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	1.	No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins. [electronic resource] by Murdoch, John D Gupta, Abha R Sanders, Stephan J Walker, Michael F Keaney, John Fernandez, Thomas V Murtha, Michael T Anyanwu, Samuel Ober, Gordon T Raubeson, Melanie J DiLullo, Nicholas M Villa, Natalie Waqar, Zainabdul Sullivan, Catherine Gonzalez, Luis Willsey, A Jeremy Choe, So-Yeon Neale, Benjamin M Daly, Mark J State, Matthew W Producer: 20150629 In: PLoS genetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder. [electronic resource] by Dong, Shan Walker, Michael F Carriero, Nicholas J DiCola, Michael Willsey, A Jeremy Ye, Adam Y Waqar, Zainulabedin Gonzalez, Luis E Overton, John D Frahm, Stephanie Keaney, John F Teran, Nicole A Dea, Jeanselle Mandell, Jeffrey D Hus Bal, Vanessa Sullivan, Catherine A DiLullo, Nicholas M Khalil, Rehab O Gockley, Jake Yuksel, Zafer Sertel, Sinem M Ercan-Sencicek, A Gulhan Gupta, Abha R Mane, Shrikant M Sheldon, Michael Brooks, Andrew I Roeder, Kathryn Devlin, Bernie State, Matthew W Wei, Liping Sanders, Stephan J Producer: 20150709 In: Cell reports vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	De novo mutations revealed by whole-exome sequencing are strongly associated with autism. [electronic resource] by Sanders, Stephan J Murtha, Michael T Gupta, Abha R Murdoch, John D Raubeson, Melanie J Willsey, A Jeremy Ercan-Sencicek, A Gulhan DiLullo, Nicholas M Parikshak, Neelroop N Stein, Jason L Walker, Michael F Ober, Gordon T Teran, Nicole A Song, Youeun El-Fishawy, Paul Murtha, Ryan C Choi, Murim Overton, John D Bjornson, Robert D Carriero, Nicholas J Meyer, Kyle A Bilguvar, Kaya Mane, Shrikant M Sestan, Nenad Lifton, Richard P Günel, Murat Roeder, Kathryn Geschwind, Daniel H Devlin, Bernie State, Matthew W Producer: 20120625 In: Nature vol. 485 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. [electronic resource] by Sanders, Stephan J Ercan-Sencicek, A Gulhan Hus, Vanessa Luo, Rui Murtha, Michael T Moreno-De-Luca, Daniel Chu, Su H Moreau, Michael P Gupta, Abha R Thomson, Susanne A Mason, Christopher E Bilguvar, Kaya Celestino-Soper, Patricia B S Choi, Murim Crawford, Emily L Davis, Lea Wright, Nicole R Davis Dhodapkar, Rahul M DiCola, Michael DiLullo, Nicholas M Fernandez, Thomas V Fielding-Singh, Vikram Fishman, Daniel O Frahm, Stephanie Garagaloyan, Rouben Goh, Gerald S Kammela, Sindhuja Klei, Lambertus Lowe, Jennifer K Lund, Sabata C McGrew, Anna D Meyer, Kyle A Moffat, William J Murdoch, John D O'Roak, Brian J Ober, Gordon T Pottenger, Rebecca S Raubeson, Melanie J Song, Youeun Wang, Qi Yaspan, Brian L Yu, Timothy W Yurkiewicz, Ilana R Beaudet, Arthur L Cantor, Rita M Curland, Martin Grice, Dorothy E Günel, Murat Lifton, Richard P Mane, Shrikant M Martin, Donna M Shaw, Chad A Sheldon, Michael Tischfield, Jay A Walsh, Christopher A Morrow, Eric M Ledbetter, David H Fombonne, Eric Lord, Catherine Martin, Christa Lese Brooks, Andrew I Sutcliffe, James S Cook, Edwin H Geschwind, Daniel Roeder, Kathryn Devlin, Bernie State, Matthew W Producer: 20110823 In: Neuron vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)