Diane S. Roe

1.5k total citations
27 papers, 1.2k citations indexed

About

Diane S. Roe is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, Diane S. Roe has authored 27 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Clinical Biochemistry, 20 papers in Molecular Biology and 8 papers in Physiology. Recurrent topics in Diane S. Roe's work include Metabolism and Genetic Disorders (27 papers), Mitochondrial Function and Pathology (13 papers) and Diet and metabolism studies (6 papers). Diane S. Roe is often cited by papers focused on Metabolism and Genetic Disorders (27 papers), Mitochondrial Function and Pathology (13 papers) and Diet and metabolism studies (6 papers). Diane S. Roe collaborates with scholars based in United States, France and Netherlands. Diane S. Roe's co-authors include Charles R. Roe, Lawrence Sweetman, Henri Brunengraber, France David, David S. Millington, Naoto Terada, Cornelis Jakobs, Donald H. Chace, Naoki Kodo and Rob Kok and has published in prestigious journals such as Journal of Clinical Investigation, Neurology and Biochemical and Biophysical Research Communications.

In The Last Decade

Diane S. Roe

27 papers receiving 1.2k citations

Peers

Diane S. Roe
C. Jakobs Netherlands
Naruji Sugiyama Japan
M. Rimoldi Italy
Mark Korson United States
A. A. M. Morris United Kingdom
Deborah Marsden United States
Kathryn Moseley United States
Carla Carducci Italy
Jennifer R. Toone Canada
María Antònia Vilaseca Spain
C. Jakobs Netherlands
Diane S. Roe
Citations per year, relative to Diane S. Roe Diane S. Roe (= 1×) peers C. Jakobs

Countries citing papers authored by Diane S. Roe

Since Specialization
Citations

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

Fields of papers citing papers by Diane S. Roe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Diane S. Roe. 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 Diane S. Roe. The network helps show where Diane S. Roe may publish in the future.

