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J. Gruen · SciRah

Researcher profile · Semantic Scholar

J. Gruen

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J. Gruen — researcher profile on SciRah

h-index: 45
Works: 155
Citations: 7,230

Most-cited papers

Family Income, Parental Education and Brain Structure in Children and Adolescents
K. Noble, Suzanne M. Houston, N. Brito, H. Bartsch +21 more
2015Nature Neuroscience1,294 citations Open access
Semantic Scholar
Neuroanatomical assessment of biological maturity
T. Brown, J. Kuperman, Yoonho Chung, M. Erhart +18 more
2012Current Biology334 citations Open access
Semantic Scholar
The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository
T. Jernigan, T. Brown, D. Hagler, N. Akshoomoff +23 more
2015NeuroImage302 citations Open access
Semantic Scholar
Multimodal imaging of the self-regulating developing brain
A. Fjell, K. Walhovd, T. Brown, J. Kuperman +25 more
2012Proceedings of the National Academy of Sciences of the United States of America222 citations Open access
Semantic Scholar
The NIH Toolbox Cognition Battery: Results from a Large Normative Developmental Sample (PING)
N. Akshoomoff, Erik Newman, W. Thompson, Connor J. McCabe +17 more
2013Neuropsychology205 citations Open access
Semantic Scholar
Long-term influence of normal variation in neonatal characteristics on human brain development
K. Walhovd, A. Fjell, T. Brown, J. Kuperman +22 more
2012Proceedings of the National Academy of Sciences of the United States of America180 citations Open access
Semantic Scholar
Discovery of 42 genome-wide significant loci associated with dyslexia
C. Doust, P. Fontanillas, E. Eising, S. Gordon +141 more
2021Nature Genetics121 citations Open access
Semantic Scholar
Genome-Wide Association Study of Shared Components of Reading Disability and Language Impairment
J. Eicher, Natalie R. Powers, L. Miller, N. Akshoomoff +26 more
2013Genes, Brain and Behavior110 citations Open access
Semantic Scholar
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people
E. Eising, Nazanin Mirza-Schreiber, E. D. de Zeeuw, Carol A. Wang +91 more
2022Proceedings of the National Academy of Sciences of the United States of America107 citations Open access
Semantic Scholar
DCDC2 Genetic Variants and Susceptibility to Developmental Dyslexia
Cecilia Marino, H. Meng, S. Mascheretti, M. Rusconi +4 more
2012Psychiatric Genetics83 citations Open access
Semantic Scholar
Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment.
Natalie R. Powers, J. Eicher, F. Butter, Y. Kong +4 more
2013American Journal of Human Genetics80 citations Open access
Semantic Scholar
Gray matter maturation and cognition in children with different APOE ε genotypes
Linda Chang, Vanessa Douet, C. Bloss, Kristin M. Lee +12 more
2016Neurology70 citations Open access
Semantic Scholar
A Dyslexia-Associated Variant in DCDC2 Changes Gene Expression
H. Meng, Natalie R. Powers, Ling Tang, N. Cope +5 more
2010Behavior Genetics69 citations Open access
Semantic Scholar
Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability
N. Cope, J. Eicher, H. Meng, C. Gibson +6 more
2012NeuroImage62 citations Open access
Semantic Scholar
Imaging-Genetics in Dyslexia: Connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments
J. Eicher, J. Gruen
2013Molecular Genetics and Metabolism59 citations Open access
Semantic Scholar
PROGRESS TOWARDS A CELLULAR NEUROBIOLOGY OF READING DISABILITY
Lisa Gabel, C. Gibson, J. Gruen, J. Loturco
2009Neurobiology of Disease57 citations Open access
Semantic Scholar
GENETIC INFLUENCES OF CORTICAL GREY MATTER IN LANGUAGE-RELATED REGIONS IN HEALTHY CONTROLS AND SCHIZOPHRENIA
S. Jamadar, Natalie R. Powers, S. Meda, J. Gelernter +2 more
2011Schizophrenia Research56 citations Open access
