David R. Beier, MD, PhD
Affiliations: | Harvard Medical School, Brigham and Women's Hospital, and Seattle Children's Research Institute |
Area:
ENU mutagenesis, forebrain and cerebral cortex developmentWebsite:
http://www.seattlechildrens.org/medical-staff/David-Randolph-Beier/Google:
"David Beier"Mean distance: 16.53 (cluster 32) | S | N | B | C | P |
Children
Sign in to add trainee| Seungshin Ha | post-doc | 2009- | Brigham and Women's Hospital and Seattle Children's Research Institute |
| Rolf W. Stottmann | post-doc | 2004-2011 | Brigham & Women's Hospital |
Collaborators
Sign in to add collaborator| Noelle Dwyer | collaborator | Brigham and Women's Hospital/ Harvard Medical School | |
| Chris A. Walsh | collaborator | Harvard Medical School | |
| Robert F. Hevner | collaborator | 2014- | University of Washington, Seattle Children's Research Institute |
BETA: Related publications
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Publications
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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 |