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B. Devlin · SciRah

Researcher profile · Semantic Scholar

B. Devlin

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B. Devlin — researcher profile on SciRah

h-index: 78
Works: 234
Citations: 42K

Most-cited papers

Identification of common genetic risk variants for autism spectrum disorder
J. Grove, S. Ripke, T. Als, M. Mattheisen +272 more
2019Nature Genetics2,146 citations Open access
Semantic Scholar
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F. Satterstrom, Jack A. Kosmicki, Jiebiao Wang, M. Breen +186 more
2019Cell2,103 citations Open access
Semantic Scholar
Gene Expression Elucidates Functional Impact of Polygenic Risk for Schizophrenia
M. Fromer, P. Roussos, S. Sieberts, Jessica S. Johnson +54 more
2016Nature Neuroscience1,097 citations Open access
Semantic Scholar
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Jack M. Fu, F. Satterstrom, Minshi Peng, H. Brand +113 more
2022Nature Genetics554 citations Open access
Semantic Scholar
Refining the role of de novo protein truncating variants in neurodevelopmental disorders using population reference samples
Jack A. Kosmicki, K. Samocha, D. Howrigan, Stephan J Sanders +12 more
2016Nature Genetics375 citations Open access
Semantic Scholar
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder
Joon-Yong An, K. Lin, Lingxue Zhu, D. Werling +31 more
2018Science298 citations Open access
Semantic Scholar
An analytical framework for whole genome sequence association studies and its implications for autism spectrum disorder
D. Werling, H. Brand, Joon-Yong An, M. Stone +43 more
2018Nature Genetics257 citations Open access
Semantic Scholar
CommonMind Consortium provides transcriptomic and epigenomic data for Schizophrenia and Bipolar Disorder
G. Hoffman, J. Bendl, G. Voloudakis, Kelsey S. Montgomery +26 more
2019Scientific Data237 citations Open access
Semantic Scholar
Gene expression imputation across multiple brain regions provides insights into schizophrenia risk.
Laura M. Huckins, Amanda Dobbyn, D. Ruderfer, G. Hoffman +25 more
2019Nature Genetics189 citations Open access
Semantic Scholar
A pleiotropic missense variant in SLC39A8 is associated with Crohn’s disease and human gut microbiome composition
Dalin Li, J. Achkar, T. Haritunians, J. Jacobs +36 more
2016Gastroenterology138 citations Open access
Semantic Scholar
Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex
D. Werling, Sirisha Pochareddy, Jinmyung Choi, Joon-Yong An +29 more
2019bioRxiv137 citations Open access
Semantic Scholar
Common risk variants identified in autism spectrum disorder
J. Grove, S. Ripke, T. Als, M. Mattheisen +71 more
2017bioRxiv105 citations Open access
Semantic Scholar
Global landscape and genetic regulation of RNA editing in cortical samples from individuals with schizophrenia
M. Breen, Amanda Dobbyn, Qin Li, P. Roussos +61 more
2019Nature Neuroscience100 citations Open access
Semantic Scholar
De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 families
Jonathan R. Belyeu, H. Brand, Harold Wang, Xue-Fang Zhao +11 more
2020bioRxiv98 citations Open access
Semantic Scholar
Investigating Shared Genetic Basis Across Tourette Syndrome and Comorbid Neurodevelopmental Disorders Along the Impulsivity-Compulsivity Spectrum
Zhiyu Yang, Hanrui Wu, P. Lee, Fotis Tsetsos +21 more
2021Biological Psychiatry84 citations Open access
Semantic Scholar
Bayesian estimation of cell type–specific gene expression with prior derived from single-cell data
Jiebiao Wang, K. Roeder, B. Devlin
2021Genome Research79 citations Open access
Semantic Scholar
Semisoft clustering of single-cell data
Lingxue Zhu, Jing Lei, L. Klei, B. Devlin +1 more
