Publications by authors named "Andrew Findlay"

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General and Spine-Specific Sarcopenia in Adult Spinal Deformity: a Narrative Overview of Current Strengths and Limitations.
Tim T Bui, Karan Joseph, Alexander T Yahanda, Andrew R Findlay, Alekos A Theologis

Global Spine J· October 2025

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Inhibition of DNAJ-HSP70 interaction improves strength in muscular dystrophy.
Rocio Bengoechea, Andrew R Findlay, Ankan K Bhadra, Hao Shao, Kevin C Stein

J Clin Invest· May 2025

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Elevated VCP ATPase Activity Correlates With Disease Onset in Multisystem Proteinopathy-1.
Sarah E Robinson, Andrew R Findlay, Shan Li, Feng Wang, Marianela Schiava

Neurol Genet· October 2024

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Dominantly inherited muscle disorders: understanding their complexity and exploring therapeutic approaches.
Andrew R Findlay

Dis Model Mech· October 2024

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DNAJB6 isoform specific knockdown: Therapeutic potential for limb girdle muscular dystrophy D1.
Andrew R Findlay, May M Paing, Jil A Daw, Meade Haller, Rocio Bengoechea

Mol Ther Nucleic Acids· June 2023

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LGMDD1 natural history and phenotypic spectrum: Implications for clinical trials.
Andrew R Findlay, Sarah E Robinson, Stephanie Poelker, Michelle Seiffert, Rocio Bengoechea

Ann Clin Transl Neurol· February 2023

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Loss of function variants in DNAJB4 cause a myopathy with early respiratory failure.
Conrad C Weihl, Ana Töpf, Rocio Bengoechea, Jennifer Duff, Richard Charlton, Andrew R Findlay

Acta Neuropathol· January 2023

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Genetic-Based Treatment Strategies for Muscular Dystrophy and Congenital Myopathies.
Andrew R Findlay, Conrad C Weihl

Continuum (Minneap Minn)· December 2022

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Clinical utility of anti-cytosolic 5'-nucleotidase 1A antibody in idiopathic inflammatory myopathies.
Chiseko Ikenaga, Andrew R Findlay, Namita A Goyal, Sarah Robinson, Jonathan Cauchi

Ann Clin Transl Neurol· March 2021

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Phenotypic diversity in an international Cure VCP Disease registry.
Chiseko Ikenaga, Andrew R Findlay, Michelle Seiffert, Allison Peck, Nathan Peck

Orphanet J Rare Dis· September 2020

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Inhibition of DNAJ-HSP70 interaction improves strength in muscular dystrophy.
Rocio Bengoechea, Andrew R Findlay, Ankan K Bhadra, Hao Shao, Kevin C Stein

J Clin Invest· August 2020

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Lithium chloride corrects weakness and myopathology in a preclinical model of LGMD1D.
Andrew R Findlay, Rocio Bengoechea, Sara K Pittman, Tsui-Fen Chou, Heather L True

Neurol Genet· April 2019

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Homozygous recessive MYH2 mutation mimicking dominant MYH2 associated myopathy.
Andrew R Findlay, Matthew B Harms, Alan Pestronk, Conrad C Weihl

Neuromuscul Disord· August 2018

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Efficient Skipping of Single Exon Duplications in DMD Patient-Derived Cell Lines Using an Antisense Oligonucleotide Approach.
Nicolas Wein, Adeline Vulin, Andrew R Findlay, Felecia Gumienny, Nianyuan Huang

J Neuromuscul Dis· April 2018

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Resistance to 6-Methylpurine is Conferred by Defective Adenine Phosphoribosyltransferase in Tetrahymena.
Takahiko Akematsu, Andrew Findlay, Yasuhiro Fukuda, Ronald E Pearlman, Josef Loidl

Genes (Basel)· March 2018

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Clinical Practice Guideline on management of older patients with chronic kidney disease stage 3b or higher (eGFR<45 mL/min/1.73 m2): a summary document from the European Renal Best Practice Group.
Ken Farrington, Adrian Covic, Ionut Nistor, Filippo Aucella, Naomi Clyne, Andrew Findlay

Nephrol Dial Transplant· January 2017

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Clinical Practice Guideline on management of older patients with chronic kidney disease stage 3b or higher (eGFR <45 mL/min/1.73 m2).
Ken Farrington, Adrian Covic, Fillipo Aucella, Naomi Clyne, Leen de Vos, Andrew Findlay

Nephrol Dial Transplant· November 2016

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The first exon duplication mouse model of Duchenne muscular dystrophy: A tool for therapeutic development.
Adeline Vulin, Nicolas Wein, Tabatha R Simmons, Andrea M Rutherford, Andrew R Findlay

Neuromuscul Disord· November 2015

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An overview of polymyositis and dermatomyositis.
Andrew R Findlay, Namita A Goyal, Tahseen Mozaffar

Muscle Nerve· May 2015

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Corrigendum: Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice.
Nicolas Wein, Adeline Vulin, Maria S Falzarano, Christina Al-Khalili Szigyarto, Baijayanta Maiti, Andrew Findlay

Nat Med· May 2015

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Clinical phenotypes as predictors of the outcome of skipping around DMD exon 45.
Andrew R Findlay, Nicolas Wein, Yuuki Kaminoh, Laura E Taylor, Diane M Dunn

Ann Neurol· April 2015

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Corrigendum: Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice.
Nicolas Wein, Adeline Vulin, Maria S Falzarano, Christina Al-Khalili Szigyarto, Baijayanta Maiti, Andrew Findlay

Nat Med· April 2015

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Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice.
Nicolas Wein, Adeline Vulin, Maria S Falzarano, Christina Al-Khalili Szigyarto, Baijayanta Maiti, Andrew Findlay

Nat Med· September 2014

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Exome sequencing identifies a DNAJB6 mutation in a family with dominantly-inherited limb-girdle muscular dystrophy.
Julien Couthouis, Alya R Raphael, Carly Siskind, Andrew R Findlay, Jason D Buenrostro

Neuromuscul Disord· May 2014

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The ZZ domain of dystrophin in DMD: making sense of missense mutations.
Adeline Vulin, Nicolas Wein, Dana M Strandjord, Eric K Johnson, Andrew R Findlay

Hum Mutat· February 2014

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