Last Updated: 09/26/2026
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Found 41 publications
Pharmacogenomic Testing: Strategies and Technical Considerations for Clinical Laboratories.
Journal: Archives of pathology & laboratory medicine
Published: October 08, 2025
Adolescent to adult health care transition for persons with intellectual and developmental disability: current barriers, next steps.
Journal: Frontiers in pediatrics
Published: August 26, 2024
A most important gift: the critical role of postmortem brain tissue in autism science.
Journal: Frontiers in neurology
Published: August 25, 2024
Fetal Fraction Methodologies and Their Clinical Use: Results of a College of American Pathologists Exercise.
Journal: The journal of applied laboratory medicine
Published: August 04, 2024
Numbers of prenatal cell-free DNA screens performed: Results of a 2022 CAP exercise.
Journal: Prenatal diagnosis
Published: November 14, 2023
Proteomic investigations of adult polyglucosan body disease: insights into the pathobiology of a neurodegenerative disorder.
Journal: Frontiers in neurology
Published: July 18, 2023
Metabolomic biomarkers in autism: identification of complex dysregulations of cellular bioenergetics.
Journal: Frontiers in psychiatry
Published: June 28, 2023
Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype.
Journal: American journal of human genetics
Published: September 01, 2022
A picture is worth a thousand words: A proposal to incorporate video into the evaluation of adults with intellectual or developmental disability living outside the home.
Journal: Frontiers in public health
Published: April 20, 2022
Climate Change and Medical Education: An Integrative Model.
Journal: Academic medicine : journal of the Association of American Medical Colleges
Published: August 25, 2021
A Metabolomics Approach to Screening for Autism Risk in the Children's Autism Metabolome Project.
Journal: Autism research : official journal of the International Society for Autism Research
Published: April 01, 2020
De Novo Variants in the ATPase Module of MORC2 Cause a Neurodevelopmental Disorder with Growth Retardation and Variable Craniofacial Dysmorphism.
Journal: American journal of human genetics
Published: February 13, 2020
Last Updated: 09/26/2026