P156: Genomic disease contribution for unknown causes of infant mortality via genome sequencing of newborn dried blood spots and semiautomated interpretation*

• Eric Ontiveros,
• Liana Protopsaltis,
• Rebecca Baer,
• Matthew Bainbridge,
• Bryant Cao,
• Yan Ding,
• Katarzyna (Kasia) Ellsworth,
• Laura Forero,
• Erwin Frise,
• Lucia Guidugli,
• YongHyun Kwon,
• Jennie Le,
• Scott Oltman,
• Mallory Owen,
• Erica Sanford Kobayashi,
• Lucita Van Der Kraan,
• Meredith Wright,
• Mark Yandell,
• Laura Jelliffe-Pawlowski,
• Gretchen Bandoli,
• Christina Chambers,
• Stephen Kingsmore

Affiliations

Eric Ontiveros

Rady Children's Institute for Genomic Medicine

Liana Protopsaltis

Rady Children's Institute for Genomic Medicine

Rebecca Baer

Department of Pediatrics, University of California San Diego

Matthew Bainbridge

Rady Children's Institute for Genomic Medicine

Bryant Cao

Rady Children's Institute for Genomic Medicine

Yan Ding

Rady Children's Institute for Genomic Medicine

Katarzyna (Kasia) Ellsworth

Rady Children's Institute for Genomic Medicine

Laura Forero

Rady Children's Institute for Genomic Medicine

Erwin Frise

Fabric Genomics, Inc

Lucia Guidugli

Rady Children's Institute for Genomic Medicine

YongHyun Kwon

Rady Children's Institute for Genomic Medicine

Jennie Le

Rady Children's Institute for Genomic Medicine

Scott Oltman

California Preterm Birth Initiative, University of California San Francisco

Mallory Owen

Rady Children's Institute for Genomic Medicine

Erica Sanford Kobayashi

Rady Children's Institute for Genomic Medicine

Lucita Van Der Kraan

Rady Children's Institute for Genomic Medicine

Meredith Wright

Rady Children's Institute for Genomic Medicine

Mark Yandell

Fabric Genomics, Inc

Laura Jelliffe-Pawlowski

California Preterm Birth Initiative, University of California San Francisco

Gretchen Bandoli

Department of Pediatrics, University of California San Diego

Christina Chambers

Department of Pediatrics, University of California San Diego

Stephen Kingsmore

Rady Children's Institute for Genomic Medicine