Year |
Citation |
Score |
2016 |
Liang D, Wang Y, Ji X, Hu H, Zhang J, Meng L, Lin Y, Ma D, Jiang T, Jiang H, Asan, Song L, Guo J, Hu P, Xu Z. Clinical application of whole-genome low-coverage next-generation sequencing to detect and characterize balanced chromosomal translocations. Clinical Genetics. PMID 27491356 DOI: 10.1111/cge.12844 |
0.675 |
|
2016 |
Li L, Ma D, Sun Y, Zhang J, Wang Y, Jiang T, Xu Z. [Mutation screening and prenatal diagnosis of methylmalonic academia in a Chinese pedigree by Ion Torrent semiconductor sequencing]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 33: 181-185. PMID 27060311 DOI: 10.3760/cma.j.issn.1003-9406.2016.02.012 |
0.658 |
|
2016 |
Wang Y, Lin Y, Luo C, Liang D, Ji X, Jiang T, Ma D, Xu Z. [Detection of TSC1/TSC2 gene mutations among patients with tuberous sclerosis complex by Ion Torrent semiconductor sequencing]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 33: 169-172. PMID 27060308 DOI: 10.3760/cma.j.issn.1003-9406.2016.02.009 |
0.656 |
|
2016 |
Ma D, Zhang J, Luo C, Lin Y, Ji X, Hu P, Xu Z. Genetic counseling for patients with nonsyndromic hearing impairment directed by gene analysis. Molecular Medicine Reports. PMID 26783197 DOI: 10.3892/mmr.2016.4769 |
0.669 |
|
2015 |
Zhang J, Ma D, Wang Y, Cao L, Wu Y, Qiao F, Liu A, Li L, Lin Y, Liu G, Liu C, Hu P, Xu Z. Analysis of chromosome 22q11 copy number variations by multiplex ligation-dependent probe amplification for prenatal diagnosis of congenital heart defect. Molecular Cytogenetics. 8: 100. PMID 26715944 DOI: 10.1186/s13039-015-0209-5 |
0.661 |
|
2015 |
Dong S, Dong S, Tian X, Xu Z, Ma D, Cui B, Ren N, Rittmann BE. Role of self-assembly coated Er(3+): YAlO3/TiO2 in intimate coupling of visible-light-responsive photocatalysis and biodegradation reactions. Journal of Hazardous Materials. 302: 386-394. PMID 26489913 DOI: 10.1016/J.Jhazmat.2015.10.007 |
0.618 |
|
2015 |
Ji X, Liang D, Sun R, Liu C, Ma D, Wang Y, Hu P, Xu Z. Molecular characterization of ring chromosome 18 by low-coverage next generation sequencing. Bmc Medical Genetics. 16: 57. PMID 26224010 DOI: 10.1186/s12881-015-0206-x |
0.658 |
|
2015 |
Cheng J, Ma D, Wu Y, Luo C, Huang C, Hu P, Zhang J, Jiang T, Xu Z. Identification of one novel CHD7 mutation in a patient from China with atypical CHARGE syndrome. Gene. PMID 26187070 DOI: 10.1016/j.gene.2015.07.042 |
0.647 |
|
2015 |
Zhou D, Xu Z, Dong S, Huo M, Dong S, Tian X, Cui B, Xiong H, Li T, Ma D. Intimate Coupling of Photocatalysis and Biodegradation for Degrading Phenol Using Different Light Types: Visible Light vs UV Light. Environmental Science & Technology. PMID 26076382 DOI: 10.1021/acs.est.5b00989 |
0.612 |
|
2015 |
Sun Y, Jiang T, Ma D, Yang G, Yang B, Wang Y, Xu Z. [Detection of pathogenic mutations for methylmalonic acidemia using new-generation semiconductor targeted sequencing]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 32: 56-9. PMID 25636100 DOI: 10.3760/cma.j.issn.1003-9406.2015.01.012 |
0.65 |
|
2015 |
Hu P, Meng L, Ma D, Qiao F, Wang Y, Zhou J, Yi L, Xu Z. A novel 11p13 microdeletion encompassing PAX6 in a Chinese Han family with aniridia, ptosis and mental retardation. Molecular Cytogenetics. 8: 3. PMID 25628759 DOI: 10.1186/s13039-015-0110-2 |
