PubRank

A Geurts van Kessel

Author PubWeight™ 90.21‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Translocation of c-ab1 oncogene correlates with the presence of a Philadelphia chromosome in chronic myelocytic leukaemia. Nature 1984 3.24
2 CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene. J Med Genet 2005 3.03
3 The human thyroglobulin gene: a polymorphic marker localized distal to C-MYC on chromosome 8 band q24. Hum Genet 1985 1.82
4 Translocation (12;22) (p13;q11) in myeloproliferative disorders results in fusion of the ETS-like TEL gene on 12p13 to the MN1 gene on 22q11. Oncogene 1995 1.70
5 Regional localization of DNA probes on the short arm of chromosome 11 using aniridia-Wilms' tumor-associated deletions. Hum Genet 1987 1.67
6 Cloning, expression and chromosomal localization of a new putative receptor-like protein tyrosine phosphatase. FEBS Lett 1991 1.66
7 Cloning, structure and expression of a cDNA encoding the human androgen receptor. Biochem Biophys Res Commun 1988 1.64
8 The gene for human complement C9 is on chromosome 5. Genomics 1989 1.40
9 Identification of two alternative fusion genes, SYT-SSX1 and SYT-SSX2, in t(X;18)(p11.2;q11.2)-positive synovial sarcomas. Hum Mol Genet 1995 1.34
10 Fusion of the transcription factor TFE3 gene to a novel gene, PRCC, in t(X;1)(p11;q21)-positive papillary renal cell carcinomas. Proc Natl Acad Sci U S A 1996 1.34
11 High resolution profiling of X chromosomal aberrations by array comparative genomic hybridisation. J Med Genet 2004 1.30
12 Quantitation of minimal residual disease in Philadelphia chromosome positive chronic myeloid leukaemia patients using real-time quantitative RT-PCR. Br J Haematol 1998 1.30
13 Chromosomal localization of the human Thy-1 gene. Proc Natl Acad Sci U S A 1985 1.30
14 Human immunodeficiency virus infection studied in CD4-expressing human-murine T-cell hybrids. Virology 1989 1.26
15 Isolation of cDNA clones for human adenosine deaminase. Gene 1983 1.24
16 Assignment of the gene coding for human beta-glucocerebrosidase to the region q21-q31 of chromosome 1 using monoclonal antibodies. Hum Genet 1983 1.22
17 SNP array analysis in constitutional and cancer genome diagnostics--copy number variants, genotyping and quality control. Cytogenet Genome Res 2011 1.17
18 Isolation and characterization of a cDNA encoding the low molecular weight insulin-like growth factor binding protein (IBP-1). EMBO J 1988 1.15
19 Comparative genomic hybridization analysis of human sarcomas: II. Identification of novel amplicons at 6p and 17p in osteosarcomas. Genes Chromosomes Cancer 1995 1.14
20 The human T cell transcription factor-1 gene. Structure, localization, and promoter characterization. J Biol Chem 1992 1.12
21 Regional localization of the gene for thyroid peroxidase to human chromosome 2pter----p12. Cytogenet Cell Genet 1988 1.10
22 Variation of CNV distribution in five different ethnic populations. Cytogenet Genome Res 2007 1.10
23 Comparative genomic hybridization of germ cell tumors of the adult testis: confirmation of karyotypic findings and identification of a 12p-amplicon. Cancer Genet Cytogenet 1996 1.05
24 Expression of nma, a novel gene, inversely correlates with the metastatic potential of human melanoma cell lines and xenografts. Int J Cancer 1996 1.04
25 Comparative genomic hybridization as a tool to define two distinct chromosome 12-derived amplification units in well-differentiated liposarcomas. Genes Chromosomes Cancer 1994 1.03
26 Nuclear localization of SYT, SSX and the synovial sarcoma-associated SYT-SSX fusion proteins. Hum Mol Genet 1997 0.99
27 Molecular mechanisms underlying the MiT translocation subgroup of renal cell carcinomas. Cytogenet Genome Res 2007 0.99
28 Detection of chromosomal DNA gains and losses in testicular germ cell tumors by comparative genomic hybridization. Genes Chromosomes Cancer 1996 0.96
29 Cloning of the cDNA encoding human skeletal-muscle fatty-acid-binding protein, its peptide sequence and chromosomal localization. Biochem J 1991 0.93
