A.L. Mosca
Impact in
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- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Craniofacial Disorders and Treatments
- Congenital Ear and Nasal Anomalies
Papers in
- Genetics 8
- Genomic variations and chromosomal abnormalities 6
- Genetics and Neurodevelopmental Disorders 2
- Genetic Syndromes and Imprinting 2
- Congenital Ear and Nasal Anomalies 2
- Dermatological and Skeletal Disorders 1
- Connective tissue disorders research 1
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- Congenital heart defects research 2
- Co-authors
- Patrick Callier (8 shared papers)Francine Mugneret (8 shared papers)Nathalie Marle (7 shared papers)Frédéric Huet (6 shared papers)Laurence Faivre (7 shared papers)Alice Masurel‐Paulet (6 shared papers)Christel Thauvin‐Robinet (5 shared papers)J. Teyssier (3 shared papers)
- Journals
- European Journal of Medical Genetics (2 papers)American Journal of Medical Genetics Part A (6 papers)
- Partner nations
- France
In The Last Decade
A.L. Mosca
8 papers receiving 68 citations
Peers
Comparison fields: 5 of 22
- Genetics 61
- Developmental Biology 2
- Pediatrics, Perinatology and Child Health 18
- Genetics 8
- Molecular Biology 30
Countries citing papers authored by A.L. Mosca
This map shows the geographic impact of A.L. Mosca'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 A.L. Mosca with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A.L. Mosca more than expected).
Fields of papers citing papers by A.L. Mosca
This network shows the impact of papers produced by A.L. Mosca. 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 A.L. Mosca. The network helps show where A.L. Mosca may publish in the future.
Co-authors
The 25 scholars most cited alongside A.L. Mosca, 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 | 2008 | 20 | |
| 2 | 2009 | 13 | |
| 3 | 2007 | 9 | |
| 4 | 2009 | 8 | |
| 5 | 2010 | 7 | |
| 6 | 2007 | 7 | |
| 7 | 2006 | 3 | |
| 8 | 2011 | 2 |
About A.L. Mosca
A.L. Mosca is a scholar working on Genetics, Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health and Plant Science, having authored 8 papers that have together received 69 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Congenital heart defects research (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Chromosomal and Genetic Variations (2 papers), Genetic Syndromes and Imprinting (2 papers), Congenital Ear and Nasal Anomalies (2 papers), Dermatological and Skeletal Disorders (1 paper) and Connective tissue disorders research (1 paper). The work is most often cited by research in Genetics (61 citations), Developmental Biology (2 citations), Pediatrics, Perinatology and Child Health (18 citations), Genetics (8 citations) and Molecular Biology (30 citations). A.L. Mosca has collaborated with scholars based in France. Frequent co-authors include Patrick Callier, Francine Mugneret, Nathalie Marle, Frédéric Huet, Laurence Faivre, Alice Masurel‐Paulet, Christel Thauvin‐Robinet, J. Teyssier, Louise Joly and Julien Guy. Their work appears in journals such as European Journal of Medical Genetics and American Journal of Medical Genetics Part A.
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.