{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,17]],"date-time":"2026-08-17T19:03:21Z","timestamp":1786993401665,"version":"build-2736575974"},"reference-count":37,"publisher":"Elsevier BV","issue":"6","license":[{"start":{"date-parts":[[2017,6,1]],"date-time":"2017-06-01T00:00:00Z","timestamp":1496275200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":["clinicalkey.jp","clinicalkey.com","clinicalkey.es","jshoulderelbow.org","clinicalkey.com.au","clinicalkey.fr","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of Shoulder and Elbow Surgery"],"published-print":{"date-parts":[[2017,6]]},"DOI":"10.1016\/j.jse.2016.11.038","type":"journal-article","created":{"date-parts":[[2017,2,3]],"date-time":"2017-02-03T04:18:23Z","timestamp":1486095503000},"page":"1103-1112","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":47,"title":["Genetic and familial predisposition to rotator cuff disease: a systematic review"],"prefix":"10.1016","volume":"26","author":[{"given":"Dominique I.","family":"Dabija","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Chan","family":"Gao","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Todd L.","family":"Edwards","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"John E.","family":"Kuhn","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nitin B.","family":"Jain","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.jse.2016.11.038_bib0010","doi-asserted-by":"crossref","first-page":"780","DOI":"10.1002\/jor.22869","article-title":"Tendon basic science: development, repair, regeneration, and healing","volume":"33","author":"Andarawis-Puri","year":"2015","journal-title":"J Orthop Res"},{"key":"10.1016\/j.jse.2016.11.038_bib0015","doi-asserted-by":"crossref","first-page":"806","DOI":"10.1093\/hmg\/ddm352","article-title":"Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p","volume":"17","author":"Broadbent","year":"2008","journal-title":"Hum Mol Genet"},{"key":"10.1016\/j.jse.2016.11.038_bib0020","doi-asserted-by":"crossref","first-page":"102","DOI":"10.1016\/j.fertnstert.2011.04.032","article-title":"Involvement of estrogen receptor\u2013related receptors in human ovarian endometriosis","volume":"96","author":"Cavallini","year":"2011","journal-title":"Fertil Steril"},{"key":"10.1016\/j.jse.2016.11.038_bib0025","doi-asserted-by":"crossref","first-page":"191","DOI":"10.1016\/j.jse.2011.10.022","article-title":"Lessons we can learn from gene expression patterns in rotator cuff tears and tendinopathies","volume":"21","author":"Chaudhury","year":"2012","journal-title":"J Shoulder Elbow Surg"},{"key":"10.1016\/j.jse.2016.11.038_bib0030","doi-asserted-by":"crossref","first-page":"125","DOI":"10.1038\/ng1507","article-title":"Mutations in the gene encoding fibroblast growth factor 10 are associated with aplasia of lacrimal and salivary glands","volume":"37","author":"Entesarian","year":"2005","journal-title":"Nat Genet"},{"key":"10.1016\/j.jse.2016.11.038_bib0035","doi-asserted-by":"crossref","first-page":"915","DOI":"10.1302\/0301-620X.91B7.22353","article-title":"Genetic influences in the progression of tears of the rotator cuff","volume":"91","author":"Gwilym","year":"2009","journal-title":"J Bone Joint Surg Br"},{"key":"10.1016\/j.jse.2016.11.038_bib0040","doi-asserted-by":"crossref","first-page":"696","DOI":"10.1302\/0301-620X.86B5.14747","article-title":"Genetic influences in the aetiology of tears of the rotator cuff. Sibling risk of a full-thickness tear","volume":"86","author":"Harvie","year":"2004","journal-title":"J Bone Joint Surg Br"},{"key":"10.1016\/j.jse.2016.11.038_bib0045","doi-asserted-by":"crossref","first-page":"2240","DOI":"10.12659\/MSM.893453","article-title":"Association between genetic polymorphisms in DEFB1 and susceptibility to digestive diseases","volume":"21","author":"Huang","year":"2015","journal-title":"Med Sci Monit"},{"key":"10.1016\/j.jse.2016.11.038_bib0050","doi-asserted-by":"crossref","first-page":"4","DOI":"10.1186\/1471-2474-15-4","article-title":"Epidemiology of musculoskeletal upper extremity ambulatory surgery in the United States","volume":"15","author":"Jain","year":"2014","journal-title":"BMC Musculoskelet Disord"},{"key":"10.1016\/j.jse.2016.11.038_bib0055","doi-asserted-by":"crossref","first-page":"6131","DOI":"10.1073\/pnas.1318948111","article-title":"Defining functional DNA elements in the human genome","volume":"111","author":"Kellis","year":"2014","journal-title":"Proc Natl Acad Sci U S A"},{"key":"10.1016\/j.jse.2016.11.038_bib0060","doi-asserted-by":"crossref","first-page":"561","DOI":"10.1214\/09-STS290","article-title":"Replication in genome-wide association