Aurora Sánchez
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- Prenatal Screening and Diagnostics 27
- Genetics top 2%
- Genomic variations and chromosomal abnormalities 28
- Genetics and Neurodevelopmental Disorders 25
- Genetic Syndromes and Imprinting 7
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- Genetic Neurodegenerative Diseases 12
- Reproductive Medicine top 5%
- Molecular Biology top 10%
- Mitochondrial Function and Pathology 9
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- Autism Spectrum Disorder Research 9
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- Chromosomal and Genetic Variations 8
Aurora Sánchez
87 papers receiving 1.8k citations
Peers
Comparison fields: 5 of 107
- Pediatrics, Perinatology and Child Health 630
- Genetics 862
- Cellular and Molecular Neuroscience 295
- Reproductive Medicine 106
- Molecular Biology 810
Countries citing papers authored by Aurora Sánchez
This map shows the geographic impact of Aurora Sánchez'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 Aurora Sánchez with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Aurora Sánchez more than expected).
Fields of papers citing papers by Aurora Sánchez
This network shows the impact of papers produced by Aurora Sánchez. 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 Aurora Sánchez. The network helps show where Aurora Sánchez may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Aurora Sánchez, 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 | 2023 | 4 | |
| 2 | 2020 | 5 | |
| 3 | 2010 | 44 | |
| 4 | 2010 | 13 | |
| 5 | 2010 | 15 | |
| 6 | 2009 | 3 | |
| 7 | 2009 | 8 | |
| 8 | 2009 | 9 | |
| 9 | 2008 | 12 | |
| 10 | 2008 | 51 | |
| 11 | 2007 | 48 | |
| 12 | 2007 | 23 | |
| 13 | 2007 | 4 | |
| 14 | 2005 | 4 | |
| 15 | 2003 | 22 | |
| 16 | 2002 | 7 | |
| 17 | 2000 | 13 | |
| 18 | 1998 | 72 | |
| 19 | [Molecular analysis of the IT15 gene in 79 Spanish families with Huntington's disease: diagnostic confirmation and presymptomatic diagnosis]. | 1997 | 3 |
| 20 | 1996 | 10 |
About Aurora Sánchez
Aurora Sánchez is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Cellular and Molecular Neuroscience, having authored 91 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (28 papers), Prenatal Screening and Diagnostics (27 papers), Genetics and Neurodevelopmental Disorders (25 papers), Genetic Neurodegenerative Diseases (12 papers), Mitochondrial Function and Pathology (9 papers), Autism Spectrum Disorder Research (9 papers), Chromosomal and Genetic Variations (8 papers) and Genetic Syndromes and Imprinting (7 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (630 citations), Genetics (862 citations) and Cellular and Molecular Neuroscience (295 citations). Aurora Sánchez has collaborated with scholars based in Spain, Mexico and Netherlands. Frequent co-authors include Anna Soler, Montserrat Milà, A. Borrell, Carmen Morales, Ester Margarit, Célia Bádenas, Irene Mademont‐Soler, Laia Rodríguez‐Revenga, V. Borobio and Irene Madrigal. Their work appears in journals such as Prenatal Diagnosis, Human Genetics, Cytogenetic and Genome Research, Journal of Neurology Neurosurgery & Psychiatry and Human Mutation.
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.