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Connection

RONIT MAROM to Osteogenesis Imperfecta

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This is a "connection" page, showing publications RONIT MAROM has written about Osteogenesis Imperfecta.
RONIT MAROM
Connection Strength
3.044
Osteogenesis Imperfecta
  1. The IFITM5 mutation in osteogenesis imperfecta type V is associated with an ERK/SOX9-dependent osteoprogenitor differentiation defect. J Clin Invest. 2024 Jun 17; 134(15).
    View in: PubMed
    Score: 0.751
  2. Dominant negative variants in KIF5B cause osteogenesis imperfecta via down regulation of mTOR signaling. PLoS Genet. 2023 Nov; 19(11):e1011005.
    View in: PubMed
    Score: 0.720
  3. Osteogenesis imperfecta: an update on clinical features and therapies. Eur J Endocrinol. 2020 Oct; 183(4):R95-R106.
    View in: PubMed
    Score: 0.581
  4. Osteogenesis imperfecta: advancements in genetics and treatment. Curr Opin Pediatr. 2019 12; 31(6):708-715.
    View in: PubMed
    Score: 0.548
  5. Pharmacological and biological therapeutic strategies for osteogenesis imperfecta. Am J Med Genet C Semin Med Genet. 2016 12; 172(4):367-383.
    View in: PubMed
    Score: 0.443
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.