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Koulischer Lucien

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Main Referenced Co-authors
Verloes, Alain  (19)
Herens, Christian  (16)
Jamar, Mauricette  (5)
Jamar, Michelle  (5)
Lesenfants, S. (4)
Main Referenced Keywords
Humans (8); Female (7); Male (7); Aged (4); Middle Aged (3);
Main Referenced Disciplines
Genetics & genetic processes (16)
Endocrinology, metabolism & nutrition (6)
Hematology (4)
Pediatrics (2)
Surgery (2)

Publications (total 31)

The most downloaded
390 downloads
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 https://hdl.handle.net/2268/10055

The most cited

182 citations (Scopus®)

VERLOES, A., SakalihasanN, N., Koulischer, L., & Limet, R. (1995). Aneurysms of the abdominal aorta: familial and genetic aspects in three hundred thirteen pedigrees. Journal of Vascular Surgery, 21 (4), 646-55. doi:10.1016/S0741-5214(95)70196-6 https://hdl.handle.net/2268/109710

Mutesa, L., Azad, A. K., Verhaeghe, C., Segers, K., Vanbellinghen, J.-F., Ngendahayo, L., Rusingiza, E. K., Mutwa, P. R., Rulisa, S., Koulischer, L., Cassiman, J.-J., Cuppens, H., & Bours, V. (2009). Genetic Analysis of Rwandan Patients With Cystic Fibrosis-Like Symptoms: Identification of Novel Cystic Fibrosis Transmembrane Conductance Regulator and Epithelial Sodium Channel Gene Variants. CHEST, 135 (5), 1233-42. doi:10.1378/chest.08-2246
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., 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

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

Poncin, J., Abs, R., Velkeniers, B., Bonduelle, M., Abramowicz, M., Legros, J.-J., Verloes, A., Meurisse, M., Van Gaal, L., Verellen, C., Koulischer, L., & Beckers, A. (1999). Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases. Human Mutation, 13 (1), 54-60. doi:10.1002/(SICI)1098-1004(1999)13:1<54::AID-HUMU6>3.0.CO;2-K
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

Schoos, R., Verloes, A., Bourguignon, J.-P., & Koulischer, L. (May 1998). Les programmes de dépistage systématique en néonatologie. Aspects pharmaco-économiques. Revue Médicale de Liège, 53 (5), 311-5.
Peer reviewed

Poncin, J., Abs, R., Velkeniers, B., Bonduelle, M., Abramowicz, M., Legros, J.-J., Verloes, A., Meurisse, M., Van Gaal, L., Koulischer, L., & Beckers, A. (1998). Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type I and related diseases. In 5th Euroregional Oncology meeting - abstract book.

Ectors, F., & Koulischer, L. (1998). La méiose chez la femelle de mammifère. In P. Popescu, H. Hayes, ... B. Dutrillaux (Eds.), Techniques de cytogénétique animale (pp. 109-114). Paris, France: INRA Editions.
Peer reviewed

Poncin, J., Abs, R., Velkeniers, B., Bonduelle, M., Abramowicz, M., Legros, J.-J., Verloes, A., Van gaal, L., Koulischer, L., & Beckers, A. (1998). Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type I and related diseases. In IV european Congress of Endocrinology - Abstract book.

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

Verloes, A., Lesenfants, S., Misson, J.-P., Galand, A., & Koulischer, L. (10 February 1997). Microcephaly, muscular build, rhizomelia, and cataracts: Description of a possible recessive syndrome and some comments on the use of electronic databases in syndromology. American Journal of Medical Genetics, 68 (4), 455-60, discussion 461. doi:10.1002/(SICI)1096-8628(19970211)68:4<455::AID-AJMG16>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.

Verloes, A., Jamblin, P., Koulischer, L., & Bourguignon, J.-P. (January 1996). A new form of skeletal dysplasia with amelogenesis imperfecta and platyspondyly. Clinical Genetics, 49 (1), 2-5. doi:10.1111/j.1399-0004.1996.tb04315.x
Peer Reviewed verified by ORBi

VERLOES, A., Sakalihasan, N., Limet, R., & Koulischer, L. (1996). Genetic aspects of abdominal aortic aneurysm. Annals of the New York Academy of Sciences, 800, 44-55. doi:10.1111/j.1749-6632.1996.tb33297.x
Peer Reviewed verified by ORBi

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

VERLOES, A., SakalihasanN, N., Koulischer, L., & Limet, R. (1995). Aneurysms of the abdominal aorta: familial and genetic aspects in three hundred thirteen pedigrees. Journal of Vascular Surgery, 21 (4), 646-55. doi:10.1016/S0741-5214(95)70196-6
Peer Reviewed verified by ORBi

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

Koulischer, L., & Bassleer, R. (March 1993). La cytogénétique humaine est née il y a 80 ans à Liège (de Winiwarter, 1912). Revue Médicale de Liège, 48 (3), 129-36.

Verloes, A., Bonneau, D., Guidi, O., Berthier, M., Oriot, D., Van Maldergem, L., & Koulischer, L. (February 1993). Brachymorphism-Onychodysplasia-Dysphalangism Syndrome. Journal of Medical Genetics, 30 (2), 158-61. doi:10.1136/jmg.30.2.158
Peer Reviewed verified by ORBi

Verloes, A., Gillerot, Y., Walczak, E., Van Maldergem, L., & Koulischer, L. (15 January 1992). Acromelic Frontonasal "Dysplasia": Further Delineation of a Subtype with Brain Malformation and Polydactyly (Toriello Syndrome). American Journal of Medical Genetics, 42 (2), 180-3. doi:10.1002/ajmg.1320420209
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., 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

Demoulin, A., Verstraelen-Proyard, J., Bourguignon, J.-P., Hustin, J., Koulischer, L., Bologne, R., & Franchimont, P. (1980). ORIGINE ET SITES D'ACTION DE L'INHIBINE. Annales d'Endocrinologie, 41 (4), 291-302.
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