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Herens Christian

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Main Referenced Co-authors
Verloes, Alain  (17)
Koulischer, Lucien  (16)
Bours, Vincent  (12)
Jamar, Mauricette  (12)
Beguin, Yves  (9)
Main Referenced Keywords
Humans (16); Male (13); Middle Aged (10); Aged (8); Female (8);
Main Referenced Unit & Research Centers
Giga-Cancer - ULiège [BE] (3)
GIGA-I3 - Giga-Infection, Immunity and Inflammation - ULiège [BE] (2)
Giga-Genetics - ULiège [BE] (1)
Giga-Signal Transduction - ULiège [BE] (1)
University of Liège, GIGA-Research, Laboratory of Human Genetics, Liège, Belgium (1)
Main Referenced Disciplines
Genetics & genetic processes (44)
Hematology (22)
Oncology (11)
Surgery (3)
Immunology & infectious disease (2)

Publications (total 76)

The most downloaded
1421 downloads
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. https://hdl.handle.net/2268/100153

The most cited

109 citations (Scopus®)

Poppe, B., Vandesompele, J., Schoch, C., Lindvall, C., Mrozek, K., Bloomfield, C. D., Beverloo, H. B., Michaux, L., Dastugue, N., Herens, C., Yigit, N., De Paepe, A., Hagemeijer, A., & Speleman, F. (01 January 2004). Expression analyses identify MLL as a prominent target of 11q23 amplification and support an etiologic role for MLL gain of function in myeloid malignancies. Blood, 103 (1), 229-235. doi:10.1182/blood-2003-06-2163 https://hdl.handle.net/2268/84465

Poulet, C., Swingland, J. T., Botta, V., Robe, P., Herens, C., Turkheimer, F., & Bours, V. (2023). Assessment of the normal cell contamination impact on tumour samples analysed with SNP arrays: The signal confusion nightmare. ORBi-University of Liège. https://orbi.uliege.be/handle/2268/302224. doi:10.1101/2023.04.04.534870

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.

SOMJA, J., Bisig, B., de Leval, L., Bonnet, C., HERENS, C., & Siebert, R. (2014). Peripheral T-cell lymphoma with t(6;14)(p25;q11.2) translocation presenting with massive splenomegaly. Virchows Archiv. doi:10.1007/s00428-014-1560-3
Peer Reviewed verified by ORBi

Bonnet, C., MENTEN, C., LAMBERT, F., Gothot, A., Baron, F., CAERS, J., HERENS, C., & Beguin, Y. (25 January 2013). Simultaneous diagnosis of CLL and CML in a single patient with evidence for two different cell clones [Poster presentation]. BHS, General Annual Meeting.

Havelange, V., Ameye, G., Theate, I., Callet-Bauchu, E., Mugneret, F., Michaux, L., Dastugue, N., Penther, D., Barin, C., Collonge-Rame, M.-A., Baranger, L., Terre, C., Nadal, N., Lippert, E., Lai, J.-L., Cabrol, C., Tigaud, I., HERENS, C., Hagemeijer, A., ... Poirel, H. A. (2013). Patterns of genomic aberrations suggest that Burkitt lymphomas with complex karyotype are distinct from other aggressive B-cell lymphomas with MYC rearrangement. Genes, Chromosomes and Cancer, 52 (1), 81-92. doi:10.1002/gcc.22008
Peer Reviewed verified by ORBi

Duhoux, F. P., Ameye, G., Montano-Almendras, C. P., Bahloula, K., Mozziconacci, M. J., Laibe, S., Wlodarska, I., Michaux, L., Talmant, P., Richebourg, S., Lippert, E., Speleman, F., HERENS, C., Struski, S., Raynaud, S., Auger, N., Nadal, N., Rack, K., Mugneret, F., ... Poirel, H. A. (2012). PRDM16 (1p36) translocations define a distinct entity of myeloid malignancies with poor prognosis but may also occur in lymphoid malignancies. British Journal of Haematology, 156 (1), 76-88. doi:10.1111/j.1365-2141.2011.08918.x
Peer Reviewed verified by ORBi

Bisig, B., Thielen, C., HERENS, C., GOFFLOT, S., Travert, M., Delfau-Larue, M.-H., Boniver, J., Gaulard, P., & de Leval, L. (2012). c-Maf expression in angioimmunoblastic T-cell lymphoma reflects follicular helper T-cell derivation rather than oncogenesis. Histopathology, 60 (2), 371-376. doi:10.1111/j.1365-2559.2011.04022.x
Peer Reviewed verified by ORBi

Max, S., HERENS, C., Schaaf-Lafontaine, N., & GOTHOT, A. (2011). Intégration des informations phénotypiques et génétiques dans le diagnostic et le suivi du myélome. In Cytométrie 2011 (pp. 128-129).

