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Zhengwen Jiang

27

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356

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Comprehensive copy number analysis of Y chromosome-linked loci for detection of structural variations and diagnosis of male infertility.

2021 Journal of Human Genetics
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A capillary electrophoresis-based variant hotspot genotyping method for rapid and reliable analysis of the phenylalanine hydroxylase gene in the Chinese Han population.

2021 Clinica Chimica Acta
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Mode-II fracture behavior evaluation for adhesively bonded pultruded GFRP/steel joint using four-point bending test

2021 Thin-walled Structures
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Integrating a GIS-Based Multi-Influence Factors Model with Hydro-Geophysical Exploration for Groundwater Potential and Hydrogeological Assessment: A Case Study in the Karak Watershed, Northern Pakistan

2021 Water
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Identification of chromosomal abnormalities in early pregnancy loss using a high-throughput ligation-dependent probe amplification-based assay.

2020 The Journal of Molecular Diagnostics
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Genetic study on small insertions and deletions in psoriasis revealed an important impact on complex human diseases

2019 Journal of Investigative Dermatology
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Intronic (TTTGA)n insertion in SAMD12 also causes familial cortical myoclonic tremor with epilepsy

2019 Movement Disorders
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Germline Duplication of SNORA18L5 Increases Risk for HBV-related Hepatocellular Carcinoma by Altering Localization of Ribosomal Proteins and Decreasing Levels of p53

2018 Gastroenterology
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A copy number variation genotyping method for aneuploidy detection in spontaneous abortion specimens.

2017 Prenatal Diagnosis
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Folate deficiency facilitates recruitment of upstream binding factor to hot spots of DNA double-strand breaks of rRNA genes and promotes its transcription.

2017 Nucleic Acids Research
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