30 Fine mapping of the 1q21 breakpoint of the papillary renal cell carcinoma-associated (X;1) translocation. Hum Genet 1996 0.92
31 Reactivity of germ cell maturation stage-specific markers in spermatocytic seminoma: diagnostic and etiological implications. Lab Invest 2001 0.92
32 Report of the first international workshop on human chromosome 18 mapping. Cytogenet Cell Genet 1993 0.91
33 The prostate-specific antigen gene and the human glandular kallikrein-1 gene are tandemly located on chromosome 19. FEBS Lett 1989 0.90
34 Renal oncocytoma with t(5;12;11), der(1)1;8) and add(19): "true" oncocytoma or chromophobe adenoma? Int J Cancer 1997 0.90
35 A familial case of renal cell carcinoma and a t(2;3) chromosome translocation. Kidney Int 1998 0.90
36 An alternative route for multistep tumorigenesis in a novel case of hereditary renal cell cancer and a t(2;3)(q35;q21) chromosome translocation. Am J Hum Genet 1998 0.89
37 Fine mapping of the human renal oncocytoma-associated translocation (5;11)(q35;q13) breakpoint. Cancer Genet Cytogenet 1997 0.89
38 Construction of a 350-kb sequence-ready 11q13 cosmid contig encompassing the markers D11S4933 and D11S546: mapping of 11 genes and 3 tumor-associated translocation breakpoints. Genomics 2000 0.89
39 The synovial sarcoma associated protein SYT interacts with the acute leukemia associated protein AF10. Oncogene 2001 0.89
40 Targeted disruption of the synovial sarcoma-associated SS18 gene causes early embryonic lethality and affects PPARBP expression. Hum Mol Genet 2006 0.89
41 Localization of a gamma-glutamyl-transferase-related gene family on chromosome 22. Hum Genet 1993 0.89
42 Amplification of chromosome subregion 12p11.2-p12.1 in a metastasis of an i(12p)-negative seminoma: relationship to tumor progression? Cancer Genet Cytogenet 1994 0.88
43 Distinct Xp11.2 breakpoints in two renal cell carcinomas exhibiting X;autosome translocations. Genes Chromosomes Cancer 1995 0.88
44 Overrepresentation of chromosome 12p sequences and karyotypic evolution in i(12p)-negative testicular germ-cell tumors revealed by fluorescence in situ hybridization. Cancer Genet Cytogenet 1993 0.87
45 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. Am J Hum Genet 1991 0.87
46 Reverse mapping of the gene encoding the human fos-related antigen-1 (fra-1) within chromosome band 11q13. Genomics 1993 0.87
47 Assignment of seven genes to distinct intervals on the midportion of human chromosome 19q surrounding the myotonic dystrophy gene region. Cytogenet Cell Genet 1990 0.86
48 Assignment of the human gene for the water channel of renal collecting duct Aquaporin 2 (AQP2) to chromosome 12 region q12-->q13. Cytogenet Cell Genet 1994 0.86
49 The human calbindin 27-kDa gene: structural organization of the 5' and 3' regions, chromosomal assignment, and restriction fragment length polymorphism. Genomics 1989 0.85
50 Long-term follow-up of persisting mixed chimerism after partially T cell-depleted allogeneic stem cell transplantation. Leukemia 2002 0.85
51 Assignment of the human gene encoding the epidermal serine proteinase inhibitor SKALP (PI3) to chromosome region 20q12-->q13. Cytogenet Cell Genet 1994 0.85
52 Structure and function of the androgen receptor. Urol Res 1989 0.83
53 Molecular cloning of the papillary renal cell carcinoma-associated translocation (X;1)(p11;q21) breakpoint. Cytogenet Cell Genet 1996 0.83
54 Translocation t(2;3)(p15-23;q26-27) in myeloid malignancies: report of 21 new cases, clinical, cytogenetic and molecular genetic features. Leukemia 2004 0.83
55 Molecular cloning of the synovial sarcoma-specific translocation (X;18)(p11.2;q11.2) breakpoint. Hum Mol Genet 1994 0.83
56 Assignment of human transcobalamin II (TC2) to chromosome 22 using somatic cell hybrids and monosomic meningioma cells. Hum Genet 1986 0.83
57 Overexpression of a cellular retinoic acid binding protein (xCRABP) causes anteroposterior defects in developing Xenopus embryos. Development 1994 0.82
