Gut microbiome modulates response to anti–PD-1 immunotherapy in melanoma patients V Gopalakrishnan, CN Spencer, L Nezi, A Reuben, MC Andrews, ... Science 359 (6371), 97-103, 2018 | 3869 | 2018 |
Preleukaemic clonal haemopoiesis and risk of therapy-related myeloid neoplasms: a case-control study K Takahashi, F Wang, H Kantarjian, D Doss, K Khanna, E Thompson, ... The Lancet Oncology 18 (1), 100-111, 2017 | 354 | 2017 |
Neoadjuvant plus adjuvant dabrafenib and trametinib versus standard of care in patients with high-risk, surgically resectable melanoma: a single-centre, open-label, randomised … RN Amaria, PA Prieto, MT Tetzlaff, A Reuben, MC Andrews, MI Ross, ... The Lancet Oncology 19 (2), 181-193, 2018 | 272 | 2018 |
Gut microbiota signatures are associated with toxicity to combined CTLA-4 and PD-1 blockade MC Andrews, CPM Duong, V Gopalakrishnan, V Iebba, WS Chen, ... Nature Medicine, 1-10, 2021 | 254 | 2021 |
Herd behavior in a complex adaptive system L Zhao, G Yang, W Wang, Y Chen, JP Huang, H Ohashi, HE Stanley Proceedings of the National Academy of Sciences 108 (37), 15058-15063, 2011 | 105 | 2011 |
Evidence for feasibility of fetal trophoblastic cell‐based noninvasive prenatal testing AM Breman, JC Chow, L U'Ren, EA Normand, S Qdaisat, L Zhao, ... Prenatal diagnosis 36 (11), 1009-1019, 2016 | 104 | 2016 |
Next-generation sequencing-based molecular diagnosis of 82 retinitis pigmentosa probands from Northern Ireland L Zhao, F Wang, H Wang, Y Li, S Alexander, K Wang, CE Willoughby, ... Human genetics 134 (2), 217-230, 2015 | 103 | 2015 |
Next-generation sequencing–based molecular diagnosis of a Chinese patient cohort with autosomal recessive retinitis pigmentosa Q Fu, F Wang, H Wang, F Xu, JE Zaneveld, H Ren, V Keser, I Lopez, ... Investigative ophthalmology & visual science 54 (6), 4158-4166, 2013 | 97 | 2013 |
Genome‐wide copy number analysis on DNA from fetal cells isolated from the blood of pregnant women S Kølvraa, R Singh, EA Normand, S Qdaisat, IB van den Veyver, ... Prenatal diagnosis 36 (12), 1127-1134, 2016 | 89 | 2016 |
Mutations in human IFT140 cause non-syndromic retinal degeneration M Xu, L Yang, F Wang, H Li, X Wang, W Wang, Z Ge, K Wang, L Zhao, ... Human genetics 134 (10), 1069-1078, 2015 | 83 | 2015 |
Molecular Analysis of Clinically Defined Subsets of High-Grade Serous Ovarian Cancer S Lee, L Zhao, C Rojas, NW Bateman, H Yao, OD Lara, J Celestino, ... Cell Reports 31 (2), 107502, 2020 | 76 | 2020 |
Mutations in the spliceosome component CWC27 cause retinal degeneration with or without additional developmental anomalies M Xu, YA Xie, H Abouzeid, CT Gordon, A Fiorentino, Z Sun, A Lehman, ... The American Journal of Human Genetics 100 (4), 592-604, 2017 | 70 | 2017 |
ATF6 Is Mutated in Early Onset Photoreceptor Degeneration With Macular Involvement M Xu, V Gelowani, A Eblimit, F Wang, MP Young, BL Sawyer, L Zhao, ... Investigative ophthalmology & visual science 56 (6), 3889-3895, 2015 | 59 | 2015 |
SeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing data Y Chen, L Zhao, Y Wang, M Cao, V Gelowani, M Xu, SA Agrawal, Y Li, ... BMC bioinformatics 18 (1), 1-9, 2017 | 57 | 2017 |
4-1BB agonist focuses CD8+ tumor-infiltrating T-cell growth into a distinct repertoire capable of tumor recognition in pancreatic cancer D Sakellariou-Thompson, MA Forget, C Creasy, V Bernard, L Zhao, ... Clinical Cancer Research 23 (23), 7263-7275, 2017 | 56 | 2017 |
ADIPOR1 Is Mutated in Syndromic Retinitis Pigmentosa M Xu, A Eblimit, J Wang, J Li, F Wang, L Zhao, X Wang, N Xiao, Y Li, ... Human mutation 37 (3), 246-249, 2016 | 48 | 2016 |
Mutations in POMGNT1 cause non-syndromic retinitis pigmentosa M Xu, T Yamada, Z Sun, A Eblimit, I Lopez, F Wang, H Manya, S Xu, ... Human molecular genetics 25 (8), 1479-1488, 2016 | 48 | 2016 |
Germline DNA Sequencing Reveals Novel Mutations Predictive of Overall Survival in a Cohort of Patients with Pancreatic Cancer JB Goldstein, L Zhao, X Wang, Y Ghelman, MJ Overman, MM Javle, ... Clinical Cancer Research 26 (6), 1385-1394, 2020 | 42 | 2020 |
Germline DNA Sequencing Reveals Novel Mutations Predictive of Overall Survival in a Cohort of Pancreatic Cancer Patients JB Goldstein, L Zhao, X Wang, Y Ghelman, MJ Overman, M Javle, ... Clinical Cancer Research, 2019 | 42* | 2019 |
Hypomorphic mutations identified in the candidate Leber congenital amaurosis gene CLUAP1 ZT Soens, Y Li, L Zhao, A Eblimit, R Dharmat, Y Li, Y Chen, M Naqeeb, ... Genetics in Medicine 18 (10), 1044-1051, 2016 | 38 | 2016 |