Population Genomic Screening for Genetic Etiologies of Neurodevelopmental/Psychiatric Disorders Demonstrates Personal Utility and Positive Participant Responses.

Wain, Karen E; Tolwinski, Kasia; Palen, Emily; Heidlebaugh, Alexis R; Holdren, Karahlyn; Walsh, Lauren Kasparson; Oetjens, Matthew T; Ledbetter, David H; Martin, Christa Lese

Wain, Karen E; Tolwinski, Kasia; Palen, Emily; Heidlebaugh, Alexis R; Holdren, Karahlyn; Walsh, Lauren Kasparson; Oetjens, Matthew T; Ledbetter, David H; Martin, Christa Lese.

Afiliación

Wain KE; Autism & Developmental Medicine Institute, Geisinger, Danville, PA 17822, USA.
Tolwinski K; Biomedical Ethics Unit, McGill University, Montreal, QC H3A 1X1, Canada.
Palen E; Autism & Developmental Medicine Institute, Geisinger, Danville, PA 17822, USA.
Heidlebaugh AR; Autism & Developmental Medicine Institute, Geisinger, Danville, PA 17822, USA.
Holdren K; Autism & Developmental Medicine Institute, Geisinger, Danville, PA 17822, USA.
Walsh LK; Autism & Developmental Medicine Institute, Geisinger, Danville, PA 17822, USA.
Oetjens MT; Autism & Developmental Medicine Institute, Geisinger, Danville, PA 17822, USA.
Ledbetter DH; Autism & Developmental Medicine Institute, Geisinger, Danville, PA 17822, USA.
Martin CL; Autism & Developmental Medicine Institute, Geisinger, Danville, PA 17822, USA.

J Pers Med ; 11(5)2021 May 01.

Article en En | MEDLINE | ID: mdl-34062946

Palabras clave

brain disorders; copy number variant; genomic screening; neuropsychiatric disorders; personal utility

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 1_ASSA2030 Problema de salud: 1_sistemas_informacao_saude Tipo de estudio: Diagnostic_studies / Etiology_studies / Qualitative_research / Screening_studies Idioma: En Revista: J Pers Med Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

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