Rune R. Frants
Publications by Year
Research Areas
Muscle Physiology and Disorders, Migraine and Headache Studies, Genetic Neurodegenerative Diseases, Lipoproteins and Cardiovascular Health, RNA Research and Splicing
Most-Cited Works
- → Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4(1996)2,331 cited
- → New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk(2010)2,224 cited
- → Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus(1994)848 cited
- → A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy(2010)763 cited
- → A Cacna1a Knockin Migraine Mouse Model with Increased Susceptibility to Cortical Spreading Depression(2004)688 cited
- → Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy(1992)678 cited
- → Localization of the gene for Cowden disease to chromosome 10q22–23(1996)669 cited
- → Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2(2012)647 cited
- → Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals(2012)508 cited
- → C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy(2007)447 cited