Lavínia Schüler‐Faccini

8.9k total citations · 2 hit papers
218 papers, 4.2k citations indexed

About

Lavínia Schüler‐Faccini is a scholar working on Public Health, Environmental and Occupational Health, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Lavínia Schüler‐Faccini has authored 218 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Public Health, Environmental and Occupational Health, 54 papers in Genetics and 48 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Lavínia Schüler‐Faccini's work include Mosquito-borne diseases and control (41 papers), Virology and Viral Diseases (19 papers) and Multiple Myeloma Research and Treatments (19 papers). Lavínia Schüler‐Faccini is often cited by papers focused on Mosquito-borne diseases and control (41 papers), Virology and Viral Diseases (19 papers) and Multiple Myeloma Research and Treatments (19 papers). Lavínia Schüler‐Faccini collaborates with scholars based in Brazil, United States and Pakistan. Lavínia Schüler‐Faccini's co-authors include Maria Teresa Vieira Sanseverino, Erlane Marques Ribeiro, Fernanda Sales Luiz Vianna, Fernando C. Barros, César G. Victora, Maria Juliana R. Doriqui, Denise P. Cavalcanti, Ana Paula Carneiro Brandalize, Marcos Vinícius da Silva Pone and Héctor Yuri Conti Wanderley and has published in prestigious journals such as New England Journal of Medicine, The Lancet and Journal of Clinical Oncology.

In The Last Decade

Lavínia Schüler‐Faccini

203 papers receiving 4.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Possible Association Between Zika Virus Infection and Microcephaly — Brazil, 2015

2016 755 citations Lavínia Schüler‐Faccini, Maria Juliana R. Doriqui et al. profile →
Congenital Zika virus syndrome in Brazil: a case series of the first 1501 livebirths with complete investigation

2016 416 citations Lavínia Schüler‐Faccini et al. profile →

Peers

Lavínia Schüler‐Faccini

PHEOH

PPCH

EPIDE

Louis Bujan France

R. Frydman France

Arijit Biswas Singapore

Ralph Nanan Australia

Hong‐Nerng Ho Taiwan

Michael Katz United States

Erlane Marques Ribeiro Brazil

Mark V. Sauer United States

Júlia Szekeres‐Barthó Hungary

G. Malinger Israel

Louis Bujan France

Lavínia Schüler‐Faccini

1.7k ×0.8

PHEOH

867 ×0.9

475 ×0.5

PPCH

386 ×0.5

EPIDE

812 ×1.4

Citations per year, relative to Lavínia Schüler‐Faccini Lavínia Schüler‐Faccini (= 1×) peers Louis Bujan

Countries citing papers authored by Lavínia Schüler‐Faccini

Since Specialization

Citations

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

Fields of papers citing papers by Lavínia Schüler‐Faccini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lavínia Schüler‐Faccini. 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 Lavínia Schüler‐Faccini. The network helps show where Lavínia Schüler‐Faccini may publish in the future.

Co-authorship network of co-authors of Lavínia Schüler‐Faccini

This figure shows the co-authorship network connecting the top 25 collaborators of Lavínia Schüler‐Faccini. A scholar is included among the top collaborators of Lavínia Schüler‐Faccini 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 Lavínia Schüler‐Faccini. Lavínia Schüler‐Faccini 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

Schüler‐Faccini, Lavínia, et al.. (2025). Infections during pregnancy: An ongoing threat. Seminars in Perinatology. 49(4). 152075–152075.

Kowalski, Thayne Woycinck, Paulo Michel Roehe, Fernanda Sales Luiz Vianna, et al.. (2024). New candidate genes potentially involved in Zika virus teratogenesis. Computers in Biology and Medicine. 173. 108259–108259.

Kowalski, Thayne Woycinck, et al.. (2023). From bench to in silico and backwards: What have we done on genetics of recurrent pregnancy loss and implantation failure and where should we go next?. Genetics and Molecular Biology. 46(3 suppl 1). e20230127–e20230127. 1 indexed citations

Vianna, Fernanda Sales Luiz, Nelson J. R. Fagundes, Marcelo Zagonel de Oliveira, et al.. (2023). HLA haplotypes and differential regional mortality caused by COVID-19 in Brazil: an ecological study based on a large bone marrow donor bank dataset. Anais da Academia Brasileira de Ciências. 95(3). e20220801–e20220801. 1 indexed citations

Schüler‐Faccini, Lavínia, et al.. (2023). Oral microbiota, co-evolution, and implications for health and disease: The case of indigenous peoples. Genetics and Molecular Biology. 46(3 suppl 1).

