Publications and communications of Aimé Lumaka Zola

Mbayabo, G., Ngole, M., Lumbala, P. K., Lumaka Zola, A., Race, V., Matthijs, G., Mikobi, T. M., Devriendt, K., Van Geet, C., & Lukusa, P. T. (December 2023). Clinical and biological profile of Sickle Cell Anemia children in a rural area in Central Africa. Hematology, 28 (1), 2193770. doi:10.1080/16078454.2023.2193770

Taruscio, D., Salvatore, M., Lumaka Zola, A., Carta, C., Cellai, L. L., Ferrari, G., Sciascia, S., Groft, S., Alanay, Y., Azam, M., Baynam, G., Cederroth, H., Cutiongco-de la Paz, E. M., Dissanayake, V. H. W., Giugliani, R., Gonzaga-Jauregui, C., Hettiarachchi, D., Kvlividze, O., Landoure, G., ... Posada, M. (02 March 2023). Undiagnosed diseases: Needs and opportunities in 20 countries participating in the Undiagnosed Diseases Network International. Frontiers in Public Health, 11, 1079601. doi:10.3389/fpubh.2023.1079601

Lumaka Zola, A., Fasquelle, C., Debray, F.-G., Alkan, S., Jacquinet, A., Harvengt, J., Boemer, F., Mulder, A., VAESSEN, S., Viellevoye, R., Gonon Rodrigues Palmeira, L., CHARLOTEAUX, B., Brysse, A., BULK, S., Rigo, V., & Bours, V. (16 February 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. doi:10.3390/ijms24044003

Sciascia, S., Roccatello, D., Salvatore, M., Carta, C., Cellai, L. L., Ferrari, G., Lumaka Zola, A., Groft, S., Alanay, Y., Azam, M., Baynam, G., Cederroth, H., Cutiongco-de la Paz, E. M., Dissanayake, V. H. W., Giugliani, R., Gonzaga-Jauregui, C., Hettiarachchi, D., Kvlividze, O., Landoure, G., ... Taruscio, D. (2023). Unmet needs in countries participating in the undiagnosed diseases network international: an international survey considering national health care and economic indicators. Frontiers in Public Health, 11, 1248260. doi:10.3389/fpubh.2023.1248260

Laetitia, M. M., Veronique, K., Mamy, N. Z., Cathy, S. M., Lumaka Zola, A., Race, V., Prosper, L. T., & Devriendt, K. (November 2022). Molecular genetic characterization of Congolese patients with oculocutaneous albinism. European Journal of Medical Genetics, 65 (11), 104611. doi:10.1016/j.ejmg.2022.104611

Mbayabo, G., Lumbala Kabuyi, P., Ngole, M., Lumaka Zola, A., Race, V., Maisin, D., Gruson, D., Matthijs, G., Minga, T. M., Devriendt, K., Van Geet, C., & Tshilobo, P. L. (2022). Value of DNA testing in the diagnosis of sickle-cell anemia in childhood in an environment with a high prevalence of other causes of anemia. Journal of Clinical Laboratory Analysis, 24593. doi:10.1002/jcla.24593

Makay, P., Mubungu, G., Mupuala, A., Bluske, K., Brown, C., Schmidt, S. A., Ngole, M., Fuanani, P., Perry, D. L., Lukusa, P., Devriendt, K., Taft, R. J., Lumaka, A., & Lumaka Zola, A. (2022). PERCHING syndrome: Clinical presentation in the first African patient confirmed by clinical whole genome sequencing. American Journal of Medical Genetics. Part A. doi:10.1002/ajmg.a.62855

Riggs, E. R., Bingaman, T. I., Barry, C.-A., Behlmann, A., Bluske, K., Bostwick, B., Bright, A., Chen, C.-A., Clause, A. R., Dharmadhikari, A. V., Ganapathi, M., Gonzaga-Jauregui, C., Grant, A. R., Hughes, M. Y., Kim, S. R., Krause, A., Liao, J., Lumaka Zola, A., Mah, M., ... Lumaka Zola, A. (2022). Clinical validity assessment of genes frequently tested on intellectual disability/autism sequencing panels. Genetics in Medicine. doi:10.1016/j.gim.2022.05.001

Ngole, M., Race, V., Mbayabo, G., Lumbala, P., Songo, C., Lukusa, P. T., Devriendt, K., Matthijs, G., & Lumaka Zola, A. (2022). DNA testing for sickle cell anemia in Africa: Implementation choices for the Democratic Republic of Congo. Journal of Clinical Laboratory Analysis, 24398. doi:10.1002/jcla.24398

Lumaka Zola, A., Carstens, N., Devriendt, K., Krause, A., Kulohoma, B., Kumuthini, J., Mubungu, G., Mukisa, J., Nel, M., Olanrewaju, T. O., Lombard, Z., Landouré, G., & as members of the Rare Disease Working Group of the H3Africa Consortium. (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. doi:10.1186/s13023-022-02391-w

Mubungu, G., Makay, P., Lumaka Zola, A., Mvuama, N., Tshika, D., Tady, B.-P., Biselele, T., Roelants, M., Tshilobo, P. L., & Devriendt, K. (February 2021). Dysmorphism and major anomalies are a main predictor of survival in newborns admitted to the neonatal intensive care unit in the Democratic Republic of Congo. American Journal of Medical Genetics. Part A, 185 (2), 453 - 460. doi:10.1002/ajmg.a.61987

Bodi, J. M., Nsibu, C. N., Longenge, R. L., Aloni, M. N., Akilimali, P. Z., Kayembe, P. K., Omar, A. H., Verhaegen, J., Tshibassu, P. M., Lukusa, P. T., Lumaka Zola, A., & Hirayama, K. (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. doi:10.1186/s12936-020-3100-8

Poaty, H., Batamba Bouya, L., Gassaye, D., Mavoungou Biatsi, K., Lumaka Zola, A., & Peko, J. (14 February 2018). Contribution of the Clinical and Histopathological Features in the Positive Diagnosis of the Juvenile Polyposis Syndrome. American Journal of Genetics & Genomics, 1 (1).

Bodi, J. M., Nsibu, C. N., Longenge, R. L., Aloni, M. N., Akilimali, P. Z., Tshibassu, P. M., Kayembe, P. K., Omar, A. H., Hirayama, K., Verhaegen, J., Lumaka Zola, A., & Lukusa, P. T. (2018). High IgG1 Malaria Antibodies Level in Children is a Possible Risk Factor of Blackwater Fever: A Case-Control Study. Pediatrics & Health Research, 3 (9). doi:10.21767/2574-2817.100034