Genetics in Medicine Open (Jan 2024)
P213: Exploring heterogeneity among gene lists proposed for newborn sequencing
- Thomas Minten,
- Sophia Adelson,
- Laura Amendola,
- David Bick,
- François Boemer,
- Alison Coffey,
- Nicolas Encina,
- Bianca Russell,
- Laurent Servais,
- Kristen Sund,
- Ryan Taft,
- Robert Green,
- Nina Gold
Affiliations
- Thomas Minten
- KU Leuven
- Sophia Adelson
- Brigham and Women’s Hospital, Stanford School of Medicine
- Laura Amendola
- Illumina Inc
- David Bick
- Genomics England
- François Boemer
- CHU Liège, University of Liège
- Alison Coffey
- Illumina Inc
- Nicolas Encina
- ICoNS, Ariadne Labs, Harvard T.H. Chan School of Public Health
- Bianca Russell
- University of California, Los Angeles
- Laurent Servais
- University of Oxford, University of Liège
- Kristen Sund
- Nurture Genomics
- Ryan Taft
- Illumina Inc
- Robert Green
- Mass General Brigham, Broad Institute, Ariadne Labs and Harvard Medical School
- Nina Gold
- Massachusetts General Hospital, Harvard Medical School
- Journal volume & issue
-
Vol. 2
p. 101110