C Beroud

Summary

Country: France

Publications

  1. ncbi [Molecular diagnostic techniques in oncogenetics]
    C Beroud
    Unité INSERM 383, Hopital Necker, 149, rue de Sevres, 75743 Paris Cedex 15, France
    Ann Med Interne (Paris) 152:326-31. 2001
  2. ncbi UMD (Universal mutation database): a generic software to build and analyze locus-specific databases
    C Beroud
    INSERM U383, Hopital Necker Enfants Malades, Clinique Maurice Lamy, Paris, France
    Hum Mutat 15:86-94. 2000
  3. ncbi Software and database for the analysis of mutations in the VHL gene
    C Beroud
    INSERM U383, Hopital Necker Enfants Malades, Universite Rene Descartes Paris V, Paris, France
    Nucleic Acids Res 26:256-8. 1998
  4. ncbi Mutations of the VHL gene in sporadic renal cell carcinoma: definition of a risk factor for VHL patients to develop an RCC
    C Gallou
    INSERM U383, Hopital Necker Enfants Malades, Paris, France
    Hum Mutat 13:464-75. 1999
  5. ncbi Assessing TP53 status in human tumours to evaluate clinical outcome
    T Soussi
    Institut Curie, Universite P and M Curie, Laboratoire de Génotoxicologie des tumeurs, Paris, France
    Nat Rev Cancer 1:233-40. 2001
  6. ncbi Software and database for the analysis of mutations in the human LDL receptor gene
    M Varret
    INSERM U383, Hopital Necker Enfants Malades, Universite Rene Descartes, Paris V, 149 161 Rue de Sèvres, 75743 Paris Cedex 15, France
    Nucleic Acids Res 25:172-80. 1997
  7. ncbi Software and database for the analysis of mutations in the human WT1 gene
    C Jeanpierre
    INSERM U383, Hopital Necker Enfants Malades, Universite Rene Descartes, Paris V, 149 rue de Sevres, 75743 Paris Cedex 15, France
    Nucleic Acids Res 26:271-4. 1998
  8. ncbi Candidate genetic modifiers of individual susceptibility to renal cell carcinoma: a study of polymorphic human xenobiotic-metabolizing enzymes
    S Longuemaux
    Institut National de la Santé et de la Recherche Médicale U458, Hopital Robert Debre, Paris, France
    Cancer Res 59:2903-8. 1999
  9. ncbi Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene
    G Collod-Beroud
    INSERM U383, Hopital Necker Enfants Malades, Universite Rene Descartes, Paris V, 149 161 Rue de Sèvres, 75743 Paris Cedex 15, France
    Nucleic Acids Res 25:147-50. 1997
  10. ncbi Software and database for the analysis of mutations in the human FBN1 gene
    G Collod
    INSERM U383, Hopital Necker Enfants Malades, Universite Rene Descartes, Paris, France
    Nucleic Acids Res 24:137-40. 1996

