Valérie Malan
- Genetics top 2%
- Genomic variations and chromosomal abnormalities 30
- Genetics and Neurodevelopmental Disorders 12
- Genomics and Rare Diseases 11
- Genetic Syndromes and Imprinting 7
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- Prenatal Screening and Diagnostics 24
- Fetal and Pediatric Neurological Disorders 9
- Molecular Biology top 10%
- Congenital heart defects research 10
- Cognitive Neuroscience top 10%
- Autism Spectrum Disorder Research 6
Valérie Malan
66 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 84
- Genetics 923
- Pediatrics, Perinatology and Child Health 333
- Molecular Biology 733
- Developmental Neuroscience 34
- Cognitive Neuroscience 148
Countries citing papers authored by Valérie Malan
This map shows the geographic impact of Valérie Malan'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 Valérie Malan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Valérie Malan more than expected).
Fields of papers citing papers by Valérie Malan
This network shows the impact of papers produced by Valérie Malan. 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 Valérie Malan. The network helps show where Valérie Malan may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Valérie Malan, 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 | 2023 | 1 | |
| 2 | 2022 | 8 | |
| 3 | 2022 | 9 | |
| 4 | 2021 | 16 | |
| 5 | 2021 | 17 | |
| 6 | 2019 | 3 | |
| 7 | 2019 | 4 | |
| 8 | 2019 | 26 | |
| 9 | 2017 | 4 | |
| 10 | 2017 | 7 | |
| 11 | 2015 | 31 | |
| 12 | 2015 | 13 | |
| 13 | 2013 | 12 | |
| 14 | 2013 | 8 | |
| 15 | 2013 | 10 | |
| 16 | 2009 | 12 | |
| 17 | 2008 | 2 | |
| 18 | 2007 | 32 | |
| 19 | 2007 | 212 | |
| 20 | 2005 | 74 |
About Valérie Malan
Valérie Malan is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 69 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (30 papers), Prenatal Screening and Diagnostics (24 papers), Genetics and Neurodevelopmental Disorders (12 papers), Genomics and Rare Diseases (11 papers), Congenital heart defects research (10 papers), Fetal and Pediatric Neurological Disorders (9 papers), Genetic Syndromes and Imprinting (7 papers) and Autism Spectrum Disorder Research (6 papers). The work is most often cited by research in Genetics (923 citations), Pediatrics, Perinatology and Child Health (333 citations) and Molecular Biology (733 citations). Valérie Malan has collaborated with scholars based in France, Belgium and Switzerland. Frequent co-authors include Michel Vekemans, Arnold Münnich, Laurence Colleaux, C Turleau, Nathalie Boddaert, Marlène Rio, Jeanne Amiel, Stanislas Lyonnet, Loïc de Pontual and Nigel P. Carter. Their work appears in journals such as JAMA, Nucleic Acids Research and The Journal of Clinical Endocrinology & Metabolism.
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.