PubRank

J Couturier

Author PubWeight™ 110.28‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 The genome of black cottonwood, Populus trichocarpa (Torr. & Gray). Science 2006 21.03
2 Interleukin 17, a T-cell-derived cytokine, promotes tumorigenicity of human cervical tumors in nude mice. Cancer Res 1999 2.23
3 [Trisomy 21 and superoxide dismutase-1 (IPO-A). Tentative localization of sub-band 21Q22.1]. Exp Cell Res 1976 2.07
4 Quality assessment of genetic markers used for therapy stratification. J Clin Oncol 2003 1.92
5 [Staining of human chromosomes with acridine orange after treatment with 5 bromodeoxyuridine]. C R Acad Sci Hebd Seances Acad Sci D 1973 1.89
6 A new member of the ETS family fused to EWS in Ewing tumors. Oncogene 1997 1.79
7 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
8 Comprehensive screening for constitutional RB1 mutations by DHPLC and QMPSF. Hum Mutat 2004 1.52
9 Bilateral renal oncocytosis with renal failure. Arch Pathol Lab Med 2001 1.41
10 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
11 Chromosomal CGH identifies patients with a higher risk of relapse in neuroblastoma without MYCN amplification. Br J Cancer 2007 1.39
12 Constitutional balanced translocations in patients with solid tumors. Cancer Genet Cytogenet 1992 1.38
13 Sequence of DNA replication in 277 R- and Q-bands of human chromosomes using a BrdU treatment. Chromosoma 1976 1.36
14 [Mosaic 14 trisomy in a female child with multiple abnormalities]. Ann Genet 1975 1.34
15 MYC activation associated with the integration of HPV DNA at the MYC locus in genital tumors. Oncogene 2006 1.31
16 Calibration of immunohistochemistry for assessment of HER2 in breast cancer: results of the French multicentre GEFPICS study. Histopathology 2003 1.23
17 [Giemsa-R-banding analysis of the trisomy 9p and report of a new case]. Humangenetik 1973 1.23
18 [Chromosome 8 : complete trisomy and segmental trisomies]. Ann Genet 1977 1.22
19 Detection of chromosome imbalances in retinoblastoma by parallel karyotype and CGH analyses. Genes Chromosomes Cancer 2000 1.21
20 hSNF5/INI1-deficient tumours and rhabdoid tumours are convergent but not fully overlapping entities. J Pathol 2007 1.20
21 Agreement between chromogenic in situ hybridisation (CISH) and FISH in the determination of HER2 status in breast cancer. Br J Cancer 2003 1.17
22 Evidence for a correlation between late replication and autosomal gene inactivation in a familial translocation t(X;21). Hum Genet 1979 1.17
23 Evidence for long-range oncogene activation by hepadnavirus insertion. EMBO J 1994 1.13
24 Surgical management of liver metastases from uveal melanoma: 16 years' experience at the Institut Curie. Eur J Surg Oncol 2009 1.11
25 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
26 Deletion of band 13q21 is compatible with normal phenotype. Hum Genet 1985 1.09
27 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
28 Multiplex PCR/liquid chromatography assay for detection of gene rearrangements: application to RB1 gene. Nucleic Acids Res 2004 1.02
29 Synaptonemal complexes in a subfertile man with a pericentric inversion in chromosome 21. Heterosynapsis without previous homosynapsis. Cytogenet Cell Genet 1988 1.02
30 [Ring chromosome 14 in monozygotic twins]. Ann Genet 1977 1.02
31 HER2 status of bone marrow micrometastasis and their corresponding primary tumours in a pilot study of 27 cases: a possible tool for anti-HER2 therapy management? Br J Cancer 2007 0.98
32 The ancestral karyotype of platyrrhine monkeys. Cytogenet Cell Genet 1981 0.95
33 Aneuploidy in human lymphocytes: an extensive study of eight individuals of various ages. Mutat Res 1993 0.94
34 Minimal focal dermal hypoplasia in a man: a case of father-to-daughter transmission. J Am Acad Dermatol 1991 0.93
35 The rate of chromosome breakage is age dependent in lymphocytes of adult controls. Hum Genet 1986 0.92
