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Natalie R. Powers, Ph.D. - Publications

Affiliations: 
2013 Genetics Yale University, New Haven, CT 
Area:
Genetics, Neuroscience Biology
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10 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2018 DeMille MMC, Tang K, Mehta CM, Geissler C, Malins JG, Powers NR, Bowen BM, Adams AK, Truong DT, Frijters JC, Gruen JR. 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. PMID 29666269 DOI: 10.1073/Pnas.1710472115  0.514
2015 Powers NR, Eicher JD, Miller LL, Kong Y, Smith SD, Pennington BF, Willcutt EG, Olson RK, Ring SM, Gruen JR. The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles. Journal of Medical Genetics. PMID 26660103 DOI: 10.1136/Jmedgenet-2015-103418  0.552
2015 Eicher JD, Stein CM, Deng F, Ciesla AA, Powers NR, Boada R, Smith SD, Pennington BF, Iyengar SK, Lewis BA, Gruen JR. The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains. Genes, Brain, and Behavior. 14: 377-85. PMID 25778907 DOI: 10.1111/Gbb.12214  0.558
2014 Eicher JD, Powers NR, Miller LL, Mueller KL, Mascheretti S, Marino C, Willcutt EG, DeFries JC, Olson RK, Smith SD, Pennington BF, Tomblin JB, Ring SM, Gruen JR. Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ. Human Genetics. 133: 869-81. PMID 24509779 DOI: 10.1007/S00439-014-1427-3  0.609
2013 Eicher JD, Powers NR, Miller LL, Akshoomoff N, Amaral DG, Bloss CS, Libiger O, Schork NJ, Darst BF, Casey BJ, Chang L, Ernst T, Frazier J, Kaufmann WE, Keating B, et al. Genome-wide association study of shared components of reading disability and language impairment. Genes, Brain, and Behavior. 12: 792-801. PMID 24024963 DOI: 10.1111/Gbb.12085  0.532
2013 Powers NR, Eicher JD, Butter F, Kong Y, Miller LL, Ring SM, Mann M, Gruen JR. Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment. American Journal of Human Genetics. 93: 19-28. PMID 23746548 DOI: 10.1016/J.Ajhg.2013.05.008  0.59
2013 Eicher JD, Powers NR, Cho K, Miller LL, Mueller KL, Ring SM, Tomblin JB, Gruen JR. Associations of prenatal nicotine exposure and the dopamine related genes ANKK1 and DRD2 to verbal language. Plos One. 8: e63762. PMID 23691092 DOI: 10.1371/Journal.Pone.0063762  0.504
2013 Jamadar S, Powers NR, Meda SA, Calhoun VD, Gelernter J, Gruen JR, Pearlson GD. 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. PMID 22669497 DOI: 10.1007/S11682-012-9168-1  0.463
2011 Jamadar S, Powers NR, Meda SA, Gelernter J, Gruen JR, Pearlson GD. Genetic influences of cortical gray matter in language-related regions in healthy controls and schizophrenia. Schizophrenia Research. 129: 141-8. PMID 21507613 DOI: 10.1016/J.Schres.2011.03.027  0.473
2011 Meng H, Powers NR, Tang L, Cope NA, Zhang PX, Fuleihan R, Gibson C, Page GP, Gruen JR. A dyslexia-associated variant in DCDC2 changes gene expression. Behavior Genetics. 41: 58-66. PMID 21042874 DOI: 10.1007/S10519-010-9408-3  0.423
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