Sarah A. Walser

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine

Robert C. Green, Katrina A.B. Goddard, Gail P. Jarvik et al. · The American Journal of Human Genetics · 2016 · 161 citations · Full text

Epidemiology, Sequencing, Medicine +7

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

Allison Werner‐Lin, Sarah A. Walser, Frances K. Barg et al. · American Journal of Medical Genetics Part A · 2016 · 70 citations

Chromosome Microarray, Medicine, Copy Number Variant +15

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

Sarah A. Walser, Katherine Kellom, Steven C. Palmer et al. · Prenatal Diagnosis · 2015 · 38 citations · Full text

Family Medicine, Reproductive Sciences, Genetic Testing +27

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

Allison Werner‐Lin, Lori Zaspel, Mae Carlson et al. · American Journal of Medical Genetics Part A · 2018 · 38 citations

Genetic Testing, Exome Sequencing, Clinical Genome +20

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

Sarah A. Walser, Allison Werner‐Lin, Amita Russell et al. · Journal of Genetic Counseling · 2016 · 33 citations · Full text