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Items: 1 to 20 of 36


Anthropologists' views on race, ancestry, and genetics.

Wagner JK, Yu JH, Ifekwunigwe JO, Harrell TM, Bamshad MJ, Royal CD.

Am J Phys Anthropol. 2017 Feb;162(2):318-327. doi: 10.1002/ajpa.23120. Epub 2016 Nov 22.


Will Precision Medicine Move Us beyond Race?

Bonham VL, Callier SL, Royal CD.

N Engl J Med. 2016 May 26;374(21):2003-5. doi: 10.1056/NEJMp1511294. No abstract available.


Disclosing Pleiotropic Effects During Genetic Risk Assessment for Alzheimer Disease: A Randomized Trial.

Christensen KD, Roberts JS, Whitehouse PJ, Royal CD, Obisesan TO, Cupples LA, Vernarelli JA, Bhatt DL, Linnenbringer E, Butson MB, Fasaye GA, Uhlmann WR, Hiraki S, Wang N, Cook-Deegan R, Green RC; REVEAL Study Group*..

Ann Intern Med. 2016 Feb 2;164(3):155-63. doi: 10.7326/M15-0187. Epub 2016 Jan 26.


A global reference for human genetic variation.

1000 Genomes Project Consortium., Auton A, Brooks LD, Durbin RM, Garrison EP, Kang HM, Korbel JO, Marchini JL, McCarthy S, McVean GA, Abecasis GR.

Nature. 2015 Oct 1;526(7571):68-74. doi: 10.1038/nature15393.


Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel.

Delaneau O, Marchini J; 1000 Genomes Project Consortium.; 1000 Genomes Project Consortium..

Nat Commun. 2014 Jun 13;5:3934. doi: 10.1038/ncomms4934.


A randomized noninferiority trial of condensed protocols for genetic risk disclosure of Alzheimer's disease.

Green RC, Christensen KD, Cupples LA, Relkin NR, Whitehouse PJ, Royal CD, Obisesan TO, Cook-Deegan R, Linnenbringer E, Butson MB, Fasaye GA, Levinson E, Roberts JS; REVEAL Study Group..

Alzheimers Dement. 2015 Oct;11(10):1222-30. doi: 10.1016/j.jalz.2014.10.014. Epub 2014 Dec 9.


Genome-wide association studies in Africans and African Americans: expanding the framework of the genomics of human traits and disease.

Peprah E, Xu H, Tekola-Ayele F, Royal CD.

Public Health Genomics. 2015;18(1):40-51. Epub 2014 Nov 26. Review.


Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences.

Colonna V, Ayub Q, Chen Y, Pagani L, Luisi P, Pybus M, Garrison E, Xue Y, Tyler-Smith C; 1000 Genomes Project Consortium., Abecasis GR, Auton A, Brooks LD, DePristo MA, Durbin RM, Handsaker RE, Kang HM, Marth GT, McVean GA.

Genome Biol. 2014 Jun 30;15(6):R88. doi: 10.1186/gb-2014-15-6-r88.


Integrative annotation of variants from 1092 humans: application to cancer genomics.

Khurana E, Fu Y, Colonna V, Mu XJ, Kang HM, Lappalainen T, Sboner A, Lochovsky L, Chen J, Harmanci A, Das J, Abyzov A, Balasubramanian S, Beal K, Chakravarty D, Challis D, Chen Y, Clarke D, Clarke L, Cunningham F, Evani US, Flicek P, Fragoza R, Garrison E, Gibbs R, Gümüs ZH, Herrero J, Kitabayashi N, Kong Y, Lage K, Liluashvili V, Lipkin SM, MacArthur DG, Marth G, Muzny D, Pers TH, Ritchie GR, Rosenfeld JA, Sisu C, Wei X, Wilson M, Xue Y, Yu F; 1000 Genomes Project Consortium., Dermitzakis ET, Yu H, Rubin MA, Tyler-Smith C, Gerstein M.

Science. 2013 Oct 4;342(6154):1235587. doi: 10.1126/science.1235587.


Would you terminate a pregnancy affected by sickle cell disease? Analysis of views of patients in Cameroon.

Wonkam A, de Vries J, Royal CD, Ramesar R, Angwafo FF 3rd.

J Med Ethics. 2014 Sep;40(9):615-20. doi: 10.1136/medethics-2013-101392. Epub 2013 Aug 5.


Personal DNA testing in college classrooms: perspectives of students and professors.

Daley LA, Wagner JK, Himmel TL, McPartland KA, Katsanis SH, Shriver MD, Royal CD.

Genet Test Mol Biomarkers. 2013 Jun;17(6):446-52. doi: 10.1089/gtmb.2012.0404. Epub 2013 Mar 28.


An integrated map of genetic variation from 1,092 human genomes.

1000 Genomes Project Consortium., Abecasis GR, Auton A, Brooks LD, DePristo MA, Durbin RM, Handsaker RE, Kang HM, Marth GT, McVean GA.

Nature. 2012 Nov 1;491(7422):56-65. doi: 10.1038/nature11632.


The serotonin transporter gene polymorphism (5HTTLPR) moderates the effect of adolescent environmental conditions on self-esteem in young adulthood: a structural equation modeling approach.

Jonassaint CR, Ashley-Koch A, Whitfield KE, Hoyle RH, Richman LS, Siegler IC, Royal CD, Williams R.

Biol Psychol. 2012 Sep;91(1):111-9. doi: 10.1016/j.biopsycho.2012.05.004. Epub 2012 Jun 1.


Tilting at windmills no longer: a data-driven discussion of DTC DNA ancestry tests.

Wagner JK, Cooper JD, Sterling R, Royal CD.

Genet Med. 2012 Jun;14(6):586-93. doi: 10.1038/gim.2011.77. Epub 2012 Mar 1.


Field of genes: an investigation of sports-related genetic testing.

Wagner JK, Royal CD.

J Pers Med. 2012 Sep 12;2(3):119-37. doi: 10.3390/jpm2030119.


Evaluation findings from genetics and family health history community-based workshops for African Americans.

Manswell Butty JA, Richardson F, Mouton CP, Royal CD, Green RD, Munroe KA.

J Community Genet. 2012 Jan;3(1):1-12. doi: 10.1007/s12687-011-0068-7. Epub 2011 Nov 5.


Living with sickle cell disease: traversing 'race' and identity.

Royal CD, Jonassaint CR, Jonassaint JC, De Castro LM.

Ethn Health. 2011 Aug-Oct;16(4-5):389-404. doi: 10.1080/13557858.2011.563283.


Differences between African American and White research volunteers in their attitudes, beliefs and knowledge regarding genetic testing for Alzheimer's disease.

Akinleye I, Roberts JS, Royal CD, Linnenbringer E, Obisesan TO, Fasaye GA, Green RC.

J Genet Couns. 2011 Dec;20(6):650-9. doi: 10.1007/s10897-011-9377-6. Epub 2011 Jun 9.


Grassroots marketing in a global era: more lessons from BiDil.

Rusert BM, Royal CD.

J Law Med Ethics. 2011 Spring;39(1):79-90. doi: 10.1111/j.1748-720X.2011.00552.x. No abstract available.


Genome-sequencing anniversary. My genome, my identity, my health.

Royal CD.

Science. 2011 Feb 11;331(6018):690-1. doi: 10.1126/science.1203123. No abstract available.

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