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Items: 15

1.

The recurrence risk of genetic complex diseases.

Bijanzadeh M.

J Res Med Sci. 2017 Mar 15;22:32. doi: 10.4103/1735-1995.202143. eCollection 2017. Review.

2.

Family health history reporting is sensitive to small changes in wording.

Conway-Pearson LS, Christensen KD, Savage SK, Huntington NL, Weitzman ER, Ziniel SI, Bacon P, Cacioppo CN, Green RC, Holm IA.

Genet Med. 2016 Dec;18(12):1308-1311. doi: 10.1038/gim.2016.45. Epub 2016 May 5.

3.

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

Tashjian RZ, Farnham JM, Granger EK, Teerlink CC, Cannon-Albright LA.

Orthop J Sports Med. 2016 Apr 12;4(4):2325967116642173. doi: 10.1177/2325967116642173. eCollection 2016 Apr.

4.

Subsequent Type 2 Diabetes in Patients with Autoimmune Disease.

Hemminki K, Liu X, Försti A, Sundquist J, Sundquist K, Ji J.

Sci Rep. 2015 Sep 9;5:13871. doi: 10.1038/srep13871.

5.

Association of gene variants with susceptibility to type 2 diabetes among Omanis.

Al-Sinani S, Woodhouse N, Al-Mamari A, Al-Shafie O, Al-Shafaee M, Al-Yahyaee S, Hassan M, Jaju D, Al-Hashmi K, Al-Abri M, Al-Rassadi K, Rizvi S, Loic Y, Froguel P, Bayoumi R.

World J Diabetes. 2015 Mar 15;6(2):358-66. doi: 10.4239/wjd.v6.i2.358.

6.

Familial Clustering of Type 2 Diabetes among Omanis.

Al-Sinani S, Al-Shafaee M, Al-Mamari A, Woodhouse N, Al-Shafie O, Hassan M, Al-Yahyaee S, Albarwani S, Jaju D, Al-Hashmi K, Al-Abri M, Rizvi S, Bayoumi R.

Oman Med J. 2014 Jan;29(1):51-4. doi: 10.5001/omj.2014.11.

7.

Genetic analysis of low BMI phenotype in the Utah Population Database.

Yates WR, Johnson C, McKee P, Cannon-Albright LA.

PLoS One. 2013 Dec 11;8(12):e80287. doi: 10.1371/journal.pone.0080287. eCollection 2013.

8.

Empiric evidence for a genetic contribution to predisposition to surgical site infection.

Lee JP, Hopf HW, Cannon-Albright LA.

Wound Repair Regen. 2013 Mar-Apr;21(2):211-5. doi: 10.1111/wrr.12024. Epub 2013 Feb 25.

9.

Extended family history of type 1 diabetes and phenotype and genotype of newly diagnosed children.

Parkkola A, Härkönen T, Ryhänen SJ, Ilonen J, Knip M; Finnish Pediatric Diabetes Register.

Diabetes Care. 2013 Feb;36(2):348-54. doi: 10.2337/dc12-0445. Epub 2012 Oct 1.

10.

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

Albright F, Teerlink C, Werner TL, Cannon-Albright LA.

BMC Cancer. 2012 Apr 3;12:138. doi: 10.1186/1471-2407-12-138. Review.

11.

Evaluation of record linkage between a large healthcare provider and the Utah Population Database.

DuVall SL, Fraser AM, Rowe K, Thomas A, Mineau GP.

J Am Med Inform Assoc. 2012 Jun;19(e1):e54-9. Epub 2011 Sep 16.

12.

Evidence for a heritable predisposition to Chronic Fatigue Syndrome.

Albright F, Light K, Light A, Bateman L, Cannon-Albright LA.

BMC Neurol. 2011 May 27;11:62. doi: 10.1186/1471-2377-11-62.

13.

Risk of cancer following hospitalization for type 2 diabetes.

Hemminki K, Li X, Sundquist J, Sundquist K.

Oncologist. 2010;15(6):548-55. doi: 10.1634/theoncologist.2009-0300. Epub 2010 May 17.

14.

Familial risks for type 2 diabetes in Sweden.

Hemminki K, Li X, Sundquist K, Sundquist J.

Diabetes Care. 2010 Feb;33(2):293-7. doi: 10.2337/dc09-0947. Epub 2009 Nov 10.

15.

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

Tashjian RZ, Farnham JM, Albright FS, Teerlink CC, Cannon-Albright LA.

J Bone Joint Surg Am. 2009 May;91(5):1136-42. doi: 10.2106/JBJS.H.00831.

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