Publications by authors named "Quinn Murphy"

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Electrochemical micro-aptasensors for exosome detection based on hybridization chain reaction amplification.
Wenfen Zhang, Zhenhua Tian, Shujie Yang, Joseph Rich, Shuaiguo Zhao, Quinn Murphy

Microsyst Nanoeng· August 2021

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SPEG binds with desmin and its deficiency causes defects in triad and focal adhesion proteins.
Shiyu Luo, Qifei Li, Jasmine Lin, Quinn Murphy, Isabelle Marty

Hum Mol Genet· February 2021

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Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation.
Amy E O'Connell, Maxim V Gerashchenko, Marie-Francoise O'Donohue, Samantha M Rosen, Eric Huntzinger, Quinn Murphy

PLoS Genet· February 2019

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Transgenic zebrafish model of DUX4 misexpression reveals a developmental role in FSHD pathogenesis.
Anna Pakula, Angela Lek, Jeffrey Widrick, Hiroaki Mitsuhashi, Katlynn M Bugda Gwilt, Quinn Murphy

Hum Mol Genet· January 2019

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De novo variant of TRRAP in a patient with very early onset psychosis in the context of non-verbal learning disability and obsessive-compulsive disorder: a case report.
Chrystal F Mavros, Catherine A Brownstein, Roshni Thyagrajan, Casie A Genetti, Sahil Tembulkar, Quinn Murphy

BMC Med Genet· November 2018

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Neonatal-Onset Chronic Diarrhea Caused by Homozygous Nonsense WNT2B Mutations.
Amy E O'Connell, Fanny Zhou, Manasvi S Shah, Quinn Murphy, Hannah Rickner

Am J Hum Genet· July 2018

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