Bing Xiao, Ph.D. - Publications

Affiliations: 
Physics Temple University, Philadelphia, PA, United States 
Area:
density-functional theory of electronic structure

43 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Xiao B, Ji X, Ye H, Liu Y, Cao Y, Sun Y, Wei W, Qiu W. [Genotypic and phenotypic analysis of a patient with de novo partial monosomy 18p and partial trisomy 18q]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 36: 484-487. PMID 31030439 DOI: 10.3760/cma.j.issn.1003-9406.2019.05.017  0.36
2019 Zhang Y, Furness JW, Xiao B, Sun J. Subtlety of TiO phase stability: Reliability of the density functional theory predictions and persistence of the self-interaction error. The Journal of Chemical Physics. 150: 014105. PMID 30621425 DOI: 10.1063/1.5055623  0.72
2018 Fan Y, Wu Y, Wang L, Wang Y, Gong Z, Qiu W, Wang J, Zhang H, Ji X, Ye J, Han L, Jin X, Shen Y, Li F, Xiao B, et al. Chromosomal microarray analysis in developmental delay and intellectual disability with comorbid conditions. Bmc Medical Genomics. 11: 49. PMID 29793483 DOI: 10.1186/s12920-018-0368-4  0.36
2018 He Y, Ji X, Yan H, Ye X, Liu Y, Wei W, Xiao B, Sun Y. Biallelic UNC80 mutations caused infantile hypotonia with psychomotor retardation and characteristic facies 2 in two Chinese patients with variable phenotypes. Gene. PMID 29572195 DOI: 10.1016/j.gene.2018.03.063  0.36
2017 Tiburcio PDB, Xiao B, Berg S, Asper S, Lyne S, Zhang Y, Zhu X, Yan H, Huang LE. Functional requirement of a wild-type allele for mutant IDH1 to suppress anchorage-independent growth through redox homeostasis. Acta Neuropathologica. PMID 29288440 DOI: 10.1007/s00401-017-1800-0  0.32
2017 Xu Y, Wang H, Xiao B, Wei W, Liu Y, Ye H, Ying XM, Chen YW, Liu XQ, Ji X, Sun Y. Novel noncontiguous duplications identified with a comprehensive mutation analysis in the DMD gene by DMD gene-targeted sequencing. Gene. PMID 29273555 DOI: 10.1016/j.gene.2017.12.037  0.36
2017 Xu H, Ji X, Xu Y, Liu X, Zhang J, Chen Y, Xiao B. [Clinical and genetic analysis of two unrelated patients with Angelman syndrome and novel UBE3A mutations]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 34: 826-830. PMID 29188609 DOI: 10.3760/cma.j.issn.1003-9406.2017.06.009  0.36
2017 Xiao B, Qiu W, Ji X, Liu X, Huang Z, Liu H, Fan Y, Xu Y, Liu Y, Yie H, Wei W, Yan H, Gong Z, Shen L, Sun Y. Marked yield of re-evaluating phenotype and exome/target sequencing data in 33 individuals with intellectual disabilities. American Journal of Medical Genetics. Part A. PMID 29159939 DOI: 10.1002/ajmg.a.38542  0.36
2017 Chen G, Xiao B, Chen L, Bai B, Zhang Y, Xu Z, Fu L, Liu Z, Li X, Zhao Y, Liang G. Discovery of new MD2-targeted anti-inflammatory compounds for the treatment of sepsis and acute lung injury. European Journal of Medicinal Chemistry. 139: 726-740. PMID 28858767 DOI: 10.1016/j.ejmech.2017.08.036  0.32
2017 Wang H, Xiao B, Ji X, Zhang J, Cao Y, Ni L, Ye H, Shen L. [Phenotypic and genetic analysis of four patients with 13q33-q34 microdeletion]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 34: 509-513. PMID 28777848 DOI: 10.3760/cma.j.issn.1003-9406.2017.04.009  0.36
