Nilsa de Deus

1.5k total citations
65 papers, 1.1k citations indexed

About

Nilsa de Deus is a scholar working on Infectious Diseases, Hepatology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Nilsa de Deus has authored 65 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Infectious Diseases, 24 papers in Hepatology and 13 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Nilsa de Deus's work include Viral gastroenteritis research and epidemiology (37 papers), Hepatitis Viruses Studies and Epidemiology (24 papers) and Child Nutrition and Water Access (13 papers). Nilsa de Deus is often cited by papers focused on Viral gastroenteritis research and epidemiology (37 papers), Hepatitis Viruses Studies and Epidemiology (24 papers) and Child Nutrition and Water Access (13 papers). Nilsa de Deus collaborates with scholars based in Mozambique, Portugal and Spain. Nilsa de Deus's co-authors include Marga Martı́n, Enric Mateu, Joaquím Segalés, Sonia Pina-Pedrero, Bibiana Peralta, Maribel Casas, Chiara Seminati, Miquel Nofrarías, Inácio Mandomando and Francisco Ruiz‐Fons and has published in prestigious journals such as PLoS ONE, The Journal of Infectious Diseases and Nutrients.

In The Last Decade

Nilsa de Deus

59 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nilsa de Deus Mozambique 19 907 686 318 148 127 65 1.1k
Anita Plenge‐Bönig Germany 12 673 0.7× 518 0.8× 128 0.4× 31 0.2× 24 0.2× 24 900
Michael O. Favorov United States 28 1.2k 1.3× 1.4k 2.1× 302 0.9× 80 0.5× 24 0.2× 49 2.0k
Remon Abu‐Elyazeed United States 21 847 0.9× 281 0.4× 17 0.1× 171 1.2× 116 0.9× 39 1.2k
Mamadou Kaba South Africa 19 925 1.0× 818 1.2× 220 0.7× 24 0.2× 23 0.2× 37 1.5k
Sanjaya Kumar Shrestha Nepal 16 438 0.5× 357 0.5× 46 0.1× 73 0.5× 49 0.4× 45 935
Hind I. Shaheen Egypt 16 513 0.6× 94 0.1× 64 0.2× 41 0.3× 42 0.3× 39 819
S. S. Gandhe India 10 535 0.6× 472 0.7× 58 0.2× 46 0.3× 35 0.3× 10 853
Abdollah Naficy United States 20 570 0.6× 188 0.3× 18 0.1× 93 0.6× 60 0.5× 26 1.1k
Edison Muñoz-Ortiz Colombia 13 313 0.3× 45 0.1× 80 0.3× 51 0.3× 77 0.6× 64 699
Élisabeth Couturier France 18 832 0.9× 461 0.7× 51 0.2× 51 0.3× 24 0.2× 40 1.2k

Countries citing papers authored by Nilsa de Deus

Since Specialization
Citations

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

Fields of papers citing papers by Nilsa de Deus

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nilsa de Deus. 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 Nilsa de Deus. The network helps show where Nilsa de Deus may publish in the future.

