PubRank

H Van Den Berghe

Author PubWeight™ 69.61‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Cytogenetic evidence of clonality in cutaneous benign fibrous histiocytomas: a report of the CHAMP study group. Histopathology 2000 3.05
2 Primary amines inhibit recycling of alpha 2M receptors in fibroblasts. Cell 1980 2.40
3 Philadelphia chromosome-positive chronic myelogenous leukemia in treated Hodgkin's disease. Cancer Genet Cytogenet 1990 1.45
4 Demonstration of an alpha2-macroglobulin receptor in human fibroblasts, absent in tumor-derived cell lines. J Biol Chem 1979 1.45
5 Stimulation of fibroblast growth factor receptor-1 occupancy and signaling by cell surface-associated syndecans and glypican. J Cell Biol 1996 1.35
6 Isochromosome 17q in blast crisis of chronic myeloid leukemia and in other hematologic malignancies is the result of clustered breakpoints in 17p11 and is not associated with coding TP53 mutations. Blood 1999 1.32
7 [Association of an anatomo-pathological syndrome of male pseudohermaphroditism, Wilms' tumor, parenchymatous nephropathy and XX/XY mosaicism]. Arch Fr Pediatr 1967 1.16
8 HMGI-C and HMGI(Y) immunoreactivity correlates with cytogenetic abnormalities in lipomas, pulmonary chondroid hamartomas, endometrial polyps, and uterine leiomyomas and is compatible with rearrangement of the HMGI-C and HMGI(Y) genes. Lab Invest 2000 1.14
9 A new characteristic karyotypic anomaly in lymphoproliferative disorders. Cancer 1979 1.13
10 Study of the synthesis and secretion of normal and artificial mutants of murine amyloid precursor protein (APP): cleavage of APP occurs in a late compartment of the default secretion pathway. J Cell Biol 1993 1.12
11 Cytogenetic, clinical, and morphologic correlations in 78 cases of fibromatosis: a report from the CHAMP Study Group. CHromosomes And Morphology. Mod Pathol 2000 1.08
12 The IL-9 receptor gene, located in the Xq/Yq pseudoautosomal region, has an autosomal origin, escapes X inactivation and is expressed from the Y. Hum Mol Genet 1997 1.08
13 Partial trisomy 14q due to familial t(14q-,11q+) translocation. Hum Genet 1977 1.07
14 A new hematologic syndrome with a distinct karyotype: the 5 q--chromosome. Blood 1975 1.05
15 Transformed mouse mammary epithelial cells synthesize undersulfated basement membrane proteoglycan. J Biol Chem 1983 1.02
16 Trisomy 17-18 and trisomy 13-15 in the African child. J Trop Med Hyg 1968 0.98
17 Interstitial deletion of the short arm of chromosome 2 in a moderately mentally retarded boy without gross clinical stigmata. Hum Genet 1979 0.97
18 Secondary chromosome changes in mantle cell lymphoma. Haematologica 1999 0.97
19 Cultured human fibroblasts contain a large pool of precursor beta 1-integrin but lack an intracellular pool of mature subunit. Eur J Biochem 1991 0.96
20 Rieger syndrome and interstitial 4q26 deletion. Genet Couns 1992 0.93
21 Endometrial stromal sarcoma t(7;17)(p15-21;q12-21) is a nonrandom chromosome change. Cancer Genet Cytogenet 1992 0.93
22 Genomic instability and recurrent breakpoints are main cytogenetic findings in Hodgkin's disease. Haematologica 1999 0.92
23 X-linked mental retardation with Marfanoid habitus: a changing phenotype with age? Genet Couns 1991 0.90
24 The clinical significance of karyotype in acute myelogenous leukemia. Cancer Genet Cytogenet 1989 0.90
25 Differences in the distribution and nature of the interstitial telomeric (TTAGGG)n sequences in the chromosomes of the Giraffidae, okapai (Okapia johnstoni), and giraffe (Giraffa camelopardalis): evidence for ancestral telomeres at the okapi polymorphic rob(5;26) fusion site. Cytogenet Cell Genet 1996 0.89
