Otterud B - Search Results

1

Genetic susceptibility in familial multiple sclerosis not linked to the myelin basic protein gene.

Rose J, Gerken S, Lynch S, Pisani P, Varvil T, Otterud B, Leppert M. Rose J, et al. Among authors: otterud b. Lancet. 1993 May 8;341(8854):1179-81. doi: 10.1016/0140-6736(93)91003-5. Lancet. 1993. PMID: 7683738

2

Description of a second microsatellite marker and linkage analysis of the muscle glycogen synthase locus in familial NIDDM.

Elbein SC, Hoffman M, Ridinger D, Otterud B, Leppert M. Elbein SC, et al. Among authors: otterud b. Diabetes. 1994 Aug;43(8):1061-5. doi: 10.2337/diab.43.8.1061. Diabetes. 1994. PMID: 7913686

3

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

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

A locus for febrile seizures (FEB3) maps to chromosome 2q23-24.

Peiffer A, Thompson J, Charlier C, Otterud B, Varvil T, Pappas C, Barnitz C, Gruenthal K, Kuhn R, Leppert M. Peiffer A, et al. Among authors: otterud b. Ann Neurol. 1999 Oct;46(4):671-8. doi: 10.1002/1531-8249(199910)46:4<671::aid-ana20>3.0.co;2-5. Ann Neurol. 1999. PMID: 10514109

6

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

7

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.

8

Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population.

Matsunami N, Hadley D, Hensel CH, Christensen GB, Kim C, Frackelton E, Thomas K, da Silva RP, Stevens J, Baird L, Otterud B, Ho K, Varvil T, Leppert T, Lambert CG, Leppert M, Hakonarson H. Matsunami N, et al. Among authors: otterud b. PLoS One. 2013;8(1):e52239. doi: 10.1371/journal.pone.0052239. Epub 2013 Jan 14. PLoS One. 2013. PMID: 23341896 Free PMC article.

9

Localization to chromosome 22 of a gene encoding a human minor histocompatibility antigen.

Gubarev MI, Jenkin JC, Leppert MF, Buchanan GS, Otterud BE, Guilbert DA, Beatty PG. Gubarev MI, et al. Among authors: otterud be. J Immunol. 1996 Dec 15;157(12):5448-54. J Immunol. 1996. PMID: 8955193

10

Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2.

Ho CY, Otterud B, Legare RD, Varvil T, Saxena R, DeHart DB, Kohler SE, Aster JC, Dowton SB, Li FP, Leppert M, Gilliland DG. Ho CY, et al. Among authors: otterud b. Blood. 1996 Jun 15;87(12):5218-24. Blood. 1996. PMID: 8652836 Free article.

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