2017 Wang H, Xu Y, Liu X, Wang L, Jiang W, Xiao B, Wei W, Chen Y, Ye W, Ji X. Prenatal diagnosis of Duchenne muscular dystrophy in 131 Chinese families with dystrophinopathy. Prenatal Diagnosis. PMID 28181689 DOI: 10.1002/pd.5019  0.36
2016 Xu H, Ji X, Ni L, Zhu Y, Chen Y, Xiao B. [Clinical features and genetic analysis of two cases with 16p13.3 microdeletion and 19q13.4 microduplication derived from familial cryptic balanced translocation]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 33: 490-3. PMID 27455004 DOI: 10.3760/cma.j.issn.1003-9406.2016.04.013  0.36
2016 Zahedi E, Xiao B, Shayestefar M. First-Principles Investigations of the Structure, Electronic, and Optical Properties of Mullite-Type Orthorhombic Bi2M4O9 (M = Al(3+), Ga(3+)). Inorganic Chemistry. PMID 27139249 DOI: 10.1021/acs.inorgchem.6b00330  0.52
2015 Zeng LL, Long L, Shen H, Fang P, Song Y, Zhang L, Xu L, Gong J, Zhang Y, Zhang Y, Xiao B, Hu D. Gray Matter Loss and Related Functional Connectivity Alterations in A Chinese Family With Benign Adult Familial Myoclonic Epilepsy. Medicine. 94: e1767. PMID 26496303 DOI: 10.1097/MD.0000000000001767  0.32
2015 Zhou L, Cao Y, Long H, Long L, Xu L, Liu Z, Zhang Y, Xiao B. ABCB1, ABCC2, SCN1A, SCN2A, GABRA1 gene polymorphisms and drug resistant epilepsy in the Chinese Han population. Die Pharmazie. 70: 416-20. PMID 26189305 DOI: 10.1691/ph.2015.4849  0.32
2015 Qu J, Yang ZQ, Zhang Y, Mao CX, Wang ZB, Mao XY, Zhou BT, Yin JY, He H, Long HY, Gong JE, Xiao B, Zhou HH, Liu ZQ. Common variants of ATP1A3 but not ATP1A2 are associated with Chinese genetic generalized epilepsies. Journal of the Neurological Sciences. 354: 56-62. PMID 26003227 DOI: 10.1016/j.jns.2015.04.045  0.32
2015 Patra A, Xiao B, Perdew JP. Short-range cut-off of the summed-up van der waals series: rare-gas dimers. Topics in Current Chemistry. 365: 53-80. PMID 25896440 DOI: 10.1007/128_2015_625  0.52
2015 Wang L, Zhang Y, Asakawa T, Li W, Han S, Li Q, Xiao B, Namba H, Lu C, Dong Q. Neuroprotective effect of neuroserpin in oxygen-glucose deprivation- and reoxygenation-treated rat astrocytes in vitro. Plos One. 10: e0123932. PMID 25874935 DOI: 10.1371/journal.pone.0123932  0.32
2015 Long L, Song Y, Zhang L, Hu C, Gong J, Xu L, Long H, Zhou L, Zhang Y, Zhang Y, Xiao B. A case-control proton magnetic resonance spectroscopy study confirms cerebellar dysfunction in benign adult familial myoclonic epilepsy. Neuropsychiatric Disease and Treatment. 11: 485-91. PMID 25750529 DOI: 10.2147/NDT.S77910  0.32
2015 Xiao B, Zhang M, Viennois E, Zhang Y, Wei N, Baker MT, Jung Y, Merlin D. Inhibition of MDR1 gene expression and enhancing cellular uptake for effective colon cancer treatment using dual-surface-functionalized nanoparticles. Biomaterials. 48: 147-60. PMID 25701040 DOI: 10.1016/j.biomaterials.2015.01.014  0.32
2015 Xu Y, Li X, Ge HJ, Xiao B, Zhang YY, Ying XM, Pan XY, Wang L, Xie WW, Ni L, Chen SP, Jiang WT, Liu P, Ye H, Cao Y, et al. Haplotype-based approach for noninvasive prenatal tests of Duchenne muscular dystrophy using cell-free fetal DNA in maternal plasma. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 25654318 DOI: 10.1038/gim.2014.207  0.36
