Center-Authored Papers

Filters: Author is Bernier, Raphael  [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
Mazina V, Gerdts J, Trinh S, Ankenman K, Ward T, Dennis MY, Girirajan S, Eichler EE, Bernier R.  2015.  Epigenetics of autism-related impairment: copy number variation and maternal infection.. Journal of developmental and behavioral pediatrics : JDBP. 36(2):61-7. Abstract
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