M A Preece

1.1k total citations
26 papers, 710 citations indexed

About

M A Preece is a scholar working on Clinical Biochemistry, Molecular Biology and Surgery. According to data from OpenAlex, M A Preece has authored 26 papers receiving a total of 710 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Clinical Biochemistry, 7 papers in Molecular Biology and 6 papers in Surgery. Recurrent topics in M A Preece's work include Metabolism and Genetic Disorders (17 papers), Amino Acid Enzymes and Metabolism (6 papers) and Neonatal Health and Biochemistry (4 papers). M A Preece is often cited by papers focused on Metabolism and Genetic Disorders (17 papers), Amino Acid Enzymes and Metabolism (6 papers) and Neonatal Health and Biochemistry (4 papers). M A Preece collaborates with scholars based in United Kingdom, United States and France. M A Preece's co-authors include H. Burton, Schuyler O. Sanderson, Patrick McKiernan, A. Green, A C J Hutchesson, Sarah Bundey, Anita MacDonald, Paul Gissen, Harry Willshaw and Saikat Santra and has published in prestigious journals such as Neurology, British Journal of Haematology and American Journal of Transplantation.

In The Last Decade

M A Preece

24 papers receiving 686 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M A Preece United Kingdom 14 420 270 160 145 126 26 710
Karine Mention France 18 280 0.7× 263 1.0× 174 1.1× 134 0.9× 76 0.6× 43 885
Gaetano Sabetta Italy 10 402 1.0× 340 1.3× 125 0.8× 174 1.2× 62 0.5× 11 631
J H Walter United Kingdom 14 277 0.7× 125 0.5× 100 0.6× 116 0.8× 46 0.4× 29 457
Barry H. Thompson United States 9 420 1.0× 291 1.1× 242 1.5× 204 1.4× 40 0.3× 15 870
Dorothea Möslinger Austria 14 358 0.9× 274 1.0× 177 1.1× 98 0.7× 52 0.4× 31 572
Leyla Tümer Türkiye 15 149 0.4× 218 0.8× 175 1.1× 126 0.9× 35 0.3× 84 663
Sabine Illsinger Germany 14 230 0.5× 227 0.8× 122 0.8× 87 0.6× 29 0.2× 32 491
Shawn E. McCandless United States 17 604 1.4× 495 1.8× 372 2.3× 299 2.1× 82 0.7× 34 1.2k
Inderneel Sahai United States 12 191 0.5× 187 0.7× 53 0.3× 134 0.9× 36 0.3× 34 530
A. Briddon United Kingdom 10 220 0.5× 169 0.6× 68 0.4× 61 0.4× 116 0.9× 25 465

Countries citing papers authored by M A Preece

Since Specialization
Citations

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

Fields of papers citing papers by M A Preece

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M A Preece. 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 M A Preece. The network helps show where M A Preece may publish in the future.

Co-authorship network of co-authors of M A Preece

This figure shows the co-authorship network connecting the top 25 collaborators of M A Preece. A scholar is included among the top collaborators of M A Preece 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 M A Preece. M A Preece 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.
Santra, Saikat, Anita MacDonald, M A Preece, Rikke Katrine Jentoft Olsen, & Brage Storstein Andresen. (2016). Long-term outcome of isobutyryl-CoA dehydrogenase deficiency diagnosed following an episode of ketotic hypoglycaemia. Molecular Genetics and Metabolism Reports. 10. 28–30. 12 indexed citations
2.
Preece, M A, et al.. (2016). How to use a controlled fast to investigate hypoglycaemia. Archives of Disease in Childhood Education & Practice. 102(1). 28–36. 4 indexed citations
3.
Charbit‐Henrion, Fabienne, Florence Lacaille, Patrick McKiernan, et al.. (2015). Early and Late Complications After Liver Transplantation for Propionic Acidemia in Children: A Two Centers Study. American Journal of Transplantation. 15(3). 786–791. 51 indexed citations
4.
Gökmen-Özel, Hülya, Anita MacDonald, Anne Daly, et al.. (2012). Dietary practices in glutaric aciduria type 1 over 16 years. Journal of Human Nutrition and Dietetics. 25(6). 514–519. 12 indexed citations
5.
Santra, Saikat, et al.. (2008). Renal tubular function in children with tyrosinaemia type I treated with nitisinone. Journal of Inherited Metabolic Disease. 31(3). 399–402. 26 indexed citations
6.
MacDonald, Anita, et al.. (2007). Prospective treatment in carnitine–acylcarnitine translocase deficiency. Journal of Inherited Metabolic Disease. 30(5). 815–815. 33 indexed citations
7.
Sanderson, Schuyler O., et al.. (2006). The incidence of inherited metabolic disorders in the West Midlands, UK. Archives of Disease in Childhood. 91(11). 896–899. 165 indexed citations
8.
Baumann, Ulrich, et al.. (2004). Hyperinsulinism in tyrosinaemia type I. Journal of Inherited Metabolic Disease. 28(2). 131–135. 41 indexed citations
9.
Gissen, Paul, M A Preece, Harry Willshaw, & Patrick McKiernan. (2003). Ophthalmic follow‐up of patients with tyrosinaemia type I on NTBC. Journal of Inherited Metabolic Disease. 26(1). 13–16. 40 indexed citations
10.
Lee, Way Seah, Patrick McKiernan, Sue V. Beath, et al.. (2001). Bile bilirubin pigment analysis in disorders of bilirubin metabolism in early infancy. Archives of Disease in Childhood. 85(1). 38–42. 10 indexed citations
11.
Holme, E., Susan Standing, M A Preece, et al.. (2001). Outcome of tyrosinaemia type III. Journal of Inherited Metabolic Disease. 24(8). 824–832. 44 indexed citations
12.
Green, A., et al.. (1999). Biochemical monitoring of treatment for galactosaemia: Biological variability in metabolite concentrations. Journal of Inherited Metabolic Disease. 22(2). 139–148. 27 indexed citations
13.
Hutchesson, A C J, et al.. (1998). A comparison of disease and gene frequencies of inborn errors of metabolism among different ethnic groups in the West Midlands, UK.. Journal of Medical Genetics. 35(5). 366–370. 58 indexed citations
14.
Baumann, Ürsula, et al.. (1996). 130 HYPERINSULINISM IN TYROSINAEMIA TYPE I. Journal of Pediatric Gastroenterology and Nutrition. 22(4). 441–441.
15.
Hutchesson, A C J, S. K. Hall, M A Preece, & A. Green. (1996). Screening for tyrosinaemia type I.. Archives of Disease in Childhood Fetal & Neonatal. 74(3). F191–F194. 19 indexed citations
16.
Buchanan, E, et al.. (1992). Intensive enteral feeding in advanced cirrhosis: reversal of malnutrition without precipitation of hepatic encephalopathy.. Archives of Disease in Childhood. 67(5). 603–607. 48 indexed citations
17.
Puntis, John W.L., et al.. (1989). Egg and breast milk based nitrogen sources compared.. Archives of Disease in Childhood. 64(10). 1472–1477. 10 indexed citations
18.
Preece, M A. (1986). Human growth after birth. Early Human Development. 14(2). 163–164. 14 indexed citations
19.
Preece, M A & R G Newall. (1977). Dextrostix-Eyetone in the insulin hypoglycaemia test.. BMJ. 2(6080). 152–154. 8 indexed citations
20.
Preece, M A & H B Valman. (1975). Vitamin D status after resection of ileum in childhood.. Archives of Disease in Childhood. 50(4). 283–285. 9 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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