  | LETE, C., FERNANDEZ CARAZO, R., MENTEN, C., BECKERS, P., KOOPMANSCH, B., FRANKE, S., DE PRIJCK, B., JAMAR, M., LAMBERT, F., & BOURS, V. (July 2021). A case of early-T-cell precursor acute lymphoblastic leukemia with e6a2 BCR-ABL1 fusion transcript [Poster presentation]. 13th European Cytogenomics Conference. |
| LETE, C., Ameye, G., BECKERS, P., Michaux, L., BOURS, V., JAMAR, M., De Bie, J., Dewaele, B., & MENTEN, C. (July 2021). CASE REPORT: the use of optical genome mapping (Bionano) to understand a complex mechanism of a KMT2A rearrangement in an AML case [Poster presentation]. 13th European Cytogenomics Conference. |
  | Muys, J., Jacquemyn, Y., Blaumeiser, B., Bourlard, L., Brison, N., BULK, S., Chiarappa, P., De Leener, A., De Rademaeker, M., Désir, J., Destrée, A., Devriendt, K., Dheedene, A., Duquenne, A., Fieuw, A., Fransen, E., GATOT, J.-S., JAMAR, M., Janssens, S., ... Janssens, K. (2020). Prenatally detected copy number variants in a national cohort: A postnatal follow-up study. Prenatal Diagnosis. doi:10.1002/pd.5751  Peer Reviewed verified by ORBi |
 | VALDES SOCIN, H. G., Rey, R., COPPENS, L., JAMAR, M., Bours, V., & Beckers, A. (2019). Le syndrome de Klinefelter : actualités cliniques et thérapeutiques. Vaisseaux, Coeur, Poumons, 24 (1). Editorial reviewed |
| JAMAR, M., HARVENGT, J., D'OTREPPE DE BOUVETTE, S., Florkin, B., & MENTEN, C. (September 2018). Diagnostic moléculaire par CGH-array + SNP d'un cas d'Anémie de Fanconi [Poster presentation]. XXIVe Colloque Association des Cytogénéticiens de Langue Française (ACLF), Saint-Malo, France. |
| JAMAR, M., MENTEN, C., GRISART, B., & GATOT, J.-S. (September 2018). Trisomie 9 détectée en DPNI : à propos de deux cas de mosaïcisme [Poster presentation]. XXIVe Colloque Association des Cytogénéticiens de Langue Française (ACLF), Saint-Malo, France. |
 | Muys, J., Blaumeiser, B., Jacquemyn, Y., Bandelier, C., Brison, N., BULK, S., Chiarappa, P., COURTENS, W., De Leener, A., De Rademaeker, M., Desir, J., Destree, A., Devriendt, K., Dheedene, A., Fieuw, A., Fransen, E., GATOT, J.-S., Holmgren, P., JAMAR, M., ... Janssens, K. (2018). The BElgian PREnatal MicroArray (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations. Prenatal Diagnosis. doi:10.1002/pd.5373 Peer Reviewed verified by ORBi |
 | Wenric, S.* , Sticca, T.* , CABERG, J.-H., Josse, C., Fasquelle, C., HERENS, C., JAMAR, M., MAX, S., GOTHOT, A., CAERS, J., & Bours, V. (2017). Exome copy number variation detection: Use of a pool of unrelated healthy tissue as reference sample. Genetic Epidemiology, 41, 35-40. doi:10.1002/gepi.22019 Peer Reviewed verified by ORBi* These authors have contributed equally to this work. |
 | Sticca, T., CABERG, J.-H., Wenric, S., Poulet, C., HERENS, C., JAMAR, M., Josse, C., El Guendi, S., MAX, S., BEGUIN, Y., GOTHOT, A., CAERS, J., & Bours, V. (2017). Genomic Studies of Multiple Myeloma Reveal an Association between X Chromosome Alterations and Genomic Profile Complexity. Genes, Chromosomes and Cancer, 56, 18-27. doi:10.1002/gcc.22397 Peer Reviewed verified by ORBi |
 | JAMAR, M., HERENS, C., MENTEN, C., Sticca, T., & CABERG, J.-H. (20 September 2016). Corrélation entre les caryotypes standard et moléculaire dans une série de 7 cas de LAL pédiatriques hyperdiploïdes [Poster presentation]. XXIIIème Colloque Association des Cytogénéticiens de Langue Française, Montpellier, France. |
 | Uwineza, A., Hitayezu, J., JAMAR, M., Caberg, J.-H., Murorunkwere, S., Janvier, N., Bours, V., & Mutesa, L. (2016). Cytogenetic Studies of Rwandan Pediatric Patients Presenting with Global Developmental Delay, Intellectual Disability and/or Multiple Congenital Anomalies. Journal of Tropical Pediatrics. doi:10.1093/tropej/fmv065 Peer Reviewed verified by ORBi |
| Daly, A., Lodish, M., Trivellin, G., Rostomyan, L., Faucz, F., Yuan, B., Naves, L. A., Choong, C., Lysy, P., Shah, N. S., Verrua, E., CABERG, J.-H., CASTERMANS, E., Zatelli, C., Schernthaner-Reiter, M., Villa, C., Metzger, D., Strebkova, N., Mazerkina, N., ... Beckers, A. (2015). Disease characteristics of patients with X-linked acrogigantism (X-LAG) syndrome. In Abstract book - ENDO 2015. |
| Trivellin, G., Daly, A., Faucz, F., Yuan, B., Rostomyan, L., Larco, D., Schernthaner-Reiter, M., Szarek, E., Leal, L., CABERG, J.-H., CASTERMANS, E., Villa, C., Dimopoulos, A., Chittiboina, P., Xekouki, P., Shah, N. S., Metzger, D., Lysy, P., Ferrante, E., ... Stratakis, C. (2015). X-Linked acro-gigantism (X-LAG) due to microduplications of chromosome Xq26 : A new disorder and implications for acromegaly. In Abstract book - ENDO 2015. |
 | Stratakis, C., Trivellin, G., Rostomyan, L., Lodish, M., Faucz, F., Naves, L. A., Choong, C., Lysy, P., Shah, N. S., Verrua, E., CABERG, J.-H., CASTERMANS, E., JAMAR, M., Zatelli, M., Schernthaner-Reiter, M., Villa, C., Metzger, D., Strebkova, N., Mazerkina, N., ... Beckers, A. (2015). X-Linked acro-gigantism (X-LAG) syndrome : a new form of infant-onset pituitary gigantism. In Abstract book - 14th International Pituitary Congress. |
 | FOGUENNE, J., SIMUL, M., KEUTGENS, A., TASSIN, F., Bonnet, C., BEGUIN, Y., JAMAR, M., LAMBERT, F., & GOTHOT, A. (2015). Multiparameter flow cytometric analysis of composite lymphoma: case report of a mantle cell lymphoma associated with a B-cell chronic lymphocytic leukemia and an aberrant T cell subset. Belgian Journal of Hematology. Peer Reviewed verified by ORBi |
 | Trivellin, G.* , Daly, A.* , Faucz, F. R., Yuan, B., Rostomyan, L., Larco, D. O., Schernthaner-Reiter, M. H., Szarek, E., Leal, L. F., CABERG, J.-H., CASTERMANS, E., Villa, C., Dimopoulos, A., Chittiboina, P., Xekouki, P., Shah, N. S., Metzger, D., Lysy, P. A., Ferrante, E., ... Stratakis, C. A.*. (2014). Gigantism and Acromegaly Due to Xq26 Microduplications and GPR101 Mutation. New England Journal of Medicine. doi:10.1056/NEJMoa1408028 Peer Reviewed verified by ORBi* These authors have contributed equally to this work. |
 | Uwineza, A., CABERG, J.-H., Hitayezu, J., JAMAR, M., DIDEBERG, V., Rusingiza, E. K., Bours, V., Mutesa, L., & Hellin, A.-C. (2014). Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies. BMC Medical Genetics, 15 (1), 79. doi:10.1186/1471-2350-15-79 Peer Reviewed verified by ORBi |
 | Teteli, R., Uwineza, A., Butera, Y., Hitayezu, J., Murorunkwere, S., Umurerwa, L., Ndinkabandi, J., Hellin, A.-C., JAMAR, M., CABERG, J.-H., Muganga, N., Mucumbitsi, J., Rusingiza, E. K., & Mutesa, L. (2014). Pattern of congenital heart diseases in Rwandan children with genetic defects. Pan African Medical Journal, 19, 85. doi:10.11604/pamj.2014.19.85.3428 Peer Reviewed verified by ORBi |
 | Uwineza, A., PIERQUIN, G., GAILLEZ, S., JAMAR, M., CABERG, J.-H., & BOURS, V. (2013). Clinical, cytogenetic and molecular characterization of two cases of mosaic ring chromosome 13. Genetic Counseling, 24 (2), 193-200. Peer Reviewed verified by ORBi |
 | Mutesa, L., JAMAR, M., PIERQUIN, G., & BOURS, V. (2012). A new 48, XXYY/47, XYY syndrome associated with multiple skeletal abnormalities, congenital heart disease and mental retardation. Indian Journal of Human Genetics, 18 (3), 352-5. doi:10.4103/0971-6866.108033 Peer Reviewed verified by ORBi |
 | Garraux, G., CABERG, J.-H., Vanbellinghen, J.-F., JAMAR, M., Bours, V., Moonen, G., & DIVE, D. (2012). Partial trisomy 4q associated with young-onset dopa-responsive parkinsonism. Archives of Neurology, 69 (3), 398-400. doi:10.1001/archneurol.2011.802 Peer Reviewed verified by ORBi |
 | Mullier, F., Daliphard, S., Garand, R., Dekeyser, M., Cornet, Y., Luquet, I., Talmant, P., Richebourg, S., JAMAR, M., Dogne, J.-M., Chatelain, C., Michaux, L., & Chatelain, B. (2012). Morphology, cytogenetics, and survival in myelodysplasia with del(20q) or ider(20q): a multicenter study. Annals of Hematology, 91 (2), 203-13. doi:10.1007/s00277-011-1286-0 Peer Reviewed verified by ORBi |
 | Thielen, C., Bisig, B., Gofflot, S., Herens, C., Fillet, G., JAMAR, M., Tassin, F., Boniver, J., Drion, P., & de Leval, L. (2011). CHIC cells: a novel ALK+ cell line derived from a relapsed anaplastic large cell lymphoma. British Journal of Haematology, 152, 356-360. doi:10.1111/j.1365-2141.2010.08414.x Peer Reviewed verified by ORBi |
 | DELVENNE, P., Deprez, M., BISIG, B., JAMAR, M., Boniver, J., Bours, V., & HERENS, C. (2010). Fish and chips. Revue Médicale de Liège, 65 Spec no., 3-10. Peer reviewed |
 | Put, N., Konings, P., Rack, K., Jamar, M., Van Roy, N., Libouton, J.-M., Vannuffel, P., Sartenaer, D., Ameye, G., Speleman, F., Herens, C., Poirel, H. A., Moreau, Y., Hagemeijer, A., Vandenberghe, P., & Michaux, L. (2009). Improved detection of chromosomal abnormalities in chronic lymphocytic leukemia by conventional cytogenetics using CpG oligonucleotide and interleukin-2 stimulation: A Belgian multicentric study. Genes, Chromosomes and Cancer, 48 (10), 843-53. doi:10.1002/gcc.20691 Peer Reviewed verified by ORBi |
 | Garraux, G., VANBELLINGHEN, J.-F., JAMAR, M., BOURS, V., Moonen, G., & DIVE, D. (2009). De novo interstitial duplication 4q associated with sporadic young-onset dopa-responsive parkinsonism. Movement Disorders, 24 (Suppl. 1), 138-S139. Peer Reviewed verified by ORBi |
 | Fournier, M., Lacrosse, S., Jamar, M., Bours, V., & Herens, C. (15 July 2005). Deletions of the 3 ' BCR and 5 ' ABL regions in patients with Philadelphia-positive chronic myeloid leukemia: a one-step process occurring in about 10% of the cases without any evidence of genetic instability in the target cells. Cancer Genetics and Cytogenetics, 160 (2), 184-187. doi:10.1016/j.cancergencyto.2005.01.002 Peer Reviewed verified by ORBi |
 | Jamar, M., Lemarchal, C., Koulischer, L., Bours, V., & LEMAIRE, V. (2003). A low rate of trisomy 21 in twin-pregnancies: A cytogenetics retrospective study of 278 cases. Genetic Counseling, 14 (4), 395-400. Peer Reviewed verified by ORBi |
 | Verloes, A., JAMAR, M., Dideberg, V., & Herens, C. (2001). Episphalosomic Syndrome : A Mca Syndrome Ressembling Fanconi Anemia, with Increased Baseline Level of Chromosome Breaks but No Hypersensivity to Clastogens. Annales de Génétique, 44 (2, Apr-Jun), 59-62. doi:10.1016/S0003-3995(01)01043-7 Peer Reviewed verified by ORBi |
 | Herens, C., Hermanne, J.-P., Tassin, F., Fassotte, M.-F., Thiry, A., Jamar, M., Schaaf-Lafontaine, N., Fillet, G., & Koulischer, L. (1999). Translocation (2;3)(p21;q26) as the sole anomaly in a case of primary myelofibrosis. Cancer Genetics and Cytogenetics, 110 (1), 62-4. doi:10.1016/S0165-4608(98)00186-1 Peer Reviewed verified by ORBi |
Herens, C., Jamar, M., Alvarez Gonzalez, M.-L., Lesenfants, S., Lombet, J., Bonnivert, J., Koulischer, L., & Verloes, A. (12 December 1997). Private Multiple Congenital Anomaly Syndromes May Result from Unbalanced Subtle Translocations: T(2q;4p) Explains the Lambotte Syndrome. American Journal of Medical Genetics, 73 (2), 127-31. doi:10.1002/(SICI)1096-8628(19971212)73:2<127::AID-AJMG5>3.0.CO;2-R Peer Reviewed verified by ORBi |
BRASSEUR, E., HERENS, C., VIERSET, L., JAMAR, M., SCHOENEN, I., & KOULISCHER, L. (17 January 1997). Loss of the Y gonosome in leukemia and preleukemia : The experience of the human genetic center of Liège [Poster presentation]. 4th Euregional Oncology meeting, Maastricht, Netherlands. |
Chapelle, J.-P., Jamar, M., & El Allaf, D. (19 October 1996). Influence of thrombolytic agents in serum levels of myocardial markers after acute myocardial infarction [Poster presentation]. 20th Symposium of the Belgian Society of Clinical Biology, Brugge, Belgium. |
 | Ectors, F., Koulischer, L., JAMAR, M., HERENS, C., VERLOES, A., Remy, B., & Beckers, J.-F. (August 1995). Cytogenetic study of bovine oocytes matured in vitro. Theriogenology, 44 (3), 445-450. doi:10.1016/0093-691X(95)00198-H Peer Reviewed verified by ORBi |