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Benjamin Michael Neale, Ph.D.

Co-Author

This page shows the publications co-authored by Benjamin Neale and Raymond Walters.
Connection Strength

1.581
  1. Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. Nat Genet. 2019 01; 51(1):63-75.
    View in: PubMed
    Score: 0.203
  2. Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders. Nat Neurosci. 2018 12; 21(12):1656-1669.
    View in: PubMed
    Score: 0.203
  3. A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder. Biol Psychiatry. 2018 06 15; 83(12):1044-1053.
    View in: PubMed
    Score: 0.189
  4. Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans. Nature. 2021 Sep; 597(7874):E3-E4.
    View in: PubMed
    Score: 0.061
  5. Genetic analyses identify widespread sex-differential participation bias. Nat Genet. 2021 05; 53(5):663-671.
    View in: PubMed
    Score: 0.060
  6. Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder. Nat Commun. 2021 Feb 15; 12(1):1166.
    View in: PubMed
    Score: 0.059
  7. Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans. Nature. 2021 Feb; 590(7846):E53.
    View in: PubMed
    Score: 0.059
  8. Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder. Nat Commun. 2021 01 25; 12(1):576.
    View in: PubMed
    Score: 0.059
  9. Examining Sex-Differentiated Genetic Effects Across Neuropsychiatric and Behavioral Traits. Biol Psychiatry. 2021 06 15; 89(12):1127-1137.
    View in: PubMed
    Score: 0.059
  10. Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations. Am J Hum Genet. 2020 10 01; 107(4):788-789.
    View in: PubMed
    Score: 0.058
  11. The mutational constraint spectrum quantified from variation in 141,456 humans. Nature. 2020 05; 581(7809):434-443.
    View in: PubMed
    Score: 0.056
  12. Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. Addict Biol. 2021 01; 26(1):e12880.
    View in: PubMed
    Score: 0.055
  13. RICOPILI: Rapid Imputation for COnsortias PIpeLIne. Bioinformatics. 2020 02 01; 36(3):930-933.
    View in: PubMed
    Score: 0.055
  14. Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants. Nat Neurosci. 2019 12; 22(12):1961-1965.
    View in: PubMed
    Score: 0.054
  15. Author Correction: Multi-trait analysis of genome-wide association summary statistics using MTAG. Nat Genet. 2019 Aug; 51(8):1295.
    View in: PubMed
    Score: 0.053
  16. Publisher Correction: Multi-trait analysis of genome-wide association summary statistics using MTAG. Nat Genet. 2019 Jul; 51(7):1190.
    View in: PubMed
    Score: 0.053
  17. Genetic Markers of ADHD-Related Variations in Intracranial Volume. Am J Psychiatry. 2019 03 01; 176(3):228-238.
    View in: PubMed
    Score: 0.052
  18. Identification of common genetic risk variants for autism spectrum disorder. Nat Genet. 2019 03; 51(3):431-444.
    View in: PubMed
    Score: 0.052
  19. Analysis of shared heritability in common disorders of the brain. Science. 2018 06 22; 360(6395).
    View in: PubMed
    Score: 0.049
  20. Multi-trait analysis of genome-wide association summary statistics using MTAG. Nat Genet. 2018 02; 50(2):229-237.
    View in: PubMed
    Score: 0.048
  21. Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations. Am J Hum Genet. 2017 Apr 06; 100(4):635-649.
    View in: PubMed
    Score: 0.045
Connection Strength
The connection strength for co-authors is the sum of the scores for each of their shared publications.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.