Xianda Wei

Nanning, China

Last Updated: 09/26/2026

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Found 15 publications

Evaluation of the diagnostic efficacy of serum DR-70 and its combination with CEA in lung cancer.

Evaluation of the diagnostic efficacy of serum DR-70 and its combination with CEA in lung cancer.

Journal: Biomarkers in medicine

Published: July 11, 2025

Corrigendum to 'Clinical validation and application of targeted long-range PCR and long-read sequencing-based analysis for haemophilia: experience from a haemophilia treatment centre in China': [JTHA, Volume 22, Issue 12, December 2024, Pages 3431-3447].

Corrigendum to 'Clinical validation and application of targeted long-range PCR and long-read sequencing-based analysis for haemophilia: experience from a haemophilia treatment centre in China': [JTHA, Volume 22, Issue 12, December 2024, Pages 3431-3447].

Journal: Journal of thrombosis and haemostasis : JTH

Published: June 22, 2025

Family trios/quartets analysis based on the Newborn Genomic Atlas for Thalassemia project in Guangxi.

Family trios/quartets analysis based on the Newborn Genomic Atlas for Thalassemia project in Guangxi.

Journal: BMC medicine

Published: May 10, 2025

The rare hemoglobin variants Hb O-Arab and Hb D-Punjab identified in population-based genetic screening throughout Guangxi, China.

The rare hemoglobin variants Hb O-Arab and Hb D-Punjab identified in population-based genetic screening throughout Guangxi, China.

Journal: Frontiers in genetics

Published: May 03, 2025

A hypomorphic SRD5A2 haplotype with a potential founder effect: composed of common variants in individuals with 5α-reductase type 2 deficiency from South China.

A hypomorphic SRD5A2 haplotype with a potential founder effect: composed of common variants in individuals with 5α-reductase type 2 deficiency from South China.

Journal: Biology of sex differences

Published: April 16, 2025

Genetic skeletal disorders: phenotypic-genotypic characteristics and RhGH therapy responses of a pediatric cohort.

Genetic skeletal disorders: phenotypic-genotypic characteristics and RhGH therapy responses of a pediatric cohort.

Journal: Scientific reports

Published: February 06, 2025

49, XXXYY: Parental Origin, Occurrence, and Clinical Phenotypes.

49, XXXYY: Parental Origin, Occurrence, and Clinical Phenotypes.

Journal: Genetics research

Published: December 18, 2024

The cryptic complex rearrangements involving the DMD gene: etiologic clues about phenotypical differences revealed by optical genome mapping.

The cryptic complex rearrangements involving the DMD gene: etiologic clues about phenotypical differences revealed by optical genome mapping.

Journal: Human genomics

Published: May 29, 2024

Clinical validation and application of targeted long-range polymerase chain reaction and long-read sequencing-based analysis for hemophilia: experience from a hemophilia treatment center in China.

Clinical validation and application of targeted long-range polymerase chain reaction and long-read sequencing-based analysis for hemophilia: experience from a hemophilia treatment center in China.

Journal: Journal of thrombosis and haemostasis : JTH

Published: March 12, 2024

Analysis of a child with DIGFAN syndrome due to variant of MORC2 gene

Analysis of a child with DIGFAN syndrome due to variant of MORC2 gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: February 04, 2024

Complex genotype-phenotype correlation of MYH11: new insights from monozygotic twins with highly variable expressivity and outcomes.

Complex genotype-phenotype correlation of MYH11: new insights from monozygotic twins with highly variable expressivity and outcomes.

Journal: BMC medical genomics

Published: July 24, 2023

Importance of comprehensive genetic testing for patients with suspected vascular Ehlers-Danlos syndrome: a family case report and literature review.

Importance of comprehensive genetic testing for patients with suspected vascular Ehlers-Danlos syndrome: a family case report and literature review.

Journal: Frontiers in genetics

Published: June 24, 2023

Showing 1-12 of 15

Last Updated: 09/26/2026