0.68 |
|
2014 |
Kim MR, Xu Z, Chen G, Ma D. Semiconductor and metallic core-shell nanostructures: synthesis and applications in solar cells and catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 11256-75. PMID 25044334 DOI: 10.1002/Chem.201402277 |
0.609 |
|
2014 |
Wang Y, Zhang J, Qin L, Meng L, Jiang T, Ma D, Hui W, Hu P, Xu Z. [Single nueleotide polymorphism array detection of Xq28 duplication in a child with mental retardation]. Zhonghua Er Ke Za Zhi. Chinese Journal of Pediatrics. 52: 227-8. PMID 24824396 |
0.627 |
|
2014 |
Ma D, Ge H, Li X, Jiang T, Chen F, Zhang Y, Hu P, Chen S, Zhang J, Ji X, Xu X, Jiang H, Chen M, Wang W, Xu Z. Haplotype-based approach for noninvasive prenatal diagnosis of congenital adrenal hyperplasia by maternal plasma DNA sequencing. Gene. 544: 252-8. PMID 24768736 DOI: 10.1016/j.gene.2014.04.055 |
0.664 |
|
2014 |
Zhang J, Hu P, Luo C, Ji Q, Zhou J, Liu A, Ma D, Xu Z. [Application of multiplex ligation-dependent probe amplification for rapid detection of aneuploidies and structural chromosomal abnormalities in prenatal diagnosis]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 31: 11-5. PMID 24510553 DOI: 10.3760/cma.j.issn.1003-9406.2014.01.003 |
0.656 |
|
2014 |
Ma D, Chen Y, Sun Y, Yang B, Cheng J, Huang M, Zhang J, Zhang J, Hu P, Lin Y, Jiang T, Xu Z. Molecular analysis of the CYP21A2 gene in Chinese patients with steroid 21-hydroxylase deficiency. Clinical Biochemistry. 47: 455-63. PMID 24503005 DOI: 10.1016/j.clinbiochem.2014.01.019 |
0.652 |
|
2011 |
Hu P, Ji X, Yang C, Zhang J, Lin Y, Cheng J, Ma D, Cao L, Yi L, Xu Z. 22q11.2 microduplication in a family with recurrent fetal congenital heart disease. European Journal of Medical Genetics. 54: e433-6. PMID 21473936 DOI: 10.1016/j.ejmg.2011.03.009 |
0.66 |
|
2011 |
Xiong Y, Zhou SF, Zhou R, Yang D, Xu ZF, Lou YT, Guo QS, Hu R, Peng T, Ma D, Li XT. Alternations of maternal and cord plasma hemostasis in preeclampsia before and after delivery. Hypertension in Pregnancy. 30: 347-58. PMID 21174589 DOI: 10.3109/10641950903572274 |
0.623 |
|
2010 |
Xu Z, Xia B, Gong Q, Bailey J, Groves B, Radeke M, Wood SA, Szumlinski KK, Ma D. Identification of a deubiquitinating enzyme as a novel AGS3-interacting protein. Plos One. 5: e9725. PMID 20305814 DOI: 10.1371/Journal.Pone.0009725 |
0.726 |
|
2009 |
Xu Z, Gong Q, Xia B, Groves B, Zimmermann M, Mugler C, Mu D, Matsumoto B, Seaman M, Ma D. A role of histone H3 lysine 4 methyltransferase components in endosomal trafficking. The Journal of Cell Biology. 186: 343-53. PMID 19651892 DOI: 10.1083/Jcb.200902146 |
0.722 |
|
2007 |
Groves B, Gong Q, Xu Z, Huntsman C, Nguyen C, Li D, Ma D. A specific role of AGS3 in the surface expression of plasma membrane proteins. Proceedings of the National Academy of Sciences of the United States of America. 104: 18103-8. PMID 17991770 DOI: 10.1073/Pnas.0709282104 |
0.73 |
|
2007 |
Gong Q, Weide M, Huntsman C, Xu Z, Jan LY, Ma D. Identification and characterization of a new class of trafficking motifs for controlling clathrin-independent internalization and recycling. The Journal of Biological Chemistry. 282: 13087-97. PMID 17331948 DOI: 10.1074/Jbc.M700767200 |
0.706 |
|
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