Combined linkage and linkage disequilibrium analysis of a motor speech phenotype within families ascertained for autism risk loci

por Flax, Judy F., Hare, Abby, Azaro, Marco A., Vieland, Veronica J., Brzustowicz, Linda M.
Publicado 2010

The Rosetta Phenotype Harmonization Method Facilitates Finding a Relationship Quantitative Trait Locus for a Complex Cognitive Trait

por Petrill, Stephen A., Klamer, Brett G., Buyske, Steven, Willcutt, Erik G., Gruen, Jeffrey R., Francis, David J., Flax, Judy F., Brzustowicz, Linda M., Bartlett, Christopher W.
Publicado 2023

MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders

por Wong, Anthony, Zhou, Anbo, Cao, Xiaolong, Mahaganapathy, Vaidhyanathan, Azaro, Marco, Gwin, Christine, Wilson, Sherri, Buyske, Steven, Bartlett, Christopher W., Flax, Judy F., Brzustowicz, Linda M., Xing, Jinchuan
Publicado 2022

Within-task variability on standardized language tests predicts autism spectrum disorder: a pilot study of the Response Dispersion Index

por Hare-Harris, Abby E., Mitchel, Marissa W., Myers, Scott M., Mitchel, Aaron D., King, Brian R., Ruocco, Brittany G., Martin, Christa Lese, Flax, Judy F., Brzustowicz, Linda M.
Publicado 2019

Structural Variations Contribute to the Genetic Etiology of Autism Spectrum Disorder and Language Impairments

por Alibutud, Rohan, Hansali, Sammy, Cao, Xiaolong, Zhou, Anbo, Mahaganapathy, Vaidhyanathan, Azaro, Marco, Gwin, Christine, Wilson, Sherri, Buyske, Steven, Bartlett, Christopher W., Flax, Judy F., Brzustowicz, Linda M., Xing, Jinchuan
Publicado 2023

Autism NPCs from both idiopathic and CNV 16p11.2 deletion patients exhibit dysregulation of proliferation and mitogenic responses

por Connacher, Robert, Williams, Madeline, Prem, Smrithi, Yeung, Percy L., Matteson, Paul, Mehta, Monal, Markov, Anna, Peng, Cynthia, Zhou, Xiaofeng, McDermott, Courtney R., Pang, Zhiping P., Flax, Judy, Brzustowicz, Linda, Lu, Che-Wei, Millonig, James H., DiCicco-Bloom, Emanuel
Publicado 2022

Autism NPCs from both idiopathic and CNV 16p11.2 deletion patients exhibit dysregulation of proliferation and mitogenic responses

por Connacher, Robert, Williams, Madeline, Prem, Smrithi, Yeung, Percy L., Matteson, Paul, Mehta, Monal, Markov, Anna, Peng, Cynthia, Zhou, Xiaofeng, McDermott, Courtney R., Pang, Zhiping P., Flax, Judy, Brzustowicz, Linda, Lu, Che-Wei, Millonig, James H., DiCicco-Bloom, Emanuel
Publicado 2022