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 |
Lumaka Zola, A. (2023). Valuable insights into hereditary spinocerebellar degeneration from clusters of homozygosity in Africa. European Journal of Human Genetics. doi:10.1038/s41431-023-01452-3 |
Lubala, T. K., Kayembe-Kitenge, T., Mubungu, G., Lumaka Zola, A., Kanteng, G., Savage, S., Luboya, O., Hagerman, R., Devriendt, K., & Lukusa-Tshilobo, P. (September 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. doi:10.1016/j.ejmg.2023.104819 |
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 |
Mubungu, G., Roelants, M., Lumaka Zola, A., Makay, P., Tshika, D., Lubala, T., Tshilobo Lukusa, P., & Devriendt, K. (2022). Objective evaluation of facial features in Congolese newborns by facial measurements. The need for population-specific measurements. American Journal of Medical Genetics. Part A. doi:10.1002/ajmg.a.62958 |
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 |
HARVENGT, J., Lumaka Zola, A., FASQUELLE, C., & BOURS, V. (26 February 2022). HIDEA Syndrome : A new case report highlighting similarities with ROHHAD Syndrome [Poster presentation]. ROHHAD International Consortium Virtual Symposium. |
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 |
Mubungu, G., Lukute, G., Makay, P., Songo, C., Lukusa, P., Devriendt, K., & Lumaka Zola, A. (2020). Phenotype and growth in Sotos syndrome patient from DR Congo (Central Africa). American Journal of Medical Genetics. Part A. doi:10.1002/ajmg.a.61617 |
Mubungu, G., Lumaka Zola, A., Mvuama, N., Tshika, D., Makay, P., Tshilobo, P. L., & Devriendt, K. (2020). Morphological characterization of newborns in Kinshasa, DR Congo: Common variants, minor, and major anomalies. American Journal of Medical Genetics. Part A. doi:10.1002/ajmg.a.61477 |
BULK, S., & Lumaka Zola, A. (22 November 2019). Preconceptional carrier screening in Belgium [Paper presentation]. 42nd Scientific Meeting Begian Society for Reproductive Medicine (BSRM), Antwerp, Belgium. |
Uyisenga, J., SEGERS, K., Lumaka Zola, A., Mugenzi, P., Boujemla, B., JOSSE, C., Mutesa, L., & BOURS, V. (26 September 2019). Germline mutations in young Rwandan with breast cancers [Paper presentation]. The Joint Minimally Invasive Surgery (MIS) & 3rd Rwanda Biotechnology Conference, Kigali, Rwanda. |
Cheng, H., Capponi, S., Wakeling, E., Marchi, E., Li, Q., Zhao, M., Weng, C., Stefan, P. G., Ahlfors, H., Kleyner, R., Rope, A., Lumaka Zola, A., Lukusa, P., Devriendt, K., Vermeesch, J., Posey, J. E., Palmer, E. E., Murray, L., Leon, E., ... Lyon, G. J. (2019). Missense variants in TAF1 and developmental phenotypes: challenges of determining pathogenicity. Human Mutation. doi:10.1002/humu.23936 |
Lumaka Zola, A., & DDD-Africa Project. (2019). Update on the Deciphering Developmental Disorders in Africa (DDD-Africa) project [Paper presentation]. 13th Meeting of the H3Africa Consortium, Tunis, Tunisia. |
Lumaka Zola, A., Lubala, T. K., Race, V., Peeters, H., Lukusa, P., & Devriendt, K. (2019). Usefulness of fragile X checklist and CGG distribution in specialized institutions in Kinshasa, DR Congo. Journal of Community Genetics, 10 (1), 153-159. doi:10.1007/s12687-018-0374-4 |
