Lista de obras -

A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics

artículo científico publicado en 2005

A multigenic approach to evaluating prostate cancer risk in a systematic replication study

artículo científico publicado en 2008

A polymorphism in the CDKN1B gene is associated with increased risk of hereditary prostate cancer

artículo científico publicado en 2004

Association between two unlinked loci at 8q24 and prostate cancer risk among European Americans

artículo científico publicado en 2007

Association of prostate cancer risk variants with clinicopathologic characteristics of the disease

artículo científico publicado en 2008

Associations between hOGG1 sequence variants and prostate cancer susceptibility

artículo científico publicado en 2002

Common sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk

artículo científico publicado en 2003

Comprehensive assessment of DNA copy number alterations in human prostate cancers using Affymetrix 100K SNP mapping array

artículo científico publicado en 2006

DNA copy number alterations in prostate cancers: a combined analysis of published CGH studies

artículo científico publicado en 2007

Evaluation of DLC1 as a prostate cancer susceptibility gene: mutation screen and association study

artículo científico publicado en 2003

Evaluation of SRD5A2 sequence variants in susceptibility to hereditary and sporadic prostate cancer ⬇️

artículo científico publicado el 15 de junio de 2003

Evidence for a general cancer susceptibility locus at 3p24 in families with hereditary prostate cancer

artículo científico publicado en 2005

Evidence for two independent prostate cancer risk-associated loci in the HNF1B gene at 17q12

artículo científico publicado en 2008

Fine mapping association study and functional analysis implicate a SNP in MSMB at 10q11 as a causal variant for prostate cancer risk

scientific article published on 19 January 2009

Genetic variability in inflammation pathways and prostate cancer risk

artículo científico publicado en 2007

Genetic variants and family history predict prostate cancer similar to prostate-specific antigen

artículo científico publicado en 2009

Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk

artículo científico publicado en 2002

Homozygous deletions and recurrent amplifications implicate new genes involved in prostate cancer

artículo científico publicado en 2008

Identification of new differentially methylated genes that have potential functional consequences in prostate cancer

artículo científico publicado en 2012

Inherited genetic markers discovered to date are able to identify a significant number of men at considerably elevated risk for prostate cancer

artículo científico publicado en 2010

Interactions of sequence variants in interleukin-1 receptor-associated kinase4 and the toll-like receptor 6-1-10 gene cluster increase prostate cancer risk

artículo científico publicado en 2006

Joint effect of HSD3B1 and HSD3B2 genes is associated with hereditary and sporadic prostate cancer susceptibility

scientific article published on 01 March 2002

Polymorphic GGC repeats in the androgen receptor gene are associated with hereditary and sporadic prostate cancer risk

scientific article published on 23 January 2002

Polymorphisms in the CYP1A1 gene are associated with prostate cancer risk

artículo científico publicado en 2003

Pooled genome linkage scan of aggressive prostate cancer: results from the International Consortium for Prostate Cancer Genetics

artículo científico publicado en 2006

Potential impact of adding genetic markers to clinical parameters in predicting prostate biopsy outcomes in men following an initial negative biopsy: findings from the REDUCE trial

artículo científico publicado en 2012

Prostate cancer risk associated loci in African Americans

scientific article published on 23 June 2009

Sequence variants at 22q13 are associated with prostate cancer risk

scientific article published on January 2009

Sequence variants of alpha-methylacyl-CoA racemase are associated with prostate cancer risk

artículo científico publicado en 2002

Sequence variants of toll-like receptor 4 are associated with prostate cancer risk: results from the CAncer Prostate in Sweden Study

artículo científico publicado en 2004

The interaction of four genes in the inflammation pathway significantly predicts prostate cancer risk

artículo científico publicado en 2005

Two independent prostate cancer risk-associated Loci at 11q13

artículo científico publicado en 2009

Lista de obras de

A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics

A multigenic approach to evaluating prostate cancer risk in a systematic replication study

A polymorphism in the CDKN1B gene is associated with increased risk of hereditary prostate cancer

Association between two unlinked loci at 8q24 and prostate cancer risk among European Americans

Association of prostate cancer risk variants with clinicopathologic characteristics of the disease

Associations between hOGG1 sequence variants and prostate cancer susceptibility

Common sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk

Comprehensive assessment of DNA copy number alterations in human prostate cancers using Affymetrix 100K SNP mapping array

DNA copy number alterations in prostate cancers: a combined analysis of published CGH studies

Evaluation of DLC1 as a prostate cancer susceptibility gene: mutation screen and association study

Evaluation of SRD5A2 sequence variants in susceptibility to hereditary and sporadic prostate cancer ⬇️

Evidence for a general cancer susceptibility locus at 3p24 in families with hereditary prostate cancer

Evidence for two independent prostate cancer risk-associated loci in the HNF1B gene at 17q12

Fine mapping association study and functional analysis implicate a SNP in MSMB at 10q11 as a causal variant for prostate cancer risk

Genetic variability in inflammation pathways and prostate cancer risk

Genetic variants and family history predict prostate cancer similar to prostate-specific antigen

Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk

Homozygous deletions and recurrent amplifications implicate new genes involved in prostate cancer

Identification of new differentially methylated genes that have potential functional consequences in prostate cancer

Inherited genetic markers discovered to date are able to identify a significant number of men at considerably elevated risk for prostate cancer

Interactions of sequence variants in interleukin-1 receptor-associated kinase4 and the toll-like receptor 6-1-10 gene cluster increase prostate cancer risk

Joint effect of HSD3B1 and HSD3B2 genes is associated with hereditary and sporadic prostate cancer susceptibility

Polymorphic GGC repeats in the androgen receptor gene are associated with hereditary and sporadic prostate cancer risk

Polymorphisms in the CYP1A1 gene are associated with prostate cancer risk

Pooled genome linkage scan of aggressive prostate cancer: results from the International Consortium for Prostate Cancer Genetics

Potential impact of adding genetic markers to clinical parameters in predicting prostate biopsy outcomes in men following an initial negative biopsy: findings from the REDUCE trial

Prostate cancer risk associated loci in African Americans

Sequence variants at 22q13 are associated with prostate cancer risk

Sequence variants of alpha-methylacyl-CoA racemase are associated with prostate cancer risk

Sequence variants of toll-like receptor 4 are associated with prostate cancer risk: results from the CAncer Prostate in Sweden Study

The interaction of four genes in the inflammation pathway significantly predicts prostate cancer risk

Two independent prostate cancer risk-associated Loci at 11q13