2018Proceedings of the National Academy of Sciences of the United States of America75 citations Open access
Semantic Scholar
Genetic Risk for Schizophrenia and Psychosis in Alzheimer Disease
M. A. DeMichele-Sweet, E. Weamer, L. Klei, D. T. Vrana +16 more
2017Molecular Psychiatry72 citations Open access
Semantic Scholar
A UNIFIED STATISTICAL FRAMEWORK FOR SINGLE CELL AND BULK RNA SEQUENCING DATA
Lingxue Zhu, Jing Lei, B. Devlin, K. Roeder
2016bioRxiv70 citations Open access
Semantic Scholar
An interactome perturbation framework prioritizes damaging missense mutations for developmental disorders
Siwei Chen, Robert Fragoza, L. Klei, Yuan Liu +4 more
2018Nature Genetics67 citations Open access
Semantic Scholar
Genome-Wide Association Identifies the First Risk Loci for Psychosis in Alzheimer Disease
M. A. DeMichele-Sweet, L. Klei, B. Creese, J. Harwood +40 more
2020Molecular Psychiatry61 citations Open access
Semantic Scholar
Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk
F. Satterstrom, Jack A. Kosmicki, Jiebiao Wang, M. Breen +153 more
2018bioRxiv60 citations Open access
Semantic Scholar
Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies.
Chelsea Lowther, E. Valkanas, J. Giordano, Harold Wang +41 more
2023American Journal of Human Genetics54 citations Open access
Semantic Scholar
Sex differences in the human brain transcriptome of cases with schizophrenia
G. Hoffman, Yixuan Ma, Kelsey S. Montgomery, J. Bendl +9 more
2020bioRxiv53 citations Open access
Semantic Scholar
Population-level variation in enhancer expression identifies disease mechanisms in the human brain
P. Dong, G. Hoffman, Pasha Apontes, J. Bendl +49 more
2022Nature Genetics49 citations Open access
Semantic Scholar
The Yin and Yang of Autism Genetics: How Rare De Novo and Common Variations Affect Liability.
P. Chaste, K. Roeder, B. Devlin
2017Annual review of genomics and human genetics (Print)49 citations Open access
Semantic Scholar
How rare and common risk variation jointly affect liability for autism spectrum disorder
L. Klei, L. McClain, B. Mahjani, K. Panayidou +12 more
2020Molecular Autism48 citations Open access
Semantic Scholar
Differential Activity of Transcribed Enhancers in the Prefrontal Cortex of 537 cases with Schizophrenia and Controls
M. Hauberg, J. Fullard, Lingxue Zhu, A. Cohain +16 more
2018Molecular Psychiatry45 citations Open access
Semantic Scholar
Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden
B. Yip, Dan Bai, B. Mahjani, L. Klei +8 more
2017Biological Psychiatry44 citations Open access
Semantic Scholar
Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder
B. Mahjani, S. de Rubeis, Christina Gustavsson Mahjani, Maureen S. Mulhern +12 more
2021Molecular Autism41 citations Open access
Semantic Scholar
Functional connectome fingerprinting accuracy in youths and adults is similar when examined on the same day and 1.5‐years apart
M. Jalbrzikowski, Fuchen Liu, William Foran, L. Klei +4 more
2020Human Brain Mapping36 citations Open access
Semantic Scholar
Maternal Effects as Causes of Risk for Obsessive-Compulsive Disorder
B. Mahjani, L. Klei, C. Hultman, H. Larsson +4 more
2020Biological Psychiatry35 citations Open access
Semantic Scholar
Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism
Jack M. Fu, F. Satterstrom, Minshi Peng, H. Brand +61 more
2021medRxiv34 citations Open access
Semantic Scholar
The genetic architecture of obsessive-compulsive disorder: alleles across the frequency spectrum contribute liability to OCD.
B. Mahjani, L. Klei, M. Mattheisen, M. Halvorsen +16 more
2021American Journal of Psychiatry33 citations Open access
Semantic Scholar
Using multiple measurements of tissue to estimate subject- and cell-type-specific gene expression
