AndrewRossFindlayMD

Neurology • Saint Louis, MO

Neuromuscular Medicine

Assistant Professor

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Office
4921 Parkview Pl
Saint Louis, MO 63110
Phone+1 314-362-6981

Fax+1 314-747-3752
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Education & Training

Washington University in St. Louis School of MedicinePost-Doctoral Fellowship, American Academy of Neurology Research Training Scholar, 2018 - 2020
Washington University/B-JH/SLCH ConsortiumFellowship, Neuromuscular Medicine (Neurology), 2017 - 2018
Washington University/B-JH/SLCH ConsortiumFellowship, Pathology-Anatomic and Clinical, 2017 - 2018
Washington University/B-JH/SLCH ConsortiumResidency, Neurology, 2013 - 2017
University of California, Irvine, School of MedicineClass of 2013
University California Santa BarbaraBS, Biochemistry, 2003 - 2007

Certifications & Licensure

IL State Medical License 2020 - 2026
MO State Medical License 2017 - 2025
American Board of Psychiatry and Neurology Neurology
American Board of Psychiatry and Neurology Neuromuscular Medicine

Publications & Presentations

PubMed

1 citations
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, Sara K Pittman, Shan Li, Feng Wang, Timothy M Miller, Heather L True, Tsui-Fen Chou, Conrad C...> ;Molecular Therapy. Nucleic Acids. 2023 Jun 13
1 citations
LGMDD1 natural history and phenotypic spectrum: Implications for clinical trials.
Andrew R Findlay, Sarah E Robinson, Stephanie Poelker, Michelle Seiffert, Rocio Bengoechea, Conrad C Weihl> ;Annals of Clinical and Translational Neurology. 2023 Feb 1
4 citations
Loss of function variants in DNAJB4 cause a myopathy with early respiratory failure.
Conrad C Weihl, Ana Töpf, Rocio Bengoechea, Jennifer Duff, Richard Charlton, Solange Kapetanovic Garcia, Cristina Domínguez-González, Abdulaziz Alsaman, Aurelio Hernán...> ;Acta Neuropathologica. 2023 Jan 1
10 citations
Clinical utility of anti-cytosolic 5'-nucleotidase 1A antibody in idiopathic inflammatory myopathies.
Chiseko Ikenaga, Andrew R. Findlay, Namita Goyal, Sarah Robinson, Jonathan Cauchi, Yessar Hussain, Leo H. Wang, Joshua C. Kershen, Brent A. Beson, Michael Wallendorf, ...> ;Annals of Clinical and Translational Neurology. 2021 Feb 8
12 citations
Phenotypic diversity in an international Cure VCP Disease registry.
Chiseko Ikenaga, Andrew R. Findlay, Michelle Seiffert, Allison Peck, Nathan Peck, Nicholas E. Johnson, Jeffrey Statland, Conrad C. Weihl> ;Orphanet Journal of Rare Diseases. 2020 Sep 29
10 citations
Inhibition of DNAJ-HSP70 interaction improves strength in muscular dystrophy
Rocio Bengoechea, Andrew R. Findlay, Ankan K. Bhadra, Hao Shao, Kevin C. Stein, Sara K. Pittman, Jil A. Wright Daw, Jason E. Gestwicki, Heather L. True, Conrad C. Weihl> ;The Journal of Clinical Investigation. 2020 Aug 3
10 citations
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, Conrad C. Weihl> ;Neurology. Genetics. 2019 Apr 1
234th ENMC International Workshop: Chaperone dysfunction in muscle disease Naarden, The Netherlands, 8-10 December 2017.
Weihl CC, Udd B, Hanna M, ENMC workshop study group> ;Neuromuscular disorders : NMD. 2018-09-25
8 citations
Homozygous recessive MYH2 mutation mimicking dominant MYH2 associated myopathy.
Andrew R. Findlay, Matthew B. Harms, Alan Pestronk, Conrad C. Weihl> ;Neuromuscular Disorders. 2018 May 21
4 citations
Resistance to 6-Methylpurine is Conferred by Defective Adenine Phosphoribosyltransferase in Tetrahymena.
Takahiko Akematsu, Andrew Findlay, Yasuhiro Fukuda, Ronald E. Pearlman, Josef Loidl, Eduardo Orias, Eileen P. Hamilton> ;Genes. 2018 Mar 23
23 citations
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, Steve D. Wilton, Kevin M. Flanigan> ;Journal of Neuromuscular Diseases. 2017 Jan 1
24 citations
The first exon duplication mouse model of Duchenne muscular dystrophy: A tool for therapeutic development
Adeline Vulin, Nicolas Wein, Tabatha R. Simmons, A. Rutherford, Andrew R. Findlay, Jacqueline A. Yurkoski, Yuuki Kaminoh, Kevin M. Flanigan> ;Neuromuscular Disorders. 2015 Nov 1
7 citations
Erratum: Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice: (Nature Medicine (2014) 20 ...
Nicolas Wein, Adeline Vulin, Maria Sofia Falzarano, Christina Al Khalili Szigyarto, Baijayanta Maiti, Andrew R. Findlay, Kristin N. Heller, Mathias Uhlén, Baskar Bakth...> ;Nature Medicine. 2015 May 1
130 citations
An overview of polymyositis and dermatomyositis.
Andrew R. Findlay, Namita Goyal, Tahseen Mozaffar> ;Muscle & Nerve. 2015 May 1
3 citations
Corrigendum: Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice (Nature Medicine (2014))
Nicolas Wein, Adeline Vulin, Maria Sofia Falzarano, Christina Al Khalili Szigyarto, Baijayanta Maiti, Andrew R. Findlay, Kristin N. Heller, Mathias Uhlén, Baskar Bakth...> ;Nature Medicine. 2015 Apr 1
33 citations
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, Jerry R. Mendell, Wendy King, Alan Pestronk, Julaine Florence, Katherine D. Mathews, Ri...> ;Annals of Neurology. 2015 Apr 1
18 citations
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, Kristin N Heller, Mathias Uhlén, Baskar Bakthavachalu...> ;Nature Medicine. 2014 Sep 1
29 citations
Exome sequencing identifies a DNAJB6 mutation in a family with dominantly-inherited limb-girdle muscular dystrophy.
Julien Couthouis, Alya R. Raphael, Carly E. Siskind, Andrew R. Findlay, Jason D. Buenrostro, William J. Greenleaf, Hannes Vogel, John W. Day, Kevin M. Flanigan, Aaron ...> ;Neuromuscular Disorders. 2014 May 1
18 citations
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, Baijayanta Maiti, Michael T. Howard, Yuuki Kaminoh, Laura E. Taylor, Tabatha R. Si...> ;Human Mutation. 2014 Feb 1
5 citations
Camptocormia as a late presentation in a manifesting carrier of duchenne muscular dystrophy.
Andrew R. Findlay, Sarah Lewis, Zarife Sahenk, Kevin M. Flanigan> ;Muscle & Nerve. 2013 Jan 1
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Press Mentions

Blocking Protein That Hinders Muscle Growth Possible Way of Treating LGMD1, Mouse Study SuggestsJune 12th, 2019
Lithium Boosts Muscle Strength in Mice with Rare Muscular DystrophyJune 3rd, 2019
The New Study Brings Good News for the People with Limb-Girdle Muscular DystrophyApril 22nd, 2019

Grant Support

K08NIAMS2019–2024
Career Development AwardAmerican Society of Gene & Cell Therapy2020–2021
Career Development AwardAmerican Society for Gene and Cell Therapy2020–2021
Neuroscience Research Training ScholarshipAmerican Academy of Neurology2018–2020