Bernie J Devlin, PhD

Professor of Psychiatry and Clinical and Translational Science

Contact Details

3811 O'Hara St.

Education & Training

Botany, Pennsylvania State University

Professional Affiliations

Fellow, American Association for the Advancement of Science
Member, American Society of Human Genetics
Member, International Society for Autism Research

Selected Honors & Awards

MERIT Award, National Institute of Mental Health
Fellow, American Association for the Advancement of Science, Statistics, Section U

Research Interests

Genetic basis of disease and disorders; Statistical genetics; Genomics, transcriptomics & proteomics
Selected Research Publications & Products
  1. Fu JM, Satterstrom FK, Peng M, Brand H, Collins RL, Dong S, Wamsley B, Klei L, Wang L, Hao SP, Stevens CR, Cusick C, Babadi M, Banks E, Collins B, Dodge S, Gabriel SB, Gauthier L, Lee SK, Liang L, Ljungdahl A, Mahjani B, Sloofman L, Smirnov AN, Barbosa M, Betancur C, Brusco A, Chung BHY, Cook EH, Cuccaro ML, Domenici E, Ferrero GB, Gargus JJ, Herman GE, Hertz-Picciotto I, Maciel P, Manoach DS, Passos-Bueno MR, Persico AM, Renieri A, Sutcliffe JS, Tassone F, Trabetti E, Campos G, Cardaropoli S, Carli D, Chan MCY, Fallerini C, Giorgio E, Girardi AC, Hansen-Kiss E, Lee SL, Lintas C, Ludena Y, Nguyen R, Pavinato L, Pericak-Vance M, Pessah IN, Schmidt RJ, Smith M, Costa CIS, Trajkova S, Wang JYT, Yu MHC; Autism Sequencing Consortium (ASC); Broad Institute Center for Common Disease Genomics (Broad-CCDG); iPSYCH-BROAD Consortium, Cutler DJ, De Rubeis S, Buxbaum JD, Daly MJ, Devlin B, Roeder K, Sanders SJ, Talkowski ME. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. Nature Genetics doi: 10.1038/s41588-022-01104-0, 2022. PMID: 35982160
  2. Wang J, Roeder K, Devlin B. Bayesian estimation of cell type-specific gene expression with prior derived from single-cell data. Genome Research 31:1807-1818, 2021. PMID: 33837133
  3. 229.Klei L, McClain LL, Mahjani B, Panayidou K, De Rubeis S, Grahnat AS, Karlsson G, Lu Y, Melhem N, Xu X, Reichenberg A, Sandin S, Hultman CM, Buxbaum JD, Roeder K, Devlin B. How rare and common risk variation jointly affect liability for autism spectrum disorder. Molecular Autism 12:66, 2021. PMID: 34615521
  4. Yurko R, GSell M, Roeder K, Devlin B. A selective inference approach for FDR control using multi-omics covariates yields insights into disease risk. Proceedings of the National Academy of Sciences, 117:15028-15035, 2020. PMID: 32522875
  5. Breen MS, Dobbyn A, Li Q, Roussos P, Hoffman GE, Stahl E, Chess A, Sklar P, Li JB, Devlin B, Buxbaum JD; Common Mind Consortium. Global landscape and genetic regulation of RNA editing in cortical samples from individuals with schizophrenia. Nature Neuroscience 22:1402-1412, 2019. PMID: 31455887