Estimating the sensitivity of genomic screening for treatable inherited metabolic disorders

Presenter: Dr Sarah Bick

Forgotten Dissenters: A Scoping Review of Parents Who Decline Newborn Screening

Presenter: Taylor Montgomery

From DBS to WGS: Rapid genomic DNA isolation from Dried Blood Spots and Whole Genome library preparation using sparQ DBS Library Prep Kit

Presenter: Dr Subrata Panja

Furthering the Dialogue on Newborn Sequencing: Insights from Neonatal Rapid Whole Genome Sequencing

Presenter: Robert Rigobello

Lessons Learned From Genomic Newborn Sequencing of 12,000+ Infants Across Two States

Presenter: Dr Paul Kruszka

Optimism and pessimism about genomic medicine among parents of infants who have received study results: Findings from the BabySeq Project

Presenter: Madison Hickingbotham

ScreenPlus parental perspectives on trust and the utilization of residual dried blood spots

Presenter: Katrina Paleologos

Whole genome sequencing from dried blood spots for newborn screening of Menkes disease and other actionable neurometabolic disorders of early infancy

Presenter: Dr Stephen Kaler

Why so different? Exploring the disorders included in newborn genome sequencing

Presenter: Dr Thomas Minten

10K Newborn Genome Screening Project in Qingdao, China: clinical findings and precision health insights

Presenter: Dr Lennart Hammarstrom

A pilot study of the Anatolian Newborn Screening Project

Presenter: Xinmeng Liao

A streamlined newborn sequencing research workflow for detecting genomic variants using a curated gene panel

Presenter: Dr Minna Niemelä

Applications of a Rapid Real Time Analysis System for Whole Genome/Exome Sequencing in Newborn Screening

Presenter: Yun-Ru Chen

Massively Parallel Biochemical Annotation of VOUS to Support Newborn Sequencing

Presenter: Dr Michael Gelb

Non-medical developmental supports following newborn sequencing: Lessons from SeqFirst

Presenter: Dr Kate MacDuffie