Year |
Citation |
Score |
2023 |
Qiao X, Grieco SF, Yu Z, Holmes TC, Xu X. Intranasal Delivery of Ketamine Induces Cortical Disinhibition. Eneuro. PMID 38164560 DOI: 10.1523/ENEURO.0107-23.2023 |
0.8 |
|
2023 |
Johnston K, Berackey BB, Tran KM, Gelber A, Yu Z, MacGregor G, Mukamel EA, Tan Z, Green K, Xu X. Single cell spatial transcriptomics reveals distinct patterns of dysregulation in non-neuronal and neuronal cells induced by the Alzheimer's risk gene mutation. Research Square. PMID 38106071 DOI: 10.21203/rs.3.rs-3656139/v1 |
0.678 |
|
2023 |
Zhang H, Sumbria RK, Chang R, Sun J, Cribbs DH, Holmes TC, Fisher MJ, Xu X. Erythrocyte-brain endothelial interactions induce microglial responses and cerebral microhemorrhages in vivo. Journal of Neuroinflammation. 20: 265. PMID 37968737 DOI: 10.1186/s12974-023-02932-5 |
0.566 |
|
2023 |
Grieco SF, Holmes TC, Xu X. Meeting report for the 2023 UC Irvine Center for Neural Circuit Mapping Conference: structure, function and development of neural circuits. Molecular Psychiatry. PMID 37919404 DOI: 10.1038/s41380-023-02308-4 |
0.731 |
|
2023 |
Anderson A, Nekanti U, Sakthivel P, Zahedi A, Creasman D, Nishi R, Dumont C, Piltti K, Guardamondo G, Hernandez N, Chen X, Song H, Lin X, Martinez J, On L, ... ... Xu X, et al. Multichannel bridges and NSC synergize to enhance axon regeneration, myelination, synaptic reconnection, and recovery after SCI. Research Square. PMID 37502943 DOI: 10.21203/rs.3.rs-3044426/v1 |
0.581 |
|
2023 |
Grieco SF, Johnston KG, Gao P, Garduño BM, Tang B, Yi E, Sun Y, Horwitz GD, Yu Z, Holmes TC, Xu X. Anatomical and molecular characterization of parvalbumin-cholecystokinin co-expressing inhibitory interneurons: implications for neuropsychiatric conditions. Molecular Psychiatry. PMID 37443194 DOI: 10.1038/s41380-023-02153-5 |
0.777 |
|
2023 |
Frantz MG, Crouse EC, Sokhadze G, Ikrar T, Stephany CÉ, Nguyen C, Xu X, McGee AW. Layer 4 Gates Plasticity in Visual Cortex Independent of a Canonical Microcircuit. Current Biology : Cb. 33: 2586. PMID 37339587 DOI: 10.1016/j.cub.2023.05.038 |
0.712 |
|
2023 |
Lin X, Cyrus N, Avila B, Holmes TC, Xu X. Hippocampal CA3 inhibitory neurons receive extensive noncanonical synaptic inputs from CA1 and subicular complex. The Journal of Comparative Neurology. PMID 37312626 DOI: 10.1002/cne.25510 |
0.748 |
|
2023 |
Chen L, Lin X, Ye Q, Nenadic Z, Holmes TC, Nitz DA, Xu X. Anatomical organization of temporally correlated neural calcium activity in the hippocampal CA1 region. Iscience. 26: 106703. PMID 37250317 DOI: 10.1016/j.isci.2023.106703 |
0.8 |
|
2023 |
Paff M, Grieco SF, Xu X. Obtaining brain tissue from living patients for psychiatry research: collaboration with patients with epilepsy and neurosurgeons. The Lancet. Psychiatry. 10: 381. PMID 37088087 DOI: 10.1016/S2215-0366(23)00142-6 |
0.593 |
|
2023 |
Grieco SF, Holmes TC, Xu X. Probing neural circuit mechanisms in Alzheimer's disease using novel technologies. Molecular Psychiatry. PMID 36959497 DOI: 10.1038/s41380-023-02018-x |
0.729 |
|
2023 |
Sun Y, Zweifel LS, Holmes TC, Xu X. Whole-brain input mapping of the lateral versus medial anterodorsal bed nucleus of the stria terminalis in the mouse. Neurobiology of Stress. 23: 100527. PMID 36861029 DOI: 10.1016/j.ynstr.2023.100527 |
0.715 |
|
2023 |
Zhao W, Johnston KG, Ren H, Xu X, Nie Q. Inferring neuron-neuron communications from single-cell transcriptomics through NeuronChat. Nature Communications. 14: 1128. PMID 36854676 DOI: 10.1038/s41467-023-36800-w |
0.688 |
|
2023 |
Birnie MT, Short AK, de Carvalho GB, Taniguchi L, Gunn BG, Pham AL, Itoga CA, Xu X, Chen LY, Mahler SV, Chen Y, Baram TZ. Stress-induced plasticity of a CRH/GABA projection disrupts reward behaviors in mice. Nature Communications. 14: 1088. PMID 36841826 DOI: 10.1038/s41467-023-36780-x |
0.763 |
|
2023 |
Zhao W, Johnston KG, Ren H, Xu X, Nie Q. Inferring neuron-neuron communications from single-cell transcriptomics through NeuronChat. Biorxiv : the Preprint Server For Biology. PMID 36712056 DOI: 10.1101/2023.01.12.523826 |
0.688 |
|
2022 |
Tan Z, Garduño BM, Aburto PF, Chen L, Ha N, Cogram P, Holmes TC, Xu X. Cognitively impaired aged Octodon degus recapitulate major neuropathological features of sporadic Alzheimer's disease. Acta Neuropathologica Communications. 10: 182. PMID 36529803 DOI: 10.1186/s40478-022-01481-x |
0.509 |
|
2022 |
Xiong F, Yang H, Song YG, Qin HB, Zhang QY, Huang X, Jing W, Deng M, Liu Y, Liu Z, Shen Y, Han Y, Lu Y, Xu X, Holmes TC, et al. An HSV-1-H129 amplicon tracer system for rapid and efficient monosynaptic anterograde neural circuit tracing. Nature Communications. 13: 7645. PMID 36496505 DOI: 10.1038/s41467-022-35355-6 |
0.516 |
|
2022 |
Zhang H, Chen L, Johnston KG, Crapser J, Green KN, Ha NM, Tenner AJ, Holmes TC, Nitz DA, Xu X. Degenerate mapping of environmental location presages deficits in object-location encoding and memory in the 5xFAD mouse model for Alzheimer's disease. Neurobiology of Disease. 176: 105939. PMID 36462718 DOI: 10.1016/j.nbd.2022.105939 |
0.788 |
|
2022 |
Grieco SF, Castrén E, Knudsen GM, Kwan AC, Olson DE, Zuo Y, Holmes TC, Xu X. Psychedelics and Neural Plasticity: Therapeutic Implications. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 42: 8439-8449. PMID 36351821 DOI: 10.1523/JNEUROSCI.1121-22.2022 |
0.718 |
|
2022 |
Zhang Y, Amaral ML, Zhu C, Grieco SF, Hou X, Lin L, Buchanan J, Tong L, Preissl S, Xu X, Ren B. Single-cell epigenome analysis reveals age-associated decay of heterochromatin domains in excitatory neurons in the mouse brain. Cell Research. PMID 36207411 DOI: 10.1038/s41422-022-00719-6 |
0.673 |
|
2022 |
Grieco SF, Holmes TC, Xu X. Meeting report for the 2022 UC Irvine Center for neural circuit mapping conference: linking brain function to cell types and circuits. Molecular Psychiatry. PMID 36198768 DOI: 10.1038/s41380-022-01810-5 |
0.74 |
|
2022 |
Hurley MJ, Urra C, Garduno BM, Bruno A, Kimbell A, Wilkinson B, Marino-Buslje C, Ezquer M, Ezquer F, Aburto PF, Poulin E, Vasquez RA, Deacon R, Avila A, Altimiras F, ... ... Xu X, et al. Genome Sequencing Variations in the , an Unconventional Natural Model of Aging and Alzheimer's Disease. Frontiers in Aging Neuroscience. 14: 894994. PMID 35860672 DOI: 10.3389/fnagi.2022.894994 |
0.461 |
|
2022 |
Ye Q, Gast G, Su X, Saito T, Saido TC, Holmes TC, Xu X. Hippocampal neural circuit connectivity alterations in an Alzheimer's disease mouse model revealed by monosynaptic rabies virus tracing. Neurobiology of Disease. 172: 105820. PMID 35843448 DOI: 10.1016/j.nbd.2022.105820 |
0.721 |
|
2022 |
Johnston KG, Grieco SF, Zhang H, Jin S, Xu X, Nie Q. Tracking longitudinal population dynamics of single neuronal calcium signal using SCOUT. Cell Reports Methods. 2: 100207. PMID 35637911 DOI: 10.1016/j.crmeth.2022.100207 |
0.784 |
|
2022 |
Lin X, Chen L, Jullienne A, Zhang H, Salehi A, Hamer M, C Holmes T, Obenaus A, Xu X. Longitudinal dynamics of microvascular recovery after acquired cortical injury. Acta Neuropathologica Communications. 10: 59. PMID 35468870 DOI: 10.1186/s40478-022-01361-4 |
0.639 |
|
2022 |
Liu YJ, Green KN, Holmes TC, Xu X. Commentary: How Do Microglia Regulate Neural Circuit Connectivity and Activity in the Adult Brain? Neuroscience Insights. 17: 26331055211071124. PMID 35098130 DOI: 10.1177/26331055211071124 |
0.579 |
|
2021 |
Lin X, Amalraj M, Blanton C, Avila B, Holmes TC, Nitz DA, Xu X. Noncanonical projections to the hippocampal CA3 regulate spatial learning and memory by modulating the feedforward hippocampal trisynaptic pathway. Plos Biology. 19: e3001127. PMID 34928938 DOI: 10.1371/journal.pbio.3001127 |
0.732 |
|
2021 |
Lin X, Chen L, Baglietto-Vargas D, Kamalipour P, Ye Q, LaFerla FM, Nitz DA, Holmes TC, Xu X. Spatial coding defects of hippocampal neural ensemble calcium activities in the triple-transgenic Alzheimer's disease mouse model. Neurobiology of Disease. 162: 105562. PMID 34838667 DOI: 10.1016/j.nbd.2021.105562 |
0.789 |
|
2021 |
Yu Z, Guindani M, Grieco SF, Chen L, Holmes TC, Xu X. Beyond t test and ANOVA: applications of mixed-effects models for more rigorous statistical analysis in neuroscience research. Neuron. PMID 34784504 DOI: 10.1016/j.neuron.2021.10.030 |
0.687 |
|
2021 |
Wong JC, Grieco SF, Dutt K, Chen L, Thelin JT, Inglis GAS, Parvin S, Garraway SM, Xu X, Goldin AL, Escayg A. Autistic-like behavior, spontaneous seizures, and increased neuronal excitability in a Scn8a mouse model. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. PMID 33658654 DOI: 10.1038/s41386-021-00985-9 |
0.74 |
|
2021 |
Grieco SF, Qiao X, Johnston KG, Chen L, Nelson RR, Lai C, Holmes TC, Xu X. Neuregulin signaling mediates the acute and sustained antidepressant effects of subanesthetic ketamine. Translational Psychiatry. 11: 144. PMID 33627623 DOI: 10.1038/s41398-021-01255-4 |
0.82 |
|
2021 |
Zheng X, Salinas KJ, Velez DXF, Nakayama T, Lin X, Banerjee D, Xu X, Gandhi SP. Host interneurons mediate plasticity reactivated by embryonic inhibitory cell transplantation in mouse visual cortex. Nature Communications. 12: 862. PMID 33558487 DOI: 10.1038/s41467-021-21097-4 |
0.786 |
|
2020 |
Liu YJ, Spangenberg E, Tang B, Holmes TC, Green KN, Xu X. Microglia elimination increases neural circuit connectivity and activity in adult mouse cortex. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 33380470 DOI: 10.1523/JNEUROSCI.2140-20.2020 |
0.652 |
|
2020 |
Yang H, Xiong F, Song YG, Jiang HF, Qin HB, Zhou J, Lu S, Grieco SF, Xu X, Zeng WB, Zhao F, Luo MH. HSV-1 H129-Derived Anterograde Neural Circuit Tracers: Improvements, Production, and Applications. Neuroscience Bulletin. PMID 33367996 DOI: 10.1007/s12264-020-00614-3 |