studies","volume":"24","author":"Kraft","year":"2009","journal-title":"Stat Sci"},{"key":"10.1016\/j.jse.2016.11.038_bib0065","doi-asserted-by":"crossref","first-page":"559","DOI":"10.1038\/ijo.2012.82","article-title":"Challenges in reproducibility of genetic association studies: lessons learned from the obesity field","volume":"37","author":"Li","year":"2013","journal-title":"Int J Obes"},{"key":"10.1016\/j.jse.2016.11.038_bib0070","doi-asserted-by":"crossref","first-page":"e1","DOI":"10.1016\/j.jclinepi.2009.06.006","article-title":"The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration","volume":"62","author":"Liberati","year":"2009","journal-title":"J Clin Epidemiol"},{"key":"10.1016\/j.jse.2016.11.038_bib0075","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1159\/000328868","article-title":"Epidemiology, genetics and biological factors of rotator cuff tears","volume":"57","author":"Longo","year":"2012","journal-title":"Med Sport Sci"},{"key":"10.1016\/j.jse.2016.11.038_bib0080","doi-asserted-by":"crossref","first-page":"2623","DOI":"10.2106\/JBJS.I.00506","article-title":"Symptomatic progression of asymptomatic rotator cuff tears: a prospective study of clinical and sonographic variables","volume":"92","author":"Mall","year":"2010","journal-title":"J Bone Joint Surg Am"},{"key":"10.1016\/j.jse.2016.11.038_bib0085","doi-asserted-by":"crossref","first-page":"296","DOI":"10.1302\/0301-620X.77B2.7706351","article-title":"Rotator-cuff changes in asymptomatic adults. The effect of age, hand dominance and gender","volume":"77","author":"Milgrom","year":"1995","journal-title":"J Bone Joint Surg Br"},{"key":"10.1016\/j.jse.2016.11.038_bib0090","doi-asserted-by":"crossref","first-page":"227","DOI":"10.1016\/j.jse.2013.07.053","article-title":"Evidence of genetic variations associated with rotator cuff disease","volume":"23","author":"Motta Gda","year":"2014","journal-title":"J Shoulder Elbow Surg"},{"key":"10.1016\/j.jse.2016.11.038_bib0095","doi-asserted-by":"crossref","first-page":"269","DOI":"10.1038\/ng1194-269","article-title":"A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome","volume":"8","author":"Muenke","year":"1994","journal-title":"Nat Genet"},{"key":"10.1016\/j.jse.2016.11.038_bib0100","first-page":"70","article-title":"Impingement lesions","author":"Neer","year":"1983","journal-title":"Clin Orthop Relat Res"},{"key":"10.1016\/j.jse.2016.11.038_bib0105","first-page":"9128","article-title":"Relevance of alpha-defensins (HNP1-3) and defensin beta-1 in diabetes","volume":"20","author":"Nemeth","year":"2014","journal-title":"World J Gastroenterol"},{"key":"10.1016\/j.jse.2016.11.038_bib0110","doi-asserted-by":"crossref","first-page":"666","DOI":"10.1093\/infdis\/jis735","article-title":"Impaired beta-defensin expression in human skin links DEFB1 promoter polymorphisms with persistent Staphylococcus aureus nasal carriage","volume":"207","author":"Nurjadi","year":"2013","journal-title":"J Infect Dis"},{"key":"10.1016\/j.jse.2016.11.038_bib0115","doi-asserted-by":"crossref","first-page":"4512","DOI":"10.1073\/pnas.0607956104","article-title":"Impaired FGF signaling contributes to cleft lip and palate","volume":"104","author":"Riley","year":"2007","journal-title":"Proc Natl Acad Sci U S A"},{"key":"10.1016\/j.jse.2016.11.038_bib0120","doi-asserted-by":"crossref","first-page":"1419","DOI":"10.1038\/sj.bjc.6603452","article-title":"Prognostic significance of downregulated expression of the candidate tumour suppressor gene SASH1 in colon cancer","volume":"95","author":"Rimkus","year":"2006","journal-title":"Br J Cancer"},{"key":"10.1016\/j.jse.2016.11.038_bib0125","doi-asserted-by":"crossref","first-page":"10","DOI":"10.2106\/00004623-199501000-00002","article-title":"Abnormal findings on magnetic resonance images of asymptomatic shoulders","volume":"77","author":"Sher","year":"1995","journal-title":"J Bone Joint Surg Am"},{"key":"10.1016\/j.jse.2016.11.038_bib0130","doi-asserted-by":"crossref","first-page":"712","DOI":"10.1046\/j.1445-2197.2003.02748.x","article-title":"Methodological index for non-randomized studies (minors): development and validation of a new instrument","volume":"73","author":"Slim","year":"2003","journal-title":"ANZ J Surg"},{"key":"10.1016\/j.jse.2016.11.038_bib0135","doi-asserted-by":"crossref","first-page":"367","DOI":"10.1534\/genetics.110.120907","article-title":"Progress and promise of genome-wide association studies for human complex trait genetics","volume":"187","author":"Stranger","year":"2011","journal-title":"Genetics"},{"key":"10.1016\/j.jse.2016.11.038_bib0140","doi-asserted-by":"crossref","first-page":"12332","DOI":"10.1074\/jbc.M114.619098","article-title":"Estrogen-related