Mubungu, G., Kadima, B., Lumaka Zola, A., Mbayabo, G., Lukusa Tshilobo, P., & Devriendt, K. (2019). Congenital lateral abdominal wall defect in two Congolese children. Clinical Dysmorphology, 28 (1), 50-52. doi:10.1097/MCD.0000000000000239 |
Uyisenga, J., SEGERS, K., Lumaka Zola, A., Mugenzi, P., FASQUELLE, C., Boujemla, B., JOSSE, C., Mutesa, L., & Bours, V. (20 September 2018). Screening of germline mutations in young Rwandan with breast cancer [Paper presentation]. Joint 11th Conference of African Society of Human Genetics (AfSHG)& 12th H3 Africa Consortium Meeting, Kigali, Rwanda. |
Uyisenga, J., SEGERS, K., Lumaka Zola, A., Mugenzi, P., FASQUELLE, C., Boujemla, B., JOSSE, C., Mutesa, L., & Bours, V. (11 September 2018). Germline mutations in young Rwandan with breast cancers [Poster presentation]. GIGA Cancer Day, Liège, Belgium. |
Lukusa-Tshilobo, P., & Lumaka Zola, A. (September 2018). Value of rare diseases research in Africa, DR Congo [Paper presentation]. Annual Meeting of the African Society for Human Genetics, Kigali, Rwanda. |
Mubungu, G., Mupuala, A., Lumaka Zola, A., Devriendt, K., & Lukusa Tshilobo, P. (September 2018). Parry-Romberg Syndrome: Clinical Presentation in a Congolese Patient [Paper presentation]. 29th EUROPEAN MEETING ON DYSMORPHOLOGY. |
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 |
Lubala, T. K., Lumaka Zola, A., Kanteng, G., Mutesa, L., Mukuku, O., Wembonyama, S., Hagerman, R., Luboya, O. N., & Lukusa Tshilobo, P. (2018). Fragile X checklists: A meta-analysis and development of a simplified universal clinical checklist. Molecular Genetics and Genomic Medicine. doi:10.1002/mgg3.398 |
Lubala, T. K., Lumaka Zola, A., Mbuyi-Musanzayi, S., Kayembe, T., Shongo, M. Y. P., Mukuku, O., Lubala, N., Malamba-Lez, D., Luboya, O. N., & Lukusa-Tshilobo, P. (2018). Fragile X syndrome with mosaic size mutation in a Bantu patient from Central Africa. Clinical Dysmorphology, 27 (2), 66-69. doi:10.1097/MCD.0000000000000208 |
Lumaka Zola, A. (2018). Comprehensive clinical and genetic study of ID/DD in DR Congo [Paper presentation]. Seminar, Johannesburg, South Africa. |
Lumaka Zola, A., Race, V., Peeters, H., Corveleyn, A., Coban-Akdemir, Z., Jhangiani, S. N., Song, X., Mubungu, G., Posey, J., Lupski, J. R., Vermeesch, J. R., Lukusa, P., & Devriendt, K. (2018). A comprehensive clinical and genetic study in 127 patients with ID in Kinshasa, DR Congo. American Journal of Medical Genetics. Part A, 176 (9), 1897-1909. doi:10.1002/ajmg.a.40382 |
Mikobi, T. M., Lukusa, P. T., Aloni, M. N., Lumaka Zola, A., Akilimali, P. Z., Devriendt, K., Matthijs, G., Mbuyi Muamba, J.-M., & Race, V. (2018). Association between sickle cell anemia and alpha thalassemia reveals a high prevalence of the alpha(3.7) triplication in congolese patients than in worldwide series. Journal of Clinical Laboratory Analysis, 32 (1). doi:10.1002/jcla.22186 |
