News & Publications for:

Christina Gurnett

Exome sequencing identifies a rare HSPG2 variant associated with familial idiopathic scoliosis

Posted on February 23, 2015

Erin E. Baschal, Cambria I. Wethey, Kandice Swindle, Robin M. Baschal, et al: 2015 G3: Genes, Genomes, Genetics; 5(2) pp167-174 Read More

Posted in: Neurogenetics, Publications Faculty:

Novel SCN3A variants associated with focal epilepsy in children

Posted on December 16, 2013

Vanoye CG, Gurnett CA, Holland KD, George AL, Kearney JA; (2014) Neurobiology of Disease, 62, pp. 313-322 Read More

Posted in: Neurogenetics, Publications Faculty:

Congratulations to Christina Gurnett

Posted on November 6, 2012

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Posted in: Neurogenetics, News Faculty:

Copy number variants and infantile spasms: evidence for abnormalities in ventral forebrain development and pathways of synaptic function

Posted on October 27, 2011

Paciorkowski AR, Thio LL, Rosenfeld JA, Gajecka M, Gurnett CA, Kulkarni S, Chung WK, Marsh ED, Gentile M, Reggin JD, Wheless JW, Balasubramanian S, Kumar R, Christian SL, Marini C, Guerrini R, Maltsev N, Shaffer LG, Dobyns WB (2011). Eur J Hum Genet, doi:10.1038/ejhg
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