Publications by authors named "Christopher T Sullivan"

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The Diagnostic Cascade of Incidental Findings: A Teachable Moment.
Linh T Nguyen, Christopher T Sullivan, Anil N Makam

JAMA Intern Med· July 2015

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Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria.
Samin A Sajan, Liliana Fernandez, Sahar Esmaeeli Nieh, Eric Rider, Polina Bukshpun, Christopher T Sullivan

PLoS Genet· March 2014

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De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes.
Jean-Baptiste Rivière, Ghayda M Mirzaa, Brian J O'Roak, Margaret Beddaoui, Diana Alcantara, Christopher T Sullivan

Nat Genet· June 2012

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De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome.
Jean-Baptiste Rivière, Bregje W M van Bon, Alexander Hoischen, Stanislav S Kholmanskikh, Brian J O'Roak, Christopher T Sullivan

Nat Genet· February 2012

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Crystal structures of DNA/RNA repair enzymes AlkB and ABH2 bound to dsDNA.
Cai-Guang Yang, Chengqi Yi, Erica M Duguid, Christopher T Sullivan, Xing Jian

Nature· April 2008

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