Rebecca C. Walsh

Participants and Study Decliners’ Perspectives About the Risks of Participating in a Clinical Trial of Whole Genome Sequencing

R. Green, A. McGuire, K. Christensen, 2016, 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 .

Deleterious variants in CRLS1 lead to cardiolipin deficiency and cause an autosomal recessive multi-system mitochondrial disease

S. Ferdinandusse, K. Boycott, J. Fletcher, 2022, Human molecular genetics.

Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants.

Robert J. Weatheritt, Stephanie L. White, N. Brown, 2021, Genetics in medicine : official journal of the American College of Medical Genetics.

Psychosocial Factors Influencing Parental Interest in Genomic Sequencing of Newborns

R. Green, S. Waisbren, C. Petty, 2016, Pediatrics.

Clinically Responsive Genomic Analysis Pipelines: Elements to improve detection rate and efficiency.

S. Sandaradura, T. Roscioli, J. Fletcher, 2021, The Journal of molecular diagnostics : JMD.

VEXAS syndrome: lessons learnt from an early Australian case series

Rebecca C. Walsh, N. W. Doo, David Heath, 2022, Internal medicine journal.

Participants and Study Decliners’ Perspectives About the Risks of Participating in a Clinical Trial of Whole Genome Sequencing

Denise L. Perry, R. Green, A. McGuire, 2016, Journal of empirical research on human research ethics : JERHRE.

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

Matthew S. Lebo, Victoria A. Miller, Jeffrey W. Pennington, 2016, American journal of human genetics.