Standout Papers

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome... 1995 2026 2005 2015 659
  1. Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome (1995)
    Andrew O.M. Wilkie, Sarah F. Slaney et al. Nature Genetics

Immediate Impact

3 by Nobel laureates 21 from Science/Nature 65 standout
Sub-graph 1 of 23

Citing Papers

Risk of Autism after Prenatal Topiramate, Valproate, or Lamotrigine Exposure
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The role of retrotransposable elements in ageing and age-associated diseases
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2 intermediate papers

Works of David J. David being referenced

Rare mutations ofFGFR2causing apert syndrome: identification of the first partial gene deletion, and anAluelement insertion from a new subfamily
2008
Prenatal exposure to phenytoin, facial development, and a possible role for vitamin K
1995

Author Peers

Author Last Decade Papers Cites
David J. David 2168 1200 178 710 106 3.0k
Ian R. Munro 1512 1407 212 449 89 3.1k
Alex A. Kane 2363 1046 100 727 119 3.3k
Samuel Stal 1368 1456 143 406 102 2.7k
Barry M. Jones 2710 2169 354 1090 109 4.5k
Samuel Pruzansky 1833 518 68 610 119 2.4k
Joseph S. Gruss 1611 2173 385 496 107 3.6k
Jeffrey A. Fearon 1895 1280 193 337 81 2.4k
Mark M. Urata 1482 939 48 923 156 2.9k
Richard E. Kirschner 1817 792 63 822 101 2.9k
Bonnie L. Padwa 2147 1279 210 595 178 3.9k

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