Lista de obras - Shannon K McDonnell - Dominio Público Uruguay

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 genetic risk score to personalize prostate cancer screening, applied to population data

scientific article published on 24 June 2020

A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer

artículo científico publicado en 2014

A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease

artículo científico publicado en 2012

Affected relative pairs and simultaneous search for two-locus linkage in the presence of epistasis

artículo científico publicado en 2007

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

artículo científico publicado en 2012

Analysis of the RNASEL gene in familial and sporadic prostate cancer

artículo científico publicado en 2002

Analysis of the prostate cancer-susceptibility locus HPC20 in 172 families affected by prostate cancer

artículo científico publicado en 2001

Assessment of genotype imputation methods

artículo científico publicado en 2009

Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

artículo científico publicado en 2018

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

Associations of prostate cancer risk variants with disease aggressiveness: results of the NCI-SPORE Genetics Working Group analysis of 18,343 cases

artículo científico publicado en 2015

Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation

artículo científico publicado en 2016

Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

scholarly article published in Nature Genetics

Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

scholarly article published in Nature Genetics

Case-control study of debrisoquine 4-hydroxylase, N-acetyltransferase 2, and apolipoprotein E gene polymorphisms in Parkinson's disease

artículo científico publicado en 2000

Case-control study of the extended tau gene haplotype in Parkinson's disease

article

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

scientific journal article

Common variants within 6p21.31 locus are associated with chronic lymphocytic leukaemia and, potentially, other non-Hodgkin lymphoma subtypes

artículo científico publicado en 2012

Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia

artículo científico publicado en 2012

Comparison of tagging single-nucleotide polymorphism methods in association analyses

artículo científico publicado en 2007

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

artículo científico publicado en 2007

Comprehensively evaluating cis-regulatory variation in the human prostate transcriptome by using gene-level allele-specific expression

artículo científico publicado en 2015

Conference Scene: Lessons learned from the 5th Statistical Analysis Workshop of the Pharmacogenetics Research Network

artículo científico publicado en 2010

Confirmation of a Positive Association between Prostate Cancer Risk and a Locus at Chromosome 8q24

artículo científico publicado en 2007

Dense genome-wide SNP linkage scan in 301 hereditary prostate cancer families identifies multiple regions with suggestive evidence for linkage

artículo científico publicado en 2009

Detecting genomic clustering of risk variants from sequence data: cases versus controls.

artículo científico publicado en 2013

Efficacy of Bilateral Prophylactic Mastectomy in Women with a Family History of Breast Cancer

article

Efficacy of bilateral prophylactic mastectomy in BRCA1 and BRCA2 gene mutation carriers

scientific article published on 01 November 2001

Efficacy of contralateral prophylactic mastectomy in women with a personal and family history of breast cancer

artículo científico publicado en 2001

Estimation of genotype relative risks from pedigree data by retrospective likelihoods

artículo científico publicado en 2010

Evaluation of Genetic Variations in the Androgen and Estrogen Metabolic Pathways as Risk Factors for Sporadic and Familial Prostate Cancer

artículo científico publicado en 2007

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

article

Experimental designs for array comparative genomic hybridization technology

artículo científico publicado en 2013

Family-based association analysis of 42 hereditary prostate cancer families identifies the Apolipoprotein L3 region on chromosome 22q12 as a risk locus ⬇️

artículo científico publicado en 2010

Fine mapping of familial prostate cancer families narrows the interval for a susceptibility locus on chromosome 22q12.3 to 1.36 Mb.

artículo científico publicado en 2007

Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants.

artículo científico publicado en 2018

Genome linkage screen for prostate cancer susceptibility loci: results from the Mayo Clinic Familial Prostate Cancer Study

artículo científico publicado en 2003

Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types

artículo científico publicado en 2016

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 of prostate cancer-specific survival

artículo científico publicado en 2015

Genome-wide linkage analyses of hereditary prostate cancer families with colon cancer provide further evidence for a susceptibility locus on 15q11-q14.