Co-authorship network of co-authors of Nilsa de Deus

This figure shows the co-authorship network connecting the top 25 collaborators of Nilsa de Deus. A scholar is included among the top collaborators of Nilsa de Deus 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 Nilsa de Deus. Nilsa de Deus 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
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Pecenka, Clint, Frédéric Debellut, Anne Schuind, et al.. (2023). Impact and Cost-Effectiveness of Alternative Human Papillomavirus Vaccines for Preadolescent Girls in Mozambique: A Modelling Study. Vaccines. 11(6). 1058–1058. 3 indexed citations
5.
Pecenka, Clint, et al.. (2022). Cost-effectiveness of rotavirus vaccination in Mozambique. Vaccine. 40(36). 5338–5346. 5 indexed citations
6.
Kellogg, Timothy A., et al.. (2020). Intestinal protozoan infections among children 0-168 months with diarrhea in Mozambique: June 2014 - January 2018. PLoS neglected tropical diseases. 14(4). e0008195–e0008195. 23 indexed citations
7.
Bhatt, Nilesh, Sádia Ali, Ilana Teruszkin Balassiano, et al.. (2017). Seroepidemiology of leptospirosis among febrile patients in a rapidly growing suburban slum and a flood-vulnerable rural district in Mozambique, 2012–2014: Implications for the management of fever. International Journal of Infectious Diseases. 64. 50–57. 19 indexed citations
8.
Bhatt, Nilesh, Ivan Manhiça, Nilsa de Deus, et al.. (2017). First serological evidence of hantavirus among febrile patients in Mozambique. International Journal of Infectious Diseases. 61. 51–55. 7 indexed citations
9.
Mandomando, Inácio, Goitom Weldegebriel, Nilsa de Deus, & Jason M. Mwenda. (2017). Feasibility of using regional sentinel surveillance to monitor the rotavirus vaccine impact, effectiveness and intussusception incidence in the African Region. Vaccine. 35(13). 1663–1667. 9 indexed citations
10.
Langa, José Paulo, et al.. (2015). Epidemic waves of cholera in the last two decades in Mozambique. The Journal of Infection in Developing Countries. 9(6). 635–641. 20 indexed citations
11.
Moraleda, Cinta, Nilsa de Deus, Montse Renom, et al.. (2013). Impact of HIV Exposure on Health Outcomes in HIV-Negative Infants Born to HIV-Positive Mothers in Sub-Saharan Africa. JAIDS Journal of Acquired Immune Deficiency Syndromes. 65(2). 182–189. 43 indexed citations
12.
Pérez‐Hoyos, Santiago, Denise Naniche, Eusébio Macete, et al.. (2011). Stabilization of HIV incidence in women of reproductive age in southern Mozambique. HIV Medicine. 12(8). 500–505. 13 indexed citations
13.
Deus, Nilsa de, et al.. (2009). La infección por el virus de la hepatitis E en el cerdo. 36–39. 1 indexed citations
14.
Peralta, Bibiana, Maribel Casas, Nilsa de Deus, et al.. (2009). Anti-HEV antibodies in domestic animal species and rodents from Spain using a genotype 3-based ELISA. Veterinary Microbiology. 137(1-2). 66–73. 60 indexed citations
15.
Casas, Maribel, Sonia Pina-Pedrero, Nilsa de Deus, et al.. (2009). Pigs orally inoculated with swine hepatitis E virus are able to infect contact sentinels. Veterinary Microbiology. 138(1-2). 78–84. 25 indexed citations
16.
Olvera, Àlex, Núria Busquets, Martı́ Cortey, et al.. (2009). Applying phylogenetic analysis to viral livestock diseases: Moving beyond molecular typing. The Veterinary Journal. 184(2). 130–137. 14 indexed citations
17.
Deus, Nilsa de, Maribel Casas, Bibiana Peralta, et al.. (2008). Hepatitis E virus infection dynamics and organic distribution in naturally infected pigs in a farrow-to-finish farm. Veterinary Microbiology. 132(1-2). 19–28. 119 indexed citations
18.
Deus, Nilsa de, Bibiana Peralta, Sonia Pina-Pedrero, et al.. (2007). Epidemiological study of hepatitis E virus infection in European wild boars (Sus scrofa) in Spain. Veterinary Microbiology. 129(1-2). 163–170. 112 indexed citations
19.
Martı́n, Marga, Joaquím Segalés, Fu‐Chen Huang, et al.. (2007). Association of hepatitis E virus (HEV) and postweaning multisystemic wasting syndrome (PMWS) with lesions of hepatitis in pigs. Veterinary Microbiology. 122(1-2). 16–24. 56 indexed citations
20.
Deus, Nilsa de, Chiara Seminati, Sonia Pina-Pedrero, et al.. (2006). Detection of hepatitis E virus in liver, mesenteric lymph node, serum, bile and faeces of naturally infected pigs affected by different pathological conditions. Veterinary Microbiology. 119(2-4). 105–114. 79 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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