| The Vibrio cholerae quorum sensing response is mediated by Hfq‐dependent sRNA/mRNA base pairing interactions JP Bardill, X Zhao, BK Hammer Molecular microbiology 80 (5), 1381-1394, 2011 | 122 | 2011 |
| Nanoparticles inhibit DNA replication by binding to DNA: modeling and experimental validation K Li, X Zhao, B K. Hammer, S Du, Y Chen ACS nano 7 (11), 9664-9674, 2013 | 103 | 2013 |
| Automated clinical exome reanalysis reveals novel diagnoses SW Baker, JR Murrell, AI Nesbitt, KB Pechter, J Balciuniene, X Zhao, Z Yu, ... The Journal of Molecular Diagnostics 21 (1), 38-48, 2019 | 82 | 2019 |
| Post‐transcriptional activation of a diguanylate cyclase by quorum sensing small RNAs promotes biofilm formation in Vibrio cholerae X Zhao, BJ Koestler, CM Waters, BK Hammer Molecular microbiology 89 (5), 989-1002, 2013 | 63 | 2013 |
| NTRK fusions identified in pediatric tumors: the frequency, fusion partners, and clinical outcome X Zhao, C Kotch, E Fox, LF Surrey, GB Wertheim, ZW Baloch, F Lin, ... JCO precision oncology 1, 204-214, 2021 | 57 | 2021 |
| Genomic analysis of dysembryoplastic neuroepithelial tumor spectrum reveals a diversity of molecular alterations dysregulating the MAPK and PI3K/mTOR pathways LF Surrey, P Jain, B Zhang, J Straka, X Zhao, BN Harding, AC Resnick, ... Journal of Neuropathology & Experimental Neurology 78 (12), 1100-1111, 2019 | 49 | 2019 |
| NFIB haploinsufficiency is associated with intellectual disability and macrocephaly I Schanze, J Bunt, JWC Lim, D Schanze, RJ Dean, M Alders, P Blanchet, ... The American Journal of Human Genetics 103 (5), 752-768, 2018 | 41 | 2018 |
| Rapid and accurate interpretation of clinical exomes using Phenoxome: a computational phenotype-driven approach C Wu, B Devkota, P Evans, X Zhao, SW Baker, R Niazi, K Cao, ... European Journal of Human Genetics 27 (4), 612-620, 2019 | 23 | 2019 |
| Genomic characterization of a PPP1CB-ALK fusion with fusion gene amplification in a congenital glioblastoma Y Zhong, F Lin, F Xu, J Schubert, J Wu, L Wainwright, X Zhao, K Cao, ... Cancer Genetics 252, 37-42, 2021 | 10 | 2021 |
| Molecular diagnostic outcomes from 700 cases: What can we learn from a retrospective analysis of clinical exome sequencing? JR Murrell, AMI Nesbitt, SW Baker, KB Pechter, J Balciuniene, X Zhao, ... The Journal of Molecular Diagnostics 24 (3), 274-286, 2022 | 8 | 2022 |
| Clinical impact of genomic characterization of 15 patients with acute megakaryoblastic leukemia–related malignancies E Lalonde, S Rentas, G Wertheim, K Cao, LF Surrey, F Lin, X Zhao, ... Molecular Case Studies 7 (2), a005975, 2021 | 8 | 2021 |
| A community approach to the cancer-variant-interpretation bottleneck K Krysiak, AM Danos, S Kiwala, JF McMichael, AC Coffman, EK Barnell, ... Nature Cancer 3 (5), 522-525, 2022 | 3 | 2022 |
| Non-coding small RNAs regulate multiple mRNA targets to control the Vibrio cholerae quorum sensing response X Zhao Georgia Institute of Technology, 2013 | 1 | 2013 |
| eP421: Development of an in-house whole transcriptome test for evaluation of splicing VUS variants: Experience and challenges in variant interpretation X Zhao, CW Wu, Y Li, A Omer, Y Feng, L Meng, C Eng, F Xia, H Dai Genetics in Medicine 24 (3), S263-S264, 2022 | | 2022 |
| eP337: Rapid Genome Sequencing (rGS) as first tier test for critically ill children with suspected genetic etiology H Dai, L Vossaert, X Zhao, K Schulze, P Liu, C Qu, V Nguyen, M Santana, ... Genetics in Medicine 24 (3), S210-S211, 2022 | | 2022 |
| 48. Crowdsourcing expert curation of somatic variants by the ClinGen Somatic Hematologic Cancer Taskforce S Rao, J Saliba, X Zhao, R He, C Kesserwan, A Danos, L Sheta, P Terraf, ... Cancer Genetics 260, 16, 2022 | | 2022 |
| Expert Curation of Somatic FLT3 Variants By the Clingen Somatic Hematologic Cancer Taskforce (ClinGen HCT) X Shao, S Rao, C Mani, J Saliba, R He, C Kesserwan, A Danos, L Sheta, ... Blood 138, 4387, 2021 | | 2021 |
| Evolution of the open-access CIViC knowledgebase is driven by the needs of the cancer variant interpretation community K Krysiak, AM Danos, S Kiwala, JF McMichael, AC Coffman, EK Barnell, ... bioRxiv, 2021.06. 13.448171, 2021 | | 2021 |
| Detection of acquired uniparental disomy in clinical exome sequencing of pediatric patients with leukemia predisposition syndromes and its clinical significance X Zhao, W Craigen, N Owen, J Dong, R Rau, W Bi, H Dai Molecular Genetics and Metabolism 132, S243-S245, 2021 | | 2021 |
| 10. The Spectrum of NTRK Fusion-associated Pediatric Tumors X Zhao, F Lin, L Surrey, M Luo, A Bauer, P Kreiger, B Pawel, J Pogoriler, ... Cancer Genetics 233, S4-S5, 2019 | | 2019 |
