Jiaxin Xue

ORCID: 0000-0002-7925-1827
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About
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Research Areas
  • Fetal and Pediatric Neurological Disorders
  • Cleft Lip and Palate Research
  • Plant Water Relations and Carbon Dynamics
  • Prenatal Screening and Diagnostics
  • Climate change and permafrost
  • Cryospheric studies and observations
  • Irrigation Practices and Water Management
  • Tree-ring climate responses
  • Dysphagia Assessment and Management
  • Neonatal Health and Biochemistry
  • Toxoplasma gondii Research Studies
  • Epilepsy research and treatment
  • Neurosurgical Procedures and Complications
  • Biomedical Research and Pathophysiology
  • Economic Growth and Productivity
  • Corrosion Behavior and Inhibition
  • Methemoglobinemia and Tumor Lysis Syndrome
  • Neurogenetic and Muscular Disorders Research
  • Soil and Unsaturated Flow
  • Concrete and Cement Materials Research
  • Tumors and Oncological Cases
  • Genetics and Neurodevelopmental Disorders
  • Spinal Cord Injury Research
  • Peatlands and Wetlands Ecology
  • Ecology and Vegetation Dynamics Studies

Shantou University
2024

Shantou University Medical College
2024

Shenzhen Maternity and Child Healthcare Hospital
2024

Heilongjiang University
2023

Guangzhou Medical University
2022-2023

Guangzhou Women and Children Medical Center
2022

Hebei Agricultural University
2022

Guangdong University of Foreign Studies
2022

Chang'an University
2021

Peking University
2017-2020

A global survey indicates that genetic syndromes affect approximately 8% of the population, but most diagnoses can only be performed after babies are born. Abnormal facial characteristics have been identified in various diseases; however, current identification technologies cannot applied to prenatal diagnosis. We developed Pgds-ResNet, a fully automated screening algorithm based on deep neural networks, detect high-risk fetuses affected by variety diseases. In for Trisomy 21, 18, 13, and...

10.3390/biomedicines11061756 article EN cc-by Biomedicines 2023-06-19

With the advancement of medicine, more and researchers have turned their attention to study fetal genetic diseases in recent years. However, it is still a challenge detect fetus, especially an area lacking access healthcare. The existing research primarily focuses on using teenagers’ or adults’ face information screen for diseases, but there are no relevant directions disease detection facial information. To fill vacancy, we designed two-stage ensemble learning model based sonography,...

10.3390/ijerph20032377 article EN International Journal of Environmental Research and Public Health 2023-01-29

The proposal of constructing the new pattern dual circulation development is product comprehensive effect internal and external factors in stage China’s development, which meets needs economic social development. Based on comparative study China United States, this paper concludes similarities differences these two countries mainly include: First, early export-oriented economy gathered strength; Second, industrial foundation relatively solid; Third, US have a strong domestic demand....

10.4236/ajibm.2022.125055 article EN American Journal of Industrial and Business Management 2022-01-01

Achieving the goal of increasing both crop yield and water-use efficiency with a better irrigation regime is major challenge in semi-arid areas. In this study, we presented two-season field experiment (October 2018–June 2019 October 2019–June 2020) that considered drought stresses, i.e., no (W0), irrigated jointing (W1), flowering (W2) after re-greening, wheat varieties (S086; J22). The results showed 45.5% excess water input did not promote (W1 vs. W2). S086 was beneficial for usage soil...

10.3390/su151310503 article EN Sustainability 2023-07-04

Objective To prospectively evaluate the prognosis of fetuses diagnosed with micrognathia using prenatal ultrasound screening. Methods Between January 2019 and December 2022, a normal range IFA to facial profile in Chinese population between 11 20 gestational weeks was established, pregnancy outcomes fetal were described. The medical records these pregnancies collected, including family history, maternal demographics, sonographic findings, genetic testing results, outcomes. Results Ultrasound...

10.1002/jum.16379 article EN Journal of Ultrasound in Medicine 2024-01-02

A global survey has revealed that genetic syndromes affect approximately 8% of the population, but most diagnoses are typically made after birth. Facial deformities commonly associated with chromosomal disorders. Prenatal diagnosis through ultrasound imaging is vital for identifying abnormal fetal facial features. However, this approach faces challenges such as inconsistent diagnostic criteria and limited coverage. To address gap, we have developed FGDS, a three-stage model utilizes images...

10.3390/bioengineering10070873 article EN cc-by Bioengineering 2023-07-23

Transaldolase (TALDO) deficiency is a rare autosomal recessive disorder caused by variants in the TALDO1 gene that commonly results multisystem dysfunction. Herein, we reported compound heterozygous Chinese prenatal case with TALDO using whole-exome sequencing (WES) for trios and Sanger sequencing. The were located on gene: NM_006755.2:c.574C > T(Chr11:g.763456C T), missense variant exon 5 paternally inherited; NM_006755.2:c.462-2A G(Chr11:g.763342A G), splicing aberration intron 4...

10.3389/fgene.2021.752272 article EN cc-by Frontiers in Genetics 2022-02-04

Lethal multiple pterygium syndrome (LMPS) is a rare disease with genetic and phenotypic heterogeneity inherited in an autosomal recessive (AR) pattern. Here, we have presented clinically significant results describing two novel mutations of CHRND gene: NM_000751.2: c.1006C>T p.(Arg336Ter) NM_000751.2:c.973_975delGTG p.(Val325del), measurement the facial angle for determining micrognathia by prenatal diagnosis first trimester pregnancy case. In conclusion, this report complements spectrum...

10.3389/fgene.2023.1005624 article EN cc-by Frontiers in Genetics 2023-01-17

The clinical features of the PCDH19 gene mutation include febrile epilepsy ranging from mild to severe, with or without intellectual disability, cognitive impairment, and psych-behavioral disorders, but there has been little research on males mosaic PCDH19. This study reported a novel, de novo, nonsense (NM_001184880: c.840C > A, p. Tyr280*) Chinese male in early middle childhood by trio whole-exome sequence (Trio-WES) confirmed Sanger sequence. proportion (c.840C was 27.9% in, buccal...

10.3389/fneur.2022.992781 article EN cc-by Frontiers in Neurology 2022-09-29

The objective is to evaluate the clinical efficacy of cross electro-nape-acupuncture (CENA) in treatment pseudobulbar palsy patients with tracheotomy intubation for severe cerebral haemorrhage and provide an innovative acupuncture method such patients.A total 126 from six trial centres who met inclusion criteria were randomly divided into three groups according random number table ratio 1 : 1, 42 each group, CENA electro-acupuncture group. Each group's lasted 30 minutes, needles removed at...

10.1155/2023/9304934 article EN cc-by Evidence-based Complementary and Alternative Medicine 2023-01-01

Abstract Recently, to achieve the goal of increasing both crop yield and water/nitrogen use efficiency with a better irrigation regime is major challenge in semi-arid areas. In this study, we presented two seasonal-field experiment that considers regimes, i.e., no (W0), irrigated jointing (W1), flowering (W2) after re-greening, varieties (S086; J22) compare response sensitivity wheat leaf physiological indicators, yield, water/N soil water consumption regimes. The results showed WUE, IWUE...

10.21203/rs.3.rs-1853075/v1 preprint EN cc-by Research Square (Research Square) 2022-07-26
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