0.618 |
|
2020 |
Li D, Yang H, Xiong F, Xu X, Zeng WB, Zhao F, Luo MH. Anterograde Neuronal Circuit Tracers Derived from Herpes Simplex Virus 1: Development, Application, and Perspectives. International Journal of Molecular Sciences. 21. PMID 32824837 DOI: 10.3390/ijms21165937 |
0.397 |
|
2020 |
Grieco SF, Qiao X, Zheng X, Liu Y, Chen L, Zhang H, Yu Z, Gavornik JP, Lai C, Gandhi SP, Holmes TC, Xu X. Subanesthetic Ketamine Reactivates Adult Cortical Plasticity to Restore Vision from Amblyopia. Current Biology : Cb. PMID 32822611 DOI: 10.1016/J.Cub.2020.07.008 |
0.833 |
|
2020 |
Xu X, Holmes TC, Luo MH, Beier KT, Horwitz GD, Zhao F, Zeng W, Hui M, Semler BL, Sandri-Goldin RM. Viral Vectors for Neural Circuit Mapping and Recent Advances in Trans-synaptic Anterograde Tracers. Neuron. PMID 32755550 DOI: 10.1016/J.Neuron.2020.07.010 |
0.592 |
|
2020 |
Frantz MG, Crouse EC, Sokhadze G, Ikrar T, Stephany CÉ, Nguyen C, Xu X, McGee AW. Layer 4 Gates Plasticity in Visual Cortex Independent of a Canonical Microcircuit. Current Biology : Cb. PMID 32589913 DOI: 10.1016/J.Cub.2020.05.067 |
0.717 |
|
2020 |
Dong X, Zhou J, Qin HB, Xin B, Huang ZL, Li YY, Xu X, Zhao F, Zhao C, Liu JJ, Luo MH, Zeng WB. Anterograde Viral Tracer HSV-1 Strain H129 Transports Primarily as Capsids in Cortical Neuron Axons. Journal of Virology. PMID 31969440 DOI: 10.1128/JVI.01957-19 |
0.354 |
|
2019 |
Guo Z, Lin X, Samaniego T, Isreb A, Cao S, Malik S, Holmes TC, Xu X. Fos-CreER Based Genetic Mapping of Forebrain Regions Activated by Acupuncture. The Journal of Comparative Neurology. PMID 31600836 DOI: 10.1002/Cne.24789 |
0.761 |
|
2019 |
Sun Y, Jin S, Lin X, Chen L, Qiao X, Jiang L, Zhou P, Johnston KG, Golshani P, Nie Q, Holmes TC, Nitz DA, Xu X. CA1-projecting subiculum neurons facilitate object-place learning. Nature Neuroscience. PMID 31548723 DOI: 10.1038/S41593-019-0496-Y |
0.806 |
|
2019 |
Gong N, Hagopian G, Holmes TC, Luo ZD, Xu X. Functional Reorganization of Local Circuit Connectivity in Superficial Spinal Dorsal Horn with Neuropathic Pain States. Eneuro. PMID 31533959 DOI: 10.1523/ENEURO.0272-19.2019 |
0.504 |
|
2019 |
Grieco SF, Wang G, Mahapatra A, Lai C, Holmes TC, Xu X. Neuregulin and ErbB expression is regulated by development and sensory experience in mouse visual cortex. The Journal of Comparative Neurology. PMID 31454079 DOI: 10.1002/cne.24762 |
0.803 |
|
2019 |
Lazaro MT, Taxidis J, Shuman T, Bachmutsky I, Ikrar T, Santos R, Marcello GM, Mylavarapu A, Chandra S, Foreman A, Goli R, Tran D, Sharma N, Azhdam M, Dong H, ... ... Xu X, et al. Reduced Prefrontal Synaptic Connectivity and Disturbed Oscillatory Population Dynamics in the CNTNAP2 Model of Autism. Cell Reports. 27: 2567-2578.e6. PMID 31141683 DOI: 10.1016/J.Celrep.2019.05.006 |
0.771 |
|
2019 |
Shi Y, Grieco SF, Holmes TC, Xu X. Development of Local Circuit Connections to Hilar Mossy Cells in the Mouse Dentate Gyrus. Eneuro. 6. PMID 30937358 DOI: 10.1523/ENEURO.0370-18.2019 |
0.805 |
|
2019 |
Itoga CA, Chen Y, Fateri C, Echeverry PA, Lai JM, Delgado J, Badhon S, Short A, Baram TZ, Xu X. New viral-genetic mapping uncovers an enrichment of corticotropin-releasing hormone-expressing neuronal inputs to the nucleus accumbens from stress-related brain regions. The Journal of Comparative Neurology. PMID 30861133 DOI: 10.1002/Cne.24676 |
0.8 |
|
2019 |
Besnard A, Gao Y, TaeWoo Kim M, Twarkowski H, Reed AK, Langberg T, Feng W, Xu X, Saur D, Zweifel LS, Davison I, Sahay A. Dorsolateral septum somatostatin interneurons gate mobility to calibrate context-specific behavioral fear responses. Nature Neuroscience. PMID 30718902 DOI: 10.1038/S41593-018-0330-Y |
0.362 |
|
2018 |
Lin X, Itoga CA, Taha S, Li MH, Chen R, Sami K, Berton F, Francesconi W, Xu X. c-Fos mapping of brain regions activated by multi-modal and electric foot shock stress. Neurobiology of Stress. 8: 92-102. PMID 29560385 DOI: 10.1016/J.Ynstr.2018.02.001 |
0.791 |
|
2018 |
Grieco SF, Holmes TC, Xu X. Neuregulin directed molecular mechanisms of visual cortical plasticity. The Journal of Comparative Neurology. PMID 29464684 DOI: 10.1002/cne.24414 |
0.791 |
|
2018 |
Sun Y, Nitz DA, Holmes TC, Xu X. Opposing and Complementary Topographic Connectivity Gradients Revealed by Quantitative Analysis of Canonical and Noncanonical Hippocampal CA1 Inputs. Eneuro. 5. PMID 29387780 DOI: 10.1523/ENEURO.0322-17.2018 |
0.691 |
|
2017 |
Chung AS, Miller SM, Sun Y, Xu X, Zweifel LS. Sexual congruency in the connectome and translatome of VTA dopamine neurons. Scientific Reports. 7: 11120. PMID 28894175 DOI: 10.1038/S41598-017-11478-5 |
0.582 |
|
2017 |
Sanathara NM, Garau C, Alachkar A, Wang L, Wang Z, Nishimori K, Xu X, Civelli O. Melanin concentrating hormone modulates oxytocin-mediated marble burying. Neuropharmacology. PMID 28888943 DOI: 10.1016/J.Neuropharm.2017.09.008 |
0.346 |
|
2017 |
Sun Y, Grieco SF, Holmes TC, Xu X. Local and Long-Range Circuit Connections to Hilar Mossy Cells in the Dentate Gyrus. Eneuro. 4. PMID 28451637 DOI: 10.1523/ENEURO.0097-17.2017 |
0.814 |
|
2017 |
Garcia-Junco-Clemente P, Ikrar T, Tring E, Xu X, Ringach DL, Trachtenberg JT. An inhibitory pull-push circuit in frontal cortex. Nature Neuroscience. PMID 28114295 DOI: 10.1038/Nn.4483 |
0.815 |
|
2016 |
Stephany CÉ, Ikrar T, Nguyen C, Xu X, McGee AW. Nogo Receptor 1 Confines a Disinhibitory Microcircuit to the Critical Period in Visual Cortex. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 36: 11006-11012. PMID 27798181 DOI: 10.1523/Jneurosci.0935-16.2016 |
0.77 |
|
2016 |
Sun Y, Ikrar T, Davis MF, Gong N, Zheng X, Luo ZD, Lai C, Mei L, Holmes TC, Gandhi SP, Xu X. Neuregulin-1/ErbB4 Signaling Regulates Visual Cortical Plasticity. Neuron. PMID 27641496 DOI: 10.1016/J.Neuron.2016.08.033 |
0.837 |
|
2016 |
Baohan A, Ikrar T, Tring E, Xu X, Trachtenberg JT. Pten and EphB4 regulate the establishment of perisomatic inhibition in mouse visual cortex. Nature Communications. 7: 12829. PMID 27611660 DOI: 10.1038/Ncomms12829 |
0.795 |
|
2016 |
Zhou QY, Burton KJ, Neal ML, Qiao Y, Kanthasamy AG, Sun Y, Xu X, Ma Y, Li X. Differential arousal regulation by prokineticin 2 signaling in the nocturnal mouse and the diurnal monkey. Molecular Brain. 9: 78. PMID 27535380 DOI: 10.1186/S13041-016-0255-X |
0.583 |
|
2016 |
Xu X, Sun Y, Holmes TC, López AJ. Noncanonical connections between the subiculum and hippocampal CA1. The Journal of Comparative Neurology. PMID 27150503 DOI: 10.1002/Cne.24024 |
0.698 |
|
2016 |
Xu X, Ikrar T, Sun Y, Santos R, Holmes TC, Francesconi W, Berton F. High-resolution and cell-type-specific photostimulation mapping shows weak excitatory versus strong inhibitory inputs in the bed nucleus of the stria terminalis. Journal of Neurophysiology. jn.01148.2015. PMID 27052587 DOI: 10.1152/Jn.01148.2015 |
0.833 |
|
2016 |
Xu X, Olivas ND, Ikrar T, Peng T, Holmes TC, Nie Q, Shi Y. Primary visual cortex shows laminar specific and balanced circuit organization of excitatory and inhibitory synaptic connectivity. The Journal of Physiology. PMID 26844927 DOI: 10.1113/Jp271891 |
0.813 |
|
2015 |
Nguyen AQ, Dela Cruz JA, Sun Y, Holmes TC, Xu X. Genetic cell targeting uncovers specific neuronal types and distinct subregions in the bed nucleus of the stria terminalis. The Journal of Comparative Neurology. PMID 26718312 DOI: 10.1002/Cne.23954 |
0.811 |
|
2015 |
Shi Y, Veidenbaum AV, Nicolau A, Xu X. Large-scale neural circuit mapping data analysis accelerated with the graphical processing unit (GPU). Journal of Neuroscience Methods. 239: 1-10. PMID 25277633 DOI: 10.1016/J.Jneumeth.2014.09.022 |
0.623 |
|
2014 |
Ozkan ED, Creson TK, Kramár EA, Rojas C, Seese RR, Babyan AH, Shi Y, Lucero R, Xu X, Noebels JL, Miller CA, Lynch G, Rumbaugh G. Reduced cognition in Syngap1 mutants is caused by isolated damage within developing forebrain excitatory neurons. Neuron. 82: 1317-33. PMID 24945774 DOI: 10.1016/J.Neuron.2014.05.015 |
0.675 |
|
2014 |
Sun Y, Nguyen AQ, Nguyen JP, Le L, Saur D, Choi J, Callaway EM, Xu X. Cell-type-specific circuit connectivity of hippocampal CA1 revealed through Cre-dependent rabies tracing. Cell Reports. 7: 269-80. PMID 24656815 DOI: 10.1016/J.Celrep.2014.02.030 |
0.82 |
|
2014 |
Parks GS, Olivas ND, Ikrar T, Sanathara NM, Wang L, Wang Z, Civelli O, Xu X. Histamine inhibits the melanin-concentrating hormone system: implications for sleep and arousal. The Journal of Physiology. 592: 2183-96. PMID 24639485 DOI: 10.1113/Jphysiol.2013.268771 |
0.796 |
|
2014 |
Shi Y, Ikrar T, Olivas ND, Xu X. Bidirectional global spontaneous network activity precedes the canonical unidirectional circuit organization in the developing hippocampus. The Journal of Comparative Neurology. 522: 2191-208. PMID 24357090 DOI: 10.1002/Cne.23528 |
0.802 |
|
2014 |
San Antonio A, Liban K, Ikrar T, Tsyganovskiy E, Xu X. Distinct physiological and developmental properties of hippocampal CA2 subfield revealed by using anti-Purkinje cell protein 4 (PCP4) immunostaining. The Journal of Comparative Neurology. 522: 1333-54. PMID 24166578 DOI: 10.1002/Cne.23486 |
0.727 |
|
2013 |
Ikrar T, Guo N, He K, Besnard A, Levinson S, Hill A, Lee HK, Hen R, Xu X, Sahay A. Adult neurogenesis modifies excitability of the dentate gyrus. Frontiers in Neural Circuits. 7: 204. PMID 24421758 DOI: 10.3389/Fncir.2013.00204 |
0.765 |
|
2013 |
Kuhlman SJ, Olivas ND, Tring E, Ikrar T, Xu X, Trachtenberg JT. A disinhibitory microcircuit initiates critical-period plasticity in the visual cortex. Nature. 501: 543-6. PMID 23975100 DOI: 10.1038/Nature12485 |
