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 |