Anna de Burca
Impact in
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- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Connective tissue disorders research
- Genetic Syndromes and Imprinting
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- Wnt/β-catenin signaling in development and cancer
- Cancer-related gene regulation
- Epigenetics and DNA Methylation
- Ubiquitin and proteasome pathways
Papers in
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- Epigenetics and DNA Methylation 1
- Muscle Physiology and Disorders 1
- Genetics 2
- Genomics and Rare Diseases 1
- Genetics and Neurodevelopmental Disorders 1
- Genetic Syndromes and Imprinting 1
- Neurogenetic and Muscular Disorders Research 1
- Co-authors
- Pedro Louro (1 shared paper)Usha Kini (1 shared paper)Victoria McKay (1 shared paper)Alan Fryer (1 shared paper)Esther Kinning (1 shared paper)John Burn (1 shared paper)Susan Tomkins (1 shared paper)Kate Chandler (1 shared paper)
- Journals
- European Journal of Medical Genetics (1 paper)PLoS ONE (1 paper)Clinical Dysmorphology (1 paper)
- Partner nations
- United KingdomItalyCanada
In The Last Decade
Anna de Burca
3 papers receiving 57 citations
Peers
Comparison fields: 5 of 19
- Genetics 28
- Molecular Biology 36
- Biological Psychiatry 1
- Neurology 3
- Genetics 3
Countries citing papers authored by Anna de Burca
This map shows the geographic impact of Anna de Burca'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 Anna de Burca with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anna de Burca more than expected).
Fields of papers citing papers by Anna de Burca
This network shows the impact of papers produced by Anna de Burca. 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 Anna de Burca. The network helps show where Anna de Burca may publish in the future.
Co-authors
The 20 scholars most cited alongside Anna de Burca, 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 | 2016 | 47 | |
| 2 | 2011 | 8 | |
| 3 | 2018 | 2 |
About Anna de Burca
Anna de Burca is a scholar working on Molecular Biology, Genetics, Genetics, Cellular and Molecular Neuroscience and Psychiatry and Mental health, having authored 3 papers that have together received 57 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (1 paper), Epigenetics and DNA Methylation (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Genetic Syndromes and Imprinting (1 paper), Neurogenetic and Muscular Disorders Research (1 paper), Muscle Physiology and Disorders (1 paper), Hereditary Neurological Disorders (1 paper) and Cerebral Palsy and Movement Disorders (1 paper). The work is most often cited by research in Genetics (28 citations), Molecular Biology (36 citations), Biological Psychiatry (1 citation), Neurology (3 citations) and Genetics (3 citations). Anna de Burca has collaborated with scholars based in United Kingdom, Italy and Canada. Frequent co-authors include Pedro Louro, Usha Kini, Victoria McKay, Alan Fryer, Esther Kinning, John Burn, Susan Tomkins, Kate Chandler, Daniela T. Pilz and Mira Kharbanda. Their work appears in journals such as European Journal of Medical Genetics, PLoS ONE and Clinical Dysmorphology.
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.