0.812 |
|
2013 |
Haettig J, Sun Y, Wood MA, Xu X. Cell-type specific inactivation of hippocampal CA1 disrupts location-dependent object recognition in the mouse. Learning & Memory (Cold Spring Harbor, N.Y.). 20: 139-46. PMID 23418393 DOI: 10.1101/Lm.027847.112 |
0.645 |
|
2013 |
Ahrar S, Nguyen TV, Shi Y, Ikrar T, Xu X, Hui EE. Optical stimulation and imaging of functional brain circuitry in a segmented laminar flow chamber. Lab On a Chip. 13: 536-41. PMID 23044655 DOI: 10.1039/C2Lc40689F |
0.795 |
|
2012 |
Clement JP, Aceti M, Creson TK, Ozkan ED, Shi Y, Reish NJ, Almonte AG, Miller BH, Wiltgen BJ, Miller CA, Xu X, Rumbaugh G. Pathogenic SYNGAP1 mutations impair cognitive development by disrupting maturation of dendritic spine synapses. Cell. 151: 709-23. PMID 23141534 DOI: 10.1016/J.Cell.2012.08.045 |
0.623 |
|
2012 |
Olivas ND, Quintanar-Zilinskas V, Nenadic Z, Xu X. Laminar circuit organization and response modulation in mouse visual cortex. Frontiers in Neural Circuits. 6: 70. PMID 23060751 DOI: 10.3389/Fncir.2012.00070 |
0.821 |
|
2012 |
Ikrar T, Shi Y, Velasquez T, Goulding M, Xu X. Cell-type specific regulation of cortical excitability through the allatostatin receptor system. Frontiers in Neural Circuits. 6: 2. PMID 22319474 DOI: 10.3389/Fncir.2012.00002 |
0.83 |
|
2011 |
Ikrar T, Olivas ND, Shi Y, Xu X. Mapping inhibitory neuronal circuits by laser scanning photostimulation. Journal of Visualized Experiments : Jove. PMID 22006064 DOI: 10.3791/3109 |
0.821 |
|
2011 |
Doretto S, Malerba M, Ramos M, Ikrar T, Kinoshita C, De Mei C, Tirotta E, Xu X, Borrelli E. Oligodendrocytes as regulators of neuronal networks during early postnatal development. Plos One. 6: e19849. PMID 21589880 DOI: 10.1371/Journal.Pone.0019849 |
0.724 |
|
2010 |
Shi Y, Nenadic Z, Xu X. Novel use of matched filtering for synaptic event detection and extraction. Plos One. 5: e15517. PMID 21124805 DOI: 10.1371/Journal.Pone.0015517 |
0.651 |
|
2010 |
Xu X, Olivas ND, Levi R, Ikrar T, Nenadic Z. High precision and fast functional mapping of cortical circuitry through a novel combination of voltage sensitive dye imaging and laser scanning photostimulation. Journal of Neurophysiology. 103: 2301-12. PMID 20130040 DOI: 10.1152/Jn.00992.2009 |
0.81 |
|
2010 |
Xu X, Roby KD, Callaway EM. Immunochemical characterization of inhibitory mouse cortical neurons: three chemically distinct classes of inhibitory cells. The Journal of Comparative Neurology. 518: 389-404. PMID 19950390 DOI: 10.1002/cne.22229 |
0.66 |
|
2009 |
Xu X, Callaway EM. Laminar specificity of functional input to distinct types of inhibitory cortical neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 70-85. PMID 19129386 DOI: 10.1523/JNEUROSCI.4104-08.2009 |
0.621 |
|
2007 |
Xu X, Anderson TJ, Casagrande VA. How do functional maps in primary visual cortex vary with eccentricity? The Journal of Comparative Neurology. 501: 741-55. PMID 17299757 DOI: 10.1002/cne.21277 |
0.585 |
|
2006 |
Xu X, Collins CE, Khaytin I, Kaas JH, Casagrande VA. Unequal representation of cardinal vs. oblique orientations in the middle temporal visual area. Proceedings of the National Academy of Sciences of the United States of America. 103: 17490-5. PMID 17088527 DOI: 10.1073/pnas.0608502103 |
0.772 |
|
2006 |
Xu X, Roby KD, Callaway EM. Mouse cortical inhibitory neuron type that coexpresses somatostatin and calretinin. The Journal of Comparative Neurology. 499: 144-60. PMID 16958092 DOI: 10.1002/cne.21101 |
0.644 |
|
2005 |
Xu X, Bosking WH, White LE, Fitzpatrick D, Casagrande VA. Functional organization of visual cortex in the prosimian bush baby revealed by optical imaging of intrinsic signals. Journal of Neurophysiology. 94: 2748-62. PMID 16000523 DOI: 10.1152/Jn.00354.2005 |
0.593 |
|
2005 |
Collins CE, Xu X, Khaytin I, Kaskan PM, Casagrande VA, Kaas JH. Optical imaging of visually evoked responses in the middle temporal area after deactivation of primary visual cortex in adult primates. Proceedings of the National Academy of Sciences of the United States of America. 102: 5594-9. PMID 15809438 DOI: 10.1073/pnas.0501762102 |
0.79 |
|
2004 |
Xu X, Bosking W, Sáry G, Stefansic J, Shima D, Casagrande V. Functional organization of visual cortex in the owl monkey. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 6237-47. PMID 15254078 DOI: 10.1523/JNEUROSCI.1144-04.2004 |
0.562 |
|
2004 |
Xu X, Collins CE, Kaskan PM, Khaytin I, Kaas JH, Casagrande VA. Optical imaging of visually evoked responses in prosimian primates reveals conserved features of the middle temporal visual area. Proceedings of the National Academy of Sciences of the United States of America. 101: 2566-71. PMID 14983049 DOI: 10.1073/pnas.0308745101 |
0.77 |
|
2004 |
Khaytin I, Xu X, Collins CE, Kaskan PM, Shima DW, Kaas JH, Casagrande VA. The Organization of the Middle Temporal Visual Area (MT) in Bush Babies and Owl Monkeys Revealed by Optical Imaging Journal of Vision. 4: 279-279. DOI: 10.1167/4.8.279 |
0.762 |
|
2003 |
Thomas A, Gallucci M, Xu X, Allison J, Stefansic J, Shima D, Casagrande V, Bonds AB. Compound stimuli promote architectural reorganization in cat striate cortex Journal of Vision. 3: 379a. DOI: 10.1167/3.9.379 |
0.643 |
|
2003 |
Emeric EE, Xu X, Mavity-Hudson J, Gallucci M, Thomas A, Barahimi B, Shima D, Stefansic J, Bonds AB, Casagrande VA. Visuotopic organization of bush baby primary visual cortex (V1) revealed by optical imaging Journal of Vision. 3: 376a. DOI: 10.1167/3.9.376 |
0.573 |
|
2003 |
Xu X, Boyd J, Gallucci M, Thomas A, Emeric E, Barahimi B, Stefansic J, Shima D, Melzer P, Allison J, Bonds AB, Casagrande V. Spatial frequency preference maps of primate visual cortex reveled by optical imaging of intrinsic signals Journal of Vision. 3: 107a. DOI: 10.1167/3.9.107 |
0.665 |
|
2002 |
Xu X, Bonds AB, Casagrande VA. Modeling receptive-field structure of koniocellular, magnocellular, and parvocellular LGN cells in the owl monkey (Aotus trivigatus). Visual Neuroscience. 19: 703-11. PMID 12688666 DOI: 10.1017/S0952523802196027 |
0.536 |
|
2002 |
Lyon DC, Xu X, Casagrande VA, Stefansic JD, Shima D, Kaas JH. Optical imaging reveals retinotopic organization of dorsal V3 in New World owl monkeys. Proceedings of the National Academy of Sciences of the United States of America. 99: 15735-42. PMID 12441399 DOI: 10.1073/pnas.242600699 |
0.714 |
|
2002 |
Xu X, Ichida J, Shostak Y, Bonds AB, Casagrande VA. Are primate lateral geniculate nucleus (LGN) cells really sensitive to orientation or direction? Visual Neuroscience. 19: 97-108. PMID 12180863 DOI: 10.1017/S0952523802191097 |
0.782 |
|
2002 |
Casagrande VA, Xu X, Sáry G. Static and dynamic views of visual cortical organization. Progress in Brain Research. 136: 389-408. PMID 12143396 DOI: 10.1016/S0079-6123(02)36032-1 |
0.667 |
|
2002 |
Xu X, Bosking W, Sáry G, Jones M, Royal D, Stefansic J, Shima D, Fitzpatrick D, Casagrande V. The functional organization of orientation maps in owl monkey V1 and V2 revealed by optical imaging of intrinsic signals Journal of Vision. 2: 99a. DOI: 10.1167/2.7.99 |
0.558 |
|
2001 |
Xu X, Ichida JM, Allison JD, Boyd JD, Bonds AB, Casagrande VA. A comparison of koniocellular, magnocellular and parvocellular receptive field properties in the lateral geniculate nucleus of the owl monkey (Aotus trivirgatus). The Journal of Physiology. 531: 203-18. PMID 11179404 DOI: 10.1111/j.1469-7793.2001.0203j.x |
0.774 |
|
2001 |
Sa'ry G, Xu X, Shostak Y, Royal D, Schall J, Casagrande V. Behavioral relevance influences LGN neurons of macaque monkey in the absence of receptive field stimulation Journal of Vision. 1: 30a. DOI: 10.1167/1.3.30 |
0.592 |
|
Low-probability matches (unlikely to be authored by this person) |
2017 |
Alachkar A, Wang L, Yoshimura R, Hamzeh AR, Wang Z, Sanathara N, Lee SM, Xu X, Abbott GW, Civelli O. Prenatal one-carbon metabolism dysregulation programs schizophrenia-like deficits. Molecular Psychiatry. PMID 28809400 DOI: 10.1038/Mp.2017.164 |
0.284 |
|
2018 |
Agarwal N, Xu X, Gopi M. Geometry Processing of Conventionally Produced Mouse Brain Slice Images. Journal of Neuroscience Methods. PMID 29689283 DOI: 10.1016/J.Jneumeth.2018.04.008 |
0.265 |
|
2024 |
Bouin A, Wu G, Koyuncu OO, Ye Q, Kim KY, Wu MY, Tong L, Chen L, Phan S, Mackey MR, Ramachandra R, Ellisman MH, Holmes TC, Semler BL, Xu X. New rabies viral resources for multi-scale neural circuit mapping. Molecular Psychiatry. PMID 38355784 DOI: 10.1038/s41380-024-02451-6 |
0.26 |
|
2016 |
Cai B, Xu X, Xing X, Jia K, Miao J, Tao D. BIT: Biologically Inspired Tracker. Ieee Transactions On Image Processing : a Publication of the Ieee Signal Processing Society. PMID 26800541 DOI: 10.1109/TIP.2016.2520358 |
0.225 |
|
2023 |
Zheng X, Wu B, Liu Y, Simmons SK, Kim K, Clarke GS, Ashiq A, Park J, Wang Z, Tong L, Wang Q, Xu X, Levin JZ, Jin X. Massively parallel Perturb-seq reveals cell type-specific transcriptional networks in cortical development. Biorxiv : the Preprint Server For Biology. PMID 37790302 DOI: 10.1101/2023.09.18.558077 |
0.215 |
|
2024 |
Grieco SF, Holmes TC, Xu X. Monosynaptic rabies tracing maps inputs to CA1 cells in old AD model mice (APP-KI). Molecular Psychiatry. 28: 4021. PMID 38291104 DOI: 10.1038/s41380-023-02393-5 |
0.196 |
|
2021 |
Shen T, Lur G, Xu X, Yu Z. To Deconvolve, or Not to Deconvolve: Inferences of Neuronal Activities using Calcium Imaging Data. Journal of Neuroscience Methods. 109431. PMID 34856319 DOI: 10.1016/j.jneumeth.2021.109431 |
0.19 |
|
2022 |
