Author

Costas Mistrellides

Boehringer Ingelheim (Germany)

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

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

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 Dmitriy DricheliD· 1 shared

Activity by Year

2023-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenetic & Genomic Medicine

Abdullah Mesut ErzurumluogluORCID

Mutual co-authors in cluster

Author profile →

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