Olaug K. Rødningen

1.9k total citations
50 papers, 949 citations indexed

About

Olaug K. Rødningen is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Olaug K. Rødningen has authored 50 papers receiving a total of 949 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 19 papers in Genetics and 17 papers in Surgery. Recurrent topics in Olaug K. Rødningen's work include Lipoproteins and Cardiovascular Health (13 papers), Genomic variations and chromosomal abnormalities (12 papers) and Genetics and Neurodevelopmental Disorders (10 papers). Olaug K. Rødningen is often cited by papers focused on Lipoproteins and Cardiovascular Health (13 papers), Genomic variations and chromosomal abnormalities (12 papers) and Genetics and Neurodevelopmental Disorders (10 papers). Olaug K. Rødningen collaborates with scholars based in Norway, United States and Denmark. Olaug K. Rødningen's co-authors include Trond P. Leren, Jan Alsner, Jens Overgaard, Serena Tonstad, Anne‐Lise Børresen‐Dale, Leiv Ose, Trevor Hastie, Asbjørg Stray‐Pedersen, Oddveig Røsby and K. Berg and has published in prestigious journals such as PLoS ONE, Genome Research and Journal of Lipid Research.

In The Last Decade

Olaug K. Rødningen

48 papers receiving 912 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Olaug K. Rødningen Norway	20	410	310	243	181	130	50	949
Matthew R. Ritter United States	15	561 1.4×	133 0.4×	259 1.1×	79 0.4×	185 1.4×	19	1.1k
Sarah McAvoy United States	17	495 1.2×	284 0.9×	85 0.3×	114 0.6×	105 0.8×	36	1.1k
Marzena Zdanowicz United States	12	990 2.4×	209 0.7×	331 1.4×	78 0.4×	46 0.4×	14	1.4k
Surya P. Rednam United States	11	322 0.8×	150 0.5×	140 0.6×	169 0.9×	33 0.3×	31	766
Jonathan P. Park United States	19	462 1.1×	267 0.9×	88 0.4×	83 0.5×	64 0.5×	36	898
Emilie Lalonde Canada	17	550 1.3×	329 1.1×	60 0.2×	246 1.4×	44 0.3×	30	1.0k
Oskar Koperek Austria	24	299 0.7×	108 0.3×	404 1.7×	143 0.8×	71 0.5×	44	1.3k
Prodipto Pal Canada	17	306 0.7×	213 0.7×	101 0.4×	166 0.9×	43 0.3×	49	956
Adriano Angioni Italy	21	739 1.8×	435 1.4×	176 0.7×	187 1.0×	19 0.1×	56	1.3k
Florian D. Vogl United States	15	278 0.7×	166 0.5×	121 0.5×	219 1.2×	77 0.6×	52	940

Countries citing papers authored by Olaug K. Rødningen

Since Specialization

Citations

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

Fields of papers citing papers by Olaug K. Rødningen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Olaug K. Rødningen. 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 Olaug K. Rødningen. The network helps show where Olaug K. Rødningen may publish in the future.

Co-authorship network of co-authors of Olaug K. Rødningen

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

All Works

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20 of 20 papers shown

Sjursen, Wenche, Anuradha Ravi, Ashish Singh, et al.. (2025). Lynch syndrome caused by SINE-VNTR-Alu-F retrotransposon insert in MSH6 confirmed after 20 years of testing: a case report and literature review. Hereditary Cancer in Clinical Practice. 23(1). 22–22.

Samarakoon, Pubudu, Hanne Sørmo Sorte, Asbjørg Stray‐Pedersen, et al.. (2016). cnvScan: a CNV screening and annotation tool to improve the clinical utility of computational CNV prediction from exome sequencing data. BMC Genomics. 17(1). 51–51. 20 indexed citations

Samarakoon, Pubudu, Hanne Sørmo Sorte, Ying Sheng, et al.. (2014). Identification of copy number variants from exome sequence data. BMC Genomics. 15(1). 661–661. 45 indexed citations

Lund, Caroline, Eylert Brodtkorb, Oddveig Røsby, Olaug K. Rødningen, & Kaja Kristine Selmer. (2013). Copy number variants in adult patients with Lennox–Gastaut syndrome features. Epilepsy Research. 105(1-2). 110–117. 29 indexed citations

