BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Hindorff LA, Bonham VL, Ohno-Machado L. Enhancing diversity to reduce health information disparities and build an evidence base for genomic medicine. Per Med 2018;15:403-12. [PMID: 30209973 DOI: 10.2217/pme-2018-0037] [Cited by in Crossref: 19] [Cited by in F6Publishing: 18] [Article Influence: 4.8] [Reference Citation Analysis]
Number Citing Articles
1 Watson J, Green MA, Giebel C, Darlington-Pollock F, Akpan A. Social and spatial inequalities in healthcare use among people living with dementia in England (2002-2016). Aging Ment Health 2022;:1-12. [PMID: 35959941 DOI: 10.1080/13607863.2022.2107176] [Reference Citation Analysis]
2 Schumacher-Schuh AF, Bieger A, Okunoye O, Mok KY, Lim SY, Bardien S, Ahmad-Annuar A, Santos-Lobato BL, Strelow MZ, Salama M, Rao SC, Zewde YZ, Dindayal S, Azar J, Prashanth LK, Rajan R, Noyce AJ, Okubadejo N, Rizig M, Lesage S, Mata IF; Global Parkinson's Genetics Program (GP2). Underrepresented Populations in Parkinson's Genetics Research: Current Landscape and Future Directions. Mov Disord 2022. [PMID: 35867623 DOI: 10.1002/mds.29126] [Reference Citation Analysis]
3 Riddle L, Karliner LS, Livaudais-Toman J, Guerra C, Roat CE, Rope AF, Wade A, Caruncho M, Zepp JM, Giang J, Wilfond BS, Joseph G. Development and evaluation of an exome sequencing training course for medical interpreters. Per Med 2022. [PMID: 35171038 DOI: 10.2217/pme-2021-0091] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Watson J, Darlington-Pollock F, Green M, Giebel C, Akpan A. The Impact of Demographic, Socio-Economic and Geographic Factors on Mortality Risk among People Living with Dementia in England (2002-2016). Int J Environ Res Public Health 2021;18:13405. [PMID: 34949010 DOI: 10.3390/ijerph182413405] [Reference Citation Analysis]
5 Norstad M, Outram S, Brown JEH, Zamora AN, Koenig BA, Risch N, Norton ME, Slavotinek A, Ackerman SL. The difficulties of broad data sharing in genomic medicine: Empirical evidence from diverse participants in prenatal and pediatric clinical genomics research. Genet Med 2021:S1098-3600(21)05349-1. [PMID: 34906477 DOI: 10.1016/j.gim.2021.09.021] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Lindberg NM, Gutierrez AM, Mittendorf KF, Ramos MA, Anguiano B, Angelo F, Joseph G. Creating accessible Spanish language materials for Clinical Sequencing Evidence-Generating Research consortium genomic projects: challenges and lessons learned. Per Med 2021;18:441-54. [PMID: 34448595 DOI: 10.2217/pme-2020-0075] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Miga KH, Wang T. The Need for a Human Pangenome Reference Sequence. Annu Rev Genomics Hum Genet 2021;22:81-102. [PMID: 33929893 DOI: 10.1146/annurev-genom-120120-081921] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
8 Pacyna JE, Shaibi GQ, Lee A, Byrne JO, Cuellar I, Sutton EJ, Hernandez V, Lindor NM, Singh D, Kullo IJ, Sharp RR. Increasing access to individualized medicine: a matched-cohort study examining Latino participant experiences of genomic screening. Genet Med 2021;23:934-41. [PMID: 33500569 DOI: 10.1038/s41436-020-01079-5] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
9 Overkleeft R, Tommel J, Evers AWM, den Dunnen JT, Roos M, Hoefmans MJ, Schrader WE, Swen JJ, Numans ME, Houwink EJF. Using Personal Genomic Data within Primary Care: A Bioinformatics Approach to Pharmacogenomics. Genes (Basel) 2020;11:E1443. [PMID: 33266138 DOI: 10.3390/genes11121443] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
10 Villanueva AG, Majumder MA. Hashtag who's missing? Lessons for genomic databases. Disabil Health J 2021;14:100945. [PMID: 32788131 DOI: 10.1016/j.dhjo.2020.100945] [Reference Citation Analysis]
11 Fernández-Rhodes L, Young KL, Lilly AG, Raffield LM, Highland HM, Wojcik GL, Agler C, Love SM, Okello S, Petty LE, Graff M, Below JE, Divaris K, North KE. Importance of Genetic Studies of Cardiometabolic Disease in Diverse Populations. Circ Res 2020;126:1816-40. [PMID: 32496918 DOI: 10.1161/CIRCRESAHA.120.315893] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
12 Cuccaro ML, Manrique CP, Quintero MA, Martinez R, McCauley JL. Understanding Participation in Genetic Research Among Patients With Multiple Sclerosis: The Influences of Ethnicity, Gender, Education, and Age. Front Genet 2020;11:120. [PMID: 32231680 DOI: 10.3389/fgene.2020.00120] [Reference Citation Analysis]
