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Connection

Astrid Rasmussen to Pedigree

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

0.467
  1. The lupus family registry and repository. Rheumatology (Oxford). 2011 Jan; 50(1):47-59.
    View in: PubMed
    Score: 0.088
  2. Anticipation and intergenerational repeat instability in spinocerebellar ataxia type 17. Ann Neurol. 2007 Jun; 61(6):607-10.
    View in: PubMed
    Score: 0.070
  3. Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population. Mov Disord. 2007 May 15; 22(7):1050-3.
    View in: PubMed
    Score: 0.070
  4. Von Hippel-Lindau disease germline mutations in Mexican patients with cerebellar hemangioblastoma. J Neurosurg. 2006 Mar; 104(3):389-94.
    View in: PubMed
    Score: 0.064
  5. Extensive cerebellar and thalamic degeneration in spinocerebellar ataxia type 10. Parkinsonism Relat Disord. 2019 09; 66:182-188.
    View in: PubMed
    Score: 0.041
  6. Expansion of the variable expression of Muenke syndrome: Hydrocephalus without craniosynostosis. Am J Med Genet A. 2016 12; 170(12):3189-3196.
    View in: PubMed
    Score: 0.033
  7. Clinical and molecular features of familial and sporadic cases of von Hippel-Lindau disease from Mexico. Clin Exp Ophthalmol. 2010 Apr; 38(3):277-83.
    View in: PubMed
    Score: 0.021
  8. Huntington's Disease-like 2 (HDL2) in North America and Japan. Ann Neurol. 2004 Nov; 56(5):670-4.
    View in: PubMed
    Score: 0.015
  9. Mutations in EFHC1 cause juvenile myoclonic epilepsy. Nat Genet. 2004 Aug; 36(8):842-9.
    View in: PubMed
    Score: 0.014
  10. Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10. Am J Hum Genet. 2004 Jun; 74(6):1216-24.
    View in: PubMed
    Score: 0.014
  11. Juvenile myoclonic epilepsy: linkage to chromosome 6p12 in Mexico families. Am J Med Genet. 2002 Dec 01; 113(3):268-74.
    View in: PubMed
    Score: 0.013
  12. Identification and mutational analysis of candidate genes for juvenile myoclonic epilepsy on 6p11-p12: LRRC1, GCLC, KIAA0057 and CLIC5. Epilepsy Res. 2002 Aug; 50(3):265-75.
    View in: PubMed
    Score: 0.012
  13. 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: 0.012
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.