Otterud B - Search Results

1

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

2

Linkage of a variant or attenuated form of adenomatous polyposis coli to the adenomatous polyposis coli (APC) locus.

Spirio L, Otterud B, Stauffer D, Lynch H, Lynch P, Watson P, Lanspa S, Smyrk T, Cavalieri J, Howard L, et al. Spirio L, et al. Among authors: otterud b. Am J Hum Genet. 1992 Jul;51(1):92-100. Am J Hum Genet. 1992. PMID: 1319115 Free PMC article.

3

Alleles of the APC gene: an attenuated form of familial polyposis.

Spirio L, Olschwang S, Groden J, Robertson M, Samowitz W, Joslyn G, Gelbert L, Thliveris A, Carlson M, Otterud B, et al. Spirio L, et al. Among authors: otterud b. Cell. 1993 Dec 3;75(5):951-7. doi: 10.1016/0092-8674(93)90538-2. Cell. 1993. PMID: 8252630

4

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.

5

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.

6

A gene for familial total anomalous pulmonary venous return maps to chromosome 4p13-q12.

Bleyl S, Nelson L, Odelberg SJ, Ruttenberg HD, Otterud B, Leppert M, Ward K. Bleyl S, et al. Among authors: otterud b. Am J Hum Genet. 1995 Feb;56(2):408-15. Am J Hum Genet. 1995. PMID: 7847375 Free PMC article.

7

A gene for distal arthrogryposis type I maps to the pericentromeric region of chromosome 9.

Bamshad M, Watkins WS, Zenger RK, Bohnsack JF, Carey JC, Otterud B, Krakowiak PA, Robertson M, Jorde LB. Bamshad M, et al. Among authors: otterud b. Am J Hum Genet. 1994 Dec;55(6):1153-8. Am J Hum Genet. 1994. PMID: 7977374 Free PMC article.

8

Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous.

Leppert M, Baird L, Anderson KL, Otterud B, Lupski JR, Lewis RA. Leppert M, et al. Among authors: otterud b. Nat Genet. 1994 May;7(1):108-12. doi: 10.1038/ng0594-108. Nat Genet. 1994. PMID: 8075632

9

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.

10

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.

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