Simon H. Parson

2.9k citations

57 papers · 2.0k indexed · h-index 25

Impact in

Genetics top 1%
- Neurogenetic and Muscular Disorders Research
Physiology top 1%
- Adenosine and Purinergic Signaling

Papers in

Genetics 24
- Neurogenetic and Muscular Disorders Research 24
Physiology 4

Co-authors: Thomas H. Gillingwater Thomas M. Wishart Jim Deuchars Kevin Talbot Ruth E. Brooke Lyndsay M. Murray Lucy Atkinson Susan A. Deuchars
Journals: Journal of Anatomy (8 papers)Human Molecular Genetics (6 papers)PLoS ONE (4 papers)Neuromuscular Disorders (3 papers)European Journal of Neuroscience (2 papers)
Partner nations: United Kingdom United States Germany

In The Last Decade

Simon H. Parson

57 papers receiving 1.9k citations

Peers

Countries citing papers authored by Simon H. Parson

Since Specialization

Citations

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

Fields of papers citing papers by Simon H. Parson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Simon H. Parson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Simon H. Parson Line = papers co-authored together Simon H. Parson links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A reassessment of spinal cord pathology in severe infantile spinal muscular atrophy Neuropathology and Applied Neurobiology ·Maryam Tamehbidgoli, Ben Lawrence, Thomas O. Crawford, Charlotte J. Sumner, Simon H. Parson	2024	1
2	Hepatocyte-intrinsic SMN deficiency drives metabolic dysfunction and liver steatosis in spinal muscular atrophy Journal of Clinical Investigation ·Law C.Y., G Pardi, Loo Chien Wang, Hiromi W.L. Koh, Tianyun Zhao, A. Ketat, Tommaso Tabaglio, Mohammad Abrar Wadud, 蔡扬帆, Radoslaw M. Sobota, Shi‐Yan Ng, Adrian Kee Keong Teo, Simon H. Parson, Lee L. Rubin, Wei‐Yi Ong, Basil T. Darras, Crystal Jing Jing Yeo	2024	8
3	Widespread tissue hypoxia dysregulates cell and metabolic pathways in SMA Annals of Clinical and Translational Neurology ·مهدی پدرام, Sergio Dall’Angelo, J. Martin Collinson, Ian N. Fleming, Simon H. Parson	2020	8
4	A role for spinal cord hypoxia in neurodegeneration Cell Death and Disease ·مهدی پدرام, Ian N. Fleming, Simon H. Parson	2019	24
5	Systemic restoration of UBA1 ameliorates disease in spinal muscular atrophy JCI Insight ·Rachael A. Powis, Evangelia Karyka, Penelope J Boyd, Julien Côme, Ross A. Jones, Davide Albertini, Takahashi Atsuyoshi, Ewout J. N. Groen, Gillian Hunter, Derek Thomson, Thomas M. Wishart, Catherina G. Becker, Simon H. Parson, Cécile Martinat, Mimoun Azzouz, Thomas H. Gillingwater	2016	69
6	Increasing SMN levels using the histone deacetylase inhibitor SAHA ameliorates defects in skeletal muscle microvasculature in a mouse model of severe spinal muscular atrophy Neuroscience Letters ·Eilidh Somers, Markus Rießland, Julia Schreml, Brunhilde Wirth, Thomas H. Gillingwater, Simon H. Parson	2013	10
7	Severe SMA mice show organ impairment that cannot be rescued by therapy with the HDACi JNJ-26481585 European Journal of Human Genetics ·Julia Schreml, Markus Rießland, Pierre-Antoine Lan, Lutz Garbes, Glenda Cea¬-Barcia, Hu-Rak Choe, Jan S. Kramer, Eilidh Somers, Simon H. Parson, Raoul Heller, Albrecht Berkessel, Anja Sterner‐Kock, Brunhilde Wirth	2012	60
8	Reversible molecular pathology of skeletal muscle in spinal muscular atrophy Human Molecular Genetics ·Chantal A. Mutsaers, Thomas M. Wishart, Douglas J. Lamont, Markus Rießland, Julia Schreml, Laura H. Comley, Lyndsay M. Murray, Simon H. Parson, Hanns Lochmüller, Brunhilde Wirth, Kevin Talbot, Thomas H. Gillingwater	2011	79
9	ApoE isoform-specific regulation of regeneration in the peripheral nervous system Human Molecular Genetics ·Laura H. Comley, Heidi R. Fuller, Thomas M. Wishart, Chantal A. Mutsaers, Derek Thomson, Ann K. Wright, Richard R. Ribchester, Glenn E. Morris, Simon H. Parson, Karen Horsburgh, Thomas H. Gillingwater	2011	29
