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Connection

Astrid Rasmussen to Myoclonic Epilepsy, Juvenile

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This is a "connection" page, showing publications Astrid Rasmussen has written about Myoclonic Epilepsy, Juvenile.
Astrid Rasmussen
Connection Strength
0.315
Myoclonic Epilepsy, Juvenile
  1. DNA variants in coding region of EFHC1: SNPs do not associate with juvenile myoclonic epilepsy. Epilepsia. 2009 May; 50(5):1184-90.
    View in: PubMed
    Score: 0.083
  2. Mutation analyses of genes on 6p12-p11 in patients with juvenile myoclonic epilepsy. Neurosci Lett. 2006 Sep 11; 405(1-2):126-31.
    View in: PubMed
    Score: 0.068
  3. Mutations in EFHC1 cause juvenile myoclonic epilepsy. Nat Genet. 2004 Aug; 36(8):842-9.
    View in: PubMed
    Score: 0.059
  4. 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: 0.053
  5. 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: 0.052
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.