2015 Tang L, Xiao B, Xu Y, Ji X, Jiang W, Liu X, Tao J. [Analysis of AGG interspersion of the FMR1 gene in fragile X syndrome]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 32: 11-5. PMID 25636091 DOI: 10.3760/cma.j.issn.1003-9406.2015.01.003  0.72
2015 Xiao B, Hu Q, Zhang Y. Finite-Time Attitude Tracking of Spacecraft With Fault-Tolerant Capability Ieee Transactions On Control Systems Technology. 23: 1338-1350. DOI: 10.1109/TCST.2014.2364124  0.32
2014 Xu Y, Xiao B, Jiang WT, Wang L, Gen HQ, Chen YW, Sun Y, Ji X. A novel mutation identified in PKHD1 by targeted exome sequencing: guiding prenatal diagnosis for an ARPKD family. Gene. 551: 33-8. PMID 25153916 DOI: 10.1016/j.gene.2014.08.032  0.36
2014 Xu H, Xiao B, Ji X, Hu Q, Chen Y, Qiu W. Nonmosaic tetrasomy 15q25.2 → qter identified with SNP microarray in a patient with characteristic facial appearance and review of the literature. European Journal of Medical Genetics. 57: 329-33. PMID 24793337 DOI: 10.1016/j.ejmg.2014.04.011  0.36
2014 Zhang Y, Zhao C, He W, Wang Z, Fang Q, Xiao B, Liu Z, Liang G, Yang S. Discovery and evaluation of asymmetrical monocarbonyl analogs of curcumin as anti-inflammatory agents. Drug Design, Development and Therapy. 8: 373-82. PMID 24741294 DOI: 10.2147/DDDT.S58168  0.32
2014 Ji X, Xing Y, Xu Y, Liu Y, Chen Y, Tao J, Xiao B. A novel mutation in MID1 in a patient with X-linked Opitz G/BBB syndrome. Gene. 537: 140-2. PMID 24374473 DOI: 10.1016/j.gene.2013.12.018  0.72
2013 Hao P, Sun J, Xiao B, Ruzsinszky A, Csonka GI, Tao J, Glindmeyer S, Perdew JP. Performance of meta-GGA Functionals on General Main Group Thermochemistry, Kinetics, and Noncovalent Interactions. Journal of Chemical Theory and Computation. 9: 355-63. PMID 26589038 DOI: 10.1021/ct300868x  0.72
2013 Sun J, Xiao B, Fang Y, Haunschild R, Hao P, Ruzsinszky A, Csonka GI, Scuseria GE, Perdew JP. Density functionals that recognize covalent, metallic, and weak bonds. Physical Review Letters. 111: 106401. PMID 25166685  0.72
2013 Xiao B, Xing Y, Ji X, Xu Y, Ni L, Zhu Y, Tao J. [Unbalanced subtelomic rearrangement involving 9q and 22q in a child with mental retardation and multiple congenital anomalies]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 30: 666-9. PMID 24327143 DOI: 10.3760/cma.j.issn.1003-9406.2013.06.007  0.72
2013 Xiao B, Ji X, Xing Y, Chen YW, Tao J. A rare case of 46, XX SRY-negative male with approximately 74-kb duplication in a region upstream of SOX9. European Journal of Medical Genetics. 56: 695-8. PMID 24140641 DOI: 10.1016/j.ejmg.2013.10.001  0.72
2013 Qu XX, Xiao B, Ji X, Jiang WT, Yang ZJ, Tao J. [A pilot study on spinal muscular atrophy carrier screening in Shanghai region using real-time PCR]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 30: 1-4. PMID 23450468 DOI: 10.3760/cma.j.issn.1003-9406.2013.01.001  0.72