Sorte, Hanne Sørmo, Elen Gjevik, Eili Sponheim, Kristin Eiklid, & Olaug K. Rødningen. (2012). Copy number variation findings among 50 children and adolescents with autism spectrum disorder. Psychiatric Genetics. 23(2). 61–69. 9 indexed citations

Selmer, Kaja Kristine, et al.. (2012). A de novo 163 kb interstitial 1q44 microdeletion in a boy with thin corpus callosum, psychomotor delay and seizures. European Journal of Medical Genetics. 55(12). 715–718. 10 indexed citations

Misceo, Doriana, Olaug K. Rødningen, Tuva Barøy, et al.. (2011). A translocation between Xq21.33 and 22q13.33 causes an intragenic SHANK3 deletion in a woman with Phelan–McDermid syndrome and hypergonadotropic hypogonadism. American Journal of Medical Genetics Part A. 155(2). 403–408. 30 indexed citations

Rødningen, Olaug K., Trine Prescott, Randi Hovland, Kristin Eiklid, & Gunnar Houge. (2010). Påvisning av kromosomavvik ved hjelp av DNA-matriser. Tidsskrift for Den norske legeforening. 130(9). 944–947.

Prescott, Trine, et al.. (2009). Two brothers with a microduplication including the MECP2 gene: rapid head growth in infancy and resolution of susceptibility to infection. Clinical Dysmorphology. 18(2). 78–82. 22 indexed citations

10.

Nahas, Shareef, et al.. (2007). Transcriptional response to ionizing radiation in human radiation sensitive cell lines. Radiotherapy and Oncology. 83(3). 256–260. 5 indexed citations

11.

Rødningen, Olaug K., Anne‐Lise Børresen‐Dale, Jan Alsner, Trevor Hastie, & Jens Overgaard. (2007). Radiation-induced gene expression in human subcutaneous fibroblasts is predictive of radiation-induced fibrosis. Radiotherapy and Oncology. 86(3). 314–320. 66 indexed citations

12.

Rødningen, Olaug K., Jens Overgaard, Jan Alsner, Trevor Hastie, & Anne‐Lise Børresen‐Dale. (2005). Microarray analysis of the transcriptional responseto single or multiple doses of ionizing radiation in human subcutaneous fibroblasts. Radiotherapy and Oncology. 77(3). 231–240. 74 indexed citations

13.

Rødningen, Olaug K., et al.. (2000). The genetic algorithm applied to haplotype data at the LDL receptor locus. Computer Methods and Programs in Biomedicine. 61(1). 1–9. 5 indexed citations

14.

Rødningen, Olaug K., Serena Tonstad, Leiv Ose, Kåre Berg, & Trond P. Leren. (1998). Effects of a 9.6-kb deletion of the LDL receptor gene (FH Helsinki) on structure and levels of mRNA. Human Mutation. 12(2). 95–102. 5 indexed citations

15.

Leren, Trond P., Serena Tonstad, Kristian Gundersen, et al.. (1997). Molecular genetics of familial hypercholesterolaemia in Norway. Journal of Internal Medicine. 241(3). 185–193. 48 indexed citations

16.

Rødningen, Olaug K. & Trond P. Leren. (1996). Application of long polymerase chain reaction in the study of the LDL receptor gene. Scandinavian Journal of Clinical and Laboratory Investigation. 56(1). 93–96. 8 indexed citations

17.

Leren, Trond P., et al.. (1994). Two founder mutations in the LDL receptor gene in Norwegian familial hypercholesterolemia subjects. Atherosclerosis. 111(2). 175–182. 50 indexed citations

18.

Leren, Trond P., et al.. (1993). Evaluation of running conditions for SSCP analysis: application of SSCP for detection of point mutations in the LDL receptor gene.. Genome Research. 3(3). 159–162. 36 indexed citations

19.

Rødningen, Olaug K., Trond P. Leren, Oddveig Røsby, et al.. (1993). Haplotype analysis at the low density lipoprotein receptor locus in normal and familial hypercholesterolemia Norwegian subjects. Clinical Genetics. 44(4). 214–220. 15 indexed citations

20.

Rødningen, Olaug K., et al.. (1992). A new polymorphism in exon 11 of the LDL receptor gene in healthy people and in familial hypercholesterolemia subjects. Clinical Genetics. 42(5). 224–228. 2 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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