David Bick

Employment

• Genomics England Clinical Advisor
  2020 - Present
• HudsonAlpha Institute for Biotechnology
  2015 - 2020

Education

Education history is unavailable.

Projects & Funding

Projects & funding information is unavailable.

Publications (9)

• Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies
  Human Genetics 2024 DOI: 10.1007/s00439-024-02657-2
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• Whole genome sequencing to screen 100 000 newborns for treatable genetic disorders
  Journal of Inherited Metabolic Disease 2024 DOI: 10.1002/jimd.12704
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• Best practices for the interpretation and reporting of clinical whole genome sequencing
  npj Genomic Medicine 2022 DOI: 10.1038/s41525-022-00295-z
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• A study of elective genome sequencing and pharmacogenetic testing in an unselected population
  Molecular Genetics & Genomic Medicine 2021 DOI: 10.1002/mgg3.1766
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• An online compendium of treatable genetic disorders
  American Journal of Medical Genetics Part C: Seminars in Medical Genetics 2021 DOI: 10.1002/ajmg.c.31874
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• Clinical utility of genomic sequencing: a measurement toolkit
  npj Genomic Medicine 2020 DOI: 10.1038/s41525-020-00164-7
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• Reducing Sanger Confirmation Testing through False Positive Prediction Algorithms
  2020 DOI: 10.1101/2020.04.30.066159
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• Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases
  Journal of Medical Genetics 2019 DOI: 10.1136/jmedgenet-2019-106111
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• A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories
  Genetics in Medicine 2017 DOI: 10.1038/gim.2016.152
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