Published in Hum Genet on December 29, 1978
Phylogenomics of African guenons. Chromosome Res (2008) 0.91
The genome of black cottonwood, Populus trichocarpa (Torr. & Gray). Science (2006) 21.03
Requirement of poly(ADP-ribose) polymerase in recovery from DNA damage in mice and in cells. Proc Natl Acad Sci U S A (1997) 5.24
[A new technic of analysis of the human karyotype]. C R Acad Sci Hebd Seances Acad Sci D (1971) 2.62
Interleukin 17, a T-cell-derived cytokine, promotes tumorigenicity of human cervical tumors in nude mice. Cancer Res (1999) 2.23
[Trisomy 21 and superoxide dismutase-1 (IPO-A). Tentative localization of sub-band 21Q22.1]. Exp Cell Res (1976) 2.07
High resolution R- and G-banding on the same preparation. Hum Genet (1981) 1.94
Quality assessment of genetic markers used for therapy stratification. J Clin Oncol (2003) 1.92
[Staining of human chromosomes with acridine orange after treatment with 5 bromodeoxyuridine]. C R Acad Sci Hebd Seances Acad Sci D (1973) 1.89
NSD3, a new SET domain-containing gene, maps to 8p12 and is amplified in human breast cancer cell lines. Genomics (2001) 1.85
LAG-3, a novel lymphocyte activation gene closely related to CD4. J Exp Med (1990) 1.83
A new member of the ETS family fused to EWS in Ewing tumors. Oncogene (1997) 1.79
Chromosomal evolution in primates: tentative phylogeny from Microcebus murinus (Prosimian) to man. Hum Genet (1979) 1.75
An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome. Hum Mol Genet (1993) 1.75
Targeted agents in metastatic Xp11 translocation/TFE3 gene fusion renal cell carcinoma (RCC): a report from the Juvenile RCC Network. Ann Oncol (2010) 1.65
A simple method for simultaneous R- or G-banding and fluorescence in situ hybridization of small single-copy genes. Cytogenet Cell Genet (1992) 1.64
Systematic analysis of 95 reciprocal translocations of autosomes. Hum Genet (1978) 1.59
Mapping of single-copy DNA sequences on human chromosomes by in situ hybridization with biotinylated probes: enhancement of detection sensitivity by intensified-fluorescence digital-imaging microscopy. Proc Natl Acad Sci U S A (1989) 1.59
Comprehensive screening for constitutional RB1 mutations by DHPLC and QMPSF. Hum Mutat (2004) 1.52
The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region. J Med Genet (2006) 1.51
[Trisomy for the distal part of the short arm of the number 3 chromosome in 3 siblings. First example of chromosomal insertion: INS(7;3)(q 31;p 21 p 26)]. Ann Genet (1972) 1.50
Mutations in OGG1, a gene involved in the repair of oxidative DNA damage, are found in human lung and kidney tumours. Oncogene (1998) 1.49
Bilateral renal oncocytosis with renal failure. Arch Pathol Lab Med (2001) 1.41
[The Dr phenotype: a study of threee cases with a ring D chromosome]. Ann Genet (1968) 1.41
[Pericentric inversion, inv(10), in a mother and aneusomy by recombination, inv(10), rec(10), in her son (author's transl)]. Cytogenet Cell Genet (1973) 1.40
Assessing HER2 gene amplification as a potential target for therapy in invasive urothelial bladder cancer with a standardized methodology: results in 1005 patients. Ann Oncol (2009) 1.40
Emergence and scattering of multiple neurofibromatosis (NF1)-related sequences during hominoid evolution suggest a process of pericentromeric interchromosomal transposition. Hum Mol Genet (1997) 1.40
Chromosomal CGH identifies patients with a higher risk of relapse in neuroblastoma without MYCN amplification. Br J Cancer (2007) 1.39
RFLP identified by the anonymous DNA segment OL VII E10 at 18q21.3 (HGM no. D18S8). Nucleic Acids Res (1987) 1.38
Constitutional balanced translocations in patients with solid tumors. Cancer Genet Cytogenet (1992) 1.38
