Matthew S. Rich

The paper introduces PhIAT, a method using PhiC31 integrase to efficiently integrate extrachromosomal arrays into C. elegans chromosomes, enabling stable genomic modifications.

The paper introduces PhIT, a recombinase-based method for modular protein tagging in C. elegans, using CRISPR to insert a landing pad and PhiC31 integrase for tag insertion.

The paper reanalyzes data from Shen et al. to argue that most synonymous mutations in yeast genes are not deleterious, challenging their original conclusions about fitness effects.

The paper shows that CaV1 and CaV2 calcium channels in C. elegans neuromuscular junctions mediate the release of distinct synaptic vesicle pools.

The paper presents C. elegans strains with constitutively expressed Cas9 from integrated transgenes, significantly improving CRISPR editing efficiency and reducing workload.