Phan-Ba, R., Bisig, B., Deprez, M., DE PRIJCK, B., DELRUE, G., HERENS, C., Moonen, G., Belachew, S., & de Leval, L. (June 2011). Primary central nervous system lymphoma in a patient treated with Natalizumab. Annals of Neurology, 69 (6), 1060-1. doi:10.1002/ana.22296
Peer Reviewed verified by ORBi

Duhoux, F. P., Ameye, G., Lambot, V., HERENS, C., LAMBERT, F., Raynaud, S., Wlodarska, I., Michaux, L., Roche-Lestienne, C., Labis, E., Taviaux, S., Chapiro, E., Khac, F. N., Struski, S., Dobbelstein, S., Dastugue, N., Lippert, E., Speleman, F., Van Roy, N., ... Poirel, H. A. (2011). Refinement of 1p36 alterations not involving PRDM16 in myeloid and lymphoid malignancies. PLoS ONE, 6 (10), 26311. doi:10.1371/journal.pone.0026311
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

Poulet, C., Hennuy, B., Robe, P., Deprez, M., HERENS, C., & Bours, V. (01 November 2010). Subclassification of diffuse glioma tumours based on gene expression and allele copy number variation [Poster presentation]. 12th EUROPEAN WORKSHOP ON CYTOGENETICS AND MOLECULAR GENETICS OF SOLID TUMORS.

Josse, C., Schoemans, R., Niessen, N.-A., Delgaudine, M., Hellin, A.-C., Herens, C., Delvenne, P., & Bours, V. (August 2010). Systematic chromosomal aberrations found in murine bone marrow-derived mesenchymal stem cells. Stem Cells and Development, 19 (8), 1167-1173. doi:10.1089/scd.2009.0264
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

Willems, E.* , Baron, F.* , Baudoux, E., Wanten, N., Seidel, L., Vanbellinghen, J.-F., Herens, C., Gothot, A., Frere, P., Bonnet, C., Hafraoui, K., Vanstraelen, G., Fillet, G., & Beguin, Y. (2009). Non-myeloablative transplantation with CD8-depleted or unmanipulated peripheral blood stem cells: a phase II randomized trial. Leukemia, 23 (3), 608-10. doi:10.1038/leu.2008.248
Peer Reviewed verified by ORBi
* These authors have contributed equally to this work.

Gervais, C., Murati, A., Helias, C., Struski, S., Eischen, A., Lippert, E., Tigaud, I., Penther, D., Bastard, C., Mugneret, F., Poppe, B., Speleman, F., Talmant, P., VanDen Akker, J., Baranger, L., Barin, C., Luquet, I., Nadal, N., Nguyen-Khac, F., ... Lessard, M. (2008). Acute myeloid leukaemia with 8p11 (MYST3) rearrangement : an integrated cytologic, cytogenetic and molecular study by the groupe francophone de cytogénétique hématologique. Leukemia, 22 (8), 1567-1575. doi:10.1038/leu.2008.128
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Luquet, I., Laï, J. L., Barin, C., Baranger, L., Bilhou-Nabera, C., Lippert, E., Gervais, C., Talmant, P., Cornillet-Lefebvre, P., Perot, C., Nadal, N., Mozziconacci, M. J., Lafage-Pochitaloff, M., Eclache, V., Mugneret, F., Lefebvre, C., Herens, C., Speleman, F., Poirel, H., ... Terre, C. (2008). Hyperdiploid karyotypes in acute myeloid leukemia define a novel entity : a study of 38 patients from the Groupe Francophone de Cytogenetique Hematologique (GFCH). Leukemia, 22 (1), 132-137. doi:10.1038/sj.leu.2404974
Peer Reviewed verified by ORBi

