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High expression levels of pyrimidine metabolic rate–limiting enzymes are adverse prognostic factors in lung adenocarcinoma: a study based on The Cancer Genome Atlas and Gene Expression Omnibus datasets

Purinergic signalling, 2020-09, Vol.16 (3), p.347-366

2020

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RUNX1 and REXO2 are associated with the heterogeneity and prognosis of IDH wild type lower grade glioma

Scientific reports, 2021-06, Vol.11 (1), p.11836-11836, Article 11836

2021

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Autophagic Network Analysis of the Dual Effect of Sevoflurane on Neurons Associated with GABARAPL1 and 2

BioMed research international, 2020, Vol.2020 (2020), p.1-12

2020

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PBX1, EMCN and ERG are associated with the sub-clusters and the prognosis of VHL mutant clear cell renal cell carcinoma

Scientific reports, 2022-05, Vol.12 (1), p.8955-8955, Article 8955

2022

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Molecular characterization of thalassemia and hemoglobinopathy in Southeastern China

Scientific reports, 2019-03, Vol.9 (1), p.3493-3493, Article 3493

2019

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Detection of copy number variation associated with ventriculomegaly in fetuses using single nucleotide polymorphism arrays

Scientific reports, 2021-03, Vol.11 (1), p.5291-5291, Article 5291

2021

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Prognostic analysis of E2F transcription factors E2F1 and E2F3 in four independent pediatric neuroblastoma cohorts

BMC pediatrics, 2022-06, Vol.22 (1), p.1-376, Article 376

2022

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Transforming growth factor-induced gene TGFBI is correlated with the prognosis and immune infiltrations of breast cancer

World journal of surgical oncology, 2024-01, Vol.22 (1), p.22-22, Article 22

2024

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Efficiency of expanded noninvasive prenatal testing in the detection of fetal subchromosomal microdeletion and microduplication in a cohort of 31,256 single pregnancies

Scientific reports, 2022-11, Vol.12 (1), p.19750-19750, Article 19750

2022

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The interactions between ineffective erythropoiesis and ferroptosis in β-thalassemia

Frontiers in physiology, 2024-02, Vol.15, p.1346173-1346173

2024

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Application of third-generation sequencing technology for identifying rare α- and β-globin gene variants in a Southeast Chinese region

BMC medical genomics, 2024-10, Vol.17 (1), p.241-10, Article 241

2024

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Genetic analysis of chorionic villus tissues in early missed abortions

Scientific reports, 2023-12, Vol.13 (1), p.21719-21719, Article 21719

2023

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The clinical value of hsa-miR-190b-5p in peripheral blood of pediatric β-thalassemia and its regulation on BCL11A expression

PloS one, 2023-10, Vol.18 (10), p.e0292031-e0292031

2023

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Prenatal genetic analysis of fetal aberrant right subclavian artery with or without additional ultrasound anomalies in a third level referral center

Scientific reports, 2023-02, Vol.13 (1), p.3414-3414, Article 3414

2023

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Etiologic evaluation and pregnancy outcomes of fetal growth restriction (FGR) associated with structural malformations

Scientific reports, 2024-04, Vol.14 (1), p.9220-9220, Article 9220

2024

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Analysis of the EGFR Amplification and CDKN2A Deletion Regulated Transcriptomic Signatures Reveals the Prognostic Significance of SPATS2L in Patients With Glioma

Frontiers in oncology, 2021-04, Vol.11, p.551160-551160

2021

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Prenatal genetic diagnosis of fetuses with dextrocardia using whole exome sequencing in a tertiary center

Scientific reports, 2024-07, Vol.14 (1), p.16266-14, Article 16266

2024

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Chromosome 1p36 candidate gene ZNF436 predicts the prognosis of neuroblastoma: a bioinformatic analysis

Italian journal of pediatrics, 2023-10, Vol.49 (1), p.1-145, Article 145

2023

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Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing

Prenatal diagnosis, 2013-05, Vol.33 (5), p.409-415

2013

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Genetic testing for fetal loss of heterozygosity using single nucleotide polymorphism array and whole-exome sequencing