36 [Herceptin, a monoclonal humanized antibody anti-HER2: a major therapeutic progress in breast cancers overexpressing this oncogene?]. Bull Cancer 1999 0.92
37 hSNF5/INI1 inactivation is mainly associated with homozygous deletions and mitotic recombinations in rhabdoid tumors. Cancer Res 1999 0.91
38 Chromosomal evolution of 19 species of sub-species of Cercopithecinae. Ann Genet 1980 0.90
39 [Prognostic factors for malignant uveal melanoma. Retrospective study on 2,241 patients and recent contribution of monosomy-3 research]. J Fr Ophtalmol 2006 0.89
40 Human papillomavirus type 16 DNA is integrated into chromosome region 12q14-q15 in a cell line derived from a vulvar intraepithelial neoplasia. Cancer Genet Cytogenet 1990 0.88
41 The neuroepithelioma breakpoint on chromosome 22 is proximal to the meningioma locus. Genomics 1990 0.88
42 Diagnosis of Xp11 translocation renal cell carcinomas in adult patients under 50 years: interest and pitfalls of automated immunohistochemical detection of TFE3 protein. Pathol Res Pract 2012 0.87
43 [X-chromosome translocations. Examination based on treatment with BUDR and staining with acridine orange]. Helv Paediatr Acta 1974 0.86
44 [Specific fluorescence of R and G bands in human chromosomes]. C R Acad Sci Hebd Seances Acad Sci D 1973 0.86
45 In neuroblastic tumours, Schwann cells do not harbour the genetic alterations of neuroblasts but may nevertheless share the same clonal origin. Oncogene 2007 0.86
46 Chromosomal aberrations induced by low-dose gamma-irradiation. Study of R-banded chromosomes of human lymphocytes. Mutat Res 1989 0.86
47 Inversion (14)(q12qter) or (q11.2q32.3): the most frequently acquired rearrangement in lymphocytes. Hum Genet 1985 0.85
48 [Comparative karyotyping of our gibbon species or subspecies (author's transl)]. Ann Genet 1982 0.85
49 [Chronology of the replication of sex chromosome bands in lymphocytes of normal subjects and patients]. Ann Genet 1978 0.85
50 Localization chromatid breaks in Fanconi's anemia, using three consecutive stains. Hum Genet 1977 0.84
51 [The r(22) syndrome, Apropos of 4 new cases]. Ann Genet 1976 0.84
52 The ancestral karyotype of Carnivora: comparison with that of platyrrhine monkeys. Cytogenet Cell Genet 1983 0.84
53 Reproductive failure and pericentric inversion in man. Andrologia 1988 0.84
54 Necrotizing cerebellitis and cerebellar atrophy caused by Neospora caninum infection: magnetic resonance imaging and clinicopathologic findings in seven dogs. J Vet Intern Med 2010 0.83
55 Conservation of replication chronology of homologous chromosome bands between four species of the genus Cebus and man. Cytogenet Cell Genet 1981 0.82
56 [Great homology of chromosome banding of the rabbit (Oryctolagus cuniculus) and primates, including man (author's transl)]. Ann Genet 1980 0.82
57 [Sterility and familial t (1q-;Xq+) translocation]. C R Acad Sci Hebd Seances Acad Sci D 1972 0.82
58 Wilms' tumor and gonadal dysgenesis in a child with the 2q37.1 deletion syndrome. Clin Genet 1998 0.82
59 Distinct patterns of alteration of myc genes associated with integration of human papillomavirus type 16 or type 45 DNA in two genital tumours. J Gen Virol 2000 0.81
60 [De novo monosomy 4q32.1 leads to 4qter in a newborn with multiple malformations (author's transl)]. Ann Genet 1979 0.81
61 [Increase of LDH A and partial trisomy 11p (author's transl)]. Ann Genet 1980 0.81
62 Partial trisomy 8q. Two case reports with maternal translocation and inverted insertion: phenotype analyses and reflections on the risk. Clin Genet 1992 0.81
63 Establishment of a human malignant fibrous histiocytoma cell line, COMA. Characterization By conventional cytogenetics, comparative genomic hybridization, and multiplex fluorescence In situ hybridization. Cancer Genet Cytogenet 2000 0.81
64 Acquired chromosome rearrangements in human lymphocytes: effect of aging. Hum Genet 1988 0.81
