K. W. Davis

Parent-of-Origin Effects in 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) Syndrome

B. Dallapiccola, M. Butler, A. Novelli, 2019, International journal of molecular sciences.

A comparison of genomic laboratory reports and observations that may enhance their clinical utility for providers and patients

E. Wassman, K. W. Davis, Megan M. Martin, 2019, Molecular genetics & genomic medicine.

Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disorders

S. Scherer, A. Prasad, M. Uddin, 2019, Neurology: Genetics.

NeuroSCORE: A Genome-wide Omics-Based Model to Identify Candidate Disease Genes of the Central Nervous System

M. Uddin, Colleen G. Bilancia, Yolanda Hom, 2021, bioRxiv.

NeuroSCORE is a genome-wide omics-based model that identifies candidate disease genes of the central nervous system

M. Uddin, Colleen G. Bilancia, Yolanda Hom, 2022, Scientific Reports.

WHAT COUNTS? THE ROLE OF NUMERACY IN INTERPRETATION OF PERSONALIZED GENOMIC RISK INFORMATION IN CORIELL PARTICIPANTS

K. W. Davis, 2016 .

Testing a best practices risk result format to communicate genetic risks.

W. Klein, D. Roter, L. Scheinfeldt, 2020, Patient education and counseling.

Genomic sequencing tests generate less uncertainty and higher diagnostic yield compared to multi-gene panel-based tests: Results of over 1.5 million tests

V. Jobanputra, C. Marshall, H. Rehm, 2022, medRxiv.