Simon Hammans

4.3k citations

45 papers · 1.7k indexed · h-index 25

Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders 15
Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases 15
- Hereditary Neurological Disorders 4
Molecular Biology top 5%
- Mitochondrial Function and Pathology 23
- ATP Synthase and ATPases Research 8
- Muscle Physiology and Disorders 7
Neurology top 10%
- Neurological diseases and metabolism 4
Neurology top 5%
- Neurological diseases and metabolism 4
Rheumatology
- Glycogen Storage Diseases and Myoclonus 5

Co-authors: A. E. Harding J A Morgan-Hughes Martin Brockington Mary G. Sweeney M G Sweeney Ian Holt T. James Beattie E M Brett
Cited by: Clinical Biochemistry Cellular and Molecular Neuroscience Molecular Biology
Journals: Brain (7 papers)Neuromuscular Disorders (5 papers)Neurology (3 papers)
Partner nations: United Kingdom United States Spain

In The Last Decade

Simon Hammans

45 papers receiving 1.7k citations

Peers

Countries citing papers authored by Simon Hammans

Since Specialization

Citations

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

Fields of papers citing papers by Simon Hammans

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Simon Hammans, 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 Hammans Line = papers co-authored together Simon Hammans links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Desminopathy presenting as late onset bilateral facial weakness, with diagnosis supported by lower limb MRI Neuromuscular Disorders ·Liam Carroll,Mark Walker,David R. Allen,H. Chen,Adam Ditchfield,Ashwin Pinto,Simon Hammans	2021	1
2	ADCY5-related dyskinesia presenting as familial myoclonus-dystonia Neurogenetics ·Andrew G. L. Douglas,Gaia Andreoletti,Kevin Talbot,Simon Hammans,Jaspal Singh,Andrea Whitney,Sarah Ennis,Nicola Foulds	2017	31
3	The UK Myotonic Dystrophy Patient Registry: facilitating and accelerating clinical research Journal of Neurology ·Libby Wood,Isabell Cordts,António Atalaia,Masanori Tashima,Paul Maddison,Margaret Phillips,Mark Roberts,Mark Rogers,Simon Hammans,Volker Straub,Richard Petty,Richard W. Orrell,Darren G. Monckton,Nikoletta Nikolenko,Cecilia Jimenez‐Moreno,Rachel Thompson,David Hilton‐Jones,Chris Turner,Hanns Lochmüller	2017	21
4	Recessive myosin myopathy with external ophthalmoplegia associated with MYH2 mutations European Journal of Human Genetics ·Homa Tajsharghi,Simon Hammans,Christopher Lindberg,Alexander Lossos,Nigel F. Clarke,Ingrid Mazanti,Leigh B. Waddell,Yakov Fellig,Nicola Foulds,Nguyen Thi Thu,Richard Webster,Olayinka Raheem,Bjarne Udd,Zohar Argov,Anders Oldfors	2013	28
5	Calpainopathy presenting as foot drop in a 41 year old Neuromuscular Disorders ·Georgina Burke,Craig Hillier,Jonathan Cole,Madeleine Sampson,Ma Chunling,Kate Bushby,Rita Barresi,Simon Hammans	2010	8
6	A treatable muscle disease Practical Neurology ·Georgina Burke,Simon Hammans,David C. Allen,Todaka Takashi,Abdullah Awad Saedi Alshammari	2009	3
7	Large scale calcium channel gene rearrangements in episodic ataxia and hemiplegic migraine: implications for diagnostic testing Journal of Medical Genetics ·Robyn Labrum,Sanjeev Rajakulendran,Tracey D. Graves,L. H. Eunson,Nickie Jamison,Mary G. Sweeney,Simon Hammans,Niall Tubridy,TC Britton,Lucinda Carr,John R. Østergaard,C Kennedy,A. Al‐Memar,Dimitri M. Kullmann,Stéphanie Schorge,I. Karen Temple,Mary B. Davis,Michael G. Hanna	2009	47
8	Clinical, pathological and genetic characterization of hereditary sensory and autonomic neuropathy type 1 (HSAN I) Brain ·Henry Houlden,R. H. M. King,Julian Blake,Mike Groves,Seth Love,Cathy E. Woodward,Simon Hammans,James A. R. Nicoll,Graham Lennox,Dominic G. O’Donovan,Carolyn Gabriel,P K Thomas,Mary M. Reilly	2005	97
9	Oculopharyngeal muscular dystrophy (OPMD): analysis of the PABPN1 gene expansion sequence in 86 patients reveals 13 different expansion types and further evidence for unequal recombination as the mutational mechanism Human Genetics ·David Robinson,Simon Hammans,강신표,Julie Sillibourne	2005	40
