Author

Andrew R. Findlay

Washington University in St. LouisORCID 0000-0002-8728-9833Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Approach:experimental assay· 2 Organism:mouse· 2 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Assay:proteomics· 1 Approach:statistical model· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Conrad Chris WeihliD· 2 shared Heather L. TrueiD· 2 shared Jil DawiD· 2 shared Rocío BengoecheaiD· 2 shared Abdulaziz Alsaman· 1 shared Ana TöpfiD· 1 shared Ankan Kumar BhadraiD· 1 shared Aurelio Hernández‐LaíniD· 1 shared

Activity by Year

2022-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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2 shared papersNeuroscience

Conrad Chris WeihlORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

DNAJB6 Isoform Specific Knockdown: Therapeutic Potential for LGMDD1

Andrew R. Findlay, May M. Paing, Jil Daw, Rocío Bengoechea, Sara K. Pittman, Shan Li, Feng Wang, Timothy M. Miller, Heather L. True, Tsui‐Fen Chou, Conrad Chris Weihl

This study investigates DNAJB6 isoform-specific knockdown as a potential therapy for LGMDD1, showing that reducing DNAJB6b levels in a mouse model corrected proteomic disease signatures.

bioRxiv · Nov 17, 2022 · PreprintNeuroscience

Loss of function variants in DNAJB4 cause a myopathy with early respiratory failure

Conrad Chris Weihl, Ana Töpf, Rocío Bengoechea, Jennifer Duff, Richard Charlton, Solange Kapetanovic García, Cristina Domínguez‐González, Abdulaziz Alsaman, Aurelio Hernández‐Laín, Luís Varona, Monica Elizabeth Ponce Sanchez, Sarah J. Beecroft, Hayley Goullée, Jil Daw, Ankan Kumar Bhadra, , Volker W. Straub

The paper identifies DNAJB4 loss of function variants causing a myopathy with early respiratory failure through exome sequencing and functional studies.

Acta Neuropathologica · Oct 20, 2022Peer-reviewedGenetics