Published in J Bone Joint Surg Am on May 01, 2009
Evidence for an inherited predisposition to lumbar disc disease. J Bone Joint Surg Am (2011) 1.53
Empiric evidence for a genetic contribution to predisposition to surgical site infection. Wound Repair Regen (2013) 1.43
Significant evidence for a heritable contribution to cancer predisposition: a review of cancer familiality by site. BMC Cancer (2012) 1.18
Evidence for a heritable predisposition to Chronic Fatigue Syndrome. BMC Neurol (2011) 0.90
Evidence of an inherited predisposition for cervical spondylotic myelopathy. Spine (Phila Pa 1976) (2012) 0.89
Natural History of Rotator Cuff Disease and Implications on Management. Oper Tech Orthop (2015) 0.82
Strong evidence for a genetic contribution to late-onset Alzheimer's disease mortality: a population-based study. PLoS One (2013) 0.81
Use of a genealogical database demonstrates heritability of pulmonary fibrosis. Lung (2013) 0.81
A heritable predisposition to pituitary tumors. Pituitary (2010) 0.77
Incidence of familial tendon dysfunction in patients with full-thickness rotator cuff tears. Open Access J Sports Med (2014) 0.77
Evidence for an Environmental and Inherited Predisposition Contributing to the Risk for Global Tendinopathies or Compression Neuropathies in Patients With Rotator Cuff Tears. Orthop J Sports Med (2016) 0.76
Matrix Metalloproteases 1 and 3 Promoter Gene Polymorphism Is Associated With Rotator Cuff Tear. Clin Orthop Relat Res (2017) 0.75
Genetic and familial predisposition to rotator cuff disease: a systematic review. J Shoulder Elbow Surg (2017) 0.75
Rotator cuff tears: An evidence based approach. World J Orthop (2015) 0.75
CURRENT CONCEPTS ON THE GENETIC FACTORS IN ROTATOR CUFF PATHOLOGY AND FUTURE IMPLICATIONS FOR SPORTS PHYSICAL THERAPISTS. Int J Sports Phys Ther (2017) 0.75
Genetic analysis of low BMI phenotype in the Utah Population Database. PLoS One (2013) 0.75
Assessment and treatment strategies for rotator cuff tears. Shoulder Elbow (2014) 0.75
Specific exercises for subacromial pain. Acta Orthop (2017) 0.75
Linkage of early-onset familial breast cancer to chromosome 17q21. Science (1990) 16.21
Anterior acromioplasty for the chronic impingement syndrome in the shoulder: a preliminary report. J Bone Joint Surg Am (1972) 5.44
Abnormal findings on magnetic resonance images of asymptomatic shoulders. J Bone Joint Surg Am (1995) 5.27
The microvascular pattern of the rotator cuff. J Bone Joint Surg Br (1970) 3.48
Rotator-cuff changes in asymptomatic adults. The effect of age, hand dominance and gender. J Bone Joint Surg Br (1995) 3.25
The demographic and morphological features of rotator cuff disease. A comparison of asymptomatic and symptomatic shoulders. J Bone Joint Surg Am (2006) 3.19
Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus. Nat Genet (1994) 3.05
Evidence for a heritable predisposition to death due to influenza. J Infect Dis (2008) 2.94
Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22. Science (1992) 2.89
Age-related prevalence of rotator cuff tears in asymptomatic shoulders. J Shoulder Elbow Surg (1999) 2.87
Familial occurrence of coronary heart disease: effect of age at diagnosis. Am J Cardiol (1979) 1.91
Pathologic evidence of degeneration as a primary cause of rotator cuff tear. Clin Orthop Relat Res (2003) 1.60
Etiology and pathophysiology of tendon ruptures in sports. Scand J Med Sci Sports (1997) 1.49
A genealogical assessment of heritable predisposition to asthma mortality. Am J Respir Crit Care Med (2007) 1.25
Familiality of diabetes mellitus. Exp Clin Endocrinol Diabetes (2007) 1.24
The COL5A1 gene and Achilles tendon pathology. Scand J Med Sci Sports (2006) 1.22
The guanine-thymine dinucleotide repeat polymorphism within the tenascin-C gene is associated with achilles tendon injuries. Am J Sports Med (2005) 1.16
Genetic influences in the aetiology of tears of the rotator cuff. Sibling risk of a full-thickness tear. J Bone Joint Surg Br (2004) 1.15
Tendon and ligament injuries: the genetic component. Br J Sports Med (2007) 1.05
Contrast-enhanced ultrasound characterization of the vascularity of the rotator cuff tendon: age- and activity-related changes in the intact asymptomatic rotator cuff. J Shoulder Elbow Surg (2008) 1.04
Distribution of blood groups in patients with tendon rupture. An analysis of 832 cases. J Bone Joint Surg Br (1989) 1.00
Cholesteryl ester transfer protein (CETP) genetic variation and early onset of non-fatal myocardial infarction. Ann Hum Genet (2008) 0.95
ABO blood groups and musculoskeletal injuries. Injury (1992) 0.87
