Geister KA - Search Results

1

A novel loss-of-function mutation in Npr2 clarifies primary role in female reproduction and reveals a potential therapy for acromesomelic dysplasia, Maroteaux type.

Geister KA, Brinkmeier ML, Hsieh M, Faust SM, Karolyi IJ, Perosky JE, Kozloff KM, Conti M, Camper SA. Geister KA, et al. Hum Mol Genet. 2013 Jan 15;22(2):345-57. doi: 10.1093/hmg/dds432. Epub 2012 Oct 12. Hum Mol Genet. 2013. PMID: 23065701 Free PMC article.

2

Advances in Skeletal Dysplasia Genetics.

Geister KA, Camper SA. Geister KA, et al. Annu Rev Genomics Hum Genet. 2015;16:199-227. doi: 10.1146/annurev-genom-090314-045904. Epub 2015 Apr 22. Annu Rev Genomics Hum Genet. 2015. PMID: 25939055 Free PMC article. Review.

3

LINE-1 Mediated Insertion into Poc1a (Protein of Centriole 1 A) Causes Growth Insufficiency and Male Infertility in Mice.

Geister KA, Brinkmeier ML, Cheung LY, Wendt J, Oatley MJ, Burgess DL, Kozloff KM, Cavalcoli JD, Oatley JM, Camper SA. Geister KA, et al. PLoS Genet. 2015 Oct 23;11(10):e1005569. doi: 10.1371/journal.pgen.1005569. eCollection 2015 Oct. PLoS Genet. 2015. PMID: 26496357 Free PMC article.

4

The Histone Methyltransferase Gene Absent, Small, or Homeotic Discs-1 Like Is Required for Normal Hox Gene Expression and Fertility in Mice.

Brinkmeier ML, Geister KA, Jones M, Waqas M, Maillard I, Camper SA. Brinkmeier ML, et al. Among authors: geister ka. Biol Reprod. 2015 Nov;93(5):121. doi: 10.1095/biolreprod.115.131516. Epub 2015 Sep 2. Biol Reprod. 2015. PMID: 26333994 Free PMC article.

5

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

Gallego-Llamas J, Timms AE, Geister KA, Lindsay A, Beier DR. Gallego-Llamas J, et al. Among authors: geister ka. BMC Genomics. 2015 Nov 9;16:913. doi: 10.1186/s12864-015-2173-1. BMC Genomics. 2015. PMID: 26552429 Free PMC article.

6

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

Geister KA, Timms AE, Beier DR. Geister KA, et al. G3 (Bethesda). 2018 Feb 2;8(2):401-409. doi: 10.1534/g3.117.300292. G3 (Bethesda). 2018. PMID: 29208648 Free PMC article.

7

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. Geister KA, et al. Dis Model Mech. 2019 Jun 17;12(6):dmm037176. doi: 10.1242/dmm.037176. Dis Model Mech. 2019. PMID: 31101663 Free PMC article.

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