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 Tarjinder Singh.
Connection Strength

0.542
  1. 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: 0.219
  2. Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders. Nat Neurosci. 2016 Apr; 19(4):571-7.
    View in: PubMed
    Score: 0.170
  3. Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations. Nat Neurosci. 2020 02; 23(2):185-193.
    View in: PubMed
    Score: 0.055
  4. De novo variants in neurodevelopmental disorders with epilepsy. Nat Genet. 2018 07; 50(7):1048-1053.
    View in: PubMed
    Score: 0.050
  5. Rare Variant, Gene-Based Association Study of Hereditary Melanoma Using Whole-Exome Sequencing. J Natl Cancer Inst. 2017 12 01; 109(12).
    View in: PubMed
    Score: 0.048
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.