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A-Z Articles Index by First Author's Last Name |
| Aarts M et al.Treatment of ischemic brain damage by perturbing NMDA receptor- PSD-95 protein interactions. Science. 2002;298(5594):846-50.PMID:12399596 [PubMed-in process] |
| Aas PA et al. Human and bacterial oxidative demethylases repair alkylation damage in both RNA and DNA. Nature 2003 Feb 20;421(6925):859-63. |
| Abi-Rached L. et al. Evidence of en bloc duplication in vertebrate genomes. Nat Genet. 2002; 31:100-105.Genet. 1997;13:90-92. |
Adams DJ et al. Mutagenic insertion and chromosome engineering resource (MICER). Nat Genet. 2004 Aug; 36 (8): 867-71. Epub 2004 Jul 04. |
| Adelfalk C. et al. Accelerated telomere shortening in Fanconi anemia fibroblasts--a longitudinal study. FEBS Lett. 2001; 506:22-26. |
| Agarwal AK et al. Zinc metalloproteinase, ZMPSTE24, is mutated in mandibuloacral dysplasia. Hum Mol Genet. 2003 Aug 15;12(16):1995-2001. |
| Agostoni C, et al. A randomized trial of long-chain polyunsaturated acid supplementation in infants with phenylketonuria. Dev Med Child Neurol. 2006 Mar;48(3):207-12 |
| Ahlgren SC et al. Sonic hedgehog rescues cranial neural crest from cell death induced by ethanol exposure. Proc Natl Acad Sci USA 2002;99:10476-81. |
| Ahmad S et al. Connexins 26 and 30 are co-assembled to form gap junctions in the cochlea of mice. Biochem Biophys Res Commun. 2003 Jul 25;307(2):362-8. |
| Alarcón M et al. Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. Am J Hum Genet. 2008 Jan;82(1):150-9. |
| Aldamiz-Echevarria L, et al. Effect of docosahexaenoic acid administration on plasma lipid profile and metabolic parameters of children with methylmalonic acidaemia. J Inherit Metab Dis. 2006 Feb;29(1):58-63 |
| Allen KJ et al. Iron-overload-related disease in HFE hereditary hemochromatosis. N Engl J Med. 2008 Jan 17;358(3):221-30. |
Amano K et al. Dosage-dependent over-expression of genes in the trisomic region of Ts1Cje mouse model for Down syndrome. Hum Mol Genet. 2004 Jul 1;13 (13): 1333-40. Epub 2004 May 11. |
| Anderson EC et al. Population-genetic basis of haplotype blocks in the 5q31 region. Am J Hum Genet. 2004 Jan; 74(1): 40-9. Epub 2003 Dec 17. |
| Anderson RR. Religious traditions and prenatal genetic counseling. 2009. AJMG p52-61. Published Online: Jan 23 2009 9:50AM DOI: 10.1002/ajmg.c.30203 |
| Aoi T, et al. Generation of pluripotent stem cells from adult mouse liver and stomach cells. Science. 2008 Feb 14 [Epub ahead of print]. |
| Arevalo E, et al. An alcohol binding site on the neural cell adhesion molecule L1. Proc Natl Acad Sci U S A. 2008 Jan 8;105(1):371-5. Epub 2007 Dec 28. |
| Ariani F et al. FOXG1 is responsible for the congenital variant of Rett syndrome. 2008. Am J Hum Genet 83, 89-93 |
| Arking DE et al. A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. Am J Hum Genet. 2008 Jan;82 (1):160-4. |
| Armstrong, S.A. et al. (2002), MLL translocations specify a distinct gene expression profile that distinguishes a unique leukemia. Nature Genetics 30:41-47. |
| ASHG Draft Statement on DTC (Direct-to-Consumer) Genetic Testing (10/10/2006) |