Chu SS, Nguyen HA, Lin D, Bhatti M, Jones-Tinsley CE, Do AH, Frostig RD, Nenadic Z, Xu X, Lim MM, Cao H. Development of highly sensitive, flexible dual L-glutamate and GABA microsensors for in vivo brain sensing. Biosensors & Bioelectronics. 222: 114941. PMID 36455372 DOI: 10.1016/j.bios.2022.114941 |
0.167 |
|
2022 |
Cheng J, Zhang X, Ni H, Li C, Xu X, Wu Z, Wang L, Lin W, Li G. Path Signature Neural Network of Cortical Features for Prediction of Infant Cognitive Scores. Ieee Transactions On Medical Imaging. PMID 35089858 DOI: 10.1109/TMI.2022.3147690 |
0.153 |
|
2024 |
Jiang Y, Ye Y, Zhang X, Yu Y, Huang L, Bao X, Xu X. Identification and characterization of CHD4-associated eRNA as a novel modulator of fetal hemoglobin levels in β-thalassemia. Biochemical and Biophysical Research Communications. 701: 149555. PMID 38325179 DOI: 10.1016/j.bbrc.2024.149555 |
0.14 |
|
2021 |
Ou H, Qing C, Xu X, Jin J. Multi-Level Context Pyramid Network for Visual Sentiment Analysis. Sensors (Basel, Switzerland). 21. PMID 33803744 DOI: 10.3390/s21062136 |
0.133 |
|
2020 |
Zhang X, Cheng J, Ni H, Li C, Xu X, Wu Z, Wang L, Lin W, Shen D, Li G. Infant Cognitive Scores Prediction with Multi-stream Attention-Based Temporal Path Signature Features. Medical Image Computing and Computer-Assisted Intervention : Miccai ... International Conference On Medical Image Computing and Computer-Assisted Intervention. 12267: 134-144. PMID 33594350 DOI: 10.1007/978-3-030-59728-3_14 |
0.131 |
|
2020 |
Huang P, Zhao Y, Zhong J, Zhang X, Liu Q, Qiu X, Chen S, Yan H, Hillyer C, Mohandas N, Pan X, Xu X. Putative regulators for the continuum of erythroid differentiation revealed by single-cell transcriptome of human BM and UCB cells. Proceedings of the National Academy of Sciences of the United States of America. PMID 32457162 DOI: 10.1073/pnas.1915085117 |
0.129 |
|
2011 |
Ma N, Huang Z, Chen X, He F, Wang K, Liu W, Zhao L, Xu X, Liao W, Ruan H, Luo S, Zhang W. Characterization of a weak allele of zebrafish cloche mutant. Plos One. 6: e27540. PMID 22132109 DOI: 10.1371/journal.pone.0027540 |
0.121 |
|
2024 |
Zhang W, Zhang X, Li L, Liao L, Zhao F, Zhong T, Pei Y, Xu X, Yang C, Zhang H, Li G. A joint brain extraction and image quality assessment framework for fetal brain MRI slices. Neuroimage. 120560. PMID 38431181 DOI: 10.1016/j.neuroimage.2024.120560 |
0.12 |
|
2024 |
Cogram P, Garduño BM, Ren B, Xu X. First International Conference on Unconventional Animal Models of Alzheimer's Disease and Aging. Journal of Alzheimer's Disease : Jad. PMID 38393919 DOI: 10.3233/JAD-249004 |
0.12 |
|
2022 |
Li Y, Zhang X, Nie J, Zhang G, Fang R, Xu X, Wu Z, Hu D, Wang L, Zhang H, Lin W, Li G. Brain Connectivity based Graph Convolutional Networks for Infant Age Prediction. Ieee Transactions On Medical Imaging. PMID 35500083 DOI: 10.1109/TMI.2022.3171778 |
0.113 |
|
2020 |
Zhang X, Ding X, Wu Z, Xia J, Ni H, Xu X, Liao L, Wang L, Li G. SIAMESE VERIFICATION FRAMEWORK FOR AUTISM IDENTIFICATION DURING INFANCY USING CORTICAL PATH SIGNATURE FEATURES. Proceedings. Ieee International Symposium On Biomedical Imaging. 2020. PMID 34422221 DOI: 10.1109/isbi45749.2020.9098385 |
0.109 |
|
2022 |
Perry Fordson H, Xing X, Guo K, Xu X. Not All Electrode Channels Are Needed: Knowledge Transfer From Only Stimulated Brain Regions for EEG Emotion Recognition. Frontiers in Neuroscience. 16: 865201. PMID 35692430 DOI: 10.3389/fnins.2022.865201 |
0.104 |
|
2021 |
Bao X, Zhang X, Wang L, Wang Z, Huang J, Zhang Q, Ye Y, Liu Y, Chen D, Zuo Y, Liu Q, Xu P, Huang B, Fang J, Lao J, ... ... Xu X, et al. Epigenetic inactivation of ERF reactivates γ-globin expression in β-thalassemia. American Journal of Human Genetics. PMID 33735615 DOI: 10.1016/j.ajhg.2021.03.005 |
0.103 |
|
2023 |
Emami MR, Espinoza A, Young CS, Ma F, Farahat PK, Felgner PL, Chamberlain JS, Xu X, Pyle AD, Pellegrini M, Villalta SA, Spencer MJ. Innate and adaptive AAV-mediated immune responses in a mouse model of Duchenne muscular dystrophy. Molecular Therapy. Methods & Clinical Development. 30: 90-102. PMID 37746243 DOI: 10.1016/j.omtm.2023.06.002 |
0.103 |
|
2019 |
Sun SC, Ma D, Li MY, Zhang RX, Huang C, Huang HJ, Xie YZ, Wang ZJ, Liu J, Cai DC, Liu CX, Yang Q, Bao FX, Gong XL, Li JR, ... ... Xu XM, et al. Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease. Brain : a Journal of Neurology. PMID 31199454 DOI: 10.1093/brain/awz151 |
0.101 |
|
2015 |
Miao J, Xu X, Qiu S, Qing C, Tao D. Temporal Variance Analysis for Action Recognition. Ieee Transactions On Image Processing : a Publication of the Ieee Signal Processing Society. PMID 26469203 DOI: 10.1109/TIP.2015.2490551 |
0.101 |
|
2016 |
Xiong F, Ji Z, Liu Y, Zhang Y, Hu L, Yang Q, Qiu Q, Zhao L, Chen D, Tian Z, Shang X, Zhang L, Wei X, Liu C, Yu Q, ... ... Xu X, et al. Mutation in SSUH2 Causes Autosomal Dominant Dentin Dysplasia Type I. Human Mutation. PMID 27680507 DOI: 10.1002/humu.23130 |
0.1 |
|
2020 |
Cheng Y, Shang X, Chen D, Pang D, Zhao C, Xu X. MicroRNA-2355-5p regulates γ-globin expression in human erythroid cells by inhibiting KLF6. British Journal of Haematology. PMID 33368182 DOI: 10.1111/bjh.17134 |
0.095 |
|
2018 |
Li Y, Liu D, Li Z, Zhang X, Ye Y, Liu Q, Shen J, Chen Z, Huang H, Liang Y, Han X, Liu J, An X, Mohandas N, Xu X. Role of tissue-specific promoter DNA methylation in regulating the human EKLF gene. Blood Cells, Molecules & Diseases. PMID 29475801 DOI: 10.1016/j.bcmd.2018.01.004 |
0.094 |
|
2022 |
Yang H, Xiong F, Qin HB, Yu QT, Sun JY, Zhao HW, Li D, Zhou Y, Zhang FK, Zhu XW, Wu T, Jiang M, Xu X, Lu Y, Shen HJ, et al. A novel H129-based anterograde monosynaptic tracer exhibits features of strong labeling intensity, high tracing efficiency, and reduced retrograde labeling. Molecular Neurodegeneration. 17: 6. PMID 35012591 DOI: 10.1186/s13024-021-00508-6 |
0.094 |
|
2014 |
Xiao J, Zhang L, Wang J, Jiang Y, Jin L, Lu J, Jin L, Zhong C, Xu X, Zhang F. Rearrangement structure-independent strategy of CNV breakpoint analysis. Molecular Genetics and Genomics : Mgg. 289: 755-63. PMID 24737421 DOI: 10.1007/S00438-014-0850-4 |
0.094 |
|
2022 |
Chen X, Calandrelli R, Girardini J, Yan Z, Tan Z, Xu X, Hiniker A, Zhong S. PHGDH expression increases with progression of Alzheimer's disease pathology and symptoms. Cell Metabolism. 34: 651-653. PMID 35508105 DOI: 10.1016/j.cmet.2022.02.008 |
0.09 |
|
2020 |
Li H, Zeng J, Zhao Y, Xu X. MZF1 regulates α-globin gene transcription via long-range interactions in erythroid differentiation. Blood Cells, Molecules & Diseases. 87: 102533. PMID 33352376 DOI: 10.1016/j.bcmd.2020.102533 |
0.085 |
|
2015 |
Ye X, Li K, Liu L, Yu F, Xiong F, Fan Y, Xu X, Zuo C, Chen D. Dentin dysplasia type I-novel findings in deciduous and permanent teeth. Bmc Oral Health. 15: 163. PMID 26693824 DOI: 10.1186/s12903-015-0149-9 |
0.085 |
|
2022 |
Ng DQ, Chan D, Agrawal P, Zhao W, Xu X, Acharya M, Chan A. EVIDENCE OF BRAIN-DERIVED NEUROTROPHIC FACTOR IN AMELIORATING CANCER-RELATED COGNITIVE IMPAIRMENT: A SYSTEMATIC REVIEW OF HUMAN STUDIES. Critical Reviews in Oncology/Hematology. 103748. PMID 35718064 DOI: 10.1016/j.critrevonc.2022.103748 |
0.083 |
|
2010 |
Sheng-Yuan Z, Xiong F, Chen YJ, Yan TZ, Zeng J, Li L, Zhang YN, Chen WQ, Bao XH, Zhang C, Xu XM. Molecular characterization of SMN copy number derived from carrier screening and from core families with SMA in a Chinese population. European Journal of Human Genetics : Ejhg. 18: 978-84. PMID 20442745 DOI: 10.1038/ejhg.2010.54 |
0.082 |
|
2015 |
Ye Y, Liang Y, Yu Q, Hu L, Li H, Zhang Z, Xu X. Analysis of human upstream open reading frames and impact on gene expression. Human Genetics. 134: 605-12. PMID 25800702 DOI: 10.1007/S00439-015-1544-7 |
0.082 |
|
2017 |
Chen D, Zuo Y, Zhang X, Ye Y, Bao X, Huang H, Tepakhan W, Wang L, Ju J, Chen G, Zheng M, Liu D, Huang S, Zong L, Li C, ... ... Xu X, et al. A Genetic Variant Ameliorates β-Thalassemia Severity by Epigenetic-Mediated Elevation of Human Fetal Hemoglobin Expression. American Journal of Human Genetics. PMID 28669403 DOI: 10.1016/j.ajhg.2017.05.012 |
0.081 |
|
2008 |
Tang L, Zeng G, Liu J, Xu X, Zhang Y, Shen G, Li Y, Liu C. Catechol determination in compost bioremediation using a laccase sensor and artificial neural networks. Analytical and Bioanalytical Chemistry. 391: 679-85. PMID 18398603 DOI: 10.1007/s00216-008-2049-1 |
0.081 |
|
2019 |
Hu A, Lu T, Chen D, Huang J, Feng W, Li Y, Guo D, Xu X, Chen D, Xiong F. Vps4b heterozygous mice do not develop tooth defects that replicate human dentin dysplasia I. Bmc Genetics. 20: 7. PMID 30634912 DOI: 10.1186/s12863-018-0699-3 |
0.078 |
|
2022 |
Perry Fordson H, Xing X, Guo K, Xu X. Emotion Recognition With Knowledge Graph Based on Electrodermal Activity. Frontiers in Neuroscience. 16: 911767. PMID 35757534 DOI: 10.3389/fnins.2022.911767 |
0.076 |
|
2015 |
Huang J, Zhang X, Liu D, Wei X, Shang X, Xiong F, Yu L, Yin X, Xu X. Compound heterozygosity for KLF1 mutations is associated with microcytic hypochromic anemia and increased fetal hemoglobin. European Journal of Human Genetics : Ejhg. PMID 25585695 DOI: 10.1038/ejhg.2014.291 |
0.076 |
|
2020 |
Gong Y, Zhang X, Zhang Q, Zhang Y, Ye Y, Yu W, Shao C, Yan T, Huang J, Zhong J, Wang L, Li Y, Wang L, Xu X. A natural DNMT1 mutation elevates the fetal hemoglobin via epigenetic de-repression of γ-globin gene in β-thalassemia. Blood. PMID 33227819 DOI: 10.1182/blood.2020006425 |
0.076 |
|
2021 |
Tao W, Liu Q, Huang S, Wang X, Qu S, Guo J, Ou D, Li G, Zhang Y, Xu X, Huang X. CABE-RY: A PAM-flexible dual-mutation base editor for reliable modeling of multi-nucleotide variants. Molecular Therapy. Nucleic Acids. 26: 114-121. PMID 34513298 DOI: 10.1016/j.omtn.2021.07.016 |
