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  1. Article

    Open Access

    Disruption in murine Eml1 perturbs retinal lamination during early development

    During mammalian development, establishing functional neural networks in stratified tissues of the mammalian central nervous system depends upon the proper migration and positioning of neurons, a process known...

    G. B. Collin, J. Won, M. P. Krebs, W. J. Hicks, J. R. Charette… in Scientific Reports (2020)

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  2. Article

    Open Access

    Human genome meeting 2016

    O1 The metabolomics approach to autism: identification of biomarkers for early detection of autism spectrum disorder

    A. K. Srivastava, Y. Wang, R. Huang, C. Skinner, T. Thompson, L. Pollard… in Human Genomics (2016)

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  3. No Access

    Article

    Alström syndrome: further evidence for linkage to human chromosome 2p13

    Alström syndrome is a rare autosomal recessive disorder characterized by retinal degeneration, sensorineural hearing loss, early-onset obesity, and non-insulin-dependent diabetes mellitus. The gene for Alströ...

    G.B. Collin, J.D. Marshall, C.F. Boerkoel, A.V. Levin, R. Weksberg… in Human Genetics (1999)

  4. No Access

    Article

    DNA pooling as a quick method for finding candidate linkages in multigenic trait analysis: an example involving susceptibility to germ cell tumors

    G. B. Collin, Y. Asada, D. S. Varnum, J. H. Nadeau in Mammalian Genome (1996)