Scientific reports, 2024-01, Vol.14 (1), p.2190-2190, Article 2190

2024

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Prognostic significance of MYCN related genes in pediatric neuroblastoma: a study based on TARGET and GEO datasets

BMC pediatrics, 2020-06, Vol.20 (1), p.314-314, Article 314

2020

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Classifying and Evaluating Fetuses With Ventriculomegaly in Genetic Etiologic Studies

Frontiers in genetics, 2021-07, Vol.12, p.682707-682707

2021

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Screening primary carnitine deficiency in 10 million Chinese newborns: a systematic review and meta-analysis

Orphanet journal of rare diseases, 2024-07, Vol.19 (1), p.248-11, Article 248

2024

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Analysis of the transcriptomic features of microsatellite instability subtype colon cancer

BMC cancer, 2019-06, Vol.19 (1), p.605-605, Article 605

2019

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Intrauterine ultrasound phenotyping, molecular characteristics, and postnatal follow-up of fetuses with the 15q11.2 BP1-BP2 microdeletion syndrome: a single-center, retrospective clinical study

BMC pregnancy and childbirth, 2024-01, Vol.24 (1), p.23-23, Article 23

2024

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High expression levels of pyrimidine metabolic rate–limiting enzymes are adverse prognostic factors in lung adenocarcinoma: a study based on The Cancer Genome Atlas and Gene Expression Omnibus datasets

RUNX1 and REXO2 are associated with the heterogeneity and prognosis of IDH wild type lower grade glioma

Autophagic Network Analysis of the Dual Effect of Sevoflurane on Neurons Associated with GABARAPL1 and 2

PBX1, EMCN and ERG are associated with the sub-clusters and the prognosis of VHL mutant clear cell renal cell carcinoma

Molecular characterization of thalassemia and hemoglobinopathy in Southeastern China

Detection of copy number variation associated with ventriculomegaly in fetuses using single nucleotide polymorphism arrays

Prognostic analysis of E2F transcription factors E2F1 and E2F3 in four independent pediatric neuroblastoma cohorts

Transforming growth factor-induced gene TGFBI is correlated with the prognosis and immune infiltrations of breast cancer

Efficiency of expanded noninvasive prenatal testing in the detection of fetal subchromosomal microdeletion and microduplication in a cohort of 31,256 single pregnancies

The interactions between ineffective erythropoiesis and ferroptosis in β-thalassemia

Application of third-generation sequencing technology for identifying rare α- and β-globin gene variants in a Southeast Chinese region

Genetic analysis of chorionic villus tissues in early missed abortions

The clinical value of hsa-miR-190b-5p in peripheral blood of pediatric β-thalassemia and its regulation on BCL11A expression

Prenatal genetic analysis of fetal aberrant right subclavian artery with or without additional ultrasound anomalies in a third level referral center

Etiologic evaluation and pregnancy outcomes of fetal growth restriction (FGR) associated with structural malformations

Analysis of the EGFR Amplification and CDKN2A Deletion Regulated Transcriptomic Signatures Reveals the Prognostic Significance of SPATS2L in Patients With Glioma

Prenatal genetic diagnosis of fetuses with dextrocardia using whole exome sequencing in a tertiary center

Chromosome 1p36 candidate gene ZNF436 predicts the prognosis of neuroblastoma: a bioinformatic analysis

Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing

Genetic testing for fetal loss of heterozygosity using single nucleotide polymorphism array and whole-exome sequencing

Prognostic significance of MYCN related genes in pediatric neuroblastoma: a study based on TARGET and GEO datasets

Classifying and Evaluating Fetuses With Ventriculomegaly in Genetic Etiologic Studies

Screening primary carnitine deficiency in 10 million Chinese newborns: a systematic review and meta-analysis

Analysis of the transcriptomic features of microsatellite instability subtype colon cancer

Intrauterine ultrasound phenotyping, molecular characteristics, and postnatal follow-up of fetuses with the 15q11.2 BP1-BP2 microdeletion syndrome: a single-center, retrospective clinical study

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