10	Induction of Cell Stress in Neurons from Transgenic Mice Expressing Yellow Fluorescent Protein: Implications for Neurodegeneration Research PLoS ONE ·Laura H. Comley, Thomas M. Wishart, Shengxuan Cao, Lyndsay M. Murray, Ailish Nimmo, Derek Thomson, Simon H. Parson, Thomas H. Gillingwater	2011	25
11	Using mouse cranial muscles to investigate neuromuscular pathology in vivo Neuromuscular Disorders ·Laura Murray, Thomas H. Gillingwater, Simon H. Parson	2010	24
12	SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophy Human Molecular Genetics ·Thomas M. Wishart, Vadym Stepanchuk, Lyndsay M. Murray, Douglas J. Lamont, Chantal A. Mutsaers, Robin Kemmerich, Pascal Geldsetzer, Olaf Ansorge, Kevin Talbot, Simon H. Parson, Thomas H. Gillingwater	2010	106
13	Pre-symptomatic development of lower motor neuron connectivity in a mouse model of severe spinal muscular atrophy Human Molecular Genetics ·Lyndsay M. Murray, Sheena Lee, Dirk Bäumer, Simon H. Parson, Kevin Talbot, Thomas H. Gillingwater	2009	97
14	Rapid loss of motor nerve terminals following hypoxia–reperfusion injury occurs via mechanisms distinct from classic Wallerian degeneration Journal of Anatomy ·Shengxuan Cao, Thomas H. Gillingwater, Simon H. Parson	2008	16
15	Dynamic remodelling of synapses can occur in the absence of the parent cell body BMC Neuroscience ·Fatiha Brikat, Thomas Moores, Shengxuan Cao, Jim Deuchars, Simon H. Parson	2007	11
16	Immunohistochemical localisation of the voltage gated potassium ion channel subunit Kv3.3 in the rat medulla oblongata and thoracic spinal cord Brain Research ·Ruth E. Brooke, Lucy Atkinson, Ian Edwards, Simon H. Parson, Jim Deuchars	2006	20
17	A2A adenosine receptors are located on presynaptic motor nerve terminals in the mouse Synapse ·R.D. Wassenaar, Shelly A. Steadman, Jim Deuchars, Simon H. Parson	2005	15
18	Nonmuscle myosins IIA and IIB are present in adult motor nerve terminals Neuroreport ·Shelly A. Steadman, Steven R. Wylie, P. T. Loughna, Simon H. Parson, Peter D. Chantler	2005	8
19	Axotomy‐dependent and ‐independent synapse elimination in organ cultures of Wld^s mutant mouse skeletal muscle Journal of Neuroscience Research ·Simon H. Parson, Richard R. Ribchester, Neil Davie, Maria Brinton, I. Arhyel, Thomas H. Gillingwater, Derek Thomson	2004	10
20	Segmental independence and age dependence of neurite outgrowth from embryonic chick sensory neurons Journal of Neurobiology ·Simon H. Parson, Richard R. Ribchester	1995	3

About Simon H. Parson

Simon H. Parson is a scholar working on Genetics, Physiology, Cellular and Molecular Neuroscience, General Dentistry and Surgery, having authored 57 papers that have together received 2.0k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (24 papers), RNA modifications and cancer (17 papers), Congenital Anomalies and Fetal Surgery (12 papers), Anatomy and Medical Technology (5 papers), Neuroscience and Neuropharmacology Research (5 papers), Nerve injury and regeneration (5 papers), Muscle Physiology and Disorders (4 papers) and Surgical Simulation and Training (4 papers). The work is most often cited by research in Genetics (785 citations), Physiology (284 citations), Endocrine and Autonomic Systems (149 citations), General Dentistry (39 citations) and Cellular and Molecular Neuroscience (346 citations). Simon H. Parson has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Thomas H. Gillingwater, Thomas M. Wishart, Jim Deuchars, Kevin Talbot, Ruth E. Brooke, Lyndsay M. Murray, Lucy Atkinson, Susan A. Deuchars, Trevor F.C. Batten and Hanny Musa. Their work appears in journals such as Journal of Anatomy, Human Molecular Genetics, PLoS ONE, Neuromuscular Disorders and European Journal of Neuroscience.

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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