Rune R. Frants

Biochemistry, Genetics and Molecular Biology · Life Sciences

90h-index31.9kcitations394works0.02yr avg
OpenAlex↗Google Scholar↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Muscle Physiology and Disorders(76), Migraine and Headache Studies(61), Genetic Neurodegenerative Diseases(49), Lipoproteins and Cardiovascular Health(43), RNA Research and Splicing(33)

Publications392 total

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
UNC Libraries·2019Open Access
Correction: Common variant burden contributes to the familial aggregation of migraine in 1,589 families
Neuron·2018
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families
Neuron·2018· 94 citedOpen Access
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
Brain·2016· 167 citedOpen Access
Early-Onset Facioscapulohumeral Muscular Dystrophy Type 1 With Some Atypical Features
Journal of Child Neurology·2014· 19 cited
RNA expression profiling in brains of familial hemiplegic migraine type 1 knock-in mice
Cephalalgia·2013· 9 cited
Genome-wide meta-analysis identifies new susceptibility loci for migraine
Nature Genetics·2013· 402 citedOpen Access
Dysferlin Regulates Cell Adhesion in Human Monocytes
Journal of Biological Chemistry·2013· 69 citedOpen Access
Intrinsic Epigenetic Regulation of the D4Z4 Macrosatellite Repeat in a Transgenic Mouse Model for FSHD
PLoS Genetics·2013· 105 citedOpen Access
Migraine without aura: genome-wide association analysis identifies several novel susceptibility
The Journal of Headache and Pain·2013· 1 citedOpen Access
Migraine is not associated with enhanced atherosclerosis
Cephalalgia·2012· 71 cited
Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2
Nature Genetics·2012· 642 citedOpen Access
Genome-wide association analysis identifies susceptibility loci for migraine without aura
Nature Genetics·2012· 339 citedOpen Access
Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals
PLoS Genetics·2012· 501 citedOpen Access
Facioscapulohumeral Muscular Dystrophy
SpringerReference·2012· 17 cited
Self‐regulated alternative splicing at the AHNAK locus
The FASEB Journal·2011· 36 cited
O.19 Facioscapulohumeral muscular dystrophy: Muscle running out of control
Neuromuscular Disorders·2011
Purkinje Cell-Specific Ablation of CaV2.1 Channels is Sufficient to Cause Cerebellar Ataxia in Mice
The Cerebellum·2011· 50 citedOpen Access
Mutations in ZBTB24 Are Associated with Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome Type 2
The American Journal of Human Genetics·2011· 195 citedOpen Access
Proteomic Analysis of the Dysferlin Protein Complex Unveils Its Importance for Sarcolemmal Maintenance and Integrity
PLoS ONE·2010· 96 citedOpen Access
page 1 of 20Next →

Frequent Co-authors

Michel D. Ferrari(16), Silvère M. van der Maarel(14), Arn M. J. M. van den Maagdenberg(14), Gisela M. Terwindt(13), George W. Padberg(12), Joost Haan(8), Richard J.L.F. Lemmers(8), Lodewijk A. Sandkuijl(8), Marten H. Hofker(6), Cisca Wijmenga(6), Boukje de Vries(6), Roel A. Ophoff(5), Nelleke A. Gruis(5), Jessica C. de Greef(5), Anine H Stam(5), Martin Dichgans(5), Ronald van Eijk(4), Sabrina Sacconi(4), Rabi Tawil(4), Jane Hewitt(4)