High frequencies of inversions and translocations of chromosomes 7 and 14 in ataxia telangiectasia. Mutat Res (1980) 1.38
Sequence of DNA replication in 277 R- and Q-bands of human chromosomes using a BrdU treatment. Chromosoma (1976) 1.36
[The mechanism of chromosome segmentation induced by BUDR (5-bromodeoxyuridine)]. Ann Genet (1974) 1.35
[Mosaic 14 trisomy in a female child with multiple abnormalities]. Ann Genet (1975) 1.34
Sensitivity to CPT-11 of xenografted human colorectal cancers as a function of microsatellite instability and p53 status. Br J Cancer (2000) 1.32
MYC activation associated with the integration of HPV DNA at the MYC locus in genital tumors. Oncogene (2006) 1.31
Detection of DNA amplification in 17 primary breast carcinomas with homogeneously staining regions by a modified comparative genomic hybridization technique. Genes Chromosomes Cancer (1994) 1.30
Physical mapping of human loci homologous to the chicken nov proto-oncogene. Oncogene (1992) 1.26
Identification of amplified DNA sequences in breast cancer and their organization within homogeneously staining regions. Genes Chromosomes Cancer (1995) 1.24
SOD2: a new type of tumor-suppressor gene? Int J Cancer (1992) 1.24
Calibration of immunohistochemistry for assessment of HER2 in breast cancer: results of the French multicentre GEFPICS study. Histopathology (2003) 1.23
[Giemsa-R-banding analysis of the trisomy 9p and report of a new case]. Humangenetik (1973) 1.23
[New system of chromosome banding: the T bands (author's transl)]. Chromosoma (1973) 1.23
Selective endoreduplication or branched chromosome? Exp Cell Res (1977) 1.22
[Chromosome 8 : complete trisomy and segmental trisomies]. Ann Genet (1977) 1.22
Detection of chromosome imbalances in retinoblastoma by parallel karyotype and CGH analyses. Genes Chromosomes Cancer (2000) 1.21
Genes occupy a fixed and symmetrical position on sister chromatids. Cell (1991) 1.20
hSNF5/INI1-deficient tumours and rhabdoid tumours are convergent but not fully overlapping entities. J Pathol (2007) 1.20
Deletion proximal to DXS68 locus (L1 probe site) in a boy with Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal hypoplasia. Hum Genet (1988) 1.18
[Four new cases of X-autosome translocation in man (author's transl)]. Humangenetik (1975) 1.17
Agreement between chromogenic in situ hybridisation (CISH) and FISH in the determination of HER2 status in breast cancer. Br J Cancer (2003) 1.17
Establishment and characterisation of a new tumorigenic cell line with a normal karyotype derived from a human breast adenocarcinoma. Br J Cancer (1990) 1.17
High glycolysis in gliomas despite low hexokinase transcription and activity correlated to chromosome 10 loss. Br J Cancer (1996) 1.17
Evidence for a correlation between late replication and autosomal gene inactivation in a familial translocation t(X;21). Hum Genet (1979) 1.17
The cell cycle of lymphocytes in Fanconi anemia. Hum Genet (1982) 1.16
[Study of progeny of individuals bearing a t(DqDq) translocation]. Ann Genet (1970) 1.15
Evidence for long-range oncogene activation by hepadnavirus insertion. EMBO J (1994) 1.13
Increased p53 protein content of colorectal tumours correlates with poor survival. Br J Cancer (1992) 1.13
Chromosomal mapping and expression of the human cyr61 gene in tumour cells from the nervous system. Mol Pathol (1997) 1.13
[Partial trisomy 21 (21q21 - 21q22.2)]. Ann Genet (1976) 1.12
Cytogenetic study of breast cancer: clinicopathologic significance of homogeneously staining regions in 84 patients. Hum Pathol (1992) 1.12
Proto-oncogene amplification and homogeneously staining regions in human breast carcinomas. Genes Chromosomes Cancer (1990) 1.11
