Olaug K. Rødningen

1.9k citations

50 papers · 949 indexed · h-index 20

Molecular Biology
Genetics top 10%
Surgery
Cancer Research top 10%
Radiology, Nuclear Medicine and Imaging top 10%

Co-authors: Trond P. Leren Jens Overgaard Jan Alsner Serena Tonstad Anne‐Lise Børresen‐Dale Leiv Ose Trevor Hastie Asbjørg Stray‐Pedersen
Topics: Lipoproteins and Cardiovascular Health (13 papers)Genomic variations and chromosomal abnormalities (12 papers)Genetics and Neurodevelopmental Disorders (10 papers)
Cited by: Cancer Research Genetics Molecular Biology
Journals: PLoS ONE Genome Research Journal of Lipid Research
Partner nations: Norway United States Denmark

In The Last Decade

Olaug K. Rødningen

48 papers receiving 912 citations

Peers

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

#	Work	Indexed citations
1	Lynch syndrome caused by SINE-VNTR-Alu-F retrotransposon insert in MSH6 confirmed after 20 years of testing: a case report and literature review 2025 ·Hereditary Cancer in Clinical Practice ·Wenche Sjursen,(unknown),(unknown),Anuradha Ravi,(unknown),Ashish Singh,Jostein Johansen,Olaug K. Rødningen,(unknown),(unknown),(unknown),Kristine Misund	0
2	cnvScan: a CNV screening and annotation tool to improve the clinical utility of computational CNV prediction from exome sequencing data 2016 ·BMC Genomics ·Pubudu Samarakoon,Hanne Sørmo Sorte,Asbjørg Stray‐Pedersen,Olaug K. Rødningen,Torbjørn Rognes,Robert Lyle	20
3	Microdeletions Including FMR1 in Three Female Patients with Intellectual Disability - Further Delineation of the Phenotype and Expression Studies 2014 ·Molecular Syndromology ·Alexander M. Zink,Eva Wohlleber,Hartmut Engels,Olaug K. Rødningen,Kirstine Ravn,Stefanie Heilmann‐Heimbach,(unknown),(unknown),Cornelia Kraus,Susanne Blichfeldt,Per Hoffmann,Heiko Reutter,F.F. Brockschmidt,Martina Kreiß‐Nachtsheim,P. H. Vogt,Trine Prescott,Zeynep Tümer,(unknown)	6
4	Haploinsufficiency of XPO1 and USP34 by a de novo 230 kb deletion in 2p15, in a patient with mild intellectual disability and cranio-facial dysmorphisms 2014 ·European Journal of Medical Genetics ·Madeleine Fannemel,Tuva Barøy,Asbjørn Holmgren,Olaug K. Rødningen,(unknown),(unknown),Eirik Frengen,Doriana Misceo	28
5	SNP in TXNRD2 Associated With Radiation-Induced Fibrosis: A Study of Genetic Variation in Reactive Oxygen Species Metabolism and Signaling 2013 ·International Journal of Radiation OncologyBiologyPhysics ·Hege Edvardsen,(unknown),Kristin V. Reinertsen,Xi Zhao,(unknown),Daniel Nebdal,Ann-Christine Syvänen,Olaug K. Rødningen,Jan Alsner,Jens Overgaard,Anne‐Lise Børresen‐Dale,Sophie D. Fosså,Vessela N. Kristensen	45
6	Copy number variation findings among 50 children and adolescents with autism spectrum disorder 2012 ·Psychiatric Genetics ·Hanne Sørmo Sorte,Elen Gjevik,Eili Sponheim,Kristin Eiklid,Olaug K. Rødningen	9
7	Severe ALG8-CDG (CDG-Ih) associated with homozygosity for two novel missense mutations detected by exome sequencing of candidate genes 2012 ·European Journal of Medical Genetics ·Hanne Sørmo Sorte,Lars Mørkrid,Olaug K. Rødningen,Mari Ann Kulseth,Asbjørg Stray‐Pedersen,Gert Matthijs,Valérie Race,Gunnar Houge,Torunn Fiskerstrand,(unknown),Robert Lyle,Trine Prescott	12
8	A de novo 163 kb interstitial 1q44 microdeletion in a boy with thin corpus callosum, psychomotor delay and seizures 2012 ·European Journal of Medical Genetics ·Kaja Kristine Selmer,(unknown),Olaug K. Rødningen,Madeleine Fannemel	10
9	A translocation between Xq21.33 and 22q13.33 causes an intragenic SHANK3 deletion in a woman with Phelan–McDermid syndrome and hypergonadotropic hypogonadism 2011 ·American Journal of Medical Genetics Part A ·Doriana Misceo,Olaug K. Rødningen,Tuva Barøy,Hanne Sørmo Sorte,Jan Roar Mellembakken,Petter Strømme,Madeleine Fannemel,Eirik Frengen	30
