Hugh Lemonde

704 total citations
15 papers, 457 citations indexed

About

Hugh Lemonde is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Hugh Lemonde has authored 15 papers receiving a total of 457 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Clinical Biochemistry, 9 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Hugh Lemonde's work include Metabolism and Genetic Disorders (12 papers), Genomics and Rare Diseases (3 papers) and Mitochondrial Function and Pathology (3 papers). Hugh Lemonde is often cited by papers focused on Metabolism and Genetic Disorders (12 papers), Genomics and Rare Diseases (3 papers) and Mitochondrial Function and Pathology (3 papers). Hugh Lemonde collaborates with scholars based in United Kingdom, United States and Netherlands. Hugh Lemonde's co-authors include Jonathan Wareham, Benjamin Hughes, Indra Joshi, Peter T. Clayton, E.G. van Grunsven, Ronald J. A. Wanders, Jerzy Adamski, D Cuebas, Lodewijk IJlst and P. Vreken and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Gut and Journal of Proteome Research.

In The Last Decade

Hugh Lemonde

14 papers receiving 440 citations

Peers

Hugh Lemonde

HEALT

COMMU

GHP

J. M. Chaves United States

Laura O’Grady Canada

Mohammad Reza Abedini Iran

Alessandra Zullo Italy

Michele Ruggiero Italy

Jennifer Collins United States

Nana Meng China

Joyce V. Lee Singapore

Christian Köhler Germany

Anne-Marie Tassé Canada

J. M. Chaves United States

Hugh Lemonde

173 ×1.0

52 ×0.4

3 ×0.0

HEALT

15 ×0.2

COMMU

21 ×0.3

GHP

Citations per year, relative to Hugh Lemonde Hugh Lemonde (= 1×) peers J. M. Chaves

Countries citing papers authored by Hugh Lemonde

Since Specialization

Citations

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

Fields of papers citing papers by Hugh Lemonde

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hugh Lemonde

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

All Works

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15 of 15 papers shown

Selvanathan, Arthavan, Sanjay Bansal, Emer Fitzpatrick, et al.. (2025). Early postnatal hepatocyte transplantation in a child with molybdenum cofactor deficiency type B. Molecular Genetics and Metabolism. 145(1). 109079–109079. 1 indexed citations

Carling, Rachel S., Anupam Chakrapani, Patricia Hall, et al.. (2024). Retrospective Review of Positive Newborn Screening Results for Isovaleric Acidemia and Development of a Strategy to Improve the Efficacy of Newborn Screening in the UK. International Journal of Neonatal Screening. 10(1). 24–24.

Lemonde, Hugh, et al.. (2019). Newborn screening for inborn errors of metabolism. Paediatrics and Child Health. 29(3). 105–110. 7 indexed citations

Moat, Stuart J., Hugh Lemonde, James R. Bonham, et al.. (2019). Performance of laboratory tests used to measure blood phenylalanine for the monitoring of patients with phenylketonuria. Journal of Inherited Metabolic Disease. 43(2). 179–188. 28 indexed citations

Davison, James, Hugh Lemonde, & Shamima Rahman. (2019). Inherited mitochondrial disease. Paediatrics and Child Health. 29(3). 116–122. 4 indexed citations

Sobczyńska‐Malefora, Agata, et al.. (2017). An infant and mother with severe B12 deficiency: vitamin B12 status assessment should be determined in pregnant women with anaemia. European Journal of Clinical Nutrition. 71(8). 1013–1015. 5 indexed citations

Lemonde, Hugh & Shamima Rahman. (2015). Inherited mitochondrial disease. Paediatrics and Child Health. 25(3). 133–138. 5 indexed citations

Lemonde, Hugh, Maureen Cleary, & Anupam Chakrapani. (2014). Newborn screening for inborn errors of metabolism. Paediatrics and Child Health. 25(3). 103–107. 8 indexed citations

Heywood, Wendy, Philippa B. Mills, Stephanie Grünewald, et al.. (2013). A New Method for the Rapid Diagnosis of Protein N-linked Congenital Disorders of Glycosylation. Journal of Proteome Research. 12(7). 3471–3479. 15 indexed citations

10.

Hughes, Benjamin, Indra Joshi, Hugh Lemonde, & Jonathan Wareham. (2009). Junior physician's use of Web 2.0 for information seeking and medical education: A qualitative study. International Journal of Medical Informatics. 78(10). 645–655. 164 indexed citations

11.

Lemonde, Hugh, et al.. (2003). Mutations in SRD5B1 ( AKR1D1 ), the gene encoding Δ ⁴ -3-oxosteroid 5β-reductase, in hepatitis and liver failure in infancy. Gut. 52(10). 1494–1499. 76 indexed citations

12.

Lemonde, Hugh, et al.. (1999). The identification of unusual bile acid metabolites by tandem mass spectrometry: use of low‐energy collision‐induced dissociation to produce informative spectra. Rapid Communications in Mass Spectrometry. 13(12). 1159–1164. 1 indexed citations

13.

Lemonde, Hugh, Andrew Johnson, & Peter T. Clayton. (1999). The identification of unusual bile acid metabolites by tandem mass spectrometry: use of low‐energy collision‐induced dissociation to produce informative spectra. Rapid Communications in Mass Spectrometry. 13(12). 1159–1164. 17 indexed citations

14.

Grunsven, E.G. van, et al.. (1998). Bifunctional protein deficiency: Complementation within the same group suggesting differential enzyme defects and clues to the underlying basis. Journal of Inherited Metabolic Disease. 21(3). 298–301. 4 indexed citations

15.

Grunsven, E.G. van, Lodewijk IJlst, P. Vreken, et al.. (1998). Peroxisomal d -hydroxyacyl-CoA dehydrogenase deficiency: Resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency. Proceedings of the National Academy of Sciences. 95(5). 2128–2133. 122 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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