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Dominique Campion

Dominique Campion

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Genetics
France
2024

D-Index & Metrics

Genetics

D-Index
89
Citations
59136
World Ranking
1092
National Ranking
38

Medicine

D-Index
90
Citations
59859
World Ranking
11947
National Ranking
370

Research.com Recognitions

  • 2024 - Research.com Genetics in France Leader Award

Overview

Dominique Campion is affiliated with the University of Rouen in France. Their research spans multiple areas within biochemistry, genetics, molecular biology, and medicine, with a primary focus on genetics and molecular biological processes. Their work is positioned at the intersection of several specialized subfields including genetics, molecular biology, physiology, neurology, and statistics and probability.

Their research primarily addresses topics related to genomics and rare diseases, Alzheimer's disease research and treatments, genomic variations and chromosomal abnormalities, genetic associations and epidemiology, genetics and neurodevelopmental disorders, epigenetics and DNA methylation, as well as bioinformatics and genomic networks.

Dominique Campion has contributed to a range of scientific publications, with frequent publication venues including:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Alzheimer s & Dementia
  • European Journal of Human Genetics
  • Translational Psychiatry
  • Acta Neuropathologica Communications

Some of their recent papers include:

  • A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts, 2021, Biological Psychiatry
  • Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease, 2022, Nature Genetics
  • Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia, 2022, JAMA Psychiatry
  • Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohorts, 2020, The Lancet Rheumatology
  • Functional correlation of genome-wide DNA methylation profiles in genetic neurodevelopmental disorders, 2022, Human Mutation

Dominique Campion frequently collaborates with several co-authors, including:

  • Gaël Nicolas
  • Camille Charbonnier
  • Anne Boland
  • David Wallon
  • Stéphane Rousseau

Best Publications

  • Biological insights from 108 schizophrenia-associated genetic loci

    Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Aiden Corvin;James T. R. Walters

  • 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

  • Genome-wide association study indentifies variants at CLU and CR1 associated with Alzheimer’s disease

    J Lambert;S Heath;G Even;D Campion

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

    Paul Hollingworth;Denise Harold;Rebecca Sims;Amy Gerrish

  • Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

    Bjarni J. Vilhjálmsson;Jian Yang;Hilary K. Finucane;Alexander Gusev

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

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

  • Genome-wide analysis of genetic loci associated with Alzheimer disease.

    Sudha Seshadri;Annette L. Fitzpatrick;M Arfan Ikram;Anita L. DeStefano

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

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

  • Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders

    Phil H. Lee;Verneri Anttila;Hyejung Won;Yen-Chen A. Feng

  • Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

    Rebecca Sims;Sven J. Van Der Lee;Adam C. Naj;Céline Bellenguez;Céline Bellenguez

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

    Dominique Campion;Cécile Dumanchin;Didier Hannequin;Bruno Dubois

  • Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

    Christian R Marshall;Daniel P Howrigan;Daniel P Howrigan;Daniele Merico;Bhooma Thiruvahindrapuram

  • APOE and Alzheimer disease: a major gene with semi-dominant inheritance

    E Genin;D Hannequin;D Wallon;K Sleegers

  • Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

    Douglas M. Ruderfer;Stephan Ripke;Stephan Ripke;Stephan Ripke;Andrew McQuillin;James Boocock

  • Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases

    Alexander Gusev;S. Hong Lee;Gosia Trynka;Hilary Finucane

  • A new highly penetrant form of obesity due to deletions on chromosome 16p11.2

    R. G. Walters;S. Jacquemont;A. Valsesia;A. Valsesia;A. Valsesia;A. J. de Smith

  • APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases

    Hélène-Marie Lanoiselée;Gaël Nicolas;David Wallon;Anne Rovelet-Lecrux

  • Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

    Sébastien Jacquemont;Alexandre Reymond;Flore Zufferey;Louise Harewood

  • Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation.

    Audrey Guilmatre;Christèle Dubourg;Anne-Laure Mosca;Solenn Legallic

  • Genome wide meta-analysis identifies genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders

    Lee Ph;Anttila;Won H

Frequent Co-Authors

Didier Hannequin
Didier Hannequin Grenoble Alpes University
Thierry Frebourg
Thierry Frebourg Grenoble Alpes University
Alexis Brice
Alexis Brice Institut du Cerveau
Florence Pasquier
Florence Pasquier University of Lille
Dan Rujescu
Dan Rujescu Medical University of Vienna
Jacques Mallet
Jacques Mallet Centre national de la recherche scientifique, CNRS
Michael John Owen
Michael John Owen Cardiff University
Tonu Esko
Tonu Esko University of Tartu
Aarno Palotie
Aarno Palotie University of Helsinki

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