Mice Lacking the Alpha9 Subunit of the Nicotinic Acetylcholine Receptor Exhibit Deficits in Frequency Difference Limens and Sound Localization

por Clause, Amanda, Lauer, Amanda M., Kandler, Karl
Publicado 2017

Transcriptional maturation of the mouse auditory forebrain

por Hackett, Troy A., Guo, Yan, Clause, Amanda, Hackett, Nicholas J., Garbett, Krassimira, Zhang, Pan, Polley, Daniel B., Mirnics, Karoly
Publicado 2015

Genome sequencing identifies three molecular diagnoses including a mosaic variant in the COL2A1 gene in an individual with Pol III–related leukodystrophy and Feingold syndrome

por Muirhead, Kayla J., Clause, Amanda R., Schlachetzki, Zinayida, Dubbs, Holly, Perry, Denise L., Hagelstrom, R. Tanner, Taft, Ryan J., Vanderver, Adeline
Publicado 2021

Autosomal Recessive ACTG2-Related Visceral Myopathy in Brothers

por Mori, Mari, Clause, Amanda R., Truxal, Kristen, Hagelstrom, R. Tanner, Manickam, Kandamurugu, Kaler, Stephen G., Prasad, Vinay, Windster, Jonathan, Alves, Maria M., Di Lorenzo, Carlo
Publicado 2022

Reactive gene curation to support interpretation and reporting of a clinical genome test for rare disease: Experience from over 1,000 cases

por Clause, Amanda R., Taylor, Julie P., Rajkumar, Revathi, Bluske, Krista, Bennett, Maren, Amendola, Laura M., Bentley, David R., Taft, Ryan J., Perry, Denise L., Coffey, Alison J.
Publicado 2023