Samantha M Baxter

6PUBLICATIONS
60CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Genetic immunologyEpigenetics (incl. genome methylation and epigenomics)
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Publications (6)

|Jul 03, 2026
Structural variant discovery and diagnostic impact in rare diseases from short-read and long-read sequencing.

|Apr 08, 2026
Unifying the Communities of Early-Onset Glycogen Storage Disease Type IV and Adult Polyglucosan Body Disease Through a Genetic Prevalence Study of GBE1-Related Disease.

Rebecca L Koch, H Orhan Akman, Erin Chown

|Oct 06, 2025
Improved allele frequencies in gnomAD through local ancestry inference.

Pragati Kore, Michael W Wilson, Grace Tiao

|Feb 19, 2024
Considerations for reporting variants in novel candidate genes identified during clinical genomic testing.

Jessica X Chong, Seth I Berger, Samantha Baxter

|Dec 06, 2023
Inferring compound heterozygosity from large-scale exome sequencing data.

Michael H Guo, Laurent C Francioli, Sarah L Stenton

|Dec 27, 2018
BRCA Challenge: BRCA Exchange as a global resource for variants in BRCA1 and BRCA2.

Melissa S Cline, Rachel G Liao, Michael T Parsons

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Frequent Collaborators

3 joint publications

Heidi L Rehm

2 joint publications

Anne O'Donnell-Luria

2 joint publications

Mark J Daly

1 joint publications

Elizabeth G Atkinson