Lista de obras - Craig Teerlink - Dominio Público Uruguay

A Genealogical Assessment of Heritable Predisposition to Asthma Mortality

artículo científico publicado en 2007

A comprehensive survey of cancer risks in extended families.

artículo científico publicado en 2012

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

A population-based description of familial clustering of Hirschsprung's disease.

artículo científico publicado en 2017

A role for the MEGF6 gene in predisposition to osteoporosis

artículo científico publicado en 2020

A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q.

artículo científico publicado en 2011

An application of the latent p value method to assess linkage in asthma pedigrees.

artículo científico publicado en 2010

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

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

artículo científico publicado en 2016

Erratum to "Significant association of full-thickness rotator cuff tears and estrogen-related receptor-β (ESRRB)" [J Shoulder Elbow Surg 2015;24:e31-e35].

artículo científico publicado en 2016

Evidence for an Environmental and Inherited Predisposition Contributing to the Risk for Global Tendinopathies or Compression Neuropathies in Patients With Rotator Cuff Tears

artículo científico publicado en 2016

Evidence for an inherited predisposition contributing to the risk for rotator cuff disease

artículo científico publicado en 2009

FANCM c5791C>T stopgain mutation (rs144567652) is a familial colorectal cancer risk factor

artículo científico publicado en 2020

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 for rotator cuff tears identifies two significant single-nucleotide polymorphisms

artículo científico publicado en 2015

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

artículo científico publicado en 2012

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

artículo científico publicado en 2013

Identification of a genetic variant associated with rotator cuff repair healing

artículo científico publicado en 2016

Identification of six loci associated with pelvic organ prolapse using genome-wide association analysis

artículo científico publicado en 2011

Identification of specific Y chromosomes associated with increased prostate cancer risk

artículo científico publicado en 2014

Linkage analysis of extended high-risk pedigrees replicates a cutaneous malignant melanoma predisposition locus on chromosome 9q21.

artículo científico publicado en 2012

Pairwise shared genomic segment analysis in three Utah high-risk breast cancer pedigrees

artículo científico publicado en 2012

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

Prostate cancer risk prediction based on complete prostate cancer family history

artículo científico publicado en 2014

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

artículo científico publicado en 2016

Significant association of full-thickness rotator cuff tears and estrogen-related receptor-β (ESRRB).

artículo científico publicado en 2014

Significant evidence for a heritable contribution to cancer predisposition: a review of cancer familiality by site

artículo científico publicado en 2012

Significant evidence for linkage to chromosome 5q13 in a genome-wide scan for asthma in an extended pedigree resource

artículo científico publicado en 2008

Significant evidence of linkage for a gene predisposing to colorectal cancer and multiple primary cancers on 22q11.

artículo científico publicado en 2014

Significant linkage evidence for a predisposition gene for pelvic floor disorders on chromosome 9q21.

artículo científico publicado en 2009

Treatment of herpes labialis: comparison of two OTC drugs and untreated controls.

artículo científico publicado en 2011

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

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 Craig Teerlink

A Genealogical Assessment of Heritable Predisposition to Asthma Mortality

A comprehensive survey of cancer risks in extended families.

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

A population-based description of familial clustering of Hirschsprung's disease.

A role for the MEGF6 gene in predisposition to osteoporosis

A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q.

An application of the latent p value method to assess linkage in asthma pedigrees.

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

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

Erratum to "Significant association of full-thickness rotator cuff tears and estrogen-related receptor-β (ESRRB)" [J Shoulder Elbow Surg 2015;24:e31-e35].

Evidence for an Environmental and Inherited Predisposition Contributing to the Risk for Global Tendinopathies or Compression Neuropathies in Patients With Rotator Cuff Tears

Evidence for an inherited predisposition contributing to the risk for rotator cuff disease

FANCM c5791C>T stopgain mutation (rs144567652) is a familial colorectal cancer risk factor

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

Genome-wide association study for rotator cuff tears identifies two significant single-nucleotide polymorphisms

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

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

Identification of a genetic variant associated with rotator cuff repair healing

Identification of six loci associated with pelvic organ prolapse using genome-wide association analysis

Identification of specific Y chromosomes associated with increased prostate cancer risk

Linkage analysis of extended high-risk pedigrees replicates a cutaneous malignant melanoma predisposition locus on chromosome 9q21.

Pairwise shared genomic segment analysis in three Utah high-risk breast cancer pedigrees

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

Prostate cancer risk prediction based on complete prostate cancer family history

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

Significant association of full-thickness rotator cuff tears and estrogen-related receptor-β (ESRRB).

Significant evidence for a heritable contribution to cancer predisposition: a review of cancer familiality by site

Significant evidence for linkage to chromosome 5q13 in a genome-wide scan for asthma in an extended pedigree resource

Significant evidence of linkage for a gene predisposing to colorectal cancer and multiple primary cancers on 22q11.

Significant linkage evidence for a predisposition gene for pelvic floor disorders on chromosome 9q21.

Treatment of herpes labialis: comparison of two OTC drugs and untreated controls.

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)

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