Lista de obras -

A Germline DNA Polymorphism Enhances Alternative Splicing of theKLF6Tumor Suppressor Gene and Is Associated with Increased Prostate Cancer Risk

article

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 novel prostate cancer susceptibility locus at 19q13

artículo científico publicado en 2009

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

artículo científico publicado en 2004

Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families ⬇️

artículo científico publicado el 19 de junio de 2012

Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease

artículo científico publicado en 2013

Association between sequence variants at 17q12 and 17q24.3 and prostate cancer risk in European and African Americans

artículo científico publicado en 2008

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

artículo científico publicado en 2007

Association of a germ-line copy number variation at 2p24.3 and risk for aggressive prostate cancer

artículo científico publicado en 2009

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

Chromosome 8q24 risk variants in hereditary and non-hereditary prostate cancer patients

artículo científico publicado en 2008

Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG

artículo científico publicado en 2011

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

artículo científico publicado en 2003

Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer

scientific journal article

Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics

artículo científico publicado en 2007

Cumulative effect of five genetic variants on prostate cancer risk in multiple study populations

artículo científico publicado en 2008

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

artículo científico publicado en 2003

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

artículo científico publicado en 2005

Evidence for a prostate cancer susceptibility locus on the X chromosome.

article

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

artículo científico publicado en 2008

Familial aggregation of bothersome benign prostatic hyperplasia symptoms

artículo científico publicado en 2003

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

Fine-mapping and family-based association analyses of prostate cancer risk variants at Xp11.

artículo científico publicado en 2009

Genetic factors influencing prostate cancer risk in Norwegian men.

artículo científico publicado en 2017

Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.

artículo científico publicado en 2016

Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.

artículo científico publicado en 2007

Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for Prostate Cancer Genetics using novel sumLINK and sumLOD analyses

artículo científico publicado en 2010

Genome-wide screen for prostate cancer susceptibility genes in men with clinically significant disease.

artículo científico publicado en 2005

Genome‐wide scan for prostate cancer susceptibility genes in the Johns Hopkins hereditary prostate cancer families ⬇️

artículo científico publicado el 1 de diciembre de 2003

Germ-line mutation of NKX3.1 cosegregates with hereditary prostate cancer and alters the homeodomain structure and function

artículo científico publicado en 2006

Germline ATBF1 mutations and prostate cancer risk

artículo científico publicado en 2006

Germline Mutations in ATM and BRCA1/2 Are Associated with Grade Reclassification in Men on Active Surveillance for Prostate Cancer

scientific article published on 08 October 2018

Germline Mutations in ATM and BRCA1/2 Distinguish Risk for Lethal and Indolent Prostate Cancer and are Associated with Early Age at Death

artículo científico publicado en 2016

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

artículo científico publicado en 2002

Germline mutations in HOXB13 and prostate-cancer risk

artículo científico publicado en 2012

Germline mutations in PPFIBP2 are associated with lethal prostate cancer

scientific article published on 24 July 2018

Germline sequence variants of the LZTS1 gene are associated with prostate cancer risk

artículo científico publicado en 2002

HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG).

artículo científico publicado en 2012

Human polymorphisms at long non-coding RNAs (lncRNAs) and association with prostate cancer risk

artículo científico publicado en 2011

Identification of a new prostate cancer susceptibility locus on chromosome 8q24.

artículo científico publicado en 2009

Individual and cumulative effect of prostate cancer risk-associated variants on clinicopathologic variables in 5,895 prostate cancer patients

artículo científico publicado en 2009

Inherited genetic variant predisposes to aggressive but not indolent prostate cancer

artículo científico publicado en 2010

Interaction effect of PTEN and CDKN1B chromosomal regions on prostate cancer linkage

artículo científico publicado en 2004

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

scientific article published on 01 March 2002

Large-scale fine mapping of the HNF1B locus and prostate cancer risk

artículo científico publicado en 2011

Mutational analysis of PINX1 in hereditary prostate cancer.

