Shedding new light on genetic dark matter

por Melhem, Nadine, Devlin, Bernie
Publicado 2010

Using multiple measurements of tissue to estimate subject- and cell-type-specific gene expression

por Wang, Jiebiao, Devlin, Bernie, Roeder, Kathryn
Publicado 2020

Bayesian estimation of cell type–specific gene expression with prior derived from single-cell data

por Wang, Jiebiao, Roeder, Kathryn, Devlin, Bernie
Publicado 2021

Intelligence, genes, and success: scientists respond to the bell curve

por Devlin, Bernie, Fienberg, Stephen, Resnick, Daniel, Roeder, Kathryn
Publicado 1997

Genetics in psychiatry: common variant association studies

por Buxbaum, Joseph D, Baron-Cohen, Simon, Devlin, Bernie
Publicado 2010

Integration of association statistics over genomic regions using Bayesian adaptive regression splines

por Zhang, Xiaohua, Roeder, Kathryn, Wallstrom, Garrick, Devlin, Bernie
Publicado 2003

A selective inference approach for false discovery rate control using multiomics covariates yields insights into disease risk

por Yurko, Ronald, G’Sell, Max, Roeder, Kathryn, Devlin, Bernie
Publicado 2020

Semisoft clustering of single-cell data

por Zhu, Lingxue, Lei, Jing, Klei, Lambertus, Devlin, Bernie, Roeder, Kathryn
Publicado 2019

O11.1. MULTIPLE GENOMIC MEASURES OF SCHIZOPHRENIA RISK ARE RELATED TO CORTICAL THICKNESS IN TYPICALLY DEVELOPING YOUTH AND YOUNG ADULTS

por Jalbrzikowski, Maria, Klei, Lambertus, Foran, William, Luna, Beatriz, Devlin, Bernie
Publicado 2020

De novo missense variants disrupting protein–protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types

por Chen, Siwei, Wang, Jiebiao, Cicek, Ercument, Roeder, Kathryn, Yu, Haiyuan, Devlin, Bernie
Publicado 2020

Functional connectome fingerprinting accuracy in youths and adults is similar when examined on the same day and 1.5‐years apart

por Jalbrzikowski, Maria, Liu, Fuchen, Foran, William, Klei, Lambertus, Calabro, Finnegan J., Roeder, Kathryn, Devlin, Bernie, Luna, Beatriz
Publicado 2020

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

The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer’s disease

por Stutzbach, Lauren D, Xie, Sharon X, Naj, Adam C, Albin, Roger, Gilman, Sid, Lee, Virginia M Y, Trojanowski, John Q, Devlin, Bernie, Schellenberg, Gerard D
Publicado 2013

Global landscape and genetic regulation of RNA editing in cortical samples from individuals with schizophrenia

por Breen, Michael S., Dobbyn, Amanda, Li, Qin, Roussos, Panos, Hoffman, Gabriel E., Stahl, Eli, Chess, Andrew, Sklar, Pamela, Li, Jin Billy, Devlin, Bernie, Buxbaum, Joseph D.
Publicado 2019

Transcriptome alterations are enriched for synapse-associated genes in the striatum of subjects with obsessive-compulsive disorder

por Piantadosi, Sean C., McClain, Lora L., Klei, Lambertus, Wang, Jiebiao, Chamberlain, Brittany L., Springer, Sara A., Lewis, David A., Devlin, Bernie, Ahmari, Susanne E.
Publicado 2021

Testing for an Unusual Distribution of Rare Variants

por Neale, Benjamin M., Rivas, Manuel A., Voight, Benjamin F., Altshuler, David, Devlin, Bernie, Orho-Melander, Marju, Kathiresan, Sekar, Purcell, Shaun M., Roeder, Kathryn, Daly, Mark J.
Publicado 2011

Incomplete response in late-life depression: getting to remission

por Lenze, Eric J., Sheffrin, Meera, Driscoll, Henry C, Mulsant, Benoit H., Pollock, Bruce G., Amanda Dew, Mary, Lotrich, Frank, Devlin, Bernie, Bies, Robert, Reynolds III, Charles F.
Publicado 2008

Schizophrenia-associated differential DNA methylation in brain is distributed across the genome and annotated to MAD1L1, a locus at which DNA methylation and transcription phenotyp...

por McKinney, Brandon C., McClain, Lora L., Hensler, Christopher M., Wei, Yue, Klei, Lambertus, Lewis, David A., Devlin, Bernie, Wang, Jiebiao, Ding, Ying, Sweet, Robert A.
Publicado 2022

Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden

por Yip, Benjamin Hon Kei, Bai, Dan, Mahjani, Behrang, Klei, Lambertus, Pawitan, Yudi, Hultman, Christina M., Grice, Dorothy E., Roeder, Kathryn, Buxbaum, Joseph D., Devlin, Bernie, Reichenberg, Abraham, Sandin, Sven
Publicado 2017

Integrated Model of De Novo and Inherited Genetic Variants Yields Greater Power to Identify Risk Genes

por He, Xin, Sanders, Stephan J., Liu, Li, De Rubeis, Silvia, Lim, Elaine T., Sutcliffe, James S., Schellenberg, Gerard D., Gibbs, Richard A., Daly, Mark J., Buxbaum, Joseph D., State, Matthew W., Devlin, Bernie, Roeder, Kathryn
Publicado 2013