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European Journal of Human Genetics : EJHG|June 26, 2019
European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac deathFlorence Fellmann, Carla G van El, Philippe Charron, et al.
Wellcome Open Research|May 20, 2022
Engaged genomic science produces better and fairer outcomes: an engagement framework for engaging and involving participants, patients and publics in genomics research and healthcare implementationMadeleine J Murtagh, Mavis Machirori, Clara L Gaff, et al.
Wellcome Open Research|November 6, 2023
Public engagement with genomicsAnna Middleton, Avery Adams, Hugbaad Aidid, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 1, 2018
Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplicationsKate Wolfe, Andrew McQuillin, Viola Alesi, et al.
European Journal of Human Genetics : EJHG|January 10, 2019
Duplication of 10q24 locus: broadening the clinical and radiological spectrumMuriel Holder-Espinasse, Aleksander Jamsheer, Fabienne Escande, et al.
Genome Medicine|May 26, 2021
Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countriesRichard Milne, Katherine I Morley, Mohamed A Almarri, et al.
American Journal of Human Genetics|September 18, 2020
Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data?Anna Middleton, Richard Milne, Mohamed A Almarri, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 7, 2022
Return of genomic results does not motivate intent to participate in research for all: Perspectives across 22 countriesRichard Milne, Katherine I Morley, Mohamed A Almarri, et al.
Nature|March 7, 2022
Whole-genome sequencing reveals host factors underlying critical COVID-19Athanasios Kousathanas, Erola Pairo-Castineira, Konrad Rawlik, et al.
The New England Journal of Medicine|November 10, 2021
100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report, Damian Smedley, Katherine R Smith, et al.
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