Richard H Scott

Summary

Affiliation: Institute of Cancer Research
Country: UK

Publications

  1. ncbi request reprint Medulloblastoma, acute myelocytic leukemia and colonic carcinomas in a child with biallelic MSH6 mutations
    Richard H Scott
    Section of Cancer Genetics, Institute of Cancer Research, 15 Cotswold Road, Sutton, Surrey SM2 5NG, UK
    Nat Clin Pract Oncol 4:130-4. 2007
  2. pmc Familial T-cell non-Hodgkin lymphoma caused by biallelic MSH2 mutations
    Richard H Scott
    Section of Cancer Genetics, Institute of Cancer Research, 15 Cotswold Road, Sutton, Surrey, UK, SM2 5NG
    J Med Genet 44:e83. 2007
  3. doi request reprint A new familial cancer syndrome including predisposition to Wilms tumor and neuroblastoma
    Fatemeh Abbaszadeh
    Section of Cancer Genetics, Institute of Cancer Research, 15 Cotswold Road, Sutton, Surrey, SM2 5NG, UK
    Fam Cancer 9:425-30. 2010
  4. pmc Stratification of Wilms tumor by genetic and epigenetic analysis
    Richard H Scott
    Division of Genetics and Epidemiology, Institute of Cancer Research and Royal Marsden Hospital, Sutton, UK
    Oncotarget 3:327-35. 2012
  5. ncbi request reprint Cancer genes associated with phenotypes in monoallelic and biallelic mutation carriers: new lessons from old players
    Nazneen Rahman
    Section of Cancer Genetics, Institute of Cancer Research, Sutton, Surrey, UK
    Hum Mol Genet 16:R60-6. 2007
  6. pmc Chromosome 6p22 locus associated with clinically aggressive neuroblastoma
    John M Maris
    Division of Oncology and the Center for Childhood Cancer Research, Children s Hospital of Philadelphia, Philadelphia, PA 19104 4318, USA
    N Engl J Med 358:2585-93. 2008

Detail Information

Publications6

  1. ncbi request reprint Medulloblastoma, acute myelocytic leukemia and colonic carcinomas in a child with biallelic MSH6 mutations
    Richard H Scott
    Section of Cancer Genetics, Institute of Cancer Research, 15 Cotswold Road, Sutton, Surrey SM2 5NG, UK
    Nat Clin Pract Oncol 4:130-4. 2007
    ..It is important to consider this diagnosis in children presenting with malignancy and abnormal skin pigmentation, even in the absence of a strong family history of tumors...
  2. pmc Familial T-cell non-Hodgkin lymphoma caused by biallelic MSH2 mutations
    Richard H Scott
    Section of Cancer Genetics, Institute of Cancer Research, 15 Cotswold Road, Sutton, Surrey, UK, SM2 5NG
    J Med Genet 44:e83. 2007
    ....
  3. doi request reprint A new familial cancer syndrome including predisposition to Wilms tumor and neuroblastoma
    Fatemeh Abbaszadeh
    Section of Cancer Genetics, Institute of Cancer Research, 15 Cotswold Road, Sutton, Surrey, SM2 5NG, UK
    Fam Cancer 9:425-30. 2010
    ..Overall, these data suggest that families with both Wilms tumor and neuroblastoma represent a previously unrecognized familial cancer syndrome in which the underlying predisposition gene(s) remain to be determined...
  4. pmc Stratification of Wilms tumor by genetic and epigenetic analysis
    Richard H Scott
    Division of Genetics and Epidemiology, Institute of Cancer Research and Royal Marsden Hospital, Sutton, UK
    Oncotarget 3:327-35. 2012
    ..001). These data provide new insights into the pattern, order, interactions and clinical associations of molecular events in Wilms tumor...
  5. ncbi request reprint Cancer genes associated with phenotypes in monoallelic and biallelic mutation carriers: new lessons from old players
    Nazneen Rahman
    Section of Cancer Genetics, Institute of Cancer Research, Sutton, Surrey, UK
    Hum Mol Genet 16:R60-6. 2007
    ..These observations raise interesting implications with respect to the identification and phenotypic characterization of cancer predisposition genes...
  6. pmc Chromosome 6p22 locus associated with clinically aggressive neuroblastoma
    John M Maris
    Division of Oncology and the Center for Childhood Cancer Research, Children s Hospital of Philadelphia, Philadelphia, PA 19104 4318, USA
    N Engl J Med 358:2585-93. 2008
    ..Neuroblastoma is a malignant condition of the developing sympathetic nervous system that most commonly affects young children and is often lethal. Its cause is not known...