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Informational Alert

Our new building on the hospital campus, Forest B, is open. Families and visitors can park in the new Forest B garage next to Emergency.

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.


  • 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

  • Variant mapping and mutation discovery in inbred mice using next-generation sequencing.

    Gallego-Llamas J, Timms AE, Geister KA, Lindsay A, Beier DR

    26552429 BMC genomics , 2015 Nov 9: 16 913 PMCID: PMC4640199

  • A forward genetic screen in mice identifies mutants with abnormal cortical patterning.

    Ha S, Stottmann RW, Furley AJ, Beier DR

    23968836 Cerebral cortex (New York, N.Y. : 1991) , 2015 Jan.: 25 (1 ) 167-79 PMCID: PMC4259276

  • Downregulating hedgehog signaling reduces renal cystogenic potential of mouse models.

    Tran PV, Talbott GC, Turbe-Doan A, Jacobs DT, Schonfeld MP, Silva LM, Chatterjee A, Prysak M, Allard BA, Beier DR

    24700869 Journal of the American Society of Nephrology : JASN , 2014 Oct.: 25 (10 ) 2201-12 PMCID: PMC4178433

  • ENU mutagenesis in the mouse.

    Stottmann R, Beier D

    25723916 Current protocols in mouse biology , 2014 Jun 16: 4 (2 ) 25-35