Herens, C., Lambert, F., Quintanilla-Martinez, L., Bisig, B., Deusings, C., & De Leval, L. (2008). Cyclin D1-negative mantle cell lymphoma with cryptic t(12;14)(p13;q32) and cyclin D2 overexpression. Blood, 111 (3), 1745-6. doi:10.1182/blood-2007-10-120824
Peer Reviewed verified by ORBi

Castermans, E.* , Baron, F.* , Willems, E., Schaaf-Lafontaine, N., Meuris, N., Gothot, A., Vanbellinghen, J.-F., Herens, C., Seidel, L., Geenen, V., Cheynier, R., & Beguin, Y. (2008). Evidence for neo-generation of T cells by the thymus after non-myeloablative conditioning. Haematologica, 93 (2), 240-7. doi:10.3324/haematol.11708
Peer Reviewed verified by ORBi
* These authors have contributed equally to this work.

Oliva, E., de Leval, L., Soslow, R. A., & Herens, C. (August 2007). High frequency of JAZF1-JJAZ1 gene fusion in endometrial stromal tumors with smooth muscle differentiation by interphase FISH detection. American Journal of Surgical Pathology, 31 (8), 1277-1284. doi:10.1097/PAS.0b013e318031f012
Peer Reviewed verified by ORBi

Lambert, F., Heimann, P., Herens, C., Chariot, A., & Bours, V. (July 2007). Consultations in molecular diagnostics - A case of FIP1L1-PDGFRA-positive chronic eosinophilic leukemia with a rare FIP1L1 breakpoint. Journal of Molecular Diagnostics, 9 (3), 414-419. doi:10.2353/jmoldx.2007.060196
Peer Reviewed verified by ORBi

Thielen, C., Herens, C., Fassotte, M.-F., Detrooz, E., Drion, P., Diss, T., Boniver, J., & de Leval, L. (October 2006). Establishment and characterisation of two novel human KSHV- and EBV-negative Burkitt cell lines, GAL-01 and GAL-02, from a primary lymphomatous effusion. European Journal of Haematology, 77 (4), 318-326. doi:10.1111/j.1600-0609.2006.00724.x
Peer Reviewed verified by ORBi

Cauwelier, B., Dastugue, N., Cools, J., Poppe, B., Herens, C., De Paepe, A., Hagemeijer, A., & Speleman, F. (July 2006). Molecular cytogenetic study of 126 unselected T-ALL cases reveals high incidence of TCR beta locus rearrangements and putative new T-cell oncogenes. Leukemia, 20 (7), 1238-1244. doi:10.1038/sj.leu.2404243
Peer Reviewed verified by ORBi

de Leval, L., Harris, N. L., Lampertz, S., & Herens, C. (June 2006). T-cell/histiocyte-rich large B-cell lymphoma associated with a near-tetraploid karyotype and complex genetic abnormalities. APMIS: Acta Pathologica, Microbiologica, et Immunologica Scandinavica, 114 (6), 474-478. doi:10.1111/j.1600-0463.2006.apm_458.x
Peer Reviewed verified by ORBi

Jeandidier, E., Dastugue, N., Mugneret, F., Lafage-Pochitaloff, M., Mozziconacci, M. J., Herens, C., Michaux, L., Verellen-Dumoulin, C., Talmant, P., Cornillet-Lefebvre, P., Luquet, I., Charrin, C., Barin, C., Collonge-Rame, M. A., Perot, C., Van den Akker, J., Gregoire, M. J., Jonveaux, P., Baranger, L., ... Berger, R. (01 April 2006). Abnormalities of the long arm of chromosome 21 in 107 patients with hematopoietic disorders: a collaborative retrospective study of the Groupe Francais de Cytogenetique Hematologique. Cancer Genetics and Cytogenetics, 166 (1), 1-11. doi:10.1016/j.cancergencyto.2005.08.005
Peer Reviewed verified by ORBi

