# Rikke S. Møller

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/rikke-s-m-ller/

## Facts

| Field | Value |
| --- | --- |
| Citations | 21,949 |
| Field | Genomics and Rare Diseases |
| h-index | 79 |
| i10-index | 233 |
| Last Known Institution | University of Southern Denmark |
| OpenAlex ID | https://openalex.org/A5071894755 |
| ORCID iD | https://orcid.org/0000-0002-9664-1448 |
| Works | 404 |

## Researcher papers

- [Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders](https://scholariq.org/papers/genetic-and-phenotypic-heterogeneity-suggest-therapeutic-implications-in-scn2a/)
- [Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies](https://scholariq.org/papers/genome-wide-mega-analysis-identifies-16-loci-and-highlights-diverse-biological/)
- [Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes](https://scholariq.org/papers/mutations-in-grin2a-cause-idiopathic-focal-epilepsy-with-rolandic-spikes/)
- [De novo variants in neurodevelopmental disorders with epilepsy](https://scholariq.org/papers/de-novo-variants-in-neurodevelopmental-disorders-with-epilepsy/)
- [A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy](https://scholariq.org/papers/a-recurrent-de-novo-mutation-in-kcnc1-causes-progressive-myoclonus-epilepsy/)
- [<i>GRIN2B</i> encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects](https://scholariq.org/papers/i-grin2b-i-encephalopathy-novel-findings-on-phenotype-variant-clustering/)
- [A catalogue of new incidence estimates of monogenic neurodevelopmental disorders caused by de novo variants](https://scholariq.org/papers/a-catalogue-of-new-incidence-estimates-of-monogenic-neurodevelopmental-disorders/)
- [The gain of function <i>SCN1A</i> disorder spectrum: novel epilepsy phenotypes and therapeutic implications](https://scholariq.org/papers/the-gain-of-function-i-scn1a-i-disorder-spectrum-novel-epilepsy-phenotypes-and/)
- [Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32](https://scholariq.org/papers/genome-wide-association-analysis-of-genetic-generalized-epilepsies-implicates/)

## Researcher topics

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Epilepsy research and treatment](https://scholariq.org/topics/epilepsy-research-and-treatment/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Neuroscience and Neuropharmacology Research](https://scholariq.org/topics/neuroscience-and-neuropharmacology-research/)

## Researcher university

- [University of Southern Denmark](https://scholariq.org/institutions/university-of-southern-denmark/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.