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Benjamin Michael Neale, Ph.D.

Co-Author

This page shows the publications co-authored by Benjamin Neale and Konrad Karczewski.
Connection Strength

1.417
  1. Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans. Nature. 2021 Feb; 590(7846):E53.
    View in: PubMed
    Score: 0.236
  2. Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power. Nat Genet. 2021 02; 53(2):195-204.
    View in: PubMed
    Score: 0.235
  3. The mutational constraint spectrum quantified from variation in 141,456 humans. Nature. 2020 05; 581(7809):434-443.
    View in: PubMed
    Score: 0.225
  4. Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum. Am J Hum Genet. 2018 06 07; 102(6):1204-1211.
    View in: PubMed
    Score: 0.196
  5. 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
  6. Human genetic analyses of organelles highlight the nucleus in age-related trait heritability. Elife. 2021 09 01; 10.
    View in: PubMed
    Score: 0.061
  7. Author Correction: A structural variation reference for medical and population genetics. Nature. 2021 Feb; 590(7846):E55.
    View in: PubMed
    Score: 0.059
  8. A structural variation reference for medical and population genetics. Nature. 2020 05; 581(7809):444-451.
    View in: PubMed
    Score: 0.056
  9. Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population. PLoS Genet. 2019 May; 15(5):e1008190.
    View in: PubMed
    Score: 0.052
  10. Base-specific mutational intolerance near splice sites clarifies the role of nonessential splice nucleotides. Genome Res. 2018 07; 28(7):968-974.
    View in: PubMed
    Score: 0.049
  11. Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population. PLoS Genet. 2018 05; 14(5):e1007329.
    View in: PubMed
    Score: 0.049
  12. Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland. Am J Hum Genet. 2018 05 03; 102(5):760-775.
    View in: PubMed
    Score: 0.049
  13. Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples. Nat Genet. 2017 Apr; 49(4):504-510.
    View in: PubMed
    Score: 0.045
  14. Analysis of protein-coding genetic variation in 60,706 humans. Nature. 2016 08 18; 536(7616):285-91.
    View in: PubMed
    Score: 0.043
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.