Berit Woldseth

502 total citations
20 papers, 253 citations indexed

About

Berit Woldseth is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Berit Woldseth has authored 20 papers receiving a total of 253 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Clinical Biochemistry and 7 papers in Physiology. Recurrent topics in Berit Woldseth's work include Metabolism and Genetic Disorders (11 papers), Amino Acid Enzymes and Metabolism (3 papers) and Biochemical and Molecular Research (3 papers). Berit Woldseth is often cited by papers focused on Metabolism and Genetic Disorders (11 papers), Amino Acid Enzymes and Metabolism (3 papers) and Biochemical and Molecular Research (3 papers). Berit Woldseth collaborates with scholars based in Norway, Sweden and Denmark. Berit Woldseth's co-authors include Bjørn O. Christophersen, Kjetil Retterstøl, Petter Strømme, Trine B. Haugen, Bjørn Tvedt, Terje Rootwelt, Ulrik Fredrik Malt, Martin P. Bogsrud, Gisle Langslet and Leiv Ose and has published in prestigious journals such as Human Molecular Genetics, Metabolism and Acta Paediatrica.

In The Last Decade

Berit Woldseth

18 papers receiving 243 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Berit Woldseth Norway 10 149 81 52 38 32 20 253
Jean Demarquoy France 8 155 1.0× 47 0.6× 28 0.5× 60 1.6× 27 0.8× 13 273
Pim de Blaauw Netherlands 10 110 0.7× 162 2.0× 64 1.2× 107 2.8× 21 0.7× 17 244
Monique Albersen Netherlands 12 109 0.7× 154 1.9× 39 0.8× 50 1.3× 10 0.3× 17 292
Stefan Koelker Germany 3 142 1.0× 214 2.6× 79 1.5× 39 1.0× 11 0.3× 3 272
Civonnia Harris United States 7 247 1.7× 112 1.4× 27 0.5× 86 2.3× 66 2.1× 9 402
Alvin D. Pewa United States 4 210 1.4× 41 0.5× 35 0.7× 87 2.3× 21 0.7× 5 301
Lisa Sniderman King United States 7 90 0.6× 191 2.4× 57 1.1× 75 2.0× 11 0.3× 12 263
Jeanne M. Hassing United States 11 91 0.6× 44 0.5× 22 0.4× 36 0.9× 15 0.5× 14 328
Natalie M. Villa United States 8 61 0.4× 184 2.3× 46 0.9× 14 0.4× 75 2.3× 17 404
Toshiaki Oura Japan 10 124 0.8× 173 2.1× 35 0.7× 37 1.0× 13 0.4× 25 277

Countries citing papers authored by Berit Woldseth

Since Specialization
Citations

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

Fields of papers citing papers by Berit Woldseth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Berit Woldseth