artículo científico publicado en 2010

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 linkage scan of prostate cancer Gleason score and confirmation of chromosome 19q

artículo científico publicado en 2007

Genome-wide transcriptional profiling reveals microRNA-correlated genes and biological processes in human lymphoblastoid cell lines

artículo científico publicado en 2009

Germline miRNA DNA variants and the risk of colorectal cancer by subtype.

artículo científico publicado en 2016

Gluthatione-S-transferase P1 polymorphism I105V in familial and sporadic prostate cancer

artículo científico publicado en 2004

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

artículo científico publicado en 2012

Head trauma preceding PD: a case-control study.

artículo científico publicado en 2003

How well do whole exome sequencing results correlate with medical findings? A study of 89 Mayo Clinic Biobank samples

artículo científico publicado en 2015

Hysterectomy, menopause, and estrogen use preceding Parkinson's disease: an exploratory case-control study.

artículo científico publicado en 2001

Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array

artículo científico publicado en 2013

Identification of candidate genes for prostate cancer-risk SNPs utilizing a normal prostate tissue eQTL data set

artículo científico publicado en 2015

Identification of novel variants in colorectal cancer families by high-throughput exome sequencing

artículo científico publicado en 2013

Identification of seven new prostate cancer susceptibility loci through a genome-wide association study

artículo científico publicado en 2009

Incidence of progressive supranuclear palsy and multiple system atrophy in Olmsted County, Minnesota, 1976 to 1990 ⬇️

artículo científico publicado el 1 de noviembre de 1997

Incorporating Functional Annotations for Fine-Mapping Causal Variants in a Bayesian Framework Using Summary Statistics.

artículo científico publicado en 2016

Lack of referral bias in genetic studies of prostate cancer

artículo científico publicado en 2002

Linkage analysis using principal components of gene expression data.

artículo científico publicado en 2007

Long-term satisfaction and psychological and social function following bilateral prophylactic mastectomy

artículo científico publicado en 2000

Luteinizing hormone beta polymorphism and risk of familial and sporadic prostate cancer.

artículo científico publicado en 2003

Microsatellite instability and 8p allelic imbalance in stage B2 and C colorectal cancers

scientific article published on 01 August 1999

Multiple genetic variant association testing by collapsing and kernel methods with pedigree or population structured data

artículo científico publicado en 2013

Multiple novel prostate cancer predisposition loci confirmed by an international study: the PRACTICAL Consortium

artículo científico publicado en 2008

Multiple novel prostate cancer susceptibility signals identified by fine-mapping of known risk loci among Europeans

artículo científico publicado en 2015

Mutational landscape of candidate genes in familial prostate cancer

artículo científico publicado en 2014

Mutations in CHEK2 associated with prostate cancer risk

artículo científico publicado en 2003

Network-directed cis-mediator analysis of normal prostate tissue expression profiles reveals downstream regulatory associations of prostate cancer susceptibility loci

artículo científico publicado en 2017

No association of germline alteration of MSR1 with prostate cancer risk

artículo científico publicado en 2003

Nonfatal cancer preceding Parkinson's disease: a case-control study

scientific article published on 01 March 2002

Pathologic characteristics of breast parenchyma in patients with hereditary breast carcinoma, including BRCA1 and BRCA2 mutation carriers

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

Post hoc Analysis for Detecting Individual Rare Variant Risk Associations Using Probit Regression Bayesian Variable Selection Methods in Case-Control Sequencing Studies

artículo científico publicado en 2016

Prediction of individual genetic risk to prostate cancer using a polygenic score

artículo científico publicado en 2015

Prostate cancer and genetic susceptibility: A genome scan incorporating disease aggressiveness

artículo científico publicado en 2006

REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants

artículo científico publicado en 2016

Regression models for linkage heterogeneity applied to familial prostate cancer

artículo científico publicado en 2001

Risk SNP-Mediated Promoter-Enhancer Switching Drives Prostate Cancer through lncRNA PCAT19

artículo científico publicado en 2018

Risk of Cognitive Impairment or Dementia in Relatives of Patients With Parkinson Disease

scientific article published on 01 October 2007

Risk of cancer after the diagnosis of Parkinson's disease: a historical cohort study

scientific article published on 01 June 2005

Risk tables for parkinsonism and Parkinson's disease.