2013 Sun J, Haunschild R, Xiao B, Bulik IW, Scuseria GE, Perdew JP. Semilocal and hybrid meta-generalized gradient approximations based on the understanding of the kinetic-energy-density dependence. The Journal of Chemical Physics. 138: 044113. PMID 23387574 DOI: 10.1063/1.4789414  0.52
2012 Ruzsinszky A, Sun J, Xiao B, Csonka GI. A meta-GGA Made Free of the Order of Limits Anomaly. Journal of Chemical Theory and Computation. 8: 2078-87. PMID 26593840 DOI: 10.1021/ct300269u  0.72
2012 Sun J, Xiao B, Ruzsinszky A. Communication: Effect of the orbital-overlap dependence in the meta generalized gradient approximation. The Journal of Chemical Physics. 137: 051101. PMID 22894323 DOI: 10.1063/1.4742312  0.72
2012 Xing Y, Ji X, Xiao B, Jiang WT, Hu Q, Hu J, Cao Y, Tao J. [Molecular and cytogenetic characterization of six 46, XX males due to translocations between the short arms of X and Y chromosomes]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 29: 408-12. PMID 22875496 DOI: 10.3760/cma.j.issn.1003-9406.2012.04.007  0.72
2012 Shen LX, Zhang JS, Ji X, Xing Y, Hu J, Tao J, Xiao B. [Clinical and genetic study of a case with Smith-Magenis syndrome]. Zhonghua Er Ke Za Zhi. Chinese Journal of Pediatrics. 50: 227-30. PMID 22801211  0.72
2011 Xiao B, Ji X, Jiang WT, Zhang JM, Hu Q, Tao J. [A case with partial trisomy 7 (q34→qter) derived from a paternal reciprocal translocation t(7;14)(q34;q32)]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 28: 654-7. PMID 22161098 DOI: 10.3760/cma.j.issn.1003-9406.2011.06.012  0.72
2011 Zhang Y, Shen J, He X, Zhang K, Wu S, Xiao B, Zhou X, Phillips RS, Gao P, Jeunemaitre X, Zhu D. A rare variant at the KYNU gene is associated with kynureninase activity and essential hypertension in the Han Chinese population. Circulation. Cardiovascular Genetics. 4: 687-94. PMID 22012986 DOI: 10.1161/CIRCGENETICS.110.959064  0.32
2011 Zhou Y, Sun W, Xiao B, Han X, Long F, Jiang WT, Ji X, Tao J. [Optimization of polymerase chain reaction assay combined with capillary electrophoresis to detect the pre- and full mutation of FMR1 gene]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 28: 401-5. PMID 21811979 DOI: 10.3760/cma.j.issn.1003-9406.2011.04.009  0.72
2011 Xiao B, Zhang JM, Ji X, Jiang WT, Hu J, Tao J. [Two cases of partial trisomy 8p derived from paternal reciprocal translocation or maternal insertion translocation: clinical features and genetic abnormalities]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 28: 247-50. PMID 21644216 DOI: 10.3760/cma.j.issn.1003-9406.2011.03.002  0.72
2009 Xiao B, Zhang Y, Niu WQ, Gao PJ, Zhu DL. Haplotype-based association of regulator of G-protein signaling 5 gene polymorphisms with essential hypertension and metabolic parameters in Chinese. Clinical Chemistry and Laboratory Medicine. 47: 1483-8. PMID 19863299 DOI: 10.1515/CCLM.2009.344  0.32
2009 Xiao B, Zhang Y, Niu W, Gao P, Zhu D. Association of ATP1B1 single-nucleotide polymorphisms with blood pressure and hypertension in a Chinese population. Clinica Chimica Acta; International Journal of Clinical Chemistry. 407: 47-50. PMID 19563793 DOI: 10.1016/j.cca.2009.06.026  0.32
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