News & Publications for:

Christina Gurnett

Mutations in Kinesin family member 6 reveal specific role in ependymal cell ciliogenesis and human neurological development

Posted on December 17, 2018

Mia J. Konjikusic, Patra Yeetong, Curtis W. Boswell, Chanjae Lee, Elle C. Roberson, Rungnapa Ittiwut, Kanya Suphapeetiporn, Brian Ciruna, Christina A. Gurnett, John B. Wallingford, Vorasuk Shotelersuk , Ryan S. Gray. PLoS Genetics, Volume 14, Issue 11, November 2018, Article number e1007817 Read More

Posted in: Neurogenetics & Transcriptomics, Publications Faculty:

A missense variant in SLC39A8 is associated with severe idiopathic scoliosis

Posted on October 8, 2018

Gabe Haller, Kevin McCall, Supak Jenkitkasemwong, Brooke Sadler, Lilian Antunes, Momchil Nikolov, Julia Whittle, Zachary Upshaw, Jimann Shin, Erin Baschal, Carlos Cruchaga, Matthew Harms, Cathleen Raggio, Jose A. Morcuende, Philip Giampietro, Nancy H. Miller, Carol Wise, Ryan S. Gray, Lila Solnica-Krezel, Mitchell Knutson, Matthew B. Dobbs & Christina A. Gurnett. Nature Communications, Volume 9, Issue 1, 1 December 2018, Article number 4171 Read More

Posted in: HPAN, Lysosome, Neurodegeneration, Neurogenetics & Transcriptomics, Publications Faculty: , ,

Gurnett named director of pediatric and developmental neurology

Posted on September 5, 2018

Physician-scientist specializes in epilepsy, neurodevelopmental disorders Read More

Posted in: Neurogenetics & Transcriptomics, News Faculty:

Massively parallel single-nucleotide mutagenesis using reversibly terminated inosine

Posted on October 3, 2016

Gabe Haller, David Alvarado, Kevin McCall, Robi D Mitra, Matthew B Dobbs & Christina A Gurnett. Nature Methods volume 13, pages 923–924 (2016)
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Posted in: Neurogenetics & Transcriptomics, Publications Faculty: , ,