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Author Details
Full Name
Natalie R Powers
Affiliation
Yale University School of Medicine
ORCID
Career Start Year
2011
Papers
17
H Index
11
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
34747456
Differential effects of two catalytic mutations on full-length PRDM9 and its isolated PR/SET domain reveal a case of pseudomodularity.
Genetics
2021
33756132
Prdm9 and meiotic cohesin proteins cooperatively promote DNA double-strand break formation in mammalian spermatocytes.
Curr Biol
2021
33097538
Sexual dimorphism in the meiotic requirement for PRDM9: A mammalian evolutionary safeguard.
Sci Adv
2020
30593494
Tissue-Specific Trans Regulation of the Mouse Epigenome.
Genetics
2019
30853435
Prdm9 and Meiotic Cohesin Proteins Cooperatively Promote DNA Double-Strand Break Formation in Mammalian Spermatocytes.
Curr Biol
2019
29666269
Worldwide distribution of the <i>DCDC2</i> READ1 regulatory element and its relationship with phoneme variation across languages.
Proc Natl Acad Sci U S A
2018
27362481
The Meiotic Recombination Activator PRDM9 Trimethylates Both H3K36 and H3K4 at Recombination Hotspots In Vivo.
PLoS Genet
2016
26660103
The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles.
J Med Genet
2016
25778907
The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains.
Genes Brain Behav
2015
26351520
Affinity-seq detects genome-wide PRDM9 binding sites and reveals the impact of prior chromatin modifications on mammalian recombination hotspot usage.
Epigenetics Chromatin
2015
24509779
Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ.
Hum Genet
2014
22669497
Genetic influences of resting state fMRI activity in language-related brain regions in healthy controls and schizophrenia patients: a pilot study.
Brain Imaging Behav
2013
24024963
Genome-wide association study of shared components of reading disability and language impairment.
Genes Brain Behav
2013
23691092
Associations of prenatal nicotine exposure and the dopamine related genes ANKK1 and DRD2 to verbal language.
PLoS One
2013
23746548
Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment.
Am J Hum Genet
2013
21042874
A dyslexia-associated variant in DCDC2 changes gene expression.
Behav Genet
2011
21507613
Genetic influences of cortical gray matter in language-related regions in healthy controls and schizophrenia.
Schizophr Res
2011
1 - 17 of 17
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The Qualcomm Institute, University of California
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Queen's Medical Center, University of Hawaii
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