Mette Gilling

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

Davina J. Hensman Moss, Antonio F. Pardiñas, Douglas R. Langbehn et al. · The Lancet Neurology · 2017 · 332 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Breakpoint Cloning and Haplotype Analysis Indicate a Single Origin of the Common Inv(10)(p11.2q21.2) Mutation among Northern Europeans

Mette Gilling, J Dullinger, Stefan Gesk et al. · The American Journal of Human Genetics · 2006 · 96 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

Linked Registries: Connecting Rare Diseases Patient Registries through a Semantic Web Layer

Pedro Sernadela, Lorena González-Castro, Claudio Carta et al. · BioMed Research International · 2017 · 56 citations · Full text

Computing, Biomedical Informatics, Health Informatics +13

Dysfunction of the Heteromeric KV7.3/KV7.5 Potassium Channel is Associated with Autism Spectrum Disorders

Mette Gilling, Hanne B. Rasmussen, Kirstine Calløe et al. · Frontiers in Genetics · 2013 · 55 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Clinical manifestations of intermediate allele carriers in Huntington disease

Esther Cubo, María A. Ramos-Arroyo, Saül Martínez‐Horta et al. · Neurology · 2016 · 54 citations

Life Sciences, Genetics, Neurology +13