0.073 |
|
2018 |
Li Y, Liu D, Zhang X, Li Z, Ye Y, Liu Q, Shen J, Chen Z, Huang H, Liang Y, Han X, Liu J, An X, Mohandas N, Xu X. miR-326 regulates HbF synthesis by targeting EKLF in human erythroid cells. Experimental Hematology. PMID 29601850 DOI: 10.1016/j.exphem.2018.03.004 |
0.073 |
|
2021 |
Lin J, Ye Y, Shang X, Zhang Y, Wei X, Xu X. TEA domain transcription factor 4 modulates repression of fetal haemoglobin by direct binding to the γ-globin gene promoters. British Journal of Haematology. PMID 34569056 DOI: 10.1111/bjh.17786 |
0.073 |
|
2023 |
Zhang Q, Lin P, Mao A, Liu Y, Shang X, Wei X, Li Y, Lin B, Xu X. An unusual case of thalassemia intermedia with inheritable complex repeats detected by single-molecule optical mapping. Haematologica. PMID 37767576 DOI: 10.3324/haematol.2023.282902 |
0.072 |
|
2012 |
Wen L, Zhu P, Liu Y, Pan Q, Qu Y, Xu X, Li X, Fu N. Development of a fluorescence immunochromatographic assay for the detection of zeta globin in the blood of (--(SEA)) α-thalassemia carriers. Blood Cells, Molecules & Diseases. 49: 128-32. PMID 22677106 DOI: 10.1016/j.bcmd.2012.05.011 |
0.071 |
|
2013 |
Qiu QW, Wu DD, Yu LH, Yan TZ, Zhang W, Li ZT, Liu YH, Zhang YP, Xu XM. Evidence of recent natural selection on the Southeast Asian deletion (--(SEA)) causing α-thalassemia in South China. Bmc Evolutionary Biology. 13: 63. PMID 23497175 DOI: 10.1186/1471-2148-13-63 |
0.071 |
|
2022 |
Li H, Zeng J, Zhao Y, Xu X. Retraction notice to "MZF1 regulates α-globin gene transcription via long-range interactions in erythroid differentiation" [Blood Cells, Mol. Dis., Volume 87, March 2021, 102533]. Blood Cells, Molecules & Diseases. 97: 102687. PMID 35738122 DOI: 10.1016/j.bcmd.2022.102687 |
0.07 |
|
2015 |
Lin L, Chen DN, Guo J, Zhou WJ, Xu XM. Development of a capillary zone electrophoresis method for rapid determination of human globin chains in α and β-thalassemia subjects. Blood Cells, Molecules & Diseases. 55: 62-7. PMID 25976469 DOI: 10.1016/j.bcmd.2015.03.003 |
0.07 |
|
2020 |
Huang H, Wang J, Liang Y, Wei X, Guo D, Sun H, Zhang X, Xu X, Xiong F. A compound heterozygous mutation of the alkaline phosphatase ALPL gene causes hypophosphatasia in a Han Chinese family. Experimental and Therapeutic Medicine. 20: 152. PMID 33093890 DOI: 10.3892/etm.2020.9281 |
0.07 |
|
2022 |
Li J, Hua H, Xu Z, Shu L, Xu X, Kuang F, Wu S. Cross-subject EEG emotion recognition combined with connectivity features and meta-transfer learning. Computers in Biology and Medicine. 145: 105519. PMID 35585734 DOI: 10.1016/j.compbiomed.2022.105519 |
0.067 |
|
2014 |
Zhou S, Hu S, Fu Y, Xu X, Yang J. Moiré interferometry with high alignment resolution in proximity lithographic process. Applied Optics. 53: 951-9. PMID 24663277 |
0.066 |
|
2019 |
Yang X, Zhou Q, Zhou W, Zhong M, Guo X, Wang X, Fan X, Yan S, Li L, Lai Y, Wang Y, Huang J, Ye Y, Zeng H, Chuan J, ... ... Xu X, et al. A Cell-free DNA Barcode-Enabled Single-Molecule Test for Noninvasive Prenatal Diagnosis of Monogenic Disorders: Application to β-Thalassemia. Advanced Science (Weinheim, Baden-Wurttemberg, Germany). 6: 1802332. PMID 31179213 DOI: 10.1002/advs.201802332 |
0.066 |
|
2022 |
Ye Y, Sun G, Ren Z, Liang Y, Luo H, Lin P, Wang X, Dong Z, Huang L, Qin L, Yu W, Wang G, Zhou Y, Tang J, Lou J, ... ... Xu X, et al. Quantification of human embryonic ζ-globin chains in Southeast Asian deletion (--) carriers. Journal of Clinical Pathology. PMID 36008105 DOI: 10.1136/jcp-2022-208159 |
0.066 |
|
2011 |
Wang HQ, Liu WY, Wu Z, Tang LJ, Xu XM, Yu RQ, Jiang JH. Homogeneous label-free genotyping of single nucleotide polymorphism using ligation-mediated strand displacement amplification with DNAzyme-based chemiluminescence detection. Analytical Chemistry. 83: 1883-9. PMID 21348511 DOI: 10.1021/ac200138v |
0.064 |
|
2015 |
Liu D, Yi S, Zhang X, Fang P, Zheng C, Lin L, Cai R, Ye Y, Zhou Y, Liang Y, Cheng F, Zhang X, Zhou W, Mohandas N, An X, ... Xu X, et al. Human STEAP3 mutations with no phenotypic red cell changes. Blood. PMID 26675350 DOI: 10.1182/blood-2015-09-670174 |
0.064 |
|
2018 |
Zhao S, Xiang J, Fan C, Asan, Shang X, Zhang X, Chen Y, Zhu B, Cai W, Chen S, Cai R, Guo X, Zhang C, Zhou Y, Huang S, ... ... Xu X, et al. Pilot study of expanded carrier screening for 11 recessive diseases in China: results from 10,476 ethnically diverse couples. European Journal of Human Genetics : Ejhg. PMID 30275481 DOI: 10.1038/S41431-018-0253-9 |
0.064 |
|
2018 |
Lu T, Li M, Xu X, Xiong J, Huang C, Zhang X, Hu A, Peng L, Cai D, Zhang L, Wu B, Xiong F. Whole exome sequencing identifies an AMBN missense mutation causing severe autosomal-dominant amelogenesis imperfecta and dentin disorders. International Journal of Oral Science. 10: 26. PMID 30174330 DOI: 10.1038/s41368-018-0027-9 |
0.063 |
|
2008 |
Zhang W, Cai WW, Zhou WP, Li HP, Li L, Yan W, Deng QK, Zhang YP, Fu YX, Xu XM. Evidence of gene conversion in the evolutionary process of the codon 41/42 (-CTTT) mutation causing beta-thalassemia in southern China. Journal of Molecular Evolution. 66: 436-45. PMID 18414926 DOI: 10.1007/s00239-008-9096-2 |
0.062 |
|
2019 |
Zhang L, Zhang Q, Tang Y, Cong P, Ye Y, Chen S, Zhang X, Chen Y, Zhu B, Cai W, Chen S, Cai R, Guo X, Zhang C, Zhou Y, ... ... Xu X, et al. LOVD-DASH: A Comprehensive LOVD Database Coupled with Diagnosis and an At-risk Assessment System for Hemoglobinopathies. Human Mutation. PMID 31286593 DOI: 10.1002/humu.23863 |
0.061 |
|
2019 |
Pang D, Shang X, Cai D, Zhu F, Cheng Y, Zhong J, Yi S, Zhang Q, Xu X. Thalassaemia intermedia caused by coinheritance of a β-thalassaemia mutation and a de novo duplication of α-globin genes in the paternal allele. British Journal of Haematology. PMID 31124576 DOI: 10.1111/bjh.15958 |
0.061 |
|
2021 |
Liang Y, Zhang X, Liu Y, Wang L, Ye Y, Tan X, Pu J, Zhang Q, Bao X, Wei X, Li D, Kurita R, Nakamura Y, Li D, Xu X. GATA zinc finger domain-containing protein 2A (GATAD2A) deficiency reactivates fetal haemoglobin in patients with β-thalassaemia through impaired formation of methyl-binding domain protein 2 (MBD2)-containing nucleosome remodelling and deacetylation (NuRD) complex. British Journal of Haematology. PMID 33997955 DOI: 10.1111/bjh.17511 |
0.061 |
|
2012 |
Zhou WJ, Liu WY, Liu D, Jiang JH, Zhou DM, Zhong ZY, Xu XM. A quantitative assay to detect α-thalassemia deletions and triplications using multiplex nested real-time quantitative polymerase chain reaction. Analytical Biochemistry. 427: 144-50. PMID 22617799 DOI: 10.1016/j.ab.2012.05.009 |
0.06 |
|
2021 |
Zhang Y, Zhang L, Hua H, Jin J, Zhu L, Shu L, Xu X, Kuang F, Liu Y. Relaxation Degree Analysis Using Frontal Electroencephalogram Under Virtual Reality Relaxation Scenes. Frontiers in Neuroscience. 15: 719869. PMID 34630012 DOI: 10.3389/fnins.2021.719869 |
0.06 |
|
2016 |
Perkins A, Xu X, Higgs DR, Patrinos GP, Arnaud L, Bieker JJ, Philipsen S. "Krüppeling" erythropoiesis: an unexpected broad spectrum of human red blood cell disorders due to KLF1 variants unveiled by genomic sequencing. Blood. PMID 26903544 DOI: 10.1182/Blood-2016-01-694331 |
0.06 |
|
2016 |
Shang X, Xu X. Update in the genetics of thalassemia: What clinicians need to know. Best Practice & Research. Clinical Obstetrics & Gynaecology. PMID 27876354 DOI: 10.1016/j.bpobgyn.2016.10.012 |
0.059 |
|
2018 |
Zhang T, Chen CLP, Chen L, Xu X, Hu B. Design of Highly Nonlinear Substitution Boxes Based on I-Ching Operators. Ieee Transactions On Cybernetics. PMID 30040668 DOI: 10.1109/TCYB.2018.2846186 |
0.058 |
|
2018 |
He F, Zhou W, Cai R, Yan T, Xu X. Systematic assessment of the performance of whole-genome amplification for SNP/CNV detection and β-thalassemia genotyping. Journal of Human Genetics. PMID 29440707 DOI: 10.1038/s10038-018-0411-5 |
0.057 |
|
2024 |
Bao X, Gao Y, Wang Z, Ye Y, Chen D, Zuo Y, Zhao C, Xu X. Activation of γ-globin expression by LncRNA-mediated ERF promoter hypermethylation in β-thalassemia. Clinical Epigenetics. 16: 12. PMID 38218889 DOI: 10.1186/s13148-023-01614-6 |
0.057 |
|
2014 |
Wang J, Xiao QZ, Chen YM, Yi S, Liu D, Liu YH, Zhang CM, Wei XF, Zhou YQ, Zhong XM, Zhao CY, Xiong F, Wei XC, Xu XM. DNA hypermethylation and X chromosome inactivation are major determinants of phenotypic variation in women heterozygous for G6PD mutations. Blood Cells, Molecules & Diseases. 53: 241-5. PMID 24958328 DOI: 10.1016/j.bcmd.2014.06.001 |
0.057 |
|
2014 |
Liu D, Zhang X, Yu L, Cai R, Ma X, Zheng C, Zhou Y, Liu Q, Wei X, Lin L, Yan T, Huang J, Mohandas N, An X, Xu X. KLF1 mutations are relatively more common in a thalassemia endemic region and ameliorate the severity of β-thalassemia. Blood. 124: 803-11. PMID 24829204 DOI: 10.1182/blood-2014-03-561779 |
0.055 |
|
2009 |
Huang SW, Li Q, Zhu SY, Li L, Xiong F, Jia YK, Xu XM. SYBR Green-based real-time PCR assay for detection of VKORC1 and CYP2C9 polymorphisms that modulate warfarin dose requirement. Clinical Chemistry and Laboratory Medicine. 47: 26-31. PMID 19117406 DOI: 10.1515/Cclm.2009.008 |
0.055 |
|
2010 |
Zhu C, Yu W, Xie J, Chen L, Ding H, Shang X, Xu X. Hemoglobin H disease due to a de novo mutation at the α2-globin gene and an inherited common α-thalassemia deletion found in a Chinese boy. Blood Cells, Molecules & Diseases. 45: 223-6. PMID 20691621 DOI: 10.1016/j.bcmd.2010.07.005 |
0.055 |
|
2019 |
Xing X, Li Z, Xu T, Shu L, Hu B, Xu X. SAE+LSTM: A New Framework for Emotion Recognition From Multi-Channel EEG. Frontiers in Neurorobotics. 13: 37. PMID 31244638 DOI: 10.3389/fnbot.2019.00037 |
0.055 |
|
2010 |
