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Author Details

Natalie R Powers
Yale University School of Medicine
2011
17
11
PMIDPaper TitleJournal TitlePublished Year
34747456Differential effects of two catalytic mutations on full-length PRDM9 and its isolated PR/SET domain reveal a case of pseudomodularity.Genetics2021
33756132Prdm9 and meiotic cohesin proteins cooperatively promote DNA double-strand break formation in mammalian spermatocytes.Curr Biol2021
33097538Sexual dimorphism in the meiotic requirement for PRDM9: A mammalian evolutionary safeguard.Sci Adv2020
30593494Tissue-Specific Trans Regulation of the Mouse Epigenome.Genetics2019
30853435Prdm9 and Meiotic Cohesin Proteins Cooperatively Promote DNA Double-Strand Break Formation in Mammalian Spermatocytes.Curr Biol2019
29666269Worldwide distribution of the <i>DCDC2</i> READ1 regulatory element and its relationship with phoneme variation across languages.Proc Natl Acad Sci U S A2018
27362481The Meiotic Recombination Activator PRDM9 Trimethylates Both H3K36 and H3K4 at Recombination Hotspots In Vivo.PLoS Genet2016
26660103The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles.J Med Genet2016
25778907The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains.Genes Brain Behav2015
26351520Affinity-seq detects genome-wide PRDM9 binding sites and reveals the impact of prior chromatin modifications on mammalian recombination hotspot usage.Epigenetics Chromatin2015
24509779Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ.Hum Genet2014
22669497Genetic influences of resting state fMRI activity in language-related brain regions in healthy controls and schizophrenia patients: a pilot study.Brain Imaging Behav2013
24024963Genome-wide association study of shared components of reading disability and language impairment.Genes Brain Behav2013
23691092Associations of prenatal nicotine exposure and the dopamine related genes ANKK1 and DRD2 to verbal language.PLoS One2013
23746548Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment.Am J Hum Genet2013
21042874A dyslexia-associated variant in DCDC2 changes gene expression.Behav Genet2011
21507613Genetic influences of cortical gray matter in language-related regions in healthy controls and schizophrenia.Schizophr Res2011
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Queen's Medical Center, University of Hawaii
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University of California
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Children's Hospital Los Angeles
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University of California San Diego
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university of massachusetts amherst Chan Medical School
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Max Planck Institute for Psycholinguistics
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