| Year |
Citation |
Score |
| 2019 |
Liang W, Zhao Y, Huang W, Gao Y, Xu W, Tao J, Yang M, Li L, Ping W, Shen H, Fu X, Chen Z, Laird PW, Cai X, Fan JB, et al. Non-invasive diagnosis of early-stage lung cancer using high-throughput targeted DNA methylation sequencing of circulating tumor DNA (ctDNA). Theranostics. 9: 2056-2070. PMID 31037156 DOI: 10.7150/Thno.28119 |
0.301 |
|
| 2018 |
Wu X, Chuan J, Hu T, Peng T, Yang M, Shen H, Laird P, Gao Y, Cai X, Xu W, Fan J, Lan P. Abstract 3310: Non-invasive diagnosis of colorectal cancer via targeted high-throughput DNA methylation sequencing of circulating tumor DNA (ctDNA) Cancer Research. 78: 3310-3310. DOI: 10.1158/1538-7445.Am2018-3310 |
0.312 |
|
| 2017 |
Janku F, Zhang S, Waters J, Liu L, Huang H, Subbiah V, Hong DS, Karp D, Fu S, Cai X, Ramzanali NM, Madwani K, Cabrilo G, Andrews DD, Zhao Y, et al. Development and validation of an ultra-deep next-generation sequencing assay for testing of plasma cell-free DNA from patients with advanced cancer. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. PMID 28536309 DOI: 10.1158/1078-0432.Ccr-17-0291 |
0.348 |
|
| 2017 |
Cai X, Gao Y, Shen H, Laird P, Fan J, Xu W, Liang W, He J. Abstract 5383: Non-invasive diagnosis of early-stage lung cancer via targeted high-throughput DNA methylation sequencing of circulating tumor DNA (ctDNA) Cancer Research. 77: 5383-5383. DOI: 10.1158/1538-7445.Am2017-5383 |
0.308 |
|
| 2015 |
Cai X, Janku F, Zhan Q, Fan JB. Accessing Genetic Information with Liquid Biopsies. Trends in Genetics : Tig. 31: 564-75. PMID 26450339 DOI: 10.1016/J.Tig.2015.06.001 |
0.301 |
|
| 2015 |
Lodato MA, Woodworth MB, Lee S, Evrony GD, Mehta BK, Karger A, Lee S, Chittenden TW, D'Gama AM, Cai X, Luquette LJ, Lee E, Park PJ, Walsh CA. Somatic mutation in single human neurons tracks developmental and transcriptional history. Science (New York, N.Y.). 350: 94-8. PMID 26430121 DOI: 10.1126/Science.Aab1785 |
0.309 |
|
| 2015 |
Evrony GD, Lee E, Mehta BK, Benjamini Y, Johnson RM, Cai X, Yang L, Haseley P, Lehmann HS, Park PJ, Walsh CA. Cell lineage analysis in human brain using endogenous retroelements. Neuron. 85: 49-59. PMID 25569347 DOI: 10.1016/J.Neuron.2014.12.028 |
0.312 |
|
| 2015 |
Janku F, Huang HJ, Ramzanali NM, Hong DS, Karp DD, Fu S, Cai X, Zhao Y, Salathia N, Waters J, Liu L, Meric-Bernstam F, Mills GB, Fan J. Ultra-deep next-generation sequencing of plasma cell-free (cf) DNA from patients with advanced cancers. Journal of Clinical Oncology. 33: 11537-11537. DOI: 10.1200/Jco.2015.33.15_Suppl.E22168 |
0.33 |
|
| 2015 |
Janku F, Huang HJ, Ramzanali NM, Hong DS, Karp DD, Cai X, Zhao Y, Salathia N, Waters J, Liu L, Klausner R, Meric-Bernstam F, Fan J. Abstract 2414: Novel, ultra deep next-generation sequencing of plasma cell-free DNA from patients with advanced cancers Cancer Research. 75: 2414-2414. DOI: 10.1158/1538-7445.Am2015-2414 |
0.35 |
|
| 2014 |
Janku F, Huang HJ, Ramzanali NM, Cai X, Klausner R, Meric-Bernstam F, Fan JB. 170 Novel, ultra-deep next-generation sequencing for BRAF mutation testing using small amount of cell-free DNA from plasma of patients with advanced cancers European Journal of Cancer. 50: 57. DOI: 10.1016/S0959-8049(14)70296-5 |
0.332 |
|
| 2013 |
Poduri A, Evrony GD, Cai X, Walsh CA. Somatic mutation, genomic variation, and neurological disease. Science (New York, N.Y.). 341: 1237758. PMID 23828942 DOI: 10.1126/Science.1237758 |
0.312 |
|
| 2012 |
Poduri A, Evrony GD, Cai X, Elhosary PC, Beroukhim R, Lehtinen MK, Hills LB, Heinzen EL, Hill A, Hill RS, Barry BJ, Bourgeois BF, Riviello JJ, Barkovich AJ, Black PM, et al. Somatic activation of AKT3 causes hemispheric developmental brain malformations. Neuron. 74: 41-8. PMID 22500628 DOI: 10.1016/J.Neuron.2012.03.010 |
0.3 |
|
| 2011 |
Alkuraya FS, Cai X, Emery C, Mochida GH, Al-Dosari MS, Felie JM, Hill RS, Barry BJ, Partlow JN, Gascon GG, Kentab A, Jan M, Shaheen R, Feng Y, Walsh CA. Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected]. American Journal of Human Genetics. 88: 536-47. PMID 21529751 DOI: 10.1016/J.Ajhg.2011.04.003 |
0.304 |
|
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