Author

Alena Stančáková

University of Eastern Finland

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetics· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 3 Assay:GWAS summary statistics· 2 Organism:human· 2 Organism:Drosophila· 1 Research Focus:fine-mapping· 1 Research Focus:GWAS / association mapping· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Markku LaaksoiD· 3 shared Andrew Tym HattersleyiD· 2 shared Jaakko TuomilehtoiD· 2 shared Jerome I. RotteriD· 2 shared Johanna KuusistoiD· 2 shared Karen L. MohlkeiD· 2 shared Leif GroopiD· 2 shared Sharon LR Kardia· 2 shared

Activity by Year

2017-2018 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetics

Markku LaaksoORCID

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3 papers

Recent·Most cited

GeneticsbioRxivPreprintOct 30, 2018

Genome-wide association and functional studies identify 46 novel loci for alcohol consumption and suggest common genetic mechanisms with neuropsychiatric disorders

Εvangelos Εvangelou, He Gao, Congying Chu…·Paul Elliott

This study identifies 46 novel genetic loci associated with alcohol consumption and suggests shared genetic mechanisms with neuropsychiatric disorders using GWAS and functional analyses.

2 citations

DrosophilaGWAS summary statistics

𝕏 PostBluesky

GenomicsbioRxivPreprintJan 9, 2018

Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

Anubha Mahajan, Daniel Taliun, Matthias Thurner…·Claudia Langenberg

This study fine-maps type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps, identifying 73 variants with >80% posterior probability of association.

37 citations

humanGWAS summary statistics

𝕏 PostBluesky

GeneticsNature CommunicationsPeer-reviewedOct 6, 2017

Heterozygous RFX6 protein truncating variants cause Maturity-Onset Diabetes of the Young (MODY) with reduced penetrance

Kashyap Amratlal Patel, Jarno L. T. Kettunen, Markku Laakso…·Michael N. Weedon

This study identifies heterozygous RFX6 protein truncating variants as a cause of MODY with reduced penetrance, using genetic analysis and cohort comparisons.

139 citationstop 1%

humanwhole-exome sequencing

𝕏 PostBluesky