Caihua Li

Shanghai, China

Last Updated: 09/26/2026

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Found 20 publications

Accu16S/AccuITS: Accurate and broadly applicable amplicon sequencing for absolute microbiome quantification.

Accu16S/AccuITS: Accurate and broadly applicable amplicon sequencing for absolute microbiome quantification.

Journal: iMeta

Published: January 30, 2026

Excessive DNA Double-Strand Breaks-Associated 3D Genome Reorganization Contributes to Neural Tube Defects with Folate Deficiency.

Excessive DNA Double-Strand Breaks-Associated 3D Genome Reorganization Contributes to Neural Tube Defects with Folate Deficiency.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)

Published: September 01, 2024

Distinct non-clock-like signatures of the basal cell carcinomas from three sisters with a lethal Gorlin-Goltz syndrome.

Distinct non-clock-like signatures of the basal cell carcinomas from three sisters with a lethal Gorlin-Goltz syndrome.

Journal: BMC medical genomics

Published: April 22, 2022

Novel variants in the RDH5 Gene in a Chinese Han family with fundus albipunctatus.

Novel variants in the RDH5 Gene in a Chinese Han family with fundus albipunctatus.

Journal: BMC ophthalmology

Published: November 26, 2021

SSR-Sequencing Reveals the Inter- and Intraspecific Genetic Variation and Phylogenetic Relationships among an Extensive Collection of Radish (Raphanus) Germplasm Resources.

SSR-Sequencing Reveals the Inter- and Intraspecific Genetic Variation and Phylogenetic Relationships among an Extensive Collection of Radish (Raphanus) Germplasm Resources.

Journal: Biology

Published: October 18, 2021

A novel 4.25 kb heterozygous deletion in PAX6 in a Chinese Han family with congenital aniridia combined with cataract and nystagmus.

A novel 4.25 kb heterozygous deletion in PAX6 in a Chinese Han family with congenital aniridia combined with cataract and nystagmus.

Journal: BMC ophthalmology

Published: February 23, 2021

High-throughput sequencing-based microsatellite genotyping for polyploids to resolve allele dosage uncertainty and improve analyses of genetic diversity, structure and differentiation: A case study of the hexaploid Camellia oleifera.

High-throughput sequencing-based microsatellite genotyping for polyploids to resolve allele dosage uncertainty and improve analyses of genetic diversity, structure and differentiation: A case study of the hexaploid Camellia oleifera.

Journal: Molecular ecology resources

Published: March 03, 2020

Aberrant Gcm1 expression mediates Wnt/β-catenin pathway activation in folate deficiency involved in neural tube defects.

Aberrant Gcm1 expression mediates Wnt/β-catenin pathway activation in folate deficiency involved in neural tube defects.

Journal: Cell death & disease

Published: September 15, 2019

Homozygous mutations in DZIP1 can induce asthenoteratospermia with severe MMAF.

Homozygous mutations in DZIP1 can induce asthenoteratospermia with severe MMAF.

Journal: Journal of medical genetics

Published: August 02, 2019

Targeted exome sequencing identifies five novel loci at genome-wide significance for modulating antidepressant response in patients with major depressive disorder.

Targeted exome sequencing identifies five novel loci at genome-wide significance for modulating antidepressant response in patients with major depressive disorder.

Journal: Translational psychiatry

Published: June 18, 2019

Homozygous mutations in SPEF2 induce multiple morphological abnormalities of the sperm flagella and male infertility.

Homozygous mutations in SPEF2 induce multiple morphological abnormalities of the sperm flagella and male infertility.

Journal: Journal of medical genetics

Published: January 12, 2019

Whole-exome sequencing reveals SALL4 variants in premature ovarian insufficiency: an update on genotype-phenotype correlations.

Whole-exome sequencing reveals SALL4 variants in premature ovarian insufficiency: an update on genotype-phenotype correlations.

Journal: Human genetics

Published: July 07, 2018

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Last Updated: 09/26/2026