Rune R. Frants

32.1k citations

317 papers · 18.5k indexed · 4 hit papers · h-index 73

Psychiatry and Mental health top 0.2%
- Migraine and Headache Studies 48
Cellular and Molecular Neuroscience top 0.2%
- Genetic Neurodegenerative Diseases 45
Neurology top 0.5%
Endocrine and Autonomic Systems top 0.5%
Genetics top 0.5%
- Neurogenetic and Muscular Disorders Research 25
Molecular Biology
- Muscle Physiology and Disorders 63
- RNA Research and Splicing 30
Surgery
- Lipoproteins and Cardiovascular Health 34
Cardiology and Cardiovascular Medicine
- Cardiomyopathy and Myosin Studies 24
Endocrinology, Diabetes and Metabolism
- Diabetes, Cardiovascular Risks, and Lipoproteins 20

Co-authors: Michel D. Ferrari Silvère M. van der Maarel George W. Padberg Arn M. J. M. van den Maagdenberg Marten H. Hofker Gisela M. Terwindt Louis M. Havekes Joost Haan
Cited by: Psychiatry and Mental health Cellular and Molecular Neuroscience Neurology
Journals: Science (1 paper)New England Journal of Medicine (1 paper)Cell (1 paper)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Rune R. Frants

315 papers receiving 18.0k citations

Hit Papers

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Peers

Countries citing papers authored by Rune R. Frants

Since Specialization

Citations

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

Fields of papers citing papers by Rune R. Frants

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rune R. Frants. 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 Rune R. Frants. The network helps show where Rune R. Frants may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Rune R. Frants, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Rune R. Frants Line = papers co-authored together Rune R. Frants links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophybreakdown → Science ·Richard J.L.F. Lemmers,Patrick J. van der Vliet,Rinse Klooster,Sabrina Sacconi,Pilar Camaño,Johannes G. Dauwerse,Lauren Snider,Kirsten R. Straasheijm,G J van Ommen,George W. Padberg,Daniel G. Miller,Stephen J. Tapscott,Rabi Tawil,Rune R. Frants,Silvère M. van der Maarel	2010	528
2	Prevalence and heritability of the metabolic syndrome and its individual components in a Dutch isolate: the Erasmus Rucphen Family study Journal of Medical Genetics ·Peter Henneman,Yurii S. Aulchenko,Rune R. Frants,Ko Willems van Dijk,Ben A. Oostra,Cornelia M. van Duijn	2008	76
3	The expression of type III hyperlipoproteinemia: involvement of lipolysis genes European Journal of Human Genetics ·Peter Henneman,Femke van der Sman-de Beer,Payman Hanifi Moghaddam,Petra E.A. Huijts,Anton F. H. Stalenhoef,John J.P. Kastelein,Cornelia M. van Duijn,Louis M. Havekes,Rune R. Frants,Ko Willems van Dijk,A.H.M. Smelt	2008	47
4	Inhibition of neointima formation by local delivery of estrogen receptor alpha and beta specific agonists Cardiovascular Research ·Yvonne D. Krom,Nuno Pires,J. Wouter Jukema,Margreet R. de Vries,Rune R. Frants,L.M. Havekes,K VANDIJK,Paul H.A. Quax	2006	18
5	Genetic Analysis of Indicators of Cholesterol Synthesis and Absorption: Lathosterol and Phytosterols in Dutch Twins and Their Parents Twin Research ·Dorret I. Boomsma,P. Hans,Rune R. Frants,J.A. Gevers Leuven,Herman-Jan M. Kempen	2003	15
6	Active genes in junk DNA? Characterization of DUX genes embedded within 3.3 kb repeated elements Gene ·Marie‐Claire Beckers,Jan Gabriëls,Silvère M. van der Maarel,Astrid De Vriese,Rune R. Frants,Désiré Collen,Alexandra Belayew	2001	35
7	Somatic Pairing Between Subtelomeric Chromosome Regions: Implications for Human Genetic Disease? Chromosome Research ·Karen Stout,Silvère M. van der Maarel,Rune R. Frants,George W. Padberg,Hans‐Hilger Ropers,Thomas Haaf	1999	28
8	Chromosomal localization of the 5-HT1F receptor gene: no evidence for involvement in response to sumatriptan in migraine patients. PubMed ·(unknown),Monique N. Vergouwe,Roel A. Ophoff,Susan L. Naylor,Hans G. Dauwerse,Pramod R. Saxena,Michel D. Ferrari,Rune R. Frants	1998	19
