Search Results - "Lingji Chen"

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  1. 1

    Molecular characterization of thalassemia and hemoglobinopathy in Southeastern China by Huang, Hailong, Xu, Liangpu, Chen, Meihuan, Lin, Na, Xue, Huili, Chen, Lingji, Wang, Yan, He, Deqin, Zhang, Min, Lin, Yuan

    Published in Scientific reports (05-03-2019)
    “…Thalassemia and hemoglobinopathy are two common inherited disorders, which are highly prevalent in southern China. However, there is little knowledge on the…”
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    Journal Article
  2. 2

    The clinical value of hsa-miR-190b-5p in peripheral blood of pediatric β-thalassemia and its regulation on BCL11A expression by Chen, Meihuan, Wang, Xinrui, Wang, Haiwei, Zhang, Min, Chen, Lingji, Chen, Hong, Pan, Yali, Zhang, Yanhong, Xu, Liangpu, Huang, Hailong

    Published in PloS one (05-10-2023)
    “…Background The B cell CLL/lymphoma 11A (BCL11A) is a key regulator of hemoglobin switching in β-thalassemia (β-thal). Previous study has suggested that…”
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    Journal Article
  3. 3

    Prenatal genetic diagnosis of fetuses with dextrocardia using whole exome sequencing in a tertiary center by Xue, Huili, Yu, Aili, Chen, Lingji, Guo, Qun, Zhang, Lin, lin, Na, Chen, Xuemei, Xu, Liangpu, Huang, Hailong

    Published in Scientific reports (15-07-2024)
    “…To evaluate the genetic etiology of fetal dextrocardia, associated ultrasound anomalies, and perinatal outcomes, we investigated the utility of whole exome…”
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    Journal Article
  4. 4

    Genetic testing for fetal loss of heterozygosity using single nucleotide polymorphism array and whole-exome sequencing by Xue, Huili, Yu, Aili, Zhang, Lin, Chen, Lingji, Guo, Qun, Lin, Min, lin, Na, Chen, Xuemei, Xu, Liangpu, Huang, Hailong

    Published in Scientific reports (25-01-2024)
    “…The study explored the clinical significance of fetal loss of heterozygosity (LOH) identified by single-nucleotide polymorphism array (SNP array). We…”
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    Journal Article
  5. 5

    Prenatal diagnosis of fetal skeletal anomalies via whole-exome sequencing in a tertiary referral center by Xue, Huili, Yu, Aili, Zhao, Wantong, Chen, Lingji, Fang, Ruqi, Ling, Wen, Zhang, Lin, Guo, Qun, lin, Na, Xu, Liangpu, Huang, Hailong

    Published in Scientific reports (09-11-2024)
    “…The accurate prenatal diagnosis of skeletal anomaly (SKA) using prenatal imaging alone remains challenging. We aimed to investigate the efficacy of whole-exome…”
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    Journal Article
  6. 6

    Clinical findings and genetic analysis of patients with copy number variants involving 17p13.3 using a single nucleotide polymorphism array: a single-center experience by Liang, Bin, Yu, Donghong, Zhao, Wantong, Wang, Yan, Wu, Xiaoqing, Chen, Lingji, Lin, Na, Huang, Hailong, Xu, Liangpu

    Published in BMC medical genomics (21-12-2022)
    “…17p13.3 microdeletions or microduplications (collectively known as copy number variants or CNVs) have been described in individuals with neurodevelopmental…”
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    Journal Article
  7. 7

    Prenatal diagnosis of fetuses with region of homozygosity detected by single nucleotide polymorphism array: a retrospective cohort study by Liang, Bin, Yu, Donghong, Zhao, Wantong, Wang, Yan, Wang, Xinrui, Wu, Xiaoqing, Chen, Lingji, Chen, Meihuan, Zhang, Min, Chen, Xuemei, Lin, Na, Huang, Hailong, Xu, Liangpu

    Published in Journal of human genetics (01-11-2022)
    “…Region of homozygosity (ROH) is classified as uniparental disomy (UPD) or identity by descent, depending on its origin. To explore the clinical relevance of…”
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    Journal Article
  8. 8

    A survey of numerical methods for nonlinear filtering problems by Budhiraja, Amarjit, Chen, Lingji, Lee, Chihoon

    Published in Physica. D (01-06-2007)
    “…The main goal of filtering is to obtain, recursively in time, good estimates of the state of a stochastic dynamical system based on noisy partial observations…”
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    Journal Article
  9. 9

    Molecular analysis and prenatal diagnosis of seven Chinese families with genetic epilepsy by Mao, Bin, Lin, Na, Guo, Danhua, He, Deqin, Xue, Huili, Chen, Lingji, He, Qianqian, Zhang, Min, Chen, Meihuan, Huang, Hailong, Xu, Liangpu

    Published in Frontiers in neuroscience (12-05-2023)
    “…Genetic epilepsy is a large group of clinically and genetically heterogeneous neurological disorders characterized by recurrent seizures, which have a clear…”
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    Journal Article
  10. 10

    Estimation under unknown correlation: covariance intersection revisited by Lingji Chen, Arambel, P.O., Mehra, R.K.

