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Nature Reviews. Genetics|November 24, 2015
Principle of proportionality in genomic data sharingCaroline F Wright, Matthew E Hurles, Helen V FirthGenetics in Medicine Open|September 30, 2024
Detection of mosaic chromosomal alterations in children with severe developmental disorders recruited to the DDD studyRuth Y Eberhardt, Caroline F Wright, David R FitzPatrick, et al.HGG Advances|December 23, 2022
IMPROVE-DD: Integrating multiple phenotype resources optimizes variant evaluation in genetically determined developmental disordersStuart Aitken, Helen V Firth, Caroline F Wright, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 5, 2020
Evaluating variants classified as pathogenic in ClinVar in the DDD StudyCaroline F Wright, Ruth Y Eberhardt, Panayiotis Constantinou, et al.European Journal of Human Genetics : EJHG|April 30, 2015
Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing researchAnna Middleton, Katherine I Morley, Eugene Bragin, et al.Journal of Medical Genetics|May 22, 2015
Potential research participants support the return of raw sequence dataAnna Middleton, Caroline F Wright, Katherine I Morley, et al.Wellcome Open Research|March 21, 2017
Returning genome sequences to research participants: Policy and practiceCaroline F Wright, Anna Middleton, Jeffrey C Barrett, et al.Nucleic Acids Research|October 24, 2013
DECIPHER: database for the interpretation of phenotype-linked plausibly pathogenic sequence and copy-number variationEugene Bragin, Eleni A Chatzimichali, Caroline F Wright, et al.Genetics in Medicine Open|December 13, 2024
Detection and characterization of copy-number variants from exome sequencing in the DDD studyPetr Danecek, Eugene J Gardner, Tomas W Fitzgerald, et al.Nature Reviews. Genetics|February 6, 2018
Paediatric genomics: diagnosing rare disease in childrenCaroline F Wright, David R FitzPatrick, Helen V FirthPageof 33