Nature and nurture in neuropsychiatric genetics: where do we stand?

por Dick, Danielle M., Riley, Brien, Kendler, Kenneth S.
Publicado 2010

Incorporating Genetics into Your Studies: A Guide for Social Scientists

por Dick, Danielle M., Latendresse, Shawn J., Riley, Brien
Publicado 2011

PATHWAY BASED ANALYSIS OF GENOTYPES IN RELATION TO ALCOHOL DEPENDENCE

por Reimers, Mark A, Riley, Brien P, Kalsi, Gursharan, Kertes, Darlene A, Kendler, Kenneth S
Publicado 2011

DIST: direct imputation of summary statistics for unmeasured SNPs

por Lee, Donghyung, Bigdeli, T. Bernard, Riley, Brien P., Fanous, Ayman H., Bacanu, Silviu-Alin
Publicado 2013

Cross-species alcohol dependence-associated gene networks: Co-analysis of mouse brain gene expression and human genome-wide association data

por Mignogna, Kristin M., Bacanu, Silviu A., Riley, Brien P., Wolen, Aaron R., Miles, Michael F.
Publicado 2019

JEPEG: a summary statistics based tool for gene-level joint testing of functional variants

por Lee, Donghyung, Williamson, Vernell S., Bigdeli, T. Bernard, Riley, Brien P., Fanous, Ayman H., Vladimirov, Vladimir I., Bacanu, Silviu-Alin
Publicado 2015

DISTMIX: direct imputation of summary statistics for unmeasured SNPs from mixed ethnicity cohorts

por Lee, Donghyung, Bigdeli, T. Bernard, Williamson, Vernell S., Vladimirov, Vladimir I., Riley, Brien P., Fanous, Ayman H., Bacanu, Silviu-Alin
Publicado 2015

Large-scale integration of DNA methylation and gene expression array platforms identifies both cis and trans relationships

por Lancaster, Eva E., Vladimirov, Vladimir I., Riley, Brien P., Landry, Joseph W., Roberson-Nay, Roxann, York, Timothy P.
Publicado 2022

Identifying potential risk genes and pathways for neuropsychiatric and substance use disorders using intermediate molecular mediator information

por Gedik, Huseyin, Nguyen, Tan Hoang, Peterson, Roseann E., Chatzinakos, Christos, Vladimirov, Vladimir I., Riley, Brien P., Bacanu, Silviu-Alin
Publicado 2023

A simple yet accurate correction for winner's curse can predict signals discovered in much larger genome scans

por Bigdeli, T. Bernard, Lee, Donghyung, Webb, Bradley Todd, Riley, Brien P., Vladimirov, Vladimir I., Fanous, Ayman H., Kendler, Kenneth S., Bacanu, Silviu-Alin
Publicado 2016

JEPEGMIX: gene-level joint analysis of functional SNPs in cosmopolitan cohorts

por Lee, Donghyung, Williamson, Vernell S., Bigdeli, T. Bernard, Riley, Brien P., Webb, Bradley T., Fanous, Ayman H., Kendler, Kenneth S., Vladimirov, Vladimir I., Bacanu, Silviu-Alin
Publicado 2016

Examining the source of increased bipolar disorder and major depressive disorder common risk variation burden in multiplex schizophrenia families

por Ahangari, Mohammad, Kirkpatrick, Robert, Nguyen, Tan-Hoang, Gillespie, Nathan, Kendler, Kenneth S., Bacanu, Silviu-Alin, Webb, Bradley T., Verrelli, Brian C., Riley, Brien P.
Publicado 2022

Schizophrenia Gene Networks and Pathways and Their Applications for Novel Candidate Gene Selection

por Sun, Jingchun, Jia, Peilin, Fanous, Ayman H., van den Oord, Edwin, Chen, Xiangning, Riley, Brien P., Amdur, Richard L., Kendler, Kenneth S., Zhao, Zhongming
Publicado 2010

Evaluating the role of common risk variation in the recurrence risk of schizophrenia in multiplex schizophrenia families

por Ahangari, Mohammad, Gentry, Amanda E., Nguyen, Tan-Hoang, Kirkpatrick, Robert, Verrelli, Brian C., Bacanu, Silviu-Alin, Kendler, Kenneth S., Webb, Bradley T., Riley, Brien P.
Publicado 2022

Relationship between polygenic risk scores and symptom dimensions of schizophrenia and schizotypy in multiplex families with schizophrenia

por Ahangari, Mohammad, Bustamante, Daniel, Kirkpatrick, Robert, Nguyen, Tan-Hoang, Verrelli, Brian C., Fanous, Ayman, Kendler, Kenneth S., Webb, Bradley T., Bacanu, Silviu-Alin, Riley, Brien P.
Publicado 2023

A serotonergic biobehavioral signature differentiates cocaine use disorder participants administered mirtazapine

por Ma, Liangsuo, Cunningham, Kathryn A., Anastasio, Noelle C., Bjork, James M., Taylor, Brian A., Arias, Albert J., Riley, Brien P., Snyder, Andrew D., Moeller, F. Gerard
Publicado 2022

Investigating the role of common and rare variants in multiplex multiple sclerosis families reveals an increased burden of common risk variation

por Everest, Elif, Ahangari, Mohammad, Uygunoglu, Ugur, Tutuncu, Melih, Bulbul, Alper, Saip, Sabahattin, Duman, Taskin, Sezerman, Ugur, Reich, Daniel S., Riley, Brien P., Siva, Aksel, Tahir Turanli, Eda
Publicado 2022

Replication of association between schizophrenia and ZNF804A in the Irish Case Control Study of Schizophrenia (ICCSS) sample

por Riley, Brien, Thiselton, Dawn, Maher, Brion S., Bigdeli, Tim, Wormley, Brandon, McMichael, G. Omari, Fanous, Ayman H., Vladimirov, Vladimir, O’Neill, F. Anthony, Walsh, Dermot, Kendler, Kenneth S.
Publicado 2009

mTADA is a framework for identifying risk genes from de novo mutations in multiple traits

por Nguyen, Tan-Hoang, Dobbyn, Amanda, Brown, Ruth C., Riley, Brien P., Buxbaum, Joseph D., Pinto, Dalila, Purcell, Shaun M., Sullivan, Patrick F., He, Xin, Stahl, Eli A.
Publicado 2020

Increasing the resolution and precision of psychiatric genome‐wide association studies by re‐imputing summary statistics using a large, diverse reference panel

por Chatzinakos, Chris, Lee, Donghyung, Cai, Na, Vladimirov, Vladimir I., Webb, Bradley T., Riley, Brien P., Flint, Jonathan, Kendler, Kenneth S., Ressler, Kerry J., Daskalakis, Nikolaos P., Bacanu, Silviu‐Alin
Publicado 2021