Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Mark Joseph Daly, Ph.D.

Co-Author

This page shows the publications co-authored by Mark Daly and Elise Robinson.
Connection Strength

2.722
  1. 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: 0.673
  2. 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: 0.608
  3. Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders. Genome Med. 2020 03 17; 12(1):28.
    View in: PubMed
    Score: 0.222
  4. 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: 0.217
  5. Paternal-age-related de novo mutations and risk for five disorders. Nat Commun. 2019 07 10; 10(1):3043.
    View in: PubMed
    Score: 0.212
  6. Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders. Nat Genet. 2017 Jul; 49(7):978-985.
    View in: PubMed
    Score: 0.182
  7. 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: 0.179
  8. A framework for the interpretation of de novo mutation in human disease. Nat Genet. 2014 Sep; 46(9):944-50.
    View in: PubMed
    Score: 0.150
  9. Identification of common genetic risk variants for autism spectrum disorder. Nat Genet. 2019 03; 51(3):431-444.
    View in: PubMed
    Score: 0.052
  10. Predicting Polygenic Risk of Psychiatric Disorders. Biol Psychiatry. 2019 07 15; 86(2):97-109.
    View in: PubMed
    Score: 0.051
  11. 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: 0.051
  12. 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: 0.044
  13. An atlas of genetic correlations across human diseases and traits. Nat Genet. 2015 Nov; 47(11):1236-41.
    View in: PubMed
    Score: 0.041
  14. Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci. Neuron. 2015 Sep 23; 87(6):1215-1233.
    View in: PubMed
    Score: 0.041
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.