Meng X, Yang X, Wang K, Guo Q, Tan Y, Mo Q, Xu X. Direct fluorescence detection of point mutations in human genomic DNA using microbead-based ligase chain reaction. Talanta. 80: 1725-9. PMID 20152403 DOI: 10.1016/j.talanta.2009.10.013 |
0.054 |
|
2017 |
Miao Y, Xiong J, Zhang X, Huang H, Yu L, Chen J, Deng W, Xu H, Liu R, Xu X, Xiang C, Xiong F. Genetic diagnosis of polycystic kidney disease, Alport syndrome and thalassemia minor in a large Chinese family. Clinical Science (London, England : 1979). PMID 28827396 DOI: 10.1042/CS20170245 |
0.054 |
|
2010 |
Xiao H, Zhu P, Liu B, Pan Q, Jiang X, Xu X, Fu N. Generation and characterization of human delta-globin-specific monoclonal antibodies. Blood Cells, Molecules & Diseases. 44: 127-32. PMID 20022528 DOI: 10.1016/j.bcmd.2009.11.003 |
0.054 |
|
2007 |
Meng X, Li H, Wang K, Tan W, Li J, Guo Q, Yang X, Mo Q, Xu X. Fidelity genotyping of point mutation by enhanced melting point difference using DNA ligase. Talanta. 73: 23-9. PMID 19071845 DOI: 10.1016/J.Talanta.2007.01.067 |
0.053 |
|
2020 |
Zhao S, Wang W, Wang Y, Han R, Fan C, Ni P, Guo F, Zeng F, Yang Q, Yang Y, Sun Y, Zhang X, Chen Y, Zhu B, Cai W, ... ... Xu X, et al. NGS-based spinal muscular atrophy carrier screening of 10,585 diverse couples in China: a pan-ethnic study. European Journal of Human Genetics : Ejhg. PMID 32884118 DOI: 10.1038/s41431-020-00714-8 |
0.053 |
|
2013 |
Huang JW, Shang X, Zhao Y, Cai R, Zhang XH, Wei XF, Xiong F, Xu XM. A novel fusion gene and a common α(0)-thalassemia deletion cause hemoglobin H disease in a Chinese family. Blood Cells, Molecules & Diseases. 51: 31-4. PMID 23481460 DOI: 10.1016/j.bcmd.2013.01.013 |
0.053 |
|
2020 |
Li Z, Shang X, Luo S, Zhu F, Wei X, Zhou W, Ye Y, Yan T, Cai R, Xu X. Characterization of two novel Alu element-mediated α-globin gene cluster deletions causing α-thalassemia by targeted next-generation sequencing. Molecular Genetics and Genomics : Mgg. PMID 31897801 DOI: 10.1007/s00438-019-01637-w |
0.053 |
|
2022 |
Wu S, Ou J, Shu L, Hu G, Song Z, Xu X, Chen Z. MhNet: Multi-scale spatio-temporal hierarchical network for real-time wearable fall risk assessment of the elderly. Computers in Biology and Medicine. 144: 105355. PMID 35286891 DOI: 10.1016/j.compbiomed.2022.105355 |
0.053 |
|
2023 |
Ren Z, Sun G, Zhang Q, Zou S, Chen J, Zhao W, Hou G, Zhong Z, Li J, Ye Y, Xu X, Lin L. LC-MS/MS-Based Absolute Quantitation of Hemoglobin Subunits from Dried Blood Spots Reveals Novel Biomarkers for α-Thalassemia Silent Carriers. Analytical Chemistry. PMID 37285171 DOI: 10.1021/acs.analchem.3c00895 |
0.052 |
|
2017 |
Jomoui W, Fucharoen G, Sanchaisuriya K, Charoenwijitkul P, Maneesarn J, Xu X, Fucharoen S. Genetic origin of α(0)-thalassemia (SEA deletion) in Southeast Asian populations and application to accurate prenatal diagnosis of Hb Bart's hydrops fetalis syndrome. Journal of Human Genetics. PMID 28381876 DOI: 10.1038/jhg.2017.41 |
0.052 |
|
2008 |
Li J, Jiang JH, Xu XM, Chu X, Jiang C, Shen G, Yu RQ. Simultaneous identification of point mutations via DNA ligase-mediated gold nanoparticle assembly. The Analyst. 133: 939-45. PMID 18575649 DOI: 10.1039/b717853k |
0.052 |
|
2016 |
Hu L, Shang X, Yi S, Cai R, Li Z, Liu C, Liang Y, Cai D, Zhang F, Xu X. Two novel copy number variations involving the α-globin gene cluster on chromosome 16 cause thalassemia in two Chinese families. Molecular Genetics and Genomics : Mgg. PMID 27000657 DOI: 10.1007/S00438-016-1193-0 |
0.052 |
|
2023 |
Li Y, Zhang Y, Qin L, Shang H, Li P, Xiao B, Ye Y, Xu X, Zhang X, Wang L. Analysis of hematological indices and splenectomy rates in 2,130 patients with Hemoglobin H diseases or β-thalassemia. Acta Haematologica. PMID 37573774 DOI: 10.1159/000533233 |
0.049 |
|
2013 |
Zhou W, Wang G, Zhao X, Xiong F, Zhou S, Peng J, Cheng Y, Xu S, Xu X. A multiplex qPCR gene dosage assay for rapid genotyping and large-scale population screening for deletional α-thalassemia. The Journal of Molecular Diagnostics : Jmd. 15: 642-51. PMID 23810501 DOI: 10.1016/j.jmoldx.2013.05.007 |
0.048 |
|
2008 |
Li L, Zhou YQ, Xiao QZ, Yan TZ, Xu XM. Development and evaluation of a reverse dot blot assay for the simultaneous detection of six common Chinese G6PD mutations and one polymorphism. Blood Cells, Molecules & Diseases. 41: 17-21. PMID 18329300 DOI: 10.1016/j.bcmd.2008.01.007 |
0.048 |
|
2021 |
Cai D, He F, Xu X, Xiong F, Zhang L. c.4621C>T variant causing Gardner's syndrome in a Han Chinese family may be inherited through maternal mosaicism. Experimental and Therapeutic Medicine. 21: 488. PMID 33790997 DOI: 10.3892/etm.2021.9919 |
0.048 |
|
2003 |
Wu G, Hua L, Zhu J, Mo QH, Xu XM. Rapid, accurate genotyping of beta-thalassaemia mutations using a novel multiplex primer extension/denaturing high-performance liquid chromatography assay. British Journal of Haematology. 122: 311-6. PMID 12846902 DOI: 10.1046/j.1365-2141.2003.04431.x |
0.047 |
|
2018 |
Lin L, Yang Q, Zhang S, Zuo Y, He S, Xu X, Chen B, Qiu X. Identification of a Novel 9.7 kb Deletion Causing α-Thalassemia in Two Pregnant Women in Southern China. Hemoglobin. 42: 209-212. PMID 30864493 DOI: 10.1080/03630269.2018.1516673 |
0.047 |
|
2019 |
Hua H, Tang W, Xu X, Feng DD, Shu L. Flexible Multi-Layer Semi-Dry Electrode for Scalp EEG Measurements at Hairy Sites. Micromachines. 10. PMID 31382695 DOI: 10.3390/Mi10080518 |
0.046 |
|
2020 |
Writing Group For Practice Guidelines For Diagnosis And Treatment Of Genetic Diseases Medical Genetics Branch Of Chinese Medical Association, Shang X, Wu X, Zhang X, Feng X, Xu X. [Clinical practice guidelines for beta-thalassemia]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 37: 243-251. PMID 32128739 DOI: 10.3760/cma.j.issn.1003-9406.2020.03.004 |
0.046 |
|
2016 |
Yang Q, Chen D, Xiong F, Chen D, Liu C, Liu Y, Yu Q, Xiong J, Liu J, Li K, Zhao L, Ye Y, Zhou H, Hu L, Tian Z, ... ... Xu X, et al. A splicing mutation in VPS4B causes dentin dysplasia I. Journal of Medical Genetics. PMID 27247351 DOI: 10.1136/jmedgenet-2015-103619 |
0.046 |
|
2009 |
Huang Y, Zhang YL, Xu X, Jiang JH, Shen GL, Yu RQ. Highly specific and sensitive electrochemical genotyping via gap ligation reaction and surface hybridization detection. Journal of the American Chemical Society. 131: 2478-80. PMID 19178278 DOI: 10.1021/ja808700d |
0.046 |
|
2003 |
Zhang J, Meng B, Liao D, Zhou L, Zhang X, Chen L, Guo Z, Peng C, Zhu B, Lee PP, Xu X, Zhou T, Deng Z, Hu Y, Li K. De novo synthesis of PCR templates for the development of SARS diagnostic assay. Molecular Biotechnology. 25: 107-12. PMID 14526121 DOI: 10.1385/MB:25:2:107 |
0.046 |
|
2008 |
Zeng Y, Miao F, Li L, Sun DH, Xu XM. A rapid and accurate DHPLC assay for determination of apolipoprotein E genotypes. Journal of Alzheimer's Disease : Jad. 12: 357-63. PMID 18198422 DOI: 10.3233/jad-2007-12409 |
0.046 |
|
2018 |
Shu L, Xie J, Yang M, Li Z, Li Z, Liao D, Xu X, Yang X. A Review of Emotion Recognition Using Physiological Signals. Sensors (Basel, Switzerland). 18. PMID 29958457 DOI: 10.3390/s18072074 |
0.046 |
|
2011 |
Wei XF, Shang X, He DQ, Huang JW, Zhang XH, Xu XM. Molecular characterization of a novel 27.6-kb deletion causing α(+) thalassemia in a Chinese family. Annals of Hematology. 90: 17-22. PMID 20645100 DOI: 10.1007/s00277-010-1030-1 |
0.046 |
|
2015 |
Liu F, Xu X, Qiu S, Qing C, Tao D. Simple to Complex Transfer Learning for Action Recognition. Ieee Transactions On Image Processing : a Publication of the Ieee Signal Processing Society. PMID 28055873 DOI: 10.1109/TIP.2015.2512107 |
0.046 |
|
2015 |
Liu F, Xu X, Qiu S, Qing C, Tao D. Simple to Complex Transfer Learning for Action Recognition. Ieee Transactions On Image Processing : a Publication of the Ieee Signal Processing Society. PMID 26841395 DOI: 10.1109/TIP.2015.2512107 |
0.046 |
|
2017 |
Shang X, Peng Z, Ye Y, Asan, Zhang X, Chen Y, Zhu B, Cai W, Chen S, Cai R, Guo X, Zhang C, Zhou Y, Huang S, Liu Y, ... ... Xu X, et al. Rapid Targeted Next-Generation Sequencing Platform for Molecular Screening and Clinical Genotyping in Subjects with Hemoglobinopathies. Ebiomedicine. PMID 28865746 DOI: 10.1016/J.Ebiom.2017.08.015 |
0.046 |
|
2004 |
Ding C, Chiu RW, Lau TK, Leung TN, Chan LC, Chan AY, Charoenkwan P, Ng IS, Law HY, Ma ES, Xu X, Wanapirak C, Sanguansermsri T, Liao C, Ai MA, et al. MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis. Proceedings of the National Academy of Sciences of the United States of America. 101: 10762-7. PMID 15247415 DOI: 10.1073/Pnas.0403962101 |
0.045 |
|
2012 |
Wan JH, Tian PL, Luo WH, Wu BY, Xiong F, Zhou WJ, Wei XC, Xu XM. Rapid determination of human globin chains using reversed-phase high-performance liquid chromatography. Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences. 901: 53-8. PMID 22727753 DOI: 10.1016/j.jchromb.2012.05.041 |
0.045 |
|
2006 |
Yan T, Cai R, Mo O, Zhu D, Ouyang H, Huang L, Zhao M, Huang F, Li L, Liang X, Xu X. Incidence and complete molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Guangxi Zhuang autonomous region of southern China: description of four novel mutations. Haematologica. 91: 1321-8. PMID 17018380 |
0.044 |
|
2022 |
Song Z, Ou J, Shu L, Hu G, Wu S, Xu X, Chen Z. Fall Risk Assessment for the Elderly Based on Weak Foot Features of Wearable Plantar Pressure. Ieee Transactions On Neural Systems and Rehabilitation Engineering : a Publication of the Ieee Engineering in Medicine and Biology Society. 30: 1060-1070. PMID 35420987 DOI: 10.1109/TNSRE.2022.3167473 |
0.044 |
|
2016 |
