Bernard Devlin, Ph.D.

Affiliations: 
Human Genetics University of Pittsburgh, Pittsburgh, PA, United States 
Area:
Human Genetics
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"Bernard Devlin"

Collaborators

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Matthew W. State collaborator UPMC (Neurotree)
Carl D. Schlichting collaborator 1985-1990 Penn State
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Publications

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Yurko R, G'Sell M, Roeder K, et al. (2020) A selective inference approach for false discovery rate control using multiomics covariates yields insights into disease risk. Proceedings of the National Academy of Sciences of the United States of America
Werling DM, Pochareddy S, Choi J, et al. (2020) Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex. Cell Reports. 31: 107489
Sanders SJ, He X, Willsey AJ, et al. (2015) Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci. Neuron. 87: 1215-1233
Cotney J, Muhle RA, Sanders SJ, et al. (2015) The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment. Nature Communications. 6: 6404
Chaste P, Klei L, Sanders SJ, et al. (2015) A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity? Biological Psychiatry. 77: 775-84
De Rubeis S, He X, Goldberg AP, et al. (2014) Synaptic, transcriptional and chromatin genes disrupted in autism. Nature. 515: 209-15
Dong S, Walker MF, Carriero NJ, et al. (2014) De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder. Cell Reports. 9: 16-23
Samocha KE, Robinson EB, Sanders SJ, et al. (2014) A framework for the interpretation of de novo mutation in human disease. Nature Genetics. 46: 944-50
Gaugler T, Klei L, Sanders SJ, et al. (2014) Most genetic risk for autism resides with common variation. Nature Genetics. 46: 881-5
Melhem NM, Lu C, Dresbold C, et al. (2014) Characterizing runs of homozygosity and their impact on risk for psychosis in a population isolate. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 165: 521-30
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