Huafang Gao

发表

Novel CRISPR/Cas12a-based genetic diagnostic approach for SLC26A4 mutation-related hereditary hearing loss.

Shasha Huang, P. Dai, Xiaohua Jin, 2021, European journal of medical genetics.

Lectin RCA-I specifically binds to metastasis-associated cell surface glycans in triple-negative breast cancer

D. Czajkowsky, Shu-juan Guo, S. Tao, 2015, Breast Cancer Research.

Screening of PAH Common Mutations in Chinese Phenylketonuria Patients Using iPLEX MALDI-TOF MS

Xu Ma, Yousheng Yan, Chuan Zhang, 2020, ACS omega.

Dysregulation of follicle fatty acid is a potential driver of human primary ovarian insufficiency

Mo Li, N. Zhang, Huafang Gao, 2020, Journal of molecular cell biology.

Evaluation of droplet digital PCR for non-invasive prenatal diagnosis of phenylketonuria

Xu Ma, F. Wang, Yousheng Yan, 2019, Analytical and Bioanalytical Chemistry.

Development of a new fluorescence immunochromatography strip for detection of chloramphenicol residues in chicken muscles.

Yunbo Luo, Wentao Xu, Kunlun Huang, 2013, Journal of the science of food and agriculture.

Mutation spectrum of PAH gene in phenylketonuria patients in Northwest China: identification of twenty novel variants

Xu Ma, Yousheng Yan, Chuan Zhang, 2019, Metabolic Brain Disease.

Establishment of primary reference measurement procedures and reference materials for EGFR variant detection in non-small cell lung cancer.

Pengyu Zhu, Lianhua Dong, Liang Li, 2021, Analytical methods : advancing methods and applications.

Increased Incidence of Mitochondrial Cytochrome C Oxidase 1 Gene Mutations in Patients with Primary Ovarian Insufficiency

J. Qiao, Bailin Wu, Cui-ling Lu, 2015, PloS one.

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

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

Noninvasive and Accurate Detection of Hereditary Hearing Loss Mutations with Buccal Swab Based on Droplet Digital PCR.

F. Wang, Junmin Pan, Xiurui Zhu, 2018, Analytical chemistry.

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.

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.

Variant analysis of 92 Chinese Han families with hearing loss

Xu Ma, Shasha Huang, P. Dai, 2022, BMC medical genomics.

Etiologic Diagnosis of Lower Respiratory Tract Bacterial Infections Using Sputum Samples and Quantitative Loop-Mediated Isothermal Amplification

Minghua Deng, Liping Wei, M. Qian, 2012, PloS one.

Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndrome

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

Mutation spectra and founder effect of TMC1 in patients with non‐syndromic deafness in Xiamen area, China

Lihua Wu, Xue Gao, Shasha Huang, 2017, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Machine-learning models utilizing CYP3A4*1G show improved prediction of hypoglycemic medication in Type 2 diabetes.

Yaping Tian, Yitian Xu, Qian Chen, 2022, Personalized Medicine.

Risk factors and methylenetetrahydrofolate reductase gene in congenital heart disease.

Bo Yang, Shiyuan Zhou, Huafang Gao, 2018, Journal of thoracic disease.