    Published in IEEE transactions on automatic control (01-11-2002)
    “…Addresses the problem of obtaining a consistent estimate (or upper bound) of the covariance matrix when combining two quantities with unknown correlation. The…”
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    Journal Article
  11. 11

    Prenatal diagnosis of BACs‐on‐Beads assay in 1520 cases from Fujian Province, China by Wang, Yan, Zhang, Min, Chen, Lingji, Huang, Hailong, Xu, Liangpu

    Published in Molecular genetics & genomic medicine (01-10-2020)
    “…Background The aim of this study was to evaluate the application of BACs‐on‐Beads (BoBs™) assay for rapid detection of chromosomal abnormalities for prenatal…”
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    Journal Article
  12. 12

    How to Tell a Bad Filter Through Monte Carlo Simulations by Lingji Chen, Chihoon Lee, Mehra, R.K.

    Published in IEEE transactions on automatic control (01-07-2007)
    “…In this note, we propose one particular method to address the issue of how to numerically evaluate nonlinear filtering algorithms and/or their software…”
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    Journal Article
  13. 13

    Comment on "One-Step Solution for the Multistep Out-of-Sequence-Measurement Problem in Tracking by Lingji Chen, Moshtagh, N., Mehra, R. K.

    “…To incorporate out-of-sequence measurements (OOSMs) in a Kalman filter, the cited paper proposed algorithms that reduced the multistep problem into a…”
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    Journal Article
  14. 14

    Identification and control of a nonlinear discrete-time system based on its linearization: a unified framework by Lingji Chen, Narendra, K.S.

    Published in IEEE transactions on neural networks (01-05-2004)
    “…This paper presents a unified theoretical framework for the identification and control of a nonlinear discrete-time dynamical system, in which the nonlinear…”
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    Journal Article
  15. 15

    A maximum weight constrained path cover algorithm for graph-based multitarget tracking by Lingji Chen, Ravichandran, Ravi

    “…In graph-based target tracking, vertices represent measurements and/or tracklets and edges represent allowable associations. Therefore a solution with a set of…”
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    Conference Proceeding
  16. 16

    The clinical value of hsa-miR-190b-5p in peripheral blood of pediatric [beta]-thalassemia and its regulation on BCL11A expression by Chen, Meihuan, Wang, Xinrui, Wang, Haiwei, Zhang, Min, Chen, Lingji, Chen, Hong, Pan, Yali, Zhang, Yanhong, Xu, Liangpu, Huang, Hailong

    Published in PloS one (05-10-2023)
    “…Background The B cell CLL/lymphoma 11A (BCL11A) is a key regulator of hemoglobin switching in [beta]-thalassemia ([beta]-thal). Previous study has suggested…”
    Get full text
    Journal Article
  17. 17

    Mutation analysis of GJB2, SLC26A4, GJB3 and mtDNA12SrRNA genes in 251 non-syndromic hearing loss patients in Fujian, China by Xiong, Yikang, Chen, Meihuan, Wang, Haiwei, Chen, Lingji, Huang, Hailong, Xu, Liangpu

    “…The molecular etiology of non-syndromic hearing loss (NSHL) in Southeastern China (Fujian) has not been precisely identified. our study selected patients with…”
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    Journal Article
  18. 18

    Automated track projection bias removal using Frechet distance and road networks by Lingji Chen, Ravichandran, Ravi

    “…When target tracks produced by a video tracker are projected to the Earth's surface, they often become a (slightly) rotated, stretched and translated version…”
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    Conference Proceeding
  19. 19

    Diagnostic accuracy and value of chromosomal microarray analysis for chromosomal abnormalities in prenatal detection: A prospective clinical study by Huang, Hailong, Wang, Yan, Zhang, Min, Lin, Na, An, Gang, He, Deqin, Chen, Meihuan, Chen, Lingji, Xu, Liangpu

    Published in Medicine (Baltimore) (21-05-2021)
    “…Chromosomal microarray analysis (CMA) has emerged as a primary diagnostic tool for the evaluation of developmental delay and structural malformations in…”
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    Journal Article
  20. 20

    Prenatal diagnosis of thalassemia in 695 pedigrees from southeastern China: a 10‐year follow‐up study by Huang, Hailong, Chen, Meihuan, Chen, Lingji, Zhang, Min, Wang, Yan, Lin, Na, Xu, Liangpu

    Published in Journal of clinical laboratory analysis (01-10-2021)
    “…Thalassaemia is highly prevalent in southeastern China. This 10‐year follow‐up study aimed to characterize the genotype and karyotype of thalassaemia in fetal…”
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    Journal Article