11 results for author:"Hodges E." in Literature citations
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| Exome sequencing and disease-network analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesis. Erlich Y., Edvardson S., Hodges E., Zenvirt S., Thekkat P., Shaag A., Dor T., Hannon G.J., Elpeleg O. |
| Mutations in the RNA granule component TDRD7 cause cataract and glaucoma. Lachke S.A., Alkuraya F.S., Kneeland S.C., Ohn T., Aboukhalil A., Howell G.R., Saadi I., Cavallesco R., Yue Y., Tsai A.C. et al. |
| Neurotrophic factor-related gene polymorphisms and adult attention deficit hyperactivity disorder (ADHD) score in a high-risk male population. Conner A.C., Kissling C., Hodges E., Hunnerkopf R., Clement R.M., Dudley E., Freitag C.M., Rosler M., Retz W., Thome J. Am. J. Med. Genet. B Neuropsychiatr. Genet. 147B:1476-1480(2008) · Mapped (16) |
| Pseudogene-derived small interfering RNAs regulate gene expression in mouse oocytes. Tam O.H., Aravin A.A., Stein P., Girard A., Murchison E.P., Cheloufi S., Hodges E., Anger M., Sachidanandam R., Schultz R.M. et al. Nature 453:534-538(2008) · Mapped (7) |
| Sorting of small RNAs into Arabidopsis argonaute complexes is directed by the 5' terminal nucleotide. Mi S., Cai T., Hu Y., Chen Y., Hodges E., Ni F., Wu L., Li S., Zhou H., Long C. et al. Cell 133:116-127(2008) · UniProtKB (4) |
| A single Hox locus in Drosophila produces functional microRNAs from opposite DNA strands. Stark A., Bushati N., Jan C.H., Kheradpour P., Hodges E., Brennecke J., Bartel D.P., Cohen S.M., Kellis M. Genes Dev. 22:8-13(2008) · Mapped (13) |
| Discovery of functional elements in 12 Drosophila genomes using evolutionary signatures. Stark A., Lin M.F., Kheradpour P., Pedersen J.S., Parts L., Carlson J.W., Crosby M.A., Rasmussen M.D., Roy S., Deoras A.N. et al. Nature 450:219-232(2007) · Mapped (67) |
| Systematic discovery and characterization of fly microRNAs using 12 Drosophila genomes. Stark A., Kheradpour P., Parts L., Brennecke J., Hodges E., Hannon G.J., Kellis M. Genome Res. 17:1865-1879(2007) · Mapped (48) |
| Recurrent finding of the FIP1L1-PDGFRA fusion gene in eosinophilia-associated acute myeloid leukemia and lymphoblastic T-cell lymphoma. Metzgeroth G., Walz C., Score J., Siebert R., Schnittger S., Haferlach C., Popp H., Haferlach T., Erben P., Mix J. et al. Leukemia 21:1183-1188(2007) · Mapped (4) |
| NovelFam3000 -- uncharacterized human protein domains conserved across model organisms. Kemmer D., Podowski R.M., Arenillas D., Lim J., Hodges E., Roth P., Sonnhammer E.L.L., Hoeoeg C., Wasserman W.W. BMC Genomics 7:48-48(2006) · UniProtKB (15) |
| A combined approach exploring gene function based on worm-human orthology. Tamas I., Hodges E., Dessi P., Johnsen R., Vaz Gomes A. BMC Genomics 6:65-65(2005) · Mapped (1) |