Liesbeth Backx
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Cleft Lip and Palate Research
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 15
- Genomic variations and chromosomal abnormalities 11
- Genetics and Neurodevelopmental Disorders 3
- Genomics and Rare Diseases 2
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- Chromosomal and Genetic Variations 6
- Co-authors
- Hilde Van Esch (9 shared papers)Joris Robert 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
- Cytogenetic and Genome Research (3 papers)European Journal of Human Genetics (3 papers)The American Journal of Human Genetics (2 papers)Molecular Cytogenetics (2 papers)European Journal of Medical Genetics (2 papers)
- Partner nations
- BelgiumUnited StatesGermany
In The Last Decade
Liesbeth Backx
16 papers receiving 628 citations
Peers
Comparison fields: 5 of 55
- Genetics 440
- Pediatrics, Perinatology and Child Health 115
- Molecular Biology 269
- Plant Science 118
- Aging 5
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 | 2007 | 255 | |
| 2 | 2010 | 79 | |
| 3 | 2011 | 49 | |
| 4 | 2010 | 47 | |
| 5 | 2007 | 41 | |
| 6 | 2008 | 40 | |
| 7 | 2009 | 32 | |
| 8 | 2010 | 31 | |
| 9 | 2010 | 29 | |
| 10 | 2019 | 29 | |
| 11 | 2011 | 12 | |
| 12 | 2008 | 11 | |
| 13 | Haploinsufficiency of the gene Quaking (QKI) is associated with the 6q terminal deletion syndrome | 2008 | 8 |
| 14 | 2009 | 7 | |
| 15 | 2009 | 5 | |
| 16 | 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, Plant Science, Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics, having authored 16 papers that have together received 676 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (6 papers), Genomics and Chromatin Dynamics (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Glycosylation and Glycoproteins Research (2 papers), Prenatal Screening and Diagnostics (2 papers), Genomics and Rare Diseases (2 papers) and Glycogen Storage Diseases and Myoclonus (1 paper). The work is most often cited by research in Genetics (440 citations), Pediatrics, Perinatology and Child Health (115 citations), Molecular Biology (269 citations), Plant Science (118 citations) and Aging (5 citations). Liesbeth Backx has collaborated with scholars based in Belgium, United States and Germany. Frequent co-authors include Hilde Van Esch, Joris Robert Vermeesch, Koenraad Devriendt, Eve Seuntjens, Jean‐Pierre Fryns, Berten Ceulemans, Nadezda Kosyakova, Thomas Liehr, Carlo Marcelis and Kathleen Freson. Their work appears in journals such as Cytogenetic and Genome Research, European Journal of Human Genetics, The American Journal of Human Genetics, 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.