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Items: 1 to 20 of 157

1.

Bridging the Gaps in Personalized Medicine Value Assessment: A Review of the Need for Outcome Metrics across Stakeholders and Scientific Disciplines.

Bush WS, Cooke Bailey JN, Beno MF, Crawford DC.

Public Health Genomics. 2019 Aug 27:1-9. doi: 10.1159/000501974. [Epub ahead of print] Review.

2.

Genetically-guided algorithm development and sample size optimization for age-related macular degeneration cases and controls in electronic health records from the VA Million Veteran Program.

Halladay CW, Hadi T, Anger MD, Greenberg PB, Sullivan JM, Konicki PE, Peachey NS, Igo RP Jr, Iyengar SK, Wu WC, Crawford DC; VA Million Veteran Program.

AMIA Jt Summits Transl Sci Proc. 2019 May 6;2019:153-162. eCollection 2019.

3.

Mind the gap: resources required to receive, process and interpret research-returned whole genome data.

Crawford DC, Cooke Bailey JN, Briggs FBS.

Hum Genet. 2019 Jul;138(7):691-701. doi: 10.1007/s00439-019-02033-5. Epub 2019 Jun 3. Review.

PMID:
31161416
4.

A Social Determinant of Health May Modify Genetic Associations for Blood Pressure: Evidence From a SNP by Education Interaction in an African American Population.

Hollister BM, Farber-Eger E, Aldrich MC, Crawford DC.

Front Genet. 2019 May 10;10:428. doi: 10.3389/fgene.2019.00428. eCollection 2019.

5.

Using Electronic Health Records To Generate Phenotypes For Research.

Pendergrass SA, Crawford DC.

Curr Protoc Hum Genet. 2019 Jan;100(1):e80. doi: 10.1002/cphg.80. Epub 2018 Dec 5.

PMID:
30516347
6.

Local genetic ancestry in CDKN2B-AS1 is associated with primary open-angle glaucoma in an African American cohort extracted from de-identified electronic health records.

Restrepo NA, Laper SM, Farber-Eger E, Crawford DC.

BMC Med Genomics. 2018 Sep 14;11(Suppl 3):70. doi: 10.1186/s12920-018-0392-4.

7.

Frequency and phenotype consequence of APOC3 rare variants in patients with very low triglyceride levels.

Crawford DC, Restrepo NA, Diggins KE, Farber-Eger E, Wells QS.

BMC Med Genomics. 2018 Sep 14;11(Suppl 3):66. doi: 10.1186/s12920-018-0387-1.

8.

The genetic underpinnings of variation in ages at menarche and natural menopause among women from the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) Study: A trans-ethnic meta-analysis.

Fernández-Rhodes L, Malinowski JR, Wang Y, Tao R, Pankratz N, Jeff JM, Yoneyama S, Carty CL, Setiawan VW, Le Marchand L, Haiman C, Corbett S, Demerath E, Heiss G, Gross M, Buzkova P, Crawford DC, Hunt SC, Rao DC, Schwander K, Chakravarti A, Gottesman O, Abul-Husn NS, Bottinger EP, Loos RJF, Raffel LJ, Yao J, Guo X, Bielinski SJ, Rotter JI, Vaidya D, Chen YI, Castañeda SF, Daviglus M, Kaplan R, Talavera GA, Ryckman KK, Peters U, Ambite JL, Buyske S, Hindorff L, Kooperberg C, Matise T, Franceschini N, North KE.

PLoS One. 2018 Jul 25;13(7):e0200486. doi: 10.1371/journal.pone.0200486. eCollection 2018.

9.

Hi-MC: a novel method for high-throughput mitochondrial haplogroup classification.

Smieszek S, Mitchell SL, Farber-Eger EH, Veatch OJ, Wheeler NR, Goodloe RJ, Wells QS, Murdock DG, Crawford DC.

PeerJ. 2018 Jun 25;6:e5149. doi: 10.7717/peerj.5149. eCollection 2018.

10.

Willingness to Participate in a National Precision Medicine Cohort: Attitudes of Chronic Kidney Disease Patients at a Cleveland Public Hospital.

Cooke Bailey JN, Crawford DC, Goldenberg A, Slaven A, Pencak J, Schachere M, Bush WS, Sedor JR, O'Toole JF.

J Pers Med. 2018 Jun 26;8(3). pii: E21. doi: 10.3390/jpm8030021.

11.

Somatic T-cell Receptor Diversity in a Chronic Kidney Disease PatientPopulation Linked to Electronic Health Records.

Crawford DC, Bailey JNC, Miskimen K, Miron P, McCauley JL, Sedor JR, ƠToole JF, Bush WS.

AMIA Jt Summits Transl Sci Proc. 2018 May 18;2017:63-71. eCollection 2018.

12.

Racial Disparities in Lung Cancer Survival: The Contribution of Stage, Treatment, and Ancestry.

Jones CC, Mercaldo SF, Blume JD, Wenzlaff AS, Schwartz AG, Chen H, Deppen SA, Bush WS, Crawford DC, Chanock SJ, Blot WJ, Grogan EL, Aldrich MC.

J Thorac Oncol. 2018 Oct;13(10):1464-1473. doi: 10.1016/j.jtho.2018.05.032. Epub 2018 Jun 6.

