Aurora Sánchez
Impact in
-
- Prenatal Screening and Diagnostics
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
- Genetics 43
- Genetics and Neurodevelopmental Disorders 22
- Genomic variations and chromosomal abnormalities 17
- Genetic Syndromes and Imprinting 7
-
- Prenatal Screening and Diagnostics 23
- Co-authors
- Anna Soler (20 shared papers)Montserrat Milà (33 shared papers)A. Borrell (20 shared papers)Ester Margarit (15 shared papers)Célia Bádenas (22 shared papers)Irene Mademont‐Soler (10 shared papers)V. Borobio (7 shared papers)Laia Rodríguez‐Revenga (17 shared papers)
- Journals
- Prenatal Diagnosis (11 papers)Human Genetics (4 papers)Cytogenetic and Genome Research (4 papers)Fertility and Sterility (3 papers)Ultrasound in Obstetrics and Gynecology (3 papers)
- Partner nations
- SpainMexicoNetherlands
In The Last Decade
Aurora Sánchez
88 papers receiving 1.9k citations
Peers
Comparison fields: 5 of 106
- Pediatrics, Perinatology and Child Health 543
- Genetics 809
- Cellular and Molecular Neuroscience 287
- Molecular Biology 729
- Neurology 131
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-authors
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
Showing the 20 most-cited of 92 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 143 | |
| 2 | 2017 | 117 | |
| 3 | 2005 | 110 | |
| 4 | 2012 | 79 | |
| 5 | 1998 | 72 | |
| 6 | 2004 | 68 | |
| 7 | 2001 | 64 | |
| 8 | 2007 | 62 | |
| 9 | 2010 | 57 | |
| 10 | 2012 | 57 | |
| 11 | 2008 | 51 | |
| 12 | 2007 | 48 | |
| 13 | 2015 | 47 | |
| 14 | 2010 | 44 | |
| 15 | 2011 | 43 | |
| 16 | 1996 | 42 | |
| 17 | 2009 | 41 | |
| 18 | 1999 | 33 | |
| 19 | 2001 | 33 | |
| 20 | 2011 | 32 |
About Aurora Sánchez
Aurora Sánchez is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Cellular and Molecular Neuroscience and Cognitive Neuroscience, having authored 92 papers that have together received 2.0k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (23 papers), Genetics and Neurodevelopmental Disorders (22 papers), Genomic variations and chromosomal abnormalities (17 papers), Genetic Neurodegenerative Diseases (13 papers), Autism Spectrum Disorder Research (8 papers), Genetic Syndromes and Imprinting (7 papers), Mitochondrial Function and Pathology (7 papers) and Chromosomal and Genetic Variations (7 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (543 citations), Genetics (809 citations), Cellular and Molecular Neuroscience (287 citations), Molecular Biology (729 citations) and Neurology (131 citations). Aurora Sánchez has collaborated with scholars based in Spain, Mexico and Netherlands. Frequent co-authors include Anna Soler, Montserrat Milà, A. Borrell, Ester Margarit, Célia Bádenas, Irene Mademont‐Soler, V. Borobio, Laia Rodríguez‐Revenga, Irene Madrigal and Xavier Estivill. Their work appears in journals such as Prenatal Diagnosis, Human Genetics, Cytogenetic and Genome Research, Fertility and Sterility and Ultrasound in Obstetrics and Gynecology.
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.