artículo científico publicado en 2002

Role of the Nijmegen breakage syndrome 1 gene in familial and sporadic prostate cancer.

artículo científico publicado en 2006

Searching for epistasis and linkage heterogeneity by correlations of pedigree-specific linkage scores

artículo científico publicado en 2008

Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study

artículo científico publicado en 2011

Single versus multiple imputation for genotypic data.

artículo científico publicado en 2009

Smoking, alcohol, and coffee consumption preceding Parkinson's disease: a case-control study.

artículo científico publicado en 2000

Survival study of Parkinson disease in Olmsted County, Minnesota

artículo científico publicado en 2003

Targeted sequencing of 36 known or putative colorectal cancer susceptibility genes.

artículo científico publicado en 2017

The Mayo Clinic family study of Parkinson's disease: study design, instruments, and sample characteristics

artículo científico publicado en 2005

The genetics of gene expression: comparison of linkage scans using two phenotype normalization methods

artículo científico publicado en 2007

The neurologic complications of B-cell chronic lymphocytic leukemia

artículo científico publicado en 1997

Time trends in the incidence of parkinsonism in Olmsted County, Minnesota

scientific article published on 01 August 2001

Truncating variants in p53AIP1 disrupting DNA damage-induced apoptosis are associated with prostate cancer risk.

artículo científico publicado en 2006

Two Common Chromosome 8q24 Variants Are Associated with Increased Risk for Prostate Cancer

artículo científico publicado en 2007

Validation of a telephone questionnaire for Parkinson's disease.

artículo científico publicado en 1998

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

Whole exome sequencing in 75 high-risk families with validation and replication in independent case-control studies identifies TANGO2, OR5H14, and CHAD as new prostate cancer susceptibility genes

artículo científico publicado en 2016

gsSKAT: Rapid gene set analysis and multiple testing correction for rare-variant association studies using weighted linear kernels

artículo científico publicado en 2017

Lista de obras de Shannon K McDonnell

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 genetic risk score to personalize prostate cancer screening, applied to population data

A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer

A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease

Affected relative pairs and simultaneous search for two-locus linkage in the presence of epistasis

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

Analysis of the RNASEL gene in familial and sporadic prostate cancer

Analysis of the prostate cancer-susceptibility locus HPC20 in 172 families affected by prostate cancer

Assessment of genotype imputation methods

Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

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

Associations of prostate cancer risk variants with disease aggressiveness: results of the NCI-SPORE Genetics Working Group analysis of 18,343 cases

Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation

Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

Case-control study of debrisoquine 4-hydroxylase, N-acetyltransferase 2, and apolipoprotein E gene polymorphisms in Parkinson's disease

Case-control study of the extended tau gene haplotype in Parkinson's disease

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

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

Common variants within 6p21.31 locus are associated with chronic lymphocytic leukaemia and, potentially, other non-Hodgkin lymphoma subtypes

Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia

Comparison of tagging single-nucleotide polymorphism methods in association analyses

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

Comprehensively evaluating cis-regulatory variation in the human prostate transcriptome by using gene-level allele-specific expression

Conference Scene: Lessons learned from the 5th Statistical Analysis Workshop of the Pharmacogenetics Research Network

Confirmation of a Positive Association between Prostate Cancer Risk and a Locus at Chromosome 8q24

Dense genome-wide SNP linkage scan in 301 hereditary prostate cancer families identifies multiple regions with suggestive evidence for linkage

Detecting genomic clustering of risk variants from sequence data: cases versus controls.