Turkheimer, F. E., Roncaroli, F., Hennuy, B., Herens, C., Nguyen Khac, M.-T., Martin, D., Evrard, A., Bours, V., Boniver, J., & Deprez, M. (2006). Chromosomal patterns of gene expression from microarray data: methodology, validation and clinical relevance in gliomas. BMC Bioinformatics, 7, 526. doi:10.1186/1471-2105-7-526
Peer Reviewed verified by ORBi

Herens, C., Ketelslegers, O., Tassin, F., Hansen, S., & Bours, V. (2006). Inositide-specific phospholipase c beta1 gene deletion is a rare event in myelodysplastic syndromes. Leukemia, 20 (3), 521-2; author reply 522-3. doi:10.1038/sj.leu.2404109
Peer Reviewed verified by ORBi

Poppe, B., De Paepe, P., Michaux, L., Dastugue, N., Bastard, C., Herens, C., Moreau, E., Cavazzini, F., Yigit, N., Van Limbergen, H., De Paepe, A., Praet, M., De Wolf-Peeters, C., Wlodarska, L., & Speleman, F. (October 2005). PAX5/IGH rearrangement is a recurrent finding in a subset of aggressive B-NHL with complex chromosomal rearrangements. Genes, Chromosomes and Cancer, 44 (2), 218-223. doi:10.1002/gcc.20214
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

Detry, O., De Roover, A., de Leval, L., Herens, C., Delwaide, J., Honore, P., & Meurisse, M. (June 2005). Transmission of an undiagnosed sarcoma to recipients of kidney and liver grafts procured in a non-heart beating donor. Liver Transplantation, 11 (6), 696-699. doi:10.1002/lt.20457
Peer Reviewed verified by ORBi

Pirottin, D., Grobet, L., Adamantidis, A., Farnir, F., Herens, C., Daa Schroder, H., & Georges, M. (2005). Transgenic engineering of male-specific muscular hypertrophy. Proceedings of the National Academy of Sciences of the United States of America, 102 (18), 6413-8. doi:10.1073/pnas.0502426102
Peer Reviewed verified by ORBi

Colige, A., Nuytinck, L., Hausser, I., van Essen, A. J., Thiry, M., Herens, C., Ades, L. C., Malfait, F., Paepe, A. D., Franck, P., Wolff, G., Oosterwijk, J. C., Smitt, J. H. S., Lapiere, C. M., & Nusgens, B. (2004). Novel types of mutation responsible for the dermatosparactic type of Ehlers-Danlos syndrome (Type VIIC) and common polymorphisms in the ADAMTS2 gene. Journal of Investigative Dermatology, 123 (4), 656-63. doi:10.1111/j.0022-202X.2004.23406.x
Peer Reviewed verified by ORBi

Poppe, B., Vandesompele, J., Schoch, C., Lindvall, C., Mrozek, K., Bloomfield, C. D., Beverloo, H. B., Michaux, L., Dastugue, N., Herens, C., Yigit, N., De Paepe, A., Hagemeijer, A., & Speleman, F. (01 January 2004). Expression analyses identify MLL as a prominent target of 11q23 amplification and support an etiologic role for MLL gain of function in myeloid malignancies. Blood, 103 (1), 229-235. doi:10.1182/blood-2003-06-2163
Peer Reviewed verified by ORBi

Herens, C., Radermecker, M., Servais, A.-M., Quatresooz, P., Jardon-Jeghers, C., Bours, V., & de Leval, L. (01 October 2003). Deletion (6)(p22p25) is a recurrent anomaly of thymoma: report of a second case and review of the literature. Cancer Genetics and Cytogenetics, 146 (1), 66-69. doi:10.1016/S0165-4608(03)00098-0
Peer Reviewed verified by ORBi

Rodriguez, L., Guardia, N. M., Herens, C., Jamar, M., Verloes, A., Lopez, F., Munoz, J. S., & Martinez-Frias, M. L. (01 October 2003). Subtle trisomy 12q24.3 and subtle monosomy 22q13.3: Three new cases and review [letter to the editor]. American Journal of Medical Genetics. Part A, 122A (2), 119-124. doi:10.1002/ajmg.a.20243
Peer Reviewed verified by ORBi

Berger, R., Dastugue, N., Busson, M., van den Akker, J., Perot, C., Ballerini, P., Hagemeijer, A., Michaux, L., Charrin, C., Pages, M. P., Mugneret, F., Andrieux, J., Talmant, P., Helias, C., Mauvieux, L., Lafage-Pochitaloff, M., Mozziconacci, M. J., Cornillet-Lefebvre, P., Radford, I., ... Bernard, O. A. (September 2003). t(5;14)/HOX11L2-positive T-cell acute lymphoblastic leukemia. A collaborative study of the Groupe Francais de Cytogenetique Hematologique (GFCH). Leukemia, 17 (9), 1851-1857. doi:10.1038/sj.leu.2403061
Peer Reviewed verified by ORBi

Defraigne, J.-O., Hermans, G., Dome, F., & Herens, C. (April 2003). Malignant solitary fibrous tumor of the pleura: report of a case with cytogenetic analysis. Virchows Archiv, 442 (4), 388-392. doi:10.1007/s00428-002-0754-2
Peer Reviewed verified by ORBi

Baron, F., Baudoux, E., Frere, P., Tourqui, S., Schaaf-Lafontaine, N., Herens, C., De Prijck, B., Fillet, G., & Beguin, Y. (2003). Low T-cell chimerism is not followed by graft rejection after nonmyeloablative stem cell transplantation (NMSCT) with CD34-selected PBSC. Bone Marrow Transplantation, 32 (8), 829-34. doi:10.1038/sj.bmt.1704220
Peer Reviewed verified by ORBi

Herens, C., Baron, F., Croisiau, C., Tassin, F., & Bours, V. (2003). Clonal chromosome aberrations in Philadelphia-negative cells from chronic myelocytic leukemia patients treated with imatinib mesylate: report of two cases. Cancer Genetics and Cytogenetics, 147 (1), 78-80. doi:10.1016/S0165-4608(03)00198-5
Peer Reviewed verified by ORBi

Detrembleur, N., Delbecque, K., Thiry, A., Boniver, J., Herens, C., & Delvenne, P. (November 2002). Le cas clinique du mois. Constipation et syndrome de masse abdominale chez une patiente de 51 ans. Revue Médicale de Liège, 57 (11), 688-91.
Peer reviewed

Baron, F., Frere, P., Herens, C., Fillet, G., & Beguin, Y. (2002). Combination of nonmyeloablative stem cell transplantation and Imatinib in accelerated phase CML. Haematologica, 87 (12), 43.
Peer Reviewed verified by ORBi

Baron, F., Baudoux, E., Frere, P., Tourqui, S., Schaaf-Lafontaine, N., Greimers, R., Herens, C., Fillet, G., & Beguin, Y. (2002). Nonmyeloablative stem cell transplantation with CD8-depleted or CD34-selected peripheral blood stem cells. Journal of Hematotherapy and Stem Cell Research, 11 (2), 301-14. doi:10.1089/152581602753658484
Peer Reviewed verified by ORBi

Herens, C., Thiry, A.-M., Dresse, M.-F., Born, J., Flagothier, C., Vanstraelen, G., Allington, N., & Bex, V. (May 2001). Translocation (16;17)(Q22;P13) Is a Recurrent Anomaly of Aneurysmal Bone Cysts. Cancer Genetics and Cytogenetics, 127 (1), 83-4. doi:10.1016/S0165-4608(00)00422-2
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

Verloes, A., Gillerot, Y., Van Maldergem, L., Schoos, R., Herens, C., Jamar, M., Dideberg, V., Lesenfants, S., & Koulischer, L. (January 2001). Major Decrease in the Incidence of Trisomy 21 at Birth in South Belgium: Mass Impact of Triple Test? European Journal of Human Genetics, 9 (1), 1-4. doi:10.1038/sj.ejhg.5200575
Peer Reviewed verified by ORBi

Scantamburlo, G., Lampertz, S., Jamar, M., Koulischer, L., & Herens, C. (September 2000). Inv(12)(Q15q24): A Nonrandom Change Associated with Myelodysplasia? Cancer Genetics and Cytogenetics, 121 (2), 206-7. doi:10.1016/S0165-4608(99)00172-7
Peer Reviewed verified by ORBi

