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Benjamin Michael Neale, Ph.D.

Co-Author

This page shows the publications co-authored by Benjamin Neale and Elise Robinson.
Connection Strength

1.567
  1. Predicting Polygenic Risk of Psychiatric Disorders. Biol Psychiatry. 2019 07 15; 86(2):97-109.
    View in: PubMed
    Score: 0.204
  2. 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
  3. Ultra-rare disruptive and damaging mutations influence educational attainment in the general population. Nat Neurosci. 2016 12; 19(12):1563-1565.
    View in: PubMed
    Score: 0.175
  4. Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population. Nat Genet. 2016 05; 48(5):552-5.
    View in: PubMed
    Score: 0.168
  5. Genetic research in autism spectrum disorders. Curr Opin Pediatr. 2015 Dec; 27(6):685-91.
    View in: PubMed
    Score: 0.165
  6. An atlas of genetic correlations across human diseases and traits. Nat Genet. 2015 Nov; 47(11):1236-41.
    View in: PubMed
    Score: 0.163
  7. Autism spectrum disorder severity reflects the average contribution of de novo and familial influences. Proc Natl Acad Sci U S A. 2014 Oct 21; 111(42):15161-5.
    View in: PubMed
    Score: 0.152
  8. The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort. Mol Psychiatry. 2015 Apr; 20(4):454-8.
    View in: PubMed
    Score: 0.150
  9. 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
  10. Identification of common genetic risk variants for autism spectrum disorder. Nat Genet. 2019 03; 51(3):431-444.
    View in: PubMed
    Score: 0.052
  11. 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
  12. A framework for the interpretation of de novo mutation in human disease. Nat Genet. 2014 Sep; 46(9):944-50.
    View in: PubMed
    Score: 0.038
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.