Conrad C. Weihl
Washington University in St. Louis(US)
Publications by Year
Research Areas
Muscle Physiology and Disorders, Genetic Neurodegenerative Diseases, Endoplasmic Reticulum Stress and Disease, Inflammatory Myopathies and Dermatomyositis, Neurogenetic and Muscular Disorders Research
Most-Cited Works
- → Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS(2013)1,475 cited
- → Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis(2014)441 cited
- → The VCP/p97 system at a glance: connecting cellular function to disease pathogenesis(2014)438 cited
- → TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementia(2008)307 cited
- → Valosin-containing protein disease: Inclusion body myopathy with Paget’s disease of the bone and fronto-temporal dementia(2009)240 cited
- → Endolysosomal sorting of ubiquitylated caveolin-1 is regulated by VCP and UBXD1 and impaired by VCP disease mutations(2011)240 cited
- → Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation(2005)194 cited
- → Exome sequencing reveals DNAJB6 mutations in dominantly‐inherited myopathy(2011)174 cited
- → Interaction with Polyglutamine Aggregates Reveals a Q/N-rich Domain in TDP-43(2010)159 cited
- → Prion-like nuclear aggregation of TDP-43 during heat shock is regulated by HSP40/70 chaperones(2013)157 cited