather than cascades? 2012 ·Clinical Genetics ·Ruth McGowan, (unknown), Sarah J. Ross, Susan Holloway, Shelagh Joss, D.E. Wilcox, Simon Holden, John Tolmie, Cheryl Longman	6
13	X‐linked VACTERL with hydrocephalus syndrome: Further delineation of the phenotype caused by FANCB mutations 2011 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), Ruth McGowan, Sulekha Rajagopalan, Alasdair G. W. Hunter, Jacques L. Michaud, Kate Gibson, Jeremy Robertson, (unknown), Stephen Abbs, Simon Holden	30
14	Penetrance for copy number variants associated with schizophrenia 2010 ·Human Molecular Genetics ·Evangelos Vassos, David Collier, Simon Holden, Christine Patch, Dan Rujescu, David St Clair, Cathryn M. Lewis	119
15	PORCNgene mutations and the protean nature of focal dermal hypoplasia 2009 ·British Journal of Dermatology ·(unknown), Jemima E. Mellerio, Simon Holden, (unknown), John A. McGrath	23
16	Prenatal diagnosis of Harlequin ichthyosis presenting as distal arthrogryposis using three‐dimensional ultrasound 2007 ·Prenatal Diagnosis ·Simon Holden, (unknown), Amanda Ogilvy‐Stuart, Helen V. Firth, C. Lees	19
17	Bipolar affective disorder associated with 11q24.2 disruption—A second report 2007 ·American Journal of Medical Genetics Part A ·William Reardon, (unknown), Simon Holden, Richard Blennerhassett	2
18	Fanconi anaemia complementation group B presenting as X linked VACTERL with hydrocephalus syndrome 2006 ·Journal of Medical Genetics ·Simon Holden, (unknown), (unknown), (unknown), (unknown), (unknown)	48
19	Cloning, genomic organization, alternative splicing and expression analysis of the human gene WNK3 (PRKWNK3) 2004 ·Gene ·Simon Holden, (unknown), F. Lucy Raymond	54
20	The human gene CXorf17 encodes a member of a novel family of putative transmembrane proteins: cDNA cloning and characterization of CXorf17 and its mouse ortholog orf34 2003 ·Gene ·Simon Holden, (unknown)	11

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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