65 Detection and quantitation by fluorescence in situ hybridization (FISH) and image analysis of HER-2/neu gene amplification in breast cancer fine-needle samples. Cancer 1999 0.81
66 [A new case of partial monosomy of chromosome 12,del(12)(p11.01 to p12.109) confirming the location of the gene for lactate dehydrogenase B]. Ann Genet 1985 0.80
67 Trisomy and tetrasomy for long arm of chromosome 1 in near-diploid human endometrial adenocarcinomas. Int J Cancer 1986 0.80
68 [Great degree of homology between the ancestral karyotype of squirrels (rodents) and that of primates and carnivores]. Ann Genet 1984 0.80
69 [Cri-du-chat syndrome and trisomy 8p due to a paternal translocation t(5;8)(p1409;p12)]. Ann Genet 1984 0.80
70 Chromosomal phylogeny of forty-two species or subspecies of cercopithecoids (Primates Catarrhini). Ann Genet 1982 0.80
71 Cytogenetical and biochemical characterization of a dG + dC-rich satellite DNA in the primate Cebus capucinus. Biochimie 1982 0.79
72 [Increased activity of adenine phosphoribosyl transferase in a child trisomic for 16q22.2 to 16qter due to malsegregation of a t(16;21) (q22.2;q22;2)pat (author's transl)]. Ann Genet 1982 0.79
73 Partial trisomy 13 (q21.3 leads to qter) resulting from a maternal translocation t (13;21). Ann Genet 1981 0.79
74 Y-autosome translocation in Cacajao calvus rubicundus (Platyrrhini). Ann Genet 1981 0.79
75 [Presence of abundant heterochromatin in the karyotype of Cebus: C. cappucinus and C. nigrivittatus]. Ann Genet 1978 0.78
76 Increased cell size and Akt activation in HER-2/neu-overexpressing invasive ductal carcinoma of the breast. Histopathology 2004 0.78
77 [Partial 11q trisomy due to missegregation of maternal t(11;22) (q23;q11.1) translocation (author's transl)]. Nouv Presse Med 1980 0.78
78 The use of high resolution banding in comparative cytogenetics: comparison between man and Lagothrix lagotricha (Cebidae). Cytogenet Cell Genet 1980 0.78
79 Two new cases of papillary renal cell carcinoma with t(X;1)(p11;q21) in females. Cancer Genet Cytogenet 1999 0.78
80 Cytogenetic study of eight new cases of radiation-induced solid tumors. Cancer Genet Cytogenet 1999 0.78
81 [Severe 5-fluorouracil toxicity in a woman treated for breast cancer with concurrent osteogenesis imperfecta and dehydrogenase deficiency]. Bull Cancer 1996 0.78
82 Chromosome study of Presbytis cristatus: presence of a complex Y-autosome rearrangement in the male. Ann Genet 1984 0.78
83 [Lethal polymalformative syndrome with 13q deletion secondary to a maternal X; 13 translocation]. J Genet Hum 1989 0.77
84 [Genomic profiling by comparative genomic hybridization: analysis of ten enucleated uveal melanoma cases]. J Fr Ophtalmol 2010 0.77
85 A novel movement disorder in related male Labrador Retrievers characterized by extreme generalized muscular stiffness. J Vet Intern Med 2011 0.77
86 Chromosomal evolution in Malagasy lemurs. VII. Phylogenic relationships between Propithecus, Avahi (Indridae), Microcebus (Cheirogaleidae), and Lemur (Lemuridae). Cytogenet Cell Genet 1983 0.76
87 [Effects of pH on the staining of human chromosomes with acridine orange]. Exp Cell Res 1974 0.76
88 Human somatic chromosome chains and rings. A preliminary note on end-to-end fusion. Cytogenet Cell Genet 1978 0.76
89 [Genomic techniques used in uveal melanoma: a literature review]. J Fr Ophtalmol 2011 0.76
90 Integration of viral sequences into the c-myc gene in two mammary adenocarcinomas induced by polyomavirus in athymic nude mice. J Virol 1995 0.76
91 Inversions in evolution of man and closely related species. Ann Genet 1986 0.75
92 'Pure' partial trisomy 2q in a male owing to malsegregation of a maternal translocation t(X;2)(p22.3;q32.1). J Med Genet 1985 0.75
93 A recurrent human papillomavirus integration site at chromosome region 12q14-q15 in SW756 and SK-v cell lines derived from genital tumors. C R Acad Sci III 1995 0.75
94 Parental origin of chromosome 22 alleles lost in meningioma. Am J Hum Genet 1990 0.75
