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A-Z Articles Index by First Author's Last Name |
| Halks-Miller M et al. CCR1 is an early and specific marker of Alzheimer's disease. Ann Neurol. 2003 Nov;54(5):638-46. |
| Halonen M et al. AIRE mutations and human leukocyte antigen genotypes as determinants of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy phenotype. J Clin Endocrinol Metab 2002;87(6):2568-74. |
| Hancock AM et al. Adaptations to Climate in Candidate Genes for Common Metabolic Disorders. 2008 PLoS Genetics 4(2): e32 |
| Hanson BJ et al. An immunocytochemical approach to detection of mitochondrial disorders. J Histochem Cytochem. 2002;50:1281-1288. |
| Hanson H et al. Telomere shortening in Fanconi anaemia demonstrated by a direct FISH approach. Cytogenet Cell Genet. 2001; 93:203-206. |
| Hao HX et al. SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma. Science. 2009 Aug 28;325(5944):1139-42. Epub 2009 Jul 23. |
Hao QL et al. In vitro identification of single CD34+CD38- cells with both lymphoid and myeloid potential. Blood. 1998 Jun 1;91(11):4145-51. |
| Hao W et al. Evidence for two apoptotic pathways in light-induced retinal degeneration. Nat Genet. 2002;32: 254-60. |
Hard ML et al. Gene-expression analysis after alcohol exposure in the developing mouse. J Lab Clin Med. 2005 Jan;145(1):47-54. |
| Hardy J & Singleton A. Genomewide association studies and human disease. N Engl J Med. 2009 Apr 23;360(17):1759-68. Epub 2009 Apr 15. |
Harikrishnan KN, et al. Brahma links the SWI/SNF chromatin-remodeling complex with MeCP2-dependent transcriptional silencing. Nat Genet. 2005 Mar;37(3):254-64. Epub 2005 Feb 6. |
| Hattar S et al. Melanopsin-containing retinal ganglion cells: architecture, projections, and intrinsic photosensitivity. Science. 2002; 295:1065-70. |
| He L et al. A microRNA polycistron as a potential human oncogene. Nature. 2005 Jun 9;435(7043):828-33. |
| Headon DJ et al. Gene defect in ectodermal dysplasia implicates a death domain adapter in development. Nature. 2001; 414:913-6. |
| Helgadottir A et al. A Common Variant on Chromosome 9p21 Affects the Risk of Myocardial Infarction. Science. 2007 May 3; [Epub ahead of print] |
| Heng HH et al. Genetic and epigenetic heterogeneity in cancer: A genome-centric perspective. J Cell Physiol. 2009 May 13. |
| Hernandez-Boussard T, et al. Pharmacogenomics: The relevance of emerging genotyping technologies. MLO Med Lab Obs. 2006 Mar;38(3):24, 26-30. |
| Higgins AW et al. Characterization of apparently balanced chromosome rearrangements from the Developmental Genome Anatomy Project. Am J Hum Genet. 2008 Mar;82(3):712-22. |
| Hinds DA et al. Common deletions and SNPs are in linkage disequilibrium in the human genome. Nat Genet. 2006 Jan;38(1):82-85. |
Hinsley TA, et al. Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome. Protein Sci. 2004 Oct;13(10):2588-99 |
| Hirano S et al. Mutator phenotype of MUTYH-null mouse embryonic stem cells. J Biol Chem. 2003 Oct 3;278(40):38121-4. |
Hirota H, et al. Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23. Genet Med. 2003 Jul-Aug;5(4):311-21 |
| Hitzler JK and Zipursky A. Origins of leukaemia in children with Down syndrome. Nat Rev Cancer. 2005 Jan;5(1):11-20. |
| Holve S et al. Metachromatic leukodystrophy in the Navajo: fallout of the American-Indian wars of the nineteenth century. Am J Med Genet. 2001 Jul 1; 101(3): 203-8. |
| Holzenberger M et al. IGF-1 receptor regulates lifespan and resistance to oxidative stress in mice. Nature. 2003 Jan 9;421(6919):182-7. |
| Hoogenraad CC et al. Targeted mutation of Cyln2 in the Williams syndrome critical region links CLIP-115 haploinsufficiency to neurodevelopmental abnormalities in mice. Nat Genet. 2002 Sep;32(1):116-27. |
| Howlett NG et al. Biallelic inactivation of BRCA2 in Fanconi anemia. Science. 2002 Jul 26;297(5581):606-9. |
| Huang TT et al. Sequential modification of NEMO/IKKgamma by SUMO-1 and ubiquitin mediates NF-kappaB activation by genotoxic stress. Cell. 2003 Nov 26;115(5):565-76. |
| Hudson G et al. Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance. Brain. 2008 Feb;131(Pt 2):329-37. Epub 2007 Dec 7. |