Tassin, F., Dewé, W., Schaaf-Lafontaine, N., Herens, C., Ravoet, C., Albert, A., Beguin, Y., & Paulus, J.-M. (2000). A four-parameter index of marrow dysplasia has predictive value for survival in myelodysplastic syndromes. Leukemia and Lymphoma, 36 (5-6), 485-96. doi:10.3109/10428190009148396
Peer Reviewed verified by ORBi

Herens, C., Tassin, F., Lemaire, V., Beguin, Y., Collard, E., Lampertz, S., Croisiau, C., Desouter-Lecomte, M., DE PRIJCK, B., Longree, L., & Koulischer, L. (2000). Deletion of the 5'-ABL region: a recurrent anomaly detected by fluorescence in situ hybridization in about 10% of Philadelphia-positive chronic myeloid leukaemia patients. British Journal of Haematology, 110 (1), 214-6. doi:10.1046/j.1365-2141.2000.02142.x
Peer Reviewed verified by ORBi

Herens, C., Brasseur, E., Jamar, M., Vierset, L., Schoenen, I., & Koulischer, L. (February 1999). Loss of the Y Chromosome in Bone Marrow Cells: Results on 1907 Consecutive Cases of Leukaemia and Preleukaemia. Clinical and Laboratory Haematology, 21 (1), 17-20. doi:10.1046/j.1365-2257.1999.00173.x
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

Verloes, A., Curry, C., Jamar, M., Herens, C., O'Lague, P., Marks, J., Sarda, P., & Blanchet, P. (November 1998). Juvenile Rheumatoid Arthritis and Del(22q11) Syndrome: A Non-Random Association. Journal of Medical Genetics, 35 (11), 943-7. doi:10.1136/jmg.35.11.943
Peer Reviewed verified by ORBi

Tassin, F., Hermanne, J.-P., Schaaf-Lafontaine, N., Herens, C., Thiry, A., Paulus, J.-M., Boniver, J., & Fillet, G. (June 1998). Les syndromes myélodysplasiques: syndromes préleucémiques. Revue Médicale de Liège, 53 (6), 357-62.
Peer reviewed

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

Koulischer, L., Verloes, A., Lesenfants, S., Jamar, M., & Herens, C. (September 1997). Genetic Risk in Natural and Medically Assisted Procreation. Early Pregnancy: Biology and Medicine, 3 (3), 164-71.
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.

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

Herens, C., Massart, S., Bouzahzah, B., Koulischer, L., & Barbason, H. (July 1995). Nuclear Lesions During Rat Hepatocarcinogenesis. II. Measuring the Micronuclei During Initiation, Promotion and Progression of Rat Hepatocarcinogenesis Induced with Diethylnitrosamine. Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 329 (2), 161-71. doi:10.1016/0027-5107(95)00025-E
Peer Reviewed verified by ORBi

Herens, C., Jacquemart, M., Koulischer, L., & Barbason, H. (July 1995). Nuclear Lesions During Rat Hepatocarcinogenesis. I. Measuring the Sister-Chromatid Exchanges During Initiation, Promotion and Progression of Rat Hepatocarcinogenesis Induced with Diethylnitrosamine. Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 329 (2), 153-9. doi:10.1016/0027-5107(95)00024-D
Peer Reviewed verified by ORBi

Verloes, A., Schoos, R., Herens, C., Vintens, A., & Koulischer, L. (January 1995). A Prenatal Trisomy 21 Screening Program Using Alpha-Fetoprotein, Human Chorionic Gonadotropin, and Free Estriol Assays on Maternal Dried Blood. American Journal of Obstetrics and Gynecology, 172 (1, Pt 1), 167-74. doi:10.1016/0002-9378(95)90108-6
Peer Reviewed verified by ORBi

Barbason, H., Herens, C., Robaye, B., Milis, G., Sulon, J., Bouzahzah, B., & Van Cantfort, J. (1995). Importance of Cell Kinetics Rhythmicity for the Control of Cell Proliferation and Carcinogenesis in Rat Liver (Review). In Vivo, 9 (6, Nov-Dec), 539-48.
Peer reviewed

Hustinx, R., Verloes, A., Grattagliano, B., Herens, C., Jamar, M., Soyeur, D., Schaaps, J.-P., & Koulischer, L. (01 September 1993). Monosomy 11q: Report of Two Familial Cases and Review of the Literature. American Journal of Medical Genetics, 47 (3), 312-7. doi:10.1002/ajmg.1320470303
Peer Reviewed verified by ORBi

