[
  {
    "title": "X-CNV: genome-wide prediction of the pathogenicity of copy number variations",
    "author": [
      {
        "given": "Lu",
        "family": "Zhang",
        "role": {},
        "email": {},
        "comment": {}
      },
      {
        "given": "Jing",
        "family": "Shi",
        "role": {},
        "email": {},
        "comment": {}
      },
      {
        "given": "Jing",
        "family": "Ouyang",
        "role": {},
        "email": {},
        "comment": {}
      },
      {
        "given": "Rui",
        "family": "Zhang",
        "role": {},
        "email": {},
        "comment": {}
      },
      {
        "given": "Yan",
        "family": "Tao",
        "role": {},
        "email": {},
        "comment": {}
      },
      {
        "given": "Dong",
        "family": "Yuan",
        "role": {},
        "email": {},
        "comment": {}
      },
      {
        "given": "Cong",
        "family": "Lv",
        "role": {},
        "email": {},
        "comment": {}
      },
      {
        "given": "Rui",
        "family": "Wang",
        "role": {},
        "email": {},
        "comment": {}
      },
      {
        "given": "Bing",
        "family": "Ning",
        "role": {},
        "email": {},
        "comment": {}
      },
      {
        "given": "Richard",
        "family": "Roberts",
        "role": {},
        "email": {},
        "comment": {}
      },
      {
        "given": "William",
        "family": "Tong",
        "role": {},
        "email": {},
        "comment": {}
      },
      {
        "given": "Zhi",
        "family": "Liu",
        "role": {},
        "email": {},
        "comment": {}
      },
      {
        "given": "Tao",
        "family": "Shi",
        "role": {},
        "email": {},
        "comment": {}
      }
    ],
    "journal": "Genome Medicine",
    "year": "2021",
    "volume": "13",
    "number": "1",
    "pages": "132",
    "doi": "10.1186/s13073-021-00945-4",
    "pmid": "34407882"
  },
  {
    "title": "Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen)",
    "author": [
      {
        "given": "Erin Rooney",
        "family": "Riggs",
        "role": {},
        "email": {},
        "comment": {}
      },
      {
        "given": "Erica F",
        "family": "Andersen",
        "role": {},
        "email": {},
        "comment": {}
      },
      {
        "given": "Athena M",
        "family": "Cherry",
        "role": {},
        "email": {},
        "comment": {}
      },
      {
        "given": "Christa Lese",
        "family": "Martin",
        "role": {},
        "email": {},
        "comment": {}
      }
    ],
    "journal": "Genetics in Medicine",
    "year": "2020",
    "volume": "22",
    "pages": "245--257",
    "doi": "10.1038/s41436-019-0686-8",
    "pmid": "31690835"
  }
]