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Author Details

Jeffrey R Gruen
Yale Medical School
1991
98
33
PMIDPaper TitleJournal TitlePublished Year
36823321Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia.Nat Genet2023
37761888The Rosetta Phenotype Harmonization Method Facilitates Finding a Relationship Quantitative Trait Locus for a Complex Cognitive Trait.Genes (Basel)2023
37214935Phonological Awareness Mediates the Relationship between DCDC2 and Reading Performance with the Influence of Home Environment.Res Sq2023
34623748D-bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia.Am J Med Genet A2022
35998220Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people.Proc Natl Acad Sci U S A2022
36266505Discovery of 42 genome-wide significant loci associated with dyslexia.Nat Genet2022
36223729Orthographic Depth May Influence the Degree of Severity of Maze Learning Performance in Children at Risk for Reading Disorder.Dev Neurosci2022
36016658Dyslexia associated gene <i>KIAA0319</i> regulates cell cycle during human neuroepithelial cell development.Front Cell Dev Biol2022
34186533Identifying Dyslexia: Link between Maze Learning and Dyslexia Susceptibility Gene, DCDC2, in Young Children.Dev Neurosci2021
34970657Sex-specific associations between traumatic experiences and resting-state functional connectivity in the Philadelphia Neurodevelopmental Cohort.JCPP Adv2021
31411106Effect of READ1 on latent profiles of reading disorder and comorbid attention and language impairment subtypes.Child Neuropsychol2020
32682798The temporal dynamics of first and second language processing: ERPs to spoken words in Mandarin-English bilinguals.Neuropsychologia2020
32486976<i>DCDC2</i> READ1 regulatory element: how temporal processing differences may shape language.Proc Biol Sci2020
30737034Genetics of bronchopulmonary dysplasia: When things do not match up, it is only the beginning.J Pediatr2019
32523329Causal Attribution Profiles as a Function of Reading Skills, Hyperactivity, and Inattention.Sci Stud Read2019
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
32523322Achievement attributions are associated with specific rather than general learning delays.Learn Individ Differ2018
29894888Increased variability of stimulus-driven cortical responses is associated with genetic variability in children with and without dyslexia.Dev Cogn Neurosci2018
30631481A molecular-genetic and imaging-genetic approach to specific comprehension difficulties in children.NPJ Sci Learn2018
29391653Reading-Related Causal Attributions for Success and Failure: Dynamic Links With Reading Skill.Read Res Q2018
26755569Executive Functions Contribute Uniquely to Reading Competence in Minority Youth.J Learn Disabil2017
28866788Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC.Hum Genet2017
27859682A method for integrating neuroimaging into genetic models of learning performance.Genet Epidemiol2017
25953057Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children.Brain Imaging Behav2016
26660103The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles.J Med Genet2016
27535846Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders.Hum Genet2016
26183468Anxiety is related to indices of cortical maturation in typically developing children and adolescents.Brain Struct Funct2016
25937488The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository.Neuroimage2016
25448322Language impairment and dyslexia genes influence language skills in children with autism spectrum disorders.Autism Res2015
26471062What is the basis for a genetic approach in neonatal disorders?Semin Perinatol2015
25778907The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains.Genes Brain Behav2015
25821911Family income, parental education and brain structure in children and adolescents.Nat Neurosci2015
24219608The NIH Toolbox Cognition Battery: results from a large normative developmental sample (PING).Neuropsychology2014
24926531The DCDC2/intron 2 deletion and white matter disorganization: focus on developmental dyslexia.Cortex2014
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
23916419Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments.Mol Genet Metab2013
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
23122624Prenatal exposure to nicotine and impaired reading performance.J Pediatr2013
21881542DCDC2 genetic variants and susceptibility to developmental dyslexia.Psychiatr Genet2012
23169628Long-term influence of normal variation in neonatal characteristics on human brain development.Proc Natl Acad Sci U S A2012
23150548Multimodal imaging of the self-regulating developing brain.Proc Natl Acad Sci U S A2012
22750057Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability.Neuroimage2012
22902750Neuroanatomical assessment of biological maturity.Curr Biol2012
22524164Molecular diagnostic testing for Klinefelter syndrome and other male sex chromosome aneuploidies.Int J Pediatr Endocrinol2012
22343285Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans.Proc Natl Acad Sci U S A2012
20850766The impact of environmental and genetic factors on neonatal late-onset sepsis.J Pediatr2011
21507613Genetic influences of cortical gray matter in language-related regions in healthy controls and schizophrenia.Schizophr Res2011
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Collaborators

Genetics and Pharmacogenomics, Merck & Co., Inc.
Co-authored papers 11
Barnard College of Columbia University
Co-authored papers 10
University of California San Diego
Co-authored papers 10
University of Maryland School of Medicine
Co-authored papers 10
Yale University School of Medicine
Co-authored papers 10
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Co-authored papers 10
University of California
Co-authored papers 10
University of California San Diego
Co-authored papers 10
University of Maryland School of Medicine
Co-authored papers 10
University of California San Diego Health System
Co-authored papers 10
university of massachusetts amherst Chan Medical School
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Co-authored papers 10
Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital
Co-authored papers 9
Center for Human Development, University of California
Co-authored papers 9
Children's Hospital Los Angeles
Co-authored papers 9
University of California San Diego
Co-authored papers 9
University of California
Co-authored papers 9
The Qualcomm Institute, University of California
Co-authored papers 8
Yale University School of Medicine.
Co-authored papers 8
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Johns Hopkins University School of Medicine
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Center for Multimodal Imaging and Genetics, University of California San Diego
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University of Washington.
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Oakfield House University of Bristol Bristol UK.
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Yale School of Medicine
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