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Earl B Robinson

Biographic Data

ID1085002
NAMEEarl B Robinson
GIVEN NAMESEarl B
FAMILY NAMERobinson
SIGNATUREROBINSON E B
AFFILIATIONSBroad Institute
ORCID0000-0003-2314-2792
VERIFIEDYes
TOTAL WORKS8
TOTAL CITATIONS0
AUTHOR COUNT8
EDITOR COUNT0
FIRST PUBLICATION YEAR1961
LATEST PUBLICATION YEAR2025
H-INDEX0
  • Socio-medical factors associated with neurodevelopmental disorders on the Kenyan coast

    Open Access•Patricia Kipkemoi, Jeanne E Savage et al.•ARTICLE•PLOS Global Public Health•2025

    Neurodevelopmental disorders (NDDs) are a group of conditions with their onset during the early developmental period and include conditions such as autism and intellectual disability. Occurrence of NDDs is thought to be determined by both genetic and environmental factors, but data on the role of environmental factors for NDD in Africa is limited. This study investigates environmental influences on NDDs in children from Kenya. This case-control s…

  • Genome-wide association meta-analysis of age at onset of walking in over 70,000 infants of European ancestry

    Open Access•Ailing Gui, Adam Hollowell et al.•ARTICLE•Nature Human Behaviour•2025•References: 126

    Age at onset of walking is an important early childhood milestone which is used clinically and in public health screening. In this genome-wide association study meta-analysis of age at onset of walking ( N = 70,560 European-ancestry infants), we identified 11 independent genome-wide significant loci. SNP-based heritability was 24.13% (95% confidence intervals = 21.86–26.40) with ~11,900 variants accounting for about 90% of it, suggesting high pol…

  • Principled distillation of UK Biobank phenotype data reveals underlying structure in human variation

    Open Access•Caitlin E Carey, Rebecca Shafee et al.•ARTICLE•Nature Human Behaviour•2024•References: 87

    Data within biobanks capture broad yet detailed indices of human variation, but biobank-wide insights can be difficult to extract due to complexity and scale. Here, using large-scale factor analysis, we distill hundreds of variables (diagnoses, assessments and survey items) into 35 latent constructs, using data from unrelated individuals with predominantly estimated European genetic ancestry in UK Biobank. These factors recapitulate known disease…

  • Cultural landscape visualization: The use of non-photorealistic 3D rendering as an analytical tool to convey change at statue of liberty national monument

    Open Access•Aidan Ackerman, John Auwaerter et al.•ARTICLE•Journal of Cultural Heritage•2023•References: 3

  • Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

    Open Access•Ditte Demontis, 23andMe Research Team et al.•ARTICLE•Nature Genetics•2019

    Attention deficit/hyperactivity disorder (ADHD) is a highly heritable childhood behavioral disorder affecting 5% of children and 2.5% of adults. Common genetic variants contribute substantially to ADHD susceptibility, but no variants have been robustly associated with ADHD. We report a genome-wide association meta-analysis of 20,183 individuals diagnosed with ADHD and 35,191 controls that identifies variants surpassing genome-wide significance in…

  • Identification of common genetic risk variants for autism spectrum disorder

    Open Access•John Grove, BUPGEN BUPGEN et al.•ARTICLE•Nature Genetics•2019

  • An atlas of genetic correlations across human diseases and traits

    Open Access•ReproGen Consortium, Brendan Bulik‐Sullivan et al.•ARTICLE•Nature Genetics•2015

  • Greek Selections from Xenophon's Anabasis and Plato's Apology, Crito, Phaedo

    Donald G Baker, Earl B Robinson•ARTICLE•The Classical World•1961

No prominent works on this page.

  • Greek Selections from Xenophon's Anabasis and Plato's Apology, Crito, Phaedo

    Donald G Baker, Earl B Robinson•ARTICLE•The Classical World•1961

  • An atlas of genetic correlations across human diseases and traits

    Open Access•ReproGen Consortium, Brendan Bulik‐Sullivan et al.•ARTICLE•Nature Genetics•2015

  • Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

    Open Access•Ditte Demontis, 23andMe Research Team et al.•ARTICLE•Nature Genetics•2019

    Attention deficit/hyperactivity disorder (ADHD) is a highly heritable childhood behavioral disorder affecting 5% of children and 2.5% of adults. Common genetic variants contribute substantially to ADHD susceptibility, but no variants have been robustly associated with ADHD. We report a genome-wide association meta-analysis of 20,183 individuals diagnosed with ADHD and 35,191 controls that identifies variants surpassing genome-wide significance in…

  • Identification of common genetic risk variants for autism spectrum disorder

    Open Access•John Grove, BUPGEN BUPGEN et al.•ARTICLE•Nature Genetics•2019

  • Cultural landscape visualization: The use of non-photorealistic 3D rendering as an analytical tool to convey change at statue of liberty national monument

    Open Access•Aidan Ackerman, John Auwaerter et al.•ARTICLE•Journal of Cultural Heritage•2023•References: 3

  • Principled distillation of UK Biobank phenotype data reveals underlying structure in human variation

    Open Access•Caitlin E Carey, Rebecca Shafee et al.•ARTICLE•Nature Human Behaviour•2024•References: 87

    Data within biobanks capture broad yet detailed indices of human variation, but biobank-wide insights can be difficult to extract due to complexity and scale. Here, using large-scale factor analysis, we distill hundreds of variables (diagnoses, assessments and survey items) into 35 latent constructs, using data from unrelated individuals with predominantly estimated European genetic ancestry in UK Biobank. These factors recapitulate known disease…

  • Socio-medical factors associated with neurodevelopmental disorders on the Kenyan coast

    Open Access•Patricia Kipkemoi, Jeanne E Savage et al.•ARTICLE•PLOS Global Public Health•2025

    Neurodevelopmental disorders (NDDs) are a group of conditions with their onset during the early developmental period and include conditions such as autism and intellectual disability. Occurrence of NDDs is thought to be determined by both genetic and environmental factors, but data on the role of environmental factors for NDD in Africa is limited. This study investigates environmental influences on NDDs in children from Kenya. This case-control s…

  • Genome-wide association meta-analysis of age at onset of walking in over 70,000 infants of European ancestry

    Open Access•Ailing Gui, Adam Hollowell et al.•ARTICLE•Nature Human Behaviour•2025•References: 126

    Age at onset of walking is an important early childhood milestone which is used clinically and in public health screening. In this genome-wide association study meta-analysis of age at onset of walking ( N = 70,560 European-ancestry infants), we identified 11 independent genome-wide significant loci. SNP-based heritability was 24.13% (95% confidence intervals = 21.86–26.40) with ~11,900 variants accounting for about 90% of it, suggesting high pol…

Biology (5 works) · Genetic Associations and Epidemiology (4 works) · Gene (3 works) · Genetics (3 works) · Genome-wide association study (3 works) · Genotype (3 works) · Single-nucleotide polymorphism (3 works) · Art (2 works) · Autism (2 works) · Autism Spectrum Disorder Research (2 works)

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