58 Assignment of the gene coding for human peroxisomal 3-oxoacyl-CoA thiolase (ACAA) to chromosome region 3p22----p23. Cytogenet Cell Genet 1989 0.81
59 Cytogenetic classification of renal cell cancer. Cancer Genet Cytogenet 1997 0.81
60 The human myoglobin gene: a third dispersed globin locus in the human genome. Nucleic Acids Res 1984 0.81
61 Isochromosome 12p-positive pineal germ cell tumor. Cancer Res 1994 0.81
62 Molecular cloning and characterization of the active human mitochondrial NADH:ubiquinone oxidoreductase 24-kDa gene (NDUFV2) and its pseudogene. Genomics 1995 0.81
63 Chromosome 3 translocations and the risk to develop renal cell cancer: a Dutch intergroup study. Genet Couns 2003 0.80
64 Clonal analysis of progenitor cells by interphase cytogenetics in patients with acute myeloid leukemia and myelodysplasia. Leukemia 1995 0.80
65 Predisposition to colorectal cancer: exploiting copy number variation to identify novel predisposing genes and mechanisms. Cytogenet Genome Res 2009 0.80
66 Fine mapping of the human bone morphogenetic protein-4 gene (BMP4) to chromosome 14q22-q23 by in situ hybridization. Genomics 1995 0.80
67 The mouse gene Ptprf encoding the leukocyte common antigen-related molecule LAR: cloning, characterization, and chromosomal localization. Genomics 1995 0.80
68 Assignment of human pepsinogen A locus to the q12-pter region of chromosome 11. Hum Genet 1985 0.80
69 Fluorescence in situ hybridization-based approaches for detection of 12p overrepresentation, in particular i(12p), in cell lines of human testicular germ cell tumors of adults. Cancer Genet Cytogenet 1996 0.80
70 Normal development, growth and reproduction in cellular retinoic acid binding protein-I (CRABPI) null mutant mice. Differentiation 1994 0.79
71 Transformation capacities of the papillary renal cell carcinoma-associated PRCCTFE3 and TFE3PRCC fusion genes. Oncogene 2001 0.79
72 Assignment of the human gene for receptor-type protein tyrosine phosphatase IA-2 (PTPRN) to chromosome region 2q35 --> q36.1 and identification of an intragenic genetic marker. Cytogenet Cell Genet 1996 0.79
73 Verification of isochromosome 12p and identification of other chromosome 12 aberrations in gonadal and extragonadal human germ cell tumors by bicolor double fluorescence in situ hybridization. Cancer Genet Cytogenet 1992 0.79
74 Isolation and characterization of the Xenopus laevis orthologs of the human papillary renal cell carcinoma-associated genes PRCC and MAD2L2 (MAD2B). Cytogenet Genome Res 2004 0.79
75 Generation of a panel of somatic cell hybrids containing fragments of human chromosome 12P by X-ray irradiation and cell fusion. Genomics 1992 0.79
76 A novel Krüppel-associated box containing the SSX gene (SSX3) on the human X chromosome is not implicated in t(X;18)-positive synovial sarcomas. Cytogenet Cell Genet 1996 0.79
77 Survival in first or second remission after lymphocyte-depleted transplantation for Philadelphia chromosome-positive CML in first chronic phase. Bone Marrow Transplant 1997 0.78
78 Assignment of the canalicular multispecific organic anion transporter gene (CMOAT) to human chromosome 10q24 and mouse chromosome 19D2 by fluorescent in situ hybridization. Cytogenet Cell Genet 1997 0.78
79 Exclusion of the phosphatidylinositol-specific phospholipase C beta 3 (PLC beta 3) gene as candidate for the multiple endocrine neoplasia type 1 (MEN 1) gene. Hum Genet 1997 0.78
80 Outcome of transplantation for standard-risk leukaemia with grafts depleted of lymphocytes after conditioning with an intensified regimen. Br J Haematol 1997 0.78
81 Molecular parameters associated with insulinoma progression: chromosomal instability versus p53 and CK19 status. Cytogenet Genome Res 2006 0.78
82 Cytogenetics of the progression of adult testicular germ cell tumors. Cancer Genet Cytogenet 1997 0.78
83 The gene (PTPN13) encoding the protein tyrosine phosphatase PTP-BL/PTP-BAS is located in mouse chromosome region 5E/F and human chromosome region 4q21. Cytogenet Cell Genet 1996 0.77
