Harvard Catalyst Profiles

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Patrick Jozef Maria Smits, Ph.D.

Co-Author

This page shows the publications co-authored by Patrick Smits and Arin Greene.
Connection Strength

2.741
  1. Endothelial MAP2K1 mutations in arteriovenous malformation activate the RAS/MAPK pathway. Biochem Biophys Res Commun. 2020 08 20; 529(2):450-454.
    View in: PubMed
    Score: 0.920
  2. EPHB4 mutation causes adult and adolescent-onset primary lymphedema. Am J Med Genet A. 2021 Jul 07.
    View in: PubMed
    Score: 0.247
  3. Lipoblastoma phenotype contains a somatic PIK3CA mutation. Pediatr Dermatol. 2021 Jan; 38(1):299-300.
    View in: PubMed
    Score: 0.234
  4. Arteriovenous malformation phenotype resembling congenital hemangioma contains KRAS mutations. Clin Genet. 2020 12; 98(6):595-597.
    View in: PubMed
    Score: 0.233
  5. Arteriovenous Malformation MAP2K1 Mutation Causes Local Cartilage Overgrowth by a Cell-Non Autonomous Mechanism. Sci Rep. 2020 03 10; 10(1):4428.
    View in: PubMed
    Score: 0.225
  6. Diffuse capillary malformation with overgrowth contains somatic PIK3CA variants. Clin Genet. 2020 05; 97(5):736-740.
    View in: PubMed
    Score: 0.223
  7. Somatic mutations in intracranial arteriovenous malformations. PLoS One. 2019; 14(12):e0226852.
    View in: PubMed
    Score: 0.222
  8. Arteriovenous malformation associated with a HRAS mutation. Hum Genet. 2019 Dec; 138(11-12):1419-1421.
    View in: PubMed
    Score: 0.219
  9. Intramuscular fast-flow vascular anomaly contains somatic MAP2K1 and KRAS mutations. Angiogenesis. 2019 11; 22(4):547-552.
    View in: PubMed
    Score: 0.217
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.