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X Qi, DH Zhang, N Wu, JH Xiao, X Wang, W Ma
Journal of medical genetics 52 (10), 710-718, 2015
|TBX6 null variants and a common hypomorphic allele in congenital scoliosis|
N Wu, X Ming, J Xiao, Z Wu, X Chen, M Shinawi, Y Shen, G Yu, J Liu, ...
New England Journal of Medicine 372 (4), 341-350, 2015
|Mechanical sensing protein PIEZO1 regulates bone homeostasis via osteoblast-osteoclast crosstalk|
L Wang, X You, S Lotinun, L Zhang, N Wu, W Zou
Nature communications 11 (1), 1-12, 2020
|Identification of tumor immune infiltration-associated lncRNAs for improving prognosis and immunotherapy response of patients with non-small cell lung cancer|
J Sun, Z Zhang, S Bao, C Yan, P Hou, N Wu, J Su, L Xu, M Zhou
Journal for immunotherapy of cancer 8 (1), 2020
|Reanalysis of clinical exome sequencing data|
P Liu, L Meng, EA Normand, F Xia, X Song, A Ghazi, J Rosenfeld, ...
New England Journal of Medicine 380 (25), 2478-2480, 2019
|Insights into genetics, human biology and disease gleaned from family based genomic studies|
JE Posey, AH O’Donnell-Luria, JX Chong, T Harel, SN Jhangiani, ...
Genetics in Medicine 21 (4), 798-812, 2019
|The copy number variation landscape of congenital anomalies of the kidney and urinary tract|
M Verbitsky, R Westland, A Perez, K Kiryluk, Q Liu, P Krithivasan, ...
Nature genetics 51 (1), 117-127, 2019
|CRISPR/Cas9 in zebrafish: an efficient combination for human genetic diseases modeling|
J Liu, Y Zhou, X Qi, J Chen, W Chen, G Qiu, Z Wu, N Wu
Human genetics 136 (1), 1-12, 2017
|Piezo1/2 mediate mechanotransduction essential for bone formation through concerted activation of NFAT-YAP1-▀-catenin|
T Zhou, B Gao, Y Fan, Y Liu, S Feng, Q Cong, X Zhang, Y Zhou, PS Yadav, ...
Elife 9, e52779, 2020
|Recurrence-associated long non-coding RNA signature for determining the risk of recurrence in patients with colon cancer|
M Zhou, L Hu, Z Zhang, N Wu, J Sun, J Su
Molecular Therapy-Nucleic Acids 12, 518-529, 2018
|The regulatory roles of microRNAs in bone remodeling and perspectives as biomarkers in osteoporosis|
M Sun, X Zhou, L Chen, S Huang, V Leung, N Wu, H Pan, W Zhen, W Lu, ...
BioMed Research International 2016, 2016
|Synovitis, acne, pustulosis, hyperostosis and osteitis syndrome: a single centre study of a cohort of 164 patients|
C Li, Y Zuo, N Wu, L Li, F Li, W Zhang, W Xu, X Zhao, H Jing, Q Pan, ...
Rheumatology 55 (6), 1023-1030, 2016
|CD146 as a new marker for an increased chondroprogenitor cell sub‐population in the later stages of osteoarthritis|
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Journal of Orthopaedic Research 33 (1), 84-91, 2015
|The genetic landscape and clinical implications of vertebral anomalies in VACTERL association|
Y Chen, Z Liu, J Chen, Y Zuo, S Liu, W Chen, G Liu, G Qiu, PF Giampietro, ...
Journal of Medical Genetics 53 (7), 431-437, 2016
|FusionCancer: a database of cancer fusion genes derived from RNA-seq data|
Y Wang, N Wu, J Liu, Z Wu, D Dong
Diagnostic pathology 10 (1), 1-4, 2015
|Perturbations of BMP/TGF-β and VEGF/VEGFR signalling pathways in non-syndromic sporadic brain arteriovenous malformations (BAVM)|
K Wang, S Zhao, B Liu, Q Zhang, Y Li, J Liu, Y Shen, X Ding, J Lin, Y Wu, ...
Journal of medical genetics 55 (10), 675-684, 2018
|Distinctive structural hallmarks and biological activities of the multiple cathelicidin antimicrobial peptides in a primitive teleost fish|
XJ Zhang, XY Zhang, N Zhang, X Guo, KS Peng, H Wu, LF Lu, N Wu, ...
The Journal of Immunology 194 (10), 4974-4987, 2015
|The role of semaphorin 3A in bone remodeling|
Z Li, J Hao, X Duan, N Wu, Z Zhou, F Yang, J Li, Z Zhao, S Huang
Frontiers in Cellular Neuroscience 11, 40, 2017
|TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 geneá…|
J Liu, N Wu, N Yang, K Takeda, W Chen, W Li, R Du, S Liu, Y Zhou, ...
Genetics in Medicine 21 (7), 1548-1558, 2019
|TBX6 compound inheritance leads to congenital vertebral malformations in humans and mice|
N Yang, N Wu, L Zhang, Y Zhao, J Liu, X Liang, X Ren, W Li, W Chen, ...
Human molecular genetics 28 (4), 539-547, 2019