P. J. Lee

548 total citations
20 papers, 366 citations indexed

About

P. J. Lee is a scholar working on Rheumatology, Clinical Biochemistry and Physiology. According to data from OpenAlex, P. J. Lee has authored 20 papers receiving a total of 366 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Rheumatology, 11 papers in Clinical Biochemistry and 7 papers in Physiology. Recurrent topics in P. J. Lee's work include Metabolism and Genetic Disorders (11 papers), Folate and B Vitamins Research (9 papers) and Glycogen Storage Diseases and Myoclonus (7 papers). P. J. Lee is often cited by papers focused on Metabolism and Genetic Disorders (11 papers), Folate and B Vitamins Research (9 papers) and Glycogen Storage Diseases and Myoclonus (7 papers). P. J. Lee collaborates with scholars based in United Kingdom, Australia and Mexico. P. J. Lee's co-authors include Robin Lachmann, A. Briddon, Ashley L. Cole, Patrick Deegan, S. Waldek, Derralynn Hughes, Helen Mundy, Paolo Muiesan, Nigel Heaton and F. Maillot and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Amino Acids and Journal of Intellectual Disability Research.

In The Last Decade

P. J. Lee

20 papers receiving 351 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
P. J. Lee United Kingdom 13 186 170 156 109 48 20 366
Sabrina Paci Italy 12 169 0.9× 196 1.2× 132 0.8× 148 1.4× 44 0.9× 31 404
J H Walter United Kingdom 14 100 0.5× 277 1.6× 97 0.6× 125 1.1× 116 2.4× 29 457
İlyas Okur Türkiye 12 136 0.7× 78 0.5× 86 0.6× 124 1.1× 42 0.9× 62 372
Surekha Pendyal United States 9 128 0.7× 158 0.9× 214 1.4× 89 0.8× 25 0.5× 21 366
Mark Sharrard United Kingdom 10 73 0.4× 178 1.0× 116 0.7× 212 1.9× 66 1.4× 21 439
Serap Sivri Türkiye 11 145 0.8× 182 1.1× 62 0.4× 120 1.1× 52 1.1× 53 342
Ayesha Ahmad United States 13 85 0.5× 120 0.7× 62 0.4× 151 1.4× 66 1.4× 37 392
Ann Wessel United States 11 141 0.8× 274 1.6× 78 0.5× 119 1.1× 56 1.2× 18 309
A Burlina Italy 7 79 0.4× 263 1.5× 92 0.6× 212 1.9× 55 1.1× 17 374
A Baldellou Spain 10 194 1.0× 163 1.0× 80 0.5× 160 1.5× 38 0.8× 23 392

Countries citing papers authored by P. J. Lee

Since Specialization
Citations

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

Fields of papers citing papers by P. J. Lee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by P. J. Lee. 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 P. J. Lee. The network helps show where P. J. Lee may publish in the future.

