Auer-Grumbach, Michaela

Top Publications

Top Publications Authored or Co-Authored by "Auer-Grumbach, Michaela"

• Transcriptional regulator PRDM12 is essential for human pain perception

  Nature Genetics, Volume 47, No. 7, Year 2015, Citations 136
• Dominant mutations in the cation channel gene transient receptor potential vanilloid 4 cause an unusual spectrum of neuropathies

  Brain, Volume 133, No. 6, Year 2010, Citations 103
• Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia

  Brain, Volume 144, No. 5, Year 2021, Citations 100
• Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes

  Nature Genetics, Volume 52, No. 5, Year 2020, Citations 94
• SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum

  Neurology, Volume 73, No. 14, Year 2009, Citations 87