Sandra Louzada

22.4k total citations
27 papers, 691 citations indexed

About

Sandra Louzada is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Sandra Louzada has authored 27 papers receiving a total of 691 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 13 papers in Genetics and 11 papers in Plant Science. Recurrent topics in Sandra Louzada's work include Chromosomal and Genetic Variations (11 papers), Genomics and Phylogenetic Studies (5 papers) and Genetic Mapping and Diversity in Plants and Animals (4 papers). Sandra Louzada is often cited by papers focused on Chromosomal and Genetic Variations (11 papers), Genomics and Phylogenetic Studies (5 papers) and Genetic Mapping and Diversity in Plants and Animals (4 papers). Sandra Louzada collaborates with scholars based in United Kingdom, Portugal and China. Sandra Louzada's co-authors include Fengtang Yang, Raquel Chaves, Filomena Adega, Ketan J. Patel, Guillaume Guilbaud, Frédéric Langevin, Sophie Roerink, Michael R. Stratton, Lee Mulderrig and Serena Nik‐Zainal and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and PLoS ONE.

In The Last Decade

Sandra Louzada

26 papers receiving 681 citations

Peers

Sandra Louzada

GENET

PFM

Guido van Mierlo Netherlands

Alexander M. Gout Australia

Xiaozhen Wang China

Anna R. Poetsch Germany

Yina Zhu China

Xiaoming Wu China

Paola Costanzo Italy

Ηλίας Στρατικόπουλος United States

N. Yu. Oparina Russia

Guido van Mierlo Netherlands

Sandra Louzada

950 ×2.1

184 ×1.1

GENET

61 ×0.4

82 ×1.0

36 ×0.6

PFM

Citations per year, relative to Sandra Louzada Sandra Louzada (= 1×) peers Guido van Mierlo

Countries citing papers authored by Sandra Louzada

Since Specialization

Citations

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

Fields of papers citing papers by Sandra Louzada

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sandra Louzada

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

All Works

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20 of 20 papers shown

Louzada, Sandra, et al.. (2024). Pericentromeric satellite RNAs as flexible protein partners in the regulation of nuclear structure. Wiley Interdisciplinary Reviews - RNA. 15(4). e1868–e1868.

Louzada, Sandra & Fengtang Yang. (2024). High-Resolution FISH Analysis Using DNA Fibers Generated by Molecular Combing. Methods in molecular biology. 2825. 185–203. 1 indexed citations

Ferreira, Daniela, et al.. (2024). Answering the Cell Stress Call: Satellite Non-Coding Transcription as a Response Mechanism. Biomolecules. 14(1). 124–124. 4 indexed citations

Louzada, Sandra, et al.. (2023). Human Satellite 1A analysis provides evidence of pericentromeric transcription. BMC Biology. 21(1). 28–28. 8 indexed citations

Hollox, Edward J. & Sandra Louzada. (2022). Genetic variation of glycophorins and infectious disease. Immunogenetics. 75(3). 201–206. 6 indexed citations

Louzada, Sandra, Luciana W. Zuccherato, Marília O. Scliar, et al.. (2020). Structural variation of the malaria-associated human glycophorin A-B-E region. BMC Genomics. 21(1). 446–446. 8 indexed citations

Gonçalves, Emanuel, Fiona M. Behan, Sandra Louzada, et al.. (2019). Structural rearrangements generate cell-specific, gene-independent CRISPR-Cas9 loss of fitness effects. Genome biology. 20(1). 27–27. 32 indexed citations

Shi, Wentao, Andrea Massaia, Sandra Louzada, et al.. (2019). Birth, expansion, and death of VCY-containing palindromes on the human Y chromosome. Genome biology. 20(1). 207–207. 13 indexed citations

Kim, Jihee, Beatrice Lana, Silvia Torelli, et al.. (2019). A new patient‐derived iPSC model for dystroglycanopathies validates a compound that increases glycosylation of α‐dystroglycan. EMBO Reports. 20(11). e47967–e47967. 16 indexed citations

10.

Garaycoechea, Juan I., Gerry P. Crossan, Frédéric Langevin, et al.. (2018). Alcohol and endogenous aldehydes damage chromosomes and mutate stem cells. Nature. 553(7687). 171–177. 272 indexed citations

11.

Louzada, Sandra, Danielle Carpenter, Anna Färnert, et al.. (2018). The Malaria-Protective Human Glycophorin Structural Variant DUP4 Shows Somatic Mosaicism and Association with Hemoglobin Levels. The American Journal of Human Genetics. 103(5). 769–776. 16 indexed citations

12.

Shi, Wentao, Andrea Massaia, Sandra Louzada, et al.. (2017). Copy number variation arising from gene conversion on the human Y chromosome. Human Genetics. 137(1). 73–83. 10 indexed citations

13.

Lee, Jake June-Koo, Sandra Louzada, Yu An, et al.. (2016). Complex chromosomal rearrangements by single catastrophic pathogenesis in NUT midline carcinoma. Annals of Oncology. 28(4). 890–897. 52 indexed citations

14.

Louzada, Sandra, et al.. (2015). A novel satellite DNA sequence in the Peromyscus genome (PMSat): Evolution via copy number fluctuation. Molecular Phylogenetics and Evolution. 92. 193–203. 12 indexed citations

15.

Skinner, Benjamin M., Carole A. Sargent, Fengtang Yang, et al.. (2015). Expansion of the HSFY gene family in pig lineages. BMC Genomics. 16(1). 442–442. 9 indexed citations

16.

Louzada, Sandra, et al.. (2015). A High-Resolution Comparative Chromosome Map of Cricetus cricetus and Peromyscus eremicus Reveals the Involvement of Constitutive Heterochromatin in Breakpoint Regions. Cytogenetic and Genome Research. 145(1). 59–67. 15 indexed citations

17.

Ding, Zhihao, Yunyun Ni, Bum-Kyu Lee, et al.. (2014). Quantitative Genetics of CTCF Binding Reveal Local Sequence Effects and Different Modes of X-Chromosome Association. PLoS Genetics. 10(11). e1004798–e1004798. 38 indexed citations

18.

Chaves, Raquel, et al.. (2012). Praomys tullbergi (Muridae, Rodentia) genome architecture decoded by comparative chromosome painting with Mus and Rattus. Chromosome Research. 20(6). 673–683. 9 indexed citations

19.

Louzada, Sandra, Filomena Adega, & Raquel Chaves. (2012). Defining the Sister Rat Mammary Tumor Cell Lines HH-16 cl.2/1 and HH-16.cl.4 as an In Vitro Cell Model for Erbb2. PLoS ONE. 7(1). e29923–e29923. 29 indexed citations

20.

Louzada, Sandra, Ana Paço, Svatava Kubı́čková, et al.. (2008). Different evolutionary trails in the related genomes Cricetus cricetus and Peromyscus eremicus (Rodentia, Cricetidae) uncovered by orthologous satellite DNA repositioning. Micron. 39(8). 1149–1155. 13 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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