Harvard Catalyst Profiles

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

Patrick Jozef Maria Smits, Ph.D.

Co-Author

This page shows the publications co-authored by Patrick Smits and Matthew Warman.
Connection Strength

0.667
  1. The skeletal phenotype of achondrogenesis type 1A is caused exclusively by cartilage defects. Development. 2018 01 08; 145(1).
    View in: PubMed
    Score: 0.194
  2. Golgi disruption and early embryonic lethality in mice lacking USO1. PLoS One. 2012; 7(11):e50530.
    View in: PubMed
    Score: 0.136
  3. Lethal skeletal dysplasia in mice and humans lacking the golgin GMAP-210. N Engl J Med. 2010 Jan 21; 362(3):206-16.
    View in: PubMed
    Score: 0.112
  4. Somatic mutations in intracranial arteriovenous malformations. PLoS One. 2019; 14(12):e0226852.
    View in: PubMed
    Score: 0.056
  5. Arteriovenous malformation associated with a HRAS mutation. Hum Genet. 2019 Dec; 138(11-12):1419-1421.
    View in: PubMed
    Score: 0.055
  6. Intramuscular fast-flow vascular anomaly contains somatic MAP2K1 and KRAS mutations. Angiogenesis. 2019 11; 22(4):547-552.
    View in: PubMed
    Score: 0.054
  7. Lubricin restoration in a mouse model of congenital deficiency. Arthritis Rheumatol. 2015 Nov; 67(11):3070-81.
    View in: PubMed
    Score: 0.042
  8. The secreted glycoprotein lubricin protects cartilage surfaces and inhibits synovial cell overgrowth. J Clin Invest. 2005 Mar; 115(3):622-31.
    View in: PubMed
    Score: 0.020
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.