Author

Klaudia Walter

Primary ORCID profile (0000-0003-4448-0301 · 19 papers)Unclaimed ORCID profile · follow to get notified of new preprints

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Klaudia WalteriD19 papers · Wellcome Sanger Institute

Biology Disciplines

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Research Focus:fine-mapping· 1 Research Focus:GWAS / association mapping· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Aarno Palotie· 1 shared Himanshu Chheda· 1 shared Mark Daly· 1 shared Matti PirineniD· 1 shared Priit PaltaiD· 1 shared Richard Durbin· 1 shared Samuli RipattiiD· 1 shared Seppo Koskinen· 1 shared

Activity by Year

2016-2016 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Aarno Palotie

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1 paper

Recent·Most cited

Whole genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United Kingdom

Himanshu Chheda, Priit Palta, Matti Pirinen, Shane McCarthy, Klaudia Walter, Seppo Koskinen, Veikko Salomaa, Mark Daly, Richard Durbin, Aarno Palotie, Tero Aittokallio, Samuli Ripatti

The paper compares genome sequences from Finnish and British populations to identify genetic variants enriched in a population bottleneck, finding significant enrichment of rare variants in Finns.

bioRxiv · Jul 12, 2016Genetics