miRNA-mediated risk for schizophrenia in 22q11.2 deletion syndrome

por Brzustowicz, Linda M., Bassett, Anne S.
Publicado 2012

Validation of a Cost-Efficient Multi-Purpose SNP Panel for Disease Based Research

por Hou, Liping, Phillips, Christopher, Azaro, Marco, Brzustowicz, Linda M., Bartlett, Christopher W.
Publicado 2011

Chronological Changes in MicroRNA Expression in the Developing Human Brain

por Moreau, Michael P., Bruse, Shannon E., Jornsten, Rebecka, Liu, Yushi, Brzustowicz, Linda M.
Publicado 2013

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

Increased Expression in Dorsolateral Prefrontal Cortex of CAPON in Schizophrenia and Bipolar Disorder

por Xu, Bin, Wratten, Naomi, Charych, Erik I, Buyske, Steven, Firestein, Bonnie L, Brzustowicz, Linda M
Publicado 2005

Meta-Analysis of Repository Data: Impact of Data Regularization on NIMH Schizophrenia Linkage Results

por Walters, Kimberly A., Huang, Yungui, Azaro, Marco, Tobin, Kathleen, Lehner, Thomas, Brzustowicz, Linda M., Vieland, Veronica J.
Publicado 2014

Autism Associated Gene, ENGRAILED2, and Flanking Gene Levels Are Altered in Post-Mortem Cerebellum

por Choi, Jiyeon, Ababon, Myka R., Soliman, Mai, Lin, Yong, Brzustowicz, Linda M., Matteson, Paul G., Millonig, James H.
Publicado 2014

Overexpression of Isoforms of Nitric Oxide Synthase 1 Adaptor Protein, Encoded by a Risk Gene for Schizophrenia, Alters Actin Dynamics and Synaptic Function

por Hernandez, Kristina, Swiatkowski, Przemyslaw, Patel, Mihir V., Liang, Chen, Dudzinski, Natasha R., Brzustowicz, Linda M., Firestein, Bonnie L.
Publicado 2016

MicroRNA Dysregulation, Gene Networks, and Risk for Schizophrenia in 22q11.2 Deletion Syndrome

por Merico, Daniele, Costain, Gregory, Butcher, Nancy J., Warnica, William, Ogura, Lucas, Alfred, Simon E., Brzustowicz, Linda M., Bassett, Anne S.
Publicado 2014

Validation of a microRNA target site polymorphism in H3F3B that is potentially associated with a broad schizophrenia phenotype

por Manley, William, Moreau, Michael P., Azaro, Marco, Siecinski, Stephen K., Davis, Gillian, Buyske, Steven, Vieland, Veronica, Bassett, Anne S., Brzustowicz, Linda
Publicado 2018

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