Otterud B - Search Results

1

A hyperactivating proinflammatory RIPK2 allele associated with early-onset osteoarthritis.

Jurynec MJ, Sawitzke AD, Beals TC, Redd MJ, Stevens J, Otterud B, Leppert MF, Grunwald DJ. Jurynec MJ, et al. Among authors: otterud b. Hum Mol Genet. 2018 Jul 1;27(13):2383-2391. doi: 10.1093/hmg/ddy132. Hum Mol Genet. 2018. PMID: 29659823 Free PMC article.

2

A hyperactivating proinflammatory RIPK2 allele associated with early-onset osteoarthritis.

Jurynec MJ, Sawitzke AD, Beals TC, Redd MJ, Stevens J, Otterud B, Leppert MF, Grunwald DJ. Jurynec MJ, et al. Among authors: otterud b. Hum Mol Genet. 2018 Jul 1;27(13):2406. doi: 10.1093/hmg/ddy196. Hum Mol Genet. 2018. PMID: 29860498 Free PMC article. No abstract available.

3

Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia: evidence for locus heterogeneity.

Heath H 3rd, Jackson CE, Otterud B, Leppert MF. Heath H 3rd, et al. Among authors: otterud b. Am J Hum Genet. 1993 Jul;53(1):193-200. Am J Hum Genet. 1993. PMID: 8317484 Free PMC article.

4

Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1.

Flanigan K, Gardner K, Alderson K, Galster B, Otterud B, Leppert MF, Kaplan C, Ptácek LJ. Flanigan K, et al. Among authors: otterud b. Am J Hum Genet. 1996 Aug;59(2):392-9. Am J Hum Genet. 1996. PMID: 8755926 Free PMC article.

5

Exome analysis of a family with pleiotropic congenital heart disease.

Arrington CB, Bleyl SB, Matsunami N, Bonnell GD, Otterud BE, Nielsen DC, Stevens J, Levy S, Leppert MF, Bowles NE. Arrington CB, et al. Among authors: otterud be. Circ Cardiovasc Genet. 2012 Apr 1;5(2):175-82. doi: 10.1161/CIRCGENETICS.111.961797. Epub 2012 Feb 15. Circ Cardiovasc Genet. 2012. PMID: 22337856 Free PMC article.

6

Colorectal adenomas and cancer link to chromosome 13q22.1-13q31.3 in a large family with excess colorectal cancer.

Neklason DW, Tuohy TM, Stevens J, Otterud B, Baird L, Kerber RA, Samowitz WS, Kuwada SK, Leppert MF, Burt RW. Neklason DW, et al. Among authors: otterud b. J Med Genet. 2010 Oct;47(10):692-9. doi: 10.1136/jmg.2009.076091. Epub 2010 Jun 3. J Med Genet. 2010. PMID: 20522424 Free PMC article.

7

Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population.

Matsunami N, Hensel CH, Baird L, Stevens J, Otterud B, Leppert T, Varvil T, Hadley D, Glessner JT, Pellegrino R, Kim C, Thomas K, Wang F, Otieno FG, Ho K, Christensen GB, Li D, Prekeris R, Lambert CG, Hakonarson H, Leppert MF. Matsunami N, et al. Among authors: otterud b. Mol Autism. 2014 Jan 27;5(1):5. doi: 10.1186/2040-2392-5-5. Mol Autism. 2014. PMID: 24467814 Free PMC article.

8

The identical 5' splice-site acceptor mutation in five attenuated APC families from Newfoundland demonstrates a founder effect.

Spirio L, Green J, Robertson J, Robertson M, Otterud B, Sheldon J, Howse E, Green R, Groden J, White R, Leppert M. Spirio L, et al. Among authors: otterud b. Hum Genet. 1999 Nov;105(5):388-98. doi: 10.1007/s004390051121. Hum Genet. 1999. PMID: 10598803

9

A novel form of juvenile recessive ALS maps to loci on 6p25 and 21q22.

Butterfield RJ, Ramachandran D, Hasstedt SJ, Otterud BE, Leppert MF, Swoboda KJ, Flanigan KM. Butterfield RJ, et al. Among authors: otterud be. Neuromuscul Disord. 2009 Apr;19(4):279-87. doi: 10.1016/j.nmd.2009.02.006. Epub 2009 Mar 21. Neuromuscul Disord. 2009. PMID: 19318250

10

Dinucleotide repeat polymorphism from a cosmid containing the human anion exchanger isoform 3 (SLC2C) gene.

Klanke CA, Su YR, Varvil TS, Otterud BE, Leppert M, Menon AG. Klanke CA, et al. Among authors: otterud be. Hum Mol Genet. 1994 Nov;3(11):2086. Hum Mol Genet. 1994. PMID: 7874147 No abstract available.

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