Co-authorship network of co-authors of P. J. Lee

This figure shows the co-authorship network connecting the top 25 collaborators of P. J. Lee. A scholar is included among the top collaborators of P. J. Lee 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 P. J. Lee. P. J. Lee 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.
Guest, Julian F., et al.. (2012). Costs and outcomes over 36 years of patients with phenylketonuria who do and do not remain on a phenylalanine‐restricted diet. Journal of Intellectual Disability Research. 57(6). 567–579. 29 indexed citations
2.
Martín‐Hernández, Elena, et al.. (2009). Long‐term needs of adult patients with organic acidaemias: outcome and prognostic factors. Journal of Inherited Metabolic Disease. 32(4). 523–533. 19 indexed citations
3.
Mundy, Helen, Jane Williams, P. J. Lee, & Mary Fewtrell. (2008). Reduction in bone mineral density in glycogenosis type III may be due to a mixed muscle and bone deficit. Journal of Inherited Metabolic Disease. 31(3). 418–423. 12 indexed citations
4.
Cole, Ashley L., P. J. Lee, Derralynn Hughes, et al.. (2007). Depression in adults with Fabry disease: A common and under‐diagnosed problem. Journal of Inherited Metabolic Disease. 30(6). 943–951. 83 indexed citations
5.
Ramachandran, Radha & P. J. Lee. (2007). Pancreatic calcification in a patient with homocystinuria. Journal of Inherited Metabolic Disease. 31(1). 124–126. 1 indexed citations
6.
Maillot, F., et al.. (2007). A practical approach to maternal phenylketonuria management. Journal of Inherited Metabolic Disease. 30(2). 198–201. 28 indexed citations
7.
Mundy, Helen, et al.. (2006). The effect of L‐alanine therapy in a patient with adult onset glycogen storage disease type II. Journal of Inherited Metabolic Disease. 29(1). 226–229. 14 indexed citations
8.
Lee, P. J. & A. Briddon. (2006). A rationale for cystine supplementation in severe homocystinuria. Journal of Inherited Metabolic Disease. 30(1). 35–38. 15 indexed citations
9.
Mundy, Helen, et al.. (2005). Exercise Capacity and Biochemical Profile during Exercise in Patients with Glycogen Storage Disease Type I. The Journal of Clinical Endocrinology & Metabolism. 90(5). 2675–2680. 8 indexed citations
10.
Haase, Claudia M., et al.. (2005). Social outcome in treated individuals with inherited metabolic disorders: UK study. Journal of Inherited Metabolic Disease. 28(6). 825–830. 16 indexed citations
11.
Cartwright, Donna, et al.. (2004). Raised HDL cholesterol in Fabry disease: Response to enzyme replacement therapy. Journal of Inherited Metabolic Disease. 27(6). 791–793. 14 indexed citations
12.
Hallam, P., M. Lilburn, & P. J. Lee. (2004). A new protein substitute for adolescents and adults with maple syrup urine disease (MSUD). Journal of Inherited Metabolic Disease. 28(5). 665–672. 1 indexed citations
13.
Lee, P. J., Paolo Muiesan, & Nigel Heaton. (2004). Successful pregnancy after combined renal–hepatic transplantation in glycogen storage disease type Ia. Journal of Inherited Metabolic Disease. 27(4). 537–538. 22 indexed citations
14.
Hargreaves, Iain P., Simon Heales, A. Briddon, John M. Land, & P. J. Lee. (2003). Blood mononuclear cell coenzyme Q10 concentration and mitochondrial respiratory chain succinate cytochrome‐c reductase activity in phenylketonuric patients. Journal of Inherited Metabolic Disease. 25(8). 673–679. 14 indexed citations
15.
Hargreaves, I., Simon Heales, A. Briddon, et al.. (2003). Primary pyruvate dehydrogenase E3 binding protein deficiency with mild hyperlactataemia and hyperalaninaemia. Journal of Inherited Metabolic Disease. 26(5). 505–506. 5 indexed citations
16.
Hargreaves, I., P. J. Lee, & A. Briddon. (2002). Homocysteine and cysteine - albumin binding in homocystinuria: assessment of cysteine status and implications for glutathione synthesis?. Amino Acids. 22(2). 109–118. 17 indexed citations
17.
Lee, P. J.. (2002). Growing older: The adult metabolic clinic. Journal of Inherited Metabolic Disease. 25(3). 252–260. 35 indexed citations
18.
Bonham, James R., Ian McDowell, P. J. Lee, et al.. (2002). Vitamin C therapy ameliorates vascular endothelial dysfunction in treated patients with homocystinuria. Journal of Inherited Metabolic Disease. 25(2). 107–118. 23 indexed citations
19.
Wilson, Callum, P. J. Lee, & J. V. Leonard. (2001). Plasma glutamine and ammonia concentrations in ornithine carbamoyltransferase deficiency and citrullinaemia. Journal of Inherited Metabolic Disease. 24(7). 691–695. 7 indexed citations
20.
Mundy, Helen, et al.. (2001). Successful pregnancy outcome in atypical hyperglycinaemia. Journal of Inherited Metabolic Disease. 24(5). 599–600. 3 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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