This figure shows the co-authorship network connecting the top 25 collaborators of Berit Woldseth. A scholar is included among the top collaborators of Berit Woldseth 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 Berit Woldseth. Berit Woldseth 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.
Rustad, Cecilie F., Paul Hoff Backe, Chunsheng Jin, et al.. (2024). A monoallelic UXS1 variant associated with short‐limbed short stature. Molecular Genetics & Genomic Medicine. 12(6). e2472–e2472.
2.
3.
Reigstad, Hallvard, Berit Woldseth, & Johannes Häberle. (2017). Normal Neurological Development During Infancy Despite Massive Hyperammonemia in Early Treated NAGS Deficiency. JIMD Reports. 37. 45–47. 5 indexed citations
4.
Bremer, Sara, et al.. (2016). Identification of a novel BCKDHA deletion causing maple syrup urine disease. Meta Gene. 10. 86–89. 2 indexed citations
5.
Barøy, Tuva, Janet Koster, Petter Strømme, et al.. (2015). A novel type of rhizomelic chondrodysplasia punctata, RCDP5, is caused by loss of the PEX5 long isoform. Human Molecular Genetics. 24(20). 5845–5854. 57 indexed citations
6.
Scheffler, Katja, et al.. (2014). Genome instability in Maple Syrup Urine Disease correlates with impaired mitochondrial biogenesis. Metabolism. 63(8). 1063–1070. 14 indexed citations
7.
Bogsrud, Martin P., Gisle Langslet, Leiv Ose, et al.. (2013). No effect of combined coenzyme Q10 and selenium supplementation on atorvastatin-induced myopathy. Scandinavian Cardiovascular Journal. 47(2). 80–87. 38 indexed citations
8.
Woldseth, Berit, et al.. (2012). Metabolic acidosis mimicking diabetic ketoacidosis after use of calorie-free mineral water. European Journal of Pediatrics. 171(9). 1405–1407. 4 indexed citations
9.
Bliksrud, Yngve Thomas, et al.. (2012). Hereditary tyrosinaemia type I in Norway: Incidence and three novel small deletions in the fumarylacetoacetase gene. Scandinavian Journal of Clinical and Laboratory Investigation. 72(5). 369–373. 14 indexed citations
10.
Bremer, Sara, Annika Ohlsson, Helge Rootwelt, et al.. (2011). A novel mucopolysaccharidosis type I associated splice site mutation and IDUA splice variants. Molecular Genetics and Metabolism. 104(3). 289–294. 2 indexed citations
11.
Backe, Paul Hoff, Magnar Bjørås, Terje Rootwelt, et al.. (2010). Four novel mutations identified in Norwegian patients result in intermittent maple syrup urine disease when combined with the R301C mutation. Molecular Genetics and Metabolism. 100(4). 324–332. 9 indexed citations
12.
Elgstøen, Katja Benedikte Prestø, et al.. (2010). Liquid chromatography-tandem mass spectrometry determination of oxalate in spot urine. Scandinavian Journal of Clinical and Laboratory Investigation. 70(3). 145–150. 9 indexed citations
13.
Woldseth, Berit, et al.. (2007). 2-methylbutyryl-CoA dehydrogenase deficiency associated with autism and mental retardation: a case report. Journal of Medical Case Reports. 1(1). 98–98. 24 indexed citations
14.
Strømme, Petter, et al.. (2007). Incidence rates of progressive childhood encephalopathy in Oslo, Norway: a population based study. BMC Pediatrics. 7(1). 25–25. 19 indexed citations
15.
Strømme, Petter, et al.. (2007). Mortality in childhood progressive encephalopathy from 1985 to 2004 in Oslo, Norway: a population‐based study. Acta Paediatrica. 97(1). 35–40. 5 indexed citations
16.
Woldseth, Berit & Terje Rootwelt. (2006). [Mitochondrial beta-oxidation defects].. PubMed. 126(6). 756–9. 5 indexed citations
17.
Retterstøl, Kjetil, Trine B. Haugen, Berit Woldseth, & Bjørn O. Christophersen. (1998). A comparative study of the metabolism of n-9, n-6 and n-3 fatty acids in testicular cells from immature rat. Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism. 1392(1). 59–72. 28 indexed citations
18.
Retterstøl, Kjetil, Berit Woldseth, & Bjørn O. Christophersen. (1996). The metabolism of 22:5(−6) and of docosahexaenoic acid [22:6(−3)] compared in rat hepatocytes. Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism. 1303(3). 180–186. 5 indexed citations
19.
Woldseth, Berit & Bjørn O. Christophersen. (1994). Biosynthesis of phospholipid molecular species in isolated liver cells studied by combining fatty acid substrates esterified in the sn-1 and sn-2 positions. Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism. 1213(1). 39–45. 4 indexed citations
20.
Woldseth, Berit, Erik Christensen, & Bjørn O. Christophersen. (1993). Incorporation of stearic acid (18:0) and palmitic acid (16:0) in phospholipid molecular species studied in isolated rat liver cells. Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism. 1167(3). 296–302. 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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