Peter Lunt

5.0k citations

98 papers · 3.1k indexed · h-index 28

Impact in

Geology top 1%
- Geological and Geophysical Studies
Genetics top 2%
- Neurogenetic and Muscular Disorders Research

Papers in ⓘ

Geology 28
- Geological and Geophysical Studies 28
Genetics 21
- Neurogenetic and Muscular Disorders Research 21

Co-authors: Peter S. Harper (8 shared papers)Meena Upadhyaya (16 shared papers)Manuela C. Koch (4 shared papers)G.W. Padberg (2 shared papers)Michel Fardeau (1 shared paper)J. Maynard (6 shared papers)Philip Jardine (7 shared papers)Willem Renema (2 shared papers)
Journals: Journal of Medical Genetics (12 papers)Journal of Asian Earth Sciences (7 papers)Neuromuscular Disorders (6 papers)Marine and Petroleum Geology (4 papers)Human Mutation (3 papers)
Partner nations: United Kingdom Netherlands Malaysia

In The Last Decade

Peter Lunt

95 papers receiving 3.0k citations

Peers

Countries citing papers authored by Peter Lunt

Since Specialization

Citations

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

Fields of papers citing papers by Peter Lunt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 98 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Hopping Hotspots: Global Shifts in Marine Biodiversity Science ·Willem Renema, David R. Bellwood, Juan C. Braga, Kate Bromfield, Robert Hall, Kenneth G. Johnson, Peter Lunt, Chris Meyer, Laura B. McMonagle, Robert J. Morley, Aaron O’Dea, Jonathan A. Todd, Frank P. Wesselingh, Moyra E.J. Wilson, John M. Pandolfi	2008	397
2	Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome) Nature Genetics ·Pia Østergaard, Michael A. Simpson, Fiona Connell, Colin G. Steward, Glen Brice, Wesley J. Woollard, Dimitra Dafou, Tatjana Kilo, Sarah Smithson, Peter Lunt, Victoria A. Murday, Shirley Hodgson, Russell Keenan, Daniela T. Pilz, Inés Martínez‐Corral, Taija Mäkinen, Peter Mortimer, Steve Jeffery, Richard C. Trembath, Sahar Mansour	2011	348
3	Diagnostic criteria for facioscapulohumeral muscular dystrophy Neuromuscular Disorders ·G.W. Padberg, Peter Lunt, Manuela C. Koch, Michel Fardeau	1991	175
4	Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD) Human Molecular Genetics ·Peter Lunt, Philip Jardine, Manuela C. Koch, J. Maynard, M. Osborn, Margaret M. Williams, P.S. Harper, Meena Upadhyaya	1995	150
5	The Opitz syndrome gene product, MID1, associates with microtubules Proceedings of the National Academy of Sciences ·Susann Schweiger, John Foerster, Tanja Lehmann, Vanessa Suckow, Yves A. Muller, Gerald Walter, T. Davies, Helen Porter, Hans van Bokhoven, Peter Lunt, Peter Traub, Hans‐Hilger Ropers	1999	106
6	Genetic counselling in facioscapulohumeral muscular dystrophy. Journal of Medical Genetics ·Peter Lunt, Peter S. Harper	1991	105
7	Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortium. PubMed ·M. Sarfarazi, Cisca Wijmenga, Meena Upadhyaya, Barbara Weiffenbach, Craig L. Hyser, Katherine D. Mathews, Jeffrey Murray, James Gilbert, M. A. Pericak‐Vance, Peter Lunt	1992	103
8	Prenatal onset spinal muscular atrophy European Journal of Paediatric Neurology ·Melanie J Macleod, Joanne Taylor, Peter Lunt, Christopher G. Mathew, S. Robb	1999	89
9	Estimation of age dependent penetrance in facioscapulohumeral muscular dystrophy by minimising ascertainment bias. Journal of Medical Genetics ·Peter Lunt, D. A. S. Compston, Peter S. Harper	1989	69
10	Genetic analysis of the G4.5 gene in families with suspected Barth syndrome The Journal of Pediatrics ·Ann M. Cantlay, Kayvan Shokrollahi, John T. Allen, Peter Lunt, Ruth Newbury‐Ecob, Colin G. Steward	1999	67
11	Application of targeted multi-gene panel testing for the diagnosis of inherited peripheral neuropathy provides a high diagnostic yield with unexpected phenotype-genotype variability BMC Medical Genetics ·Thalia Antoniadi, Chris Buxton, Gemma Dennis, Natalie Forrester, Debbie Smith, Peter Lunt, Sarah Burton‐Jones	2015	64
12	A systematic review of interventions to provide genetics education for primary care BMC Family Practice ·Milena Paneque, Daniela Turchetti, Leigh Jackson, Peter Lunt, Elisa J. F. Houwink, Heather Skirton	2016	55
13	A three generation family with fibrodysplasia ossificans progressiva. Journal of Medical Genetics ·J. M. Connor, Heather Skirton, Peter Lunt	1993	54
14	Autosomal Dominant Inheritance of Autoantibodies to Thyroid Peroxidase and Thyroglobulin—Studies in Families Not Selected for Autoimmune Thyroid Disease* The Journal of Clinical Endocrinology & Metabolism ·David Phillips, Louise Prentice, Meena Upadhyaya, Peter Lunt, Susan Chamberlain, D. F. Roberts, Sandra M. McLachlan, Bernard Rees Smith	1991	52
15	Improved molecular diagnosis of facioscapulohumeral muscular dystrophy (FSHD): validation of the differential double digestion for FSHD. Journal of Medical Genetics ·Meena Upadhyaya, J. Maynard, Mark T. Rogers, Peter Lunt, Philip Jardine, David Ravine, Peter S. Harper	1997	51
16	Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophy Muscle & Nerve ·Peter Lunt, Philip Jardine, Manuela C. Koch, J. Maynard, Micheal Osborn, Maggie Williams, Peter S. Harper, Meena Upadhyaya	1995	46
17	Best practice guidelines on genetic diagnostics of Facioscapulohumeral muscular dystrophy: Workshop 9th June 2010, LUMC, Leiden, The Netherlands Neuromuscular Disorders ·Richard J.L.F. Lemmers, Suzanne O’Shea, George W. Padberg, Peter Lunt, Silvère M. van der Maarel	2011	39
18	Ehlers-Danlos Syndrome with Severe Early-Onset Periodontal Disease (EDS-VIII) Is a Distinct, Heterogeneous Disorder with One Predisposition Gene at Chromosome 12p13 The American Journal of Human Genetics ·Nazneen Rahman, Melanie Dunstan, M. Dawn Teare, Sandra Hanks, Jenny Douglas, Kim Coleman, William E. Bottomly, Mary Ellen Campbell, Britta Berglund, Magnus Nordenskjöld, Bengt Forssell, Nigel Burrows, Peter Lunt, Ian Young, Nigel Williams, Graham R. Bignell, P. Andrew Futreal, F M Pope	2003	38
19	An unusually severe phenotype for familial adenomatous polyposis Archives of Disease in Childhood ·Diana Eccles, Peter Lunt, Yvonne Wallis, Mike Griffiths, Bhupinder Sandhu, Sean McKay, Dion Morton, J Shea-Simonds, Fiona MacDonald	1997	34
20	44th ENMC International Workshop: Facioscapulohumeral Muscular Dystrophy: Molecular Studies Neuromuscular Disorders ·Peter Lunt	1998	34

About Peter Lunt

Peter Lunt is a scholar working on Geology, Genetics, Geophysics, Paleontology and Earth-Surface Processes, having authored 98 papers that have together received 3.1k indexed citations. Recurring topics across this work include Geological and Geophysical Studies (28 papers), Muscle Physiology and Disorders (23 papers), Neurogenetic and Muscular Disorders Research (21 papers), Cardiomyopathy and Myosin Studies (12 papers), Hydrocarbon exploration and reservoir analysis (9 papers), earthquake and tectonic studies (8 papers), Seismic Imaging and Inversion Techniques (7 papers) and Paleontology and Stratigraphy of Fossils (7 papers). The work is most often cited by research in Geology (291 citations), Genetics (512 citations), Cellular and Molecular Neuroscience (483 citations), Paleontology (177 citations) and Molecular Biology (1.6k citations). Peter Lunt has collaborated with scholars based in United Kingdom, Netherlands and Malaysia. Frequent co-authors include Peter S. Harper, Meena Upadhyaya, Manuela C. Koch, G.W. Padberg, Michel Fardeau, J. Maynard, Philip Jardine, Willem Renema, P.S. Harper and Moyra E.J. Wilson. Their work appears in journals such as Journal of Medical Genetics, Journal of Asian Earth Sciences, Neuromuscular Disorders, Marine and Petroleum Geology and Human Mutation.

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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