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Localized JNK signaling regulates organ size during development.
Published in:
eLife, 2016, p. 1, doi. 10.7554/eLife.11491
By:
- Willsey, Helen Rankin;
- Xiaoyan Zheng;
- Pastor-Pareja, José Carlos;
- Willsey, A. Jeremy;
- Beachy, Philip A.;
- Tian Xu
Publication type:
Article
Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15 q11.2, Specifically Breakpoints 1 to 2.
Published in:
Autism Research: Official Journal of the International Society for Autism Research, 2014, v. 7, n. 3, p. 355, doi. 10.1002/aur.1378
By:
- Chaste, Pauline;
- Sanders, Stephan J.;
- Mohan, Kommu N.;
- Klei, Lambertus;
- Song, Youeun;
- Murtha, Michael T.;
- Hus, Vanessa;
- Lowe, Jennifer K.;
- Willsey, A. Jeremy;
- Moreno‐De‐Luca, Daniel;
- Yu, Timothy W.;
- Fombonne, Eric;
- Geschwind, Daniel;
- Grice, Dorothy E.;
- Ledbetter, David H.;
- Lord, Catherine;
- Mane, Shrikant M.;
- Martin, Donna M.;
- Morrow, Eric M.;
- Walsh, Christopher A.
Publication type:
Article
The female protective effect in autism spectrum disorder is not mediated by a single genetic locus.
Published in:
Molecular Autism, 2015, v. 6, n. 1, p. 1, doi. 10.1186/s13229-015-0014-3
By:
- Gockley, Jake;
- Willsey, A. Jeremy;
- Shan Dong;
- Dougherty, Joseph D.;
- Constantino, John N.;
- Sanders, Stephan J.
Publication type:
Article
DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics.
Published in:
Molecular Autism, 2014, v. 5, n. 1, p. 1, doi. 10.1186/2040-2392-5-22
By:
- Li Liu;
- Jing Lei;
- Sanders, Stephan J.;
- Willsey, Arthur Jeremy;
- Yan Kou;
- Cicek, Abdullah Ercument;
- Klei, Lambertus;
- Cong Lu;
- Xin He;
- Mingfeng Li;
- Muhle, Rebecca A.;
- Ma'ayan, Avi;
- Noonan, James P.;
- Sestan, Nenad;
- McFadden, Kathryn A.;
- State, Matthew W.;
- Buxbaum, Joseph D.;
- Devlin, Bernie;
- Roeder, Kathryn
Publication type:
Article
Common genetic variants, acting additively, are a major source of risk for autism.
Published in:
Molecular Autism, 2012, v. 3, n. 1, p. 1, doi. 10.1186/2040-2392-3-9
By:
- Klei, Lambertus;
- Sanders, Stephan J.;
- Murtha, Michael T.;
- Hus, Vanessa;
- Lowe, Jennifer K.;
- Jeremy Willsey, A.;
- Moreno-De-Luca, Daniel;
- Yu, Timothy W.;
- Fombonne, Eric;
- Geschwind, Daniel;
- Grice, Dorothy E.;
- Ledbetter, David H.;
- Lord, Catherine;
- Mane, Shrikant M.;
- Martin, Christa Lese;
- Martin, Donna M.;
- Morrow, Eric M.;
- Walsh, Christopher A.;
- Melhem, Nadine M.;
- Chaste, Pauline
Publication type:
Article
The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery.
Published in:
Frontiers in Neuroscience, 2016, p. 1, doi. 10.3389/fnins.2016.00351
By:
- Georgitsi, Marianthi;
- Willsey, A. Jeremy;
- Mathews, Carol A.;
- State, Matthew;
- Scharf, Jeremiah M.;
- Paschou, Peristera;
- Maniadaki, Katerina;
- Kandasamy, Preeti
Publication type:
Article
The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery.
Published in:
Frontiers in Neuroscience, 2016, p. 1, doi. 10.3389/fnins.2016.00351
By:
- Georgitsi, Marianthi;
- Willsey, A. Jeremy;
- Mathews, Carol A.;
- State, Matthew;
- Scharf, Jeremiah M.;
- Paschou, Peristera;
- Maniadaki, Katerina;
- Kandasamy, Preeti
Publication type:
Article
The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment.
Published in:
Nature Communications, 2015, v. 6, n. 3, p. 6404, doi. 10.1038/ncomms7404
By:
- Cotney, Justin;
- Muhle, Rebecca A.;
- Sanders, Stephan J.;
- Liu, Li;
- Willsey, A. Jeremy;
- Niu, Wei;
- Liu, Wenzhong;
- Klei, Lambertus;
- Lei, Jing;
- Yin, Jun;
- Reilly, Steven K.;
- Tebbenkamp, Andrew T.;
- Bichsel, Candace;
- Pletikos, Mihovil;
- Sestan, Nenad;
- Roeder, Kathryn;
- State, Matthew W.;
- Devlin, Bernie;
- Noonan, James P.
Publication type:
Article
De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Published in:
Nature, 2012, v. 485, n. 7397, p. 237, doi. 10.1038/nature10945
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.
Publication type:
Article
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.
Published in:
PLoS Genetics, 2015, v. 11, n. 1, p. 1, doi. 10.1371/journal.pgen.1004852
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.
Publication type:
Article

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