Aimé Lumaka

690 total citations
46 papers, 293 citations indexed

About

Aimé Lumaka is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Aimé Lumaka has authored 46 papers receiving a total of 293 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 11 papers in Pediatrics, Perinatology and Child Health and 10 papers in Molecular Biology. Recurrent topics in Aimé Lumaka's work include Prenatal Screening and Diagnostics (10 papers), Genomic variations and chromosomal abnormalities (9 papers) and Genomics and Rare Diseases (8 papers). Aimé Lumaka is often cited by papers focused on Prenatal Screening and Diagnostics (10 papers), Genomic variations and chromosomal abnormalities (9 papers) and Genomics and Rare Diseases (8 papers). Aimé Lumaka collaborates with scholars based in Belgium, Democratic Republic of the Congo and United States. Aimé Lumaka's co-authors include Koenraad Devriendt, Prosper Lukusa-Tshilobo, Léon Mutesa, Vincent Bours, Hilde Peeters, Corinne Fasquelle, Valérie Race, T. Lukusa, Joris Vermeesch and Adeline Jacquinet and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Aimé Lumaka

43 papers receiving 282 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Aimé Lumaka 155 89 44 38 34 46 293
Ayala Aviram 161 1.0× 168 1.9× 75 1.7× 55 1.4× 23 0.7× 9 328
Arlene Buller 138 0.9× 154 1.7× 82 1.9× 36 0.9× 31 0.9× 27 453
Jean P. Pfotenhauer 156 1.0× 211 2.4× 16 0.4× 51 1.3× 19 0.6× 9 438
Mamoru Ozaki 142 0.9× 152 1.7× 38 0.9× 63 1.7× 10 0.3× 38 389
Alessandra Splendore 227 1.5× 172 1.9× 58 1.3× 30 0.8× 11 0.3× 16 392
Rob Elles 192 1.2× 203 2.3× 31 0.7× 68 1.8× 10 0.3× 20 437
A Mavrou 104 0.7× 172 1.9× 23 0.5× 26 0.7× 21 0.6× 16 290
Lara Cresswell 134 0.9× 83 0.9× 29 0.7× 28 0.7× 19 0.6× 9 317
Iskra Petković 164 1.1× 179 2.0× 28 0.6× 24 0.6× 11 0.3× 31 305
Marie‐Pierre Cordier 189 1.2× 168 1.9× 59 1.3× 119 3.1× 17 0.5× 34 438

