| Year |
Citation |
Score |
| 2021 |
Taliun D, Harris DN, Kessler MD, Carlson J, Szpiech ZA, Torres R, Taliun SAG, Corvelo A, Gogarten SM, Kang HM, Pitsillides AN, LeFaive J, Lee SB, Tian X, Browning BL, ... ... Minear MA, et al. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program. Nature. 590: 290-299. PMID 33568819 DOI: 10.1038/s41586-021-03205-y |
0.353 |
|
| 2017 |
Afshari NA, Igo RP, Morris NJ, Stambolian D, Sharma S, Pulagam VL, Dunn S, Stamler JF, Truitt BJ, Rimmler J, Kuot A, Croasdale CR, Qin X, Burdon KP, Riazuddin SA, ... ... Minear MA, et al. Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy. Nature Communications. 8: 14898. PMID 28358029 DOI: 10.1038/Ncomms14898 |
0.606 |
|
| 2015 |
Minear MA, Alessi S, Allyse M, Michie M, Chandrasekharan S. Noninvasive Prenatal Genetic Testing: Current and Emerging Ethical, Legal, and Social Issues. Annual Review of Genomics and Human Genetics. 16: 369-98. PMID 26322648 DOI: 10.1146/Annurev-Genom-090314-050000 |
0.326 |
|
| 2015 |
Katsanis SH, Minear MA, Vorderstrasse A, Yang N, Reeves JW, Rakhra-Burris T, Cook-Deegan R, Ginsburg GS, Simmons LA. Perspectives on genetic and genomic technologies in an academic medical center: the duke experience. Journal of Personalized Medicine. 5: 67-82. PMID 25854543 DOI: 10.3390/Jpm5020067 |
0.416 |
|
| 2015 |
Allyse M, Minear MA, Berson E, Sridhar S, Rote M, Hung A, Chandrasekharan S. Non-invasive prenatal testing: a review of international implementation and challenges. International Journal of Women's Health. 7: 113-26. PMID 25653560 DOI: 10.2147/Ijwh.S67124 |
0.37 |
|
| 2014 |
Li YJ, Minear MA, Qin X, Rimmler J, Hauser MA, Allingham RR, Igo RP, Lass JH, Iyengar SK, Klintworth GK, Afshari NA, Gregory SG. Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy. Investigative Ophthalmology & Visual Science. 55: 4577-84. PMID 24917144 DOI: 10.1167/Iovs.13-13517 |
0.579 |
|
| 2014 |
Chandrasekharan S, Minear MA, Hung A, Allyse M. Noninvasive prenatal testing goes global. Science Translational Medicine. 6: 231fs15. PMID 24718856 DOI: 10.1126/Scitranslmed.3008704 |
0.329 |
|
| 2013 |
Minear MA, Li YJ, Rimmler J, Balajonda E, Watson S, Allingham RR, Hauser MA, Klintworth GK, Afshari NA, Gregory SG. Genetic screen of African Americans with Fuchs endothelial corneal dystrophy. Molecular Vision. 19: 2508-16. PMID 24348007 |
0.507 |
|
| 2011 |
Li YJ, Minear MA, Rimmler J, Zhao B, Balajonda E, Hauser MA, Allingham RR, Eghrari AO, Riazuddin SA, Katsanis N, Gottsch JD, Gregory SG, Klintworth GK, Afshari NA. Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy. Plos One. 6: e18044. PMID 21533127 DOI: 10.1371/Journal.Pone.0018044 |
0.62 |
|
| 2011 |
Minear MA, Crosslin DR, Sutton BS, Connelly JJ, Nelson SC, Gadson-Watson S, Wang T, Seo D, Vance JM, Sketch MH, Haynes C, Goldschmidt-Clermont PJ, Shah SH, Kraus WE, Hauser ER, et al. Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease. Human Genetics. 129: 641-54. PMID 21298289 DOI: 10.1007/S00439-011-0959-Z |
0.569 |
|
| 2010 |
Riazuddin SA, Zaghloul NA, Al-Saif A, Davey L, Diplas BH, Meadows DN, Eghrari AO, Minear MA, Li YJ, Klintworth GK, Afshari N, Gregory SG, Gottsch JD, Katsanis N. Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p. American Journal of Human Genetics. 86: 45-53. PMID 20036349 DOI: 10.1016/J.Ajhg.2009.12.001 |
0.562 |
|
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