artículo científico publicado en 2004

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

Prostate cancer risk associated loci in African Americans

scientific article published on 23 June 2009

Rare Germline Pathogenic Mutations of DNA Repair Genes Are Most Strongly Associated with Grade Group 5 Prostate Cancer

scientific article published on 13 January 2020

Sequence variants at 22q13 are associated with prostate cancer risk

scientific article published on January 2009

Sequence variants in the human 25-hydroxyvitamin D3 1-alpha-hydroxylase (CYP27B1) gene are not associated with prostate cancer risk

artículo científico publicado en 2002

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

artículo científico publicado en 2002

Two genome-wide association studies of aggressive prostate cancer implicate putative prostate tumor suppressor gene DAB2IP

scientific article published on 11 December 2007

Two independent prostate cancer risk-associated Loci at 11q13

artículo científico publicado en 2009

Two-locus genome-wide linkage scan for prostate cancer susceptibility genes with an interaction effect

article

Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG)

artículo científico publicado en 2011

Lista de obras de

A Germline DNA Polymorphism Enhances Alternative Splicing of theKLF6Tumor Suppressor Gene and Is Associated with Increased Prostate Cancer Risk

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

A novel prostate cancer susceptibility locus at 19q13

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

Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families ⬇️

Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease

Association between sequence variants at 17q12 and 17q24.3 and prostate cancer risk in European and African Americans

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

Association of a germ-line copy number variation at 2p24.3 and risk for aggressive prostate cancer

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

Associations between hOGG1 sequence variants and prostate cancer susceptibility

Chromosome 8q24 risk variants in hereditary and non-hereditary prostate cancer patients

Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG

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

Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer

Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics

Cumulative effect of five genetic variants on prostate cancer risk in multiple study populations

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

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

Evidence for a prostate cancer susceptibility locus on the X chromosome.

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

Familial aggregation of bothersome benign prostatic hyperplasia symptoms

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

Fine-mapping and family-based association analyses of prostate cancer risk variants at Xp11.

Genetic factors influencing prostate cancer risk in Norwegian men.

Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.

Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.

Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for Prostate Cancer Genetics using novel sumLINK and sumLOD analyses

Genome-wide screen for prostate cancer susceptibility genes in men with clinically significant disease.

Genome‐wide scan for prostate cancer susceptibility genes in the Johns Hopkins hereditary prostate cancer families ⬇️

Germ-line mutation of NKX3.1 cosegregates with hereditary prostate cancer and alters the homeodomain structure and function

Germline ATBF1 mutations and prostate cancer risk

Germline Mutations in ATM and BRCA1/2 Are Associated with Grade Reclassification in Men on Active Surveillance for Prostate Cancer

Germline Mutations in ATM and BRCA1/2 Distinguish Risk for Lethal and Indolent Prostate Cancer and are Associated with Early Age at Death

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

Germline mutations in HOXB13 and prostate-cancer risk

Germline mutations in PPFIBP2 are associated with lethal prostate cancer

Germline sequence variants of the LZTS1 gene are associated with prostate cancer risk

HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG).

Human polymorphisms at long non-coding RNAs (lncRNAs) and association with prostate cancer risk

Identification of a new prostate cancer susceptibility locus on chromosome 8q24.

Individual and cumulative effect of prostate cancer risk-associated variants on clinicopathologic variables in 5,895 prostate cancer patients

Inherited genetic variant predisposes to aggressive but not indolent prostate cancer

Interaction effect of PTEN and CDKN1B chromosomal regions on prostate cancer linkage

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

Large-scale fine mapping of the HNF1B locus and prostate cancer risk

Mutational analysis of PINX1 in hereditary prostate cancer.

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

Prostate cancer risk associated loci in African Americans

Rare Germline Pathogenic Mutations of DNA Repair Genes Are Most Strongly Associated with Grade Group 5 Prostate Cancer

Sequence variants at 22q13 are associated with prostate cancer risk

Sequence variants in the human 25-hydroxyvitamin D3 1-alpha-hydroxylase (CYP27B1) gene are not associated with prostate cancer risk

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

Two genome-wide association studies of aggressive prostate cancer implicate putative prostate tumor suppressor gene DAB2IP

Two independent prostate cancer risk-associated Loci at 11q13

Two-locus genome-wide linkage scan for prostate cancer susceptibility genes with an interaction effect

Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG)