John Dean

8.6k citations

103 papers · 3.5k indexed · h-index 30

Impact in

Genetics top 1%
- Connective tissue disorders research
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders

Papers in ⓘ

Genetics 36
- Connective tissue disorders research 8
- Genomics and Rare Diseases 8
- Genomic variations and chromosomal abnormalities 7
Developmental Biology 2

Co-authors: D. J. Lloyd (1 shared paper)Susan Moore (8 shared papers)Peter D. Turnpenny (12 shared papers)Z Miedzybrodzka (7 shared papers)Lisa Strain (2 shared papers)Mark P.R. Hamilton (1 shared paper)David T. Bonthron (1 shared paper)Kathleen W. Rao (1 shared paper)
Journals: Journal of Medical Genetics (17 papers)Heart (6 papers)Clinical Genetics (6 papers)Developmental Medicine & Child Neurology (4 papers)The American Journal of Human Genetics (4 papers)
Partner nations: United Kingdom United States Canada

In The Last Decade

John Dean

100 papers receiving 3.3k citations

Peers

Countries citing papers authored by John Dean

Since Specialization

Citations

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

Fields of papers citing papers by John Dean

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside John Dean, 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 John Dean Line = papers co-authored together John Dean 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 103 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Characteristics of fetal anticonvulsant syndrome associated autistic disorder Developmental Medicine & Child Neurology ·AD Rasalam, H. Hailey, JHG Williams, SJ Moore, PD Turnpenny, D. J. Lloyd, John Dean	2005	335
2	Heterozygous Mutations in TREX1 Cause Familial Chilblain Lupus and Dominant Aicardi-Goutières Syndrome The American Journal of Human Genetics ·Gillian Rice, William G. Newman, John Dean, Teresa Patrick, Rekha Parmar, Kim Flintoff, Peter Robins, Scott Harvey, Thomas Hollis, Ann M. O’Hara, Ariane L. Herrick, A P Bowden, Fred W. Perrino, Tomas Lindahl, Deborah E. Barnes, Yanick J. Crow	2007	266
3	Clinical and genetic epidemiology of Bardet-Biedl syndrome in Newfoundland: A 22-year prospective, population-based, cohort study American Journal of Medical Genetics Part A ·Susan Moore, Jane S. Green, Yanli Fan, Ashvinder K. Bhogal, Elizabeth Dicks, Bridget A. Fernandez, Mark Stefanelli, Christopher Murphy, B. Cramer, John Dean, Philip L. Beales, Nicholas Katsanis, Anne S. Bassett, William S. Davidson, Patrick S. Parfrey	2005	230
4	ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency Brain ·Rikke Katrine Jentoft Olsen, S. E. Olpin, Brage Storstein Andresen, Z Miedzybrodzka, Morteza Pourfarzam, B. Merinero, Frank E. Frerman, Michael W. Beresford, John Dean, Nanna Cornelius, Oluf Andersen, Anders Oldfors, Elisabeth Holme, Niels Gregersen, Douglass M. Turnbull, Andrew A.M. Morris	2007	215
5	Marfan syndrome: clinical diagnosis and management European Journal of Human Genetics ·John Dean	2007	188
6	Long term health and neurodevelopment in children exposed to antiepileptic drugs before birth Journal of Medical Genetics ·John Dean, (unknown), (unknown), (unknown), (unknown), (unknown)	2002	178
7	Preliminary phenotypic map of chromosome 4p16 based on 4p deletions American Journal of Medical Genetics ·Laurel L. Estabrooks, Kathleen W. Rao, Deborah A. Driscoll, Barbara F. Crandall, John Dean, Elina Ikonen, Bruce R. Korf, Arthur S. Aylsworth	1995	158
8	Elastin: mutational spectrum in supravalvular aortic stenosis European Journal of Human Genetics ·Kay Metcalfe, Agnes K Rucka, Leslie Smoot, Guenter Hofstadler, Gerald Tuzler, Pascal McKeown, Victoria Mok Siu, Anita Rauch, John Dean, N R Dennis, Ian O. Ellis, William Reardon, Cheryl Cytrynbaum, Lucy R. Osborne, John R.W. Yates, Andrew Read, Dian Donnai, Mayada Tassabehji	2000	110
9	A True Hermaphrodite Chimera Resulting from Embryo Amalgamation after in Vitro Fertilization New England Journal of Medicine ·Lisa Strain, John Dean, Mark P.R. Hamilton, David T. Bonthron	1998	100
10	Kabuki make-up (Niikawa-Kuroki) syndrome Clinical Dysmorphology ·N. Philip, Peter Meinecke, Allou Konan David, John Dean, Ségolène Aymé, Rebecca I. Clark, Eva Gross‐Kieselstein, D. Hosenfeld, A. Moncla, Daniel Bortolin Muller, Mary Porteous, Helena G. Dos Santos, Isabel Cordeiro, Angelo Selicorni, Margherita Silengo, Gholamali Tariverdian	1992	85
11	Ascertainment and severity of Marfan syndrome in a Scottish population. Journal of Medical Genetics ·J. Gray, A. B. Bridges, M.J.W. Faed, TH Pringle, P S Baines, John Dean, M. Boxer	1994	81
12	Aortic distensibility and stiffness index measured by magnetic resonance imaging in patients with Marfan's syndrome. Heart ·Jacqueline Adams, Melissa Brooks, Thomas W. Redpath, F. W. Smith, John Dean, J.A. Gray, Steven A. Walton, R. J. Trent	1995	71
13	Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosis. Journal of Medical Genetics ·William Reardon, David Wilkes, Paul Rutland, Louise J. Pulleyn, S Malcolm, John Dean, Robert D. Evans, Barry M. Jones, Richard Hayward, C. Michael Hall, N C Nevin, M Baraister, R M Winter	1997	70
14	Antenatal screening for carriers of cystic fibrosis: randomised trial of stepwise v couple screening BMJ ·Z Miedzybrodzka, M H Hall, Jill Mollison, Allan Templeton, I T Russell, John Dean, Kevin F. Kelly, Theresa M. Marteau, N E Haites	1995	65
15	Management of Marfan syndrome Heart ·John Dean	2002	58
16	Fetal anticonvulsant syndrome and mutation in the maternal MTHFR gene Clinical Genetics ·John Dean, Susan Moore, Aileen Osborne, Jonathan D. Howe, Peter D. Turnpenny	1999	52
17	Cardiac involvement in Emery Dreifuss muscular dystrophy: a case series Heart ·Aidan Buckley, John Dean, I R Mahy	1999	52
18	Life expectancy in British Marfan syndrome populations Clinical Genetics ·J.A. Gray, A. B. Bridges, RR West, L. McLeish, Graham Stuart, John Dean, MEM Porteous, M. Boxer, SJ Davies	1998	51
19	Mitochondrial DNA reveals phylogenetic structuring and cryptic diversity in Australian freshwater macroinvertebrate assemblages Marine and Freshwater Research ·Andrew Baker, Jane M. Hughes, John Dean, Stuart E. Bunn	2004	46
20	Type III collagen mutations cause fragile cerebral arteries British Journal of Neurosurgery ·F M Pope, B. E. Kendall, G. I. Slapak, Ravish Kapoor, W. I. McDonald, D. A. S. Compston, R. Mitchell, Daniel Hope, M.W. Millar‐Craig, John Dean, Alan Johnston, Patrick Lynch, Padmini Sarathchandra, P Narcisi, A C Nicholls, Allan J. Richards, J. L. Mackenzie	1991	45

