Heather Mason-Suares

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 5

Top Topics

Dna Methylation

Hypertrophic Cardiomyopathy

Top Venues

Molecular genetics & genomic medicine

Clinical chemistry

This page only lists publications with an associated author ORCID identifier.

Publications

Laura M Sack, Lauren Mertens, Elissa Murphy, Laura Hutchinson, Anne B S Giersch, Heather Mason-Suares
Leveraging Unique Chromosomal Microarray Probes to Accurately Detect Copy Number at the Highly Homologous 15q15.3 Deafness-Infertility Syndrome Locus. Clinical chemistry (2023)
Samantha L P Schilit, Courtney Studwell, Pamela Flatley, Marc Listewnik, Lauren Mertens, Azra H Ligon, Heather Mason-Suares
Chromosomal microarray analysis in pregnancy loss: Is it time for a consensus approach? Prenatal diagnosis 42 (12) (2022)
Leora Witkowski, Mitchell W Dillon, Elissa Murphy, Matthew S Lebo, Heather Mason-Suares
Expanding the Noonan spectrum/RASopathy NGS panel: Benefits of adding NF1 and SPRED1. Molecular genetics & genomic medicine 8 (4) (2020)
Ahmad N Abou Tayoun, Heather Mason-Suares
Considerations for whole exome sequencing unique to prenatal care. Human genetics 139 (9) (2019)
Ozge Ceyhan-Birsoy, Maya M Miatkowski, Elizabeth Hynes, Birgit H Funke, Heather Mason-Suares
NGS testing for cardiomyopathy: Utility of adding RASopathy-associated genes. Human mutation 39 (7) (2018)