84 A synovial sarcoma with a complex t(X;18;5;4) and a break in the ornithine aminotransferase (OAT)L1 cluster on Xp11.2. Genes Chromosomes Cancer 1994 0.77
85 EcoRI RFLP at the creatine kinase-brain type gene locus (CKBB, chromosome 14). Nucleic Acids Res 1987 0.77
86 Derivative (y)t(Y;1)(q12;q12),+9 in a patient with polycythemia vera during transition into myelodysplasia. Cancer Genet Cytogenet 1996 0.77
87 Report of the Fourth International Workshop on Human Chromosome 18 Mapping. Boston, Massachusetts, October 7-9, 1996. Cytogenet Cell Genet 1996 0.77
88 Chromosomal localization of three human genes encoding members of the TGF-beta superfamily of type I serine/threonine kinase receptors. Mamm Genome 1998 0.77
89 The gene for the human putative apoE receptor is on chromosome 12 in the segment q13-14. Genomics 1989 0.76
90 Assignment1 of the PTP-SL/PTPBR7 gene (Ptprr/PTPRR) to mouse chromosome region 8A2 by in situ hybridization. Cytogenet Cell Genet 1999 0.76
91 Assignment of the gene encoding the latent TGF-beta 1-binding protein (LTBP1) to human chromosome 2, region p12-->q22. Cytogenet Cell Genet 1994 0.76
92 A polymorphic DNA probe from chromosome 19 (19cen-q11). Nucleic Acids Res 1989 0.75
93 Report of the Third International Workshop on human chromosome 18 mapping 1995. Cytogenet Cell Genet 1995 0.75
94 A cytogenetic classification of germ cell tumors, and its biological relevance. Eur Urol 1993 0.75
95 Uniparental origin of i(12p) in human germ cell tumors. Genes Chromosomes Cancer 1993 0.75
96 Comparison of chromosome studies on PHA-stimulated blood and unstimulated bone marrow cells in recipients of lymphocyte depleted grafts using counterflow centrifugation. Bone Marrow Transplant 1993 0.75
97 Exclusion of the nuclear factor-kappa B3 (REL A) gene as candidate for the multiple endocrine neoplasia type 1 (MEN 1) gene. Biochem Mol Med 1997 0.75
98 Refined mapping of the human Ets-related gene Elk-1 to Xp11.2-p11.4, distal to the OATL1 region. Hum Genet 1994 0.75
99 Common origin of the human synovial sarcoma associated SS18 and SS18L1 gene loci. Cytogenet Genome Res 2006 0.75
100 Identification of a yeast artificial chromosome that spans the human papillary renal cell carcinoma-associated t(X;1) breakpoint in Xp11.2. Cancer Genet Cytogenet 1993 0.75
101 Assignment of casein kinase 2 alpha sequences to two different human chromosomes. Hum Genet 1992 0.75
102 Red blood cell phenotyping is a sensitive technique for monitoring chronic myeloid leukaemia patients after T-cell-depleted bone marrow transplantation and after donor leucocyte infusion. Br J Haematol 2000 0.75
103 A 46,XY female with mixed gonadal dysgenesis and a 48,XY, +7, +i(12p) chromosome pattern in a primary gonadal tumor. Cancer Genet Cytogenet 1991 0.75
104 A long-lasting, complete hematologic and cytogenetic remission of chronic myelogenous leukemia after treatment with busulfan alone. Ann Hematol 1996 0.75
105 Towards the isolation of a human malignant extragonadal germ cell tumour-associated breakpoint in chromosome 11q13. APMIS 1998 0.75
106 Fine mapping of the human receptor-like protein tyrosine phosphatase gene (PTPRM) to 18p11.2 by fluorescence in situ hybridization. Cytogenet Cell Genet 1993 0.75
107 Assignment of the human protein tyrosine phosphatase epsilon (PTPRE) gene to chromosome 10q26 by fluorescence in situ hybridization. Genomics 1995 0.75
108 Isolation of osteosarcoma-associated amplified DNA sequences using representational difference analysis. Genes Chromosomes Cancer 1997 0.75
109 Generation and characterization of radiation reduced cell hybrids and isolation of probes from the proximal short arm of the human X chromosome. Hum Genet 1992 0.75
110 Genomic structure, chromosomal localization, and embryonic expression of the mouse homolog of PRCC, a gene associated with papillary renal cell carcinoma. Cytogenet Cell Genet 2001 0.75
111 Genomic cloning of the human histo-blood group ABO locus. Biochem Biophys Res Commun 1995 0.75