| Year |
Citation |
Score |
| 2018 |
Dong X, Shi M, Lee M, Toro R, Gravina S, Han W, Yasuda S, Wang T, Zhang Z, Vijg J, Suh Y, Spivack SD. Global, integrated analysis of methylomes and transcriptomes from laser capture microdissected bronchial and alveolar cells in human lung. Epigenetics. 1-22. PMID 29465290 DOI: 10.1080/15592294.2018.1441650 |
0.3 |
|
| 2015 |
Nadel J, Athanasiadou R, Lemetre C, Wijetunga NA, Ó Broin P, Sato H, Zhang Z, Jeddeloh J, Montagna C, Golden A, Seoighe C, Greally JM. RNA:DNA hybrids in the human genome have distinctive nucleotide characteristics, chromatin composition, and transcriptional relationships. Epigenetics & Chromatin. 8: 46. PMID 26579211 DOI: 10.1186/S13072-015-0040-6 |
0.32 |
|
| 2015 |
Chung JH, Cai J, Suskin BG, Zhang Z, Coleman K, Morrow BE. Whole-Genome Sequencing and Integrative Genomic Analysis Approach on Two 22q11.2 Deletion Syndrome Family Trios for Genotype to Phenotype Correlations. Human Mutation. 36: 797-807. PMID 25981510 DOI: 10.1002/Humu.22814 |
0.328 |
|
| 2012 |
Golden A, McLellan AS, Dubin RA, Jing Q, O Broin P, Moskowitz D, Zhang Z, Suzuki M, Hargitai J, Calder RB, Greally JM. The Einstein Genome Gateway using WASP - a high throughput multi-layered life sciences portal for XSEDE. Studies in Health Technology and Informatics. 175: 182-91. PMID 22942009 DOI: 10.3233/978-1-61499-054-3-182 |
0.321 |
|
| 2009 |
Korbel JO, Abyzov A, Mu XJ, Carriero N, Cayting P, Zhang Z, Snyder M, Gerstein MB. PEMer: a computational framework with simulation-based error models for inferring genomic structural variants from massive paired-end sequencing data. Genome Biology. 10: R23. PMID 19236709 DOI: 10.1186/Gb-2009-10-2-R23 |
0.327 |
|
| 2009 |
Zhang ZD, Nayar M, Ammons D, Rampersad J, Fox GE. Rapid in vivo exploration of a 5S rRNA neutral network. Journal of Microbiological Methods. 76: 181-7. PMID 19041908 DOI: 10.1016/J.Mimet.2008.10.010 |
0.484 |
|
| 2008 |
Wu JQ, Du J, Rozowsky J, Zhang Z, Urban AE, Euskirchen G, Weissman S, Gerstein M, Snyder M. Systematic analysis of transcribed loci in ENCODE regions using RACE sequencing reveals extensive transcription in the human genome. Genome Biology. 9: R3. PMID 18173853 DOI: 10.1186/Gb-2008-9-1-R3 |
0.352 |
|
| 2006 |
Muzny DM, Scherer SE, Kaul R, Wang J, Yu J, Sudbrak R, Buhay CJ, Chen R, Cree A, Ding Y, Dugan-Rocha S, Gill R, Gunaratne P, Harris RA, Hawes AC, ... ... Zhang Z, et al. The DNA sequence, annotation and analysis of human chromosome 3. Nature. 440: 1194-8. PMID 16641997 DOI: 10.1038/Nature04728 |
0.326 |
|
| 2006 |
Zhang Z, Jackson GW, Fox GE, Willson RC. Microbial identification by mass cataloging. Bmc Bioinformatics. 7: 117. PMID 16524471 DOI: 10.1186/1471-2105-7-117 |
0.503 |
|
| 2004 |
Gibbs RA, Weinstock GM, Metzker ML, Muzny DM, Sodergren EJ, Scherer S, Scott G, Steffen D, Worley KC, Burch PE, Okwuonu G, Hines S, Lewis L, DeRamo C, Delgado O, ... ... Zhang Z, et al. Genome sequence of the Brown Norway rat yields insights into mammalian evolution. Nature. 428: 493-521. PMID 15057822 DOI: 10.1038/Nature02426 |
0.338 |
|
| 2003 |
Zhang Z, D'Souza LM, Lee YH, Fox GE. Common 5S rRNA variants are likely to be accepted in many sequence contexts. Journal of Molecular Evolution. 56: 69-76. PMID 12569424 DOI: 10.1007/S00239-002-2381-6 |
0.547 |
|
| 2002 |
Zhang Z, Willson RC, Fox GE. Identification of characteristic oligonucleotides in the bacterial 16S ribosomal RNA sequence dataset. Bioinformatics (Oxford, England). 18: 244-50. PMID 11847072 DOI: 10.1093/Bioinformatics/18.2.244 |
0.542 |
|
| 2002 |
Nagaswamy U, Larios-Sanz M, Hury J, Collins S, Zhang Z, Zhao Q, Fox GE. NCIR: a database of non-canonical interactions in known RNA structures. Nucleic Acids Research. 30: 395-7. PMID 11752347 DOI: 10.1093/Nar/30.1.395 |
0.519 |
|
| 2000 |
Nagaswamy U, Voss N, Zhang Z, Fox GE. Database of non-canonical base pairs found in known RNA structures. Nucleic Acids Research. 28: 375-6. PMID 10592279 DOI: 10.1093/Nar/28.1.375 |
0.499 |
|
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