About John Dean

John Dean is a scholar working on Genetics, Developmental Biology, Pediatrics, Perinatology and Child Health, Cardiology and Cardiovascular Medicine and Ecological Modeling, having authored 103 papers that have together received 3.5k indexed citations. Recurring topics across this work include Freshwater macroinvertebrate diversity and ecology (11 papers), Pharmacological Effects and Toxicity Studies (9 papers), Connective tissue disorders research (8 papers), Prenatal Screening and Diagnostics (8 papers), Genomics and Rare Diseases (8 papers), Invertebrate Taxonomy and Ecology (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Tracheal and airway disorders (6 papers). The work is most often cited by research in Genetics (1.4k citations), Clinical Biochemistry (219 citations), Pediatrics, Perinatology and Child Health (575 citations), Developmental Neuroscience (104 citations) and Cardiology and Cardiovascular Medicine (452 citations). John Dean has collaborated with scholars based in United Kingdom, United States and Canada. Frequent co-authors include D. J. Lloyd, Susan Moore, Peter D. Turnpenny, Z Miedzybrodzka, Lisa Strain, Mark P.R. Hamilton, David T. Bonthron, Kathleen W. Rao, Barbara F. Crandall and Arthur S. Aylsworth. Their work appears in journals such as Journal of Medical Genetics, Heart, Clinical Genetics, Developmental Medicine & Child Neurology and The American Journal of Human Genetics.

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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