Items where Author is "Ercan-Sencicek, AG"

Article

Dong, S and Walker, MF and Carriero, NJ and DiCola, M and Willsey, AJ and Ye, AY and Waqar, Z and Gonzalez, LE and Overton, JD and Frahm, S and Keaney, JF and Teran, NA and Dea, J and Mandell, JD and HusBal, V and Sullivan, CA and DiLullo, NM and Khalil, RO and Gockley, J and Yuksel, Z and Sertel, SM and Ercan-Sencicek, AG and Gupta, AR and Mane, SM and Sheldon, M and Brooks, AI and Roeder, K and Devlin, B and State, MW and Wei, L and Sanders, SJ (2014) De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder. Cell Reports, 9 (1). 16 - 23.

Gupta, AR and Pirruccello, M and Cheng, F and Kang, HJ and Fernandez, TV and Baskin, JM and Choi, M and Liu, L and Ercan-Sencicek, AG and Murdoch, JD and Klei, L and Neale, BM and Franjic, D and Daly, MJ and Lifton, RP and De Camilli, P and Zhao, H and Šestan, N and State, MW (2014) Rare deleterious mutations of the gene EFR3A in autism spectrum disorders. Molecular Autism, 5 (1).