Connection

Co-Authors

This is a "connection" page, showing publications co-authored by SEEMA LALANI and KIM WORLEY.
Connection Strength

0.630
  1. Clinical exome sequencing uncovers a high frequency of Mendelian disorders in infants with stroke: A retrospective analysis. Am J Med Genet A. 2022 11; 188(11):3184-3190.
    View in: PubMed
    Score: 0.202
  2. LMOD2-related dilated cardiomyopathy presenting in late infancy. Am J Med Genet A. 2022 06; 188(6):1858-1862.
    View in: PubMed
    Score: 0.195
  3. Heterozygous variants in PLCG1 affect hearing, vision, cardiac, and immune function. Elife. 2025 Aug 27; 13.
    View in: PubMed
    Score: 0.062
  4. Heterozygous variants in PLCG1 affect hearing, vision, cardiac, and immune function. medRxiv. 2025 May 29.
    View in: PubMed
    Score: 0.061
  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: 0.056
  6. Dominant negative variants in IKZF2 cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delay. J Med Genet. 2023 11; 60(11):1092-1104.
    View in: PubMed
    Score: 0.053
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.