Jiebiao Wang, B. Devlin, K. Roeder
2019Bioinform.33 citations Open access
Semantic Scholar
Transcriptome alterations are enriched for synapse-associated genes in the striatum of subjects with obsessive-compulsive disorder
Sean C. Piantadosi, L. McClain, L. Klei, Jiebiao Wang +5 more
2020bioRxiv30 citations Open access
Semantic Scholar
De novo missense variants disrupting protein–protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types
Si-Wei Chen, Jiebiao Wang, E. Cicek, K. Roeder +2 more
2020Molecular Autism28 citations Open access
Semantic Scholar
Cognitive and default mode networks support developmental stability in functional connectome fingerprinting through adolescence
M. Jalbrzikowski, Fuchen Liu, William Foran, L. Klei +4 more
2019bioRxiv22 citations Open access
Semantic Scholar
H-MAGMA, inheriting a shaky statistical foundation, yields excess false positives
Ronald Yurko, K. Roeder, B. Devlin, Max G'Sell
2020bioRxiv21 citations Open access
Semantic Scholar
Transcriptomic Imputation of Bipolar Disorder and Bipolar subtypes reveals 29 novel associated genes
Laura M. Huckins, Amanda Dobbyn, Whitney Mcfadden, Wei-Qing Wang +16 more
2017bioRxiv20 citations Open access
Semantic Scholar
Schizophrenia-associated differential DNA methylation in brain is distributed across the genome and annotated to MAD1L1, a locus at which DNA methylation and transcription phenotypes share genetic variation with schizophrenia risk
B. McKinney, L. McClain, C. Hensler, Yue Wei +6 more
2022Translational Psychiatry19 citations Open access
Semantic Scholar
Cohort profile: Epidemiology and Genetics of Obsessive–compulsive disorder and chronic tic disorders in Sweden (EGOS)
B. Mahjani, Karin Dellenvall, Anna-Carin Säll Grahnat, G. Karlsson +11 more
2020Social Psychiatry and Psychiatric Epidemiology18 citations
Semantic Scholar
A method to exploit the structure of genetic ancestry space to enhance case-control studies
Corneliu Bodea, B. Neale, S. Ripke, M. Daly +2 more
2016bioRxiv18 citations Open access
Semantic Scholar
Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families
D. Werling, H. Brand, Joon-Yong An, M. Stone +41 more
2017bioRxiv16 citations Open access
Semantic Scholar
A selective inference approach for false discovery rate control using multiomics covariates yields insights into disease risk
Ronald Yurko, Max G'Sell, K. Roeder, B. Devlin
2020Proceedings of the National Academy of Sciences of the United States of America15 citations Open access
Semantic Scholar
Not All Autism Genes Are Created Equal: A Response to Myers et al.
J. Buxbaum, D. Cutler, M. Daly, B. Devlin +2 more
2020American Journal of Human Genetics14 citations Open access
Semantic Scholar
Comment on: What genes are differentially expressed in individuals with schizophrenia? A systematic review
G. Hoffman, A. Jaffe, Michael Jeffrey Gandal, L. Collado-Torres +5 more
2022Molecular Psychiatry12 citations Open access
Semantic Scholar
Systematic evaluation of genome sequencing for the assessment of fetal structural anomalies
Chelsea Lowther, E. Valkanas, J. Giordano, Harold Wang +41 more
2020bioRxiv12 citations Open access
Semantic Scholar
Cross-disorder GWAS meta-analysis for Attention Deficit/Hyperactivity Disorder, Autism Spectrum Disorder, Obsessive Compulsive Disorder, and Tourette Syndrome
Zhiyu Yang, Hanrui Wu, P. Lee, Fotis Tsetsos +21 more
201911 citations Open access
Semantic Scholar
Gene expression imputation across multiple brain regions reveals schizophrenia risk throughout development
Laura M. Huckins, Amanda Dobbyn, D. Ruderfer, G. Hoffman +24 more
2017bioRxiv10 citations Open access
Semantic Scholar

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