Espinosa, Mariano Martínez, et al.. (2022). Recent dengue virus infection: epidemiological survey on risk factors associated with infection in a medium-sized city in Mato Grosso. LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas). 5 indexed citations

Luza, André Luís, et al.. (2021). Mapeamento dinâmico da probabilidade de infestação por vetores urbanos de arbovírus nos municípios do Rio Grande do Sul, 2016-2017. Epidemiologia e Serviços de Saúde. 30(2). e2020154–e2020154. 3 indexed citations

Santin, Juliana Tosetto, et al.. (2021). Prevalence and antimicrobial resistance profile of Staphylococcus aureus in inherited epidermolysis bullosa: a cross‐sectional multicenter study in Brazil. International Journal of Dermatology. 60(9). 1126–1130. 6 indexed citations

Barros, Sérgio Estelita, et al.. (2021). Development of dentofacial characteristics related to Incontinentia Pigmenti syndrome: A repeated cross-sectional study. American Journal of Orthodontics and Dentofacial Orthopedics. 160(1). 66–76. 1 indexed citations

10.

Kiszewski, Ana Elisa, et al.. (2021). Gene panel for the diagnosis of epidermolysis bullosa: proposal for a viable and efficient approach. Anais Brasileiros de Dermatologia. 96(2). 155–162. 9 indexed citations

11.

Schüler‐Faccini, Lavínia, et al.. (2020). Prevalence of congenital anomalies at birth among live births in the state of Maranhão from 2001 to 2016: temporal and spatial analysis. Revista Brasileira de Epidemiologia. 24(suppl 1). e210020–e210020. 6 indexed citations

12.

Espinosa, Mariano Martínez, et al.. (2020). Sociodemographic and sanitary profile of chikungunya virus infection in medium-sized municipality in Mato Grosso, from January to March 2018, Brasil.. SHILAP Revista de lepidopterología. 1 indexed citations

13.

Santin, Juliana Tosetto, et al.. (2020). Genotype‐phenotype correlations on epidermolysis bullosa with congenital absence of skin: A comprehensive review. Clinical Genetics. 99(1). 29–41. 13 indexed citations

14.

Santin, Juliana Tosetto, et al.. (2020). Inherited epidermolysis bullosa: update on the clinical and genetic aspects. Anais Brasileiros de Dermatologia. 95(5). 551–569. 54 indexed citations

15.

Santin, Juliana Tosetto, et al.. (2019). An overview of the genetic basis of epidermolysis bullosa in Brazil: discovery of novel and recurrent disease‐causing variants. Clinical Genetics. 96(3). 189–198. 21 indexed citations

16.

Bisso‐Machado, Rafael, et al.. (2019). HLA diversity in Brazil. HLA. 95(1). 3–14. 15 indexed citations

17.

Oliveira, Marcelo Zagonel de, Mariana Jobim, Luiz Gonzaga, et al.. (2018). Spatial analyzes of HLA data in Rio Grande do Sul, south Brazil: genetic structure and possible correlation with autoimmune diseases. International Journal of Health Geographics. 17(1). 34–34. 8 indexed citations

18.

Nunes, José Manuel, Stéphane Bühler, Marcelo Zagonel de Oliveira, et al.. (2016). The HLA‐A, ‐B and ‐DRB1 polymorphism in a large dataset of South Brazil bone marrow donors from Rio Grande do Sul. HLA. 89(1). 29–38. 7 indexed citations

19.

Vianna, Fernanda Sales Luiz, Maria Teresa Vieira Sanseverino, & Lavínia Schüler‐Faccini. (2014). Thalidomide Analogs in Brazil: Concern About Teratogenesis. LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas). 2 indexed citations

20.

Schwartz, Ida Vanessa Döederlein, et al.. (2014). Clinical genetics and public policies: how should rare diseases be managed?. SHILAP Revista de lepidopterología. 7 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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