Alexandre Mathieu

1.3k citations
7 papers · 156 · h-index 6

Impact in

    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Genomics and Rare Diseases
    • Genetic Associations and Epidemiology
    • Autism Spectrum Disorder Research

Papers in

    • Genomic variations and chromosomal abnormalities 5
    • Genetics and Neurodevelopmental Disorders 3
    • Genomics and Rare Diseases 2
    • Congenital heart defects research 3
    • Advanced biosensing and bioanalysis techniques 1
    • Biochemical and Molecular Research 1

Alexandre Mathieu

6 papers receiving 155 citations

Peers

Alexandre Mathieu
Comparison fields: 5 of 49
  • Genetics 97
  • Cognitive Neuroscience 48
  • Developmental Neuroscience 5
  • Molecular Biology 81
  • Cellular and Molecular Neuroscience 16
Replace Nathan P. Achilly with:
Nathan P. Achilly United States
Jordana Weissman United States
Ramalakshmi Ramasamy United States
Gérald Bussy France
Elysa J. Marco United States
Marta Codina‐Solà Spain
Laura C. Murphy United Kingdom
Tianyun Wang China
Anna Mikhailov Canada
Marion Pilorge France
Alexandre Mathieu relative to Nathan P. Achilly United States Nathan P. Achilly's profile →
Citations per field
00.5×3.4×
Nathan P. Achilly · 1×
Citations per year

Countries citing papers authored by Alexandre Mathieu

Since Specialization
Citations

This map shows the geographic impact of Alexandre Mathieu's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Alexandre Mathieu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alexandre Mathieu more than expected).

Fields of papers citing papers by Alexandre Mathieu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alexandre Mathieu. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Alexandre Mathieu. The network helps show where Alexandre Mathieu may publish in the future.

Co-authors

The 25 scholars most cited alongside Alexandre Mathieu, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Alexandre Mathieu Line = papers co-authored together Alexandre Mathieu links everyone, so they are left out of the graph.

All Works

7 of 7 papers shown
#Work
1 201952
2 201845
3 202118
4 201517
5 202314
6 201810
7 20250

About Alexandre Mathieu

Alexandre Mathieu is a scholar working on Genetics, Molecular Biology, Surgery, Cardiology and Cardiovascular Medicine and Clinical Psychology, having authored 7 papers that have together received 156 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Congenital heart defects research (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genomics and Rare Diseases (2 papers), Tryptophan and brain disorders (1 paper), Pancreatic function and diabetes (1 paper), Advanced biosensing and bioanalysis techniques (1 paper) and Biochemical and Molecular Research (1 paper). The work is most often cited by research in Genetics (97 citations), Cognitive Neuroscience (48 citations), Developmental Neuroscience (5 citations), Molecular Biology (81 citations) and Cellular and Molecular Neuroscience (16 citations). Alexandre Mathieu has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Thomas Bourgeron, Claire S. Leblond, Guillaume Huguet, Nathalie Lemière, Freddy Cliquet, Christopher Gillberg, Richard Delorme, Jean‐François Deleuze, Julien Buratti and Thierry Bienvenu. Their work appears in journals such as European Journal of Medical Genetics, JAMA Psychiatry, npj Genomic Medicine, Translational Psychiatry and Journal of Applied Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact