Publications by authors named "Anson Cheng"

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Connecting cilium, stress response, and proteostasis abnormalities inform variant and therapy assessment in RPGRIP1 retinal organoids.
To Ha Loi, Anson Cheng, Hani Jieun Kim, Milan Fernando, Benjamin M Nash

Stem Cell Reports· December 2025

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Selective disruption of Drp1-independent mitophagy and mitolysosome trafficking by an Alzheimer's disease relevant tau modification in a novel Caenorhabditis elegans model.
Sanjib Guha, Anson Cheng, Trae Carroll, Dennisha King, Shon A Koren

Genetics· August 2022

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Evaluation for Retinal Therapy for Variation Assessed in hiPSC Retinal Pigment Epithelial Cells.
Benjamin M Nash, To Ha Loi, Milan Fernando, Amin Sabri, James Robinson, Anson Cheng

Stem Cells Int· December 2021

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Genome sequencing in congenital cataracts improves diagnostic yield.
Alan Ma, John R Grigg, Maree Flaherty, James Smith, Andre E Minoche, Anson Cheng

Hum Mutat· September 2021

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Revealing hidden genetic diagnoses in the ocular anterior segment disorders.
Alan Ma, Saira Yousoof, John R Grigg, Maree Flaherty, Andre E Minoche, Anson Cheng

Genet Med· October 2020

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A T231E Mutant that Mimics Pathologic Phosphorylation of Tau in Alzheimer's disease Causes Activation of the Mitochondrial Unfolded Protein Response in touch neurons.
Sanjib Guha, Sarah Fischer, Anson Cheng, Gail V W Johnson, Keith Nehrke

MicroPubl Biol· September 2020

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The role of transglutaminase 2 in mediating glial cell function and pathophysiology in the central nervous system.
Jacob Rudlong, Anson Cheng, Gail V W Johnson

Anal Biochem· February 2020

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ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder.
Lloyd B Williams, Asif Javed, Amin Sabri, Denise J Morgan, Chad D Huff, Anson Cheng

Genet Med· September 2019

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Sporadic and Familial Congenital Cataracts: Mutational Spectrum and New Diagnoses Using Next-Generation Sequencing.
Alan S Ma, John R Grigg, Gladys Ho, Ivan Prokudin, Elizabeth Farnsworth, Anson Cheng

Hum Mutat· April 2016

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Mutations in SIPA1L3 cause eye defects through disruption of cell polarity and cytoskeleton organization.
Rebecca Greenlees, Marija Mihelec, Saira Yousoof, Daniel Speidel, Selwin K Wu, Anson Cheng

Hum Mol Genet· October 2015

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Sequence of age-associated changes to the mouse neuromuscular junction and the protective effects of voluntary exercise.
Anson Cheng, Marco Morsch, Yui Murata, Nazanin Ghazanfari, Stephen W Reddel

PLoS One· February 2014

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