Neus Baena

1.1k total citations
31 papers, 470 citations indexed

About

Neus Baena is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Neus Baena has authored 31 papers receiving a total of 470 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 13 papers in Molecular Biology and 12 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Neus Baena's work include Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Neus Baena is often cited by papers focused on Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Neus Baena collaborates with scholars based in Spain, France and United Kingdom. Neus Baena's co-authors include Míriam Guitart, Elisabeth Gabau, Claude Stoll, C. De Vigan, E Cariati, M. Clementi, M.R. Caballı́n, Joan Blanco, J. Egozcue and Francesca Vidal and has published in prestigious journals such as PLoS ONE, The American Journal of Human Genetics and The British Journal of Psychiatry.

In The Last Decade

Neus Baena

29 papers receiving 411 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Neus Baena Spain 13 286 199 132 92 47 31 470
Chiara Palka Italy 10 210 0.7× 136 0.7× 255 1.9× 48 0.5× 46 1.0× 34 468
Alida C. Knegt Netherlands 14 257 0.9× 232 1.2× 271 2.1× 71 0.8× 120 2.6× 35 652
Irene Mademont‐Soler Spain 16 186 0.7× 220 1.1× 224 1.7× 55 0.6× 56 1.2× 28 572
Anne M. Bandholz United States 6 355 1.2× 332 1.7× 154 1.2× 70 0.8× 15 0.3× 8 515
Ioannis Papoulidis Greece 13 251 0.9× 195 1.0× 116 0.9× 40 0.4× 33 0.7× 52 388
E. Robert Wassman United States 13 375 1.3× 136 0.7× 223 1.7× 83 0.9× 31 0.7× 23 603
Sandra Peacock United States 9 308 1.1× 207 1.0× 183 1.4× 25 0.3× 16 0.3× 11 489
Nathalie Leporrier France 15 167 0.6× 251 1.3× 153 1.2× 94 1.0× 32 0.7× 24 478
Louis Lello United States 11 238 0.8× 159 0.8× 87 0.7× 21 0.2× 45 1.0× 18 409
F. R. Sergovich Canada 13 348 1.2× 172 0.9× 232 1.8× 48 0.5× 38 0.8× 20 548

