Connection

JIMMY HOLDER JR to Developmental Disabilities

This is a "connection" page, showing publications JIMMY HOLDER JR has written about Developmental Disabilities.
Connection Strength

0.241
  1. De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome. Genome Med. 2019 02 28; 11(1):12.
    View in: PubMed
    Score: 0.105
  2. A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and Seizures. Cell. 2018 02 22; 172(5):924-936.e11.
    View in: PubMed
    Score: 0.098
  3. Chronic Catatonia in an Individual With a De Novo Missense SHANK1 Variant. Am J Med Genet A. 2025 Apr; 197(4):e63943.
    View in: PubMed
    Score: 0.039
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.