Mikobi, T. M., Tshilobo Lukusa, P., Aloni, M. N., Lumaka Zola, A., Kaba, D. K., Devriendt, K., Matthijs, G., Mbuyi Muamba, J. M., & Race, V. (2018). Protective BCL11A and HBS1L-MYB polymorphisms in a cohort of 102 Congolese patients suffering from sickle cell anemia. Journal of Clinical Laboratory Analysis, 32 (1). doi:10.1002/jcla.22207 |
Lumaka Zola, A., Cosemans, N., Lulebo Mampasi, A., Mubungu, G., Mvuama, N., Lubala, T., Mbuyi-Musanzayi, S., Breckpot, J., Holvoet, M., de Ravel, T., Van Buggenhout, G., Peeters, H., Donnai, D., Mutesa, L., Verloes, A., Lukusa Tshilobo, P., & Devriendt, K. (2017). Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator. Clinical Genetics, 92 (2), 166-171. doi:10.1111/cge.12948 |
Lumaka Zola, A., Mubungu, G., Race, V., Peeters, H., Lukusa-Tshilobo, P., & Devriendt, K. (2017). Clinical and molecular screening for the fragile X syndrome in specialized institutions in Kinshasa, DR Congo [Paper presentation]. Annual Meeting of the African Society for Human Genetics. |
Mbuyi-Musanzayi, S., Lumaka Zola, A., Kasole, T. L., Ilunga, E. K., Asani, B. Y., Tshilobo, P. L., Muenze, P. K., Reychler, H., Katombe, F. T., & Devriendt, K. (2017). Wolf-Hirschhorn Syndrome: Clinical and Genetic Data from a First Case Diagnosed in Central Africa. Journal of Pediatric Genetics, 6 (3), 186-190. doi:10.1055/s-0037-1599194 |
Kershenovich, R., & Lumaka Zola, A. (2016). Highlighting phenotypic differences of Down Syndrome and Turner (45X) Syndrome Patients from different ethnic groups using computer-aided facial dysmorphology analysis [Poster presentation]. Annual Meeting of the American College of Medical Genetics and Genomics (ACMG), Tampa, Florida, United States. |
Lumaka Zola, A., Cosemans, N., Lulebo Mampasi, A., Mubungu, G., Lubala, T., Mbuyi-Musanzayi, S., Breckpot, J., Holvoet, M., de Ravel de l’Argentière, T., Van Buggenhout, G., Donnai, D., Peeters, H., Mutesa, L., Verloes, A., Lukusa-Tshilobo, P., & Devriendt, K. (2016). Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator [Paper presentation]. 17th Manchester Dysmorphology Conference, Manchester, United Kingdom. |
Lumaka Zola, A., COSMANS, N., LULEBO MAMPASI, A., Peeters, H., Holvoet, M., Tshilobo LUKUSA, P., & DEVRIENDT, K. (2016). DETECTION OF FACIAL DYSMORPHISM IN CENTRAL AFRICAN PATIENTS. Genetic Counseling. |
Lumaka Zola, A., Lukoo, R., Mubungu, G., Lumbala, P., Mbayabo, G., Mupuala, A., Tshilobo, P. L., & Devriendt, K. (2016). Williams-Beuren syndrome: pitfalls for diagnosis in limited resources setting. Clinical Case Reports, 4 (3), 294-7. doi:10.1002/ccr3.476 |
MUBUNGU, G., Lumaka Zola, A., NGIYULU, R., DEVRIENDT, K., CORVELEYN, A., & LUKUSA TSHILOBO, P. (2016). DOOR SYNDROME: deafness, onychdystrophy, osteodystrophy, and mental retardation. Genetic Counseling. |
Lubala K., T., Lumaka Zola, A., Shongo, M., Mbuyi-Musanzayi, S., Ndua-Musole, M., Mukuku, O., Yogolelo Asani, B., Lubala N., Kayembe-Kitenge, T., Lalamba-Lez, uboya, Devriendt, K., & Lukusa-Tshilobo, P. (2015). Molecular evidence for full mutations in the FMR1 gene and fragile X syndrome in the Bantu-speaking population in Central Africa [Paper presentation]. 2nd Congress of the Congolese Society for Human Genetics, Lubumbashi, Congo - Brazzaville. |
Lumaka Zola, A., Cosemans, N., Peeters, H., Lukusa-Tshilobo, P., & Devriendt, K. (2015). A study of facial morphology of Congolese down syndrome patients with FACE2GENE [Paper presentation]. 2nd Congress of the Congolese Society for Human Genetics, Lubumbashi, Congo - Brazzaville. |
Lumaka Zola, A., PEETERS, H., LUKUSA-Tshilobo, & DEVRIENDT, K. (2015). COPY NUMBER VARIATIONS IN CONGOLESE PATIENTS WITH ID [Poster presentation]. Annual meeting of the Belgian Society for Human Genetics, Charleroi, Belgium. |
Lumaka Zola, A., Peeters, H., Lukusa-Tshilobo, P., & Devriendt, K. (2015). A genetic etiological study of intellectual disability in Kinshasa - DR CONGO [Paper presentation]. 2nd Congress of the Congolese Society for Human Genetics, Lubumbashi, Congo - Brazzaville. |
Mbuyi-Musanzayi, S., Lubala K., T., Lumaka Zola, A., Kayembe K., Kabamba N., Kalenga, Lukusa-Tshilobo, P., Tshilombo K., Banza-Lubaba N., & Devriendt, K. (2015). Meningocele in a Congolese femald with Beckwith-Wiedemann phenotype [Paper presentation]. 2nd Congress of the Congolese Society for Human Genetics, Lubumbashi, Congo - Brazzaville. |
Mbuyi-Musanzayi, S., Lumaka Zola, A., Lubala K., T., Kasamba, E., Yogolelo A., B., Lukusa-Tshilobo, P., Kalenga M., Lukusa-Tshilombo, P., & Devriendt, K. (2015). Wolf-Hirschhorn Syndrome: clinical and genetic data from a first case diagnosed in Central Africa [Paper presentation]. 2nd Congeress of the Congolese Society for Hulman Genetics, Lubumbashi, Congo - Brazzaville. |
Mikobi, T., Race, V., Aloni N, M., Lumaka Zola, A., Kaba K., D., Mbuyi-Muamba, J.-M., Lukusa-Tshilobo, P., Matthijs, G., & Devriendt, K. (2015). Etude génétique des loci régulateurs de l’hémoglobine foetale chez les drépanocytaires congolais [Paper presentation]. 2nd Congress of the Congolese Society for Human Genetics, Lubumbashi, Congo - Brazzaville. |
Mubungu, G., Lumaka Zola, A., Devriendt, K., & Lukusa-Tshilobo, P. (2015). An unknown syndrome of congenital hypoplasia of the lateral abdominal wall muscles. Genetic Counseling, 1 (1). |
Mubungu, G., Lumaka Zola, A., Kadima, B., Nsaman, S., Devriendt, K., & Lukusa-Tshilobo, P. (2015). Un syndrome inconnu avec hypoplasia congénitale des muscles de la paroi latéro-abdominale [Paper presentation]. 2nd Congress of the Congolese Society for Human Genetics, Lubumbashi, Congo - Brazzaville. |
Mubungu, G., Lumaka Zola, A., Ngiyulu, R., Devriendt, K., Corveleyn, A., & Lukusa-Tshilobo, P. (2015). Door syndrome: deafness, onychdystrophy, osteodystrophy, and mental retardation [Paper presentation]. 2nd Congress of the Congolese Society for Human Genetics, Lubumbashi, Congo - Brazzaville. |
Lumaka Zola, A., Mubungu, G., Mukaba, P., Mutantu, P., Luyeye, G., Corveleyn, A., Tady, B.-P., Lukusa Tshilobo, P., & Devriendt, K. (2014). A novel heterozygous mutation of three consecutive nucleotides causing Apert syndrome in a Congolese family. European Journal of Medical Genetics, 57 (4), 169-73. doi:10.1016/j.ejmg.2014.01.004 |
Lumaka Zola, A., THOELEN, R., BRISON, N., PEETERS, H., LUKUSA TSHILOBO, P., VERMEESCH, J., & DEVRIENDT, K. (2014). Making Array CHG technology accessible for Congolese patients using Stripped slides [Poster presentation]. BeMGI Annual Meeting 2014, Liège, Belgium. |
Mbuyi-Musanzayi, S., Lubala Kasole, T., Lumaka Zola, A., Kayembe Kitenge, T., Kabamba Ngombe, L., Kalenga Muenze, P., Lukusa Tshilobo, P., Tshilombo Katombe, F., Banza Lubaba Nkulu, C., & Devriendt, K. (2014). Meningocele in a congolese female with beckwith-wiedemann phenotype. Case Reports in Genetics, 2014, 989425. doi:10.1155/2014/989425 |
Mbuyi-Musanzayi, S., Lumaka Zola, A., Yogolelo Asani, B., Lubala Kasole, T., Lukusa Tshilobo, P., Kalenga Muenze, P., Tshilombo Katombe, F., & Devriendt, K. (2014). Preaxial polydactyly of the foot: variable expression of trisomy 13 in a case from central Africa. Case Reports in Genetics, 2014, 365031. doi:10.1155/2014/365031 |
Mubungu, G., Lumaka Zola, A., Matondo, R., Mbayabo, G., Tuka, D., Kayembe, C., Mulowhe, D., Molua, A., Tady, B.-P., Nkidiaka, E., Bunga, P., Lukusa Tshilobo, P., & Devriendt, K. (2014). Skinfold over toenail is pathognomonic for the popliteal pterygium syndrome in a Congolese family with large intrafamilial variability. Clinical Case Reports, 2 (6), 250-3. doi:10.1002/ccr3.101 |
Lumaka Zola, A., Peeters, H., Lukusa-Tshilobo, P., & Devriendt, K. (May 2013). Genetic causes of intellectual disability among males in Kinshasa [Paper presentation]. 1st Congrès de la société Congolaise de Génétique Humaine. Kinshasa. |
Tshika, D., Mubungu, G., Kayembe, C., Mabela, T., Lumaka Zola, A., Devriendt, K., & Lukusa-Tshilobo, P. (May 2013). Ostéogénèse imparfaite: observations cliniques à propos d’une famille Congolaise [Paper presentation]. 1st Congress of the Congolese Society for Human Genetics, Kinshasa, Congo - Brazzaville. |
Lumaka Zola, A., Mubungu, G., Mutantu, P., Mukaba, P., Luyeye, G., Tady, B., Corveleyn, A., Lukusa-Tshilobo, P., & Devriendt, K. (2013). A novel heterozygous mutation of three consecutive nucleotides causing Apert syndrome in a Congolese family. Genetic Counseling, 25 (1). |
Lumaka Zola, A., MUBUNGU, G., MUTANTU, P., MUKABA, P., LUYEYE, G., TADY, B.-P., CORVENLEYN, A., LUKUSA-Tshilobo, P., & DEVRIENT, K. (2013). A novel heterozygous mutation of three consecutive nucleotides causing Apert syndrome in a Congolese family [Poster presentation]. Annual meeting of the Belgian Society for Human Genetics (BeSHG). |
Mbayabo, G., Lumaka Zola, A., Lukoo, R., Mubungu, G., Mukendi, D., Lukusa-Tshilobo, P., & Devriendt, K. (2013). Syndrome de Williams Beuren: difficultés pour le diagnostic dans un patient Congolais [Paper presentation]. 1st Congress of the Congolese Society for Human Genetics, Kinshasa, Congo - Brazzaville. |
Mubungu, G., Lumaka Zola, A., Mukaba, P., Mutantu, P., Luyeye, G., Tady., B., Corveleyn, A., Lukusa-Tshilobo, P., & Devriendt, K. (2013). Nouvelle mutation hétérozygote de trois nuclétides consecutifs causant le syndrome d’Apert dans une famille Congolaise [Paper presentation]. 1st Congress of the Congolese Society for Human Genetics, Kinshasa, Congo - Brazzaville. |
