Standout Papers

Mutations in the <i>DJ-1</i> Gene Associated with Autosomal Recessive Ea... 1996 2026 2006 2016 2.1k
  1. Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism (2003)
    Vincenzo Bonifati, Patrizia Rizzu et al. Science
  2. APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy (2005)
    Anne Rovelet‐Lecrux, Didier Hannequin et al. Nature Genetics
  3. Causal relation between α-synuclein locus duplication as a cause of familial Parkinson's disease (2004)
    Pablo Ibáñez, Ebba Lohmann et al. The Lancet
  4. Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia (1996)
    Alexandra Dürr, Mireille Cossée et al. New England Journal of Medicine
  5. Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2 (2000)
    Andrew Escayg, Bryan T. MacDonald et al. Nature Genetics
  6. Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats (1996)
    Georges Imbert, Frédéric Saudou et al. Nature Genetics
  7. Parkinson's disease: from monogenic forms to genetic susceptibility factors (2009)
    Suzanne Lesage, Alexis Brice Human Molecular Genetics
  8. Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies (2011)
    Michael A. Nalls, Vincent Plagnol et al. The Lancet
  9. Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion (1997)
    Gilles David, Nacer Abbas et al. Nature Genetics
  10. First genetic evidence of GABAA receptor dysfunction in epilepsy: a mutation in the γ2-subunit gene (2001)
    Stéphanie Baulac, Gilles Huberfeld et al. Nature Genetics
  11. Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias (1995)
    Yvon Trottier, Yves Lutz et al. Nature
  12. Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum (1999)
    Dominique Campion, Cécile Dumanchin et al. The American Journal of Human Genetics
  13. G51D α‐synuclein mutation causes a novel Parkinsonian–pyramidal syndrome (2013)
    Suzanne Lesage, Mathieu Anheim et al. Annals of Neurology

Immediate Impact

3 by Nobel laureates 29 from Science/Nature 103 standout
Sub-graph 1 of 16

Citing Papers

The Human and Mouse Enteric Nervous System at Single-Cell Resolution
2020 Standout
Spatiotemporal dynamics of molecular pathology in amyotrophic lateral sclerosis
2019 StandoutScience
3 intermediate papers

Works of Alexis Brice being referenced

Inhibition of Lysosome Membrane Recycling Causes Accumulation of Gangliosides that Contribute to Neurodegeneration
2018
Loss of function of C9orf72 causes motor deficits in a zebrafish model of amyotrophic lateral sclerosis
2013
and 2 more

Author Peers

Author Last Decade Papers Cites
Alexis Brice 18576 15926 16673 535 35.0k
Patrik Brundin 17482 15185 14307 361 34.7k
Donald L. Price 16227 9744 16722 362 43.7k
James F. Gusella 13880 10292 22076 460 40.6k
Olle Lindvall 23677 7354 15711 360 42.1k
Serge Przedborski 15116 21509 14134 257 40.8k
M. Flint Beal 14927 11599 19598 271 35.8k
Guy A. Rouleau 7610 13004 14128 652 32.8k
Gen Sobue 9446 11411 12236 750 27.5k
Jeffrey D. Rothstein 14827 12187 15518 233 36.6k
Christian Haass 9602 9853 23797 383 49.1k

All Works

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2026