Author

Michio Inoue

Washington University in St. LouisORCID 0000-0003-2757-3266Unclaimed 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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Approach:experimental assay· 2 Organism:mouse· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Conrad Chris WeihliD· 2 shared Rocío BengoecheaiD· 2 shared Abdulaziz Alsaman· 1 shared Ana TöpfiD· 1 shared Andrew R. FindlayiD· 1 shared Ankan Kumar BhadraiD· 1 shared Aritoshi IidaiD· 1 shared Aurelio Hernández‐LaíniD· 1 shared

Activity by Year

2022-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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2 shared papersNeuroscience

Conrad Chris WeihlORCID

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2 papers

Recent·Most cited

NeuroscienceActa NeuropathologicaPeer-reviewedDec 13, 2022

Distinct chaperonopathy in skeletal muscle associated with the dominant variant in DNAJB4

Michio Inoue, S. Noguchi, Yukiko Inoue…·Ichizo Nishino

The paper identifies a DNAJB4 variant causing chaperonopathy in skeletal muscle, leading to muscle weakness and specific pathological features in type 1 fibers.

18 citations

mouseexperimental assay

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GeneticsActa NeuropathologicaPeer-reviewedOct 20, 2022

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

Conrad Chris Weihl, Ana Töpf, Rocío Bengoechea…·Volker W. Straub

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

30 citations

humanmouse

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