Author

Ingrid Brænne

Boehringer Ingelheim (Germany)ORCID 0000-0003-4591-0326Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Abdullah Mesut ErzurumluogluiD· 1 shared Aleksandr Kantorovich· 1 shared Boehringer Ingelheim – Global Computational Biology and Digital Sciences· 1 shared Boris BartholdyiD· 1 shared Boris NoyvertiD· 1 shared Christian BeckeriD· 1 shared Clive R. Wood· 1 shared Costas Mistrellides· 1 shared

Activity by Year

2023-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Abdullah Mesut ErzurumluogluORCID

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1 paper

Recent·Most cited

Imputation of structural variants using a multi-ancestry long-read sequencing panel enables identification of disease associations

Boris Noyvert, Abdullah Mesut Erzurumluoglu, Dmitriy Drichel, Steffen Omland, Till F. M. Andlauer, Stefanie Mueller, Lau Sennels, Christian Becker, Aleksandr Kantorovich, Boris Bartholdy, Ingrid Brænne, Julio Cesar Bolivar-Lopez, Costas Mistrellides, Gillian M. Belbin, Jeremiah H. Li, , Zhihao Ding

The paper imputes structural variants using a multi-ancestry long-read sequencing panel and identifies disease associations in large-scale datasets.

medRxiv · Dec 20, 2023 · PreprintGenetic & Genomic Medicine