Standout Papers

LOVD v.2.0: the next generation in gene variant data... 1999 2026 2008 2017 680
  1. LOVD v.2.0: the next generation in gene variant databases (2011)
    Ivo F.A.C. Fokkema, Peter E.M. Taschner et al. Human Mutation
  2. Mutations in the O-Mannosyltransferase Gene POMT1 Give Rise to the Severe Neuronal Migration Disorder Walker-Warburg Syndrome (2002)
    Sophie Currier, Alice Steinbrecher et al. The American Journal of Human Genetics
  3. Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC Syndrome (1999)
    Jacopo Celli, Pascal H. G. Duijf et al. Cell

Immediate Impact

13 by Nobel laureates 28 from Science/Nature 59 standout
Sub-graph 1 of 22

Citing Papers

Human TKTL1 implies greater neurogenesis in frontal neocortex of modern humans than Neanderthals
2022 StandoutScienceNobel
The changing landscape of atherosclerosis
2021 StandoutNature
2 intermediate papers

Works of Jacopo Celli being referenced

Low‐Density Lipoprotein Receptor Gene Familial Hypercholesterolemia Variant Database: Update and Pathological Assessment
2012
Mutations in the O-Mannosyltransferase Gene POMT1 Give Rise to the Severe Neuronal Migration Disorder Walker-Warburg Syndrome
2002 Standout

Author Peers

Author Last Decade Papers Cites
Jacopo Celli 1571 803 363 401 16 2.4k
Anita Farhi 2286 1041 277 362 14 3.5k
Lisa Garrett‐Beal 2425 703 347 662 17 3.4k
Frieder Schwenk 2466 760 267 424 19 4.1k
Charles P. Harris 1933 450 441 341 25 2.7k
Elizabeth Robertson 2159 717 372 232 12 3.6k
Ruchi Bajpai 2827 627 317 231 25 3.5k
Pleasantine Mill 2413 773 215 397 32 3.3k
Donald A. Glass 2283 538 220 752 38 3.2k
Juha Saharinen 1910 710 194 469 34 3.0k
Peter Bialek 2350 534 187 718 18 3.1k

All Works

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2026