Search Results - "Lingji Chen"
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1
Molecular characterization of thalassemia and hemoglobinopathy in Southeastern China
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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2
The clinical value of hsa-miR-190b-5p in peripheral blood of pediatric β-thalassemia and its regulation on BCL11A expression
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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3
Prenatal genetic diagnosis of fetuses with dextrocardia using whole exome sequencing in a tertiary center
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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4
Genetic testing for fetal loss of heterozygosity using single nucleotide polymorphism array and whole-exome sequencing
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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Prenatal diagnosis of fetal skeletal anomalies via whole-exome sequencing in a tertiary referral center
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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Clinical findings and genetic analysis of patients with copy number variants involving 17p13.3 using a single nucleotide polymorphism array: a single-center experience
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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Prenatal diagnosis of fetuses with region of homozygosity detected by single nucleotide polymorphism array: a retrospective cohort study
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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8
A survey of numerical methods for nonlinear filtering problems
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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9
Molecular analysis and prenatal diagnosis of seven Chinese families with genetic epilepsy
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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10
Estimation under unknown correlation: covariance intersection revisited
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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Prenatal diagnosis of BACs‐on‐Beads assay in 1520 cases from Fujian Province, China
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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12
How to Tell a Bad Filter Through Monte Carlo Simulations
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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13
Comment on "One-Step Solution for the Multistep Out-of-Sequence-Measurement Problem in Tracking
Published in IEEE transactions on aerospace and electronic systems (01-07-2011)“…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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14
Identification and control of a nonlinear discrete-time system based on its linearization: a unified framework
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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15
A maximum weight constrained path cover algorithm for graph-based multitarget tracking
Published in 2015 18th International Conference on Information Fusion (Fusion) (01-07-2015)“…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
The clinical value of hsa-miR-190b-5p in peripheral blood of pediatric [beta]-thalassemia and its regulation on BCL11A expression
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…”
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Journal Article -
17
Mutation analysis of GJB2, SLC26A4, GJB3 and mtDNA12SrRNA genes in 251 non-syndromic hearing loss patients in Fujian, China
Published in International journal of pediatric otorhinolaryngology (01-01-2024)“…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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18
Automated track projection bias removal using Frechet distance and road networks
Published in 17th International Conference on Information Fusion (FUSION) (01-07-2014)“…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
Diagnostic accuracy and value of chromosomal microarray analysis for chromosomal abnormalities in prenatal detection: A prospective clinical study
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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Prenatal diagnosis of thalassemia in 695 pedigrees from southeastern China: a 10‐year follow‐up study
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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