Liesbeth Backx
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Congenital heart defects research
- Chromatin Remodeling and Cancer
- Genomics and Chromatin Dynamics
Papers in
- Genetics 13
- Genomic variations and chromosomal abnormalities 10
- Genetics and Neurodevelopmental Disorders 3
- Genomics and Rare Diseases 2
- Connective tissue disorders research 1
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- Genomics and Chromatin Dynamics 3
- Glycosylation and Glycoproteins Research 2
- Co-authors
- Hilde Van Esch (9 shared papers)Joris Vermeesch (12 shared papers)Koenraad Devriendt (6 shared papers)Eve Seuntjens (3 shared papers)Jean‐Pierre Fryns (3 shared papers)Berten Ceulemans (1 shared paper)Nadezda Kosyakova (4 shared papers)Thomas Liehr (3 shared papers)
- Journals
- European Journal of Human Genetics (3 papers)Cytogenetic and Genome Research (3 papers)Molecular Cytogenetics (2 papers)European Journal of Medical Genetics (2 papers)The American Journal of Human Genetics (1 paper)
- Partner nations
- BelgiumPortugalUnited States
In The Last Decade
Liesbeth Backx
14 papers receiving 327 citations
Peers
Comparison fields: 5 of 47
- Genetics 196
- Molecular Biology 183
- Aging 4
- Cell Biology 31
- Developmental Biology 4
Countries citing papers authored by Liesbeth Backx
This map shows the geographic impact of Liesbeth Backx'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 Liesbeth Backx with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Liesbeth Backx more than expected).
Fields of papers citing papers by Liesbeth Backx
This network shows the impact of papers produced by Liesbeth Backx. 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 Liesbeth Backx. The network helps show where Liesbeth Backx may publish in the future.
Co-authors
The 25 scholars most cited alongside Liesbeth Backx, 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 | 72 | |
| 2 | 2010 | 45 | |
| 3 | 2007 | 35 | |
| 4 | 2008 | 34 | |
| 5 | 2009 | 29 | |
| 6 | 2019 | 26 | |
| 7 | 2010 | 26 | |
| 8 | 2010 | 25 | |
| 9 | 2011 | 12 | |
| 10 | 2008 | 10 | |
| 11 | Haploinsufficiency of the gene Quaking (QKI) is associated with the 6q terminal deletion syndrome | 2008 | 7 |
| 12 | 2009 | 7 | |
| 13 | 2009 | 4 | |
| 14 | Fas-associated factor-1, a protein involved in apoptosis, causes cleft lip and palate | 2008 | 1 |
About Liesbeth Backx
Liesbeth Backx is a scholar working on Genetics, Molecular Biology, Plant Science, Pediatrics, Perinatology and Child Health and Genetics, having authored 14 papers that have together received 333 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Chromosomal and Genetic Variations (7 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genomics and Chromatin Dynamics (3 papers), Prenatal Screening and Diagnostics (2 papers), Genomics and Rare Diseases (2 papers), Glycosylation and Glycoproteins Research (2 papers) and Connective tissue disorders research (1 paper). The work is most often cited by research in Genetics (196 citations), Molecular Biology (183 citations), Aging (4 citations), Cell Biology (31 citations) and Developmental Biology (4 citations). Liesbeth Backx has collaborated with scholars based in Belgium, Portugal and United States. Frequent co-authors include Hilde Van Esch, Joris Vermeesch, Koenraad Devriendt, Eve Seuntjens, Jean‐Pierre Fryns, Berten Ceulemans, Nadezda Kosyakova, Thomas Liehr, Kathleen Freson and Connie Schrander‐Stumpel. Their work appears in journals such as European Journal of Human Genetics, Cytogenetic and Genome Research, Molecular Cytogenetics, European Journal of Medical Genetics and The American Journal of Human 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.