Collaborators

Detail Information

Publications12

  1. ncbi [Molecular diagnostic techniques in oncogenetics]
    C Beroud
    Unité INSERM 383, Hopital Necker, 149, rue de Sevres, 75743 Paris Cedex 15, France
    Ann Med Interne (Paris) 152:326-31. 2001
    ..A few definitions Exploration methods (unknown mutations) Diagnostic methods (known mutations) New technologies and perspectives What should be done when no mutation can be identified? Research strategies in oncogenitics..
  2. ncbi UMD (Universal mutation database): a generic software to build and analyze locus-specific databases
    C Beroud
    INSERM U383, Hopital Necker Enfants Malades, Clinique Maurice Lamy, Paris, France
    Hum Mutat 15:86-94. 2000
    ..Four new LSDBs are under construction (VLCAD, MCAD, KIR6, and COL4A5). Finally, the data can be transferred to core databases...
  3. ncbi Software and database for the analysis of mutations in the VHL gene
    C Beroud
    INSERM U383, Hopital Necker Enfants Malades, Universite Rene Descartes Paris V, Paris, France
    Nucleic Acids Res 26:256-8. 1998
    ..The current database and the analysis software are accessible via the internet and world wide web interface at the URL:http://www.umd.necker.fr..
  4. ncbi Mutations of the VHL gene in sporadic renal cell carcinoma: definition of a risk factor for VHL patients to develop an RCC
    C Gallou
    INSERM U383, Hopital Necker Enfants Malades, Paris, France
    Hum Mutat 13:464-75. 1999
    ..05). Thus, mutations resulting in truncated proteins may lead to a higher risk of RCC in VHL patients...
  5. ncbi Assessing TP53 status in human tumours to evaluate clinical outcome
    T Soussi
    Institut Curie, Universite P and M Curie, Laboratoire de Génotoxicologie des tumeurs, Paris, France
    Nat Rev Cancer 1:233-40. 2001
    ..What simple steps can be taken to ensure that patients benefit from our understanding of TP53?..
  6. ncbi Software and database for the analysis of mutations in the human LDL receptor gene
    M Varret
    INSERM U383, Hopital Necker Enfants Malades, Universite Rene Descartes, Paris V, 149 161 Rue de Sèvres, 75743 Paris Cedex 15, France
    Nucleic Acids Res 25:172-80. 1997
    ..To facilitate the mutational analysis of the LDLR gene, and promote the analysis of the relationship between genotype and phenotype, a software package along with a computerized database (currently listing 210 entries) have been created...
  7. ncbi Software and database for the analysis of mutations in the human WT1 gene
    C Jeanpierre
    INSERM U383, Hopital Necker Enfants Malades, Universite Rene Descartes, Paris V, 149 rue de Sevres, 75743 Paris Cedex 15, France
    Nucleic Acids Res 26:271-4. 1998
    ..To facilitate the genotype-phenotype correlation analyses, we have created a software package along with a computerized database of germline (70 entries) and somatic (28 entries) mutations reported in the literature...
  8. ncbi Candidate genetic modifiers of individual susceptibility to renal cell carcinoma: a study of polymorphic human xenobiotic-metabolizing enzymes
    S Longuemaux
    Institut National de la Santé et de la Recherche Médicale U458, Hopital Robert Debre, Paris, France
    Cancer Res 59:2903-8. 1999
    ..These positive findings suggest that interindividual variation in the metabolic pathways involved in the functionalization and detoxification of specific xenobiotics is an important susceptibility factor for RCC in Caucasians...
  9. ncbi Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene
    G Collod-Beroud
    INSERM U383, Hopital Necker Enfants Malades, Universite Rene Descartes, Paris V, 149 161 Rue de Sèvres, 75743 Paris Cedex 15, France
    Nucleic Acids Res 25:147-50. 1997
    ..The second version of the computerized Marfan database contains 89 entries. The software has been modified to accomodate new functions and routines...
  10. ncbi Software and database for the analysis of mutations in the human FBN1 gene
    G Collod
    INSERM U383, Hopital Necker Enfants Malades, Universite Rene Descartes, Paris, France
    Nucleic Acids Res 24:137-40. 1996
    ..To facilitate mutational analysis of the FBN1 gene, a software package along with a computerized database (currently listing 63 entries) have been created...
  11. ncbi p53 website and analysis of p53 gene mutations in human cancer: forging a link between epidemiology and carcinogenesis
    T Soussi
    Institut Curie, UMR 218 CNRS, Paris, France
    Hum Mutat 15:105-13. 2000
    ..This software includes an optimized structure to assist and secure data entry and to allow the input of various clinical data...
  12. ncbi Isolation of kidney complementary DNAs down-expressed in Wilms' tumor by a subtractive hybridization approach
    E Austruy
    INSERM U73, Chateau de Longchamp, Paris, France
    Cancer Res 53:2888-94. 1993
    ..We propose that these clones could be helpful for an improved histological characterization of Wilms' tumors...