Ference J. Loupatty

524 total citations
9 papers, 395 citations indexed

About

Ference J. Loupatty is a scholar working on Molecular Biology, Clinical Biochemistry and Surgery. According to data from OpenAlex, Ference J. Loupatty has authored 9 papers receiving a total of 395 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 5 papers in Clinical Biochemistry and 1 paper in Surgery. Recurrent topics in Ference J. Loupatty's work include Metabolism and Genetic Disorders (5 papers), Mitochondrial Function and Pathology (4 papers) and ATP Synthase and ATPases Research (3 papers). Ference J. Loupatty is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Mitochondrial Function and Pathology (4 papers) and ATP Synthase and ATPases Research (3 papers). Ference J. Loupatty collaborates with scholars based in Netherlands, Switzerland and Australia. Ference J. Loupatty's co-authors include Ronald J. A. Wanders, Marinus Durán, Jos P.N. Ruiter, Lodewijk IJlst, W. Lehnert, Marcel J.W. Janssen, Madelon M. Buijs, F.A.L. van der Horst, Jos P.M. Wielders and Annemieke C. Heijboer and has published in prestigious journals such as The American Journal of Human Genetics, Clinical Chemistry and NMR in Biomedicine.

In The Last Decade

Ference J. Loupatty

9 papers receiving 386 citations

Peers

Ference J. Loupatty
Ference J. Loupatty
Citations per year, relative to Ference J. Loupatty Ference J. Loupatty (= 1×) peers Khalid Mehmood Raja

Countries citing papers authored by Ference J. Loupatty

Since Specialization
Citations

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

Fields of papers citing papers by Ference J. Loupatty

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ference J. Loupatty

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

All Works

9 of 9 papers shown
1.
2.
Janssen, Marcel J.W., Jos P.M. Wielders, Lianne S.M. Boesten, et al.. (2012). Multicenter comparison study of current methods to measure 25-hydroxyvitamin D in serum. Steroids. 77(13). 1366–1372. 72 indexed citations
3.
Wanders, Ronald J. A., Marinus Durán, & Ference J. Loupatty. (2010). Enzymology of the branched‐chain amino acid oxidation disorders: the valine pathway. Journal of Inherited Metabolic Disease. 35(1). 5–12. 67 indexed citations
4.
Loupatty, Ference J., Peter T. Clayton, Jos P.N. Ruiter, et al.. (2006). Mutations in the Gene Encoding 3-Hydroxyisobutyryl-CoA Hydrolase Results in Progressive Infantile Neurodegeneration. The American Journal of Human Genetics. 80(1). 195–199. 66 indexed citations
5.
Loupatty, Ference J., Annemarie van der Steen, Lodewijk IJlst, et al.. (2006). Clinical, biochemical, and molecular findings in three patients with 3-hydroxyisobutyric aciduria. Molecular Genetics and Metabolism. 87(3). 243–248. 15 indexed citations
6.
Engelke, Udo F. H., Berry Kremer, Leo A. J. Kluijtmans, et al.. (2006). NMR spectroscopic studies on the late onset form of 3‐methylglutaconic aciduria type I and other defects in leucine metabolism. NMR in Biomedicine. 19(2). 271–278. 45 indexed citations
7.
Rosa, Gabriella Di, Federica Deodato, Ference J. Loupatty, et al.. (2006). Hypertrophic cardiomyopathy, cataract, developmental delay, lactic acidosis: A novel subtype of 3‐methylglutaconic aciduria. Journal of Inherited Metabolic Disease. 29(4). 546–550. 24 indexed citations
8.
Loupatty, Ference J., Jos P.N. Ruiter, Lodewijk IJlst, Marinus Durán, & Ronald J. A. Wanders. (2004). Direct Nonisotopic Assay of 3-Methylglutaconyl-CoA Hydratase in Cultured Human Skin Fibroblasts to Specifically Identify Patients with 3-Methylglutaconic Aciduria Type I. Clinical Chemistry. 50(8). 1447–1450. 9 indexed citations
9.
IJlst, Lodewijk, Ference J. Loupatty, Jos P.N. Ruiter, et al.. (2002). 3-Methylglutaconic Aciduria Type I Is Caused by Mutations in AUH. The American Journal of Human Genetics. 71(6). 1463–1466. 57 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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