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Stephen Kingsmore

Chair

Cleveland Clinic

United States

Research Interests

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Professors in United States

Articles (20)

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Collaborators (13)

Kit Sing Au

Associate Professor

University of Texas Medical School at Houston

UNITED STATES

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Nikolaus Rieber

Professor

Technical University of Munich

GERMANY

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Edgar Hernandez

Research Assistant Professor

University of Utah

UNITED STATES

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Kimberley Tolias

Professor

Stanford University

UNITED STATES

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John B. Wallingford

University of Texas at Austin

UNITED STATES

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Bruce Gelb

Director

Icahn School of Medicine at Mount Sinai

UNITED STATES

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Xiaoxu Yang

Assistant Professor

University of Utah

UNITED STATES

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Vaidehi Jobanputra

Columbia University Irving Medical Center

UNITED STATES

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Pietro Caironi

Associate Professor of Anesthesia and Intensive Care

Università degli Studi di Torino

ITALY

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Ryan Taft

Chief Scientific Officer

UNITED STATES

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Martin Werner Breuss

Assistant Professor

University of Colorado Anschutz Medical Campus

UNITED STATES

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Sangwoo Kim

Assistant professor

Yonsei University College of Medicine

SOUTH KOREA

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Nicole Coufal

Associate Professor

University of California, San Diego

UNITED STATES

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Stephen Kingsmore

Research Interests

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Articles (20)

Systematic review and meta-analysis of humoral immunity proteins and mortality in sepsis

Developmental organization of sensory and sympathetic ganglia

MPSE identifies newborns for whole genome sequencing within 48 h of NICU admission

The contribution of de novo coding mutations to meningomyelocele.

Rapid Genome Sequencing Compared with a Gene Panel in Critically Ill Infants with a Suspected Genetic Disorder: An Economic Evaluation.

A phenotypic brain organoid atlas and biobank for neurodevelopmental disorders

A phenotypic brain organoid atlas for neurodevelopmental disorders

Clinical characterization of Collagen XII-related disease caused by biallelic <i>COL12A1</i> variants

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

Long-term follow-up of children who received rapid genomic sequencing

Palliative Care Outcomes for Critically ill Children After Rapid Whole Genome Sequencing

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

The diagnosis and treatment of rare genetic disorders in neonates, infants, and children: the time is now

Cell-type-resolved mosaicism reveals clonal dynamics of the human forebrain

Advancing access to genome sequencing for rare genetic disorders: recent progress and call to action

Biallelic Loss of Function Variants in SENP7 Cause Immunodeficiency with Neurologic and Muscular Phenotypes.

Early Newborn Metabolic Patterning and Sudden Infant Death Syndrome

Genome sequencing detects a wide range of clinically relevant copy-number variants and other genomic alterations

Genome-based newborn screening for severe childhood genetic diseases has high positive predictive value and sensitivity in a NICU pilot trial

Genomic mosaicism reveals developmental organization of trunk neural crest-derived ganglia

Collaborators (13)

Kit Sing Au

Nikolaus Rieber

Edgar Hernandez

Kimberley Tolias

John B. Wallingford

Bruce Gelb

Xiaoxu Yang

Vaidehi Jobanputra

Pietro Caironi

Ryan Taft

Martin Werner Breuss

Sangwoo Kim

Nicole Coufal

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