DNA hypomethylation in breast cancer: an independent parameter of tumor progression? Cancer Genet Cytogenet (1997) 1.11
Surgical management of liver metastases from uveal melanoma: 16 years' experience at the Institut Curie. Eur J Surg Oncol (2009) 1.11
Gliomas are driven by glycolysis: putative roles of hexokinase, oxidative phosphorylation and mitochondrial ultrastructure. Anticancer Res (1997) 1.10
Segmental chromosomal alterations lead to a higher risk of relapse in infants with MYCN-non-amplified localised unresectable/disseminated neuroblastoma (a SIOPEN collaborative study). Br J Cancer (2011) 1.09
Deletion of band 13q21 is compatible with normal phenotype. Hum Genet (1985) 1.09
Cytogenetics of colorectal adenocarcinomas. Cancer Genet Cytogenet (1990) 1.08
Loss of alleles on chromosome 18 and on the short arm of chromosome 17 in polyploid colorectal carcinomas. Int J Cancer (1988) 1.08
[Translocation 46,XX, t(15; 21) (q13; q22,1) in the mother of 2 children with partial trisomy 15 and monosomy 21]. Ann Genet (1973) 1.08
An unbalanced 4q-21q translocation identified by the R but not by the G and Q chromosome banding techniques. Ann Genet (1973) 1.07
Simultaneous monitoring of P53 protein and DNA content of colorectal adenocarcinomas by flow cytometry. Int J Cancer (1990) 1.07
Comparison of RBG-banded karyotypes of cattle, sheep, and goats. Cytogenet Cell Genet (1991) 1.06
Amplification of DNA sequences from chromosome 19q13.1 in human pancreatic cell lines. Genomics (1998) 1.06
Highly recurrent der(1;16)(q10;p10) and other 16q arm alterations in lobular breast cancer. Genes Chromosomes Cancer (1998) 1.06
Specific induction of uncoiling and recombination by azacytidine in classical satellite-containing constitutive heterochromatin. Cytogenet Cell Genet (1993) 1.05
Alterations of DNA methylation patterns in germ cells and Sertoli cells from developing mouse testis. Cytogenet Cell Genet (1999) 1.05
Deletion of the pseudoautosomal region and lack of sex-chromosome pairing at pachytene in two infertile men carrying an X;Y translocation. Cytogenet Cell Genet (1990) 1.04
[Ring 15 chromosome: r(15). Identification by controlled denaturation]. Ann Genet (1972) 1.03
Assignment of human desmin gene to band 2q35 by nonradioactive in situ hybridization. Hum Genet (1989) 1.03
Reconstruction of the ancestral karyotype of eutherian mammals. Chromosome Res (2003) 1.02
Multiplex PCR/liquid chromatography assay for detection of gene rearrangements: application to RB1 gene. Nucleic Acids Res (2004) 1.02
Intracellular pH governs the subcellular distribution of hexokinase in a glioma cell line. Biochem J (1996) 1.02
Synaptonemal complexes in a subfertile man with a pericentric inversion in chromosome 21. Heterosynapsis without previous homosynapsis. Cytogenet Cell Genet (1988) 1.02
[Ring chromosome 14 in monozygotic twins]. Ann Genet (1977) 1.02
Osteosarcoma following retinoblastoma: age at onset and latency period. Ophthalmic Genet (2001) 1.01
Characterization of SRp46, a novel human SR splicing factor encoded by a PR264/SC35 retropseudogene. Mol Cell Biol (1998) 1.01
Variations of chromosome radiation sensitivity in fetal and adult mice during gestation. Mutat Res (1991) 1.01
Z-DNA immunoreactivity in fixed metaphase chromosomes of primates. Proc Natl Acad Sci U S A (1983) 1.01
Consistent deficiencies of chromosome 18 and of the short arm of chromosome 17 in eleven cases of human large bowel cancer: a possible recessive determinism. Ann Genet (1985) 1.00
Common methylation characteristics of sex chromosomes in somatic and germ cells from mouse, lemur and human. Chromosome Res (2000) 1.00