Karen E Wain

Publication Activity (10 Years)

Years Active: 2019-2021
Publications (10 Years): 5

Top Topics

Tandem Mass Spectrometry

Autism Spectrum Disorder

Dna Methylation

Top Venues

Journal of personalized medicine

Genetics in medicine : official journal of the American College of Medical Genetics

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

Publications

Karen E Wain, Kasia Tolwinski, Emily Palen, Alexis R Heidlebaugh, Karahlyn Holdren, Lauren Kasparson Walsh, Matthew T Oetjens, David H Ledbetter, Christa Lese Martin
Population Genomic Screening for Genetic Etiologies of Neurodevelopmental/Psychiatric Disorders Demonstrates Personal Utility and Positive Participant Responses. Journal of personalized medicine 11 (5) (2021)
Kelly E Ormond, Maia J Borensztein, Miranda L G Hallquist, Adam H Buchanan, William Andrew Faucett, Holly L Peay, Maureen E Smith, Eric P Tricou, Wendy R Uhlmann, Karen E Wain, Curtis R Coughlin, null On Behalf Of The Clinical Genome CADRe Workgroup
Defining the Critical Components of Informed Consent for Genetic Testing. Journal of personalized medicine 11 (12) (2021)
Karen E Wain, Danielle R Azzariti, Jennifer L Goldstein, Amy Knight Johnson, Patti Krautscheid, Brianna Lepore, Julianne M O'Daniel, Deborah Ritter, Juliann M Savatt, Erin Rooney Riggs, Christa Lese Martin
Variant interpretation is a component of clinical practice among genetic counselors in multiple specialties. Genetics in medicine : official journal of the American College of Medical Genetics 22 (4) (2019)
Karen E Wain, Emily Palen, Juliann M Savatt, Devin Shuman, Brenda Finucane, Andrea Seeley, Thomas D Challman, Scott M Myers, Christa Lese Martin
The value of genomic variant ClinVar submissions from clinical providers: Beyond the addition of novel variants. Human mutation 39 (11) (2019)
Juliann M Savatt, Danielle R Azzariti, William Andrew Faucett, Steven M Harrison, Jennifer Hart, Brandi Kattman, Melissa J Landrum, David H Ledbetter, Vanessa Rangel Miller, Emily Palen, Michael J Bamshad, Jud Rhode, Stefanie Turner, Jo Anne Vidal, Karen E Wain, Erin Rooney Riggs, Christa Lese Martin
ClinGen's GenomeConnect registry enables patient-centered data sharing. Human mutation 39 (11) (2019)