Shihao Zhou

Hunan Provincial Key Laboratory Of Regional Hereditary Birth Defects Prevention And Control
Changsha, China

Last Updated: 09/26/2026

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Found 28 publications

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

Journal: Clinica chimica acta; international journal of clinical chemistry
Published: July 08, 2026

A comparative study of SNPscan/CNVplex assay and routine PCR in genetic analysis of thalassemia.

A comparative study of SNPscan/CNVplex assay and routine PCR in genetic analysis of thalassemia.

Journal: Frontiers in genetics
Published: February 28, 2026

Learning an Adaptive Sparse Transformer for Efficient Image Restoration.

Learning an Adaptive Sparse Transformer for Efficient Image Restoration.

Journal: IEEE transactions on pattern analysis and machine intelligence
Published: August 01, 2025

Genetic rare disease prevention and control: Family-based screening and reproductive interventions in Changsha.

Genetic rare disease prevention and control: Family-based screening and reproductive interventions in Changsha.

Journal: HGG advances
Published: February 06, 2025

Cost-effectiveness of different screening strategies for Down syndrome: a real-world analysis in 140,472 women.

Cost-effectiveness of different screening strategies for Down syndrome: a real-world analysis in 140,472 women.

Journal: Frontiers in public health
Published: November 27, 2024

Determining the origin of genome aberrations improves the positive predictive value of NIPT for 22q11.2 deletion syndrome.

Determining the origin of genome aberrations improves the positive predictive value of NIPT for 22q11.2 deletion syndrome.

Journal: Scientific reports
Published: November 22, 2024

A retrospective single center analysis of fetuses with region of homozygosity detected by single nucleotide polymorphism array.

A retrospective single center analysis of fetuses with region of homozygosity detected by single nucleotide polymorphism array.

Journal: Scientific reports
Published: August 11, 2024

A prospective multicenter birth cohort in China: pregnancy health atlas.

A prospective multicenter birth cohort in China: pregnancy health atlas.

Journal: European journal of epidemiology
Published: June 28, 2024

Results of a Pilot External Quality Assessment Scheme for Genetic Testing of Newborns with Spinal Muscular Atrophy.

Results of a Pilot External Quality Assessment Scheme for Genetic Testing of Newborns with Spinal Muscular Atrophy.

Journal: Clinical laboratory
Published: May 15, 2024

Strategic Implementation of Fragile X Carrier Screening in China: A Focused Pilot Study.

Strategic Implementation of Fragile X Carrier Screening in China: A Focused Pilot Study.

Journal: The Journal of molecular diagnostics : JMD
Published: March 02, 2024

The genetics and clinical outcomes in 151 cases of fetal growth restriction: A Chinese single-center study.

The genetics and clinical outcomes in 151 cases of fetal growth restriction: A Chinese single-center study.

Journal: European journal of obstetrics, gynecology, and reproductive biology
Published: November 28, 2023

Analysis of screening results for genetic metabolic diseases among 352 449 newborns from Changsha

Analysis of screening results for genetic metabolic diseases among 352 449 newborns from Changsha

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 29, 2023
Showing 1-12 of 28

Last Updated: 09/26/2026