mGluR5-Antagonist Mediated Reversal of Elevated Stereotyped, Repetitive Behaviors in the VPA Model of Autism

por Mehta, Mili V., Gandal, Michael J., Siegel, Steven J.
Publicado 2011

A Critical Appraisal of Imaging Transcriptomics

por Mandal, Ayan S., Gandal, Michael, Seidlitz, Jakob, Alexander-Bloch, Aaron
Publicado 2022

Measuring the Maturity of the Fast-Spiking Interneuron Transcriptional Program in Autism, Schizophrenia, and Bipolar Disorder

por Gandal, Michael J., Nesbitt, Addie May, McCurdy, Richard M., Alter, Mark D.
Publicado 2012

Profiling allele specific gene expression in brains from individuals with autism spectrum disorder reveals preferential minor allele usage

por Lee, Changhoon, Kang, Eun Yong, Gandal, Michael J., Eskin, Eleazar, Geschwind, Daniel H.
Publicado 2019

GeneticsMakie.jl: a versatile and scalable toolkit for visualizing locus-level genetic and genomic data

por Kim, Minsoo, Vo, Daniel D, Kumagai, Michi E, Jops, Connor T, Gandal, Michael J
Publicado 2022

Neuron-specific transcriptomic signatures indicate neuroinflammation and altered neuronal activity in ASD temporal cortex

por Zhang, Pan, Omanska, Alicja, Ander, Bradley P., Gandal, Michael J., Stamova, Boryana, Schumann, Cynthia M.
Publicado 2023

Convergence of circuit dysfunction in ASD: a common bridge between diverse genetic and environmental risk factors and common clinical electrophysiology

por Port, Russell G., Gandal, Michael J., Roberts, Timothy P. L., Siegel, Steven J., Carlson, Gregory C.
Publicado 2014

Leveraging eQTLs to identify individual-level tissue of interest for a complex trait

por Majumdar, Arunabha, Giambartolomei, Claudia, Cai, Na, Haldar, Tanushree, Schwarz, Tommer, Gandal, Michael, Flint, Jonathan, Pasaniuc, Bogdan
Publicado 2021

Strong correlation of downregulated genes related to synaptic transmission and mitochondria in post-mortem autism cerebral cortex

por Schwede, Matthew, Nagpal, Shailender, Gandal, Michael J., Parikshak, Neelroop N., Mirnics, Karoly, Geschwind, Daniel H., Morrow, Eric M.
Publicado 2018

White matter microstructure shows sex differences in late childhood: Evidence from 6797 children

por Lawrence, Katherine E., Abaryan, Zvart, Laltoo, Emily, Hernandez, Leanna M., Gandal, Michael J., McCracken, James T., Thompson, Paul M.
Publicado 2022

150 risk variants for diverticular disease of intestine prioritize cell types and enable polygenic prediction of disease susceptibility

por Wu, Yeda, Goleva, Slavina B., Breidenbach, Lindsay B., Kim, Minsoo, MacGregor, Stuart, Gandal, Michael J., Davis, Lea K., Wray, Naomi R.
Publicado 2023

Association between resting-state functional brain connectivity and gene expression is altered in autism spectrum disorder

por Berto, Stefano, Treacher, Alex H., Caglayan, Emre, Luo, Danni, Haney, Jillian R., Gandal, Michael J., Geschwind, Daniel H., Montillo, Albert A., Konopka, Genevieve
Publicado 2022

Comparison of gene expression in living and postmortem human brain

por Collado-Torres, Leonardo, Klei, Lambertus, Liu, Chunyu, Kleinman, Joel E., Hyde, Thomas M., Geschwind, Daniel H., Gandal, Michael J., Devlin, Bernie, Weinberger, Daniel R.
Publicado 2023

Decoupling Sleep and Brain Size in Childhood: An Investigation of Genetic Covariation in the Adolescent Brain Cognitive Development Study

por Hernandez, Leanna M., Kim, Minsoo, Hernandez, Cristian, Thompson, Wesley, Fan, Chun Chieh, Galván, Adriana, Dapretto, Mirella, Bookheimer, Susan Y., Fuligni, Andrew, Gandal, Michael J.
Publicado 2022

Integrative genomics identifies a convergent molecular subtype that links epigenomic with transcriptomic differences in autism

por Ramaswami, Gokul, Won, Hyejung, Gandal, Michael J., Haney, Jillian, Wang, Jerry C., Wong, Chloe C. Y., Sun, Wenjie, Prabhakar, Shyam, Mill, Jonathan, Geschwind, Daniel H.
Publicado 2020

Brain gene co-expression networks link complement signaling with convergent synaptic pathology in schizophrenia

por Kim, Minsoo, Haney, Jillian R., Zhang, Pan, Hernandez, Leanna M., Wang, Lee-kai, Perez-Cano, Laura, Olde Loohuis, Loes M., de la Torre-Ubieta, Luis, Gandal, Michael J.
Publicado 2021

Multi-ancestry phenome-wide association of complement component 4 variation with psychiatric and brain phenotypes in youth

por Hernandez, Leanna M., Kim, Minsoo, Zhang, Pan, Bethlehem, Richard A. I., Hoftman, Gil, Loughnan, Robert, Smith, Diana, Bookheimer, Susan Y., Fan, Chun Chieh, Bearden, Carrie E., Thompson, Wesley K., Gandal, Michael J.
Publicado 2023

Spatial fine-mapping for gene-by-environment effects identifies risk hot spots for schizophrenia

por Fan, Chun Chieh, McGrath, John J., Appadurai, Vivek, Buil, Alfonso, Gandal, Michael J., Schork, Andrew J., Mortensen, Preben Bo, Agerbo, Esben, Geschwind, Sandy A., Geschwind, Daniel, Werge, Thomas, Thompson, Wesley K., Pedersen, Carsten Bøcker
Publicado 2018

Integrative network analysis reveals biological pathways associated with Williams syndrome

por Kimura, Ryo, Swarup, Vivek, Tomiwa, Kiyotaka, Gandal, Michael J., Parikshak, Neelroop N., Funabiki, Yasuko, Nakata, Masatoshi, Awaya, Tomonari, Kato, Takeo, Iida, Kei, Okazaki, Shin, Matsushima, Kanae, Kato, Toshihiro, Murai, Toshiya, Heike, Toshio, Geschwind, Daniel H., Hagiwara, Masatoshi
Publicado 2018

Associations between patterns in comorbid diagnostic trajectories of individuals with schizophrenia and etiological factors

por Krebs, Morten Dybdahl, Themudo, Gonçalo Espregueira, Benros, Michael Eriksen, Mors, Ole, Børglum, Anders D., Hougaard, David, Mortensen, Preben Bo, Nordentoft, Merete, Gandal, Michael J., Fan, Chun Chieh, Geschwind, Daniel H., Schork, Andrew J., Werge, Thomas, Thompson, Wesley K.
Publicado 2021