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Anxiety and Depression in Chinese Students During the COVID-19 Pandemic: A Meta-Analysis

Frontiers in public health, 2021-08, Vol.9, p.697642-697642

2021

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Different effects of anxiety and avoidance dimensions of attachment on interpersonal trust: A multilevel meta-analysis

Journal of social and personal relationships, 2022-06, Vol.39 (7), p.2069-2093

2022

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Abnormal hemoglobin anti-Lepore Hong Kong compound with β0-thalassemia ameliorate thalassemia severity when co-inherited with α-thalassemia

Scientific reports, 2024-03, Vol.14 (1), p.6682-6682, Article 6682

2024

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Hb Q-Thailand heterozygosity unlinked with the (-α4.2/) α+-thalassemia deletion allele identified by long-read SMRT sequencing: hematological and molecular analyses

Hematology (Luxembourg), 2023-12, Vol.28 (1), p.2184118-2184118

2023

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Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden (HBA2:c.178G>C) and Hb Quong Sze (HBA2:c.377T>C)

Journal of international medical research, 2021-07, Vol.49 (7), p.30006052110314-3000605211031429

2021

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First study to describe a novel HbA2: c.400A > C mutation and Hb Dongguan heterozygote in two unrelated Chinese families

Hematology (Luxembourg), 2022-12, Vol.27 (1), p.867-873

2022

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Accurate detection of α-globin gene copy number variants with two reactions using droplet digital PCR

Hematology (Luxembourg), 2022-12, Vol.27 (1), p.198-203

2022

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Identification of four novel large deletions and complex variants in the α-globin locus in Chinese population

Human genomics, 2023-04, Vol.17 (1), p.38-38, Article 38

2023

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Activation of γ-globin expression by LncRNA-mediated ERF promoter hypermethylation in β-thalassemia

Clinical epigenetics, 2024-01, Vol.16 (1), p.12-12, Article 12

2024

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Two novel deletion mutations in β-globin gene cause β-thalassemia trait in two Chinese families

Human genomics, 2023-12, Vol.17 (1), p.111-111, Article 111

2023

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The -α3.7III subtype of α+-thalassemia was identified in China

Hematology (Luxembourg), 2022-12, Vol.27 (1), p.826-830

2022

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Compounded with hemoglobin Port Phillip and ‐α4.2 or ‐‐SEA deletions were identified in Chinese population

Molecular genetics & genomic medicine, 2021-09, Vol.9 (9), p.e1699-n/a

2021

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Identification and characterization of CHD4-associated eRNA as a novel modulator of fetal hemoglobin levels in β-thalassemia

Biochemical and biophysical research communications, 2024-03, Vol.701, p.149555-149555, Article 149555

2024

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Temporal characteristics of emotional conflict processing: the modulation role of attachment styles

International journal of psychophysiology, 2023-11, Vol.193, p.112243-112243, Article 112243

2023

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DNA methylation patterns of β-globin cluster in β-thalassemia patients

Clinical epigenetics, 2020-12, Vol.12 (1), p.187-187, Article 187

2020

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Activation of [gamma]-globin expression by LncRNA-mediated ERF promoter hypermethylation in [beta]-thalassemia

Clinical epigenetics, 2024-01, Vol.16 (1)

2024

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The -α 3.7III subtype of α + -thalassemia was identified in China

Hematology (Luxembourg), 2022-12, Vol.27 (1), p.826-830

2022

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Epigenetic inactivation of ERF reactivates γ-globin expression in β-thalassemia

American journal of human genetics, 2021-04, Vol.108 (4), p.709-721

2021

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DNA methylation patterns of [beta]-globin cluster in [beta]-thalassemia patients

Clinical epigenetics, 2020-12, Vol.12 (1)

2020

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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, 2021-06, Vol.193 (6), p.1220-1227

2021

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Abnormal hemoglobin anti-Lepore Hong Kong compound with β 0 -thalassemia ameliorate thalassemia severity when co-inherited with α-thalassemia

Scientific reports, 2024-03, Vol.14 (1), p.6682

2024

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Downregulation by CNNM2 of ATP5MD expression in the 10q24.32 schizophrenia-associated locus involved in impaired ATP production and neurodevelopment

NPJ schizophrenia, 2021-05, Vol.7 (1), p.27-27, Article 27

2021

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A Genetic Variant Ameliorates β-Thalassemia Severity by Epigenetic-Mediated Elevation of Human Fetal Hemoglobin Expression

American journal of human genetics, 2017-07, Vol.101 (1), p.130-138

2017

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Compounded with hemoglobin Port Phillip and -α 4.2 or -- SEA deletions were identified in Chinese population

Molecular genetics & genomic medicine, 2021-09, Vol.9 (9), p.e1699

2021

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Analysis of SSRs Derived from an EST Library of Half-Smooth Tongue Sole Cynoglossus semilaevis

Journal of Ocean University of China, 2008-08, Vol.7 (3), p.339-342

2008

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Anxiety and Depression in Chinese Students During the COVID-19 Pandemic: A Meta-Analysis

Different effects of anxiety and avoidance dimensions of attachment on interpersonal trust: A multilevel meta-analysis

Abnormal hemoglobin anti-Lepore Hong Kong compound with β0-thalassemia ameliorate thalassemia severity when co-inherited with α-thalassemia

Hb Q-Thailand heterozygosity unlinked with the (-α4.2/) α+-thalassemia deletion allele identified by long-read SMRT sequencing: hematological and molecular analyses

Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden (HBA2:c.178G>C) and Hb Quong Sze (HBA2:c.377T>C)

First study to describe a novel HbA2: c.400A > C mutation and Hb Dongguan heterozygote in two unrelated Chinese families

Accurate detection of α-globin gene copy number variants with two reactions using droplet digital PCR

Identification of four novel large deletions and complex variants in the α-globin locus in Chinese population

Activation of γ-globin expression by LncRNA-mediated ERF promoter hypermethylation in β-thalassemia

Two novel deletion mutations in β-globin gene cause β-thalassemia trait in two Chinese families

The -α3.7III subtype of α+-thalassemia was identified in China

Compounded with hemoglobin Port Phillip and ‐α4.2 or ‐‐SEA deletions were identified in Chinese population

Identification and characterization of CHD4-associated eRNA as a novel modulator of fetal hemoglobin levels in β-thalassemia

Temporal characteristics of emotional conflict processing: the modulation role of attachment styles

DNA methylation patterns of β-globin cluster in β-thalassemia patients

Activation of [gamma]-globin expression by LncRNA-mediated ERF promoter hypermethylation in [beta]-thalassemia

The -α 3.7III subtype of α + -thalassemia was identified in China

Epigenetic inactivation of ERF reactivates γ-globin expression in β-thalassemia

DNA methylation patterns of [beta]-globin cluster in [beta]-thalassemia patients

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

Abnormal hemoglobin anti-Lepore Hong Kong compound with β 0 -thalassemia ameliorate thalassemia severity when co-inherited with α-thalassemia

Downregulation by CNNM2 of ATP5MD expression in the 10q24.32 schizophrenia-associated locus involved in impaired ATP production and neurodevelopment

A Genetic Variant Ameliorates β-Thalassemia Severity by Epigenetic-Mediated Elevation of Human Fetal Hemoglobin Expression

Compounded with hemoglobin Port Phillip and -α 4.2 or -- SEA deletions were identified in Chinese population

Analysis of SSRs Derived from an EST Library of Half-Smooth Tongue Sole Cynoglossus semilaevis

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