13 Morales A, Kinnamon DD, Jordan E, Platt J, Vatta M, Dorschner MO, Starkey CA, Mead JO, Ai T, Burke W, Gastier-Foster J, Jarvik GP, Rehm HL, Nickerson DA, Hershberger RE; DCM Precision Medicine study of the DCM Consortium., DCM Consortium institutions and personnel participating in this study: Study Principal Investigator and Co-Investigators,DCM Consortium Clinical Site Principal Investigators and Clinical Site Other Significant Contributors (OSC). The following clinical sites and individuals contributed to the submission of RO 1 H L 128857 as Site Principal Investigators (Site Pl) or as Other Significant Contributors (OSC),Dr. Huggins also served as study co-principal investigator,The following clinical site was added following approval of NHGRI supplemental funding but prior to initiation of enrollment,The following clinical sites were added following study activation. Variant Interpretation for Dilated Cardiomyopathy: Refinement of the American College of Medical Genetics and Genomics/ClinGen Guidelines for the DCM Precision Medicine Study. Circ Genom Precis Med 2020;13:e002480. [PMID: 32160020 DOI: 10.1161/CIRCGEN.119.002480] [Cited by in Crossref: 16] [Cited by in F6Publishing: 11] [Article Influence: 8.0] [Reference Citation Analysis]
14 Ridgeway JL, Albertie M, Pantoja E, Prescott D, Zhu X, Breitkopf CR. Understanding Diverse Perspectives on Genetic Research Through Focus Group Talk. International Journal of Qualitative Methods 2019;18:160940691989247. [DOI: 10.1177/1609406919892476] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
15 Wagner JK. Ethical and Legal Considerations for the Inclusion of Underserved and Underrepresented Immigrant Populations in Precision Health and Genomic Research in the United States. Ethn Dis 2019;29:641-50. [PMID: 31889769 DOI: 10.18865/ed.29.S3.641] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
16 Lee SS, Fullerton SM, Saperstein A, Shim JK. Ethics of inclusion: Cultivate trust in precision medicine. Science 2019;364:941-2. [PMID: 31171685 DOI: 10.1126/science.aaw8299] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
17 Popejoy AB. Diversity In Precision Medicine And Pharmacogenetics: Methodological And Conceptual Considerations For Broadening Participation. Pharmgenomics Pers Med 2019;12:257-71. [PMID: 31686892 DOI: 10.2147/PGPM.S179742] [Cited by in Crossref: 3] [Cited by in F6Publishing: 10] [Article Influence: 1.0] [Reference Citation Analysis]
18 Peterson RE, Kuchenbaecker K, Walters RK, Chen CY, Popejoy AB, Periyasamy S, Lam M, Iyegbe C, Strawbridge RJ, Brick L, Carey CE, Martin AR, Meyers JL, Su J, Chen J, Edwards AC, Kalungi A, Koen N, Majara L, Schwarz E, Smoller JW, Stahl EA, Sullivan PF, Vassos E, Mowry B, Prieto ML, Cuellar-Barboza A, Bigdeli TB, Edenberg HJ, Huang H, Duncan LE. Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and Recommendations. Cell 2019;179:589-603. [PMID: 31607513 DOI: 10.1016/j.cell.2019.08.051] [Cited by in Crossref: 96] [Cited by in F6Publishing: 78] [Article Influence: 32.0] [Reference Citation Analysis]
19 Behring M, Hale K, Ozaydin B, Grizzle WE, Sodeke SO, Manne U. Inclusiveness and ethical considerations for observational, translational, and clinical cancer health disparity research. Cancer 2019;125:4452-61. [PMID: 31502259 DOI: 10.1002/cncr.32495] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
20 Koehly LM, Persky S, Philip Shaw, Bonham VL, Marcum CS, Sudre GP, Lea DE, Davis SK. Social and behavioral science at the forefront of genomics: Discovery, translation, and health equity. Soc Sci Med 2021;271:112450. [PMID: 31558303 DOI: 10.1016/j.socscimed.2019.112450] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
21 Nugent A, Conatser KR, Turner LL, Nugent JT, Sarino EMB, Ricks-Santi LJ. Reporting of race in genome and exome sequencing studies of cancer: a scoping review of the literature. Genet Med 2019;21:2676-80. [PMID: 31160752 DOI: 10.1038/s41436-019-0558-2] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 3.3] [Reference Citation Analysis]
22 Bien SA, Wojcik GL, Hodonsky CJ, Gignoux CR, Cheng I, Matise TC, Peters U, Kenny EE, North KE. The Future of Genomic Studies Must Be Globally Representative: Perspectives from PAGE. Annu Rev Genomics Hum Genet 2019;20:181-200. [PMID: 30978304 DOI: 10.1146/annurev-genom-091416-035517] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 3.7] [Reference Citation Analysis]
23 Bentley AR, Callier S, Rotimi C. The Emergence of Genomic Research in Africa and New Frameworks for Equity in Biomedical Research. Ethn Dis 2019;29:179-86. [PMID: 30906167 DOI: 10.18865/ed.29.S1.179] [Cited by in Crossref: 13] [Cited by in F6Publishing: 8] [Article Influence: 4.3] [Reference Citation Analysis]
24 Rubinstein WS. CancerLinQ: Cutting the Gordian Knot of Interoperability. JOP 2019;15:3-6. [DOI: 10.1200/jop.18.00612] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.7] [Reference Citation Analysis]