Matthew W. State

University of California, San Francisco, San Francisco, CA 
 2009 Yale University, New Haven, CT 
Genetics and genomics of developmental neuropsychiatric disorders
"Matthew State"
Mean distance: 16.84
Cross-listing: GenetiTree


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Richard P. Lifton grad student Yale (GenetiTree)
David Christian Ward grad student 2001 Yale (Chemistry Tree)
 (Evaluation of a chromosome 18 locus associated with Tourette syndrome phenotypes: Breakpoint characterization, transcript assessment, and candidate gene analysis.)


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Thomas Fernandez grad student Yale Med Sch (GenetiTree)
Abha R. Gupta grad student UCSF (Cell & Gene Therapy Tree)
Stephan J. Sanders grad student Yale
Brian J. O'Roak grad student 2009 Yale
Althea A. Stillman grad student 2009 Yale
John Daniel Murdoch grad student 2012 Yale
Ellen J. Hoffman grad student 2014 Yale
Arthur J. Willsey grad student 2014 Yale
Christopher Mason post-doc Cornell University, Weill Medical College, Burke Res. Institute (GenetiTree)
Donna M. Werling post-doc


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Murat Gunel collaborator Yale Med Sch
John L. R. Rubenstein collaborator
Nenad Sestan collaborator
BETA: Related publications


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Markenscoff-Papadimitriou E, Whalen S, Przytycki P, et al. (2020) A Chromatin Accessibility Atlas of the Developing Human Telencephalon. Cell
Willsey HR, Xu Y, Everitt A, et al. (2020) Neurodevelopmental disorder risk gene is required for ciliogenesis and brain size in embryos. Development (Cambridge, England)
Fazel Darbandi S, Robinson Schwartz SE, Pai EL, et al. (2020) Enhancing WNT Signaling Restores Cortical Neuronal Spine Maturation and Synaptogenesis in Tbr1 Mutants. Cell Reports. 31: 107495
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
Satterstrom FK, Kosmicki JA, Wang J, et al. (2020) Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism. Cell
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
Li M, Santpere G, Imamura Kawasawa Y, et al. (2018) Integrative functional genomic analysis of human brain development and neuropsychiatric risks. Science (New York, N.Y.). 362
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
Sestan N, State MW. (2018) Lost in Translation: Traversing the Complex Path from Genomics to Therapeutics in Autism Spectrum Disorder. Neuron. 100: 406-423
Fazel Darbandi S, Robinson Schwartz SE, Qi Q, et al. (2018) Neonatal Tbr1 Dosage Controls Cortical Layer 6 Connectivity. Neuron
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