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 70 standout
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Works of Johan Östman being referenced

SCN9A Mutations in Paroxysmal Extreme Pain Disorder: Allelic Variants Underlie Distinct Channel Defects and Phenotypes
2006 Standout

Author Peers

Author Last Decade Papers Cites
Johan Östman 527 465 259 5 776
L Caroline Stirling 448 457 281 7 730
Elda Tzoumaka 512 433 356 7 769
Fay Heblich 567 287 410 9 842
Anne Pizzoccaro 461 451 238 12 896
Joseph G. McGivern 588 400 342 15 860
Stéphane Lolignier 462 477 278 20 892
Sriyani Pathirathna 442 599 348 10 844
Michel Lazdunski 625 218 385 15 898
Andrew D. Piekarz 467 284 368 12 701
W. N. Hormuzdiar 448 451 350 6 674

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