Connection

HONGZHENG DAI to Polymorphism, Single Nucleotide

This is a "connection" page, showing publications HONGZHENG DAI has written about Polymorphism, Single Nucleotide.
  1. Exploring the complexity of systemic sclerosis etiology by trio whole genome sequencing. Hum Mol Genet. 2024 09 19; 33(19):1643-1647.
    View in: PubMed
    Score: 0.467
  2. Integrative exome sequencing and machine learning identify MICB and interferon pathway genes as contributors to SSc risk. Ann Rheum Dis. 2025 Aug; 84(8):1363-1374.
    View in: PubMed
    Score: 0.031
  3. De novo variants in RYBP are associated with a severe neurodevelopmental disorder and congenital anomalies. Genet Med. 2025 Apr; 27(4):101369.
    View in: PubMed
    Score: 0.030
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.