Stephen Kingsmore

20PUBLICATIONS
70CO-AUTHORS
Major global burdens of diseaseNeonatologyInfant and child healthGene expression (incl. microarray and other genome-wide approaches)Cell and nuclear division
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Publications (20)

|Dec 08, 2025
Genome x Environment analysis of Sudden Unexpected Infant Death unveils etiologic heterogeneity and strong cannabis and genetic disease risks.

Stephen F Kingsmore, Gretchen Bandoli, Daniel C Helbling

|Nov 14, 2025
Clinical utility and cost-effectiveness of BeginNGS newborn screening by genome sequencing and standard newborn screening for severe childhood genetic diseases: an adaptive, international and comparative clinical trial.

Rebecca Reimers, Miranda Bailey, Chester Brown

|Apr 29, 2025
Rapid Genome Sequencing Compared to a Gene Panel in Critically Ill Infants with a Suspected Genetic Disorder: An Economic Evaluation.

Tara A Lavelle, Jill L Maron, Stephen F Kingsmore

|Apr 18, 2025
Rapid Whole-Genome Sequencing as a First-Line Test Is Likely to Significantly Reduce the Cost of Acute Care in a Private Payer System.

Christy Moore, Madison Arenchild, Bryce Waldman

|Oct 10, 2024
Genomic mosaicism reveals developmental organization of trunk neural crest-derived ganglia.

Keng Ioi Vong, Yanina D Alvarez, Geoffroy Noel

|Mar 28, 2024
Advancing access to genome sequencing for rare genetic disorders: recent progress and call to action.

Vaidehi Jobanputra, Brock Schroeder, Heidi L Rehm

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Frequent Collaborators

5 joint publications

David P Dimmock

5 joint publications

Sergey Batalov

4 joint publications

Narayanan Veeraraghavan

3 joint publications

Nathaly M Sweeney