Countries citing papers authored by Neus Baena

Since Specialization
Citations

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

Fields of papers citing papers by Neus Baena

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Neus Baena

This figure shows the co-authorship network connecting the top 25 collaborators of Neus Baena. A scholar is included among the top collaborators of Neus Baena 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 Neus Baena. Neus Baena 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.
Spataro, Nino, Elisabeth Gabau, Juan Pablo Trujillo‐Quintero, et al.. (2024). Case report: Identification of a novel variant p.Gly215Arg in the CHN1 gene causing Moebius syndrome. Frontiers in Genetics. 15. 1291063–1291063. 1 indexed citations
2.
Capel, Ismael, Neus Baena, María Rosa Bella, et al.. (2023). Genetic testing for familial hyperparathyroidism: clinical-genetic profile in a Mediterranean cohort. Frontiers in Endocrinology. 14. 3 indexed citations
3.
Spataro, Nino, Juan Pablo Trujillo‐Quintero, Elisabeth Gabau, et al.. (2023). High Performance of a Dominant/X-Linked Gene Panel in Patients with Neurodevelopmental Disorders. Genes. 14(3). 708–708. 3 indexed citations
4.
Capel, Ismael, Neus Baena, María Rosa Bella, et al.. (2022). Novel germline variants of CDKN1B and CDKN2C identified during screening for familial primary hyperparathyroidism. Journal of Endocrinological Investigation. 46(4). 829–840. 6 indexed citations
5.
Gabau, Elisabeth, Carme Brun i Gasca, Steven Laurie, et al.. (2021). New genes involved in Angelman syndrome-like: Expanding the genetic spectrum. PLoS ONE. 16(10). e0258766–e0258766. 14 indexed citations
6.
Castellanos, Elisabeth, Bernat Gel, Andreu Alibés, et al.. (2019). Mutational spectrum by phenotype: panel‐based NGS testing of patients with clinical suspicion of RASopathy and children with multiple café‐au‐lait macules. Clinical Genetics. 97(2). 264–275. 12 indexed citations
7.
Pintó, Xavier, et al.. (2019). Genetic contribution to lipid target achievement with statin therapy: a prospective study. The Pharmacogenomics Journal. 20(3). 494–504. 7 indexed citations
8.
Pintó, Xavier, et al.. (2018). KIF6 gene as a pharmacogenetic marker for lipid-lowering effect in statin treatment. PLoS ONE. 13(10). e0205430–e0205430. 11 indexed citations
9.
Esteba‐Castillo, Susanna, Neus Baena, Anna Ruiz, et al.. (2018). High Incidence of Copy Number Variants in Adults with Intellectual Disability and Co-morbid Psychiatric Disorders. Behavior Genetics. 48(4). 323–336. 16 indexed citations
10.
García-Ramallo, Eva, Neus Baena, Míriam Guitart, et al.. (2017). RNA editing independently occurs at three mir-376a-1 sites and may compromise the stability of the microRNA hairpin. Gene. 628. 109–116. 4 indexed citations
11.
Baena, Neus, Elisabeth Gabau, Adrijan Sarajlija, et al.. (2017). Novel intragenic deletions within the UBE3A gene in two unrelated patients with Angelman syndrome: case report and review of the literature. BMC Medical Genetics. 18(1). 137–137. 5 indexed citations
12.
Bueno, Marta, Susanna Esteba‐Castillo, Ramón Novell, et al.. (2016). Lack of Postprandial Peak in Brain-Derived Neurotrophic Factor in Adults with Prader-Willi Syndrome. PLoS ONE. 11(9). e0163468–e0163468. 24 indexed citations
13.
Colobrán, Roger, Clara Franco‐Jarava, Andrea Martín‐Nalda, et al.. (2016). Novel Mutations Causing C5 Deficiency in Three North-African Families. Journal of Clinical Immunology. 36(4). 388–396. 7 indexed citations
14.
Ruiz, Anna, Gemma Llort, Neus Baena, et al.. (2014). Genetic Testing in Hereditary Breast and Ovarian Cancer Using Massive Parallel Sequencing. BioMed Research International. 2014. 1–8. 13 indexed citations
15.
Caballı́n, M.R., et al.. (2005). Characterization of six marker chromosomes by comparative genomic hybridization. American Journal of Medical Genetics Part A. 136A(2). 169–174. 2 indexed citations
16.
Garne, Ester, Maria Loane, Catherine De Vigan, et al.. (2004). Prenatal diagnostic procedures used in pregnancies with congenital malformations in 14 regions of Europe. Prenatal Diagnosis. 24(11). 908–912. 14 indexed citations
17.
Baena, Neus, et al.. (2001). Fetal and placenta chromosome constitution in 237 pregnancy losses. Annales de Génétique. 44(2). 83–88. 9 indexed citations
18.
Vigan, C. De, Neus Baena, E Cariati, M. Clementi, & Claude Stoll. (2001). Contribution of ultrasonographic examination to the prenatal detection of chromosomal abnormalities in 19 centres across Europe. Annales de Génétique. 44(4). 209–217. 48 indexed citations
19.
Durán, Carmina, et al.. (1998). Incidència del reflux vesicoureteral als controls d'hidronefrosi prenatal. 58(3). 156–160. 1 indexed citations
20.
Blanco, Joan, Elisabeth Gabau, Neus Baena, et al.. (1998). Chromosome 21 Disomy in the Spermatozoa of the Fathers of Children with Trisomy 21, in a Population with a High Prevalence of Down Syndrome: Increased Incidence in Cases of Paternal Origin. The American Journal of Human Genetics. 63(4). 1067–1072. 88 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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