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

Journal of shoulder and elbow surgery, 2016-02, Vol.25 (2), p.174-179

2016

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Evidence for pelvic organ prolapse predisposition genes on chromosomes 10 and 17

American journal of obstetrics and gynecology, 2015-06, Vol.212 (6), p.771.e1-771.e7

2015

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Erratum to “Genome-wide association study for rotator cuff tears identifies two significant single-nucleotide polymorphisms” [J Shoulder Elbow Surg 2016;25:174-179]

Journal of shoulder and elbow surgery, 2016-10, Vol.25 (10), p.1731-1731

2016

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Increased risk for other cancers in individuals with Ewing sarcoma and their relatives

Cancer medicine (Malden, MA), 2019-12, Vol.8 (18), p.7924-7930

2019

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Relative risk for Alzheimer disease based on complete family history

Neurology, 2019-04, Vol.92 (15), p.e1745

2019

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Replication of the 10q11 and Xp11 Prostate Cancer Risk Variants: Results from a Utah Pedigree-Based Study

Cancer epidemiology, biomarkers & prevention, 2009-04, Vol.18 (4), p.1290-1294

2009

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

BMC genomics, 2012-11, Vol.13 (1), p.676-676, Article 676

2012

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A Nonsynonymous Variant in the GOLM1 Gene in Cutaneous Malignant Melanoma

JNCI : Journal of the National Cancer Institute, 2018-12, Vol.110 (12), p.1380-1385

2018

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A population‐based study of testicular cancer risk among children and young adults from Norway and Utah, USA

International journal of cancer, 2020-09, Vol.147 (6), p.1604-1611

2020

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Population-based risks for cancer in patients with ALS

Neurology, 2016-07, Vol.87 (3), p.289-294

2016

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Comorbidity and Cancer Disease Rates among Those at High-Risk for Alzheimer's Disease: A Population Database Analysis

International journal of environmental research and public health, 2022-12, Vol.19 (24), p.16419

2022

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

Journal of bone and joint surgery. American volume, 2009-05, Vol.91 (5), p.1136-1142

2009

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Germline Variant in SLCO2B1 and Response to Abiraterone Acetate Plus Prednisone (AA) in New-onset Metastatic Castration-resistant Prostate Cancer (mCRPC)

Molecular cancer therapeutics, 2019-03, Vol.18 (3), p.726-729

2019

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Similar survival of patients with multiple versus single primary melanomas based on Utah Surveillance, Epidemiology, and End Results data (1973-2011)

Journal of the American Academy of Dermatology, 2018-08, Vol.79 (2), p.238-244

2018

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Inherited Variants in SULT1E1 and Response to Abiraterone Acetate in Men with Metastatic Castration Refractory Prostate Cancer

The Journal of urology, 2016-10, Vol.196 (4), p.1112-1116

2016

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Genome-wide analysis of high-risk primary brain cancer pedigrees identifies PDXDC1 as a candidate brain cancer predisposition gene

Neuro-oncology (Charlottesville, Va.), 2021-02, Vol.23 (2), p.277-283

2021

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Colorectal cancer risk based on extended family history and body mass index

Genetic epidemiology, 2020-10, Vol.44 (7), p.778-784

2020

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

Obstetrics and gynecology (New York. 1953), 2011-12, Vol.118 (6), p.1345-1353

2011

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Genome-wide linkage analysis in Spanish melanoma-prone families identifies a new familial melanoma susceptibility locus at 11q

European journal of human genetics : EJHG, 2018-08, Vol.26 (8), p.1188-1193

2018

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Significant Linkage Evidence for a Predisposition Gene for Pelvic Floor Disorders on Chromosome 9q21

American journal of human genetics, 2009-05, Vol.84 (5), p.678-682

2009

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Identification of specific Y chromosomes associated with increased prostate cancer risk

The Prostate, 2014-06, Vol.74 (9), p.991-998

2014

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No evidence of BRCA2 mutations in chromosome 13q-linked Utah high-risk prostate cancer pedigrees

BMC research notes, 2009-05, Vol.2 (1), p.94-94

2009

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Linkage Analysis of Extended High-Risk Pedigrees Replicates a Cutaneous Malignant Melanoma Predisposition Locus on Chromosome 9q21

Journal of investigative dermatology, 2013-01, Vol.133 (1), p.128-134

2013

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

Orthopaedic journal of sports medicine, 2016-04, Vol.4 (4), p.2325967116642173-2325967116642173

2016

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Localization of a prostate cancer predisposition gene to an 880-kb region on chromosome 22q12.3 in utah high-risk pedigrees

Cancer research (Chicago, Ill.), 2006-10, Vol.66 (20), p.10205-10212

2006

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

Evidence for pelvic organ prolapse predisposition genes on chromosomes 10 and 17

Erratum to “Genome-wide association study for rotator cuff tears identifies two significant single-nucleotide polymorphisms” [J Shoulder Elbow Surg 2016;25:174-179]

Increased risk for other cancers in individuals with Ewing sarcoma and their relatives

Relative risk for Alzheimer disease based on complete family history

Replication of the 10q11 and Xp11 Prostate Cancer Risk Variants: Results from a Utah Pedigree-Based Study

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

A Nonsynonymous Variant in the GOLM1 Gene in Cutaneous Malignant Melanoma

A population‐based study of testicular cancer risk among children and young adults from Norway and Utah, USA

Population-based risks for cancer in patients with ALS

Comorbidity and Cancer Disease Rates among Those at High-Risk for Alzheimer's Disease: A Population Database Analysis

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

Germline Variant in SLCO2B1 and Response to Abiraterone Acetate Plus Prednisone (AA) in New-onset Metastatic Castration-resistant Prostate Cancer (mCRPC)

Similar survival of patients with multiple versus single primary melanomas based on Utah Surveillance, Epidemiology, and End Results data (1973-2011)

Inherited Variants in SULT1E1 and Response to Abiraterone Acetate in Men with Metastatic Castration Refractory Prostate Cancer

Genome-wide analysis of high-risk primary brain cancer pedigrees identifies PDXDC1 as a candidate brain cancer predisposition gene

Colorectal cancer risk based on extended family history and body mass index

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

Genome-wide linkage analysis in Spanish melanoma-prone families identifies a new familial melanoma susceptibility locus at 11q

Significant Linkage Evidence for a Predisposition Gene for Pelvic Floor Disorders on Chromosome 9q21

Identification of specific Y chromosomes associated with increased prostate cancer risk

No evidence of BRCA2 mutations in chromosome 13q-linked Utah high-risk prostate cancer pedigrees

Linkage Analysis of Extended High-Risk Pedigrees Replicates a Cutaneous Malignant Melanoma Predisposition Locus on Chromosome 9q21

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

Localization of a prostate cancer predisposition gene to an 880-kb region on chromosome 22q12.3 in utah high-risk pedigrees

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