Conrad C. Weihl

TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementia

Conrad C. Weihl, Sara Miller, Gerald F. Watts et al. · Journal of Neurology Neurosurgery & Psychiatry · 2008 · 306 citations · Full text

Genetics, Pathology, Disease Gene Identification +20

Endolysosomal sorting of ubiquitylated caveolin-1 is regulated by VCP and UBXD1 and impaired by VCP disease mutations

Danilo Ritz, Maja Vuk, Philipp Kirchner et al. · Nature Cell Biology · 2011 · 238 citations

Chromatin, Endolysosomal Sorting, Genetics +6

Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation

Conrad C. Weihl, Seema Dalal, Alan Pestronk et al. · Human Molecular Genetics · 2005 · 192 citations

Ubiquitinated Proteins, Molecular Biology, Cytoskeleton +16

Exome sequencing reveals <i>DNAJB6</i> mutations in dominantly‐inherited myopathy

Matthew B. Harms, R. Brian Sommerville, Peggy Allred et al. · Annals of Neurology · 2011 · 172 citations · Full text

Interaction with Polyglutamine Aggregates Reveals a Q/N-rich Domain in TDP-43

Rodrigo A. Fuentealba, Maria Udan, Shaughn Bell et al. · Journal of Biological Chemistry · 2010 · 158 citations · Full text

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Molecular Neuroscience +14