| Year |
Citation |
Score |
| 2018 |
Grishin D, Obbad K, Estep P, Quinn K, Zaranek SW, Zaranek AW, Vandewege W, Clegg T, César N, Cifric M, Church G. Accelerating Genomic Data Generation and Facilitating Genomic Data Access Using Decentralization, Privacy-Preserving Technologies and Equitable Compensation Blockchain in Healthcare Today. 1: 1-23. DOI: 10.30953/BHTY.V1.34 |
0.709 |
|
| 2017 |
Chan Y, Tung M, Garruss AS, Zaranek SW, Chan YK, Lunshof JE, Zaranek AW, Ball MP, Chou MF, Lim ET, Church GM. An unbiased index to quantify participant's phenotypic contribution to an open-access cohort. Scientific Reports. 7: 46148. PMID 28387241 DOI: 10.1038/Srep46148 |
0.506 |
|
| 2017 |
Lubin IM, Aziz N, Babb LJ, Ballinger D, Bisht H, Church DM, Cordes S, Eilbeck K, Hyland F, Kalman L, Landrum M, Lockhart ER, Maglott D, Marth G, Pfeifer JD, ... ... Zaranek AW, et al. Principles and Recommendations for Standardizing the Use of the Next-Generation Sequencing Variant File in Clinical Settings. The Journal of Molecular Diagnostics : Jmd. PMID 28315672 DOI: 10.1016/J.Jmoldx.2016.12.001 |
0.583 |
|
| 2016 |
Mao Q, Ciotlos S, Zhang RY, Ball MP, Chin R, Carnevali P, Barua N, Nguyen S, Agarwal MR, Clegg T, Connelly A, Vandewege W, Zaranek AW, Estep PW, Church GM, et al. The whole genome sequences and experimentally phased haplotypes of over 100 personal genomes. Gigascience. 5: 42. PMID 27724973 DOI: 10.1186/S13742-016-0148-Z |
0.83 |
|
| 2016 |
Zook JM, Catoe D, McDaniel J, Vang L, Spies N, Sidow A, Weng Z, Liu Y, Mason CE, Alexander N, Henaff E, McIntyre AB, Chandramohan D, Chen F, Jaeger E, ... ... Zaranek AW, et al. Extensive sequencing of seven human genomes to characterize benchmark reference materials. Scientific Data. 3: 160025. PMID 27271295 DOI: 10.1038/Sdata.2016.25 |
0.827 |
|
| 2014 |
Ball MP, Bobe JR, Chou MF, Clegg T, Estep PW, Lunshof JE, Vandewege W, Zaranek A, Church GM. Harvard Personal Genome Project: lessons from participatory public research. Genome Medicine. 6: 10. PMID 24713084 DOI: 10.1186/Gm527 |
0.806 |
|
| 2012 |
Ball MP, Thakuria JV, Zaranek AW, Clegg T, Rosenbaum AM, Wu X, Angrist M, Bhak J, Bobe J, Callow MJ, Cano C, Chou MF, Chung WK, Douglas SM, Estep PW, et al. A public resource facilitating clinical use of genomes. Proceedings of the National Academy of Sciences of the United States of America. 109: 11920-7. PMID 22797899 DOI: 10.1073/Pnas.1201904109 |
0.687 |
|
| 2012 |
Peters BA, Kermani BG, Sparks AB, Alferov O, Hong P, Alexeev A, Jiang Y, Dahl F, Tang YT, Haas J, Robasky K, Zaranek AW, Lee JH, Ball MP, Peterson JE, et al. Accurate whole-genome sequencing and haplotyping from 10 to 20 human cells. Nature. 487: 190-5. PMID 22785314 DOI: 10.1038/Nature11236 |
0.782 |
|
| 2012 |
Thakuria JV, Zaranek AW, Church GM, Berry GT. Back to the future: from genome to metabolome. Human Mutation. 33: 809-12. PMID 22431014 DOI: 10.1002/Humu.22073 |
0.693 |
|
| 2011 |
Dewey FE, Chen R, Cordero SP, Ormond KE, Caleshu C, Karczewski KJ, Whirl-Carrillo M, Wheeler MT, Dudley JT, Byrnes JK, Cornejo OE, Knowles JW, Woon M, Sangkuhl K, Gong L, ... ... Zaranek AW, et al. Phased whole-genome genetic risk in a family quartet using a major allele reference sequence. Plos Genetics. 7: e1002280. PMID 21935354 DOI: 10.1371/Journal.Pgen.1002280 |
0.687 |
|
| 2011 |
Zaranek AW, Clegg T, Vandewege W, Thakuria JV. Comments and Suggestions for Improvement of the Archon Genomics X PRIZE Validation Protocol Nature Precedings. 6: 1-1. DOI: 10.1038/Npre.2011.5766.1 |
0.366 |
|
| 2010 |
Zaranek AW, Levanon EY, Zecharia T, Clegg T, Church GM. A survey of genomic traces reveals a common sequencing error, RNA editing, and DNA editing. Plos Genetics. 6: e1000954. PMID 20531933 DOI: 10.1371/Journal.Pgen.1000954 |
0.64 |
|
| 2010 |
Ashley EA, Butte AJ, Wheeler MT, Chen R, Klein TE, Dewey FE, Dudley JT, Ormond KE, Pavlovic A, Morgan AA, Pushkarev D, Neff NF, Hudgins L, Gong L, Hodges LM, ... ... Zaranek AW, et al. Clinical assessment incorporating a personal genome. Lancet (London, England). 375: 1525-35. PMID 20435227 DOI: 10.1016/S0140-6736(10)60452-7 |
0.802 |
|
| 2010 |
Drmanac R, Sparks AB, Callow MJ, Halpern AL, Burns NL, Kermani BG, Carnevali P, Nazarenko I, Nilsen GB, Yeung G, Dahl F, Fernandez A, Staker B, Pant KP, Baccash J, ... ... Zaranek AW, et al. Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays. Science (New York, N.Y.). 327: 78-81. PMID 19892942 DOI: 10.1126/Science.1181498 |
0.824 |
|
| 2009 |
Kim JI, Ju YS, Park H, Kim S, Lee S, Yi JH, Mudge J, Miller NA, Hong D, Bell CJ, Kim HS, Chung IS, Lee WC, Lee JS, Seo SH, ... ... Zaranek AW, et al. A highly annotated whole-genome sequence of a Korean individual. Nature. 460: 1011-5. PMID 19587683 DOI: 10.1038/Nature08211 |
0.793 |
|
| 2009 |
Whiteford N, Skelly T, Curtis C, Ritchie ME, Löhr A, Zaranek AW, Abnizova I, Brown C. Swift: primary data analysis for the Illumina Solexa sequencing platform. Bioinformatics (Oxford, England). 25: 2194-9. PMID 19549630 DOI: 10.1093/Bioinformatics/Btp383 |
0.407 |
|
| 2009 |
Li JB, Gao Y, Aach J, Zhang K, Kryukov GV, Xie B, Ahlford A, Yoon JK, Rosenbaum AM, Zaranek AW, LeProust E, Sunyaev SR, Church GM. Multiplex padlock targeted sequencing reveals human hypermutable CpG variations. Genome Research. 19: 1606-15. PMID 19525355 DOI: 10.1101/Gr.092213.109 |
0.758 |
|
| 2008 |
Zaranek AW, Clegg T, Vandewege W, Church GM. Free Factories: Unified Infrastructure for Data Intensive Web Services. Proceedings of the Usenix ... Annual Technical Conference. Usenix Technical Conference. 2008: 391-404. PMID 20514356 |
0.325 |
|
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