Standout Papers

A forkhead-domain gene is mutated in a severe speech and language disorder 1996 2026 2006 2016 1.2k
  1. A forkhead-domain gene is mutated in a severe speech and language disorder (2001)
    Cecilia Lai, Simon E. Fisher et al. Nature
  2. Molecular evolution of FOXP2, a gene involved in speech and language (2002)
    Wolfgang Enard, Molly Przeworski et al. Nature
  3. Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations (2011)
    Brian J. O’Roak, Pelagia Deriziotis et al. Nature Genetics
  4. A common molecular basis for three inherited kidney stone diseases (1996)
    Sarah E. Lloyd, Simon H. S. Pearce et al. Nature

Immediate Impact

53 by Nobel laureates 56 from Science/Nature 83 standout
Sub-graph 1 of 21

Citing Papers

Accurate proteome-wide missense variant effect prediction with AlphaMissense
2023 StandoutScienceNobel
Human TKTL1 implies greater neurogenesis in frontal neocortex of modern humans than Neanderthals
2022 StandoutScienceNobel
4 intermediate papers

Works of Simon E. Fisher being referenced

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
2011 Standout
A Functional Genetic Link between Distinct Developmental Language Disorders
2008
and 1 more

Author Peers

Author Last Decade Papers Cites
Simon E. Fisher 5288 4756 4064 4263 220 13.8k
Faraneh Vargha‐Khadem 1803 1453 3435 6718 152 12.6k
Anthony P. Monaco 10103 15427 3530 3562 574 32.4k
Albert M. Galaburda 1273 1401 4045 7477 168 13.3k
Ursula Bellugi 1225 1661 5150 3964 202 13.8k
Norman Geschwind 1127 901 4637 12864 126 18.3k
William T. Greenough 5441 6481 938 8404 200 22.9k
Glenn D. Rosen 1209 3400 2659 3575 190 12.1k
Stephen J. Suomi 1318 1320 2109 3086 361 16.3k
Kenneth K. Kídd 9708 6958 428 1688 381 23.4k
Chet C. Sherwood 764 2042 583 3248 223 9.0k

All Works

Loading papers...

Rankless by CCL
2026