E. Young

1.1k total citations
23 papers, 768 citations indexed

About

E. Young is a scholar working on Physiology, Molecular Biology and Epidemiology. According to data from OpenAlex, E. Young has authored 23 papers receiving a total of 768 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Physiology, 7 papers in Molecular Biology and 6 papers in Epidemiology. Recurrent topics in E. Young's work include Lysosomal Storage Disorders Research (17 papers), Trypanosoma species research and implications (6 papers) and Carbohydrate Chemistry and Synthesis (5 papers). E. Young is often cited by papers focused on Lysosomal Storage Disorders Research (17 papers), Trypanosoma species research and implications (6 papers) and Carbohydrate Chemistry and Synthesis (5 papers). E. Young collaborates with scholars based in United Kingdom, India and Netherlands. E. Young's co-authors include Ashok Vellodi, Bryan Winchester, Victoria Lidchi, Kevin Mills, C. Phillip Morris, Stephen Waldek, J. E. Wraith, Alan Cooper, Johannes Rainer and A. D. Patrick and has published in prestigious journals such as Journal of Nutrition, Journal of Neurology Neurosurgery & Psychiatry and Archives of Disease in Childhood.

In The Last Decade

E. Young

22 papers receiving 736 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
E. Young United Kingdom 15 664 281 179 175 148 23 768
Ya. V. Voznyi Russia 12 592 0.9× 248 0.9× 171 1.0× 206 1.2× 105 0.7× 19 685
Cordula Steglich Germany 16 609 0.9× 358 1.3× 132 0.7× 226 1.3× 158 1.1× 24 805
R J Desnick United States 12 778 1.2× 309 1.1× 205 1.1× 245 1.4× 212 1.4× 20 941
Josanne Cox‐Brinkman Netherlands 9 886 1.3× 375 1.3× 285 1.6× 242 1.4× 200 1.4× 11 991
Rosanna Gatti Italy 17 422 0.6× 141 0.5× 167 0.9× 298 1.7× 195 1.3× 35 808
A. H. Fensom United Kingdom 14 329 0.5× 111 0.4× 76 0.4× 175 1.0× 63 0.4× 31 725
Norberto Guelbert Argentina 16 514 0.8× 216 0.8× 105 0.6× 148 0.8× 232 1.6× 39 651
Robert Dobrovolný Czechia 13 640 1.0× 302 1.1× 208 1.2× 154 0.9× 180 1.2× 17 753
Shuan-Pei Lin Taiwan 19 371 0.6× 210 0.7× 65 0.4× 239 1.4× 206 1.4× 39 793
Shu-Chuan Chiang Taiwan 10 426 0.6× 179 0.6× 102 0.6× 208 1.2× 197 1.3× 20 721

Countries citing papers authored by E. Young

Since Specialization
Citations

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

Fields of papers citing papers by E. Young

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E. Young

This figure shows the co-authorship network connecting the top 25 collaborators of E. Young. A scholar is included among the top collaborators of E. Young 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 E. Young. E. Young 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.
Young, E., Kevin Mills, C. Phillip Morris, et al.. (2005). Is globotriaosylceramide a useful biomarker in Fabry disease?. Acta Paediatrica. 94(s447). 51–54. 102 indexed citations
2.
Jackson, Marie, Peter T. Clayton, Stephanie Grünewald, et al.. (2005). Elevation of plasma aspartylglucosaminidase is a useful marker for the congenital disorders of glycosylation type I (CDG I). Journal of Inherited Metabolic Disease. 28(6). 1197–1198. 9 indexed citations
3.
Young, E., Kevin Mills, C. Phillip Morris, et al.. (2005). Is globotriaosylceramide a useful biomarker in Fabry disease?. Acta Paediatrica. 94(0). 51–54. 68 indexed citations
4.
Mills, Kevin, C. Phillip Morris, Ashok Vellodi, et al.. (2005). Measurement of urinary CDH and CTH by tandem mass spectrometry in patients hemizygous and heterozygous for Fabry disease. Journal of Inherited Metabolic Disease. 28(1). 35–48. 56 indexed citations
5.
Vellodi, Ashok, E. Young, Alan Cooper, et al.. (1999). Long‐term follow‐up following bone marrow transplantation for Hunter disease. Journal of Inherited Metabolic Disease. 22(5). 638–648. 128 indexed citations
6.
Voznyi, Ya. V., J. L. M. Keulemans, Grazia M.S. Mancini, et al.. (1999). A new simple enzyme assay for pre- and postnatal diagnosis of infantile neuronal ceroid lipofuscinosis (INCL) and its variants. Journal of Medical Genetics. 36(6). 471–474. 29 indexed citations
7.
Young, E., et al.. (1999). Bone marrow transplantation for Maroteaux–Lamy syndrome (MPS VI): Long‐term follow‐up. Journal of Inherited Metabolic Disease. 22(1). 50–62. 100 indexed citations
8.
Cragg, Helen, Magali Williamson, E. Young, et al.. (1997). Fucosidosis: genetic and biochemical analysis of eight cases.. Journal of Medical Genetics. 34(2). 105–110. 16 indexed citations
9.
10.
Grider, Arthur & E. Young. (1996). The Acrodermatitis Enteropathica Mutation Transiently Affects Zinc Metabolism in Human Fibroblasts. Journal of Nutrition. 126(1). 219–224. 10 indexed citations
11.
Vellodi, Ashok, Helen Cragg, Bryan Winchester, et al.. (1995). Allogeneic bone marrow transplantation for fucosidosis.. PubMed. 15(1). 153–8. 38 indexed citations
12.
Williamson, Magali, Helen Cragg, Keith A. Kretz, et al.. (1993). A 5' splice site mutation in fucosidosis.. Journal of Medical Genetics. 30(3). 218–223. 14 indexed citations
13.
Malcolm, S, et al.. (1993). The molecular detection of the pseudodeficiency allele for arylsulphatase A in patients with neurological symptoms and low arylsulphatase A activity. Journal of Inherited Metabolic Disease. 16(6). 1048–1049. 2 indexed citations
14.
Vellodi, Ashok, et al.. (1992). Bone marrow transplantation for Sanfilippo disease type B. Journal of Inherited Metabolic Disease. 15(6). 911–918. 44 indexed citations
15.
Diggelen, O. P. van, et al.. (1990). Prenatal diagnosis of morquio disease type a using a simple fluorometric enzyme assay. Prenatal Diagnosis. 10(2). 85–91. 19 indexed citations
16.
Thomas, P. K., E. Young, & R. H. M. King. (1989). Sandhoff disease mimicking adult-onset bulbospinal neuronopathy.. Journal of Neurology Neurosurgery & Psychiatry. 52(9). 1103–1106. 17 indexed citations
17.
Lane, A.B., et al.. (1980). Segregation of Tay-Sachs and Sandhoff alleles in a non-Jewish family.. PubMed. 32(6). 920–6. 1 indexed citations
18.
Young, E., et al.. (1975). Variability of acid hydrolase activities in cultured skin fibroblasts and amniotic fluid cells.. Journal of Medical Genetics. 12(3). 224–229. 25 indexed citations
19.
Young, E., John Wilson, A. D. Patrick, & L. Crome. (1972). Galactocerebrosidase Deficiency in Globoid Cell Leucodystrophy of Late Onset. Archives of Disease in Childhood. 47(253). 449–450. 12 indexed citations
20.
Young, E., et al.. (1972). Leukocyte -galactosidase activity in GM 1 -gangliosidosis.. PubMed. 50(3). 502–3. 8 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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