PMID:
29885480
13.

Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) study.

Kocarnik JM, Richard M, Graff M, Haessler J, Bien S, Carlson C, Carty CL, Reiner AP, Avery CL, Ballantyne CM, LaCroix AZ, Assimes TL, Barbalic M, Pankratz N, Tang W, Tao R, Chen D, Talavera GA, Daviglus ML, Chirinos-Medina DA, Pereira R, Nishimura K, Bužková P, Best LG, Ambite JL, Cheng I, Crawford DC, Hindorff LA, Fornage M, Heiss G, North KE, Haiman CA, Peters U, Le Marchand L, Kooperberg C.

Hum Mol Genet. 2018 Aug 15;27(16):2940-2953. doi: 10.1093/hmg/ddy211.

14.

Trans-ethnic analysis of metabochip data identifies two new loci associated with BMI.

Gong J, Nishimura KK, Fernandez-Rhodes L, Haessler J, Bien S, Graff M, Lim U, Lu Y, Gross M, Fornage M, Yoneyama S, Isasi CR, Buzkova P, Daviglus M, Lin DY, Tao R, Goodloe R, Bush WS, Farber-Eger E, Boston J, Dilks HH, Ehret G, Gu CC, Lewis CE, Nguyen KH, Cooper R, Leppert M, Irvin MR, Bottinger EP, Wilkens LR, Haiman CA, Park L, Monroe KR, Cheng I, Stram DO, Carlson CS, Jackson R, Kuller L, Houston D, Kooperberg C, Buyske S, Hindorff LA, Crawford DC, Loos RJF, Le Marchand L, Matise TC, North KE, Peters U.

Int J Obes (Lond). 2018 Mar;42(3):384-390. doi: 10.1038/ijo.2017.304. Epub 2017 Dec 21.

15.

INTEGRATING COMMUNITY-LEVEL DATA RESOURCES FOR PRECISION MEDICINE RESEARCH.

Bush WS, Crawford DC, Briggs F, Freedman D, Sloan C.

Pac Symp Biocomput. 2018;23:618-622.

16.

Local ancestry transitions modify snp-trait associations.

Fish AE, Crawford DC, Capra JA, Bush WS.

Pac Symp Biocomput. 2018;23:424-435.

17.

Two Novel Susceptibility Loci for Prostate Cancer in Men of African Ancestry.

Conti DV, Wang K, Sheng X, Bensen JT, Hazelett DJ, Cook MB, Ingles SA, Kittles RA, Strom SS, Rybicki BA, Nemesure B, Isaacs WB, Stanford JL, Zheng W, Sanderson M, John EM, Park JY, Xu J, Stevens VL, Berndt SI, Huff CD, Wang Z, Yeboah ED, Tettey Y, Biritwum RB, Adjei AA, Tay E, Truelove A, Niwa S, Sellers TA, Yamoah K, Murphy AB, Crawford DC, Gapstur SM, Bush WS, Aldrich MC, Cussenot O, Petrovics G, Cullen J, Neslund-Dudas C, Stern MC, Jarai ZK, Govindasami K, Chokkalingam AP, Hsing AW, Goodman PJ, Hoffmann T, Drake BF, Hu JJ, Clark PE, Van Den Eeden SK, Blanchet P, Fowke JH, Casey G, Hennis AJM, Han Y, Lubwama A, Thompson IM Jr, Leach R, Easton DF, Schumacher F, Van den Berg DJ, Gundell SM, Stram A, Wan P, Xia L, Pooler LC, Mohler JL, Fontham ETH, Smith GJ, Taylor JA, Srivastava S, Eeles RA, Carpten J, Kibel AS, Multigner L, Parent ME, Menegaux F, Cancel-Tassin G, Klein EA, Brureau L, Stram DO, Watya S, Chanock SJ, Witte JS, Blot WJ, Henderson BE, Haiman CA; PRACTICAL/ELLIPSE Consortium.

J Natl Cancer Inst. 2017 Aug 1;109(8). doi: 10.1093/jnci/djx084.

18.

Reducing Clinical Noise for Body Mass Index Measures Due to Unit and Transcription Errors in the Electronic Health Record.

Goodloe R, Farber-Eger E, Boston J, Crawford DC, Bush WS.

AMIA Jt Summits Transl Sci Proc. 2017 Jul 26;2017:102-111. eCollection 2017.

19.

Extracting Country-of-Origin from Electronic Health Records for Gene- Environment Studies as Part of the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) Study.

Farber-Eger E, Goodloe R, Boston J, Bush WS, Crawford DC.

AMIA Jt Summits Transl Sci Proc. 2017 Jul 26;2017:50-57. eCollection 2017.

20.

Germline Genetic Variants and Lung Cancer Survival in African Americans.

Jones CC, Bush WS, Crawford DC, Wenzlaff AS, Schwartz AG, Wiencke JK, Wrensch MR, Blot WJ, Chanock SJ, Grogan EL, Aldrich MC.

Cancer Epidemiol Biomarkers Prev. 2017 Aug;26(8):1288-1295. doi: 10.1158/1055-9965.EPI-16-0998. Epub 2017 Jun 15.

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