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Connection

William Dobyns to Gene Expression Regulation, Developmental

This is a "connection" page, showing publications William Dobyns has written about Gene Expression Regulation, Developmental.
  1. A developmental and genetic classification for midbrain-hindbrain malformations. Brain. 2009 Dec; 132(Pt 12):3199-230.
    View in: PubMed
    Score: 0.266
  2. Mutations in MAST1 Cause Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations. Neuron. 2018 12 19; 100(6):1354-1368.e5.
    View in: PubMed
    Score: 0.123
  3. PARD3 dysfunction in conjunction with dynamic HIPPO signaling drives cortical enlargement with massive heterotopia. Genes Dev. 2018 06 01; 32(11-12):763-780.
    View in: PubMed
    Score: 0.030
  4. Hypomorphic Recessive Variants in SUFU Impair the Sonic Hedgehog Pathway and Cause Joubert Syndrome with Cranio-facial and Skeletal Defects. Am J Hum Genet. 2017 Oct 05; 101(4):552-563.
    View in: PubMed
    Score: 0.029
  5. CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar development. Nat Genet. 2012 Nov; 44(11):1260-4.
    View in: PubMed
    Score: 0.020
  6. Polymicrogyria includes fusion of the molecular layer and decreased neuronal populations but normal cortical laminar organization. J Neuropathol Exp Neurol. 2011 Jun; 70(6):438-43.
    View in: PubMed
    Score: 0.018
  7. Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia. Neuron. 1998 Dec; 21(6):1315-25.
    View in: PubMed
    Score: 0.008
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.