Sarah A Walser

“Something Extra on Chromosome 5”: Parents’ Understanding of Positive Prenatal Chromosomal Microarray Analysis (CMA) Results

B. Bernhardt, R. Wapner, Sarah A Walser, 2016, Journal of Genetic Counseling.

A Comprehensive Review of Neurologic Manifestations of COVID-19 and Management of Pre-existing Neurologic Disorders in Children

Rohit Jain, Sarah A Walser, Sarah A. Walser, 2020, Journal of child neurology.

An Observational Study of Children’s Involvement in Informed Consent for Exome Sequencing Research

Victoria A. Miller, B. Bernhardt, Sawona Biswas, 2017, Journal of empirical research on human research ethics : JERHRE.

Erratum: Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine (American Journal of Human Genetics (2016) 98(6) (1067–1076) (S0002929716301069) (10.1016/j.ajhg.2016.04.011))

Sara Chandros Hull, Robert C. Green, Sean D. Mooney, 2016 .

Comparing genetic counselor's and patient's perceptions of needs in prenatal chromosomal microarray testing

B. Bernhardt, S. Palmer, K. Kellom, 2015, Prenatal diagnosis.

Complementary and Alternative Medicine (CAM) use in Children with Epilepsy

E. Lehman, Sarah A Walser, Sarah A. Walser, 2022, Journal of child neurology.

Research participants’ experiences with return of genetic research results and preferences for web‐based alternatives

K. Nathanson, S. Domchek, J. Stopfer, 2019, Molecular genetics & genomic medicine.

Gratitude, protective buffering, and cognitive dissonance: How families respond to pediatric whole exome sequencing in the absence of actionable results

B. Bernhardt, Rebecca Mueller, Sarah A Walser, 2018, American journal of medical genetics. Part A.

“They Can't Find Anything Wrong with Him, Yet”: Mothers’ experiences of parenting an infant with a prenatally diagnosed copy number variant (CNV)

B. Bernhardt, F. Barg, Sarah A Walser, 2017, American journal of medical genetics. Part A.