Genome-wide association study identifies three loci associated with melanoma risk. Nat Genet (2009) 3.89
Genome-wide association study identifies three new melanoma susceptibility loci. Nat Genet (2011) 2.29
HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG). Hum Genet (2012) 2.18
A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics. Am J Hum Genet (2005) 1.96
Shared predispositions of parkinsonism and cancer: a population-based pedigree-linked study. Arch Neurol (2012) 1.87
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia. Nat Genet (2013) 1.85
Pooled genome linkage scan of aggressive prostate cancer: results from the International Consortium for Prostate Cancer Genetics. Hum Genet (2006) 1.70
Population-based family history-specific risks for colorectal cancer: a constellation approach. Gastroenterology (2009) 1.61
A genealogical assessment of heritable predisposition to aneurysms. J Neurosurg (2003) 1.60
Identification of excess clustering of coronary heart diseases among extended pedigrees in a genealogical population database. Am Heart J (2006) 1.60
Meta association of colorectal cancer confirms risk alleles at 8q24 and 18q21. Cancer Epidemiol Biomarkers Prev (2009) 1.60
The role of dual-degree programs in colleges and schools of pharmacy: the report of the 2008-09 Research and Graduate Affairs Committee. Am J Pharm Educ (2009) 1.57
Evidence for an inherited predisposition to lumbar disc disease. J Bone Joint Surg Am (2011) 1.53
Longitudinal assessment of the nevus phenotype in a melanoma kindred. J Invest Dermatol (2004) 1.44
Empiric evidence for a genetic contribution to predisposition to surgical site infection. Wound Repair Regen (2013) 1.43
Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium. Cancer Epidemiol Biomarkers Prev (2009) 1.29
A genealogical assessment of heritable predisposition to asthma mortality. Am J Respir Crit Care Med (2007) 1.25
Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics. Hum Mol Genet (2007) 1.20
Lobular breast cancer: excess familiality observed in the Utah Population Database. Int J Cancer (2005) 1.20
Significant evidence for a heritable contribution to cancer predisposition: a review of cancer familiality by site. BMC Cancer (2012) 1.18
Extracolonic cancers associated with hereditary nonpolyposis colorectal cancer in the Utah Population Database. Am J Gastroenterol (2006) 1.17
Significant linkage evidence for a predisposition gene for pelvic floor disorders on chromosome 9q21. Am J Hum Genet (2009) 1.16
Localization of a prostate cancer predisposition gene to an 880-kb region on chromosome 22q12.3 in Utah high-risk pedigrees. Cancer Res (2006) 1.16
Comparison of compliance for colorectal cancer screening and surveillance by colonoscopy based on risk. Genet Med (2011) 1.13
A role for XRCC2 gene polymorphisms in breast cancer risk and survival. J Med Genet (2011) 1.10
Genetic variants in XRCC2: new insights into colorectal cancer tumorigenesis. Cancer Epidemiol Biomarkers Prev (2009) 1.10
Genome-wide linkage analyses of extended Utah pedigrees identifies loci that influence recurrent, early-onset major depression and anxiety disorders. Am J Med Genet B Neuropsychiatr Genet (2005) 1.08
Familiality in brain tumors. Neurology (2008) 1.06
A comprehensive survey of cancer risks in extended families. Genet Med (2012) 1.06
Population-based prevalence of CDKN2A mutations in Utah melanoma families. J Invest Dermatol (2006) 1.05
Population-based analysis of prognostic factors and survival in familial melanoma. J Clin Oncol (2005) 1.04
Genomic search for prostate cancer predisposition loci in Utah pedigrees. Prostate (2005) 1.02
Evidence for a heritable component in death resulting from aortic and mitral valve diseases. Circulation (2004) 1.02
Identification of six loci associated with pelvic organ prolapse using genome-wide association analysis. Obstet Gynecol (2011) 0.98
A population-based description of familial clustering of pancreatic cancer. Clin Gastroenterol Hepatol (2010) 0.97
Characterization of linkage disequilibrium structure, mutation history, and tagging SNPs, and their use in association analyses: ELAC2 and familial early-onset prostate cancer. Genet Epidemiol (2005) 0.96
Statistical recombinant mapping in extended high-risk Utah pedigrees narrows the 8q24 prostate cancer locus to 2.0 Mb. Prostate (2007) 0.95
Familial myeloma. N Engl J Med (2008) 0.94
Fine-mapping CASP8 risk variants in breast cancer. Cancer Epidemiol Biomarkers Prev (2011) 0.94
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. Hum Genet (2013) 0.93
Replication of the 10q11 and Xp11 prostate cancer risk variants: results from a Utah pedigree-based study. Cancer Epidemiol Biomarkers Prev (2009) 0.93
