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Items: 1 to 20 of 23

1.

Innovative designs of point-of-care comparative effectiveness trials.

Shih MC, Turakhia M, Lai TL.

Contemp Clin Trials. 2015 Nov;45(Pt A):61-8. doi: 10.1016/j.cct.2015.06.014. Epub 2015 Jun 19. Review.

PMID:
26099528
2.

Rare genetic variant analysis on blood pressure in related samples.

Chen H, Choi SH, Hong J, Lu C, Milton JN, Allard C, Lacey SM, Lin H, Dupuis J.

BMC Proc. 2014 Jun 17;8(Suppl 1):S35. doi: 10.1186/1753-6561-8-S1-S35. eCollection 2014.

3.

Confirmation of genetic variants associated with lethal prostate cancer in a cohort of men from hereditary prostate cancer families.

Karyadi DM, Zhao S, He Q, McIntosh L, Wright JL, Ostrander EA, Feng Z, Stanford JL.

Int J Cancer. 2015 May 1;136(9):2166-71. doi: 10.1002/ijc.29241. Epub 2014 Oct 13.

4.

Testing genetic association with rare and common variants in family data.

Chen H, Malzahn D, Balliu B, Li C, Bailey JN.

Genet Epidemiol. 2014 Sep;38 Suppl 1:S37-43. doi: 10.1002/gepi.21823.

5.

Efficient mapping and geographic disparities in breast cancer mortality at the county-level by race and age in the U.S.

Chien LC, Yu HL, Schootman M.

Spat Spatiotemporal Epidemiol. 2013 Jun;5:27-37. doi: 10.1016/j.sste.2013.03.002. Epub 2013 Mar 27.

6.

Unstable mutations in the FMR1 gene and the phenotypes.

Loesch D, Hagerman R.

Adv Exp Med Biol. 2012;769:78-114. Review.

7.

Genome scan in familial late-onset Alzheimer's disease: a locus on chromosome 6 contributes to age-at-onset.

Zhao W, Marchani EE, Cheung CY, Steinbart EJ, Schellenberg GD, Bird TD, Wijsman EM.

Am J Med Genet B Neuropsychiatr Genet. 2013 Mar;162B(2):201-12. doi: 10.1002/ajmg.b.32133. Epub 2013 Jan 25.

8.

The modifying effect of patient location on stage-specific survival following colorectal cancer using geosurvival models.

Chien LC, Schootman M, Pruitt SL.

Cancer Causes Control. 2013 Mar;24(3):473-84. doi: 10.1007/s10552-012-0134-4. Epub 2013 Jan 10.

9.

Genotype×age interaction in human transcriptional ageing.

Kent JW Jr, Göring HH, Charlesworth JC, Drigalenko E, Diego VP, Curran JE, Johnson MP, Dyer TD, Cole SA, Jowett JB, Mahaney MC, Comuzzie AG, Almasy L, Moses EK, Blangero J, Williams-Blangero S.

Mech Ageing Dev. 2012 Sep-Oct;133(9-10):581-90. doi: 10.1016/j.mad.2012.07.005. Epub 2012 Jul 31.

10.

Genetic analyses of smoking initiation, persistence, quantity, and age-at-onset of regular cigarette use in Brazilian families: the Baependi Heart Study.

Horimoto AR, Oliveira CM, Giolo SR, Soler JP, de Andrade M, Krieger JE, Pereira AC.

BMC Med Genet. 2012 Jan 30;13:9. doi: 10.1186/1471-2350-13-9.

12.

Change in vascular access and hospitalization risk in long-term hemodialysis patients.

Lacson E Jr, Wang W, Lazarus JM, Hakim RM.

Clin J Am Soc Nephrol. 2010 Nov;5(11):1996-2003. doi: 10.2215/CJN.08961209. Epub 2010 Sep 30.

13.

Cumulative exposure to air pollution and long term outcomes after first acute myocardial infarction: a population-based cohort study. Objectives and methodology.

Gerber Y, Myers V, Broday DM, Koton S, Steinberg DM, Drory Y.

BMC Public Health. 2010 Jun 24;10:369. doi: 10.1186/1471-2458-10-369.

14.

A Variance-Component Framework for Pedigree Analysis of Continuous and Categorical Outcomes.

Epstein MP, Hunter JE, Allen EG, Sherman SL, Lin X, Boehnke M.

Stat Biosci. 2009 Nov;1(2):181-198.

15.

New score tests for age-at-onset linkage analysis in general pedigrees.

Callegaro A, Uh HW, Helmer Q, Houwing-Duistermaat JJ.

BMC Proc. 2009 Dec 15;3 Suppl 7:S97.

16.

Robust age at onset linkage analysis in nuclear families.

Callegaro A, van Houwelingen JC, Houwing-Duistermaat JJ.

Hum Hered. 2010;69(2):80-90. doi: 10.1159/000264446. Epub 2009 Dec 4.

17.

Investigation of innate immunity genes CARD4, CARD8 and CARD15 as germline susceptibility factors for colorectal cancer.

Möckelmann N, von Schönfels W, Buch S, von Kampen O, Sipos B, Egberts JH, Rosenstiel P, Franke A, Brosch M, Hinz S, Röder C, Kalthoff H, Fölsch UR, Krawczak M, Schreiber S, Bröring CD, Tepel J, Schafmayer C, Hampe J.

BMC Gastroenterol. 2009 Oct 20;9:79. doi: 10.1186/1471-230X-9-79.

18.
19.

Fragile X-associated primary ovarian insufficiency: evidence for additional genetic contributions to severity.

Hunter JE, Epstein MP, Tinker SW, Charen KH, Sherman SL.

Genet Epidemiol. 2008 Sep;32(6):553-9. doi: 10.1002/gepi.20329.

20.

A genomic scan for age at onset of Alzheimer's disease in 437 families from the NIMH Genetic Initiative.

Dickson MR, Li J, Wiener HW, Perry RT, Blacker D, Bassett SS, Go RC.

Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):784-92. doi: 10.1002/ajmg.b.30689.

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