Claudine Junien
Impact in
-
- Birth, Development, and Health
- Prenatal Screening and Diagnostics
- Obstetrics and Gynecology top 0.5%
Papers in
-
- Epigenetics and DNA Methylation 39
- Renal and related cancers 35
- Genetics 80
- Genetic Syndromes and Imprinting 25
- Genomic variations and chromosomal abnormalities 23
- Co-authors
- Anne Gabory (21 shared papers)Catherine Gallou‐Kabani (13 shared papers)Linda Attig (8 shared papers)Cathérine Boileau (26 shared papers)Isabelle Henry (28 shared papers)Jean‐Pierre Rabès (13 shared papers)Alexandre Vigé (13 shared papers)Jean‐Christophe Fournet (12 shared papers)
- Journals
- Human Genetics (32 papers)Human Mutation (12 papers)Genomics (11 papers)European Journal of Human Genetics (6 papers)Journal of Medical Genetics (5 papers)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
Claudine Junien
235 papers receiving 10.4k citations
Claudine Junien's Hit Papers
Peers
Comparison fields: 5 of 143
- Pediatrics, Perinatology and Child Health 2.3k
- Obstetrics and Gynecology 642
- Endocrinology, Diabetes and Metabolism 1.4k
- Genetics 2.4k
- Molecular Biology 5.0k
Countries citing papers authored by Claudine Junien
This map shows the geographic impact of Claudine Junien'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 Claudine Junien with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Claudine Junien more than expected).
Fields of papers citing papers by Claudine Junien
This network shows the impact of papers produced by Claudine Junien. 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 Claudine Junien. The network helps show where Claudine Junien may publish in the future.
Co-authors
The 25 scholars most cited alongside Claudine Junien, 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 242 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome Hit paper breakdown → | 1991 | 718 |
| 2 | Child Health, Developmental Plasticity, and Epigenetic Programming Hit paper breakdown → | 2010 | 457 |
| 3 | 1991 | 331 | |
| 4 | 2013 | 269 | |
| 5 | 1997 | 234 | |
| 6 | 1998 | 230 | |
| 7 | 2009 | 230 | |
| 8 | 1999 | 214 | |
| 9 | 2009 | 200 | |
| 10 | 2005 | 195 | |
| 11 | 2010 | 191 | |
| 12 | 2007 | 189 | |
| 13 | 2015 | 189 | |
| 14 | Myotonic dystrophy: size- and sex-dependent dynamics of CTG meiotic instability, and somatic mosaicism. | 1993 | 189 |
| 15 | 2005 | 165 | |
| 16 | 1998 | 164 | |
| 17 | 2000 | 157 | |
| 18 | 2012 | 156 | |
| 19 | 2003 | 154 | |
| 20 | 2000 | 148 |
About Claudine Junien
Claudine Junien is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Surgery and Cellular and Molecular Neuroscience, having authored 242 papers that have together received 10.7k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (39 papers), Renal and related cancers (35 papers), Birth, Development, and Health (30 papers), Genetic Syndromes and Imprinting (25 papers), Genomic variations and chromosomal abnormalities (23 papers), Genetic Neurodegenerative Diseases (22 papers), Prenatal Screening and Diagnostics (20 papers) and Lipoproteins and Cardiovascular Health (16 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (2.3k citations), Obstetrics and Gynecology (642 citations), Endocrinology, Diabetes and Metabolism (1.4k citations), Genetics (2.4k citations) and Molecular Biology (5.0k citations). Claudine Junien has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Anne Gabory, Catherine Gallou‐Kabani, Linda Attig, Cathérine Boileau, Isabelle Henry, Jean‐Pierre Rabès, Alexandre Vigé, Jean‐Christophe Fournet, Marie‐Sylvie Gross and Marc Jeanpierre. Their work appears in journals such as Human Genetics, Human Mutation, Genomics, European Journal of Human Genetics and Journal of Medical Genetics.
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.