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| Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes D Liang, DS Cram, HU Tan, S Linpeng, Y Liu, H Sun, Y Zhang, F Tian, ... Genetics in Medicine 21 (9), 1998-2006, 2019 | 206 | 2019 |
| Pregnancy-related complications and adverse pregnancy outcomes in multiple pregnancies resulting from assisted reproductive technology: a meta-analysis of cohort studies J Qin, H Wang, X Sheng, D Liang, H Tan, J Xia Fertility and sterility 103 (6), 1492-1508. e7, 2015 | 177 | 2015 |
| Non‐invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing D Liang, W Lv, H Wang, L Xu, J Liu, H Li, L Hu, Y Peng, L Wu Prenatal diagnosis 33 (5), 409-415, 2013 | 168 | 2013 |
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| Common genetic variants on 1p13. 2 associate with risk of autism K Xia, H Guo, Z Hu, G Xun, L Zuo, Y Peng, K Wang, Y He, Z Xiong, L Sun, ... Molecular psychiatry 19 (11), 1212-1219, 2014 | 112 | 2014 |
| Assisted reproductive technology and risk of congenital malformations: a meta-analysis based on cohort studies J Qin, X Sheng, H Wang, D Liang, H Tan, J Xia Archives of gynecology and obstetrics 292, 777-798, 2015 | 111 | 2015 |
| MicroRNAs expression in ox-LDL treated HUVECs: MiR-365 modulates apoptosis and Bcl-2 expression B Qin, B Xiao, D Liang, J Xia, Y Li, H Yang Biochemical and biophysical research communications 410 (1), 127-133, 2011 | 111 | 2011 |
| Noninvasive prenatal testing for Wilson disease by use of circulating single-molecule amplification and resequencing technology (cSMART) W Lv, X Wei, R Guo, Q Liu, Y Zheng, J Chang, T Bai, H Li, J Zhang, ... Clinical Chemistry 61 (1), 172-181, 2015 | 109 | 2015 |
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| Seamless Genetic Conversion of SMN2 to SMN1 via CRISPR/Cpf1 and Single-Stranded Oligodeoxynucleotides in Spinal Muscular Atrophy Patient-Specific … M Zhou, Z Hu, L Qiu, T Zhou, M Feng, Q Hu, B Zeng, Z Li, Q Sun, Y Wu, ... Human gene therapy 29 (11), 1252-1263, 2018 | 64 | 2018 |
| XRCC2 mutation causes meiotic arrest, azoospermia and infertility Y Yang, J Guo, L Dai, Y Zhu, H Hu, L Tan, W Chen, D Liang, J He, M Tu, ... Journal of medical genetics 55 (9), 628-636, 2018 | 64 | 2018 |
| MicroRNA let-7c inhibits Bcl-xl expression and regulates ox-LDL-induced endothelial apoptosis B Qin, B Xiao, D Liang, Y Li, T Jiang, H Yang BMB reports 45 (8), 464-469, 2012 | 64 | 2012 |
| Mutation in PITX2 is associated with ring dermoid of the cornea K Xia, L Wu, X Liu, X Xi, D Liang, D Zheng, F Cai, Q Pan, Z Long, H Dai, ... Journal of medical genetics 41 (12), e129-e129, 2004 | 60 | 2004 |
| In situ genetic correction of F8 intron 22 inversion in hemophilia A patient-specific iPSCs Y Wu, Z Hu, Z Li, J Pang, M Feng, X Hu, X Wang, S Lin-Peng, B Liu, ... Scientific reports 6 (1), 18865, 2016 | 58 | 2016 |
| TALE nickase mediates high efficient targeted transgene integration at the human multi-copy ribosomal DNA locus Y Wu, T Gao, X Wang, Y Hu, X Hu, Z Hu, J Pang, Z Li, J Xue, M Feng, ... Biochemical and biophysical research communications 446 (1), 261-266, 2014 | 57 | 2014 |
| Molecular analysis of hearing loss associated with enlarged vestibular aqueduct in the mainland Chinese: a unique SLC26A4 mutation spectrum H Hu, L Wu, Y Feng, Q Pan, Z Long, J Li, H Dai, K Xia, D Liang, N Niikawa, ... Journal of Human Genetics 52 (6), 492-497, 2007 | 56 | 2007 |
| DMD mutation spectrum analysis in 613 Chinese patients with dystrophinopathy R Guo, G Zhu, H Zhu, R Ma, Y Peng, D Liang, L Wu Journal of human genetics 60 (8), 435-442, 2015 | 54 | 2015 |
| A novel de novo POGZ mutation in a patient with intellectual disability BO Tan, Y Zou, Y Zhang, R Zhang, J Ou, Y Shen, J Zhao, X Luo, J Guo, ... Journal of human genetics 61 (4), 357-359, 2016 | 51 | 2016 |
| A study on a cohort of 301 Chinese patients with isolated methylmalonic acidemia L Kang, Y Liu, M Shen, YI Liu, R He, J Song, Y Jin, M Li, Y Zhang, H Dong, ... Journal of inherited metabolic disease 43 (3), 409-423, 2020 | 50 | 2020 |
daisuke satoHokkaido University在 huhp.hokudai.ac.jp 的电子邮件经过验证
