Standout Papers

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathi... 1997 2026 2006 2016 689
  1. Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome (1997)
    Ercole Rao, Birgit Weiß et al. Nature Genetics

Immediate Impact

45 by Nobel laureates 62 from Science/Nature 70 standout
Sub-graph 1 of 21

Citing Papers

Single-cell brain organoid screening identifies developmental defects in autism
2023 StandoutNature
Human TKTL1 implies greater neurogenesis in frontal neocortex of modern humans than Neanderthals
2022 StandoutScienceNobel
4 intermediate papers

Works of Gudrun Rappold being referenced

Mitochondrial dysfunction and oxidative stress contribute to cognitive and motor impairment in FOXP1 syndrome
2022
Homozygous loss of CHRNA7 on chromosome 15q13.3 causes severe encephalopathy with seizures and hypotonia
2010
and 2 more

Author Peers

Author Last Decade Papers Cites
Gudrun Rappold 5774 4990 1081 215 9.8k
Hans‐Hilger Ropers 8943 7113 897 287 14.8k
Christine M. Distèche 10412 6837 2313 224 17.0k
Orsetta Zuffardi 6726 6968 2105 323 11.7k
Paul S. Burgoyne 7116 6434 1926 136 10.9k
P. Pearson 6199 4607 1403 207 10.6k
Eden R. Martin 4315 3996 438 236 10.9k
Charles E. Schwartz 7453 6100 809 316 12.7k
B.M. Cattanach 5811 5383 919 135 9.3k
Ethylin Wang Jabs 8505 7695 633 236 14.4k
Ben C.J. Hamel 6502 5878 364 199 11.1k

All Works

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2026