Tepakhan W, Yamsri S, Sanchaisuriya K, Fucharoen G, Xu X, Fucharoen S. Nine known and five novel mutations in the erythroid transcription factor KLF1 gene and phenotypic expression of fetal hemoglobin in hemoglobin E disorder. Blood Cells, Molecules & Diseases. 59: 85-91. PMID 27282573 DOI: 10.1016/j.bcmd.2016.04.010 |
0.044 |
|
2020 |
Shu L, Yu Y, Chen W, Hua H, Li Q, Jin J, Xu X. Wearable Emotion Recognition Using Heart Rate Data from a Smart Bracelet. Sensors (Basel, Switzerland). 20. PMID 32012920 DOI: 10.3390/s20030718 |
0.043 |
|
2011 |
Wang Z, Xu X, Ding X, Xiao H, Huang Y, Liu J, Xing X, Wang H, Liao DJ. Extraction of prostatic lumina and automated recognition for prostatic calculus image using PCA-SVM. Computational and Mathematical Methods in Medicine. 2011: 831278. PMID 21461364 DOI: 10.1155/2011/831278 |
0.043 |
|
2022 |
Tan J, Zhang X, Qing C, Xu X. Fourier Domain Robust Denoising Decomposition and Adaptive Patch MRI Reconstruction. Ieee Transactions On Neural Networks and Learning Systems. PMID 37015441 DOI: 10.1109/TNNLS.2022.3222394 |
0.043 |
|
2021 |
Wang J, Zhou S, He F, Zhang X, Lu J, Zhang J, Zhang F, Xu X, Yang F, Xiong F. Familial Translocation t(2;4) (q37.3;p16.3), Resulting in a Partial Trisomy of 2q (or 4p) and a Partial Monosomy of 4p (or 2q), Causes Dysplasia. Frontiers in Genetics. 12: 741607. PMID 34887900 DOI: 10.3389/fgene.2021.741607 |
0.042 |
|
2011 |
Yan TZ, Mo QH, Cai R, Chen X, Zhang CM, Liu YH, Chen YJ, Zhou WJ, Xiong F, Xu XM. Reliable detection of paternal SNPs within deletion breakpoints for non-invasive prenatal exclusion of homozygous α-thalassemia in maternal plasma. Plos One. 6: e24779. PMID 21980356 DOI: 10.1371/journal.pone.0024779 |
0.042 |
|
2009 |
Huang SW, Chen HS, Wang XQ, Huang L, Xu DL, Hu XJ, Huang ZH, He Y, Chen KM, Xiang DK, Zou XM, Li Q, Ma LQ, Wang HF, Chen BL, ... ... Xu XM, et al. Validation of VKORC1 and CYP2C9 genotypes on interindividual warfarin maintenance dose: a prospective study in Chinese patients. Pharmacogenetics and Genomics. 19: 226-34. PMID 19177029 DOI: 10.1097/Fpc.0B013E328326E0C7 |
0.042 |
|
2007 |
Li B, Zhao Y, Xu X, Zhou H, He B, Wu Z, Zhang Z. A simple method for the preparation of containing Sb nano- and microcrystallines via an ultrasound agitation. Ultrasonics Sonochemistry. 14: 557-62. PMID 17097908 DOI: 10.1016/j.ultsonch.2006.09.007 |
0.042 |
|
2002 |
Mo Q, Xu X, Zhong X, Liu Z. [An improved PCR-based megaprimer method for site-directed mutagenesis]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 19: 68-71. PMID 11836693 |
0.041 |
|
2019 |
Cheng Y, Cai D, Shang X, Pang D, Wei X, Zhong J, Xu X. A combination of the (αα) and -- deletions causing a severe form of hemoglobin H disease. International Journal of Laboratory Hematology. PMID 31756043 DOI: 10.1111/ijlh.13122 |
0.041 |
|
2008 |
Zhang P, Chu X, Xu X, Shen G, Yu R. Electrochemical detection of point mutation based on surface ligation reaction and biometallization. Biosensors & Bioelectronics. 23: 1435-41. PMID 18242973 DOI: 10.1016/j.bios.2007.12.011 |
0.04 |
|
2015 |
Fang P, Li L, Zeng J, Zhou WJ, Wu WQ, Zhong ZY, Yan TZ, Xie JS, Huang J, Lin L, Zhao Y, Xu XM. Molecular characterization and copy number of SMN1, SMN2 and NAIP in Chinese patients with spinal muscular atrophy and unrelated healthy controls. Bmc Musculoskeletal Disorders. 16: 11. PMID 25888055 DOI: 10.1186/s12891-015-0457-x |
0.04 |
|
2011 |
Xiong F, Huang Q, Chen X, Zhou Y, Zhang X, Cai R, Chen Y, Xie J, Feng S, Wei X, Xiao Q, Zhang T, Luo S, Yang X, Hao Y, ... ... Xu X, et al. A melting curve analysis--based PCR assay for one-step genotyping of β-thalassemia mutations a multicenter validation. The Journal of Molecular Diagnostics : Jmd. 13: 427-35. PMID 21704277 DOI: 10.1016/j.jmoldx.2011.03.005 |
0.039 |
|
2022 |
Chen T, Zhang Q, Shang X, Zou S, Qin J, Li K, Lin B, Tao Z, Long X, Xu X. Diamond-Blackfan anaemia caused by a de novo initiation codon mutation resulting in a shorter isoform of GATA1. Clinical Genetics. PMID 36029112 DOI: 10.1111/cge.14218 |
0.039 |
|
2023 |
Zhou Y, Zhao Y, Xiang Z, Yan Z, Shu L, Xu X, Zhang L, Tian X. A dual-task-embedded virtual reality system for intelligent quantitative assessment of cognitive processing speed. Frontiers in Human Neuroscience. 17: 1158650. PMID 37063104 DOI: 10.3389/fnhum.2023.1158650 |
0.038 |
|
2008 |
Liu JX, Zhou WJ, Gong JL, Tang L, Zhang Y, Yu HY, Wang B, Xu XM, Zeng GM. An electrochemical sensor for detection of laccase activities from Penicillium simplicissimum in compost based on carbon nanotubes modified glassy carbon electrode. Bioresource Technology. 99: 8748-51. PMID 18511270 DOI: 10.1016/j.biortech.2008.04.029 |
0.038 |
|
2022 |
Tan XM, Liu YH, Shang X, Ye YH, Xu XM. A Novel Hemoglobin Variant Hb Liaobu [α107(G14)Val→Leu, : c.322G>C] Detected by Matrix-Assisted Laser Desorption Ionization-Time-of-Flight Mass Spectrometry. Hemoglobin. 1-4. PMID 35322741 DOI: 10.1080/03630269.2022.2036186 |
0.038 |
|
2013 |
Liu YH, Shang X, Li ZT, Wu YM, Li LF, Xu XM. A novel COL7A1 gene mutation causing pretibial epidermolysis bullosa: report of a Chinese family with intra-familial phenotypical diversity. Gene. 524: 377-80. PMID 23624125 DOI: 10.1016/j.gene.2013.03.143 |
0.038 |
|
2008 |
Li Q, Li LY, Huang SW, Li L, Chen XW, Zhou WJ, Xu XM. Rapid genotyping of known mutations and polymorphisms in beta-globin gene based on the DHPLC profile patterns of homoduplexes and heteroduplexes. Clinical Biochemistry. 41: 681-7. PMID 18339318 DOI: 10.1016/j.clinbiochem.2008.02.008 |
0.037 |
|
2017 |
Guo K, Liu L, Xu X, Xu D, Tao D. GoDec+: Fast and Robust Low-Rank Matrix Decomposition Based on Maximum Correntropy. Ieee Transactions On Neural Networks and Learning Systems. PMID 28436892 DOI: 10.1109/Tnnls.2016.2643286 |
0.037 |
|
2022 |
Zhou C, He S, Liu D, Zuo Y, Chen Q, Wang L, Chen B, Chen F, Luo J, Xu X, Lin L. Reference intervals for erythrocyte parameters and hemoglobin electrophoresis parameters for young children in Guangxi. International Journal of Laboratory Hematology. PMID 36064301 DOI: 10.1111/ijlh.13965 |
0.037 |
|
2011 |
Wu HM, Li L, Yuan XW, Zhou YQ, Xiao QZ, Liu WY, Zhou WJ, Xu XM. Rapid, accurate detection of TMPRSS6 gene causative mutations with a high-resolution melting assay. Blood Cells, Molecules & Diseases. 47: 198-204. PMID 21783390 DOI: 10.1016/j.bcmd.2011.06.004 |
0.037 |
|
2023 |
Liu Y, Zhuang Y, Chen J, Zhong Z, Fang J, Li X, Xiao B, Li P, Lin B, Tao Z, Liang Y, Lin P, Wang X, Song M, Luo H, ... ... Xu X, et al. Quantitative evaluation of the clinical severity of hemoglobin H disease in a cohort of 591 patients using a scoring system based on regression analysis. Haematologica. PMID 37646667 DOI: 10.3324/haematol.2023.283211 |
0.036 |
|
2005 |
Li L, Mo QH, Xu XM. Rapid, accurate genotyping of alcohol dehydrogenase-1B and aldehyde dehydrogenase-2 based on the use of denaturing HPLC Clinical Chemistry and Laboratory Medicine : Cclm / Fescc.. 43: 1334-1338. PMID 16309369 |
0.036 |
|
2005 |
Mo QH, Zhu H, Li LY, Xu XM. Reliable and high-throughput mutation screening for beta-thalassemia by a single-base extension/fluorescence polarization assay. Genetic Testing. 8: 257-62. PMID 15727248 DOI: 10.1089/gte.2004.8.257 |
0.036 |
|
2016 |
Li L, Zhou WJ, Fang P, Zhong ZY, Xie JS, Yan TZ, Zeng J, Tan XH, Xu XM. Evaluation and comparison of three assays for molecular detection of spinal muscular atrophy. Clinical Chemistry and Laboratory Medicine. PMID 27754957 DOI: 10.1515/cclm-2016-0275 |
0.035 |
|
2010 |
Sun MN, Xiong F, Zhang XH, Lou JW, Xu XM. [Analysis of the phenotype-genotype relationship of Hb Constant Spring]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 27: 481-3. PMID 20931520 DOI: 10.3760/cma.j.issn.1003-9406.2010.05.001 |
0.034 |
|
2005 |
Zhou Y, Zhang Y, Li L, Li W, Mo Q, Zheng Q, Xu X. [Rapid detection of three common deletional alpha thalassemias in Chinese by single-tube multiplex PCR]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 22: 180-4. PMID 15793780 |
0.033 |
|
2005 |
Hua L, Zhu H, Li XR, Li J, Mo QH, Liao C, Hou YX, Zhong M, Xu XM. [Accurate and rapid prenatal diagnosis of beta-thalassemia by a multiplex primer extension and denaturing high-performance liquid chromatography technique]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 21: 600-3. PMID 15583991 |
0.032 |
|
2008 |
Mao X, Jiang J, Xu X, Chu X, Luo Y, Shen G, Yu R. Enzymatic amplification detection of DNA based on "molecular beacon" biosensors. Biosensors & Bioelectronics. 23: 1555-61. PMID 18304797 DOI: 10.1016/j.bios.2008.01.019 |
0.032 |
|
2018 |
Hu A, Li X, Chen D, Lu T, Huang J, Xu X, Chen D, Xiong F. [Analysis of DSPP gene mutation in a Chinese pedigree affected with hereditary dentinogenesis imperfecta]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 35: 511-514. PMID 30098245 DOI: 10.3760/cma.j.issn.1003-9406.2018.04.011 |
0.032 |
|
2018 |
Pu J, Zhang L, Wei X, Xu X. Clinical Genotyping by Next Generation Sequencing Reveals a Novel, De Novo β-Globin Gene Mutation Causing Hemolytic Anemia in a Chinese Individual. Hemoglobin. 1-5. PMID 30277086 DOI: 10.1080/03630269.2018.1496928 |
0.032 |
|
2020 |
Writing Group For Practice Guidelines For Diagnosis And Treatment Of Genetic Diseases Medical Genetics Branch Of Chinese Medical Association, Shang X, Zhang X, Yang F, Xu X. [Clinical practice guidelines for alpha-thalassemia]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 37: 235-242. PMID 32128738 DOI: 10.3760/cma.j.issn.1003-9406.2020.03.003 |
0.031 |
|
2019 |
Zhu F, Wei X, Cai D, Pang D, Zhong J, Liang M, Zuo Y, Xu X, Shang X. A novel 223 kb deletion in the beta-globin gene cluster was identified in a Chinese thalassemia major patient. International Journal of Laboratory Hematology. PMID 30945812 DOI: 10.1111/ijlh.13021 |