10	Two brothers with a microduplication including the MECP2 gene: rapid head growth in infancy and resolution of susceptibility to infection 2009 ·Clinical Dysmorphology ·Trine Prescott,Olaug K. Rødningen,(unknown),Asbjørg Stray‐Pedersen	22
11	Transcriptional response to ionizing radiation in human radiation sensitive cell lines 2007 ·Radiotherapy and Oncology ·(unknown),Shareef Nahas,Jørgen Aarøe,Richard A. Gatti,(unknown),Olaug K. Rødningen	5
12	Radiation-induced gene expression in human subcutaneous fibroblasts is predictive of radiation-induced fibrosis 2007 ·Radiotherapy and Oncology ·Olaug K. Rødningen,Anne‐Lise Børresen‐Dale,Jan Alsner,Trevor Hastie,Jens Overgaard	66
13	Ocular findings in Norwegian patients with ataxia‐telangiectasia: a 5 year prospective cohort study 2007 ·Acta Ophthalmologica Scandinavica ·Ruth Riise,Jan Ygge,(unknown),Asbjørg Stray‐Pedersen,Toke Bek,Olaug K. Rødningen,Arvid Heiberg	16
14	Microarray analysis of the transcriptional responseto single or multiple doses of ionizing radiation in human subcutaneous fibroblasts 2005 ·Radiotherapy and Oncology ·Olaug K. Rødningen,Jens Overgaard,Jan Alsner,Trevor Hastie,Anne‐Lise Børresen‐Dale	74
15	Molecular genetics of familial hypercholesterolaemia in Norway 1997 ·Journal of Internal Medicine ·Trond P. Leren,Serena Tonstad,Kristian Gundersen,(unknown),Olaug K. Rødningen,Hilde Sundvold,Leiv Ose,K. Berg	48
16	Application of long polymerase chain reaction in the study of the LDL receptor gene 1996 ·Scandinavian Journal of Clinical and Laboratory Investigation ·Olaug K. Rødningen,Trond P. Leren	8
17	Two founder mutations in the LDL receptor gene in Norwegian familial hypercholesterolemia subjects 1994 ·Atherosclerosis ·Trond P. Leren,(unknown),Olaug K. Rødningen,Serena Tonstad,Leiv Ose	50
18	Evaluation of running conditions for SSCP analysis: application of SSCP for detection of point mutations in the LDL receptor gene. 1993 ·Genome Research ·Trond P. Leren,(unknown),Olaug K. Rødningen,Leiv Ose,Serena Tonstad,K. Berg	36
19	Haplotype analysis at the low density lipoprotein receptor locus in normal and familial hypercholesterolemia Norwegian subjects 1993 ·Clinical Genetics ·Olaug K. Rødningen,Trond P. Leren,Oddveig Røsby,Serena Tonstad,Leiv Ose,Kåre Berg	15
20	A 9.6 kilobase deletion in the low density lipoprotein receptor gene in Norwegian familial hypercholesterolemia subjects 1992 ·Clinical Genetics ·Olaug K. Rødningen,(unknown),Serena Tonstad,Leiv Ose,Kåre Berg,(unknown)	12

About Olaug K. Rødningen

Olaug K. Rødningen is a scholar working on Cancer Research, Genetics and Developmental Biology, having authored 50 papers that have together received 949 indexed citations. Recurring topics across this work include Lipoproteins and Cardiovascular Health (13 papers), Genomic variations and chromosomal abnormalities (12 papers) and Genetics and Neurodevelopmental Disorders (10 papers). The work is most often cited by research in Cancer Research (181 citations), Genetics (310 citations) and Molecular Biology (410 citations). Olaug K. Rødningen has collaborated with scholars based in Norway, United States and Denmark. Frequent co-authors include Trond P. Leren, Jens Overgaard, Jan Alsner, Serena Tonstad, Anne‐Lise Børresen‐Dale, Leiv Ose, Trevor Hastie, Asbjørg Stray‐Pedersen, Oddveig Røsby and Hanne Sørmo Sorte. Their work appears in journals such as PLoS ONE, Genome Research and Journal of Lipid Research.

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