Wilson A - Search Results

1

Hyperhomocysteinemia due to methionine synthase deficiency, cblG: structure of the MTR gene, genotype diversity, and recognition of a common mutation, P1173L.

Watkins D, Ru M, Hwang HY, Kim CD, Murray A, Philip NS, Kim W, Legakis H, Wai T, Hilton JF, Ge B, Doré C, Hosack A, Wilson A, Gravel RA, Shane B, Hudson TJ, Rosenblatt DS. Watkins D, et al. Among authors: wilson a. Am J Hum Genet. 2002 Jul;71(1):143-53. doi: 10.1086/341354. Epub 2002 May 30. Am J Hum Genet. 2002. PMID: 12068375 Free PMC article.

2

Functionally null mutations in patients with the cblG-variant form of methionine synthase deficiency.

Wilson A, Leclerc D, Saberi F, Campeau E, Hwang HY, Shane B, Phillips JA 3rd, Rosenblatt DS, Gravel RA. Wilson A, et al. Am J Hum Genet. 1998 Aug;63(2):409-14. doi: 10.1086/301976. Am J Hum Genet. 1998. PMID: 9683607 Free PMC article.

3

Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism.

Wilson A, Leclerc D, Rosenblatt DS, Gravel RA. Wilson A, et al. Hum Mol Genet. 1999 Oct;8(11):2009-16. doi: 10.1093/hmg/8.11.2009. Hum Mol Genet. 1999. PMID: 10484769

4

Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria.

Leclerc D, Wilson A, Dumas R, Gafuik C, Song D, Watkins D, Heng HH, Rommens JM, Scherer SW, Rosenblatt DS, Gravel RA. Leclerc D, et al. Among authors: wilson a. Proc Natl Acad Sci U S A. 1998 Mar 17;95(6):3059-64. doi: 10.1073/pnas.95.6.3059. Proc Natl Acad Sci U S A. 1998. PMID: 9501215 Free PMC article.

5

A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida.

Wilson A, Platt R, Wu Q, Leclerc D, Christensen B, Yang H, Gravel RA, Rozen R. Wilson A, et al. Mol Genet Metab. 1999 Aug;67(4):317-23. doi: 10.1006/mgme.1999.2879. Mol Genet Metab. 1999. PMID: 10444342

6

Identification of the gene responsible for the cblA complementation group of vitamin B12-responsive methylmalonic acidemia based on analysis of prokaryotic gene arrangements.

Dobson CM, Wai T, Leclerc D, Wilson A, Wu X, Doré C, Hudson T, Rosenblatt DS, Gravel RA. Dobson CM, et al. Among authors: wilson a. Proc Natl Acad Sci U S A. 2002 Nov 26;99(24):15554-9. doi: 10.1073/pnas.242614799. Epub 2002 Nov 15. Proc Natl Acad Sci U S A. 2002. PMID: 12438653 Free PMC article.

7

Molecular cloning, expression and physical mapping of the human methionine synthase reductase gene.

Leclerc D, Odièvre M, Wu Q, Wilson A, Huizenga JJ, Rozen R, Scherer SW, Gravel RA. Leclerc D, et al. Among authors: wilson a. Gene. 1999 Nov 15;240(1):75-88. doi: 10.1016/s0378-1119(99)00431-x. Gene. 1999. PMID: 10564814

8

Integration of physical, genetic and cytogenetic maps of human chromosome 7: isolation and analysis of yeast artificial chromosome clones for 117 mapped genetic markers.

Green ED, Idol JR, Mohr-Tidwell RM, Braden VV, Peluso DC, Fulton RS, Massa HF, Magness CL, Wilson AM, Kimura J, et al. Green ED, et al. Among authors: wilson am. Hum Mol Genet. 1994 Mar;3(3):489-501. doi: 10.1093/hmg/3.3.489. Hum Mol Genet. 1994. PMID: 8012362

9

Patient-Informed Value Elements in Cost-Effectiveness Analyses of Major Depressive Disorder Treatment: A Literature Review and Synthesis.

Slejko JF, Mattingly TJ 2nd, Wilson A, Xie R, Chapman RH, Amill-Rosario A, dosReis S. Slejko JF, et al. Among authors: wilson a. Value Health. 2024 Jun 7:S1098-3015(24)02404-5. doi: 10.1016/j.jval.2024.05.017. Online ahead of print. Value Health. 2024. PMID: 38852668

10

Patient-Provider Satisfaction and Communication in U.S. Prenatal Care: A Systematic Review.

Leyser-Whalen O, Ambert PA, Wilson AL, Quaney V, Estrella F, Gomez M, Monteblanco AD. Leyser-Whalen O, et al. Among authors: wilson al. Matern Child Health J. 2024 Jun 8. doi: 10.1007/s10995-024-03952-0. Online ahead of print. Matern Child Health J. 2024. PMID: 38850378 Review.

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