A de novo gain-of-function mutation in SCN11A causes loss of pain perceptionEnrico Leipold, Ingo Kurth, Christian A. Hübner et al.|Nature Genetics|2013Cited by 304
Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathyIngo Kurth, Christian A. Hübner, Torsten Pamminger et al.|Nature Genetics|2009Cited by 256
Transcriptional regulator PRDM12 is essential for human pain perceptionYa-Chun Chen, Jonathan Baets, Michaela Auer‐Grumbach et al.|Nature Genetics|2015Cited by 172
Dominant mutations in the cation channel gene transient receptor potential vanilloid 4 cause an unusual spectrum of neuropathiesPeter De Jonghe, Jonathan Baets, Michaela Auer‐Grumbach et al.|Brain|2010Cited by 134
Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3Uwe Kornak, Ingo Kurth, Inès Mademan et al.|Brain|2014Cited by 107