Author

Alexander Dietl

University Hospital RegensburgORCID 0000-0002-4091-8620Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Physiology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 1 Research Focus:development & morphogenesis· 1 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Research Focus:metabolism & bioenergetics· 1

Frequent Co-Authors

Alessandra ChesiiD· 1 shared Alessandro DelitalaiD· 1 shared Alexander G. NickeliD· 1 shared Aliki‐Eleni FarmakiiD· 1 shared Alireza AniiD· 1 shared Amy L MooreiD· 1 shared Anders Ulrik EliaseniD· 1 shared Andrej Kasakow· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetics

Alessandra ChesiORCID

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2 papers

Recent·Most cited

Mitochondrial reactive oxygen species cause arrhythmias in hypertrophic cardiomyopathy

Michael Kohlhaas, Vasco Sequeira, Shan S. Parikh, Alexander Dietl, Olga Richter, Johannes Bay, Edoardo Bertero, Julia Schwemmlein, Xiao Yu Tian, Felix W. Friedrich, Frederik Flenner, Alexander G. Nickel, Felix Michael Alscher, Maithily S. Nanadikar, Raghav Venkataraman, , Christoph Maack

This study shows that mitochondrial reactive oxygen species contribute to arrhythmias in hypertrophic cardiomyopathy by disrupting calcium handling and electrical conduction.

bioRxiv · Oct 2, 2024 · PreprintPhysiology

A Saturated Map of Common Genetic Variants Associated with Human Height from 5.4 Million Individuals of Diverse Ancestries

Loïc Yengo, Sailaja Vedantam, Eirini Marouli, Julia Sidorenko, Eric Bartell, Saori Sakaue, Marielisa Graff, Anders Ulrik Eliasen, Yunxuan Jiang, Sridharan Raghavan, Jenkai Miao, Joshua D. Arias, Ronen E. Mukamel, Cassandra Nichole Spracklen, Xianyong Yin, , Thomas Folkmann Hansen

This study identifies 12,111 SNPs associated with height from 5.4 million individuals, explaining most common SNP-based heritability and showing ancestry-specific prediction accuracy.

bioRxiv · Jan 7, 2022 · PreprintGenetics