Standout Papers

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal domi... 1993 2026 2004 2015 518
  1. A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis (1993)
    Ethylin Wang Jabs, Ulrich Müller et al. Cell

Immediate Impact

4 by Nobel laureates 31 from Science/Nature 68 standout
Sub-graph 1 of 21

Citing Papers

YAP/TAZ activity in stromal cells prevents ageing by controlling cGAS–STING
2022 StandoutNature
The single-cell transcriptional landscape of mammalian organogenesis
2019 StandoutNature
2 intermediate papers

Works of Wen Luo being referenced

Premature suture closure and ectopic cranial bone in mice expressing Msx2 transgenes in the developing skull.
1995
Regulation of the Msx2 homeobox gene during mouse embryogenesis: A transgene with 439 bp of 5′ flanking sequence is expressed exclusively in the apical ectodermal ridge of the developing limb
1994

Author Peers

Author Last Decade Papers Cites
Wen Luo 1545 112 271 725 72 2.1k
Tetsuo Kunieda 1235 174 158 749 129 2.3k
R.T. Taggart 1255 72 149 409 53 2.0k
Xiayi Ke 901 116 190 1063 54 2.6k
Chunsheng Han 1345 125 364 564 68 2.2k
Bernard Jost 1579 211 291 430 48 2.2k
Martin Bergmann 1139 119 222 486 72 2.7k
Charles R. Farber 1593 84 370 892 90 2.8k
Keesook Lee 1317 62 221 699 74 2.6k
Jeroen F. J. Laros 1194 49 248 753 44 1.8k
Haixu Chen 1423 287 231 299 55 2.3k

All Works

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