Anna Abulí

979 total citations
23 papers, 301 citations indexed

About

Anna Abulí is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Anna Abulí has authored 23 papers receiving a total of 301 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Anna Abulí's work include Genomics and Rare Diseases (6 papers), Prenatal Screening and Diagnostics (6 papers) and Genetic factors in colorectal cancer (6 papers). Anna Abulí is often cited by papers focused on Genomics and Rare Diseases (6 papers), Prenatal Screening and Diagnostics (6 papers) and Genetic factors in colorectal cancer (6 papers). Anna Abulí collaborates with scholars based in Spain, United States and Qatar. Anna Abulí's co-authors include Sergi Castellvı́-Bel, Antoni Castells, Paola Martinelli, Marta Sevillano, Francisco X. Real, Gavin Whissell, Alexandre Calon, Guillermo P. Vicent, A. Silvina Nacht and Xavier Hernando‐Momblona and has published in prestigious journals such as Nature Communications, Journal of Clinical Oncology and SHILAP Revista de lepidopterología.

In The Last Decade

Anna Abulí

21 papers receiving 298 citations

Peers

Anna Abulí
Angela Apessos Greece
Ruthann Pfau United States
Estela G. Toraño Spain
G. Wendell Richmond United States
Tatiana Burjanivová Slovakia
Hiroto Ueda Japan
Gilles Thomas France
Xiaojing Zhang China
Detlef Trost France
Gerald L. Arthur United States
Angela Apessos Greece
Anna Abulí
Citations per year, relative to Anna Abulí Anna Abulí (= 1×) peers Angela Apessos

