Muriel Holder
Impact in
- Sensory Systems top 5%
- Hearing, Cochlea, Tinnitus, Genetics
- Genetics top 10%
- Genetic and Kidney Cyst Diseases
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 8
- Cleft Lip and Palate Research 2
- Craniofacial Disorders and Treatments 2
- Congenital Ear and Nasal Anomalies 2
- Blood disorders and treatments 2
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- DNA Repair Mechanisms 1
- Co-authors
- Pierre Sarda (2 shared papers)M. Durand (1 shared paper)Sabine Sigaudy (1 shared paper)Vincent Marion (1 shared paper)Corinne Stoetzel (1 shared paper)Christian P. Hamel (1 shared paper)Christian Brandt (1 shared paper)Bruno Moulin (1 shared paper)
- Journals
- The American Journal of Human Genetics (2 papers)Human Mutation (1 paper)Clinical Journal of the American Society of Nephrology (1 paper)European Journal of Human Genetics (1 paper)Pediatric and Developmental Pathology (1 paper)
- Partner nations
- FranceUnited KingdomUnited States
In The Last Decade
Muriel Holder
14 papers receiving 409 citations
Peers
Comparison fields: 5 of 50
- Sensory Systems 93
- Genetics 171
- Molecular Biology 236
- Genetics 23
- Otorhinolaryngology 9
Countries citing papers authored by Muriel Holder
This map shows the geographic impact of Muriel Holder'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 Muriel Holder with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Muriel Holder more than expected).
Fields of papers citing papers by Muriel Holder
This network shows the impact of papers produced by Muriel Holder. 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 Muriel Holder. The network helps show where Muriel Holder may publish in the future.
Co-authors
The 25 scholars most cited alongside Muriel Holder, 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 | 2010 | 92 | |
| 2 | 2007 | 86 | |
| 3 | 2012 | 67 | |
| 4 | 2014 | 55 | |
| 5 | 2013 | 30 | |
| 6 | 2012 | 28 | |
| 7 | 2014 | 18 | |
| 8 | 2013 | 9 | |
| 9 | 2011 | 8 | |
| 10 | 2011 | 6 | |
| 11 | 2012 | 6 | |
| 12 | 2003 | 3 | |
| 13 | 2019 | 2 | |
| 14 | 2015 | 1 |
About Muriel Holder
Muriel Holder is a scholar working on Genetics, Molecular Biology, Cell Biology, Physiology and Genetics, having authored 14 papers that have together received 411 indexed citations. Recurring topics across this work include Cellular transport and secretion (3 papers), Cleft Lip and Palate Research (2 papers), Oral and Maxillofacial Pathology (2 papers), Craniofacial Disorders and Treatments (2 papers), Congenital Ear and Nasal Anomalies (2 papers), Lysosomal Storage Disorders Research (2 papers), Blood disorders and treatments (2 papers) and DNA Repair Mechanisms (1 paper). The work is most often cited by research in Sensory Systems (93 citations), Genetics (171 citations), Molecular Biology (236 citations), Genetics (23 citations) and Otorhinolaryngology (9 citations). Muriel Holder has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Pierre Sarda, M. Durand, Sabine Sigaudy, Vincent Marion, Corinne Stoetzel, Christian P. Hamel, Christian Brandt, Bruno Moulin, Hélène Dollfus and Anne Vielle. Their work appears in journals such as The American Journal of Human Genetics, Human Mutation, Clinical Journal of the American Society of Nephrology, European Journal of Human Genetics and Pediatric and Developmental Pathology.
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.