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David R. Beier, MD, PhD

Harvard Medical School, Brigham and Women's Hospital, and Seattle Children's Research Institute 
ENU mutagenesis, forebrain and cerebral cortex development
"David Beier"
Mean distance: 16.53 (cluster 32)
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Huang X, Henck J, Qiu C, et al. (2023) Single-cell, whole-embryo phenotyping of mammalian developmental disorders. Nature
Jamet S, Ha S, Ho TH, et al. (2022) The Arginine Methyltransferase Carm1 is Necessary for Heart Development. G3 (Bethesda, Md.)
Ha S, Tripathi PP, Daza RA, et al. (2020) Reelin Mediates Hippocampal Cajal-Retzius Cell Positioning and Infrapyramidal Blade Morphogenesis. Journal of Developmental Biology. 8
Bittermann E, Abdelhamed Z, Liegel RP, et al. (2019) Differential requirements of tubulin genes in mammalian forebrain development. Plos Genetics. 15: e1008243
Geister KA, Lopez-Jimenez AJ, Houghtaling S, et al. (2019) Loss of function of disrupts collagen post-translational modification and causes musculoskeletal defects. Disease Models & Mechanisms
Weghorn D, Balick DJ, Cassa C, et al. (2019) Applicability of the mutation-selection balance model to population genetics of heterozygous protein-truncating variants in humans. Molecular Biology and Evolution
Abdelhamed Z, Vuong SM, Hill L, et al. (2018) A mutation in Ccdc39 causes neonatal hydrocephalus with abnormal motile cilia development in mice. Development (Cambridge, England). 145
Geister KA, Timms AE, Beier DR. (2017) Optimizing Genomic Methods for Mapping and Identification of Candidate Variants in ENU Mutagenesis Screens Using Inbred Mice. G3 (Bethesda, Md.)
Strassman A, Schnütgen F, Dai Q, et al. (2017) Generation of a multipurpose Prdm16 allele by targeted trapping. Disease Models & Mechanisms
Cassa CA, Weghorn D, Balick DJ, et al. (2017) Estimating the selective effects of heterozygous protein-truncating variants from human exome data. Nature Genetics
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