Familial clustering of endometrial cancer in a well-defined population. Gynecol Oncol (2011) 0.92
Significant evidence for linkage to chromosome 5q13 in a genome-wide scan for asthma in an extended pedigree resource. Eur J Hum Genet (2008) 0.90
A role for XRCC4 in age at diagnosis and breast cancer risk. Cancer Epidemiol Biomarkers Prev (2006) 0.90
Evidence for a heritable predisposition to Chronic Fatigue Syndrome. BMC Neurol (2011) 0.90
Confirmation of chromosome 7q11 locus for predisposition to intracranial aneurysm. Hum Genet (2003) 0.90
A familial component to human rectal cancer, independent of colon cancer risk. Clin Gastroenterol Hepatol (2007) 0.90
Evidence of an inherited predisposition for cervical spondylotic myelopathy. Spine (Phila Pa 1976) (2012) 0.89
Population-based assessment of non-melanoma cancer risk in relatives of cutaneous melanoma probands. J Invest Dermatol (2006) 0.88
Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for Prostate Cancer Genetics using novel sumLINK and sumLOD analyses. Prostate (2010) 0.88
High-resolution characterization of linkage disequilibrium structure and selection of tagging single nucleotide polymorphisms: application to the cholesteryl ester transfer protein gene. Ann Hum Genet (2006) 0.85
Prostate cancer risk prediction based on complete prostate cancer family history. Prostate (2014) 0.84
Joint effects of common genetic variants from multiple genes and pathways on the risk of premature coronary artery disease. Am Heart J (2010) 0.83
A population-based analysis of clustering identifies a strong genetic contribution to lethal prostate cancer. Front Genet (2013) 0.83
Dissecting the genetic etiology of major depressive disorder using linkage analysis. Trends Mol Med (2005) 0.83
Examination of ELN as a candidate gene in the Utah intracranial aneurysm pedigrees. Stroke (2005) 0.82
The familiality of pelvic organ prolapse in the Utah Population Database. Int Urogynecol J (2012) 0.82
Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG. Prostate (2011) 0.81
Associations of ATR and CHEK1 single nucleotide polymorphisms with breast cancer. PLoS One (2013) 0.81
Failure to detect differences in proliferation status of nevi from CDKN2A mutation carriers and non-carriers. J Invest Dermatol (2002) 0.81
Strong evidence for a genetic contribution to late-onset Alzheimer's disease mortality: a population-based study. PLoS One (2013) 0.81
Co-prevalence of other tumors in patients harboring pituitary tumors. J Neurosurg (2014) 0.80
Multiple primary melanomas in a CDKN2A mutation carrier exposed to ionizing radiation. Arch Dermatol (2007) 0.80
Complex genotype sarcomas display familial inheritance independent of known cancer predisposition syndromes. Cancer Epidemiol Biomarkers Prev (2011) 0.80
A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twins. Hum Reprod (2010) 0.80
Increased melanocytic nevi and nevus density in a G-34T CDKN2A/p16 melanoma-prone pedigree. J Invest Dermatol (2008) 0.79
Extracting disease risk profiles from expression data for linkage analysis: application to prostate cancer. BMC Proc (2007) 0.79
How well does family history predict who will get colorectal cancer? Implications for cancer screening and counseling. Genet Med (2011) 0.79
A cautionary note on the appropriateness of using a linkage resource for an association study. BMC Genet (2003) 0.79
Utah Population Database: a tool to study the hereditary element of nonsyndromic neurosurgical diseases. Neurosurg Focus (2010) 0.78
Nevus distribution in a Utah melanoma kindred with a temperature-sensitive CDKN2A mutation. J Invest Dermatol (2005) 0.78
Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families. BMC Med Genet (2012) 0.76
Identification of specific Y chromosomes associated with increased prostate cancer risk. Prostate (2014) 0.75
The impact of family history on the risk of colorectal neoplasia: don't change the guidelines just yet! Dig Dis Sci (2012) 0.75
Linkage analysis of extended high-risk pedigrees replicates a cutaneous malignant melanoma predisposition locus on chromosome 9q21. J Invest Dermatol (2012) 0.75
Pairwise shared genomic segment analysis in three Utah high-risk breast cancer pedigrees. BMC Genomics (2012) 0.75
No evidence of BRCA2 mutations in chromosome 13q-linked Utah high-risk prostate cancer pedigrees. BMC Res Notes (2009) 0.75
A parallel genetic algorithm to discover patterns in genetic markers that indicate predisposition to multifactorial disease. Comput Biol Med (2008) 0.75
Corrigendum: Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients. Nat Commun (2015) 0.75