Herens, C., Alvarez Gonzalez, M.-L., & Barbason, H. (May 1992). Cytogenetic Changes in Hepatocarcinomas from Rats Treated with Chronic Exposure to Diethylnitrosamine. Cancer Genetics and Cytogenetics, 60 (1), 45-52. doi:10.1016/0165-4608(92)90232-W
Peer Reviewed verified by ORBi

Lapiere, J. C., Verloes, A., Herens, C., Delfortrie, J., Van Maldergem, L., Gillerot, Y., & Koulischer, L. (1992). Combined 10pter-->P11 and 18pter-->Q11 Trisomy in a 7-Year-Old Child. Genetic Counseling, 3 (3), 155-9.
Peer Reviewed verified by ORBi

Koulischer, L., Schoos, R., Verloes, A., & Herens, C. (December 1991). Le dépistage prénatal de la trisomie 21 sur sérum maternel. Mise au point. Revue Médicale de Liège, 46 (12), 625-32.
Peer reviewed

Verloes, A., Schaaps, J.-P., Herens, C., Soyeur, D., Hustin, J., & Dodinval, P. (February 1991). Prenatal Diagnosis of Cystic Hygroma and Chorioangioma in the Wolf-Hirschhorn Syndrome. Prenatal Diagnosis, 11 (2), 129-32. doi:10.1002/pd.1970110209
Peer Reviewed verified by ORBi

Verloes, A., Seret, N., Bernier, V., Gonzales, M., Herens, C., & Koulischer, L. (1991). Branchial Arch Anomalies in Trisomy 18. Annales de Génétique, 34 (1), 22-4.
Peer Reviewed verified by ORBi

Herens, C., Verloes, A., Laloux, F., & Van Maldergem, L. (May 1990). Trisomy 20q. A New Case and Further Phenotypic Delineation. Clinical Genetics, 37 (5), 363-6. doi:10.1111/j.1399-0004.1990.tb03520.x
Peer Reviewed verified by ORBi

Herens, C., Pierquin, G., Verloes, A., Schaaps, J.-P., & Frederic, J. (May 1989). Mosaicism of 46,Xx/47,Xx,+9/47,Xx,+?Mar in the Same Amniotic Fluid with Apparent Loss of One Cell Line after Delivery. Prenatal Diagnosis, 9 (5), 373-5. doi:10.1002/pd.1970090513
Peer Reviewed verified by ORBi

Barbason, H., Bouzahzah, B., Herens, C., Marchandise, J., Sulon, J., & Van Cantfort, J. (1989). Circadian Synchronization of Liver Regeneration in Adult Rats: The Role Played by Adrenal Hormones. Cell and Tissue Kinetics, 22 (6), 451-460. doi:10.1111/j.1365-2184.1989.tb00228.x
Peer Reviewed verified by ORBi

Verloes, A., Herens, C., Van Maldergem, L., Retz, M. C., & Dodinval, P. (1989). Roberts-Sc Phocomelia Syndrome with Exencephaly. Annales de Génétique, 32 (3), 169-70.
Peer Reviewed verified by ORBi

Pierquin, G., Herens, C., Dodinval, P., Frederic, J., Weber, I., Senterre, J., & Fryns, J. P. (May 1988). Partial Trisomy 20q Due to Paternal T(8;20) Translocation. Case Report and Review of the Literature. Clinical Genetics, 33 (5), 386-9. doi:10.1111/j.1399-0004.1988.tb03466.x
Peer Reviewed verified by ORBi

Cloes, J.-M., Herens, C., Nys, M., Calberg-Bacq, C. M., François, C., & Rentier, B. (1988). Production of heterobispecific monoclonal antibodies by mouse hybrid hybridomas (quadromas). Archives Internationales de Physiologie et de Biochimie, 96, 143.

Verloes, A., Herens, C., Lambotte, C., & Frederic, J. (1987). Chromosome 22 Mosaic Monosomy (46,Xy/45,Xy,-22). Annales de Génétique, 30 (3), 178-9.
Peer Reviewed verified by ORBi

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