Connection

MONIKA WEISZ HUBSHMAN to Female

This is a "connection" page, showing publications MONIKA WEISZ HUBSHMAN has written about Female.
Connection Strength

0.070
  1. Novel WWOX deleterious variants cause early infantile epileptic encephalopathy, severe developmental delay and dysmorphism among Yemenite Jews. Eur J Paediatr Neurol. 2019 May; 23(3):418-426.
    View in: PubMed
    Score: 0.019
  2. Whole-exome sequencing reveals POC5 as a novel gene associated with autosomal recessive retinitis pigmentosa. Hum Mol Genet. 2018 02 15; 27(4):614-624.
    View in: PubMed
    Score: 0.018
  3. Homozygous deletion of RAG1, RAG2 and 5' region TRAF6 causes severe immune suppression and atypical osteopetrosis. Clin Genet. 2017 Jun; 91(6):902-907.
    View in: PubMed
    Score: 0.017
  4. Detection of copy number variations in epilepsy using exome data. Clin Genet. 2018 03; 93(3):577-587.
    View in: PubMed
    Score: 0.004
  5. Is one diagnosis the whole story? patients with double diagnoses. Am J Med Genet A. 2016 09; 170(9):2338-48.
    View in: PubMed
    Score: 0.004
  6. Re-evaluation of bone pain in patients with type 1 Gaucher disease suggests that bone crises occur in small bones as well as long bones. Blood Cells Mol Dis. 2016 09; 60:65-72.
    View in: PubMed
    Score: 0.004
  7. Homozygous MED25 mutation implicated in eye-intellectual disability syndrome. Hum Genet. 2015 Jun; 134(6):577-87.
    View in: PubMed
    Score: 0.004
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.