Browse by Publication

Messinger, DS and Young, GS and Webb, SJ and Ozonoff, S and Bryson, SE and Carter, A and Carver, L and Charman, T and Chawarska, K and Curtin, S and Dobkins, K and Hertz-Picciotto, I and Hutman, T and Iverson, JM and Landa, R and Nelson, CA and Stone, WL and Tager-Flusberg, H and Zwaigenbaum, L (2016) Commentary: Sex difference differences? A reply to Constantino Dr Meng-Chuan Lai. Molecular Autism, 7 (1).

Siegel, M and Smith, KA and Mazefsky, C and Gabriels, RL and Erickson, C and Kaplan, D and Morrow, EM and Wink, L and Santangelo, SL (2015) The autism inpatient collection: Methods and preliminary sample description. Molecular Autism, 6 (1).

Kana, RK and Maximo, JO and Williams, DL and Keller, TA and Schipul, SE and Cherkassky, VL and Minshew, NJ and Just, MA (2015) Aberrant functioning of the theory-of-mind network in children and adolescents with autism. Molecular Autism, 6 (1).

Messinger, DS and Young, GS and Webb, SJ and Ozonoff, S and Bryson, SE and Carter, A and Carver, L and Charman, T and Chawarska, K and Curtin, S and Dobkins, K and Hertz-Picciotto, I and Hutman, T and Iverson, JM and Landa, R and Nelson, CA and Stone, WL and Tager-Flusberg, H and Zwaigenbaum, L (2015) Early sex differences are not autism-specific: A Baby Siblings Research Consortium (BSRC) study. Molecular Autism, 6 (1).

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).

Liu, L and Lei, J and Sanders, SJ and Willsey, AJ and Kou, Y and Cicek, AE and Klei, L and Lu, C and He, X and Li, M and Muhle, RA and Ma'Ayan, A and Noonan, JP and Šestan, N and McFadden, KA and State, MW and Buxbaum, JD and Devlin, B and Roeder, K (2014) DAWN: A framework to identify autism genes and subnetworks using gene expression and genetics. Molecular Autism, 5 (1).

Klei, L and Sanders, SJ and Murtha, MT and Hus, V and Lowe, JK and Willsey, AJ and Moreno-De-Luca, D and Yu, TW and Fombonne, E and Geschwind, D and Grice, DE and Ledbetter, DH and Lord, C and Mane, SM and Martin, CL and Martin, DM and Morrow, EM and Walsh, CA and Melhem, NM and Chaste, P and Sutcliffe, JS and State, MW and Cook, EH and Roeder, K and Devlin, B (2012) Common genetic variants, acting additively, are a major source of risk for autism. Molecular Autism, 3 (1).