Philip Jardine

3.0k total citations
33 papers, 1.6k citations indexed

About

Philip Jardine is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Philip Jardine has authored 33 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 10 papers in Neurology and 7 papers in Genetics. Recurrent topics in Philip Jardine's work include Muscle Physiology and Disorders (8 papers), Neurogenetic and Muscular Disorders Research (6 papers) and Genetic Neurodegenerative Diseases (5 papers). Philip Jardine is often cited by papers focused on Muscle Physiology and Disorders (8 papers), Neurogenetic and Muscular Disorders Research (6 papers) and Genetic Neurodegenerative Diseases (5 papers). Philip Jardine collaborates with scholars based in United Kingdom, Netherlands and Australia. Philip Jardine's co-authors include Peter Lunt, J. Maynard, Meena Upadhyaya, Manuela C. Koch, Joost Haan, E. E. Kors, Arn M. J. M. van den Maagdenberg, Robin B. Fitzsimons, Rune R. Frants and Michel D. Ferrari and has published in prestigious journals such as Journal of Clinical Investigation, Brain and Annals of Neurology.

In The Last Decade

Philip Jardine

33 papers receiving 1.5k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Philip Jardine United Kingdom 18 747 371 343 299 275 33 1.6k
Byung Chan Lim South Korea 23 750 1.0× 244 0.7× 244 0.7× 436 1.5× 481 1.7× 165 1.8k
Florian Stögbauer Germany 25 410 0.5× 525 1.4× 377 1.1× 184 0.6× 187 0.7× 69 1.8k
Sabrina W. Yum United States 25 880 1.2× 297 0.8× 543 1.6× 138 0.5× 85 0.3× 63 1.8k
Agathe Roubertie France 28 769 1.0× 713 1.9× 618 1.8× 359 1.2× 424 1.5× 114 2.1k
Michael C. Kruer United States 25 746 1.0× 901 2.4× 449 1.3× 412 1.4× 342 1.2× 74 2.2k
Maria Kinali United Kingdom 31 1.8k 2.4× 147 0.4× 338 1.0× 344 1.2× 234 0.9× 57 2.4k
Robin B. Fitzsimons Australia 18 1.2k 1.6× 171 0.5× 274 0.8× 115 0.4× 223 0.8× 29 1.7k
Satoko Kumada Japan 20 630 0.8× 260 0.7× 289 0.8× 423 1.4× 202 0.7× 86 1.4k
Yeşim Parman Türkiye 23 580 0.8× 637 1.7× 482 1.4× 171 0.6× 99 0.4× 98 1.6k
Pierre Labauge France 23 716 1.0× 1.2k 3.1× 294 0.9× 147 0.5× 190 0.7× 119 2.4k

