Center-Authored Papers

Filters: Author is Stessman, Holly A  [Clear All Filters]
2014
Stessman HA, Bernier R, Eichler EE.  2014.  A genotype-first approach to defining the subtypes of a complex disease.. Cell. 156(5):872-7. Abstract
Bernier R, Golzio C, Xiong B, Stessman HA, Coe BP, Penn O, Witherspoon K, Gerdts J, Baker C, Vulto-van Silfhout AT et al..  2014.  Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development.. Cell. Abstract
2015
Krumm N, Turner TN, Baker C, Vives L, Mohajeri K, Witherspoon K, Raja A, Coe BP, Stessman HA, He Z-X et al..  2015.  Excess of rare, inherited truncating mutations in autism.. Nature genetics. Abstract
Chen D-H, Méneret A, Friedman JR, Korvatska O, Gad A, Bonkowski ES, Stessman HA, Doummar D, Mignot C, Anheim M et al..  2015.  ADCY5-related dyskinesia: Broader spectrum and genotype-phenotype correlations.. Neurology. Abstract