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Connection

Astrid Rasmussen to Adolescent

This is a "connection" page, showing publications Astrid Rasmussen has written about Adolescent.
Connection Strength

0.350
  1. Comparison of the American-European Consensus Group Sjogren's syndrome classification criteria to newly proposed American College of Rheumatology criteria in a large, carefully characterised sicca cohort. Ann Rheum Dis. 2014 Jan; 73(1):31-8.
    View in: PubMed
    Score: 0.065
  2. Uptake of genetic testing and long-term tumor surveillance in von Hippel-Lindau disease. BMC Med Genet. 2010 Jan 12; 11:4.
    View in: PubMed
    Score: 0.051
  3. Clinical and genetic characteristics of Mexican Huntington's disease patients. Mov Disord. 2009 Oct 15; 24(13):2012-5.
    View in: PubMed
    Score: 0.050
  4. Anticipation and intergenerational repeat instability in spinocerebellar ataxia type 17. Ann Neurol. 2007 Jun; 61(6):607-10.
    View in: PubMed
    Score: 0.042
  5. Clinical heterogeneity of recessive ataxia in the Mexican population. J Neurol Neurosurg Psychiatry. 2006 Dec; 77(12):1370-2.
    View in: PubMed
    Score: 0.041
  6. Von Hippel-Lindau disease germline mutations in Mexican patients with cerebellar hemangioblastoma. J Neurosurg. 2006 Mar; 104(3):389-94.
    View in: PubMed
    Score: 0.039
  7. Childhood-onset of primary Sjögren's syndrome: phenotypic characterization at diagnosis of 158 children. Rheumatology (Oxford). 2021 10 02; 60(10):4558-4567.
    View in: PubMed
    Score: 0.029
  8. Impact of genetic ancestry and sociodemographic status on the clinical expression of systemic lupus erythematosus in American Indian-European populations. Arthritis Rheum. 2012 Nov; 64(11):3687-94.
    View in: PubMed
    Score: 0.015
  9. Progressive GAA expansions in dorsal root ganglia of Friedreich's ataxia patients. Ann Neurol. 2007 Jan; 61(1):55-60.
    View in: PubMed
    Score: 0.010
  10. Genotype-phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive deficit subphenotype. Hum Mol Genet. 2002 May 15; 11(11):1263-71.
    View in: PubMed
    Score: 0.007
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.