Countries citing papers authored by Philip Jardine

Since Specialization
Citations

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

Fields of papers citing papers by Philip Jardine

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Philip Jardine

This figure shows the co-authorship network connecting the top 25 collaborators of Philip Jardine. A scholar is included among the top collaborators of Philip Jardine 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 Philip Jardine. Philip Jardine is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Hacohen, Yael, Michael Absoud, Mark Woodhall, et al.. (2013). Autoantibody biomarkers in childhood-acquired demyelinating syndromes: results from a national surveillance cohort. Journal of Neurology Neurosurgery & Psychiatry. 85(4). 456–461. 60 indexed citations
2.
Shah, Siddharth, Sian Ellard, Rachel Kneen, et al.. (2012). Childhood presentation of COL4A1 mutations. Developmental Medicine & Child Neurology. 54(6). 569–574. 53 indexed citations
3.
Proudfoot, Malcolm J., Philip Jardine, Rupert Noad, et al.. (2012). Long-Term Follow-up of a Successfully Treated Case of Congenital Pyridoxine-Dependent Epilepsy. JIMD Reports. 10. 103–106. 13 indexed citations
4.
Williams, Cathy, et al.. (2010). Optic disc drusen masquerading as papilloedema. Archives of Disease in Childhood. 95(8). 629–629. 8 indexed citations
5.
Fong, Choong Yi, Andrew Mumford, Marcus Likeman, & Philip Jardine. (2010). Cerebral palsy in siblings caused by compound heterozygous mutations in the gene encoding protein C. Developmental Medicine & Child Neurology. 52(5). 489–493. 28 indexed citations
6.
Shah, Siddharth, Y Kumar, Brendan McLean, et al.. (2009). A dominantly inherited mutation in collagen IV A1 (COL4A1) causing childhood onset stroke without porencephaly. European Journal of Paediatric Neurology. 14(2). 182–187. 48 indexed citations
7.
Kurian, Manju A., Juan Zhen, Shuyuan Cheng, et al.. (2009). Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia. Journal of Clinical Investigation. 119(6). 1595–603. 148 indexed citations
8.
Khan, Sadaquate, Ingram Wright, Shazia Javed, et al.. (2009). High frequency stimulation of the mamillothalamic tract for the treatment of resistant seizures associated with hypothalamic hamartoma. Epilepsia. 50(6). 1608–1611. 50 indexed citations
9.
Rankin, Julia, Michaela Auer‐Grumbach, Warwick Bagg, et al.. (2008). Extreme phenotypic diversity and nonpenetrance in families with the LMNA gene mutation R644C. American Journal of Medical Genetics Part A. 146A(12). 1530–1542. 80 indexed citations
10.
Majumdar, Anirban, Pilar Póo, J. Colomer, et al.. (2008). Syndrome of fixed dystonia in adolescents – Short term outcome in 4 cases. European Journal of Paediatric Neurology. 13(5). 466–472. 9 indexed citations
11.
Barth, P. G., Monique M. Ryan, Richard Webster, et al.. (2007). Rhabdomyolysis in pontocerebellar hypoplasia type 2 (PCH-2). Neuromuscular Disorders. 18(1). 52–58. 11 indexed citations
12.
Goede, Christian G E L De, Philip Jardine, Paul Eunson, et al.. (2006). Severe progressive late onset myelopathy and arachnoiditis following neonatal meningitis. European Journal of Paediatric Neurology. 10(1). 31–36. 8 indexed citations
13.
Evans, Julie, Hayley Archer, James Colley, et al.. (2005). Early onset seizures and Rett-like features associated with mutations in CDKL5. European Journal of Human Genetics. 13(10). 1113–1120. 135 indexed citations
14.
McDonald, Denise, Maria Kinali, Andrew Gallagher, et al.. (2002). Fracture prevalence in Duchenne muscular dystrophy. Developmental Medicine & Child Neurology. 44(10). 695–8. 133 indexed citations
15.
Kors, E. E., Gisela M. Terwindt, Robin B. Fitzsimons, et al.. (2001). Delayed cerebral edema and fatal coma after minor head trauma: Role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine. Annals of Neurology. 49(6). 753–760. 269 indexed citations
16.
Howells, Rachel, Andrew Curran, Philip Jardine, Ruth Newbury‐Ecob, & Bhupinder Sandhu. (2000). Mesenteric angina complicating a mesodermal anomaly. European Journal of Paediatric Neurology. 4(4). 181–183. 4 indexed citations
17.
18.
Jardine, Philip, et al.. (1994). The association between Coffin‐Lowry syndrome and psychosis: a family study. Journal of Intellectual Disability Research. 38(5). 469–473. 14 indexed citations
19.
Jardine, Philip, Meena Upadhyaya, J. Maynard, Peter S. Harper, & Peter Lunt. (1994). A scapular onset muscular dystrophy without facial involvement: Possible allelism with facioscapulohumeral muscular dystrophy. Neuromuscular Disorders. 4(5-6). 477–482. 18 indexed citations
20.
Jardine, Philip, Manuela C. Koch, Peter Lunt, et al.. (1994). De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1).. Archives of Disease in Childhood. 71(3). 221–227. 25 indexed citations

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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