receptor beta reduces the subnuclear mobility of estrogen receptor alpha and suppresses estrogen-dependent cellular function","volume":"290","author":"Tanida","year":"2015","journal-title":"J Biol Chem"},{"key":"10.1016\/j.jse.2016.11.038_bib0145","doi-asserted-by":"crossref","first-page":"589","DOI":"10.1016\/j.csm.2012.07.001","article-title":"Epidemiology, natural history, and indications for treatment of rotator cuff tears","volume":"31","author":"Tashjian","year":"2012","journal-title":"Clin Sports Med"},{"key":"10.1016\/j.jse.2016.11.038_bib0150","doi-asserted-by":"crossref","first-page":"1136","DOI":"10.2106\/JBJS.H.00831","article-title":"Evidence for an inherited predisposition contributing to the risk for rotator cuff disease","volume":"91","author":"Tashjian","year":"2009","journal-title":"J Bone Joint Surg Am"},{"key":"10.1016\/j.jse.2016.11.038_bib0155","doi-asserted-by":"crossref","first-page":"174","DOI":"10.1016\/j.jse.2015.07.005","article-title":"Genome-wide association study for rotator cuff tears identifies two significant single-nucleotide polymorphisms","volume":"25","author":"Tashjian","year":"2016","journal-title":"J Shoulder Elbow Surg"},{"key":"10.1016\/j.jse.2016.11.038_bib0160","doi-asserted-by":"crossref","first-page":"137","DOI":"10.2147\/OAJSM.S63656","article-title":"Incidence of familial tendon dysfunction in patients with full-thickness rotator cuff tears","volume":"5","author":"Tashjian","year":"2014","journal-title":"Open Access J Sports Med"},{"key":"10.1016\/j.jse.2016.11.038_bib0165","doi-asserted-by":"crossref","first-page":"e31","DOI":"10.1016\/j.jse.2014.06.052","article-title":"Significant association of full-thickness rotator cuff tears and estrogen-related receptor-beta (ESRRB)","volume":"24","author":"Teerlink","year":"2015","journal-title":"J Shoulder Elbow Surg"},{"key":"10.1016\/j.jse.2016.11.038_bib0170","doi-asserted-by":"crossref","first-page":"338","DOI":"10.1086\/510920","article-title":"Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia","volume":"80","author":"Tekin","year":"2007","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.jse.2016.11.038_bib0175","doi-asserted-by":"crossref","first-page":"2125","DOI":"10.1007\/s11357-012-9500-0","article-title":"In vitro tenocyte metabolism in aging and oestrogen deficiency","volume":"35","author":"Torricelli","year":"2013","journal-title":"Age (Dordr)"},{"key":"10.1016\/j.jse.2016.11.038_bib0180","doi-asserted-by":"crossref","first-page":"81","DOI":"10.1186\/1471-2350-15-81","article-title":"Role of estrogen related receptor beta (ESRRB) in DFN35B hearing impairment and dental decay","volume":"15","author":"Weber","year":"2014","journal-title":"BMC Med Genet"},{"key":"10.1016\/j.jse.2016.11.038_bib0185","doi-asserted-by":"crossref","first-page":"361","DOI":"10.1086\/427956","article-title":"Mutations that cause osteoglophonic dysplasia define novel roles for FGFR1 in bone elongation","volume":"76","author":"White","year":"2005","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.jse.2016.11.038_bib0190","doi-asserted-by":"crossref","first-page":"2972","DOI":"10.1038\/sj.onc.1206474","article-title":"SASH1: a candidate tumor suppressor gene on chromosome 6q24.3 is downregulated in breast cancer","volume":"22","author":"Zeller","year":"2003","journal-title":"Oncogene"}],"container-title":["Journal of Shoulder and Elbow Surgery"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1058274616306115?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1058274616306115?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,9,18]],"date-time":"2019-09-18T02:46:19Z","timestamp":1568774779000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1058274616306115"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017,6]]},"references-count":37,"journal-issue":{"issue":"6","published-print":{"date-parts":[[2017,6]]}},"alternative-id":["S1058274616306115"],"URL":"https:\/\/doi.org\/10.1016\/j.jse.2016.11.038","relation":{},"ISSN":["1058-2746"],"issn-type":[{"value":"1058-2746","type":"print"}],"subject":[],"published":{"date-parts":[[2017,6]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Genetic and familial predisposition to rotator cuff disease: a systematic review","name":"articletitle","label":"Article Title"},{"value":"Journal of Shoulder and Elbow Surgery","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jse.2016.11.038","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2016 Journal of Shoulder and Elbow Surgery Board of Trustees. All rights reserved.","name":"copyright","label":"Copyright"}]}}