Standout Papers

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon ... 1992 2026 2003 2014 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
  2. Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy (1992)
    J. David Brook, S.A. Rundle et al. Nature
  3. Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome (1994)
    William Reardon, Robin M. Winter et al. Nature Genetics

Immediate Impact

10 by Nobel laureates 19 from Science/Nature 59 standout
Sub-graph 1 of 18

Citing Papers

Small RNAs are modified with N-glycans and displayed on the surface of living cells
2021 StandoutNobel
Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association
2018 Standout
15 intermediate papers

Works of William Reardon being referenced

The spectrum of congenital cardiac malformations encountered in six children with Kabuki syndrome
2006
Elastin: mutational spectrum in supravalvular aortic stenosis
2000
and 14 more

Author Peers

Author Last Decade Papers Cites
William Reardon 5127 6477 1211 1774 193 11.7k
Patrick J. Willems 3763 5314 623 781 206 9.7k
William J. Kimberling 3484 6248 887 3843 186 11.4k
Paul Coucke 3658 3261 481 1343 260 7.8k
Sally A. Camper 3563 6946 783 860 217 12.8k
Frans P.M. Cremers 3867 13575 279 1250 293 15.9k
Thomas Gridley 2524 12699 1529 995 143 17.5k
Mireille Claustres 1811 4270 414 827 220 8.0k
Dominique Weil 1396 6577 663 2513 184 9.6k
Lisbeth Tranebjærg 2195 3526 400 818 159 6.5k
Susan H. Blanton 2223 2775 527 806 187 6.1k

All Works

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2026