A Moncla
Impact in
- Genetics top 5%
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
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- Epigenetics and DNA Methylation
- RNA modifications and cancer
- Congenital heart defects research
Papers in
- Genetics 3
- Genetic Syndromes and Imprinting 2
- Connective tissue disorders research 1
- Craniofacial Disorders and Treatments 1
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- Hedgehog Signaling Pathway Studies 1
- Co-authors
- Arthur L. Beaudet (2 shared papers)Jane Summers (2 shared papers)Albert Schinzel (2 shared papers)Charles A. Williams (2 shared papers)Laura Laan (2 shared papers)Jill Clayton‐Smith (2 shared papers)Joseph Wagstaff (2 shared papers)R. Ellen Magenis (2 shared papers)
- Journals
- American Journal of Medical Genetics Part A (1 paper)American Journal of Medical Genetics (1 paper)PubMed (2 papers)
- Partner nations
- FranceSwedenNetherlands
In The Last Decade
A Moncla
6 papers receiving 451 citations
Peers
Comparison fields: 5 of 52
- Genetics 411
- Molecular Biology 318
- Pediatrics, Perinatology and Child Health 89
- Cognitive Neuroscience 47
- Developmental Biology 4
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 21 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
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 420 | |
| 2 | 1998 | 29 | |
| 3 | Cerebrofaciothoracic dysplasia: a new family. | 1992 | 8 |
| 4 | Conference Report Angelman Syndrome 2005: Updated Consensus for Diagnostic Criteria | 2006 | 5 |
| 5 | [Diagnosis of minor chromosome modifications by molecular cytogenetics]. | 1989 | 3 |
| 6 | Physical mapping of the 17p chromosomal region relationship with the charcot marie tooth disease | 1991 | 2 |
About A Moncla
A Moncla is a scholar working on Genetics, Molecular Biology, Epidemiology, Rheumatology and Endocrinology, Diabetes and Metabolism, having authored 6 papers that have together received 467 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (2 papers), MicroRNA in disease regulation (1 paper), Connective tissue disorders research (1 paper), Moyamoya disease diagnosis and treatment (1 paper), Cancer-related molecular mechanisms research (1 paper), Craniofacial Disorders and Treatments (1 paper), T-cell and Retrovirus Studies (1 paper) and Hedgehog Signaling Pathway Studies (1 paper). The work is most often cited by research in Genetics (411 citations), Molecular Biology (318 citations), Pediatrics, Perinatology and Child Health (89 citations), Cognitive Neuroscience (47 citations) and Developmental Biology (4 citations). A Moncla has collaborated with scholars based in France, Sweden and Netherlands. Frequent co-authors include Arthur L. Beaudet, Jane Summers, Albert Schinzel, Charles A. Williams, Laura Laan, Jill Clayton‐Smith, Joseph Wagstaff, R. Ellen Magenis, Joan H.M. Knoll and Ségolène Aymé. Their work appears in journals such as American Journal of Medical Genetics Part A, American Journal of Medical 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.