Amparo Sanchís

1.2k total citations
4 papers, 34 citations indexed

About

Amparo Sanchís is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Amparo Sanchís has authored 4 papers receiving a total of 34 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Molecular Biology, 2 papers in Pediatrics, Perinatology and Child Health and 2 papers in Genetics. Recurrent topics in Amparo Sanchís's work include RNA modifications and cancer (2 papers), Prenatal Screening and Diagnostics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Amparo Sanchís is often cited by papers focused on RNA modifications and cancer (2 papers), Prenatal Screening and Diagnostics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Amparo Sanchís collaborates with scholars based in Spain. Amparo Sanchís's co-authors include Eva Bermejo, Carlos A. Valverde, Elvira Rodríguez‐Pinilla, John M. Opitz, James F. Reynolds, Miguel Urioste, Esperanza Such, Francisco Martı́nez, Mónica Rosello and Laia Pedrola and has published in prestigious journals such as International Journal of Molecular Sciences, American Journal of Medical Genetics and Revista chilena de obstetricia y ginecología.

In The Last Decade

Amparo Sanchís

2 papers receiving 34 citations

Peers

Amparo Sanchís

GENET

PPCH

DB

RHEUM

PHEOH

Melissa Lorenzo Canada

Madelena Martin United States

Renee Bend United States

Elisa Savin Italy

Renata Lúcia Leite Ferreira de Lima Brazil

Hali Wright United States

Vasil Mico United States

Pavandip Singh Wasan Singapore

Ruzan Mkrtchyan Armenia

Geòrgia Escaramís Spain

Melissa Lorenzo Canada

Amparo Sanchís

17 ×0.9

GENET

5 ×0.3

PPCH

0 ×0.0

DB

8 ×0.7

RHEUM

7 ×0.7

PHEOH

Citations per year, relative to Amparo Sanchís Amparo Sanchís (= 1×) peers Melissa Lorenzo

Countries citing papers authored by Amparo Sanchís

Since Specialization

Citations

This map shows the geographic impact of Amparo Sanchís'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 Amparo Sanchís with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Amparo Sanchís more than expected).

Fields of papers citing papers by Amparo Sanchís

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Amparo Sanchís. 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 Amparo Sanchís. The network helps show where Amparo Sanchís may publish in the future.

Co-authorship network of co-authors of Amparo Sanchís

This figure shows the co-authorship network connecting the top 25 collaborators of Amparo Sanchís. A scholar is included among the top collaborators of Amparo Sanchís based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Amparo Sanchís. Amparo Sanchís is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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4 of 4 papers shown

1.

Orellana, Carmen, Mónica Rosello, Amparo Sanchís, et al.. (2025). Utility of Optical Genome Mapping for Accurate Detection and Fine-Mapping of Structural Variants in Elusive Rare Diseases. International Journal of Molecular Sciences. 26(3). 1244–1244.

2.

Sanchís, Amparo, et al.. (2018). Diagnostico prenatal en Sindrome de Cornelia de Lange a propósito de 2 casos. Revista chilena de obstetricia y ginecología. 83(1). 93–98.

3.

Urioste, Miguel, et al.. (1996). Epidemiological analysis of multi-site closure failure of neural tube in humans. American Journal of Medical Genetics. 66(1). 64–68. 15 indexed citations

4.

Sanchís, Amparo, et al.. (1985). Duplication of hands and feet, multiple joint dislocations, absence of corpus callosum and hypsarrhythmia: Acrocallosal syndrome?. American Journal of Medical Genetics. 20(1). 123–130. 19 indexed citations

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.

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