26 Comparative cytogenetic study of spindle cell and pleomorphic leiomyosarcomas of soft tissues: a report from the CHAMP Study Group. Cancer Genet Cytogenet 2000 0.88
27 Six-year follow-up of the clinical significance of karyotype in acute lymphoblastic leukemia. Cancer Genet Cytogenet 1989 0.87
28 Cytogenetic and clinical investigations in 76 cases with therapy-related leukemia and myelodysplastic syndrome. Cancer Genet Cytogenet 1989 0.87
29 Genetic abnormalities in marginal zone B-cell lymphoma. Hematol Oncol 2000 0.87
30 Partial distal 12q trisomy. Ann Genet 1980 0.87
31 Philadelphia chromosome in human multiple myeloma. J Natl Cancer Inst 1979 0.87
32 Cytogenetic investigation of a case of congenital fibrosarcoma. Cancer Genet Cytogenet 1989 0.86
33 On the excess of mental retardation and/or congenital malformations in apparently balanced reciprocal translocations. A critical review of the Leuven data 1966-1991. Genet Couns 1991 0.86
34 Marginal zone B-cell lymphomas including mucosa-associated lymphoid tissue type lymphoma (MALT), monocytoid B-cell lymphoma and splenic marginal zone cell lymphoma and their relation to the reactive marginal zone. Leuk Lymphoma 1997 0.85
35 Translocation (15;17)(q22;q21) in a patient with Klinefelter syndrome. Cancer Genet Cytogenet 1996 0.85
36 XY/XXY mosaicism and fragile X syndrome. Ann Genet 1983 0.85
37 Clinical-cytogenetic correlations in myelodysplasia (preleukemia). Cancer Genet Cytogenet 1989 0.84
38 Brief clinical report: the Dubowitz syndrome in a teenager. Am J Med Genet 1979 0.84
39 Cytogenetic and immunohistochemical evidence that giant cell fibroblastoma is related to dermatofibrosarcoma protuberans. Genes Chromosomes Cancer 1996 0.84
40 Increased head circumference and facial cleft as presenting signs of the nevoid basal-cell carcinoma syndrome. Genet Couns 1991 0.84
41 Ring chromosome 15: follow-up data on physical and psychological development. Genet Couns 1990 0.83
42 Chromosome changes in a case of hibernoma. Genes Chromosomes Cancer 1992 0.83
43 Triploid-diploid mosaïcism in a deeply mentally retarded adult. Ann Genet 1980 0.82
44 Partial distal 1q trisomy. A distinct clinical dysmorphic syndrome in adulthood. Ann Genet 1980 0.82
45 Dicentric (1;15) in myeloid disorders. Cancer Genet Cytogenet 1996 0.82
46 The foetal alcohol syndrome. Acta Paediatr Belg 1977 0.82
47 Exchanging the extracellular domain of amyloid precursor protein for horseradish peroxidase does not interfere with alpha-secretase cleavage of the beta-amyloid region, but randomizes secretion in Madin-Darby canine kidney cells. J Biol Chem 1995 0.81
48 Solitary fibrous tumour of the pleura with t(4;15)(q13;q26) Histopathology 1999 0.81
49 Chromosome abnormalities in acute promyelocytic leukemia (APL). Cancer 1979 0.81
50 Transmission of ring chromosome 18 46,XX/46,XX,r(18) mosaicism in a mother and ring chromosome 18 syndrome in her son. Ann Genet 1992 0.81
51 Partners of Huntington patients: implications of the disease and opinions about predictive testing and prenatal diagnosis. Genet Couns 1990 0.80
52 BCL-6 expression in reactive lymphoid tissue and in B-cell non-Hodgkin's lymphomas. J Pathol 1996 0.80
53 Anterior basal encephalocele in the median cleft face syndrome. Comments on nosology and treatment. Genet Couns 1990 0.80
54 The 6p21 chromosome region is nonrandomly involved in endometrial polyps. Gynecol Oncol 1992 0.79
55 Ring chromosome 6 as the only change in a thymoma. Genes Chromosomes Cancer 1993 0.79
