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Genetics
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2026

D-Index & Metrics

Best Scientists

D-Index
169
Citations
127847
World Ranking
904
National Ranking
18

Medicine

D-Index
173
Citations
134670
World Ranking
470
National Ranking
12

Genetics

D-Index
169
Citations
129157
World Ranking
71
National Ranking
1

Alexis Brice publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Alexis Brice sits on this spectrum.

45–54 publications: 6 scientists 55–64 publications: 10 scientists 65–74 publications: 35 scientists 75–84 publications: 84 scientists 85–94 publications: 102 scientists 95–104 publications: 151 scientists 105–114 publications: 175 scientists 115–124 publications: 203 scientists 125–134 publications: 217 scientists 135–144 publications: 205 scientists 145–154 publications: 193 scientists 155–164 publications: 188 scientists 165–174 publications: 170 scientists 175–184 publications: 178 scientists 185–194 publications: 164 scientists 195–204 publications: 173 scientists 205–214 publications: 159 scientists 215–224 publications: 134 scientists 225–234 publications: 143 scientists 235–244 publications: 105 scientists 245–254 publications: 114 scientists 255–264 publications: 92 scientists 265–274 publications: 88 scientists 275–284 publications: 87 scientists 285–294 publications: 80 scientists 295–304 publications: 62 scientists 305–314 publications: 75 scientists 315–324 publications: 67 scientists 325–334 publications: 60 scientists 335–344 publications: 52 scientists 345–354 publications: 40 scientists 355–364 publications: 48 scientists 365–374 publications: 47 scientists 375–384 publications: 46 scientists 385–394 publications: 31 scientists 395–404 publications: 27 scientists 405–414 publications: 40 scientists 415–424 publications: 30 scientists 425–434 publications: 43 scientists 435–444 publications: 29 scientists 445–454 publications: 14 scientists 455–464 publications: 28 scientists 465–474 publications: 21 scientists 475–484 publications: 21 scientists 485–494 publications: 22 scientists 495–504 publications: 17 scientists 505–514 publications: 12 scientists 515–524 publications: 11 scientists 525–534 publications: 8 scientists 535–544 publications: 8 scientists 545–554 publications: 14 scientists 555–564 publications: 4 scientists 565–574 publications: 11 scientists 575–584 publications: 5 scientists 585–594 publications: 11 scientists 595–604 publications: 12 scientists 605–614 publications: 7 scientists 615–624 publications: 6 scientists 625–634 publications: 10 scientists 635–644 publications: 9 scientists 645–654 publications: 10 scientists 655–664 publications: 6 scientists 665–674 publications: 6 scientists 675–684 publications: 6 scientists 685–694 publications: 4 scientists 695–702 publications: 6 scientists 703+ publications: 100 scientists
45 publications 703+

This scientist: 932 publications — 99th percentile

99% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 703 publications or more.

Alexis Brice D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where Alexis Brice sits on this spectrum.

40–41 D-Index: 24 scientists 42–43 D-Index: 52 scientists 44–45 D-Index: 84 scientists 46–47 D-Index: 112 scientists 48–49 D-Index: 118 scientists 50–51 D-Index: 141 scientists 52–53 D-Index: 143 scientists 54–55 D-Index: 145 scientists 56–57 D-Index: 179 scientists 58–59 D-Index: 162 scientists 60–61 D-Index: 175 scientists 62–63 D-Index: 191 scientists 64–65 D-Index: 172 scientists 66–67 D-Index: 184 scientists 68–69 D-Index: 164 scientists 70–71 D-Index: 158 scientists 72–73 D-Index: 150 scientists 74–75 D-Index: 136 scientists 76–77 D-Index: 127 scientists 78–79 D-Index: 127 scientists 80–81 D-Index: 111 scientists 82–83 D-Index: 110 scientists 84–85 D-Index: 110 scientists 86–87 D-Index: 84 scientists 88–89 D-Index: 102 scientists 90–91 D-Index: 66 scientists 92–93 D-Index: 72 scientists 94–95 D-Index: 70 scientists 96–97 D-Index: 54 scientists 98–99 D-Index: 60 scientists 100–101 D-Index: 49 scientists 102–103 D-Index: 55 scientists 104–105 D-Index: 45 scientists 106–107 D-Index: 42 scientists 108–109 D-Index: 28 scientists 110–111 D-Index: 39 scientists 112–113 D-Index: 25 scientists 114–115 D-Index: 31 scientists 116–117 D-Index: 29 scientists 118–119 D-Index: 34 scientists 120–121 D-Index: 29 scientists 122–123 D-Index: 29 scientists 124–125 D-Index: 18 scientists 126–127 D-Index: 27 scientists 128–129 D-Index: 22 scientists 130–131 D-Index: 16 scientists 132–133 D-Index: 11 scientists 134–135 D-Index: 17 scientists 136–137 D-Index: 12 scientists 138–139 D-Index: 21 scientists 140–141 D-Index: 4 scientists 142–143 D-Index: 9 scientists 144–145 D-Index: 14 scientists 146–147 D-Index: 6 scientists 148–149 D-Index: 10 scientists 150–151 D-Index: 7 scientists 152–153 D-Index: 9 scientists 154–155 D-Index: 8 scientists 156–157 D-Index: 8 scientists 158–159 D-Index: 9 scientists 160+ D-Index: 96 scientists
40 D-Index 160+

This scientist: 169 D-Index — 98th percentile

98% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 160 D-Index or more.

