Engineering microdeletions and microduplications by targeting segmental duplications with CRISPR. Tai D.J., Ragavendran A., Manavalan P., Stortchevoi A., Seabra C.M., Erdin S., Collins R.L., Blumenthal I., Chen X., Shen Y., Sahin M., Zhang C., Lee C. C., Gusella J., Talkowski M.

Recurrent de novo mutations implicate novel genes underlying simplex autism risk. O'Roak B., Stessman H., Boyle E.A., Witherspoon K.T., Martin B., Lee C. C., Vives L., Baker C., Hiatt J.B., Nickerson D.A., Bernier R., Shendure J., Eichler E.

Cryptic and complex chromosomal aberrations in early-onset neuropsychiatric disorders. Brand H., Pillalamarri V., Collins R.L., Eggert S., O'Dushlaine C., Braaten E.B., Stone M.R., Chambert K., Doty N.D., Hanscom C., Rosenfeld J.A., Ditmars H., Blais J., Mills R., Lee C. C., Gusella J., McCarroll S., Smoller J.W., Talkowski M., Doyle A.E.