Author

Tania Kümpfel

Institut für Klinische NeuroimmunologieORCID 0000-0001-7509-5268Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Abdulrahman SalhabiD· 1 shared Adam SantanielloiD· 1 shared An GorisiD· 1 shared Anne Haney CrossiD· 1 shared Anne SpurklandiD· 1 shared Antonios BayasiD· 1 shared Ashley Harris BeechamiD· 1 shared Benedicte A. LieiD· 1 shared

Activity by Year

2018-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenomics

Abdulrahman SalhabORCID

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2 papers

Recent·Most cited

GenomicsNature CommunicationsPeer-reviewedMay 7, 2019

DNA methylation signatures of a large cohort monozygotic twins clinically discordant for multiple sclerosis

Nicole Y. Souren, Lisa Ann Gerdes, Pavlo Lutsik…·Jörn Walter

The paper identifies DNA methylation differences in monozygotic twins discordant for multiple sclerosis, highlighting treatment effects and genetic confounders.

88 citationstop 1%

humanDNA methylation

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GeneticsCellPeer-reviewedOct 18, 2018

Low frequency and rare coding variation contributes to multiple sclerosis risk

Mitja Mitrovič, Nikolaos A. Patsopoulos, Ashley Harris Beecham…·Hakon H. Hakonarson

The paper identifies low-frequency coding variants contributing to multiple sclerosis risk using a large case-control study.

173 citationstop 1%

humanGWAS summary statistics

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