9	Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4breakdown → Cell ·Roel A. Ophoff,Gisela M. Terwindt,Monique N. Vergouwe,Ronald van Eijk,Peter J. Oefner,Susan M.G. Hoffman,Jane E. Lamerdin,Harvey W. Mohrenweiser,Dennis E. Bulman,Maurizio Ferrari,Joost Haan,Dick Lindhout,Gert‐Jan B. van Ommen,Marten H. Hofker,Michel D. Ferrari,Rune R. Frants	1996	1758
10	Variable expression of familial dysbetalipoproteinemia in apolipoprotein E2 (Lys146-->Gln) Allele carriers. Journal of Clinical Investigation* ·Peter de Knijff,Arn M. J. M. van den Maagdenberg,D.I. Boomsma,Anton F. H. Stalenhoef,A.H.M. Smelt,John J.P. Kastelein,A. David Marais,Rune R. Frants,Louis M. Havekes	1994	18
11	Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral musculatur dystrophy (FSHD) Human Genetics ·S. Cacurri,Giancarlo Deidda,N. Piazzo,Andrea Novelletto,I. La Cesa,Serenella Servidei,Giuliana Galluzzi,Cisca Wijmenga,Rune R. Frants,L. Felicetti	1994	12
12	Linkage and apparent heterogeneity in proximal spinal muscular atrophies Neuromuscular Disorders ·Jan M. Cobben,Hans Scheffer,Marjolein Visser,Jan Osinga,Rune R. Frants,Gerrit van der Steege,Cisca Wijmenga,Leo P. ten Kate,Gert‐Jan B. van Ommen,Charles H.C.M. Buys	1993	8
13	Heparan sulphate proteoglycans are involved in the lipoprotein lipase-mediated enhancement of the cellular binding of very low density and low density lipoproteins Biochemical and Biophysical Research Communications ·Monique Mulder,Paola Lombardi,Hans Jansen,Theo J.C. van Berkel,Rune R. Frants,Louis M. Havekes	1992	106
14	Dinucleotide repeat polymorphism adjacent to the ANT1 gene on 4q35 Nucleic Acids Research ·Cisca Wijmenga,Larry L. Deaven,Rune R. Frants	1992	3
15	The familial hypercholesterolemia (FH)-North Karelia mutation of the low density lipoprotein receptor gene deletes seven nucleotides of exon 6 and is a common cause of FH in Finland. Journal of Clinical Investigation ·Ulla‐Maija Koivisto,Hannu Turtola,Katriina Aalto‐Setälä,Bert Top,Rune R. Frants,Petri T. Kovanen,A C Syvänen,Kimmo Kontula	1992	90
16	Familial dysbetalipoproteinemia associated with apolipoprotein E3-Leiden in an extended multigeneration pedigree. Journal of Clinical Investigation ·Peter de Knijff,Arn M. J. M. van den Maagdenberg,A.F.H. Stalenhoef,J.A. Gevers Leuven,Pierre N.M. Demacker,L. P. Kuyt,Rune R. Frants,Louis M. Havekes	1991	84
17	Characterisation of the LDL receptor in Epstein-Barr virus transformed lymphocytes Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism ·Paola Lombardi,E. de Wit,Rune R. Frants,Louis M. Havekes	1990	5
18	Salivary Protein Polymorphism in Kenya: Evidence for a New <i>AMY1 </i>Allele Human Heredity ·Jan C. Pronk,Wim J. Jansen,Appolo Pronk,Christien F.A.M.v.d. Pol,Rune R. Frants,Aldur W. Eriksson	1984	14
19	A New Unstable PI M Variant of a<sub>1</sub>-Antitrypsin in a Finnish Isolate Human Heredity ·Rune R. Frants,Aldur W. Eriksson	1980	5
20	Reliable Classification of Six Pi M Subtypes by Separator Isoelectric Focusing Human Heredity ·Rune R. Frants,Aldur W. Eriksson	1978	65

About Rune R. Frants

Rune R. Frants is a scholar working on Psychiatry and Mental health, Cellular and Molecular Neuroscience and Genetics, having authored 317 papers that have together received 18.5k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (63 papers), Migraine and Headache Studies (48 papers), Genetic Neurodegenerative Diseases (45 papers), Lipoproteins and Cardiovascular Health (34 papers), RNA Research and Splicing (30 papers), Neurogenetic and Muscular Disorders Research (25 papers), Cardiomyopathy and Myosin Studies (24 papers) and Diabetes, Cardiovascular Risks, and Lipoproteins (20 papers). The work is most often cited by research in Psychiatry and Mental health (4.0k citations), Cellular and Molecular Neuroscience (3.5k citations) and Neurology (1.4k citations). Rune R. Frants has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Michel D. Ferrari, Silvère M. van der Maarel, George W. Padberg, Arn M. J. M. van den Maagdenberg, Marten H. Hofker, Gisela M. Terwindt, Louis M. Havekes, Joost Haan, Lodewijk A. Sandkuijl and Roel A. Ophoff. Their work appears in journals such as Science, New England Journal of Medicine and Cell.

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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