Research.com Recognitions

  • 2026 - Research.com Genetics in France Leader Award
  • 2026 - Research.com Medicine in France Leader Award
  • 2025 - Research.com Best Scientists Award
  • 2025 - Research.com Genetics in France Leader Award
  • 2025 - Research.com Medicine in France Leader Award
  • 2024 - Research.com Genetics in France Leader Award
  • 2024 - Research.com Genetics and Molecular Biology in France Leader Award
  • 2023 - Research.com Genetics in France Leader Award
  • 2023 - Research.com Genetics and Molecular Biology in France Leader Award
  • 2023 - Research.com Medicine in France Leader Award
  • 2022 - Research.com Genetics and Molecular Biology in France Leader Award

Overview

Alexis Brice is affiliated with the Institut du Cerveau in France and has contributed extensively to research in medicine, biochemistry, genetics, molecular biology, and neuroscience. Their work primarily spans neurology, molecular biology, cellular and molecular neuroscience, genetics, and physiology.

The scientist's research topics focus on Parkinson's disease mechanisms and treatments, genetic neurodegenerative diseases, neurological diseases and metabolism, mitochondrial function and pathology, nuclear receptors and signaling, neurological disorders and treatments, and amyotrophic lateral sclerosis research.

Frequent publication venues for Alexis Brice include bioRxiv (Cold Spring Harbor Laboratory), Movement Disorders, Brain, npj Parkinson's Disease, and Neurology.

Collaborations have been established with several frequent co-authors including Jean-Christophe Corvol, Suzanne Lesage, Alexandra Dürr, Huw R. Morris, and Andrew Singleton.

Recent notable papers include:

  • Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology, 2021, Nature Genetics
  • Finding genetically-supported drug targets for Parkinson's disease using Mendelian randomization of the druggable genome, 2021, Nature Communications
  • Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets, 2021, JAMA Neurology
  • Genome-wide survival study identifies a novel synaptic locus and polygenic score for cognitive progression in Parkinson's disease, 2021, Nature Genetics
  • Differences in the Presentation and Progression of Parkinson's Disease by Sex, 2020, Movement Disorders

Alexis Brice has authored a book published by Springer International Publishing titled Trials for Cerebellar Ataxias in 2023.

Best Publications

  • Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

    Jean-Charles Lambert;Jean-Charles Lambert;Jean-Charles Lambert;Carla A Ibrahim-Verbaas;Denise Harold;Adam C Naj

  • Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism

    Vincenzo Bonifati;Vincenzo Bonifati;Patrizia Rizzu;Marijke J. van Baren;Onno Schaap

  • Friedreich's Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat Expansion

    Victoria Campuzano;Laura Montermini;Maria Dolores Moltò;Luigi Pianese

  • Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease

    Ellen Sidransky;Michael A. Nalls;Jan O. Aasly;Judith Aharon-Peretz

  • Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies

    Mike A Nalls;Cornelis Blauwendraat;Costanza L Vallerga;Karl Heilbron

  • Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.

    Paul Hollingworth;Denise Harold;Rebecca Sims;Amy Gerrish

  • Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

    Mike A Nalls;Nathan Pankratz;Christina M. Lill;Chuong B. Do

  • Association between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene

    CB Lucking;A Durr;Bonifati;J Vaughan

  • Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

    Daniel G Healy;Mario Falchi;Sean S O'Sullivan;Vincenzo Bonifati

  • APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

    Anne Rovelet-Lecrux;Didier Hannequin;Gregory Raux;Nathalie Le Meur

  • Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease.

    Valentina Escott-Price;Céline Bellenguez;Li-San Wang;Seung-Hoan Choi

  • Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

    Elisa Majounie;Alan E. Renton;Kin Mok;Elise G. P. Dopper;Elise G. P. Dopper

  • Causal relation between α-synuclein locus duplication as a cause of familial Parkinson's disease

    P Ibáñez;A-M Bonnet;B Débarges;E Lohmann

  • Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.

    Andrew Escayg;Bryan T. MacDonald;Miriam H. Meisler;Stéphanie Baulac

  • Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia

    Alexandra Dürr;Mireille Cossee;Yves Agid;Victoria Campuzano

  • Parkinson's disease: from monogenic forms to genetic susceptibility factors

    Suzanne Lesage;Alexis Brice

  • Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum

    Dominique Campion;Cécile Dumanchin;Didier Hannequin;Bruno Dubois

  • First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene.

    Stéphanie Baulac;Gilles Huberfeld;Isabelle Gourfinkel-An;Georgia Mitropoulou

  • Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats

    Georges Imbert;Frédéric Saudou;Frédéric Saudou;Gaël Yvert;Gaël Yvert;Didier Devys;Didier Devys

  • Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.

    Michael A Nalls;Vincent Plagnol;Dena G Hernandez

Frequent Co-Authors

Alexandra Durr
Alexandra Durr Sorbonne University
Giovanni Stevanin
Giovanni Stevanin Inserm : Institut national de la santé et de la recherche médicale
Yves Agid
Yves Agid Institut du Cerveau
Didier Hannequin
Didier Hannequin Grenoble Alpes University
Thomas Gasser
Thomas Gasser University of Tübingen
Eric LeGuern
Eric LeGuern Institut du Cerveau
Suzanne Lesage
Suzanne Lesage Université Paris Cité
Nicholas W. Wood
Nicholas W. Wood University College London
Peter Heutink
Peter Heutink German Center for Neurodegenerative Diseases
Andrew B. Singleton
Andrew B. Singleton National Institutes of Health

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Related Online Degrees & Career Pathways

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Nurses looking to further specialize can explore some of the best online bsn to dnp programs, integrating advanced practice nursing with genetics competencies. Additionally, it’s important to understand the cost of rn to bsn options, ensuring you find a pathway that fits both your career goals and budget.

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