Countries citing papers authored by Aimé Lumaka

Since Specialization
Citations

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

Fields of papers citing papers by Aimé Lumaka

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aimé Lumaka

This figure shows the co-authorship network connecting the top 25 collaborators of Aimé Lumaka. A scholar is included among the top collaborators of Aimé Lumaka 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 Aimé Lumaka. Aimé Lumaka 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.
Souche, Erika, Prosper Lukusa-Tshilobo, Chris Van Geet, et al.. (2024). Genetic modulators of diversity in biological expression of sickle cell anemia in patients from democratic republic of Congo. Mediterranean Journal of Hematology and Infectious Diseases. 17(1). e2025001–e2025001.
2.
Fasquelle, Corinne, Keith Durkin, Maria Artesi, et al.. (2024). Genetic evaluation of patients with multiple primary cancers. Oncology Letters. 29(1). 4–4. 1 indexed citations
3.
Kayembe‐Kitenge, Tony, Aimé Lumaka, Oscar Numbi Luboya, et al.. (2023). Usefulness of automated image analysis for recognition of the fragile X syndrome gestalt in Congolese subjects. European Journal of Medical Genetics. 66(9). 104819–104819. 2 indexed citations
4.
Lumaka, Aimé, Valérie Race, Gert Matthijs, et al.. (2023). Hydroxyurea treatment for adult sickle cell anemia patients in Kinshasa. SHILAP Revista de lepidopterología. 4(3). 595–601. 3 indexed citations
5.
Lumaka, Aimé, Corinne Fasquelle, François‐Guillaume Debray, et al.. (2023). Rapid Whole Genome Sequencing Diagnoses and Guides Treatment in Critically Ill Children in Belgium in Less than 40 Hours. International Journal of Molecular Sciences. 24(4). 4003–4003. 10 indexed citations
6.
Lumaka, Aimé, et al.. (2023). PMS2 Pathogenic Variant in Lynch Syndrome-Associated Colorectal Cancer with Polyps. SHILAP Revista de lepidopterología. 10(1). 1–5. 3 indexed citations
7.
Harvengt, Julie, et al.. (2023). HIDEA syndrome: A new case report highlighting similarities with ROHHAD syndrome. Frontiers in Genetics. 14. 1137767–1137767. 3 indexed citations
8.
Lumaka, Aimé, et al.. (2022). Molecular genetic characterization of Congolese patients with oculocutaneous albinism. European Journal of Medical Genetics. 65(11). 104611–104611. 1 indexed citations
9.
Lumaka, Aimé, Koenraad Devriendt, Amanda Krause, et al.. (2022). Increasing African genomic data generation and sharing to resolve rare and undiagnosed diseases in Africa: a call-to-action by the H3Africa rare diseases working group. Orphanet Journal of Rare Diseases. 17(1). 230–230. 25 indexed citations
10.
Lumaka, Aimé, Valérie Race, Gert Matthijs, et al.. (2022). Clinical and laboratory characterization of adult sickle cell anemia patients in Kinshasa. PLoS ONE. 17(12). e0278478–e0278478. 3 indexed citations
11.
Lumaka, Aimé, et al.. (2021). BMPR1A and SMAD4 mutations in juvenile polyposis syndrome: clinicopathological and genetic data from two congolese patients. Gene Reports. 23. 101141–101141. 3 indexed citations
12.
Nsibu, Célestin N., Michel Ntetani Aloni, Pierre Akilimali, et al.. (2020). Exploring association between MBL2 gene polymorphisms and the occurrence of clinical blackwater fever through a case–control study in Congolese children. Malaria Journal. 19(1). 25–25. 1 indexed citations
13.
Lumaka, Aimé, et al.. (2018). Contribution of the Clinical and Histopathological Features in the Positive Diagnosis of the Juvenile Polyposis Syndrome. Open Repository and Bibliography (University of Liège). 1 indexed citations
14.
Aloni, Michel Ntetani, Pierre Akilimali, Patrick Kayembé, et al.. (2018). High IgG1 Malaria Antibodies Level in Children is a Possible Risk Factor of Blackwater Fever: A Case-Control Study. Open Repository and Bibliography (University of Liège). 3(3). 2 indexed citations
15.
Lumaka, Aimé, et al.. (2018). Fragile X syndrome with mosaic size mutation in a Bantu patient from Central Africa. Clinical Dysmorphology. 27(2). 66–69. 3 indexed citations
16.
Lumaka, Aimé, et al.. (2018). Usefulness of fragile X checklist and CGG distribution in specialized institutions in Kinshasa, DR Congo. Journal of Community Genetics. 10(1). 153–159. 3 indexed citations
17.
Lumaka, Aimé, et al.. (2014). A novel heterozygous mutation of three consecutive nucleotides causing Apert syndrome in a Congolese family. European Journal of Medical Genetics. 57(4). 169–173. 5 indexed citations
18.
Lumaka, Aimé, et al.. (2014). Preaxial Polydactyly of the Foot: Variable Expression of Trisomy 13 in a Case from Central Africa. SHILAP Revista de lepidopterología. 2014. 1–5. 3 indexed citations
19.
Lumaka, Aimé, Ingele Casteels, Els Ortibus, et al.. (2012). Variability in expression of a familial 2.79 Mb microdeletion in chromosome14q22.1–22.2. American Journal of Medical Genetics Part A. 158A(6). 1381–1387. 19 indexed citations
20.
Lumaka, Aimé, et al.. (2011). X-linked adrenal hypoplasia congenita: a novel DAX1 missense mutation and challenges for clinical diagnosis in Africa. European Journal of Pediatrics. 171(2). 267–270. 6 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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