M. Jacquemont
Impact in
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- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Papers in
- Genetics 2
- Genomic variations and chromosomal abnormalities 1
- Animal Genetics and Reproduction 1
- Congenital Ear and Nasal Anomalies 1
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- Genomics and Chromatin Dynamics 1
- Co-authors
- Valérie Malan (2 shared papers)Damien Sanlaville (1 shared paper)Jean‐Louis Taillemite (1 shared paper)Christian Grillon (1 shared paper)Azarnouche Ardalan (1 shared paper)Lydie Bürglen (1 shared paper)Julie Steffann (1 shared paper)Bérénice Doray (1 shared paper)
- Journals
- Clinical Genetics (1 paper)PubMed (1 paper)
- Partner nations
- France
In The Last Decade
M. Jacquemont
2 papers receiving 30 citations
Peers
Comparison fields: 5 of 15
- Genetics 14
- Pediatrics, Perinatology and Child Health 4
- Pulmonary and Respiratory Medicine 6
- Genetics 2
- Surgery 8
Countries citing papers authored by M. Jacquemont
This map shows the geographic impact of M. Jacquemont'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 M. Jacquemont with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Jacquemont more than expected).
Fields of papers citing papers by M. Jacquemont
This network shows the impact of papers produced by M. Jacquemont. 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 M. Jacquemont. The network helps show where M. Jacquemont may publish in the future.
Co-authors
The 15 scholars most cited alongside M. Jacquemont, 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 | 2015 | 16 | |
| 2 | A new case of a severe clinical phenotype of the cat-eye syndrome. | 2004 | 14 |
About M. Jacquemont
M. Jacquemont is a scholar working on Genetics, Molecular Biology, Genetics, Immunology and Allergy and Plant Science, having authored 2 papers that have together received 30 indexed citations. Recurring topics across this work include Cell Adhesion Molecules Research (1 paper), Genomics and Chromatin Dynamics (1 paper), Genomic variations and chromosomal abnormalities (1 paper), Chromosomal and Genetic Variations (1 paper), Animal Genetics and Reproduction (1 paper) and Congenital Ear and Nasal Anomalies (1 paper). The work is most often cited by research in Genetics (14 citations), Pediatrics, Perinatology and Child Health (4 citations), Pulmonary and Respiratory Medicine (6 citations), Genetics (2 citations) and Surgery (8 citations). M. Jacquemont has collaborated with scholars based in France. Frequent co-authors include Valérie Malan, Damien Sanlaville, Jean‐Louis Taillemite, Christian Grillon, Azarnouche Ardalan, Lydie Bürglen, Julie Steffann, Bérénice Doray, Serge Romana and C Turleau. Their work appears in journals such as Clinical Genetics and PubMed.
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.