LaBuda MC - Search Results

1

Genetic anticipation in Crohn's disease.

Bayless TM, Picco MF, LaBuda MC. Bayless TM, et al. Among authors: labuda mc. Am J Gastroenterol. 1998 Dec;93(12):2322-5. doi: 10.1111/j.1572-0241.1998.02322.x. Am J Gastroenterol. 1998. PMID: 9860387 Review. No abstract available.

2

Identification of novel susceptibility loci for inflammatory bowel disease on chromosomes 1p, 3q, and 4q: evidence for epistasis between 1p and IBD1.

Cho JH, Nicolae DL, Gold LH, Fields CT, LaBuda MC, Rohal PM, Pickles MR, Qin L, Fu Y, Mann JS, Kirschner BS, Jabs EW, Weber J, Hanauer SB, Bayless TM, Brant SR. Cho JH, et al. Among authors: labuda mc. Proc Natl Acad Sci U S A. 1998 Jun 23;95(13):7502-7. doi: 10.1073/pnas.95.13.7502. Proc Natl Acad Sci U S A. 1998. PMID: 9636179 Free PMC article.

3

Linkage mapping by simultaneous screening of multiple polymorphic loci using Alu oligonucleotide-directed PCR.

Zietkiewicz E, Labuda M, Sinnett D, Glorieux FH, Labuda D. Zietkiewicz E, et al. Proc Natl Acad Sci U S A. 1992 Sep 15;89(18):8448-51. doi: 10.1073/pnas.89.18.8448. Proc Natl Acad Sci U S A. 1992. PMID: 1528850 Free PMC article.

4

Two hereditary defects related to vitamin D metabolism map to the same region of human chromosome 12q13-14.

Labuda M, Fujiwara TM, Ross MV, Morgan K, Garcia-Heras J, Ledbetter DH, Hughes MR, Glorieux FH. Labuda M, et al. J Bone Miner Res. 1992 Dec;7(12):1447-53. doi: 10.1002/jbmr.5650071212. J Bone Miner Res. 1992. PMID: 1336301 Free article.

5

Mapping autosomal recessive vitamin D dependency type I to chromosome 12q14 by linkage analysis.

Labuda M, Morgan K, Glorieux FH. Labuda M, et al. Am J Hum Genet. 1990 Jul;47(1):28-36. Am J Hum Genet. 1990. PMID: 1971995 Free PMC article.

6

Linkage disequilibrium analysis in young populations: pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians.

Labuda M, Labuda D, Korab-Laskowska M, Cole DE, Zietkiewicz E, Weissenbach J, Popowska E, Pronicka E, Root AW, Glorieux FH. Labuda M, et al. Am J Hum Genet. 1996 Sep;59(3):633-43. Am J Hum Genet. 1996. PMID: 8751865 Free PMC article.

7

Osteogenesis imperfecta type VII maps to the short arm of chromosome 3.

Labuda M, Morissette J, Ward LM, Rauch F, Lalic L, Roughley PJ, Glorieux FH. Labuda M, et al. Bone. 2002 Jul;31(1):19-25. doi: 10.1016/s8756-3282(02)00808-6. Bone. 2002. PMID: 12110407

8

Human 25-hydroxyvitamin D 24-hydroxylase cytochrome P450 subunit maps to a different chromosomal location than that of pseudovitamin D-deficient rickets.

Labuda M, Lemieux N, Tihy F, Prinster C, Glorieux FH. Labuda M, et al. J Bone Miner Res. 1993 Nov;8(11):1397-406. doi: 10.1002/jbmr.5650081114. J Bone Miner Res. 1993. PMID: 8266831 Free article.

9

Unique origin and specific ethnic distribution of the Friedreich ataxia GAA expansion.

Labuda M, Labuda D, Miranda C, Poirier J, Soong BW, Barucha NE, Pandolfo M. Labuda M, et al. Neurology. 2000 Jun 27;54(12):2322-4. doi: 10.1212/wnl.54.12.2322. Neurology. 2000. PMID: 10881262

10

The genetic clock and the age of the founder effect in growing populations: a lesson from French Canadians and Ashkenazim.

Labuda D, Zietkiewicz E, Labuda M. Labuda D, et al. Am J Hum Genet. 1997 Sep;61(3):768-71. Am J Hum Genet. 1997. PMID: 9326343 Free PMC article. No abstract available.

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