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Genetics|November 17, 2021
A motor independent requirement for dynein light chain in Caenorhabditis elegans meiotic synapsisSara M Fielder, Tori Kent, Huiping Ling, et al.
Micropublication Biology|December 22, 2025
Null Mutant mig-15(udn323) Shows Touch Receptor Neuron Migration Defects in C. elegansSara DaCunha, Gary A Silverman, Tim Schedl, et al.
Molecular Genetics and Metabolism|April 1, 2022
Functional analysis of a novel de novo variant in PPP5C associated with microcephaly, seizures, and developmental delaySara M Fielder, Jill A Rosenfeld, Lindsay C Burrage, et al.
Autophagy Reports|July 29, 2024
A fluorescent reporter for rapid assessment of autophagic flux reveals unique autophagy signatures during C. elegans post-embryonic development and identifies compounds that modulate autophagyZachary D Dawson, Hemalatha Sundaramoorthi, Suk Regmi, et al.
Human Molecular Genetics|December 30, 2025
Phenotypic expansion of CALM1/2-associated disorders to include neurologic phenotypes without arrhythmiaHieu D Hoang, Rebecca C Spillmann, Daniel J Wegner, et al.
Medrxiv : the Preprint Server for Health Sciences|July 17, 2025
Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disordersSara M Fielder, Marisa W Friederich, Daniella H Hock, et al.
EMBO Molecular Medicine|August 26, 2025
Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disordersSara M Fielder, Marisa W Friederich, Daniella H Hock, et al.
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