forestSV: structural variant discovery through statistical learning

por Michaelson, Jacob J., Sebat, Jonathan
Publicado 2012

SLINGER: large-scale learning for predicting gene expression

por Vervier, Kévin, Michaelson, Jacob J.
Publicado 2016

TiSAn: estimating tissue-specific effects of coding and non-coding variants

por Vervier, Kévin, Michaelson, Jacob J
Publicado 2018

cerebroViz: an R package for anatomical visualization of spatiotemporal brain data

por Bahl, Ethan, Koomar, Tanner, Michaelson, Jacob J
Publicado 2017

Forecasting risk gene discovery in autism with machine learning and genome-scale data

por Brueggeman, Leo, Koomar, Tanner, Michaelson, Jacob J.
Publicado 2020

Author Correction: Forecasting risk gene discovery in autism with machine learning and genome-scale data

por Brueggeman, Leo, Koomar, Tanner, Michaelson, Jacob J.
Publicado 2020

Data-driven assessment of eQTL mapping methods

por Michaelson, Jacob J, Alberts, Rudi, Schughart, Klaus, Beyer, Andreas
Publicado 2010

Teamwork: Improved eQTL Mapping Using Combinations of Machine Learning Methods

por Ackermann, Marit, Clément-Ziza, Mathieu, Michaelson, Jacob J., Beyer, Andreas
Publicado 2012

Integrated genetic and epigenetic prediction of coronary heart disease in the Framingham Heart Study

por Dogan, Meeshanthini V., Grumbach, Isabella M., Michaelson, Jacob J., Philibert, Robert A.
Publicado 2018

Whole-genome sequencing in a family with twin boys with autism and intellectual disability suggests multimodal polygenic risk

por McKenna, Brooke, Koomar, Tanner, Vervier, Kevin, Kremsreiter, Jamie, Michaelson, Jacob J.
Publicado 2018

Estimating the Prevalence and Genetic Risk Mechanisms of ARFID in a Large Autism Cohort

por Koomar, Tanner, Thomas, Taylor R., Pottschmidt, Natalie R., Lutter, Michael, Michaelson, Jacob J.
Publicado 2021

Altered hippocampal transcriptome dynamics following sleep deprivation

por Gaine, Marie E., Bahl, Ethan, Chatterjee, Snehajyoti, Michaelson, Jacob J., Abel, Ted, Lyons, Lisa C.
Publicado 2021

Clinical autism subscales have common genetic liabilities that are heritable, pleiotropic, and generalizable to the general population

por Thomas, Taylor R., Koomar, Tanner, Casten, Lucas G., Tener, Ashton J., Bahl, Ethan, Michaelson, Jacob J.
Publicado 2022

Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language Development

por Mueller, Kathryn L., Murray, Jeffrey C., Michaelson, Jacob J., Christiansen, Morten H., Reilly, Sheena, Tomblin, J. Bruce
Publicado 2016

Mapping the spatial transcriptomic signature of the hippocampus during memory consolidation

por Vanrobeys, Yann, Mukherjee, Utsav, Langmack, Lucy, Bahl, Ethan, Lin, Li-Chun, Michaelson, Jacob J, Abel, Ted, Chatterjee, Snehajyoti
Publicado 2023

Novel and ultra-rare damaging variants in neuropeptide signaling are associated with disordered eating behaviors

por Lutter, Michael, Bahl, Ethan, Hannah, Claire, Hofammann, Dabney, Acevedo, Summer, Cui, Huxing, McAdams, Carrie J., Michaelson, Jacob J.
Publicado 2017

Mapping the spatial transcriptomic signature of the hippocampus during memory consolidation

por Vanrobaeys, Yann, Mukherjee, Utsav, Langmack, Lucy, Beyer, Stacy E., Bahl, Ethan, Lin, Li-Chun, Michaelson, Jacob J., Abel, Ted, Chatterjee, Snehajyoti
Publicado 2023

Community attitudes on genetic research of gender identity, sexual orientation, and mental health

por Thomas, Taylor R., Hofammann, Dabney, McKenna, Brooke G., I. R. van der Miesen, Anna, Stokes, Mark A., Daniolos, Peter, Michaelson, Jacob J.
Publicado 2020

Integrative Analysis of Low- and High-Resolution eQTL

por Loguercio, Salvatore, Overall, Rupert W., Michaelson, Jacob J., Wiltshire, Tim, Pletcher, Mathew T., Miller, Brooke H., Walker, John R., Kempermann, Gerd, Su, Andrew I., Beyer, Andreas
Publicado 2010

Transcriptional signatures of regulatory and toxic responses to benzo-[a]-pyrene exposure

por Michaelson, Jacob J, Trump, Saskia, Rudzok, Susanne, Gräbsch, Carolin, Madureira, Danielle J, Dautel, Franziska, Mai, Juliane, Attinger, Sabine, Schirmer, Kristin, von Bergen, Martin, Lehmann, Irina, Beyer, Andreas
Publicado 2011