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Center for Developmental Biology and Regenerative Medicine
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Publications

Dr. David Beier has authored dozens of research papers, including the selected publications listed below. To see more of his publications, view a complete list on PubMed.

  • The arginine methyltransferase Carm1 is necessary for heart development.

    Jamet S, Ha S, Ho TH, Houghtaling S, Timms A, Yu K, Paquette A, Maga AM, Greene NDE, Beier DR

    G3 (Bethesda) , 2022 Jul 29: 12 (8 ) jkac155

  • Spiny mice activate unique transcriptional programs after severe kidney injury regenerating organ function without fibrosis.

    Okamura DM, Brewer CM, Wakenight P, Bahrami N, Bernardi K, Tran A, Olson J, Shi X, Yeh SY, Piliponsky A, Collins SJ, Nguyen ED, Timms AE, MacDonald JW, Bammler TK, Nelson BR, Millen KJ, Beier DR, Majesky MW

    iScience , 2021 Nov 3: 24 (11 ) 103269

  • Reelin Mediates Hippocampal Cajal-Retzius Cell Positioning and Infrapyramidal Blade Morphogenesis.

    Ha S, Tripathi PP, Daza RA, Hevner RF, Beier DR

    J Dev Biol , 2020 Sep 18: 8 (3 ) E20

  • Loss of function of Colgalt1 disrupts collagen post-translational modification and causes musculoskeletal defects.

    Geister KA, Lopez-Jimenez AJ, Houghtaling S, Ho TH, Vanacore R, Beier DR

    Dis Model Mech , 2019: 12 (6 )

  • Optimizing Genomic Methods for Mapping and Identification of Candidate Variants in ENU Mutagenesis Screens Using Inbred Mice.

    Geister KA, Timms AE, Beier DR

    29208648 G3 (Bethesda, Md.) , 2018 Feb 2: 8 (2 ) 401-409 PMCID: PMC5919724

  • Estimating the selective effects of heterozygous protein-truncating variants from human exome data.

    Cassa CA, Weghorn D, Balick DJ, Jordan DM, Nusinow D, Samocha KE, O'Donnell-Luria A, MacArthur DG, Daly MJ, Beier DR, Sunyaev SR

    28369035 Nature genetics , 2017 May: 49 (5 ) 806-810 PMCID: PMC5618255

  • C-Terminal Region Truncation of RELN Disrupts an Interaction with VLDLR, Causing Abnormal Development of the Cerebral Cortex and Hippocampus.

    Ha S, Tripathi PP, Mihalas AB, Hevner RF, Beier DR

    28123028 The Journal of neuroscience : the official journal of the Society for Neuroscience , 2017 Jan 25: 37 (4 ) 960-971 PMCID: PMC5296787

  • High-resolution genetic localization of a modifying locus affecting disease severity in the juvenile cystic kidneys (jck) mouse model of polycystic kidney disease.

    Beier DR

    27114383 Mammalian genome : official journal of the International Mammalian Genome Society , 2016 June: 27 (5-6 ) 191-9

  • Reduction of ciliary length through pharmacologic or genetic inhibition of CDK5 attenuates polycystic kidney disease in a model of nephronophthisis.

    Husson H, Moreno S, Smith LA, Smith MM, Russo RJ, Pitstick R, Sergeev M, Ledbetter SR, Bukanov NO, Lane M, Zhang K, Billot K, Carlson G, Shah J, Meijer L, Beier DR, Ibraghimov-Beskrovnaya O

    27053712 Human molecular genetics , 2016 Apr 5

  • Improvement of ENU Mutagenesis Efficiency Using Serial Injection and Mismatch Repair Deficiency Mice.

    Gallego-Llamas J, Timms AE, Pitstick R, Peters J, Carlson GA, Beier DR

    27441645 PloS one , 2016: 11 (7 ) e0159377 PMCID: PMC4956170

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