Natalie R. Powers, Ph.D.

Affiliations: 
2013 Genetics Yale University, New Haven, CT 
Area:
Genetics, Neuroscience Biology
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"Natalie Powers"
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Parents

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Jeffery Grven grad student 2013 Yale
 (Discovery of the 6p21.3 Reading Disability Gene.)
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Publications

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DeMille MMC, Tang K, Mehta CM, et al. (2018) Worldwide distribution of the READ1 regulatory element and its relationship with phoneme variation across languages. Proceedings of the National Academy of Sciences of the United States of America
Powers NR, Eicher JD, Miller LL, et al. (2015) The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles. Journal of Medical Genetics
Eicher JD, Stein CM, Deng F, et al. (2015) The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains. Genes, Brain, and Behavior. 14: 377-85
Eicher JD, Powers NR, Miller LL, et al. (2014) Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ. Human Genetics. 133: 869-81
Eicher JD, Powers NR, Miller LL, et al. (2013) Genome-wide association study of shared components of reading disability and language impairment. Genes, Brain, and Behavior. 12: 792-801
Powers NR, Eicher JD, Butter F, et al. (2013) Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment. American Journal of Human Genetics. 93: 19-28
Eicher JD, Powers NR, Cho K, et al. (2013) Associations of prenatal nicotine exposure and the dopamine related genes ANKK1 and DRD2 to verbal language. Plos One. 8: e63762
Jamadar S, Powers NR, Meda SA, et al. (2013) Genetic influences of resting state fMRI activity in language-related brain regions in healthy controls and schizophrenia patients: a pilot study. Brain Imaging and Behavior. 7: 15-27
Jamadar S, Powers NR, Meda SA, et al. (2011) Genetic influences of cortical gray matter in language-related regions in healthy controls and schizophrenia. Schizophrenia Research. 129: 141-8
Meng H, Powers NR, Tang L, et al. (2011) A dyslexia-associated variant in DCDC2 changes gene expression. Behavior Genetics. 41: 58-66
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