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J.J. Cassiman

Observed names: J J Cassiman, J. -J. Cassiman, J. J. CASSIMAN, J. J. Cassiman, J.-J. Cassiman, J.J. CASSIMAN, JEAN‐JACQUES CASSIMAN, Jean-Jacques Cassiman, Jean‐Jacques Cassiman
Institution: KU Leuven
OpenAlex ID: A5111475730
Histiocyte-Rich B-Cell Lymphoma
1992 · J. Delabie, E. Vandenberghe, et al. · The American Journal of Surgical Pathology · 145
D90A heterozygosity in the SOD1 gene is associated with familial and apparently sporadic amyotrophic lateral sclerosis
1996 · W. Robberecht, T. Aguirre, et al. · Neurology · 131
In Vitro Cultivation of Human Tumor Tissues II. Morphological and Virological Characterization of Three Cell Lines
2009 · H. Heremans, A. Billiau, et al. · Oncology · 109
Mantle cell lymphoma: a clinicopathological study of 55 cases
1995 · S. PITTALUGA, I. WLODARSKA, et al. · Histopathology · 100
Primary role of the HLA class II DRB1*0301 allele in graves disease
2000 · Mahdi Zamani, Marijke Spaepen, et al. · American Journal of Medical Genetics · 88
Philadelphia chromosome-positive acute myeloid leukemia: cytoimmunologic and cytogenetic features.
1996 · A Cuneo, A Ferrant, et al. · PubMed · 83
Genes that determine immunology and inflammation modify the basic defect of impaired ion conductance in cystic fibrosis epithelia
2010 · Frauke Stanke, Tim Becker, et al. · Journal of Medical Genetics · 78
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Demonstration of the genuine iso-12p character of the standard marker chromosome of testicular germ cell tumors and identification of further chromosome 12 aberrations by competitive in situ hybridization.
1991 · R F Suijkerbuijk, A Y van de Veen, et al. · Europe PMC (PubMed Central) · 67
Myelodysplastic syndromes with bone marrow fibrosis: a myelodysplastic disorder with proliferative features
1991 · G. E. G. Verhoef, C. De Wolf-Peeters, et al. · Annals of Hematology · 65
Non‐radioactive in situ hybridization for the detection and monitoring of trisomy 12 in B‐cell chronic lymphocytic leukaemia
1992 · A. Cuneo, I. Wlodarska, et al. · British Journal of Haematology · 61
Mutation analysis in adenylosuccinate lyase deficiency: Eight novel mutations in the re-evaluated full ADSL coding sequence
1999 · Sandrine Marie, Harry Cuppens, et al. · Human Mutation · 52
BCL6 gene rearrangements also occur in marginal zone B‐cell lymphoma
1997 · JUDITH DIERLAMM, STEFANIA PITTALUGA, et al. · British Journal of Haematology · 49
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Incorporation of dITP or 7-deaza dGTP during PCR improves sequencing of the product
1993 · Herman Dierick, Michel Stul, et al. · Nucleic Acids Research · 46
Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome.
1997 · K Devriendt, P Petit, et al. · Journal of Medical Genetics · 38
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Importance of HLA-DRB1 and DQA1 genes and of the amino acid polymorphisms in the functional domain of DRβ1 chain in multiple sclerosis
1995 · M.Zamani Ghabanbasani, X.x. Gu, et al. · Journal of Neuroimmunology · 34
Cytogenetic and clinicobiological features of acute leukemia with stem cell phenotype: Study of nine cases
1996 · Antonio Cuneo, Augustine Ferrant, et al. · Cancer Genetics and Cytogenetics · 30
Differential splicing of COL4A5 mRNA in kidney and white blood cells: A complex mutation in the COL4A5 gene of an Alport patient deletes the NC1 domain
1993 · Caiying Guo, Boudewijn Van Damme, et al. · Kidney International · 30
Trisomy 3 is a consistent chromosome change in malignant lymphoproliferative disorders preceded by cold agglutinin disease
1995 · L. Michaux, J. Dierlamm, et al. · British Journal of Haematology · 29
Y-chromosomal STR haplotypes in three major population groups in Bulgaria
2001 · Boriana Zaharova, Silvia Andonova, et al. · Forensic Science International · 28
HLA and T-cell receptor polymorphisms in Belgian multiple sclerosis patients: No evidence for disease association with the T-cell receptor
1994 · C. Vandevyver, I. Buyse, et al. · Journal of Neuroimmunology · 26
Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3–p22.2 (MRX49) and Xp11.3–p11.21 (MRX50)
1997 · S. Claes, A. Vogels, et al. · American Journal of Medical Genetics · 25
Functional interaction between TRP4 and CFTR in mouse aorta endothelial cells
2001 · Lin Wei, Marc Freichel, et al. · BMC Physiology · 23
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Family Planning Decisions after the Birth of a Cystic Fibrosis Child: The Impact of Prenatal Diagnosis
1988 · G. Evers-Kiebooms, L. Denayer, et al. · Scandinavian Journal of Gastroenterology · 23
Trisomy 12p due to familial t(12p-,6q+) translocation
1974 · J.P. Fryns, H. Berghe, et al. · Human Genetics · 23
Tertiary partial 14 trisomy 47, XX, +14q-
1974 · J. P. Fryns, J. J. Cassiman, et al. · Human Genetics · 23
Works count: 70
Citation count: 1,758
H-index: 23
I10-index: 43
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