Arthur J. Willsey, Ph.D.

Affiliations: 
2014 Yale University, New Haven, CT 
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"Arthur Willsey"
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Matthew W. State grad student 2014 Yale
 (A spatiotemporal systems biology approach to understanding autism spectrum disorder.)
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Rosenthal SB, Willsey HR, Xu Y, et al. (2021) A convergent molecular network underlying autism and congenital heart disease. Cell Systems
Yu D, Sul JH, Tsetsos F, et al. (2019) Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. The American Journal of Psychiatry. 176: 217-227
Wang S, Mandell JD, Kumar Y, et al. (2018) De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis. Cell Reports. 25: 3544
An JY, Lin K, Zhu L, et al. (2018) Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder. Science (New York, N.Y.). 362
Wang S, Mandell JD, Kumar Y, et al. (2018) De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis. Cell Reports. 24: 3441-3454.e12
Willsey AJ, Morris MT, Wang S, et al. (2018) The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders. Cell. 174: 505-520
Werling DM, Brand H, An JY, et al. (2018) An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder. Nature Genetics
Sanders SJ, Neale BM, Huang H, et al. (2018) Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium. Nature Neuroscience
Sanders SJ, Neale BM, Huang H, et al. (2017) Whole genome sequencing in psychiatric disorders: the WGSPD consortium. Nature Neuroscience. 20: 1661-1668
Willsey AJ, Fernandez TV, Yu D, et al. (2017) De Novo Coding Variants Are Strongly Associated with Tourette Disorder. Neuron. 94: 486-499.e9
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