Connection

Co-Authors

This is a "connection" page, showing publications co-authored by SHAMIKA KETKAR and LINDSAY BURRAGE.
Connection Strength

0.715
  1. RNA Sequencing as a Diagnostic Tool. JAMA. 2023 01 03; 329(1):85-86.
    View in: PubMed
    Score: 0.220
  2. A novel, de novo intronic variant in POGZ causes White-Sutton syndrome. Am J Med Genet A. 2022 07; 188(7):2198-2203.
    View in: PubMed
    Score: 0.209
  3. Exploring the complexity of systemic sclerosis etiology by trio whole genome sequencing. Hum Mol Genet. 2024 Sep 19; 33(19):1643-1647.
    View in: PubMed
    Score: 0.062
  4. Recessive loss-of-function variants in DPH1 identified as the molecular cause in a sibling pair previously diagnosed with Fine-Lubinsky syndrome. Am J Med Genet A. 2024 Aug 21; e63845.
    View in: PubMed
    Score: 0.062
  5. The clinical utility and diagnostic implementation of human subject cell transdifferentiation followed by RNA sequencing. Am J Hum Genet. 2024 05 02; 111(5):841-862.
    View in: PubMed
    Score: 0.060
  6. TMEM161B regulates cerebral cortical gyration, Sonic Hedgehog signaling, and ciliary structure in the developing central nervous system. Proc Natl Acad Sci U S A. 2023 Jan 24; 120(4):e2209964120.
    View in: PubMed
    Score: 0.055
  7. Transcriptome-directed analysis for Mendelian disease diagnosis overcomes limitations of conventional genomic testing. J Clin Invest. 2021 01 04; 131(1).
    View in: PubMed
    Score: 0.048
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.