Aster V. E. Harder

MedicineNeuroscienceBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 7 papers. Top paper: “Genotype-phenotype correlations in SCN8A -related disorders reveal prognostic and therapeutic implications”.

Genotype-phenotype correlations in SCN8A -related disorders reveal prognostic and therapeutic implications

Brain(2021)10.1093/brain/awab321

N/A

2.9DataRank · unranked

149 citations

Yuanyuan Liu, Mahmoud Koko, Cathrine E. Gjerulfsen, Lukas Sonnenberg, Julian Schubert +95 more

Diagnosing migraine from genome-wide genotype data: a machine learning analysis

Brain(2025)10.1093/brain/awaf172

N/A

0.269DataRank · unranked

5 citations

Tjaša Kumelj, Bendik S Winsvold, Marte‐Helene Bjørk, Parashkev Nachev, Manjit Matharu +70 more

Genotype-phenotype correlations in SCN8A -related disorders reveal prognostic and therapeutic implications

medRxiv(2021)10.1101/2021.03.22.21253711

N/A

0DataRank · unranked

5 citations

Yuanyuan Liu, Cathrine E. Gjerulfsen, Mahmoud Koko, Lukas Sonnenberg, Julian Schubert +95 more

Migraine, inflammatory bowel disease and celiac disease: A Mendelian randomization study

Headache The Journal of Head and Face Pain(2023)10.1111/head.14470

N/A

0DataRank · unranked

13 citations

Gull Rukh, Mathias Rask‐Andersen, Aster V. E. Harder, Arn M. J. M. van den Maagdenberg, Helgi B. Schiöth +2 more

Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene

European Journal of Human Genetics(2023)10.1038/s41431-023-01489-4

N/A

0DataRank · unranked

8 citations

Francesco Danilo Tiziano, Mohamad A. Mikati, Lisanne S. Vijfhuizen, Sophie Nicole, Gaëtan Lesca +19 more

Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles

Nature Genetics(2022)10.1038/s41588-021-00990-0

N/A

0DataRank · unranked

399 citations

Bendik Slagsvold Winsvold, Sanni Ruotsalainen, Gyða Björnsdóttir, Aster V. E. Harder, Lisette J. A. Kogelman +68 more

Genetic Susceptibility Loci in Genomewide Association Study of Cluster Headache

Annals of Neurology(2021)10.1002/ana.26146

N/A

0DataRank · unranked

64 citations

Bendik Slagsvold Winsvold, Raymond Noordam, Lisanne S. Vijfhuizen, Sigrid Børte, Lisette J. A. Kogelman +18 more