Standout Papers

SCN9A Mutations in Paroxysmal Extreme Pain Disorder: Allelic Variants Underlie Distinct Channel... 2006 2026 2012 2019 547
  1. SCN9A Mutations in Paroxysmal Extreme Pain Disorder: Allelic Variants Underlie Distinct Channel Defects and Phenotypes (2006)
    Caroline Fertleman, Mark D. Baker et al. Neuron

Immediate Impact

25 by Nobel laureates 33 from Science/Nature 60 standout
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Works of Frances Elmslie being referenced

Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss
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SCN9A Mutations in Paroxysmal Extreme Pain Disorder: Allelic Variants Underlie Distinct Channel Defects and Phenotypes
2006 Standout
and 1 more

Author Peers

Author Last Decade Papers Cites
Frances Elmslie 1222 554 712 28 2.0k
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Mary Kay Koenig 1100 257 535 59 1.9k
Chunling Zhang 1097 216 311 49 2.7k
Shinji Hatakeyama 1599 158 845 43 2.6k
Omolara O. Ogunshola 1099 254 449 54 2.7k
Tilman Breiderhoff 1335 187 568 29 2.3k
Brad T. Tinkle 577 1020 416 16 2.2k
Rachel A. Gibson 1201 538 301 51 2.1k

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