Efficacy of Bilateral Prophylactic Mastectomy in Women with a Family History of Breast Cancer

Efficacy of bilateral prophylactic mastectomy in BRCA1 and BRCA2 gene mutation carriers

Efficacy of contralateral prophylactic mastectomy in women with a personal and family history of breast cancer

Estimation of genotype relative risks from pedigree data by retrospective likelihoods

Evaluation of Genetic Variations in the Androgen and Estrogen Metabolic Pathways as Risk Factors for Sporadic and Familial Prostate Cancer

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

Experimental designs for array comparative genomic hybridization technology

Family-based association analysis of 42 hereditary prostate cancer families identifies the Apolipoprotein L3 region on chromosome 22q12 as a risk locus ⬇️

Fine mapping of familial prostate cancer families narrows the interval for a susceptibility locus on chromosome 22q12.3 to 1.36 Mb.

Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants.

Genome linkage screen for prostate cancer susceptibility loci: results from the Mayo Clinic Familial Prostate Cancer Study

Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types

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

Genome-wide association study of prostate cancer-specific survival

Genome-wide linkage analyses of hereditary prostate cancer families with colon cancer provide further evidence for a susceptibility locus on 15q11-q14.

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 linkage scan of prostate cancer Gleason score and confirmation of chromosome 19q

Genome-wide transcriptional profiling reveals microRNA-correlated genes and biological processes in human lymphoblastoid cell lines

Germline miRNA DNA variants and the risk of colorectal cancer by subtype.

Gluthatione-S-transferase P1 polymorphism I105V in familial and sporadic prostate cancer

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

Head trauma preceding PD: a case-control study.

How well do whole exome sequencing results correlate with medical findings? A study of 89 Mayo Clinic Biobank samples

Hysterectomy, menopause, and estrogen use preceding Parkinson's disease: an exploratory case-control study.

Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array

Identification of candidate genes for prostate cancer-risk SNPs utilizing a normal prostate tissue eQTL data set

Identification of novel variants in colorectal cancer families by high-throughput exome sequencing

Identification of seven new prostate cancer susceptibility loci through a genome-wide association study

Incidence of progressive supranuclear palsy and multiple system atrophy in Olmsted County, Minnesota, 1976 to 1990 ⬇️

Incorporating Functional Annotations for Fine-Mapping Causal Variants in a Bayesian Framework Using Summary Statistics.

Lack of referral bias in genetic studies of prostate cancer

Linkage analysis using principal components of gene expression data.

Long-term satisfaction and psychological and social function following bilateral prophylactic mastectomy

Luteinizing hormone beta polymorphism and risk of familial and sporadic prostate cancer.

Microsatellite instability and 8p allelic imbalance in stage B2 and C colorectal cancers

Multiple genetic variant association testing by collapsing and kernel methods with pedigree or population structured data

Multiple novel prostate cancer predisposition loci confirmed by an international study: the PRACTICAL Consortium

Multiple novel prostate cancer susceptibility signals identified by fine-mapping of known risk loci among Europeans

Mutational landscape of candidate genes in familial prostate cancer

Mutations in CHEK2 associated with prostate cancer risk

Network-directed cis-mediator analysis of normal prostate tissue expression profiles reveals downstream regulatory associations of prostate cancer susceptibility loci

No association of germline alteration of MSR1 with prostate cancer risk

Nonfatal cancer preceding Parkinson's disease: a case-control study

Pathologic characteristics of breast parenchyma in patients with hereditary breast carcinoma, including BRCA1 and BRCA2 mutation carriers

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

Post hoc Analysis for Detecting Individual Rare Variant Risk Associations Using Probit Regression Bayesian Variable Selection Methods in Case-Control Sequencing Studies

Prediction of individual genetic risk to prostate cancer using a polygenic score

Prostate cancer and genetic susceptibility: A genome scan incorporating disease aggressiveness

REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants

Regression models for linkage heterogeneity applied to familial prostate cancer