Standout Papers
- Lamin A Truncation in Hutchinson-Gilford Progeria (2003)
- Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family (1997)
- Somatic and germline activating mutations of the ALK kinase receptor in neuroblastoma (2008)
- SOX10 mutations in patients with Waardenburg-Hirschsprung disease (1998)
- Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome (2003)
- Mutations of the RET proto-oncogene in Hirschsprung's disease (1994)
Immediate Impact
13 by Nobel laureates 32 from Science/Nature 65 standout
Citing Papers
Computational design of soluble and functional membrane protein analogues
2024 StandoutNatureNobel
Human TKTL1 implies greater neurogenesis in frontal neocortex of modern humans than Neanderthals
2022 StandoutScienceNobel
Works of Stanislas Lyonnet being referenced
Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesis
2007
Claudin-1 gene mutations in neonatal sclerosing cholangitis associated with ichthyosis: A tight junction disease
2004
Author Peers
| Author | Last Decade | Papers | Cites | |||
|---|---|---|---|---|---|---|
| Stanislas Lyonnet | 8677 | 4506 | 4065 | 310 | 16.3k | |
| Jeanne Amiel | 6357 | 3151 | 3213 | 316 | 13.9k | |
| Simon J. Conway | 10299 | 1591 | 3129 | 211 | 22.3k | |
| Cynthia C. Morton | 8600 | 2855 | 1255 | 277 | 18.6k | |
| Frank Costantini | 17357 | 5490 | 3188 | 143 | 24.3k | |
| Ron G. Rosenfeld | 9117 | 6100 | 2209 | 435 | 22.6k | |
| Rune R. Frants | 10089 | 1908 | 2332 | 317 | 18.1k | |
| Sherri J. Bale | 14268 | 12453 | 1872 | 140 | 28.8k | |
| Thomas Meitinger | 11034 | 5431 | 1169 | 314 | 18.7k | |
| Urban Lendahl | 15240 | 2186 | 2534 | 215 | 24.5k | |
| David Bick | 10084 | 9850 | 1661 | 83 | 21.0k |
All Works
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