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Hannah S. Seidel

Researcher at Eastern Michigan University

Publications -  23
Citations -  1351

Hannah S. Seidel is an academic researcher from Eastern Michigan University. The author has contributed to research in topics: Germline & Stem cell. The author has an hindex of 12, co-authored 20 publications receiving 1205 citations. Previous affiliations of Hannah S. Seidel include University of Wisconsin-Madison & Princeton University.

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Widespread genetic incompatibility in C. elegans maintained by balancing selection.

TL;DR: The data suggest that long-term maintenance of a balanced polymorphism has permitted the incompatibility in Caenorhabditis elegans to persist despite gene flow across the rest of the genome.
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Population genomic analysis of outcrossing and recombination in yeast.

TL;DR: A method to infer the evolutionary history of a species from genome sequences of multiple individuals was developed and applied to whole-genome sequence data from three strains of Saccharomyces cerevisiae and the sister species SacCharomyces paradoxus and provides the initial foundation for population studies of association between genotype and phenotype in S. cerevisia.

A Novel Sperm-Delivered Toxin Causes Late-Stage Embryo Lethality and Transmission Ratio Distortion in C. elegans

TL;DR: A sperm-delivered toxin and an embryo-expressed antidote form a co-adapted gene complex in C. elegans that promotes its own transmission to the detriment of organisms carrying it.
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A Novel Sperm-Delivered Toxin Causes Late-Stage Embryo Lethality and Transmission Ratio Distortion in C. elegans

TL;DR: In this paper, a sperm-delivered toxin, peel-1, and an embryo-expressed antidote, zeel-1 are shown to gain a transmission advantage through a combination of paternal-effect killing and zygotic self-rescue.
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A Powerful New Quantitative Genetics Platform, Combining Caenorhabditis elegans High-Throughput Fitness Assays with a Large Collection of Recombinant Strains

TL;DR: This new strain collection removes variation in the neuropeptide receptor gene npr-1, known to have large physiological and behavioral effects on C. elegans, and mitigates the hybrid strain incompatibility caused by zeel-1 and peel- 1, allowing for identification of quantitative trait loci that otherwise would have been masked by those effects.