10	MNGIE neuropathy: Five cases mimicking chronic inflammatory demyelinating polyneuropathy Muscle & Nerve ·Richard Bedlack,Tuan Vu,Simon Hammans,Toby Zerner,Bennett Myers,Joel C. Morgenlander,Michio Hirano	2004	48
11	Oculopharyngeal muscular dystrophy Brain ·M. E. Hill,NUL – INA M. ABDULHAKIM,Tristan F. W. McMullan,Anthony G. Tyers,David Hilton‐Jones,David Robinson,Simon Hammans	2001	61
12	X‐linked cerebellar ataxia and sideroblastic anaemia associated with a missense mutation in the ABC7 gene predicting V411L British Journal of Haematology ·Ramon Amenós Cos,徹切無沢,Simon Hammans,Alison May	2001	51
13	A clinical and genetic study of a manifesting heterozygote with X-linked myotubular myopathy Neuromuscular Disorders ·Simon Hammans,David Robinson,Céline Moutou,Colin Kennedy,N R Dennis,PJ Hughes,D. W. Ellison	2000	33
14	Ataxia with isolated vitamin E deficiency presenting as mutation negative Friedreich's ataxia Journal of Neurology Neurosurgery & Psychiatry ·Simon Hammans,C Kennedy	1998	16
15	The mitochondrial DNA transfer RNA ^Leu(UUR) A→G(3243) mutation: A clinical and genetic study Brain ·Simon Hammans,Mary G. Sweeney,Michael G. Hanna,Martin Brockington,J A Morgan-Hughes,A. E. Harding	1995	123
16	Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·J A Morgan-Hughes,M G Sweeney,Jonathan M. Cooper,Simon Hammans,Martin Brockington,Anthony H.V. Schapira,A E Harding,N. Schell	1995	69
17	Mitochondrial DNA mutation underlying Leigh's syndrome: Clinical, pathological, biochemical, and genetic studies of a patient presenting with progressive myoclonic epilepsy Journal of the Neurological Sciences ·Mary G. Sweeney,Simon Hammans,L. W. Duchen,Jonathan M. Cooper,Anthony H.V. Schapira,Colin Kennedy,Jeanne M. E. Jacobs,B.D. Youl,J A Morgan-Hughes,A. E. Harding	1994	43
18	The mitochondrial DNA transfer RNA^LysA→G^[8344] mutation and the syndrome of myoclonic epilepsy with ragged red fibres [MERRF] Brain ·Simon Hammans,Mary G. Sweeney,Martin Brockington,Graham Lennox,N F Lawton,Colin Kennedy,J A Morgan-Hughes,A E Harding	1993	114
19	A tandem duplication in the D–loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathies Nature Genetics ·Martin Brockington,Mary G. Sweeney,Simon Hammans,J A Morgan-Hughes,Anita E. Harding	1993	61
20	A MOLECULAR GENETIC STUDY OF FOCAL HISTOCHEMICAL DEFECTS IN MITOCHONDRIAL ENCEPHALOMYOPATHIES Brain ·Simon Hammans,Mary G. Sweeney,David Wicks,J A Morgan-Hughes,A. E. Harding	1992	40

About Simon Hammans

Simon Hammans is a scholar working on Clinical Biochemistry, Cellular and Molecular Neuroscience and Neurology, having authored 45 papers that have together received 1.7k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (23 papers), Metabolism and Genetic Disorders (15 papers), Genetic Neurodegenerative Diseases (15 papers), ATP Synthase and ATPases Research (8 papers), Muscle Physiology and Disorders (7 papers), Glycogen Storage Diseases and Myoclonus (5 papers), Neurological diseases and metabolism (4 papers) and Hereditary Neurological Disorders (4 papers). The work is most often cited by research in Clinical Biochemistry (825 citations), Cellular and Molecular Neuroscience (425 citations) and Molecular Biology (1.4k citations). Simon Hammans has collaborated with scholars based in United Kingdom, United States and Spain. Frequent co-authors include A. E. Harding, J A Morgan-Hughes, Martin Brockington, Mary G. Sweeney, M G Sweeney, Ian Holt, T. James Beattie, E M Brett, A E Harding and David Robinson. Their work appears in journals such as Brain, Neuromuscular Disorders, Neurology, Journal of Neurology Neurosurgery & Psychiatry and Journal of Inherited Metabolic Disease.

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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