List of works - Daniel J. Schaid

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

scientific article

A comprehensive examination of CYP19 variation and risk of breast cancer using two haplotype-tagging approaches

scientific article

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

scientific article published on 14 September 2014

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

scientific article

A review of kernel methods for genetic association studies

scientific article published on 02 January 2019

A weighted U-statistic for genetic association analyses of sequencing data.

scientific article

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

scientific article published on June 19, 2012

Anticipation in familial Parkinson's disease: a reanalysis of 13 United Kingdom kindreds

scientific article published on December 1996

Application of sequential haplotype scan methods to case-control data

scientific article

Aromatase inhibitor-associated bone fractures: a case-cohort GWAS and functional genomics

scientific article

Associations between measles antibody levels and the protein structure of class II human leukocyte antigens.

scientific article published in July 2003

Citalopram and escitalopram plasma drug and metabolite concentrations: genome-wide associations

scientific article

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

scientific journal article

Comparison of microsatellites versus single-nucleotide polymorphisms in a genome linkage screen for prostate cancer-susceptibility Loci

scientific article

Complex segregation analysis of Parkinson's disease: The Mayo Clinic Family Study

scientific article published in May 2006

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

scientific article

Estimation of genotype relative risks from pedigree data by retrospective likelihoods

scientific article

Familial recurrence risk with varying amount of family history

scientific article published on 11 February 2019

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

scientific article

Fast and robust adjustment of cell mixtures in epigenome-wide association studies with SmartSVA

scientific article

Fine-mapping the HOXB region detects common variants tagging a rare coding allele: evidence for synthetic association in prostate cancer

scientific article

Genetic association with overall survival of taxane-treated lung cancer patients - a genome-wide association study in human lymphoblastoid cell lines followed by a clinical association study

scientific article

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

scientific article published in September 2016

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

scientific article

Genotype determination for polymorphisms in linkage disequilibrium

scientific article

Glutathione pathway genetic polymorphisms and lung cancer survival after platinum-based chemotherapy

scientific article

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

scientific article published on 12 October 2012

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

scientific article

Identifying single-nucleotide polymorphisms responsible for the linkage signal of rheumatoid arthritis on chromosome 6 by joint modeling of linkage and association

scientific article

Incorporating a Genetic Risk Score Into Coronary Heart Disease Risk Estimates: Effect on Low-Density Lipoprotein Cholesterol Levels (the MI-GENES Clinical Trial)

scientific article

Kernel methods for large-scale genomic data analysis

scientific article

Lessons learned in the analysis of high-dimensional data in vaccinomics

scientific article

Merging pharmacometabolomics with pharmacogenomics using '1000 Genomes' single-nucleotide polymorphism imputation: selective serotonin reuptake inhibitor response pharmacogenomics

scientific article

Methods to impute missing genotypes for population data

scientific article

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

scientific article

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

scientific article

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

scientific article published on 29 May 2015

Mutational landscape of candidate genes in familial prostate cancer

scientific article

Next generation analytic tools for large scale genetic epidemiology studies of complex diseases

scientific article

No association of germline alteration of MSR1 with prostate cancer risk

scientific article (publication date: October 2003)

Nonparametric tests of association of multiple genes with human disease

scientific article

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

scientific article published in December 2016

PedBLIMP: extending linear predictors to impute genotypes in pedigrees

scientific article

Penalized models for analysis of multiple mediators

scientific article published on 27 April 2020

Polymorphisms in mitochondrial genes and prostate cancer risk

scientific article

Regularized rare variant enrichment analysis for case-control exome sequencing data

scientific article

Robust multipoint identical-by-descent mapping for affected relative pairs

scientific article

Score tests for association between traits and haplotypes when linkage phase is ambiguous

scientific article (publication date: February 2002)

Testing genetic linkage with relative pairs and covariates by quasi-likelihood score statistics

scientific article

The impact of HLA-DRB1 genes on extra-articular disease manifestations in rheumatoid arthritis

scientific article

The kinship2 R package for pedigree data

scientific 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)

scientific article published on 25 December 2011

Variation in anastrozole metabolism and pharmacodynamics in women with early breast cancer

scientific article

List of works by Daniel J. Schaid

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

A comprehensive examination of CYP19 variation and risk of breast cancer using two haplotype-tagging approaches

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

A review of kernel methods for genetic association studies

A weighted U-statistic for genetic association analyses of sequencing data.

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

Anticipation in familial Parkinson's disease: a reanalysis of 13 United Kingdom kindreds

Application of sequential haplotype scan methods to case-control data

Aromatase inhibitor-associated bone fractures: a case-cohort GWAS and functional genomics

Associations between measles antibody levels and the protein structure of class II human leukocyte antigens.

Citalopram and escitalopram plasma drug and metabolite concentrations: genome-wide associations

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

Comparison of microsatellites versus single-nucleotide polymorphisms in a genome linkage screen for prostate cancer-susceptibility Loci

Complex segregation analysis of Parkinson's disease: The Mayo Clinic Family Study

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

Estimation of genotype relative risks from pedigree data by retrospective likelihoods

Familial recurrence risk with varying amount of family history

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

Fast and robust adjustment of cell mixtures in epigenome-wide association studies with SmartSVA

Fine-mapping the HOXB region detects common variants tagging a rare coding allele: evidence for synthetic association in prostate cancer

Genetic association with overall survival of taxane-treated lung cancer patients - a genome-wide association study in human lymphoblastoid cell lines followed by a clinical association 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 linkage analyses of hereditary prostate cancer families with colon cancer provide further evidence for a susceptibility locus on 15q11-q14.

Genotype determination for polymorphisms in linkage disequilibrium

Glutathione pathway genetic polymorphisms and lung cancer survival after platinum-based chemotherapy

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

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

Identifying single-nucleotide polymorphisms responsible for the linkage signal of rheumatoid arthritis on chromosome 6 by joint modeling of linkage and association

Incorporating a Genetic Risk Score Into Coronary Heart Disease Risk Estimates: Effect on Low-Density Lipoprotein Cholesterol Levels (the MI-GENES Clinical Trial)

Kernel methods for large-scale genomic data analysis

Lessons learned in the analysis of high-dimensional data in vaccinomics

Merging pharmacometabolomics with pharmacogenomics using '1000 Genomes' single-nucleotide polymorphism imputation: selective serotonin reuptake inhibitor response pharmacogenomics

Methods to impute missing genotypes for population data

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

Next generation analytic tools for large scale genetic epidemiology studies of complex diseases

No association of germline alteration of MSR1 with prostate cancer risk

Nonparametric tests of association of multiple genes with human disease

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

PedBLIMP: extending linear predictors to impute genotypes in pedigrees

Penalized models for analysis of multiple mediators

Polymorphisms in mitochondrial genes and prostate cancer risk

Regularized rare variant enrichment analysis for case-control exome sequencing data

Robust multipoint identical-by-descent mapping for affected relative pairs

Score tests for association between traits and haplotypes when linkage phase is ambiguous

Testing genetic linkage with relative pairs and covariates by quasi-likelihood score statistics

The impact of HLA-DRB1 genes on extra-articular disease manifestations in rheumatoid arthritis

The kinship2 R package for pedigree data

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)

Variation in anastrozole metabolism and pharmacodynamics in women with early breast cancer