• 43 Citations
  • 3 h-Index
20172020

Research output per year

If you made any changes in Pure these will be visible here soon.

Personal profile

Area of Expertise

My major research interest is the methodological development of statistical genetics, including detecting gene – environment interaction, controlling for population stratification in genome-wide association studies and developing powerful genetic association tests.
I am actively seeking opportunities for collaboration with scientific and clinical investigators in biostatistics or statistical genetics. I have been involved in various genetic studies for human complex diseases, such as heart disease, Alzheimer's disease, fatty liver disease, and Fuch’s endothelial corneal dystrophy.

Education/Academic qualification

BS in Mathematics , Beijing Institute of Technology

MS in Statistics, Southern Methodist University

PhD in Biostatistics, Southern Methodist University

Fingerprint Dive into the research topics where Zhengyang Zhou is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 8 Similar Profiles

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Projects

Research Output

  • 43 Citations
  • 3 h-Index
  • 12 Article
  • 1 Letter
Open Access
  • Two-stage Bayesian GWAS of 9576 individuals identifies SNP regions that are targeted by miRNAs inversely expressed in Alzheimer's and cancer

    for the Alzheimer's Disease Neuroimaging Initiative, Breast and Prostate Cancer Cohort Consortium, and Alzheimer's Disease Genetics Consortium, 1 Jan 2020, In : Alzheimer's and Dementia. 16, 1, p. 162-177 16 p.

    Research output: Contribution to journalArticle

    Open Access
  • 1 Scopus citations

    A meta-analysis of the association between the presence of Helicobacter pylori and periodontal diseases

    Chen, Z., Cai, J., Chen, Y. M., Wei, J., Li, H. B., Lu, Y., Zhou, Z. & Chen, X. L., 1 May 2019, In : Medicine. 98, 22, p. e15922

    Research output: Contribution to journalArticle

    Open Access
  • 3 Scopus citations

    A novel autosomal recessive lipodystrophy syndrome due to homozygous LMNA variant

    Patni, N., Hatab, S., Xing, C., Zhou, Z., Quittner, C. & Garg, A., 1 Jan 2019, (Accepted/In press) In : Journal of Medical Genetics. 106395.

    Research output: Contribution to journalArticle

  • 2 Scopus citations