Paper Details

Paper Title

Recommendations for clinical interpretation of variants found in non-coding regions of the genome.

Paper Journal Title

Genome Med

Paper Citation Count

Paper Publication Year

2022

Bio Mention

candidate regulatory elements, genetic disorders, genome, monogenic disease, non-coding region variants, non-coding regions, protein-coding regions

Mesh Descriptor

Author Name	Affiliation
Jamie M Ellingford	University of Manchester
Jamie M Ellingford	St Mary's Hospital, Manchester University NHS Foundation Trust
Jamie M Ellingford
Kate Downes	Cambridge University Hospitals NHS Foundation Trust
Sian Ellard	Institute of Biomedical and Clinical Science, University of Exeter Medical School
Sian Ellard	Royal Devon and Exeter NHS Foundation Trust
David R FitzPatrick	Institute of Genetics and Cancer, University of Edinburgh, Western General Hospital
John M Greally	Children's Hospital at Montefiore/Montefiore Medical Center/Albert, Einstein College of Medicine
Hilary C Martin	Wellcome Sanger Institute
Hilary C Martin	Wellcome Sanger Institute
Anne O'Donnell-Luria	Broad Institute of MIT and Harvard
Anne O'Donnell-Luria	Massachusetts General Hospital
Anne O'Donnell-Luria	Boston Children's Hospital
Anne O'Donnell-Luria	Broad Institute of MIT and Harvard
Anne O'Donnell-Luria	Boston Children's Hospital
Anne O'Donnell-Luria	Massachusetts General Hospital
Heidi L Rehm	Broad Institute of MIT and Harvard
Heidi L Rehm	Massachusetts General Hospital
Heidi L Rehm	Broad Institute of MIT and Harvard
Heidi L Rehm	Massachusetts General Hospital
Moriel Singer-Berk	Broad Institute of MIT and Harvard
Jenny C Taylor	National Institute for Health Research Oxford Biomedical Research Centre, University of Oxford
Jenny C Taylor	University of Oxford
Caroline F Wright	Institute of Biomedical and Clinical Science, University of Exeter Medical School

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