56 High incidence of mental retardation in Turner syndrome patients with ring chromosome X formation. Genet Couns 1990 0.79
57 BCL3 rearrangement and t(14;19)(q32;q13) in lymphoproliferative disorders. Genes Chromosomes Cancer 1996 0.79
58 Morphological characteristics of epithelial and fibroblastic cells growing out from biopsies of human skin. J Invest Dermatol 1980 0.79
59 Langer type of mesomelic dwarfism as the possible homozygous expression of dyschondrosteosis. Hum Genet 1979 0.79
60 Involvement of 19q13 in follicular thyroid adenoma. Cancer Genet Cytogenet 1992 0.78
61 Differences in agglutinability of adult and fetal human fibroblasts using phytohemagglutinin. Cell Differ 1977 0.78
62 Is the chromosome band 1p36 another hot-spot for rearrangements in uterine leiomyoma? Genes Chromosomes Cancer 1990 0.78
63 "Jumping" translocation of 9q in a case of follicular lymphoma. Cancer Genet Cytogenet 1994 0.78
64 "Adult" form of polycystic kidney disease in neonates. Clin Genet 1979 0.78
65 i(12p) in a malignant ovarian tumor. Cancer Genet Cytogenet 1990 0.78
66 Application of crossed immunoelectrophoresis to the visualization and characterization of human fibroblast antigens. Cell Mol Biol Incl Cyto Enzymol 1981 0.77
67 A physical map of the region spanning the chromosome 12 translocation breakpoint in a mesothelioma with a t(X;12)(q22;p13). Cytogenet Cell Genet 1995 0.77
68 Chromosomes and causation of human cancer and leukemia: XXXI. Dq- deletions and their significance in proliferative disorders. Cancer 1979 0.77
69 A new cytogenetic subgroup in tenosynovial giant cell tumors (nodular tenosynovitis) is characterized by involvement of 16q24. Cancer Genet Cytogenet 1996 0.76
70 Trisomy 12p due to familial t(12p-,6q plus) translocation. Humangenetik 1974 0.76
71 Psychological profile and behavioural characteristics in 12 patients with Prader-Willi syndrome. Genet Couns 1990 0.76
72 Aspects of the neoplasms observed in patients with constitutional autosomal trisomy. Cancer Genet Cytogenet 1996 0.75
73 Aggregation-induced alterations in fibroblast morphology. An ultrastructural study. Cell Tissue Res 1976 0.75
74 A variant translocation t(2;18) in follicular lymphoma involves the 5' end of bcl-2 and Ig kappa light chain gene. Oncogene 1991 0.75
75 Unknown syndrome: nasal hypoplasia, sparse hair, truncal obesity, genital hypoplasia, and severe mental retardation. J Med Genet 1992 0.75
76 Computer-assisted karyotyping with human interaction. J Histochem Cytochem 1977 0.75
77 Isolated peripheral thrombocytopenia as presenting symptom in preleukemia: a report of two cases with 11q+. Cancer Genet Cytogenet 1982 0.75
78 Clinicopathological evolution and multilineage involvement in erythroleukemia: report of a case. Haematologica 1992 0.75
79 [XXXX syndrome. Apropos of a further case observed since birth]. Union Med Can 1975 0.75
80 Twin pregnancies after medically assisted reproduction: epidemiology, comparative perinatal morbidity and mortality. J Perinat Med 1991 0.75
81 Partial monosomy of the long arm of chromosome 16: a distinct clinical entity? Hum Genet 1979 0.75
82 5q- anomaly in lymphoid disorders. Leukemia 1990 0.75
83 Modulation of the effect of colchicine and cytochalasin B on fibroblast aggregates by the substratum. J Cell Sci 1978 0.75
84 [Simultaneous study of karyotype and bone marrow histology in chronic myeloid leukemia with Ph1 chromsome. (author's transl)]. Nouv Rev Fr Hematol 1976 0.75
85 Hyperdiploidy in benign breast lesions. Cancer Genet Cytogenet 1998 0.75
86 Zygosity determination at birth: a plea to the obstetrician. J Perinat Med 1991 0.75
87 Design of a special interpreter for the classification of human chromosomes. IEEE Trans Pattern Anal Mach Intell 1979 0.75
88 5q- anomaly in a patient with disseminated teratoma. Cancer Genet Cytogenet 1983 0.75
89 [Refractory anemia and chromosome 5 q -: a new syndrome]. Bull Mem Acad R Med Belg 1975 0.75
90 Primary parauterine leiomyoma with a t(6;14) Genes Chromosomes Cancer 1999 0.75
91 The 5q- and additional chromosome anomalies in two patients with acute myeloid leukemia. Ann Genet 1979 0.75
92 Hypomelanosis of Ito and severe sensorineural deafness. Genet Couns 1992 0.75
93 The Wolf-Hirschhorn syndrome. Deletion of the short arm of chromosome 4. Acta Paediatr Belg 1979 0.75
94 Anomalous alpha 2-macroglobulin-protease complexes in cystic fibrosis: decreased uptake of the complexes by fibroblasts in culture. Pediatr Res 1979 0.75
95 The otopalatodigital syndrome. Acta Paediatr Belg 1978 0.75
96 Mosaic 46, XY/47,XY, + der(18)t(Y;18)(q11.22;q11.2) karyotype, moderate mental retardation and non-specific dysmorphism. Genet Couns 1990 0.75
97 A patient with Langer type of mesomelic dwarfism. Acta Paediatr Belg 1977 0.75
98 Cytogenetic characterization of three cases of unusual B-cell non-Hodgkin's lymphoma. Cancer Genet Cytogenet 1991 0.75
99 Chromosomes in plasma-cell malignancies. Eur J Haematol Suppl 1989 0.75
100 OKT8-positive T-cell lymphoma associated with a chromosome rearrangement t(2;17) possibly involving the T8 locus. N Engl J Med 1985 0.75
101 Involvement of 6p in an endometrial polyp. Cancer Genet Cytogenet 1991 0.75
102 Cytogenetic and molecular studies of the Philadelphia translocation in myelodysplastic syndromes. Report of two cases and review of the literature. Cancer Genet Cytogenet 1992 0.75
103 Cytogenetic studies in T-cell malignancies. Cancer Genet Cytogenet 1988 0.75
104 del(1)(q12) in adenocarcinomas of the prostate. Cancer Genet Cytogenet 1996 0.75
105 On the recurrence risk of 18 trisomy. Ann Genet 1991 0.75
106 Molecular cytogenetic analysis discloses complex genetic imbalance in a t(11;21) myelodysplastic syndrome. Cancer Genet Cytogenet 1990 0.75
107 Atypical chromosome abnormalities in a renal oncocytoma. Cancer Genet Cytogenet 1999 0.75
108 Fluorescence in situ hybridization for the detection and monitoring of the Ph-positive clone in chronic myelogenous leukemia: comparison with metaphase banding analysis. Leukemia 1998 0.75
109 Involvement of chromosomes 1 and 18 in renal cell tumors. Cancer Genet Cytogenet 2000 0.75
110 [Comparative study on the value of exfoliative vaginal cytology in determination of the radiosensitivity of cancer of the cervix]. Arch Anat Pathol (Paris) 1967 0.75
111 New chromosomal syndromes. I. Partial trisomy of the distal portion of the long arm of chromosome number 10 (10q24 leads to 10qter): a clinical entity. Acta Paediatr Belg 1979 0.75
112 Isodicentric (X)(q13): a new characteristic chromosomal anomaly in myeloproliferative syndrome? Cancer Genet Cytogenet 1982 0.75
113 Translocation t(8;16)(p11;p13) in acute non-lymphocytic leukemia: report on two new cases and review of the literature. Leuk Lymphoma 1996 0.75
114 Osteodysplasty a rare skeletal dysplasia. Acta Paediatr Belg 1979 0.75
115 Martin-Bell phenotype in males with acquired central nervous system lesions. 15 males diagnosed during a systematic etiological study of 274 mentally retarded males. Genet Couns 1990 0.75
116 Penile enlargement in tetrasomy 18p: an additional feature? Ann Genet 1990 0.75