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Andersen, Erica

https://orcid.org/0000-0002-7205-0600

A5079874169 | I223532165

Mayo Clinic

University of Utah

Citations 3

Utilizing ClinGen gene‐disease validity and dosage sensitivity curations to inform variant classification

Human Mutation | October 25, 2021 | Volume: 43 | Issue: 8 | Pages: 1031-1040

10.1002/humu.24291 | PMID 34694049

Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features

Human Mutation | February 29, 2020 | Volume: 41 | Issue: 7 | Pages: 1238-1249

10.1002/humu.24009 | PMID 32112660

Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar

Human Mutation | August 10, 2018 | Volume: 39 | Issue: 11 | Pages: 1650-1659

10.1002/humu.23610 | PMID 30095202