Zongfu Cao

发表

VarfromPDB: An Automated and Integrated Tool to Mine Disease-Gene-Variant Relations from the Public Databases and Literature

Lei Wang, Zongfu Cao, Yilu Chen, 2017 .

Detailed pedigree analyses and prenatal diagnosis for a family with mucopolysaccharidosis type II

Zongfu Cao, L. Hui, Chuan Zhang, 2021, BMC medical genomics.

Functional collagen conduits combined with human mesenchymal stem cells promote regeneration after sciatic nerve transection in dogs

Zongfu Cao, Zhifeng Xiao, J. Dai, 2018, Journal of tissue engineering and regenerative medicine.

Maternal UPD of chromosome 7 in a patient with Silver‐Russell syndrome and Pendred syndrome

Zongfu Cao, Xu Ma, Chuan Zhang, 2020, Journal of clinical laboratory analysis.

Spatial pattern and variations in the prevalence of congenital heart disease in children aged 4-18 years in the Qinghai-Tibetan Plateau.

Z. Ren, Zongfu Cao, Binbin Wang, 2018, The Science of the total environment.

Developmental mechanisms of arsenite toxicity in zebrafish (Danio rerio) embryos.

Zongfu Cao, Xu Ma, Hong-Fei Xia, 2009, Aquatic toxicology.

MicroRNA expression and regulation in the uterus during embryo implantation in rat

Zongfu Cao, Xu Ma, Hong-Fei Xia, 2014, The FEBS journal.

Mutation screening of crystallin genes in Chinese families with congenital cataracts

Zongfu Cao, Juhua Yang, Lijuan Liu, 2019, Molecular vision.

A Novel Missense Variant in the Gene PPP2R5D Causes a Rare Neurodevelopmental Disorder with Increased Phenotype

Zongfu Cao, Xiangchun Yang, Haibo Li, 2021, BioMed research international.

The implication of p66shc in oxidative stress induced by deltamethrin.

Zongfu Cao, Xu Ma, Hongyu Jin, 2017, Chemico-biological interactions.

Molecular diagnose of a large hearing loss population from China by targeted genome sequencing

Yang Wang, Quanfei Huang, Zongfu Cao, 2022, Journal of Human Genetics.

Mutation Analysis of 63 Northwest Chinese Probands with Oculocutaneous Albinism

Zongfu Cao, Xu Ma, Z. Chuan, 2020, Current eye research.

A multiplex droplet digital PCR assay for non-invasive prenatal testing of fetal aneuploidies.

F. Wang, Zongfu Cao, Xiurui Zhu, 2019, The Analyst.

Clinical heterogeneity and intrafamilial variability of Joubert syndrome in two siblings with CPLANE1 variants

Zongfu Cao, Ruikun Cai, Yufei Yu, 2021, Molecular genetics & genomic medicine.

Whole exome sequencing reveals novel CEP104 mutations in a Chinese patient with Joubert syndrome

Zongfu Cao, Ruikun Cai, Yufei Yu, 2019, Molecular genetics & genomic medicine.

Mutation analysis of TCOF1 gene in Chinese Treacher Collins syndrome patients

Zongfu Cao, Cuixia Chen, Xu Ma, 2020, Journal of clinical laboratory analysis.

Novel mutations in HSF4 cause congenital cataracts in Chinese families

Zongfu Cao, Juhua Yang, Lijuan Liu, 2018, BMC Medical Genetics.

Identification of two novel pathogenic variants of PIBF1 by whole exome sequencing in a 2-year-old boy with Joubert syndrome

Yun Peng, Zongfu Cao, Ruikun Cai, 2020, BMC medical genetics.

Prevention and Control of Pathogens Based on Big-Data Mining and Visualization Analysis

Hao Lin, Zongfu Cao, Ruikun Cai, 2021, Frontiers in Molecular Biosciences.

Mutation analysis, treatment and prenatal diagnosis of Chinese cases of methylmalonic acidemia

Zongfu Cao, Cuixia Chen, Xu Ma, 2020, Scientific Reports.

Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndrome

Zongfu Cao, Ruikun Cai, Xu Ma, 2021, Genetics in Medicine.

MiR‐98 is involved in rat embryo implantation by targeting Bcl‐xl

Zongfu Cao, Xu Ma, Xiaohua Jin, 2014, FEBS letters.

Folic acid supplementation, preconception body mass index, and preterm delivery: findings from the preconception cohort data in a Chinese rural population

Zongfu Cao, Yuan He, Ying Yang, 2015, BMC Pregnancy and Childbirth.

[Wiedemann-Steiner syndrome due to novel nonsense variant of KMT2A gene in a case].

Zongfu Cao, Chuan Zhang, H. Xue, 2021, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

[Standardization for sharing and utilization of Chinese genetic resources].

Zongfu Cao, Xu Ma, Zuoqi Peng, 2008, Yi chuan = Hereditas.

Novel Compound Heterozygous Variants in MKS1 Leading to Joubert Syndrome

Zongfu Cao, Xu Ma, Guangyu Zhang, 2020, Frontiers in Genetics.

A novel 1.38-kb deletion combined with a single nucleotide variant in KIAA0586 as a cause of Joubert syndrome

Zongfu Cao, Cuixia Chen, Xu Ma, 2023, BMC Medical Genomics.

The spectrum of phenylalanine hydroxylase variants and genotype–phenotype correlation in phenylketonuria patients in Gansu, China

Zongfu Cao, Xu Ma, Yousheng Yan, 2023, Human Genomics.

Identification of deep intronic variants of PAH in phenylketonuria using full-length gene sequencing

Zongfu Cao, Xu Ma, Yousheng Yan, 2023, Orphanet Journal of Rare Diseases.

A novel nonsense mutation in CRYBB1 associated with autosomal dominant congenital cataract

Zongfu Cao, Feng Gu, Juhua Yang, 2008, Molecular vision.

The novel G10680A mutation is associated with complete penetrance of the LHON/T14484C family.

Zongfu Cao, Juhua Yang, Xu Ma, 2009, Mitochondrion.

Random forest classifier improving phenylketonuria screening performance in two Chinese populations

Zongfu Cao, Xu Ma, Dan-yan Zhuang, 2022, Frontiers in Molecular Biosciences.

MiR‐98 is involved in rat embryo implantation by targeting Bcl‐xl

Zongfu Cao, Xu Ma, Xiaohua Jin, 2014, FEBS letters.

[Study on newborn screening for Duchenne muscular dystrophy and diagnostic strategy].

Zongfu Cao, Dan-yan Zhuang, Haibo Li, 2021, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Proteomics & Bioinformatics

Lei Wang, Zongfu Cao, Yilu Chen, 2022 .