Marie‐Pierre Moizard
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research
Papers in
- Genetics 13
- Genetics and Neurodevelopmental Disorders 7
- Genetic Syndromes and Imprinting 5
- Genomic variations and chromosomal abnormalities 5
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- RNA modifications and cancer 5
- Ubiquitin and proteasome pathways 3
- Muscle Physiology and Disorders 3
- Congenital heart defects research 3
- Epigenetics and DNA Methylation 2
- Co-authors
- Claude Moraine (9 shared papers)Martine Raynaud (10 shared papers)Christian Andrés (2 shared papers)Annick Toutain (11 shared papers)Nathalie Ronce (9 shared papers)Sylvain Briault (5 shared papers)Hans‐Hilger Ropers (2 shared papers)Frédéric Laumonnier (3 shared papers)
- Journals
- European Journal of Human Genetics (3 papers)Clinical Genetics (2 papers)The American Journal of Human Genetics (2 papers)Human Mutation (2 papers)Human Genetics (1 paper)
- Partner nations
- FranceGermanyNetherlands
In The Last Decade
Marie‐Pierre Moizard
18 papers receiving 1.0k citations
Marie‐Pierre Moizard's Hit Papers
Peers
Comparison fields: 5 of 76
- Genetics 515
- Cognitive Neuroscience 313
- Aging 18
- Molecular Biology 662
- Cellular and Molecular Neuroscience 166
Countries citing papers authored by Marie‐Pierre Moizard
This map shows the geographic impact of Marie‐Pierre Moizard'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 Marie‐Pierre Moizard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marie‐Pierre Moizard more than expected).
Fields of papers citing papers by Marie‐Pierre Moizard
This network shows the impact of papers produced by Marie‐Pierre Moizard. 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 Marie‐Pierre Moizard. The network helps show where Marie‐Pierre Moizard may publish in the future.
Co-authors
The 25 scholars most cited alongside Marie‐Pierre Moizard, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family Hit paper breakdown → | 2004 | 552 |
| 2 | 2006 | 155 | |
| 3 | 1998 | 99 | |
| 4 | 2000 | 87 | |
| 5 | 2013 | 30 | |
| 6 | 2018 | 22 | |
| 7 | 2000 | 17 | |
| 8 | 2008 | 15 | |
| 9 | 1994 | 14 | |
| 10 | 2021 | 14 | |
| 11 | 1996 | 12 | |
| 12 | 1999 | 10 | |
| 13 | 2019 | 10 | |
| 14 | 2002 | 9 | |
| 15 | 2013 | 5 | |
| 16 | 1997 | 4 | |
| 17 | Novel nonsense mutation of GPC3 gene in a patient with Simpson-Golabi-Behmel syndrome. | 2011 | 2 |
| 18 | 2024 | 1 | |
| 19 | 2025 | 0 |
About Marie‐Pierre Moizard
Marie‐Pierre Moizard is a scholar working on Genetics, Molecular Biology, Genetics, Surgery and Pediatrics, Perinatology and Child Health, having authored 19 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (7 papers), Genetic Syndromes and Imprinting (5 papers), RNA modifications and cancer (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Ubiquitin and proteasome pathways (3 papers), Muscle Physiology and Disorders (3 papers), Congenital heart defects research (3 papers) and Epigenetics and DNA Methylation (2 papers). The work is most often cited by research in Genetics (515 citations), Cognitive Neuroscience (313 citations), Aging (18 citations), Molecular Biology (662 citations) and Cellular and Molecular Neuroscience (166 citations). Marie‐Pierre Moizard has collaborated with scholars based in France, Germany and Netherlands. Frequent co-authors include Claude Moraine, Martine Raynaud, Christian Andrés, Annick Toutain, Nathalie Ronce, Sylvain Briault, Hans‐Hilger Ropers, Frédéric Laumonnier, Marie Gomot and Jamel Chelly. Their work appears in journals such as European Journal of Human Genetics, Clinical Genetics, The American Journal of Human Genetics, Human Mutation and Human 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.