Publications and communications of Mauricette JAMAR

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.

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.

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

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).

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

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

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
* These authors have contributed equally to this work.

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

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.

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.

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.

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.

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

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
* 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

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.

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

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

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

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

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.

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.

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

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

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.

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

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

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

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