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Connection

Astrid Rasmussen to Molecular Sequence Data

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This is a "connection" page, showing publications Astrid Rasmussen has written about Molecular Sequence Data.
Astrid Rasmussen
Connection Strength
0.054
Molecular Sequence Data
  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: 0.017
  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: 0.014
  3. Mutations in EFHC1 cause juvenile myoclonic epilepsy. Nat Genet. 2004 Aug; 36(8):842-9.
    View in: PubMed
    Score: 0.012
  4. 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: 0.011
Connection Strength

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Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.