Standout Papers

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy 1995 2026 2005 2015 572
  1. Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy (1998)
    Bernard Brais, Jean‐Pierre Bouchard et al. Nature Genetics
  2. Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy (1995)
    A. Leclerc, Xu Zhang et al. Nature Genetics

Immediate Impact

8 by Nobel laureates 39 from Science/Nature 72 standout
Sub-graph 1 of 18

Citing Papers

Muscular dystrophies
2019 Standout
A new era for understanding amyloid structures and disease
2018 Standout
28 intermediate papers

Works of F.M.S. Tomé being referenced

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy
1998 Standout
Morphological changes in muscle fibers in oculopharyngeal muscular dystrophy
1997
and 22 more

Author Peers

Author Last Decade Papers Cites
F.M.S. Tomé 3811 1506 919 72 4.3k
Eijiro Ozawa 4106 1113 1081 99 4.6k
Roger A. Williamson 3782 963 782 96 6.2k
Yoshihide Sunada 3853 958 1014 143 5.1k
Luc A. Sabourin 4580 1649 730 57 5.6k
Silvia Torelli 3959 724 505 79 4.4k
Daniel E. Michele 3480 620 762 69 4.5k
Marina Mora 4643 1049 1001 157 6.5k
Ronald D. Cohn 3338 604 665 36 4.3k
Rita Barresi 2732 612 515 52 3.4k
Kiichi Arahata 6388 1508 1201 138 8.1k

All Works

Loading papers...

Rankless by CCL
2026