Semantic Scholar
Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans
Trygve E Bakken, J. Roddey, S. Djurovic, N. Akshoomoff +20 more
2012Proceedings of the National Academy of Sciences of the United States of America55 citations Open access
Semantic Scholar
Genetic Contribution to Patent Ductus Arteriosus in the Premature Newborn
V. Bhandari, Gongfu Zhou, M. Bizzarro, C. Buhimschi +3 more
2009Pediatrics53 citations Open access
Semantic Scholar
Anxiety is related to indices of cortical maturation in typically developing children and adolescents
Erik Newman, W. Thompson, H. Bartsch, D. Hagler +23 more
2015Brain Structure and Function52 citations Open access
Semantic Scholar
Prenatal exposure to nicotine and impaired reading performance
Kelly Cho, Jan C. Frijters, He-Ping Zhang, L. Miller +1 more
2012Jornal de Pediatria51 citations Open access
Semantic Scholar
Pleiotropic Effects of DCDC2 and DYX1C1 Genes on Language and Mathematics Traits in Nuclear Families of Developmental Dyslexia
Cecilia Marino, S. Mascheretti, Valentina Riva, F. Cattaneo +6 more
2010Behavior Genetics49 citations Open access
Semantic Scholar
Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ
J. Eicher, Natalie R. Powers, L. Miller, K. Mueller +10 more
2014Human Genetics46 citations Open access
Semantic Scholar
The DCDC2/intron 2 deletion and white matter disorganization: Focus on developmental dyslexia
Cecilia Marino, P. Scifo, P. D. Della Rosa, S. Mascheretti +8 more
2014Cortex; a journal devoted to the study of the nervous system and behavior45 citations Open access
Semantic Scholar
Language impairment and dyslexia genes influence language skills in children with autism spectrum disorders
J. Eicher, J. Gruen
2014Autism Research43 citations Open access
Semantic Scholar
Executive Functions Contribute Uniquely to Reading Competence in Minority Youth
Lisa A. Jacobson, Taylor A Koriakin, Paul H. Lipkin, R. Boada +9 more
2016Journal of Learning Disabilities38 citations Open access
Semantic Scholar
The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles
Natalie R. Powers, J. Eicher, L. Miller, Y. Kong +6 more
2015Journal of Medical Genetics37 citations Open access
Semantic Scholar
The Impact of Environmental and Genetic Factors on Neonatal Late-Onset Sepsis
M. Bizzarro, Yuan Jiang, N. Hussain, J. Gruen +2 more
2010Jornal de Pediatria37 citations Open access
Semantic Scholar
Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African–American youth
Dongnhu T. Truong, A. K. Adams, Steven Paniagua, Jan C. Frijters +15 more
2019Journal of Medical Genetics34 citations Open access
Semantic Scholar
Increased variability of stimulus-driven cortical responses is associated with genetic variability in children with and without dyslexia
T. Centanni, D. Pantazis, Dongnhu T. Truong, J. Gruen +2 more
2018Developmental Cognitive Neuroscience34 citations Open access
Semantic Scholar
Functional impact of a single nucleotide polymorphism in the OPRD1 promoter region
Hui-Ping Zhang, J. Gelernter, J. Gruen, H. Kranzler +2 more
2010Journal of Human Genetics33 citations Open access
Semantic Scholar
Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children
J. Eicher, Angela M. Montgomery, N. Akshoomoff, D. Amaral +22 more
2015Brain Imaging and Behavior30 citations Open access
Semantic Scholar
Associations of Prenatal Nicotine Exposure and the Dopamine Related Genes ANKK1 and DRD2 to Verbal Language
J. Eicher, Natalie R. Powers, Kelly Cho, L. Miller +4 more
2013PLoS ONE29 citations Open access
Semantic Scholar
Genetic Influences of Resting State fMRI Activity in Language-Related Brain Regions in Healthy Controls and Schizophrenia Patients: A Pilot Study
S. Jamadar, Natalie R. Powers, S. Meda, V. Calhoun +3 more