Mubungu, G., Matondo, R., Mbayabo, G., Tuka, D., Nkidiaka, E., Bunga, P., Lumaka Zola, A., Tady, B., Lukusa-Tshilobo, P., & Devriendt, K. (2013). Popliteal pterygium syndrome: observations cliniques dans une famille Congolaise [Paper presentation]. 1st Congress of the COngolese Society for Human Genetics. |
Mutantu, P., Nkuku, C., Lumaka Zola, A., Mikobi, T., Race, V., Muyembe T., Lukusa-Tshilobo, P., Devriendt, K., & Matthijs, G. (2013). Extraction de l’ADN humain par la méthode du salting-out. Challenge et opportunités [Paper presentation]. 1st Congress of the Congolese Society for Human Genetics, Kinshasha, Congo - Brazzaville. |
Tshamala, H., Lumaka Zola, A., Bodi, J., Itokwa, K., Noki, I., Devriendt, K., Lukusa-Tshilobo, P., & Gini, J.-L. (2013). Leucémie myéloïde chronique juvenile: à propos d’un cas chez un adolescent Congolais de 15 ans [Paper presentation]. 1st Congress of the Congolese Society for Human Genetics, Kinshasa, Congo - Brazzaville. |
Lumaka Zola, A., Lukusa-Tshilobo, P., Peeters, H., & Devriendt, K. (2012). A genetic-etiological study of intellectual disability in the Democratic Republic of Congo. Initial results. Genetic Counseling, 24 (1). |
Lumaka Zola, A., Mubungu, G., Nsibu, C., Tady, B.-P., Lukusa, T., & Devriendt, K. (2012). X-linked adrenal hypoplasia congenita: a novel DAX1 missense mutation and challenges for clinical diagnosis in Africa. European Journal of Pediatrics, 171 (2), 267-70. doi:10.1007/s00431-011-1523-5 |
Lumaka Zola, A., Van Hole, C., Casteels, I., Ortibus, E., De Wolf, V., Vermeesch, J. R., Lukusa, T., & Devriendt, K. (2012). Variability in expression of a familial 2.79 Mb microdeletion in chromosome 14q22.1-22.2. American Journal of Medical Genetics. Part A, 158A (6), 1381-7. doi:10.1002/ajmg.a.35353 |
Lumaka Zola, A., Vanhole, C., Casteels, I., Ortibus, E., Vermeesch, J., Lukusa-Tshilobo, P., & Devriendt, K. (2011). Variability in expression of a familial 2.79 Mb microdeletion in chr14q22.1-22.2. Genetic Counseling, 23 (1), 90. |
Lumaka Zola, A., Mubungu, G., Nsibu Ndosimao, C., Tady Muyala, B., Lukusa Tshilobo, P., & Devriendt, K. (July 2009). Insiffisance Surrénaliènne Congénitale liée au Chromosome X [Paper presentation]. Congrès de la Socièté de Pédiatrie du Congo Démocratique, Kinshasa, Congo - Brazzaville. |
Lumaka Zola, A. (2009). Proposal for an African reference Database for rare disease [Paper presentation]. 13th Meeting of the H3Africa Consortium, Tunis, Tunisia. |
Lumaka Zola, A., Bone, D., Lukoo, R., Mujinga, N., Senga, I., Tady, B., Matthijs, G., & Lukusa, T. P. (2009). Werdnig-Hoffmann disease: report of the first case clinically identified and genetically confirmed in central Africa (Kinshasa-Congo). Genetic Counseling, 20 (4), 349-58. |
Lumaka Zola, A. (September 2008). Some current issues for NGS variants classification in Rare diseases in Africa. Annual Meeting of the African Society for Human Genetics, 18 Septembre 2018. Kigali, Ruanda [Paper presentation]. Annual Meeting of the African Society for Human Genetics, Kigali, Rwanda. |