A. Moncla
Impact in
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
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- Epigenetics and DNA Methylation
- RNA modifications and cancer
Papers in
- Genetics 20
- Genomic variations and chromosomal abnormalities 9
- Genetics and Neurodevelopmental Disorders 8
- Genetic Syndromes and Imprinting 6
- Neurogenetic and Muscular Disorders Research 4
- Connective tissue disorders research 3
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- Epigenetics and DNA Methylation 5
- Co-authors
- Perrine Malzac (6 shared papers)Marie‐Geneviève Mattéi (9 shared papers)D. Depétris (3 shared papers)Cécile Mignon‐Ravix (3 shared papers)Laurent Villard (4 shared papers)N. Philip (7 shared papers)Marie‐Antoinette Voelckel (3 shared papers)André Mégarbané (2 shared papers)
- Journals
- Journal of Medical Genetics (5 papers)European Journal of Pediatrics (2 papers)European Journal of Human Genetics (2 papers)European Journal of Medical Genetics (1 paper)Neuromuscular Disorders (1 paper)
- Partner nations
- FranceItalyUnited Kingdom
In The Last Decade
A. Moncla
29 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 75
- Genetics 737
- Molecular Biology 589
- Pediatrics, Perinatology and Child Health 148
- Developmental Neuroscience 32
- Pharmacy 26
Countries citing papers authored by A. Moncla
This map shows the geographic impact of A. Moncla'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. Moncla with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A. Moncla more than expected).
Fields of papers citing papers by A. Moncla
This network shows the impact of papers produced by A. Moncla. 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. Moncla. The network helps show where A. Moncla may publish in the future.
Co-authors
The 25 scholars most cited alongside A. Moncla, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 30 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1998 | 122 | |
| 2 | 2006 | 104 | |
| 3 | Triplet repeat expansion at the FRAXE locus and X-linked mild mental handicap. | 1994 | 90 |
| 4 | 2004 | 89 | |
| 5 | 2008 | 88 | |
| 6 | 1992 | 86 | |
| 7 | 2009 | 74 | |
| 8 | 2000 | 66 | |
| 9 | 2005 | 57 | |
| 10 | New domains of neural cell-adhesion molecule L1 implicated in X-linked hydrocephalus and MASA syndrome. | 1995 | 57 |
| 11 | 1996 | 54 | |
| 12 | 1993 | 42 | |
| 13 | 2009 | 33 | |
| 14 | 1991 | 32 | |
| 15 | 1995 | 29 | |
| 16 | 2000 | 23 | |
| 17 | 1999 | 20 | |
| 18 | The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21). | 1993 | 15 |
| 19 | 1992 | 11 | |
| 20 | 1998 | 10 |
About A. Moncla
A. Moncla is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Genetics and Pediatrics, Perinatology and Child Health, having authored 30 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (8 papers), Genetic Syndromes and Imprinting (6 papers), Hereditary Neurological Disorders (5 papers), Epigenetics and DNA Methylation (5 papers), Neurogenetic and Muscular Disorders Research (4 papers), Connective tissue disorders research (3 papers) and Autism Spectrum Disorder Research (3 papers). The work is most often cited by research in Genetics (737 citations), Molecular Biology (589 citations), Pediatrics, Perinatology and Child Health (148 citations), Developmental Neuroscience (32 citations) and Pharmacy (26 citations). A. Moncla has collaborated with scholars based in France, Italy and United Kingdom. Frequent co-authors include Perrine Malzac, Marie‐Geneviève Mattéi, D. Depétris, Cécile Mignon‐Ravix, Laurent Villard, N. Philip, Marie‐Antoinette Voelckel, André Mégarbané, Mark C. Hirst and Kay E. Davies. Their work appears in journals such as Journal of Medical Genetics, European Journal of Pediatrics, European Journal of Human Genetics, European Journal of Medical Genetics and Neuromuscular Disorders.
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.