Alice Goldenberg
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Connective tissue disorders research
- Developmental Biology top 10%
Papers in
-
- Congenital heart defects research 4
- RNA modifications and cancer 4
- Epigenetics and DNA Methylation 3
- Genetics 21
- Genomic variations and chromosomal abnormalities 9
- Genetics and Neurodevelopmental Disorders 6
- Co-authors
- Valérie Cormier‐Daire (9 shared papers)Pascale Saugier-Véber (11 shared papers)Arnold Münnich (6 shared papers)Caroline Michot (4 shared papers)Thierry Frébourg (10 shared papers)Muriel Holder‐Espinasse (4 shared papers)Marlène Rio (2 shared papers)Joris Andrieux (3 shared papers)
- Journals
- European Journal of Human Genetics (5 papers)Human Mutation (4 papers)Journal of Medical Genetics (3 papers)Acta Neuropathologica Communications (2 papers)Pediatric Nephrology (2 papers)
- Partner nations
- FranceSwitzerlandUnited States
In The Last Decade
Alice Goldenberg
48 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 80
- Genetics 562
- Developmental Biology 37
- Molecular Biology 776
- Cellular and Molecular Neuroscience 126
- Clinical Biochemistry 45
Countries citing papers authored by Alice Goldenberg
This map shows the geographic impact of Alice Goldenberg'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 Alice Goldenberg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alice Goldenberg more than expected).
Fields of papers citing papers by Alice Goldenberg
This network shows the impact of papers produced by Alice Goldenberg. 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 Alice Goldenberg. The network helps show where Alice Goldenberg may publish in the future.
Co-authors
The 25 scholars most cited alongside Alice Goldenberg, 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 49 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 181 | |
| 2 | 2009 | 165 | |
| 3 | 2013 | 103 | |
| 4 | 2012 | 93 | |
| 5 | 2009 | 85 | |
| 6 | 2014 | 70 | |
| 7 | 2018 | 57 | |
| 8 | 2010 | 44 | |
| 9 | 2011 | 44 | |
| 10 | 2003 | 41 | |
| 11 | 2018 | 34 | |
| 12 | 2012 | 29 | |
| 13 | 2018 | 29 | |
| 14 | 2006 | 28 | |
| 15 | 2017 | 28 | |
| 16 | 2018 | 27 | |
| 17 | 2016 | 24 | |
| 18 | 2012 | 24 | |
| 19 | 2009 | 23 | |
| 20 | 2008 | 22 |
About Alice Goldenberg
Alice Goldenberg is a scholar working on Molecular Biology, Genetics, Surgery, Pediatrics, Perinatology and Child Health and Cellular and Molecular Neuroscience, having authored 49 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (6 papers), Congenital heart defects research (4 papers), RNA modifications and cancer (4 papers), Cholesterol and Lipid Metabolism (3 papers), Epigenetics and DNA Methylation (3 papers), Prenatal Screening and Diagnostics (3 papers) and Congenital limb and hand anomalies (3 papers). The work is most often cited by research in Genetics (562 citations), Developmental Biology (37 citations), Molecular Biology (776 citations), Cellular and Molecular Neuroscience (126 citations) and Clinical Biochemistry (45 citations). Alice Goldenberg has collaborated with scholars based in France, Switzerland and United States. Frequent co-authors include Valérie Cormier‐Daire, Pascale Saugier-Véber, Arnold Münnich, Caroline Michot, Thierry Frébourg, Muriel Holder‐Espinasse, Marlène Rio, Joris Andrieux, Geneviève Baujat and Nathalie Le Meur. Their work appears in journals such as European Journal of Human Genetics, Human Mutation, Journal of Medical Genetics, Acta Neuropathologica Communications and Pediatric Nephrology.
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.