{
  "abstract": null,
  "abstract_shown": false,
  "affiliations": [
    "Population, Policy and Practice, UCL Great Ormond Street Institute of Child Health, London, UK",
    "UCL Great Ormond Street Institute of Child Health",
    "Rapid Research Evaluation and Appraisal Lab (RREAL), University College London, London, UK",
    "Warwick University",
    "Warwick Medical School, University of Warwick, Coventry, UK",
    "Queen Mary University of London",
    "University College London",
    "Health Economics and Policy Research Unit (HEPRU), Queen Mary University of London, London, UK",
    "National Institute for Health and Care Research Barts Biomedical Research Centre, London, UK",
    "Genetic Alliance UK",
    "Genetic Alliance UK, London, UK",
    "Alstrom Syndrome UK",
    "Department of Population Health Sciences, University of Leicester, Leicester, UK",
    "Great Ormond Street Hospital for Children NHS Foundation Trust",
    "Alström Syndrome UK and Breaking Down Barriers, Torquay, UK",
    "NHS North Thames Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK",
    "Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London, UK"
  ],
  "article_type": null,
  "arxiv": null,
  "author_total": 18,
  "authors": [
    {
      "affs": [
        0,
        1
      ],
      "name": "Celine Lewis",
      "orcid": "0000-0001-7169-1521"
    },
    {
      "affs": [
        2,
        3
      ],
      "name": "Emma Beecham",
      "orcid": "0000-0002-1832-0286"
    },
    {
      "affs": [
        4,
        5
      ],
      "name": "Felicity Boardman",
      "orcid": "0000-0002-3268-6276"
    },
    {
      "affs": [
        2,
        6
      ],
      "name": "Gráinne Brady",
      "orcid": "0009-0002-2141-781X"
    },
    {
      "affs": [
        7,
        8,
        6
      ],
      "name": "James P. Buchanan",
      "orcid": "0000-0003-2528-0638"
    },
    {
      "affs": [
        2,
        1
      ],
      "name": "Sigrún Eyrúnardóttir Clark",
      "orcid": "0000-0001-5679-2535"
    },
    {
      "affs": [
        2,
        9
      ],
      "name": "Katie Gilchrist",
      "orcid": "0000-0002-8529-4997"
    },
    {
      "affs": [
        0,
        9
      ],
      "name": "Pia Hardelid",
      "orcid": "0000-0002-0154-1306"
    },
    {
      "affs": [
        10,
        11
      ],
      "name": "Amy Hunter"
    },
    {
      "affs": [
        12,
        10,
        13
      ],
      "name": "Jennifer Jones"
    },
    {
      "affs": [
        14,
        6
      ],
      "name": "Kerry Leeson‐Beevers",
      "orcid": "0000-0001-8826-5086"
    },
    {
      "affs": [
        15,
        5
      ],
      "name": "Bethany Stafford‐Smith"
    },
    {
      "affs": [
        0,
        13
      ],
      "name": "Joachim Tan",
      "orcid": "0000-0003-0462-4761"
    },
    {
      "affs": [
        2,
        1
      ],
      "name": "Cecilia Vindrola‐Padros",
      "orcid": "0000-0001-7859-1646"
    },
    {
      "affs": [
        7,
        13
      ],
      "name": "Martin Vu",
      "orcid": "0000-0001-5918-1692"
    },
    {
      "affs": [
        16,
        15
      ],
      "name": "Wing Han Wu",
      "orcid": "0009-0001-8998-4944"
    },
    {
      "affs": [
        0
      ],
      "name": "Ania Zylbersztejn",
      "orcid": "0000-0003-1035-1448"
    },
    {
      "affs": [
        16,
        15
      ],
      "name": "Melissa K. Hill",
      "orcid": "0000-0003-3900-1425"
    }
  ],
  "bibtex": "https://research.draconitic.com/paper/dj70xwgvec5h3.bib",
  "cited_by": 12,
  "doi": "10.1530/ey.23.15.1",
  "fulltext_url": null,
  "id": "dj70xwgvec5h3",
  "issns": [
    "1662-3991",
    "1662-4009"
  ],
  "landing_url": "https://doi.org/10.1101/2024.05.14.24307295",
  "language": "en",
  "licence": "unknown",
  "licence_label": "Licence not stated",
  "licence_source": "unknown",
  "licence_url": null,
  "metadata_licence": null,
  "native_subjects": [
    [
      "openalex",
      "1311|Genomics and Rare Diseases"
    ]
  ],
  "openalex": "W4396933505",
  "pdf_url": null,
  "pmcid": null,
  "pmid": null,
  "published": "2026-09-03",
  "publisher": "Bioscientifica",
  "ris": "https://research.draconitic.com/paper/dj70xwgvec5h3.ris",
  "sources": [
    {
      "first_seen": "2026-10-30T13:26:46Z",
      "native_id": "W4396933505",
      "source": "openalex",
      "url": "https://doi.org/10.1101/2024.05.14.24307295"
    }
  ],
  "subjects": [
    {
      "field": "biology",
      "origin": "openalex:1311|Genomics and Rare Diseases",
      "subfield": "genetics-genomics"
    }
  ],
  "title": "Exploring the feasibility, acceptability and impact of genomic newborn screening for rare diseases in England: A study protocol for the Generation Study - Process and Impact Evaluation (Version 2)",
  "title_text": "Exploring the feasibility, acceptability and impact of genomic newborn screening for rare diseases in England: A study protocol for the Generation Study - Process and Impact Evaluation (Version 2)",
  "type": "peer-reviewed",
  "updated_at": "2026-11-08T13:20:43Z",
  "url": "https://research.draconitic.com/paper/dj70xwgvec5h3",
  "venue": "Yearbook of pediatric endocrinology",
  "versions": []
}