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  1. No Access

    Article

    Chromosomal Copy Number Variation Analysis in Pregnancy Products from Recurrent and Sporadic Miscarriage Using Next-Generation Sequencing

    Chromosomal abnormality is one of the causes of fetal miscarriage. The potential differences of fetal chromosomal abnormalities in sporadic miscarriage (SM) and recurrent miscarriage (RM) remain unclear. The p...

    **a Zhang, Heming Wu, Zhonghang Gu, Zhikang Yu, Liubing Lan… in Reproductive Sciences (2022)

  2. Article

    Open Access

    GSTP1 c.313A > G mutation is an independent risk factor for neutropenia hematotoxicity induced by anthracycline-/paclitaxel-based chemotherapy in breast cancer patients

    The link between glutathione S-transferase P1 (GSTP1) c.313A > G polymorphism and chemotherapy-related adverse events remains controversial. The goal of this study was to assess how this variant affected the t...

    Juanzi Zeng, Heming Wu, Donghua Liu, Liang Li… in World Journal of Surgical Oncology (2022)

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  3. Article

    Open Access

    Association of ALDH2 rs671 and MTHFR rs1801133 polymorphisms with hypertension among Hakka people in Southern China

    Genetic factors play an important role in susceptibility to hypertension. Herein, the association between acetaldehyde dehydrogenase 2 (ALDH2) and methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms...

    Heming Wu, Qingyan Huang, Zhikang Yu, Zhixiong Zhong in BMC Cardiovascular Disorders (2022)

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