Rosenblatt DS - Search Results

1

Human methylenetetrahydrofolate reductase: isolation of cDNA mapping and mutation identification.

Goyette P, Sumner JS, Milos R, Duncan AM, Rosenblatt DS, Matthews RG, Rozen R. Goyette P, et al. Among authors: rosenblatt ds. Nat Genet. 1994 Aug;7(4):551. Nat Genet. 1994. PMID: 7951330 No abstract available.

2

Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification.

Goyette P, Sumner JS, Milos R, Duncan AM, Rosenblatt DS, Matthews RG, Rozen R. Goyette P, et al. Among authors: rosenblatt ds. Nat Genet. 1994 Jun;7(2):195-200. doi: 10.1038/ng0694-195. Nat Genet. 1994. PMID: 7920641

3

Severe and mild mutations in cis for the methylenetetrahydrofolate reductase (MTHFR) gene, and description of five novel mutations in MTHFR.

Goyette P, Christensen B, Rosenblatt DS, Rozen R. Goyette P, et al. Among authors: rosenblatt ds. Am J Hum Genet. 1996 Dec;59(6):1268-75. Am J Hum Genet. 1996. PMID: 8940272 Free PMC article.

4

Correlation of a common mutation in the methylenetetrahydrofolate reductase gene with plasma homocysteine in patients with premature coronary artery disease.

Christensen B, Frosst P, Lussier-Cacan S, Selhub J, Goyette P, Rosenblatt DS, Genest J Jr, Rozen R. Christensen B, et al. Among authors: rosenblatt ds. Arterioscler Thromb Vasc Biol. 1997 Mar;17(3):569-73. doi: 10.1161/01.atv.17.3.569. Arterioscler Thromb Vasc Biol. 1997. PMID: 9102178

5

Seven novel mutations in the methylenetetrahydrofolate reductase gene and genotype/phenotype correlations in severe methylenetetrahydrofolate reductase deficiency.

Goyette P, Frosst P, Rosenblatt DS, Rozen R. Goyette P, et al. Among authors: rosenblatt ds. Am J Hum Genet. 1995 May;56(5):1052-9. Am J Hum Genet. 1995. PMID: 7726158 Free PMC article.

6

Homocystinuria (methylenetetrahydrofolate reductase deficiency) and mutation of factor V gene.

Goyette P, Rosenblatt D, Rozen R. Goyette P, et al. J Inherit Metab Dis. 1998 Aug;21(6):690-1. doi: 10.1023/a:1005457206323. J Inherit Metab Dis. 1998. PMID: 9762613 No abstract available.

7

Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders.

Leclerc D, Campeau E, Goyette P, Adjalla CE, Christensen B, Ross M, Eydoux P, Rosenblatt DS, Rozen R, Gravel RA. Leclerc D, et al. Among authors: rosenblatt ds. Hum Mol Genet. 1996 Dec;5(12):1867-74. doi: 10.1093/hmg/5.12.1867. Hum Mol Genet. 1996. PMID: 8968737

8

Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects.

Christensen B, Arbour L, Tran P, Leclerc D, Sabbaghian N, Platt R, Gilfix BM, Rosenblatt DS, Gravel RA, Forbes P, Rozen R. Christensen B, et al. Among authors: rosenblatt ds. Am J Med Genet. 1999 May 21;84(2):151-7. doi: 10.1002/(sici)1096-8628(19990521)84:2<151::aid-ajmg12>3.0.co;2-t. Am J Med Genet. 1999. PMID: 10323741

9

Prenatal diagnosis for severe methylenetetrahydrofolate reductase deficiency by linkage analysis and enzymatic assay.

Morel CF, Scott P, Christensen E, Rosenblatt DS, Rozen R. Morel CF, et al. Among authors: rosenblatt ds. Mol Genet Metab. 2005 Jun;85(2):115-20. doi: 10.1016/j.ymgme.2005.03.001. Epub 2005 Apr 1. Mol Genet Metab. 2005. PMID: 15896655

10

Characterization of six novel mutations in the methylenetetrahydrofolate reductase (MTHFR) gene in patients with homocystinuria.

Sibani S, Christensen B, O'Ferrall E, Saadi I, Hiou-Tim F, Rosenblatt DS, Rozen R. Sibani S, et al. Among authors: rosenblatt ds. Hum Mutat. 2000;15(3):280-7. doi: 10.1002/(SICI)1098-1004(200003)15:3<280::AID-HUMU9>3.0.CO;2-I. Hum Mutat. 2000. PMID: 10679944

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