95 Chromosome imbalances in endometrial adenocarcinomas: a possible adaptation to abnormal metabolic pathways. Ann Genet 1986 0.75
96 Pleomorphic medium-sized T-cell lymphoma following Hodgkin's disease (nodular sclerosis type). Arch Pathol Lab Med 1997 0.75
97 A possible tetracycline-risperidone-sertraline interaction in an adolescent. Can J Clin Pharmacol 1999 0.75
98 [Ring of the chromosome 4. I - With 4p- phenotype]. Ann Genet 1977 0.75
99 Cytogenetic aspects of Primate evolution. Prog Clin Biol Res 1982 0.75
100 [Cytogenetics of two Lorisidae (Nycticebus coucang and Perodicticus potto). Comparison with the lemurs and the simians (author's transl)]. Ann Genet 1979 0.75
101 Inherited Xq duplication due to a zygotic translocation t(X;X)(q23;q27). Ann Genet 1988 0.75
102 [Modification of chromatids before fixation: production of G bands by various stains]. Ann Genet 1976 0.75
103 Aberrations of the synaptonemal complexes in a male 46,XY,-14,+der(14)t(Y;14). Ann Genet 1985 0.75
104 [Possible localization of the glutathione reductase (EC 1.6.4.2) on the 8p21 band]. Ann Genet 1977 0.75
105 [Increased activity of adenine phosphoribosyl transferase in a child trisomic for 16q22.2 to 16qter due to malsegregation of a t(16;21) (q22.2;q22;2)pat]. Sem Hop 1982 0.75
106 [Attenuated phenotype of trisomy 4p by translocation t(X;4)(p21.2;p13)]. Ann Genet 1982 0.75
107 [Non random position of metaphasic chromosomes. II. Effect of condensation on the position of X chromosomes]. Ann Genet 1982 0.75
108 [The karyotypes of Colobus vellersus and of C. palliatus: comparison with Cercopithecidae and man]. Ann Genet 1981 0.75
109 [Demonstration and electrophysiological analysis of the blinking reflex in the rat. Value of the animal model]. Ann Otolaryngol Chir Cervicofac 1993 0.75
110 [The karyotype of sterile and infertile men]. Bull Assoc Anat (Nancy) 1987 0.75
111 Isoacentric and isocentric chromosomes originating after deletions of human chromosomes. Hum Genet 1987 0.75
112 Radiation induced inversions in human somatic cells. Ann Genet 1986 0.75
113 [Renal medullary carcinoma, a new clinico-pathological entity. Immunohistochemical, ultrastructural, flow cytometric and cytogenetic study of a case]. Ann Pathol 1999 0.75
114 Identity of euchromatic bands from man to cercopithecidae (Cercopithecus aethiops, Cercopithecus sabaeus, Erythrocebus patas, and Miopithecus talapoin). Hum Genet 1978 0.75
115 [Cavitary choroidal melanoma in a child]. J Fr Ophtalmol 2006 0.75
116 [Chromosome sites of papillomavirus genome integration in genital tumors]. Ann Pathol 1992 0.75
117 Inactive X chromosome gene reactivation induced by 5-azacytidine, is not correlated with the modification of the pattern of replication. Ann Genet 1987 0.75
118 [Cytogenetics of Cercopithecus (mona) campbelli. Comparison with other cercopithecus species and man (author's transl)]. Ann Genet 1981 0.75
119 [Injection of collagen in recurrent paralysis after thoracic surgery]. Ann Chir 1992 0.75
120 [Trisomy 6p due to a de-novo t(6;12) translocation]. Ann Pediatr (Paris) 1988 0.75
121 Detailed cell cycle analysis in human lymphocytes; application to gamma-irradiated cells. Hum Genet 1984 0.75
122 Chromosomal evolution in "lemurs". VI. Chromosomal banding studies of Galago senegalensis, Galago alleni, Galago demidovii and Euoticus elegantulus. Folia Primatol (Basel) 1982 0.75
123 The karyotype of Galago crassicaudatus is ancestral for lorisiforms. Folia Primatol (Basel) 1983 0.75
124 Bilateral MALT-type ocular adnexal lymphoma with marginal zone lymphoma leukaemic cells and ophthalmological diffuse large B cell lymphoma. Br J Ophthalmol 2008 0.75
125 [Partial trisomy for the long arm of chromosome 2 due to malsegregation of a maternal insertion : ins(6;2)(p22;q24q34)]. Ann Genet 1977 0.75
126 Renal cell carcinoma: recent progress. Adv Nephrol Necker Hosp 1994 0.75
127 [Technics of chromosome analysis]. Ann Biol Clin (Paris) 1973 0.75