Author

Raymond C. Chan

Color (United States)

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Assay:DNA methylation· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Alexandra MartinsiD· 1 shared Álvaro N.A. MonteiroiD· 1 shared Amanda B. SpurdleiD· 1 shared Amanda Ewart TolandiD· 1 shared Arjen R. MensenkampiD· 1 shared Bing FengiD· 1 shared Bryony A. ThompsoniD· 1 shared Clare TurnbulliD· 1 shared

Activity by Year

2024-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alexandra MartinsORCID

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Author profile →

1 paper

Recent·Most cited

Evidence-based recommendations for gene-specific ACMG/AMP variant classification from the ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel

Michael T. Parsons, Miguel de la Hoya, Marcy E. Richardson, Emma Tudini, Michael G. Anderson, Windy Berkofsky‐Fessler, Sandrine M. Caputo, Raymond C. Chan, Melissa Cline, Bing Feng, Cristina Fortuño, Encarna B. Gómez-García, Johanna S. Hadler, Susan C. Hiraki, Megan A. Holdren, , Amanda B. Spurdle

The paper refines ACMG/AMP variant classification criteria for BRCA1 and BRCA2 by calibrating evidence strength and improving classification consistency through expert panel review.

The American Journal of Human Genetics · Aug 13, 2024Peer-reviewedGenetic & Genomic Medicine