2012Brain Imaging and Behavior27 citations Open access
Semantic Scholar
A highly sensitive, high-throughput assay for the detection of Turner syndrome.
S. Rivkees, Karl Hager, S. Hosono, Anastasia Wise +3 more
2011Journal of Clinical Endocrinology and Metabolism27 citations Open access
Semantic Scholar
Reading-Related Causal Attributions for Success and Failure: Dynamic Links With Reading Skill
Jan C. Frijters, Kimberley C. Tsujimoto, R. Boada, S. Gottwald +8 more
2017Reading Research Quarterly18 citations Open access
Semantic Scholar
Schizophrenia-risk variant rs6994992 in the neuregulin-1 gene on brain developmental trajectories in typically developing children
Vanessa Douet, Linda Chang, A. Pritchett, K. Lee +14 more
2014Translational Psychiatry18 citations Open access
Semantic Scholar
Family income, parental education and brain structure in children and adolescents
K. Noble, Suzanne M. Houston, N. Brito, H. Bartsch +21 more
201517 citations
Semantic Scholar
Dyslexia associated gene KIAA0319 regulates cell cycle during human neuroepithelial cell development
Steven Paniagua, Bilal Cakir, Yue Hu, Ferdi Ridvan Kiral +5 more
2022Frontiers in Cell and Developmental Biology14 citations Open access
Semantic Scholar
Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities
K. Price, K. Wigg, E. Eising, Yu Feng +86 more
2022Translational Psychiatry13 citations Open access
Semantic Scholar
Effects on developmental outcomes after cesarean birth versus vaginal birth in Chinese children aged 1–59 months: a cross-sectional community-based survey
Hong Zhou, Yuan Ding, Yuning Yang, Si-Yu Zou +327 more
2019PeerJ13 citations Open access
Semantic Scholar
Worldwide distribution of the DCDC2 READ1 regulatory element and its relationship with phoneme variation across languages
M. DeMille, Kevin Tang, C. Mehta, Christopher Geissler +7 more
2018Proceedings of the National Academy of Sciences of the United States of America13 citations Open access
Semantic Scholar
A molecular-genetic and imaging-genetic approach to specific comprehension difficulties in children
Miao Li, J. Malins, M. DeMille, M. Lovett +14 more
2018npj Science of Learning12 citations Open access
Semantic Scholar
Causal Attribution Profiles as a Function of Reading Skills, Hyperactivity, and Inattention
Kimberley C. Tsujimoto, R. Boada, S. Gottwald, D. Hill +8 more
2018Scientific Studies of Reading12 citations Open access
Semantic Scholar
Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders
Dongnhu T. Truong, L. Shriberg, S. D. Smith, Kathy L. Chapman +7 more
2016Human Genetics12 citations Open access
Semantic Scholar
Genome-wide association analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people
E. Eising, Nazanin Mirza-Schreiber, E. D. de Zeeuw, Carol A. Wang +86 more
202111 citations Open access
Semantic Scholar
The temporal dynamics of first and second language processing: ERPs to spoken words in Mandarin-English bilinguals
Jin Xue, Ban-Ban Li, R. Yan, J. Gruen +3 more
2020Neuropsychologia11 citations Open access
Semantic Scholar
A method for integrating neuroimaging into genetic models of learning performance
C. Mehta, J. Gruen, He-Ping Zhang
2016Genetic Epidemiology11 citations Open access
Semantic Scholar
The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains
J. Eicher, Catherine M. Stein, Fenghua Deng, Allison A. Vrich Ciesla +7 more
2015Genes, Brain and Behavior10 citations Open access
Semantic Scholar
Specificity, Co-Occurrence, and Growth: Math and Reading Skill Development in Children With Learning Disabilities
Kate Connors, Emily L. Guertin, Melissa Nichol, J. Bosson-Heenan +2 more
2025Journal of Learning Disabilities9 citations Open access
Semantic Scholar

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