Luisa Herrera

1.0k total citations
33 papers, 567 citations indexed

About

Luisa Herrera is a scholar working on Molecular Biology, Genetics and Clinical Psychology. According to data from OpenAlex, Luisa Herrera has authored 33 papers receiving a total of 567 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Clinical Psychology. Recurrent topics in Luisa Herrera's work include Reproductive Biology and Fertility (3 papers), Child and Adolescent Psychosocial and Emotional Development (3 papers) and Personality Disorders and Psychopathology (3 papers). Luisa Herrera is often cited by papers focused on Reproductive Biology and Fertility (3 papers), Child and Adolescent Psychosocial and Emotional Development (3 papers) and Personality Disorders and Psychopathology (3 papers). Luisa Herrera collaborates with scholars based in Chile, United States and Italy. Luisa Herrera's co-authors include David Schlessinger, Antonino Forabosco, Massimo Pellegrini, Steven Mumm, Giuseppe Pilia, Laura Crisponi, Antonio Percesepe, Ramaiah Nagaraja, P. Carvallo and Verónica Mericq and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and FEBS Letters.

In The Last Decade

Luisa Herrera

33 papers receiving 549 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Luisa Herrera Chile 14 213 190 134 53 50 33 567
Tuck C. Ngun United States 8 220 1.0× 225 1.2× 110 0.8× 89 1.7× 24 0.5× 8 581
Staci E. Pollack United States 9 160 0.8× 83 0.4× 196 1.5× 125 2.4× 46 0.9× 29 602
Negar Ghahramani United States 6 169 0.8× 182 1.0× 80 0.6× 42 0.8× 22 0.4× 6 464
Abigail Woodroffe United States 10 187 0.9× 172 0.9× 85 0.6× 93 1.8× 15 0.3× 12 510
Eileen M. Resnick United States 11 150 0.7× 228 1.2× 55 0.4× 92 1.7× 83 1.7× 14 631
W. Knogler Austria 12 73 0.3× 91 0.5× 100 0.7× 63 1.2× 70 1.4× 23 662
Lisa Yang United Kingdom 17 256 1.2× 56 0.3× 84 0.6× 183 3.5× 68 1.4× 49 976
Ichiko Nishijima Japan 17 604 2.8× 263 1.4× 136 1.0× 17 0.3× 44 0.9× 41 1.2k
Suzanne McKenna United States 13 269 1.3× 101 0.5× 46 0.3× 100 1.9× 112 2.2× 20 933
M.V. Gomes Brazil 11 239 1.1× 137 0.7× 78 0.6× 25 0.5× 58 1.2× 20 492

Countries citing papers authored by Luisa Herrera

Since Specialization
Citations

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

Fields of papers citing papers by Luisa Herrera

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luisa Herrera

This figure shows the co-authorship network connecting the top 25 collaborators of Luisa Herrera. A scholar is included among the top collaborators of Luisa Herrera 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 Luisa Herrera. Luisa Herrera 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.
Booij, Linda, et al.. (2022). Potential epigenetic mechanisms in psychotherapy: a pilot study on DNA methylation and mentalization change in borderline personality disorder. Frontiers in Human Neuroscience. 16. 955005–955005. 12 indexed citations
2.
Troncoso, M., et al.. (2021). Hypomyelination and Congenital Cataract: Identification of a Novel likely pathogenic c.414+1G>A in FAM126A gene Variant. SHILAP Revista de lepidopterología. 9(5). e04171–e04171. 1 indexed citations
3.
Castillo, Silvia, et al.. (2020). Knobloch syndrome in a patient from Chile. American Journal of Medical Genetics Part A. 182(10). 2239–2242. 4 indexed citations
4.
Silva, Hernán, et al.. (2020). SERT and BDNF polymorphisms interplay on neuroticism in borderline personality disorder. BMC Research Notes. 13(1). 61–61. 4 indexed citations
5.
Jiménez, Juan Pablo, et al.. (2019). Sintomatologia depresiva y bienestar psicológico en estudiantes universitarios chilenos. Revista médica de Chile. 147(5). 579–588. 28 indexed citations
6.
Jiménez, Juan Pablo, Luisa Herrera, Jaime R. Silva, et al.. (2018). Psychotherapy and Genetic Neuroscience: An Emerging Dialog. Frontiers in Genetics. 9. 257–257. 30 indexed citations
7.
Bustamante, M. Leonor, Luisa Herrera, Pablo A. Gaspar, et al.. (2017). Shifting the focus toward rare variants in schizophrenia to close the gap from genotype to phenotype. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 174(7). 663–670. 11 indexed citations
8.
González, Sergio, Sergio Aguilera, Cecilia Alliende, et al.. (2011). Alterations in type I hemidesmosome components suggestive of epigenetic control in the salivary glands of patients with Sjögren's syndrome. Arthritis & Rheumatism. 63(4). 1106–1115. 35 indexed citations
9.
Moraga, Mauricio, et al.. (2010). Different phenotypes of lattice corneal dystrophy type I in patients with 417C>T (R124C) and 1762A>G (H572R) mutations in TGFBI (BIGH3).. PubMed. 16. 1601–9. 5 indexed citations
10.
Herrera, Luisa, et al.. (2008). Anticipation in familial lattice corneal dystrophy type I with R124C mutation in the TGFBI (BIGH3) gene.. PubMed. 14. 829–35. 11 indexed citations
11.
Perez-Pastene, Carolina, Rebecca Graumann, Marcelo Miranda, et al.. (2007). Association of GST M1 null polymorphism with Parkinson's disease in a Chilean population with a strong Amerindian genetic component. Neuroscience Letters. 418(2). 181–185. 33 indexed citations
12.
13.
Herrera, Luisa, Chris Ottolenghi, José Elías García‐Ortíz, et al.. (2005). Mouse ovary developmental RNA and protein markers from gene expression profiling. Developmental Biology. 279(2). 271–290. 52 indexed citations
14.
Schlessinger, David, Luisa Herrera, Laura Crisponi, et al.. (2002). Genes and translocations involved in POF. American Journal of Medical Genetics. 111(3). 328–333. 109 indexed citations
15.
Mumm, Steven, Luisa Herrera, Paul Waeltz, et al.. (2001). χ/Autosomal Translocations in the χq Critical Region Associated with Premature Ovarian Failure Fall within and outside Genes. Genomics. 76(1-3). 30–36. 33 indexed citations
16.
Kleinsteuber, Karin, et al.. (2000). Mialgias post ejercicio como forma de presentación de una distrofinopatía. Revista médica de Chile. 128(7). 772–777. 1 indexed citations
17.
Echeverrı́a, Valentina, et al.. (1997). Molecular cloning and expression of an adenylyl cyclase from Xenopus laevis oocytes1. FEBS Letters. 404(1). 91–94. 9 indexed citations
18.
Herrera, Luisa, et al.. (1997). Two different 5′ splice site mutations in the growth hormone gene causing autosomal dominant growth hormone deficiency. Human Genetics. 101(1). 113–117. 31 indexed citations
19.
Herrera, Luisa, et al.. (1997). Dual transduction signaling by a Xenopus muscarinic receptor: Adenylyl cyclase inhibition and MAP kinase activation. Journal of Cellular Biochemistry. 65(1). 75–82. 3 indexed citations
20.
Herrera, Luisa, Pilar Carvallo, Marcelo Antonelli, & Juan Olate. (1994). Cloning of a Xenopus laevis muscarinic receptor encoded by an intronless gene. FEBS Letters. 352(2). 175–179. 5 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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