Pages that link to "Q56953402"
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The following pages link to Shannon K McDonnell (Q56953402):
Displaying 50 items.
- Genome-wide transcriptional profiling reveals microRNA-correlated genes and biological processes in human lymphoblastoid cell lines (Q21143768) (← links)
- No association of germline alteration of MSR1 with prostate cancer risk (Q28205246) (← links)
- Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types (Q28388497) (← links)
- Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer (Q28943505) (← links)
- Identification of seven new prostate cancer susceptibility loci through a genome-wide association study (Q29417022) (← links)
- Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study (Q29417074) (← links)
- Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array (Q29417155) (← links)
- Multiple novel prostate cancer predisposition loci confirmed by an international study: the PRACTICAL Consortium (Q30491647) (← links)
- Multiple genetic variant association testing by collapsing and kernel methods with pedigree or population structured data (Q30621608) (← links)
- Detecting genomic clustering of risk variants from sequence data: cases versus controls. (Q30654520) (← links)
- Identification of candidate genes for prostate cancer-risk SNPs utilizing a normal prostate tissue eQTL data set (Q31028555) (← links)
- Linkage analysis using principal components of gene expression data. (Q31154947) (← links)
- The genetics of gene expression: comparison of linkage scans using two phenotype normalization methods (Q33332867) (← links)
- Comparison of tagging single-nucleotide polymorphism methods in association analyses (Q33333026) (← links)
- Assessment of genotype imputation methods (Q33519327) (← links)
- Single versus multiple imputation for genotypic data. (Q33519363) (← links)
- Estimation of genotype relative risks from pedigree data by retrospective likelihoods (Q33521055) (← links)
- A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics (Q34015399) (← links)
- Regression models for linkage heterogeneity applied to familial prostate cancer (Q34020676) (← links)
- Genome-wide linkage analyses of hereditary prostate cancer families with colon cancer provide further evidence for a susceptibility locus on 15q11-q14. (Q34065183) (← links)
- Mutational landscape of candidate genes in familial prostate cancer (Q34079517) (← links)
- Family-based association analysis of 42 hereditary prostate cancer families identifies the Apolipoprotein L3 region on chromosome 22q12 as a risk locus (Q34112200) (← links)
- Analysis of the prostate cancer-susceptibility locus HPC20 in 172 families affected by prostate cancer (Q34113343) (← links)
- Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families (Q34308746) (← links)
- Incidence of progressive supranuclear palsy and multiple system atrophy in Olmsted County, Minnesota, 1976 to 1990 (Q34446721) (← links)
- Hysterectomy, menopause, and estrogen use preceding Parkinson's disease: an exploratory case-control study. (Q34464847) (← links)
- Head trauma preceding PD: a case-control study. (Q35138182) (← links)
- A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer (Q35248192) (← links)
- Multiple novel prostate cancer susceptibility signals identified by fine-mapping of known risk loci among Europeans (Q35646703) (← links)
- Comprehensively evaluating cis-regulatory variation in the human prostate transcriptome by using gene-level allele-specific expression (Q35689802) (← links)
- How well do whole exome sequencing results correlate with medical findings? A study of 89 Mayo Clinic Biobank samples (Q35884217) (← links)
- Associations of prostate cancer risk variants with disease aggressiveness: results of the NCI-SPORE Genetics Working Group analysis of 18,343 cases (Q36100579) (← links)
- Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia (Q36141922) (← links)
- Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for Prostate Cancer Genetics using novel sumLINK and sumLOD analyses (Q36190531) (← links)
- A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease (Q36477652) (← links)
- HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG). (Q36503369) (← links)
- 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) (Q36503573) (← links)
- Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG (Q36599631) (← links)
- Common variants within 6p21.31 locus are associated with chronic lymphocytic leukaemia and, potentially, other non-Hodgkin lymphoma subtypes (Q36734692) (← links)
- Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation (Q36792641) (← links)
- Identification of novel variants in colorectal cancer families by high-throughput exome sequencing (Q36991821) (← links)
- Experimental designs for array comparative genomic hybridization technology (Q37058063) (← links)
- Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics (Q37121925) (← links)
- Dense genome-wide SNP linkage scan in 301 hereditary prostate cancer families identifies multiple regions with suggestive evidence for linkage (Q37166267) (← links)
- Searching for epistasis and linkage heterogeneity by correlations of pedigree-specific linkage scores (Q37172187) (← links)
- Mutations in CHEK2 associated with prostate cancer risk (Q37219438) (← links)
- REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants (Q37342106) (← links)
- Analysis of the RNASEL gene in familial and sporadic prostate cancer (Q37361805) (← links)
- Germline miRNA DNA variants and the risk of colorectal cancer by subtype. (Q37594185) (← links)
- 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 (Q37623732) (← links)