Co-authorship network of co-authors of Diane S. Roe

This figure shows the co-authorship network connecting the top 25 collaborators of Diane S. Roe. A scholar is included among the top collaborators of Diane S. Roe 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 Diane S. Roe. Diane S. Roe 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.
Roe, Charles R., et al.. (2008). Carnitine palmitoyltransferase II deficiency. Neurology. 71(4). 260–264. 70 indexed citations
2.
Roe, Charles R., et al.. (2007). Choice of oils for essential fat supplements can enhance production of abnormal metabolites in fat oxidation disorders. Molecular Genetics and Metabolism. 92(4). 346–350. 13 indexed citations
3.
Pedersen, Christina B., Claus Bischoff, Ernst Christensen, et al.. (2006). Variations in IBD (ACAD8) in Children with Elevated C4-Carnitine Detected by Tandem Mass Spectrometry Newborn Screening. Pediatric Research. 60(3). 315–320. 26 indexed citations
4.
Roe, Diane S., et al.. (2005). Differentiation of long-chain fatty acid oxidation disorders using alternative precursors and acylcarnitine profiling in fibroblasts. Molecular Genetics and Metabolism. 87(1). 40–47. 20 indexed citations
5.
Gargus, J. Jay, et al.. (2003). Respiratory complex II defect in siblings associated with a symptomatic secondary block in fatty acid oxidation. Journal of Inherited Metabolic Disease. 26(7). 659–670. 13 indexed citations
6.
Roe, Charles R., Lawrence Sweetman, Diane S. Roe, France David, & Henri Brunengraber. (2002). Treatment of cardiomyopathy and rhabdomyolysis in long-chain fat oxidation disorders using an anaplerotic odd-chain triglyceride. Journal of Clinical Investigation. 110(2). 259–269. 186 indexed citations
7.
Roe, Charles R., Lawrence Sweetman, Diane S. Roe, France David, & Henri Brunengraber. (2002). Treatment of cardiomyopathy and rhabdomyolysis in long-chain fat oxidation disorders using an anaplerotic odd-chain triglyceride. Journal of Clinical Investigation. 110(2). 259–269. 4 indexed citations
8.
Tiến, Nguyễn Văn, Brage Storstein Andresen, Thomas J. Corydon, et al.. (2002). Identification of isobutyryl-CoA dehydrogenase and its deficiency in humans. Molecular Genetics and Metabolism. 77(1-2). 68–79. 51 indexed citations
9.
Yang, Bing-Zhi, Diane S. Roe, M. Brivet, et al.. (2001). Carnitine/Acylcarnitine Translocase Deficiency (Neonatal Phenotype): Successful Prenatal and Postmortem Diagnosis Associated with a Novel Mutation in a Single Family. Molecular Genetics and Metabolism. 73(1). 64–70. 27 indexed citations
10.
Roe, Diane S., Christine Vianey‐Saban, Shailja Sharma, M. T. Zabot, & Charles R. Roe. (2001). Oxidation of unsaturated fatty acids by human fibroblasts with very-long-chain acyl-CoA dehydrogenase deficiency: aspects of substrate specificity and correlation with clinical phenotype. Clinica Chimica Acta. 312(1-2). 55–67. 22 indexed citations
11.
Chisholm, Christian A., Mark A. Lovell, Lawrence Sweetman, et al.. (2001). Prenatal diagnosis of multiple acyl‐CoA dehydrogenase deficiency: association with elevated α‐fetoprotein and cystic renal changes. Prenatal Diagnosis. 21(10). 856–859. 9 indexed citations
12.
Roe, Diane S., Charles R. Roe, M. Brivet, & Lawrence Sweetman. (2000). Evidence for a Short-Chain Carnitine–Acylcarnitine Translocase in Mitochondria Specifically Related to the Metabolism of Branched-Chain Amino Acids. Molecular Genetics and Metabolism. 69(1). 69–75. 33 indexed citations
13.
Roe, Charles R. & Diane S. Roe. (2000). Detection of Gene Defects in Branched-Chain Amino Acid Metabolism by Tandem Mass Spectrometry of Carnitine Esters Produced by Cultured Fibroblasts. Methods in enzymology on CD-ROM/Methods in enzymology. 324. 424–431. 5 indexed citations
14.
Gibson, K. Michael, T. Burlingame, Boris M. Hogema, et al.. (2000). 2-Methylbutyryl-Coenzyme A Dehydrogenase Deficiency: A New Inborn Error of L-Isoleucine Metabolism. Pediatric Research. 47(6). 830–833. 70 indexed citations
15.
Roe, Charles R. & Diane S. Roe. (1999). Recent Developments in the Investigation of Inherited Metabolic Disorders Using Cultured Human Cells. Molecular Genetics and Metabolism. 68(2). 243–257. 53 indexed citations
16.
Roe, Charles R., Stephen D. Cederbaum, Diane S. Roe, et al.. (1998). Isolated Isobutyryl-CoA Dehydrogenase Deficiency: An Unrecognized Defect in Human Valine Metabolism. Molecular Genetics and Metabolism. 65(4). 264–271. 59 indexed citations
17.
Yang, Bing-Zhi, Jia-Huan Ding, Diane S. Roe, et al.. (1998). Identification of Four Novel Mutations in Patients with Carnitine Palmitoyltransferase II (CPT II) Deficiency. Molecular Genetics and Metabolism. 64(4). 229–236. 25 indexed citations
18.
Roe, Charles R., Eduard A. Struys, Rob Kok, et al.. (1998). Methylmalonic Semialdehyde Dehydrogenase Deficiency: Psychomotor Delay and Methylmalonic Aciduria without Metabolic Decompensation. Molecular Genetics and Metabolism. 65(1). 35–43. 28 indexed citations
19.
Yang, Bing-Zhi, et al.. (1998). A Novel Mutation Identified in Carnitine Palmitoyltransferase II Deficiency. Molecular Genetics and Metabolism. 63(2). 110–115. 26 indexed citations
20.
Kahler, Stephen G., David S. Millington, Diane S. Roe, et al.. (1994). Intravenous L-Carnitine and Acetyl-L-Carnitine in Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency and Isovaleric Acidemia. Pediatric Research. 35(1). 96–101. 16 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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