Countries citing papers authored by Anna Abulí

Since Specialization
Citations

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

Fields of papers citing papers by Anna Abulí

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Abulí

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Abulí. A scholar is included among the top collaborators of Anna Abulí 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 Anna Abulí. Anna Abulí is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Rodó, Carlota, Nerea Maíz, David Gómez‐Andrés, et al.. (2024). Parental or Trio Magnetic Resonance Imaging to Improve Prenatal Counseling in Brain Anomalies. Prenatal Diagnosis. 44(12). 1435–1443. 1 indexed citations
2.
Abulí, Anna, Juan José Guillén, Joaquı́n Rueda, et al.. (2024). Population-based genetic carrier screening. A consensus statement from the Spanish societies: AEGH, AEDP, ASEBIR, SEAGEN, SEF and SEGCD. European Journal of Human Genetics. 33(4). 402–412.
3.
Paneque, Milena, et al.. (2024). Thirty-years of genetic counselling education in Europe: a growing professional area. European Journal of Human Genetics. 32(11). 1500–1505. 6 indexed citations
4.
Abulí, Anna, E. Antolín, A. Borrell, et al.. (2024). Guidelines for NGS procedures applied to prenatal diagnosis by the Spanish Society of Gynecology and Obstetrics and the Spanish Association of Prenatal Diagnosis. Journal of Medical Genetics. 61(8). 727–733. 4 indexed citations
5.
Abulí, Anna, et al.. (2023). The diagnosis communication process in spinal muscular atrophy: A cross-cutting view of the new challenges facing the therapeutic era. SHILAP Revista de lepidopterología. 1(1). 100825–100825. 1 indexed citations
6.
Abulí, Anna, et al.. (2023). Staying alert with polyhydramnios; an Ondine syndrome case. Case Reports in Perinatal Medicine. 12(1). 20220026–20220026.
7.
Abulí, Anna, Marta Codina‐Solà, Irene Valenzuela, et al.. (2022). Experience using singleton exome sequencing of probands as an approach to preconception carrier screening in consanguineous couples. Journal of Medical Genetics. 60(6). 540–546. 1 indexed citations
8.
Becker, Philipp, Cristina Frías-López, Marc Dabad, et al.. (2022). A method for multiplexed full-length single-molecule sequencing of the human mitochondrial genome. Nature Communications. 13(1). 5902–5902. 17 indexed citations
9.
Carrasco, Estela, Adrià López‐Fernández, Marta Codina‐Solà, et al.. (2022). Clinical and psychological implications of secondary and incidental findings in cancer susceptibility genes after exome sequencing in patients with rare disorders. Journal of Medical Genetics. 60(7). 685–691. 6 indexed citations
10.
Abulí, Anna, et al.. (2021). Current Status of Genetic Counselling for Rare Diseases in Spain. Diagnostics. 11(12). 2320–2320. 2 indexed citations
11.
Plaja, Alberto, Carlota Rodó, Irene Valenzuela, et al.. (2020). Chromosomal microarray analysis in fetuses with central nervous system anomalies: An 8‐year long observational study from a tertiary care university hospital. Prenatal Diagnosis. 41(1). 123–135. 13 indexed citations
12.
Abulí, Anna, Marta Codina‐Solà, Irene Valenzuela, et al.. (2020). Beyond the disease itself: A cross‐cutting educational initiative for patients and families with rare diseases. Journal of Genetic Counseling. 30(3). 693–700. 2 indexed citations
13.
Alías, Laura, Sara Bernal, Maite Calucho, et al.. (2018). Utility of two SMN1 variants to improve spinal muscular atrophy carrier diagnosis and genetic counselling. European Journal of Human Genetics. 26(10). 1554–1557. 26 indexed citations
14.
Abulí, Anna, Montserrat Boada, Elísabet Clua, et al.. (2017). Cribado ampliado de portadores en un programa de donación de ovocitos: Implementación de un nuevo test y resultados tras dos años de experiencia. 4(3). 113–121. 2 indexed citations
15.
Abulí, Anna, Antoni Castells, Luís Bujanda, et al.. (2016). Genetic Variants Associated with Colorectal Adenoma Susceptibility. PLoS ONE. 11(4). e0153084–e0153084. 11 indexed citations
16.
Whissell, Gavin, Paola Martinelli, Xavier Hernando‐Momblona, et al.. (2014). The transcription factor GATA6 enables self-renewal of colon adenoma stem cells by repressing BMP gene expression. Nature Cell Biology. 16(7). 695–707. 102 indexed citations
17.
Castellvı́-Bel, Sergi, Clara Ruíz-Ponte, Ceres Fernández–Rozadilla, et al.. (2012). Seeking genetic susceptibility variants for colorectal cancer: the EPICOLON consortium experience. Mutagenesis. 27(2). 153–159. 7 indexed citations
18.
Fernández–Rozadilla, Ceres, Luisa de Castro, Juan Clofent, et al.. (2010). Single Nucleotide Polymorphisms in the Wnt and BMP Pathways and Colorectal Cancer Risk in a Spanish Cohort. PLoS ONE. 5(9). e12673–e12673. 35 indexed citations
19.
Fernández–Rozadilla, Ceres, Rosa Tarrı́o, Juan Clofent, et al.. (2010). Colorectal Cancer Susceptibility Quantitative Trait Loci in Mice as a Novel Approach to Detect Low-Penetrance Variants in Humans: A Two-Stage Case-Control Study. Cancer Epidemiology Biomarkers & Prevention. 19(2). 619–623. 5 indexed citations
20.

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Angela Apessos Breakdown of academic impact, for papers by Ruthann Pfau Breakdown of academic impact, for papers by Estela G. Toraño Breakdown of academic impact, for papers by G. Wendell Richmond Breakdown of academic impact, for papers by Tatiana Burjanivová Breakdown of academic impact, for papers by Hiroto Ueda Breakdown of academic impact, for papers by Gilles Thomas Breakdown of academic impact, for papers by Xiaojing Zhang Breakdown of academic impact, for papers by Detlef Trost Breakdown of academic impact, for papers by Gerald L. Arthur
Rankless by CCL
2026