0.031 |
|
2009 |
Zhou WJ, Zhou SY, Huang SW, Zhou JP, Xu XM. [Identification of a missense mutation in SEDL gene from a Chinese family with X-linked spondyloepiphyseal dysplasia tarda]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 25: 15-8. PMID 18247296 |
0.031 |
|
2013 |
Xiong F, Li Q, Zhang C, Chen Y, Li P, Wei X, Li Q, Zhou W, Li L, Shang X, Xu X. Analyses of GATA4, NKX2.5, and TFAP2B genes in subjects from southern China with sporadic congenital heart disease. Cardiovascular Pathology : the Official Journal of the Society For Cardiovascular Pathology. 22: 141-5. PMID 22959235 DOI: 10.1016/j.carpath.2012.07.001 |
0.031 |
|
2004 |
Kong QP, Yao YG, Sun C, Zhu CL, Zhong L, Wang CY, Cai WW, Xu XM, Xu AL, Zhang YP. Phylogeographic analysis of mitochondrial DNA haplogroup F2 in China reveals T12338C in the initiation codon of the ND5 gene not to be pathogenic Journal of Human Genetics. 49: 414-423. PMID 15278763 DOI: 10.1007/s10038-004-0170-3 |
0.031 |
|
2009 |
Li LY, Mo QH, Xu XM. [Rapid diagnosis of non-deletion alpha-thalassemias by reverse dot blot]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 20: 345-7. PMID 12903049 |
0.03 |
|
2018 |
Zhang Q, Zhang Y, Xu H, Xu M, Wen X, Xu X, Zhou W. [Genetic and phenotypic analysis of a rare case with homozygous Chinese Gγ (Aγδβ)-thal deletion]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 35: 553-556. PMID 30098255 DOI: 10.3760/cma.j.issn.1003-9406.2018.04.021 |
0.03 |
|
2019 |
Zhang Q, Zhang Y, Xu X, Zhou W, Fan X. [Establishment of a system for rapid detection of JAK2 V617F mutation in myeloproliferative diseases]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 36: 980-984. PMID 31598940 DOI: 10.3760/cma.j.issn.1003-9406.2019.10.007 |
0.03 |
|
2023 |
Wu S, Shu L, Song Z, Xu X. SFDA: Domain Adaptation with Source Subject Fusion Based On Multi-source And Single-target Fall Risk Assessment. Ieee Transactions On Neural Systems and Rehabilitation Engineering : a Publication of the Ieee Engineering in Medicine and Biology Society. PMID 38032785 DOI: 10.1109/TNSRE.2023.3337861 |
0.028 |
|
2011 |
Wang LH, Huang YQ, Shang X, Su QX, Xiong F, Yu QY, Lin HP, Wei ZS, Hong MF, Xu XM. Mutation analysis of 73 southern Chinese Wilson's disease patients: identification of 10 novel mutations and its clinical correlation. Journal of Human Genetics. 56: 660-5. PMID 21796144 DOI: 10.1038/jhg.2011.76 |
0.028 |
|
2022 |
Zhang Q, Wang G, Sun D, Lin W, Yan T, Wu Y, Wu M, Chen J, Zou S, Xie W, Zhou Y, Wang Y, He L, Liu Y, Qiu Z, ... ... Xu X, et al. MALDI-TOF-MS for Rapid Screening and Typing of β-Globin Variant and β-Thalassemia through Direct Measurements of Intact Globin Chains. Clinical Chemistry. PMID 36226750 DOI: 10.1093/clinchem/hvac151 |
0.028 |
|
2013 |
Yuan XW, Zhou WJ, Shang X, Li L, Liu YH, Xu XM. Rapid simultaneous genotyping of polymorphisms in ADH1B and ALDH2 using high resolution melting assay. Clinical Chemistry and Laboratory Medicine. 51: e75-7. PMID 23001317 DOI: 10.1515/cclm-2012-0509 |
0.028 |
|
2023 |
Wang G, Zou S, Li J, Wang X, Wu H, Tao Z, Zhang Q, Xu X, Zhou Y. The diagnosis and molecular analysis of a novel 27.2 kb deletion causing α-thalassemia. Clinical Biochemistry. PMID 36878345 DOI: 10.1016/j.clinbiochem.2023.03.002 |
0.027 |
|
2012 |
Zhou YQ, Shang X, Yin BM, Xiong F, Xiao QZ, Zhou WJ, Zhang YL, Xu XM. [Large-scale population-based genetic screening and prenatal diagnosis for thalassemias in Zhuhai City of Guangdong Province]. Zhonghua Fu Chan Ke Za Zhi. 47: 90-5. PMID 22455738 |
0.027 |
|
2021 |
Lin W, Zhang Q, Shen Z, Qu X, Wang Q, Wei L, Qiu Y, Yang J, Xu X, Lao J. Molecular and phenotype characterization of an elongated β-globin variant produced by HBB:C.313delA. International Journal of Laboratory Hematology. PMID 34271589 DOI: 10.1111/ijlh.13639 |
0.026 |
|
2007 |
Chen XW, Mo QH, Li Q, Zeng R, Xu XM. A novel mutation of -73(A-->T) in the CCAAT box of the beta-globin gene identified in a patient with the mild beta-thalassemia intermedia. Annals of Hematology. 86: 653-7. PMID 17516066 DOI: 10.1007/s00277-007-0312-8 |
0.026 |
|
2010 |
Wang Z, Yu W, Li Y, Shang X, Zhang X, Xiong F, Xu X. Analysis of alpha-hemoglobin-stabilizing protein (AHSP) gene as a genetic modifier to the phenotype of beta-thalassemia in Southern China. Blood Cells, Molecules & Diseases. 45: 128-32. PMID 20627634 DOI: 10.1016/j.bcmd.2010.04.005 |
0.026 |
|
2016 |
Liu C, Tian Z, Yang Q, Ma Q, Xu X, Xiong F. [Screening of CTSC gene mutations in a Chinese pedigree affected with Papillon-Lefevre syndrome]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 33: 150-154. PMID 27060303 DOI: 10.3760/cma.j.issn.1003-9406.2016.02.005 |
0.026 |
|
2004 |
Yang LL, Ou YH, Xu XM. [Rapid molecular diagnosis of trisomy 21 using the PCR-STR-SSCP technique]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 21: 466-9. PMID 15476172 |
0.023 |
|
2010 |
Chen W, Zhang X, Shang X, Cai R, Li L, Zhou T, Sun M, Xiong F, Xu X. The molecular basis of beta-thalassemia intermedia in southern China: genotypic heterogeneity and phenotypic diversity. Bmc Medical Genetics. 11: 31. PMID 20181291 DOI: 10.1186/1471-2350-11-31 |
0.023 |
|
2008 |
Yi P, Yu F, Huang S, Zhong C, Li Q, Yang Y, Zhang W, Xiao C, Xu X. Identification of a novel frameshift mutation at codon 53 (-T) in the beta-globin gene causing dominantly inherited beta-thalassemia in a Chinese Miao family. Blood Cells, Molecules & Diseases. 41: 56-9. PMID 18381244 DOI: 10.1016/j.bcmd.2008.02.001 |
0.023 |
|
2009 |
Zhou YQ, Mo QH, Lu JH, Li LY, Liang X, Jia SQ, Xiao GF, Zhou WJ, Xiao QZ, Xu XM. [A community-based genetic screening of large-scale population and prenatal diagnosis for alpha and beta thalassemia in Zhuhai city of Guangdong province]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 25: 256-61. PMID 18543211 |
0.02 |
|
2003 |
Jia S, Lao X, Li W, Ma J, Mo Q, Xu X. A rare beta-thalassaemia mutation (C-T) at position -90 of the beta-globin gene discovered in a Chinese family. Haematologica. 88: 1191-3. PMID 14555318 |
0.02 |
|
2010 |
Lou JW, Li Q, Wei XF, Huang JW, Xu XM. Identification of the linkage of a 1.357 KB beta-globin gene deletion and A gamma-globin gene triplication in a Chinese family. Hemoglobin. 34: 343-53. PMID 20642332 DOI: 10.3109/03630269.2010.486357 |
0.02 |
|
2004 |
Li WJ, Lao XW, Jai SQ, Liang FA, Mo QH, Ma JY, Xu XM. [A rare transcription mutation (-90 C-->T) in a Chinese family with beta-thalassemia]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 20: 468-70. PMID 14669211 |
0.019 |
|
2020 |
Pang D, Shang X, Cai D, Yang F, Lu H, Cheng Y, Wei X, He F, Xu X. Unusual survival of a twin with homozygous α0-thalassemia due to Chimerism. Haematologica. 0. PMID 33124788 DOI: 10.3324/haematol.2020.262600 |
0.019 |
|
2013 |
Zhao Y, Shang X, Xiong F, Liu YH, Lou JW, Xu XM. [Analysis of clinical phenotypes of compound heterozygotes of Hb J-Bangkok and β-thalassemia]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 30: 148-51. PMID 23568723 DOI: 10.3760/cma.j.issn.1003-9406.2013.04.005 |
0.019 |
|
2020 |
Wang D, Ouyang J, Zhou P, Yan J, Shu L, Xu X. A Novel Low-Cost Wireless Footwear System for Monitoring Diabetic Foot Patients. Ieee Transactions On Biomedical Circuits and Systems. PMID 33296308 DOI: 10.1109/TBCAS.2020.3043538 |
0.019 |
|
2002 |
Cai R, Li L, Liang X, Liu Z, Su L, Li W, Zhu Q, Mo Q, Pan L, Ouyang H, Huang L, Xu X. [Prevalence survey and molecular characterization of alpha and beta thalassemia in Liuzhou city of Guangxi]. Zhonghua Liu Xing Bing Xue Za Zhi = Zhonghua Liuxingbingxue Zazhi. 23: 281-5. PMID 12411074 |
0.017 |
|
2021 |
Zhou X, Chen T, Zhang Q, Qi M, Zhang L, Du J, Chi H, Shen B, Xu X, Lu Y. De novo HBB frameshift mutation in a patient with dominant β-thalassemia major. International Journal of Laboratory Hematology. PMID 34323379 DOI: 10.1111/ijlh.13669 |
0.014 |
|
2004 |
Hua L, Li J, Liu ZY, Zhong HZ, Liao C, Xu XM. [Use of capillary electrophoresis to determine hemoglobin A2 in healthy adults and alpha- and beta-thalassemia carriers]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 20: 421-4. PMID 14556197 |
0.013 |
|
2005 |
Liao C, Mo QH, Li J, Li LY, Huang YN, Hua L, Li QM, Zhang JZ, Feng Q, Zeng R, Zhong HZ, Jia SQ, Cui YY, Xu XM. Carrier screening for alpha- and beta-thalassemia in pregnancy: the results of an 11-year prospective program in Guangzhou Maternal and Neonatal hospital. Prenatal Diagnosis. 25: 163-71. PMID 15712323 DOI: 10.1002/pd.1079 |
0.011 |
|
2002 |
Zhou YQ, Xiao GF, Li LY, Li WD, Liu ZY, Zhu LF, Mo QH, Qu XJ, Xu XM. Evaluation of clinical application of gap-PCR as a routine method for alpha-thalassemia carrier detection. Di 1 Jun Yi Da Xue Xue Bao = Academic Journal of the First Medical College of Pla. 22: 434-6. PMID 12390707 |
0.011 |
|
2012 |
Xiong F, Lou JW, Wei XF, Sun MN, Huang JW, Shang X, Zhang XH, Xu XM. [Analysis of hematological characteristics on the 79 co-inheritance of α-thalassemia and β-thalassemia carriers in Guangxi]. Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi. 33: 856-60. PMID 23384911 |
0.01 |
|
2012 |
Xu XM, Yu YH. [Prenatal diagnosis for thalassemias]. Zhonghua Fu Chan Ke Za Zhi. 47: 81-4. PMID 22455736 |
0.01 |
|
2004 |
Tan JR, Li WJ, Ma JY, Mo QH, Li LY, Jia SQ, Lao XW, Li LY, He RQ, Xu XM. Molecular epidemiological study of alpha- and beta-thalassemia in Sihui city. Di 1 Jun Yi Da Xue Xue Bao = Academic Journal of the First Medical College of Pla. 23: 716-9. PMID 12865230 |
0.01 |
|
Hide low-probability matches. |