Rapid genomic sequencing for genetic disease diagnosis and therapy in intensive care units: a review by Stephen F. Kingsmore, Russell Nofsinger, Kasia Ellsworth

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620 Clinical management of lupus in the United States: a claims-based analysis by Peter E Lipsky, Kathryn M Kingsmore, John Zent

Cephalic arch stenosis: an analysis of outcome by type of first intervention by Umberto Pisano, Karen Stevenson, Ram Kasthuri, David Kingsmore

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A novel index for measuring the impact of devices on hypertension by D. B. Kingsmore, B. Edgar, M. Rostron, C. Delles, A. J. B. Brady

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1104 Machine learning to determine the endotype of SLE patients: a validation study by Peter E Lipsky, Prathyusha Bachali, Amrie C Grammer, Kathryn M Kingsmore, Erika L Hubbard

The Genomic landscape of short tandem repeats across multiple ancestries. by Prashanth Vijayaraghavan, Sergey Batalov, Yan Ding, Erica Sanford, Stephen F Kingsmore, David Dimmock, Charlotte Hobbs, Matthew Bainbridge

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Whole genome sequencing of an African American family highlights toll like receptor 6 variants in Kawasaki disease susceptibility. by Jihoon Kim, Chisato Shimizu, Stephen F Kingsmore, Stephen F Kingsmore, Narayanan Veeraraghavan, Eric Levy, Andre M Ribeiro Dos Santos, Hai Yang, Jay Flatley, Long Truong Hoang, Martin L Hibberd, Adriana H Tremoulet, Olivier Harismendy, Lucila Ohno-Machado, Jane C Burns

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Publisher Correction: Analysis of transcriptomic features reveals molecular endotypes of SLE with clinical implications by Erika L. Hubbard, Prathyusha Bachali, Kathryn M. Kingsmore, Yisha He, Michelle D. Catalina, Amrie C. Grammer, Peter E. Lipsky

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Analysis of transcriptomic features reveals molecular endotypes of SLE with clinical implications by Erika L. Hubbard, Prathyusha Bachali, Kathryn M. Kingsmore, Yisha He, Michelle D. Catalina, Amrie C. Grammer, Peter E. Lipsky

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What are the observed procedural costs of vascular access surgery? Protocol for a systematic review by Karen Stevenson, Andrew Jackson, Catrin Jones, Peter Thomson, Ram Kasthuri, David Kingsmore, Lucian Gaianu, Emma Aitken, Ben Edgar, Callum Stove

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NBSTRN Tools to Advance Newborn Screening Research and Support Newborn Screening Stakeholders by Kee Chan, Zhanzhi Hu, Lynn W. Bush, Heidi Cope, Ingrid A. Holm, Stephen F. Kingsmore, Kevin Wilhelm, Curt Scharfe, Amy Brower

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Realtime monitoring of thrombus formation in vivo using a self-reporting vascular access graft by Daniel Hoare, David Kingsmore, Michael Holsgrove, Ewan Russell, Mahmut T. Kirimi, Jakub Czyzewski, Nosrat Mirzai, Simon Kennedy, Steven L. Neale, John R. Mercer

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Exploration of treatment burden through examination of workload and patient capacity during transition onto kidney replacement therapy: a systematic review of qualitative research by Catrin Jones, Ross Cairns, Heather Walker, Silje Welsh, Benjamin Edgar, Karen Stevenson, Bhautesh D. Jani, Patrick B. Mark, David Kingsmore, Katie I. Gallacher

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P610: Identification of trinucleotide repeat expansions in DMPK using rapid whole genome sequencing by Lucia Guidugli, Monia Hammer, Bryant Cao, Joseph Shen, Daniel Rito, Claire Botsford, David Chitayat, Jerica Lenberg, Kristen Wigby, Kelly Watkins, Stephen Kingsmore, Mari Tokita

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Genomic sequencing has a high diagnostic yield in children with congenital anomalies of the heart and urinary system by Erika T. Allred, Erika T. Allred, Elliot A. Perens, Nicole G. Coufal, Nicole G. Coufal, Erica Sanford Kobayashi, Erica Sanford Kobayashi, Stephen F. Kingsmore, David P. Dimmock

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Hypertensive load predicts recovery of renal function for patients undergoing revascularisation for renal artery stenosis by Ben Edgar, Rob Pearson, Andrew Jackson, Callum Stove, Ram Kasthuri, Keith Hussey, Christian Delles, Colin Geddes, Patrick Mark, Giles Roditi, Linsay McCallum, David B. Kingsmore

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Molecular mechanisms governing the progression of nephritis in lupus prone mice and human lupus patients by Andrea R. Daamen, Hongyang Wang, Hongyang Wang, Prathyusha Bachali, Nan Shen, Kathryn M. Kingsmore, Robert D. Robl, Amrie C. Grammer, Shu Man Fu, Shu Man Fu, Peter E. Lipsky

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Isolated Absent Aortic Valve: A Unique Fetal Case With Echocardiographic, Pathologic, and Genetic Correlation by Eleanor L. Schuchardt, MD, Paul Grossfeld, MD, Stephen Kingsmore, MD, DSc, Yan Ding, MD, Lisa A. Vargas, RDCS, Dan A. Dyar, MA, RDCS, Arturo Mendoza, MD, Kirsten B. Dummer, MD

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Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learning by Bennet Peterson, Edgar Javier Hernandez, Charlotte Hobbs, Sabrina Malone Jenkins, Barry Moore, Edwin Rosales, Samuel Zoucha, Erica Sanford, Matthew N. Bainbridge, Erwin Frise, Albert Oriol, Luca Brunelli, Stephen F. Kingsmore, Mark Yandell

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Advancing access to genome sequencing for rare genetic disorders: recent progress and call to action by Vaidehi Jobanputra, Brock Schroeder, Heidi L. Rehm, Wei Shen, Elizabeth Spiteri, Ghunwa Nakouzi, Stacie Taylor, Christian R. Marshall, Linyan Meng, Stephen F. Kingsmore, Katarzyna Ellsworth, Euan Ashley, Ryan J. Taft, on behalf of the Medical Genome Initiative

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