Sandra Corbani
Impact in
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- Genetic Syndromes and Imprinting
- Connective tissue disorders research
- Genetics and Neurodevelopmental Disorders
- Genetic and Kidney Cyst Diseases
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- Diabetes, Cardiovascular Risks, and Lipoproteins
- Growth Hormone and Insulin-like Growth Factors
Papers in
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- Wnt/β-catenin signaling in development and cancer 2
- Hedgehog Signaling Pathway Studies 2
- Connective Tissue Growth Factor Research 2
- Epigenetics and DNA Methylation 2
- Genetics 12
- Genetics and Neurodevelopmental Disorders 5
- Genomic variations and chromosomal abnormalities 4
- Connective tissue disorders research 3
- Genetic Syndromes and Imprinting 3
- Co-authors
- Éliane Chouery (20 shared papers)André Mégarbané (21 shared papers)Nabiha Salem (6 shared papers)Valérie Delague (5 shared papers)Nadine Jalkh (7 shared papers)Joelle Abou Ghoch (6 shared papers)Marie‐Paule Lefranc (4 shared papers)Claudine Junien (1 shared paper)
- Journals
- European Journal of Human Genetics (2 papers)Clinical Genetics (2 papers)Journal of Intellectual Disability Research (1 paper)Molecular Cytogenetics (1 paper)European Journal of Medical Genetics (1 paper)
- Partner nations
- LebanonFranceSwitzerland
In The Last Decade
Sandra Corbani
21 papers receiving 379 citations
Peers
Comparison fields: 5 of 61
- Genetics 163
- Endocrinology, Diabetes and Metabolism 63
- Molecular Biology 225
- Immunology 51
- Surgery 88
Countries citing papers authored by Sandra Corbani
This map shows the geographic impact of Sandra Corbani'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 Sandra Corbani with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sandra Corbani more than expected).
Fields of papers citing papers by Sandra Corbani
This network shows the impact of papers produced by Sandra Corbani. 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 Sandra Corbani. The network helps show where Sandra Corbani may publish in the future.
Co-authors
The 25 scholars most cited alongside Sandra Corbani, 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 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 77 | |
| 2 | 2012 | 48 | |
| 3 | 2005 | 46 | |
| 4 | 2005 | 43 | |
| 5 | 2006 | 43 | |
| 6 | 2011 | 35 | |
| 7 | Clinical and molecular findings in three Lebanese families with Bietti crystalline dystrophy: report on a novel mutation. | 2012 | 22 |
| 8 | 2018 | 12 | |
| 9 | 2008 | 10 | |
| 10 | 2013 | 9 | |
| 11 | 2015 | 6 | |
| 12 | 2011 | 6 | |
| 13 | 2017 | 6 | |
| 14 | 2015 | 6 | |
| 15 | 2010 | 5 | |
| 16 | 2020 | 4 | |
| 17 | 2018 | 4 | |
| 18 | 2011 | 2 | |
| 19 | 2024 | 1 | |
| 20 | 2024 | 1 |
About Sandra Corbani
Sandra Corbani is a scholar working on Molecular Biology, Genetics, Surgery, Pulmonary and Respiratory Medicine and Hematology, having authored 23 papers that have together received 387 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Connective tissue disorders research (3 papers), Genetic Syndromes and Imprinting (3 papers), Wnt/β-catenin signaling in development and cancer (2 papers), Hedgehog Signaling Pathway Studies (2 papers), Connective Tissue Growth Factor Research (2 papers) and Epigenetics and DNA Methylation (2 papers). The work is most often cited by research in Genetics (163 citations), Endocrinology, Diabetes and Metabolism (63 citations), Molecular Biology (225 citations), Immunology (51 citations) and Surgery (88 citations). Sandra Corbani has collaborated with scholars based in Lebanon, France and Switzerland. Frequent co-authors include Éliane Chouery, André Mégarbané, Nabiha Salem, Valérie Delague, Nadine Jalkh, Joelle Abou Ghoch, Marie‐Paule Lefranc, Claudine Junien, Mathilde Varret and Cathérine Boileau. Their work appears in journals such as European Journal of Human Genetics, Clinical Genetics, Journal of Intellectual Disability Research, Molecular Cytogenetics and European 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.